#Dyslipidemia Therapeutics Market Size
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vijukumar · 1 year ago
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Navigating the Cardiovascular Landscape: Trends, Technologies, and Transformations
The cardiovascular field stands at the forefront of medical innovation, with dynamic growth in various sectors, including cardiovascular devices, drugs, diagnostics, and safety services. In this blog, we will explore the multifaceted landscape of the cardiovascular market, uncovering market trends, major players, and the pivotal role of technological advancements in reshaping cardiovascular healthcare.
Cardiovascular Devices Market: A Dynamic Frontier
Market Size and Demand:
The global cardiovascular devices market is undergoing significant expansion, with a projected valuation of USD 65.4 billion by 2025. This growth is propelled by a surge in demand for cutting-edge technologies aimed at addressing cardiovascular diseases, which remain a leading cause of morbidity and mortality worldwide.
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Innovation Driving Market Dynamics:
Innovative cardiovascular devices, such as implantable cardioverter-defibrillators (ICDs), transcatheter heart valves, and wearable cardiac monitors, are redefining the landscape. The demand for these advanced technologies underscores the industry's commitment to providing more efficient and patient-friendly solutions.
Cardiovascular Drugs Market: A Pillar of Therapeutic Advancements
Market Size and Major Players:
The cardiovascular drugs market, valued at USD 83.95 billion in 2020, is anticipated to witness a compound annual growth rate (CAGR) of 4.3% from 2021 to 2028. Key players, including Pfizer, Novartis, and AstraZeneca, continue to drive innovation in pharmaceutical interventions for cardiovascular diseases, contributing significantly to market growth.
Focus on Cardiovascular Disease Drugs:
With an increasing prevalence of cardiovascular diseases, there is a growing focus on the development of drugs targeting specific cardiovascular conditions. This includes medications addressing hypertension, dyslipidemia, and heart failure, among others.
Cardiovascular Diagnostic Devices Market: Precision in Diagnosis
Market Research Reports and Industry Trends:
The cardiovascular diagnostic devices market is evolving rapidly, with a projected CAGR of 5.4% from 2021 to 2026. Comprehensive industry research reports highlight emerging trends such as the integration of artificial intelligence (AI) in diagnostic tools, offering precision and efficiency in cardiovascular disease diagnosis.
Cardiac Safety Services Market: Ensuring Patient Well-being
Ensuring Safety in Cardiovascular Therapies:
Cardiac safety services have become integral to the development and monitoring of cardiovascular drugs. These services play a crucial role in assessing and managing potential cardiac risks associated with pharmaceutical interventions, ensuring patient safety throughout the drug development process.
Cardiovascular Surgery Market: Advancing Surgical Interventions
Technological Innovations in Surgery:
The cardiovascular surgery market is witnessing transformative advancements, with minimally invasive procedures, robotic-assisted surgeries, and innovative surgical devices leading the way. These developments aim to enhance patient outcomes, reduce recovery times, and improve overall surgical experiences.
Conclusion: Navigating the Future of Cardiovascular Health
In conclusion, the cardiovascular landscape is undergoing a paradigm shift fueled by technological innovations, dynamic market trends, and the tireless efforts of industry leaders. As cardiovascular devices, drugs, and diagnostics continue to evolve, the collective goal remains clear – to improve patient outcomes, enhance diagnostic precision, and reduce the global burden of cardiovascular diseases. The collaborative efforts of major players, coupled with ongoing research and development, promise a future where cardiovascular health is at the forefront of medical progress.
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aditi-us · 6 years ago
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Global Dyslipidemia Therapeutics Market Size, Trends, Share, Key Player & Forecast until 2023
A Comprehensive research study conducted by KD Market Insights on " Dyslipidemia Therapeutics Market – By Product Type (Low-density Lipoproteins (LDL), Triglycerides), By Drug Class (Statins, Non-Statins, Combinations Drugs), By Distribution Channel (Hospitals Pharmacies, Drug Stores, Retail Stores, Mail Order Pharmacies) & Global Market Size, Trends, Share & Forecast 2018-2023" report offers extensive and highly detailed historical, current and future market trends in the global and regional/market. The Dyslipidemia Therapeutics Market report includes market size, growth drivers, barriers, opportunities, trends and other information which helps to find new opportunities in this market for the growth of the business through new technologies and developments. Global Dyslipidemia Therapeutics market witnessed a market value of USD XX Million in 2017 and is estimated to reach USD XX million in 2023, registering a compound annual growth rate (CAGR) of XX% between 2017 and 2023. The market research report demonstrates market dynamics which includes growth drivers, restraining factors and opportunities and trends spearheading current nature and future status of this market. Our general approach is to target several individuals with specific questions that we believed would satisfy our research objective. Further, to speed up the data collection process, we employed an online survey, delivered via email. The research team analyzed the results to identify potential opportunities and risks for the market. Request for Sample @ https://www.kdmarketinsights.com/sample/3070 In addition, the report offers recent industry activities and value chain analysis for the Dyslipidemia Therapeutics Market. Moreover, Porter’s Five Forces analysis demonstrates the five forces which include buyers bargaining power, suppliers bargaining power, the threat of new entrants, the threat of substitutes, and degree of competition in Dyslipidemia Therapeutics Market. Along with figures and tables, a market attractiveness and BPS analysis has been provided for every segment in the report. The report analyses the market by geographies i.e. North America, Europe, Asia Pacific, Latin America & Middle East & Africa. Further, the geographies are fragmented into the country and regional groupings: - North America (U.S. & Canada) - Europe (Germany, United Kingdom, France, Italy, Spain, Russia and Rest of Europe) - Asia Pacific (China, India, Japan, South Korea, Indonesia, Taiwan, Australia, New Zealand and Rest of Asia Pacific) - Latin America (Brazil, Mexico, Argentina and Rest of Latin America) - Middle East & Africa (GCC, North Africa, South Africa and Rest of Middle East & Africa) Segmentation The research offers a comprehensive analysis of global Dyslipidemia Therapeutics market with respect to following sub-markets: Based on Product Type: - Low-density Lipoproteins (LDL) - Triglycerides Based on Drug Class: - Statins - Non-Statins - - - PCSK9 inhibitors - - - Cholesterol absorption inhibitors - - - Bile Acid resins - - - Fibrate - - - Others - Combinations Drugs Based on Distribution Channel: - Hospitals Pharmacies - Drug Stores - Retail Stores - Mail Order Pharmacies Competitive Landscape The report includes profiles of leading companies in the global Dyslipidemia Therapeutics market. Some of the key players profiled include: - AstraZeneca - Kowa Pharmaceuticals America, Inc - Merck & Co - Pfizer - Amgen - Sanofi - Novelion Therapeutics - Mylan - Abbott Laboratories - Novartis AG - Other Major & Niche Key Players Browse Full Report with TOC @ https://www.kdmarketinsights.com/product/dyslipidemia-therapeutics-market Table of Contents: Research Methodology Market Definition and List of Abbreviations 1. Executive Summary 2. Growth Drivers & Issues in Global Dyslipidemia Therapeutics Market 3. Global Dyslipidemia Therapeutics Market Trends 4. Opportunities in Global Dyslipidemia Therapeutics Market 5. Recent Industry Activities, 2017 6. Porter's Five Forces Analysis 7. Market Value Chain and Supply Chain Analysis 8. Global Dyslipidemia Therapeutics Market Size (USD Million), Forecast & Y-o-Y Growth Analysis, 2017-2023 9. Global Dyslipidemia Therapeutics Market Segmentation Analysis, By Product Type 9.1. Introduction 9.2. Market Attractiveness, By Product Type 9.3. BPS Analysis, By Product Type 9.4. Low-density Lipoproteins (LDL) Market Size (USD Million), Forecast & Y-o-Y Growth Analysis, 2017-2023 9.5. Triglycerides Market Size (USD Million), Forecast & Y-o-Y Growth Analysis, 2017-2023 10. Global Dyslipidemia Therapeutics Market Segmentation Analysis, By Drug Class 10.1. Introduction 10.2. Market Attractiveness, By Drug Class 10.3. BPS Analysis, By Drug Class 10.4. Statins Market Size (USD Million), Forecast & Y-o-Y Growth Analysis, 2017-2023 10.5. Non-Statins Market Size (USD Million), Forecast & Y-o-Y Growth Analysis, 2017-2023 10.5.1. PCSK9 inhibitors Market Size (USD Million), Forecast & Y-o-Y Growth Analysis, 2017-2023 10.5.2. Cholesterol absorption inhibitors Market Size (USD Million), Forecast & Y-o-Y Growth Analysis, 2017-2023 10.5.3. Bile Acid resins Market Size (USD Million), Forecast & Y-o-Y Growth Analysis, 2017-2023 10.5.4. Fibrate Market Size (USD Million), Forecast & Y-o-Y Growth Analysis, 2017-2023 10.5.5. Others Market Size (USD Million), Forecast & Y-o-Y Growth Analysis, 2017-2023 10.6. Combinations Drugs Market Size (USD Million), Forecast & Y-o-Y Growth Analysis, 2017-2023 11. Global Dyslipidemia Therapeutics Market Segmentation Analysis, By Distribution Channel 11.1. Introduction 11.2. Market Attractiveness, By Distribution Channel 11.3. BPS Analysis, By Distribution Channel 11.4. Hospitals Pharmacies Market Size (USD Million), Forecast & Y-o-Y Growth Analysis, 2017-2023 11.5. Drug Stores Market Size (USD Million), Forecast & Y-o-Y Growth Analysis, 2017-2023 11.6. Retail Stores Market Size (USD Million), Forecast & Y-o-Y Growth Analysis, 2017-2023 11.7. Mail Order Pharmacies Market Size (USD Million), Forecast & Y-o-Y Growth Analysis, 2017-2023 Continue… Check for Discount @ https://www.kdmarketinsights.com/discount/3070 About Us: KD Market Insights offers a comprehensive database of syndicated research studies, customized reports, and consulting services. These reports are created to help in making smart, instant and crucial decisions based on extensive and in-depth quantitative information, supported by extensive analysis and industry insights. Our dedicated in-house team ensures the reports satisfy the requirement of the client. We aim at providing value service to our clients. Our reports are backed by extensive industry coverage and is made sure to give importance to the specific needs of our clients. The main idea is to enable our clients to make an informed decision, by keeping them and ourselves up to date with the latest trends in the market. Contact Us: KD Market Insights 150 State Street, Albany, New York, USA 12207 +1 (518) 300-1215 Email: [email protected] Website: www.kdmarketinsights.com
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sophiajhon-blog · 6 years ago
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Global Dyslipidemia Therapeutics Market Size, Share, News, Trend, Demand, Opportunity by the end of 2023
A recent report by KD market insights titled as " Dyslipidemia Therapeutics Market – By Product Type (Low-density Lipoproteins (LDL), Triglycerides), By Drug Class (Statins, Non-Statins, Combinations Drugs), By Distribution Channel (Hospitals Pharmacies, Drug Stores, Retail Stores, Mail Order Pharmacies) & Global Market Size, Trends, Share & Forecast 2018-2023" provides the key trends, opportunities and challenges market will face in the forecasted period of 6 years i.e. 2019-2023. The study also provides the Dyslipidemia Therapeutics Market. competitors share and region wise analysis around the globe. Global Dyslipidemia Therapeutics market witnessed a market value of USD XX Million in 2017 and is estimated to reach USD XX million in 2023, registering a compound annual growth rate (CAGR) of XX% between 2017 and 2023. The market research report demonstrates market dynamics which includes growth drivers, restraining factors and opportunities and trends spearheading current nature and future status of this market. Our general approach is to target several individuals with specific questions that we believed would satisfy our research objective. Further, to speed up the data collection process, we employed an online survey, delivered via email. The research team analyzed the results to identify potential opportunities and risks for the market. Request for Sample @ https://www.kdmarketinsights.com/sample/3070 The report begins with an overview for Dyslipidemia Therapeutics Market. The research report broadly covers analysis of key market drivers, challenges, opportunities and trends. The study also provides separate analysis to understand market size, projections and macroeconomic indicators of global regions that affects the market share. The report also offers an extensive coverage of various industry players along with their recent product launches and market activities. The report also goes through porter’s five analyses for getting a better understanding about the forces that shape competition within the industry. There is a timeline considered for useful analysis i.e. 2017 is considered as base year, 2018 as estimated year and 2019-2023 as forecasted year. The market is divided into various segments and further sub-segments to drive the useful insights that can be utilized for company revenue growth and business. The Dyslipidemia Therapeutics Market is segmented on the basis of - Based on Product Type: - Low-density Lipoproteins (LDL) - Triglycerides Based on Drug Class: - Statins - Non-Statins - - - PCSK9 inhibitors - - - Cholesterol absorption inhibitors - - - Bile Acid resins - - - Fibrate - - - Others - Combinations Drugs Based on Distribution Channel: - Hospitals Pharmacies - Drug Stores - Retail Stores - Mail Order Pharmacies The research also does a separate geographical analysis that comprises both the region wise and country wise analysis. The geography covered in the report is North America (U.S. & Canada), Europe (Germany, United Kingdom, France, Italy, Spain, Russia and Rest of Europe) , Asia Pacific (China, India, Japan, South Korea, Indonesia, Taiwan, Australia, New Zealand and Rest of Asia Pacific) Latin America (Brazil, Mexico, Argentina and Rest of Latin America) and Middle East & Africa (GCC, North Africa, South Africa and Rest of Middle East & Africa). As per the report, Asia Pacific is likely to be the market giant in the upcoming years. Considering the competition, the major vendors providing Dyslipidemia Therapeutics Market across the globe are - - AstraZeneca - Kowa Pharmaceuticals America, Inc - Merck & Co - Pfizer - Amgen - Sanofi - Novelion Therapeutics - Mylan - Abbott Laboratories - Novartis AG - Other Major & Niche Key Players These vendors have adopted various types of organic and inorganic growth strategies, such as new product launches, business expansions, partnerships and collaborations, and mergers and acquisitions, to expand their offerings and further expand their presence in the Dyslipidemia Therapeutics Market. Browse Full Report With TOC@ https://www.kdmarketinsights.com/product/dyslipidemia-therapeutics-market Table of Content Research Methodology Market Definition and List of Abbreviations 1. Executive Summary 2. Growth Drivers & Issues in Global Dyslipidemia Therapeutics Market 3. Global Dyslipidemia Therapeutics Market Trends 4. Opportunities in Global Dyslipidemia Therapeutics Market 5. Recent Industry Activities, 2017 6. Porter's Five Forces Analysis 7. Market Value Chain and Supply Chain Analysis 8. Global Dyslipidemia Therapeutics Market Size (USD Million), Forecast & Y-o-Y Growth Analysis, 2017-2023 9. Global Dyslipidemia Therapeutics Market Segmentation Analysis, By Product Type 9.1. Introduction 9.2. Market Attractiveness, By Product Type 9.3. BPS Analysis, By Product Type 9.4. Low-density Lipoproteins (LDL) Market Size (USD Million), Forecast & Y-o-Y Growth Analysis, 2017-2023 9.5. Triglycerides Market Size (USD Million), Forecast & Y-o-Y Growth Analysis, 2017-2023 10. Global Dyslipidemia Therapeutics Market Segmentation Analysis, By Drug Class 10.1. Introduction 10.2. Market Attractiveness, By Drug Class 10.3. BPS Analysis, By Drug Class 10.4. Statins Market Size (USD Million), Forecast & Y-o-Y Growth Analysis, 2017-2023 10.5. Non-Statins Market Size (USD Million), Forecast & Y-o-Y Growth Analysis, 2017-2023 10.5.1. PCSK9 inhibitors Market Size (USD Million), Forecast & Y-o-Y Growth Analysis, 2017-2023 10.5.2. Cholesterol absorption inhibitors Market Size (USD Million), Forecast & Y-o-Y Growth Analysis, 2017-2023 10.5.3. Bile Acid resins Market Size (USD Million), Forecast & Y-o-Y Growth Analysis, 2017-2023 10.5.4. Fibrate Market Size (USD Million), Forecast & Y-o-Y Growth Analysis, 2017-2023 10.5.5. Others Market Size (USD Million), Forecast & Y-o-Y Growth Analysis, 2017-2023 10.6. Combinations Drugs Market Size (USD Million), Forecast & Y-o-Y Growth Analysis, 2017-2023 11. Global Dyslipidemia Therapeutics Market Segmentation Analysis, By Distribution Channel 11.1. Introduction 11.2. Market Attractiveness, By Distribution Channel 11.3. BPS Analysis, By Distribution Channel 11.4. Hospitals Pharmacies Market Size (USD Million), Forecast & Y-o-Y Growth Analysis, 2017-2023 11.5. Drug Stores Market Size (USD Million), Forecast & Y-o-Y Growth Analysis, 2017-2023 11.6. Retail Stores Market Size (USD Million), Forecast & Y-o-Y Growth Analysis, 2017-2023 11.7. Mail Order Pharmacies Market Size (USD Million), Forecast & Y-o-Y Growth Analysis, 2017-2023 12. Geographical Analysis 12.1. Introduction 12.2. North America Dyslipidemia Therapeutics Market Size (USD Million), Forecast & Y-o-Y Growth Analysis, 2017-2023 12.2.1. By Product Type 12.2.2. By Drug Class 12.2.3. By Distribution Channel 12.2.4. By Country 12.2.4.1. Market Attractiveness, By End-user 12.2.4.2. BPS Analysis, By End-User 12.2.4.3. U.S. Market Size (USD Million), Forecast & Y-o-Y Growth Analysis, 2017-2023 12.2.4.4. Canada Market Size (USD Million), Forecast & Y-o-Y Growth Analysis, 2017-2023 12.3. Europe Dyslipidemia Therapeutics Market Size (USD Million), Forecast & Y-o-Y Growth Analysis, 2017-2023 12.3.1. By Product Type 12.3.2. By Drug Class 12.3.3. By Distribution Channel 12.3.4. By Country 12.3.4.1. Market Attractiveness, By Country 12.3.4.2. BPS Analysis, By Country 12.3.4.3. Germany Market Size (USD Million), Forecast & Y-o-Y Growth Analysis, 2017-2023 12.3.4.4. United Kingdom Market Size (USD Million), Forecast & Y-o-Y Growth Analysis, 2017-2023 12.3.4.5. France Market Size (USD Million), Forecast & Y-o-Y Growth Analysis, 2017-2023 12.3.4.6. Italy Market Size (USD Million), Forecast & Y-o-Y Growth Analysis, 2017-2023 Continue.... Check for Discount @ https://www.kdmarketinsights.com/discount/3070 About KD Market Insights KD Market Insights has come with the idea of helping business by intelligent decision making and thorough understanding of the industry. We offer a comprehensive database of syndicated research, customized reports as well as consulting services to help a business grow in their respective domain. At KD Market Insights, we offer our client a deep Market research reports accompanied by business consulting services that can help them to reach on top of the corporate world. Our customized reports are built by keeping all factors of the industry in mind. Contact Us 150 State Street, 3rd Floor, Albany, New York United States (12207) Telephone: +1-518-300-1215 Email: - [email protected] Website: - www.kdmarketinsights.com
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healthcaremrr · 2 years ago
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globalaircraftgalley · 2 years ago
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Cardiometabolic Diseases Market Competitive Strategies, Advertising Trends, & Market Analysis by 2028
The Cardiometabolic Diseases Market is grow at a rate of 5.90% CAGR in the forecast period of 2021 to 2028.  DBMR Research Report provide analysis & insight regarding various factor expected to be prevalent throughout the forecast period while providing their impacts on the market’s growth.
Cardiometabolic illnesses are a group of metabolic conditions that raise the risk of individuals developing cardiovascular disease. Hypertension, central obesity, insulin resistance, dyslipidemia and glucose tolerance are some of these conditions. Patients are more likely to suffer from stroke, diabetes, or various types of heart disease as a result of these illnesses.
High consumption of fast food due to changing lifestyle which will result in higher rate of obesity and rising usage of biomarkers for diagnostic and risk assessment procedures are the driving factors which will influence the market growth rate. Furthermore, growing number of patients adopting pharmaceuticals and therapeutics owing to the proliferation of digital modes of drug delivery and innovations as well as advancements in technologies used for the drug delivery in healthcare industry are the factors that will expand the cardiometabolic diseases market. Also, increase in the proliferation of AI technology in the healthcare industry resulting in improved support services to the industry will act as a market driver and accelerate the growth rate.
Rise in the research and development activities and emerging markets will provide beneficial opportunities for the cardiometabolic diseases market in the forecast period of 2021-2028.
Cardiometabolic Diseases Market Insight
This Cardiometabolic Diseases market report provides details of new recent developments, trade regulations, import export analysis, production analysis, value chain optimization, market share, impact of domestic and localized market players, analyses opportunities in terms of emerging revenue pockets, changes in market regulations, strategic market growth analysis, market size, category market growths, application niches and dominance, product approvals, product launches, geographic expansions, technological innovations in the market. To gain more info Cardiometabolic Diseases market contact Data Bridge Market Research for an Analyst Brief, our team will help you take an informed market decision to achieve market growth. 
Cardiometabolic Diseases Trends Segmentation
It is fragmented on the basis of -
Type
chronic/congestive heart failure,  hypertension, type 2 diabetes, and obesity.
Treatment
ACE inhibitors, diuretics, glucophage,  liposuction and others.
End user
clinic, hospital and others.
 Request Access for Cardiometabolic Diseases Market Sample Report: https://www.databridgemarketresearch.com/request-a-sample/?dbmr=global-cardiometabolic-diseases-market
Cardiometabolic Diseases Industry Country Level Analysis
The countries covered in the global Cardiometabolic Diseases market report are the U.S., Canada and Mexico in North America, Brazil, Argentina and Rest of South America as part of South America, Germany, Italy, U.K., France, Spain, Netherlands, Belgium, Switzerland, Turkey, Russia, Rest of Europe in Europe, Japan, China, India, South Korea, Australia, Singapore, Malaysia, Thailand, Indonesia, Philippines, Rest of Asia-Pacific (APAC)  in the Asia-Pacific (APAC), Saudi Arabia, U.A.E, South Africa, Egypt, Israel, Rest of Middle East and Africa (MEA) as a part of Middle East and Africa (MEA).  
Cardiometabolic Diseases Industry Share Analysis
·         The major players covered in the Cardiometabolic Diseases market report are
·         Alnylam Pharmaceuticals, Inc.;
·         Arrowhead Pharmaceuticals, Inc.;
·         Dicerna Pharmaceuticals, Inc.;
·         Cardax, Inc.;
·         Novartis AG;
·         Novo Nordisk A/S;
·         Boehringer Ingelheim International GmbH;
·         Kowa Company, Ltd.
 Access Full Report:- https://www.databridgemarketresearch.com/reports/global-cardiometabolic-diseases-market
 Major TOC of the Cardiometabolic Diseases Report
Chapter One:
Chapter Two:
 Get TOC of the Report: https://www.databridgemarketresearch.com/toc/?dbmr=global-cardiometabolic-diseases-market
About Us:
Data Bridge Market Research set forth itself as an unconventional and neoteric Market research and consulting firm with unparalleled level of resilience and integrated approaches. We are determined to unearth the best market opportunities and foster efficient information for your business to thrive in the market
Contact:
Data Bridge Market Research
Tel: +1-888-387-2818
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globalaircraft · 3 years ago
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Cardiometabolic Diseases Market Business Opportunities in 2022
The Alkylamines Market is grow at a rate of 5.90% CAGR in the forecast period of 2021 to 2028. DBMR Research Report provide analysis & insight regarding various factor expected to be prevalent throughout the forecast period while providing their impacts on the market’s growth.
Cardiometabolic illnesses are a group of metabolic conditions that raise the risk of individuals developing cardiovascular disease. Hypertension, central obesity, insulin resistance, dyslipidemia and glucose tolerance are some of these conditions. Patients are more likely to suffer from stroke, diabetes, or various types of heart disease as a result of these illnesses.
High consumption of fast food due to changing lifestyle which will result in higher rate of obesity and rising usage of biomarkers for diagnostic and risk assessment procedures are the driving factors which will influence the market growth rate. Furthermore, growing number of patients adopting pharmaceuticals and therapeutics owing to the proliferation of digital modes of drug delivery and innovations as well as advancements in technologies used for the drug delivery in healthcare industry are the factors that will expand the cardiometabolic diseases market. Also, increase in the proliferation of AI technology in the healthcare industry resulting in improved support services to the industry will act as a market driver and accelerate the growth rate.
Rise in the research and development activities and emerging markets will provide beneficial opportunities for the cardiometabolic diseases market in the forecast period of 2021-2028.
📷
Cardiometabolic Diseases Market Insight
This Cardiometabolic Diseases market report provides details of new recent developments, trade regulations, import export analysis, production analysis, value chain optimization, market share, impact of domestic and localized market players, analyses opportunities in terms of emerging revenue pockets, changes in market regulations, strategic market growth analysis, market size, category market growths, application niches and dominance, product approvals, product launches, geographic expansions, technological innovations in the market. To gain more info Cardiometabolic Diseases market contact Data Bridge Market Research for an Analyst Brief, our team will help you take an informed market decision to achieve market growth.
Cardiometabolic Diseases Trends Segmentation
It is fragmented on the basis of-
Type
chronic/congestive heart failure, hypertension, type 2 diabetes, and obesity.
Treatment
ACE inhibitors, diuretics, glucophage, liposuction and others.
End user
clinic, hospital and others.
Request Access for Cardiometabolic Diseases Market Sample Report: https://www.databridgemarketresearch.com/request-a-sample/?dbmr=global-cardiometabolic-diseases-market
Cardiometabolic Diseases Industry Country Level Analysis
The countries covered in the global Cardiometabolic Diseases market report are the U.S., Canada and Mexico in North America, Brazil, Argentina and Rest of South America as part of South America, Germany, Italy, U.K., France, Spain, Netherlands, Belgium, Switzerland, Turkey, Russia, Rest of Europe in Europe, Japan, China, India, South Korea, Australia, Singapore, Malaysia, Thailand, Indonesia, Philippines, Rest of Asia-Pacific (APAC) in the Asia-Pacific (APAC), Saudi Arabia, U.A.E, South Africa, Egypt, Israel, Rest of Middle East and Africa (MEA) as a part of Middle East and Africa (MEA).
Cardiometabolic Diseases Industry Share Analysis
The major players covered in the Cardiometabolic Diseases market report are
Alnylam Pharmaceuticals, Inc.;
Arrowhead Pharmaceuticals, Inc.;
Dicerna Pharmaceuticals, Inc.;
Cardax, Inc.;
Novartis AG;
Novo Nordisk A/S;
Boehringer Ingelheim International GmbH;
Kowa Company, Ltd.
Access Full Report:- https://www.databridgemarketresearch.com/reports/global-cardiometabolic-diseases-market
Major TOC of the Cardiometabolic Diseases Report
Chapter One:
Chapter Two:
Get TOC of the Report: https://www.databridgemarketresearch.com/toc/?dbmr=global-cardiometabolic-diseases-market
About Us:
Data Bridge Market Research set forth itself as an unconventional and neoteric Market research and consulting firm with unparalleled level of resilience and integrated approaches. We are determined to unearth the best market opportunities and foster efficient information for your business to thrive in the market
Contact:
Data Bridge Market Research
Tel: +1-888-387-2818
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pavanghage · 4 years ago
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Dyslipidemia Drugs Market 2021 Global Industry Analysis by Trends, Size, Share, Company Overview, Growth and Forecast by 2027
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Dyslipidemia Drugs Market is analyzed with industry experts in mind to maximize return on investment by providing clear information needed for informed business decisions. This research will help both established and new entrants to identify and analyze market needs, market size and competition. It explains the supply and demand situation, the competitive scenario, and the challenges for market growth, market opportunities and the threats faced by key players.
Sample Copy of This Report:https://axelreports.com/request-sample/61500
A 360 degree outline of the competitive scenario of the Global Dyslipidemia Drugs Market is presented by Axel Reports Market Insights. It has a massive data allied to the recent product and technological developments in the markets.
It has a wide-ranging analysis of the impact of these advancements on the market’s future growth, wide-ranging analysis of these extensions on the market’s future growth. The research report studies the market in a detailed manner by explaining the key facets of the market that are foreseeable to have a countable stimulus on its developing extrapolations over the forecast period.
Reasons for buying this report:
It offers an analysis of changing competitive scenario.
For making informed decisions in the businesses, it offers analytical data with strategic planning methodologies.
It offers seven-year assessment of Global Dyslipidemia Drugs
It helps in understanding the major key product segments.
Researchers throw light on the dynamics of the market such as drivers, restraints, trends, and opportunities.
It offers regional analysis of Global Dyslipidemia Drugs Market along with business profiles of several stakeholders.
It offers massive data about trending factors that will influence the progress of the Global Dyslipidemia Drugs
Get ToC for the overview of the premium report @ https://axelreports.com/industry-analysis/2021-2027-global-and-regional-dyslipidem/61500
By Market Players: AstraZeneca Bristol-Myers Squibb Sanofi Merck Amgen Pfizer Cerenis Amarin Corporation Alnylam Pharmaceuticals Catabasis Pharmaceuticals Daiichi Sankyo GlaxoSmithKline Cipla Kadmon Pharmaceuticals Eli Lilly Daewoong Pharmaceutical CJ HealthCare JW Pharmaceuticals Esperion Therapeutics CKD Bio Lupin Pharmaceuticals By Type Statins Cholesterol absorption inhibitors Dyslipidemia injectable By Application Hospitals and Clinics Medical Laboratories Drug Stores Others
A detailed outline of the Global Dyslipidemia Drugs Market includes a comprehensive analysis of different verticals of businesses. North America, Latin America, Asia-Pacific, Africa, and Europe have been considered for the studies on the basis of several terminologies.
This is anticipated to drive the Global Dyslipidemia Drugs Market over the forecast period. This research report covers the market landscape and its progress prospects in the near future. After studying key companies, the report focuses on the new entrants contributing to the growth of the market. Most companies in the Global Dyslipidemia Drugs Market are currently adopting new technological trends in the market.
Finally, the researchers throw light on different ways to discover the strengths, weaknesses, opportunities, and threats affecting the growth of the Global Dyslipidemia Drugs Market. The feasibility of the new report is also measured in this research report.
Make an Enquiry for purchasing this Report :https://axelreports.com/enquiry-before-buying/61500
Table of Contents:
Global Dyslipidemia Drugs Market Overview
Economic Impact on Industry
Market Competition by Manufacturers
Production, Revenue (Value) by Region
Production, Revenue (Value), Price Trend by Type
Market Analysis by Application
Cost Analysis
Industrial Chain, Sourcing Strategy and Downstream Buyers
Marketing Strategy Analysis, Distributors/Traders
Market Effect Factors Analysis
Global Dyslipidemia Drugs Market Forecast
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pratikwadekar2 · 5 years ago
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Dyslipidemia Market Strategic Insights and key Business Influencing Factors | Major Players – Alnylam Pharmaceuticals, Amarin Corporation,  Amgen, Bristol-Myers Squibb, Catabasis Pharmaceuticals.
Dyslipidemia Market is a condition in which the levels of lipids (cholesterol, triglycerides, or both) or low high-density lipoprotein (HDL) cholesterol level elevated due to multiple reasons including lifestyle, genetics-disorders, drugs etc. According to World Health Organization, there were approximately 17.9 million people in 2016, who died from cardiovascular diseases, almost more than half of these cases could have been avoided with the availability of proper medical treatment. This significant number is expected to act as a driver to the market growth.
Global Dyslipidemia is expected to rise gradually to an estimated value of USD 27.52 billion by 2026, registering a CAGR of 10.50% in the forecast period of 2019-2026 with the annual sales of USD 12.38 billion in the year of 2018. This rise in market value can be attributed to the increase in prevalence and awareness along with concerns regarding the health of patients.
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https://www.databridgemarketresearch.com/request-a-sample/?dbmr=global-dyslipidemia-market
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Competitive Analysis: Global Dyslipidemia Market
Few of the major competitors currently working in Global Dyslipidemia Market are AstraZeneca (UK), Merck, Pfizer, Sanofi, Alnylam Pharmaceuticals, Amarin Corporation,  Amgen, Bristol-Myers Squibb, Catabasis Pharmaceuticals, Cerenis, Cipla Inc., CJ HealthCare, CKD Bio, Daewoong Pharmaceutical, Daiichi Sankyo, Eli Lilly, Esperion Therapeutics, GlaxoSmithKline, JW Pharmaceuticals, Kadmon Pharmaceuticals, Lupin Pharmaceuticals and few among others.
 Key Pointers Covered in the Global Dyslipidemia Market Trends and Forecast to 2026
Global   Dyslipidemia Market New Sales Volumes
Global   Dyslipidemia  Market Replacement Sales Volumes
Global   Dyslipidemia Market Installed Base
Global   Dyslipidemia Market By Brands
Global   Dyslipidemia Market Size
Global   Dyslipidemia  Market Procedure Volumes
Global   Dyslipidemia Market Product Price Analysis
Global   Dyslipidemia Market Healthcare Outcomes
Global   Dyslipidemia Market Cost of Care Analysis
Global   Dyslipidemia Market Regulatory Framework and Changes
Global   Dyslipidemia Market Prices and Reimbursement Analysis
Global   Dyslipidemia Market Shares in Different Regions
Recent Developments for Global   Dyslipidemia Market Competitors
Global   Dyslipidemia Market Upcoming Applications
Global   Dyslipidemia Market Innovators Study
Get Detailed TOC:
https://www.databridgemarketresearch.com/toc/?dbmr=global-dyslipidemia-market
Key Developments in the Market:
In the year 2018, Sanofi and Regeneron Pharmaceuticals, Inc. announced that Praluent (alirocumab) in phase 3 clinical trialdemonstrated the risk of major adverse cardiovascular events (MACE) in patients who had suffered a recent acute coronary syndrome (ACS) event such as a heart attack.
In the year 2018, Amgen Inc. announced the launch of Repatha (Evolocumab) in the US for the indication of heart attacks and stroke due to high cholesterol at a reduced price to gain more customers.
In the year 2015, WuXi PharmaTech announced its partnership with Eli Lilly to develop, manufacture, and commercializes in China a Lilly-discovered oral experimental drug for cardiovascular risk in patients with dyslipidemia.
Market Drivers
Increase in global geriatric population
Increase in prevalence of lifestyle diseases
Rise in acceptance of telemental health
Increase in availability of generic drugs
Market Restraints
Lack of R&D initiatives in this area.
patent expiry for some blockbuster drugs
Fewer Government initiatives taken in this direction.
 Inquire Before Buying:
https://www.databridgemarketresearch.com/inquire-before-buying/?dbmr=global-dyslipidemia-market
Key insights in the report:
Complete and distinct analysis of the market drivers and restraints
Key Market players involved in this industry
Detailed analysis of the Market Segmentation
Competitive analysis of the key players involved
About Us:
Data Bridge Market Research set forth itself as an unconventional and neoteric Market research and consulting firm with unparalleled level of resilience and integrated approaches. We are determined to unearth the best market opportunities and foster efficient information for your business to thrive in the market.
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Glomerular Disease Therapeutics Market
Asia Pacific Drug Delivery Devices Market
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thesittingduck · 4 years ago
Text
caduet tablets Uses, Dosage, Side Effects, Precautions & Warnings
Drug Online
caduet Generic drug of the Therapeutic class: Cardiology and angiology Active ingredients: Amlodipine , Atorvastatin
what is caduet medication?
This medication is supplied as blue, oval-shaped, film-coated tablets debossed with “Pfizer” on one side and “CDT 101” on the other side.
Boxes of 7, 10, 14, 20, 28, 30, 50, 56, 60, 90, 100 or 200 tablets.
Not all presentations may be marketed.
what is caduet medication used for and   indication?
CADUET is indicated for the prevention of cardiovascular events in hypertensive patients with 3 associated cardiovascular risk factors, with normal to moderately elevated cholesterol without established coronary artery disease, and in whom, according to current recommendations, the concomitant use of amlodipine and a low dose of atorvastatin is suitable .
CADUET should be used when the response to regimen and other non-pharmacological measures is inadequate.
caduet dosage
Oral route
The usual starting dose is 5 mg / 10 mg once daily.
If tighter blood pressure control is required, a dosage of 10 mg / 10 mg once daily may be administered.
The tablets can be taken at any time of the day, with or without food.
CADUET can be used alone or in combination with other antihypertensive drugs, but it must not be used in combination with other calcium channel blockers or another statin.
The combination of CADUET and fibrates should generally be avoided (see sections 4.4 and Interactions with other medicinal products and other forms of interaction ).
Patients with renal impairment : No dosage adjustment is necessary in patients with impaired renal function (see sections 4.4 and Pharmacokinetic properties ).
Patients with hepatic impairment : CADUET is contraindicated in patients with active hepatic disease.
Children / Adolescents : The safety and efficacy of CADUET have not been established in children / adolescents. Therefore, the use of CADUET is not recommended in this population.
Elderly : It does not appear necessary to adjust the dose in the elderly (see section Pharmacokinetic properties ).
Combination with other medicinal products : In combination with ciclosporin, the dose of atorvastatin should not exceed 10 mg (see section Interactions with other medicinal products and other forms of interaction ).
Contraindications
CADUET is contraindicated in patients:
Being hypersensitive to dihydropyridines *, to amlodipine, to atorvastatin or to any of the excipients of this medicine,
have active liver disease or a persistent and unexplained increase in serum transaminases exceeding 3 times the upper limit of normal,
In women who are pregnant, breastfeeding or of childbearing potential and not using reliable contraceptive methods (see section Pregnancy and breast-feeding ),
In combination with itraconazole, ketoconazole, telithromycin (see section Interactions with other medicinal products and other forms of interactions ),
having severe hypotension,
Having shock (including cardiogenic shock),
Having an obstruction of the efferent pathway to the left ventricle (for example severe aortic stenosis),
With haemodynamically unstable heart failure after acute myocardial infarction.
* amlodipine is a calcium channel blocker derived from dihydropyridine.
HOW TO TAKE CADUET?
Always take this medicine exactly as your doctor or pharmacist has told you. Check with your doctor or pharmacist if in doubt.
Adults
The recommended starting dose of CADUET is one 5 mg / 10 mg tablet per day. Your doctor may increase the dose if necessary to 1 tablet of CADUET 10 mg / 10 mg per day.
The tablets should be swallowed whole with a glass of water. They can be taken at any time of the day, with or without food. However, it is best to take them at the same time each day.
Continue to follow your doctor’s dietary advice, especially to eat a low fat diet, avoid tobacco, and exercise regularly.
If you have the impression that the effect of CADUET tablets is too strong or too weak, talk to your doctor or pharmacist.
Use in children and adolescents
This medication is not recommended for children and adolescents.
If you take more CADUET 10 mg / 10 mg film-coated tablets than you should
If you accidentally take too many CADUET tablets (more than your usual dose), ask your doctor or the nearest hospital for advice. Take any remaining tablets, the carton or the whole carton with you so that hospital staff can quickly identify which medicine you have taken.
If you forget to take CADUET 10 mg / 10 mg film-coated tablets
If you forget to take your dose of CADUET, take your next dose at the normal time.
Do not take a double dose to make up for the dose you forgot to take.
If you stop taking CADUET 10 mg / 10 mg film-coated tablets
Do not stop taking CADUET unless your doctor tells you to.
If you have any further questions on the use of this medicine or want to stop taking your treatment, ask your doctor or pharmacist for more information.
How To Store Caduet?
Keep this medication out of the sight and reach of children.
Do not use this medicine after the expiry date which is stated on the blister, the carton and the vial after “EXP”. The expiration date refers to the last day of that month.
Store at a temperature not exceeding 30 ° C.
Do not throw away any medicines via a wastewater treatment plant or with household waste. Ask your pharmacist how to throw away the medicines you no longer use. These measures will help protect the environment.
caduet side effects
The safety of CADUET has been evaluated in double-blind, placebo-controlled studies in 1092 patients treated for concomitant hypertension and dyslipidemia. During clinical trials with CADUET, no specific adverse events specific to this combination were observed.
Adverse events were limited to those previously reported for amlodipine and / or atorvastatin (see table of adverse events below).
In controlled clinical trials, discontinuation of treatment due to clinical adverse events or laboratory abnormalities was observed in 5.1% of patients treated with amlodipine and atorvastatin versus 4.0% of patients treated with amlodipine and atorvastatin. patients taking a placebo.
The adverse events below, listed according to MedDRA system organ classification and frequency order, relate to amlodipine and atorvastatin individually.
Very common: ³ 1/10, common: ³ 1/100 and <1/10, infrequent: ³ 1/1000 and <1/100, rare: ³ 1/10000 and <1/1000, very rare: < 1 / 10,000, frequency not known (cannot be estimated from the available data).
MedDRA
System organ classes
Side effects
Frequency
Amlodipine
Atorvastatin
Infections and infestations
Nasopharyngitis
Frequent
Blood and lymphatic system disorders
Leukopenia
Very rare
Thrombocytopenia
Very rare
Rare
Immune system disorders
hypersensitivity
Very rare
Frequent
Anaphylaxis
Very rare
Metabolism and nutrition disorders
Hyperglycemia *
Very rare
Frequent
Weight gain
Infrequent
Infrequent
Weightloss
Infrequent
Hypoglycemia
Infrequent
Anorexia
Infrequent
Psychiatric disorders
Insomnia
Infrequent
Infrequent
Mood disorders (including anxiety)
Infrequent
Nightmares
Infrequent
Depression
Infrequent
Frequency not known
Confusion
Rare
Disorders of the system nervous
Drowsiness
Frequent
Dizziness
Frequent
Infrequent
Headache (especially at the start of treatment)
Frequent
Frequent
Tremors
Infrequent
Hypoesthesias, paresthesias
Infrequent
Infrequent
Syncope
Infrequent
Hypertonia
Very rare
Peripheral neuropathy
Very rare
Rare
Amnesia
Infrequent
Dysgeusia
Infrequent
Infrequent
Extrapyramidal syndrome
Frequency not known
Eye disorders
Blurred vision
Infrequent
Visual disturbances (including diplopia)
Infrequent
Rare
Ear and labyrinth disease
Tinnitus
Infrequent
Infrequent
Hearing loss
Very rare
Cardiac disorders
Palpitations
Frequent
Angina pectoris
Rare
Myocardial infarction
Very rare
Arrhythmia (including bradycardia, ventricular tachycardia and atrial fibrillation)
Very rare
Vascular disorders
Flushing
Frequent
Hypotension
Infrequent
Vasculitis
Very rare
Respiratory, thoracic and mediastinal disorders
Pharyngolaryngeal pain
Frequent
Epistaxis
Frequent
Dyspnea
Infrequent
Rhinitis
Infrequent
Cough
Very rare
Interstitial lung disease, especially during long-term treatment
Frequency not known
Gastrointestinal disorders
Gingival hyperplasia
Very rare
Nausea
Frequent
Frequent
Upper and lower abdominal pain
Frequent
Infrequent
Vomiting
Infrequent
Infrequent
Dyspepsia
Infrequent
Frequent
Changes in intestinal transit (including diarrhea and constipation)
Infrequent
Dry mouth
Infrequent
Dysgeusia
Infrequent
Diarrhea, constipation, gas
Frequent
Gastritis
Very rare
Pancreatitis
Very rare
Infrequent
Eructation
Infrequent
Hepatobiliary disorders
Hepatitis
Very rare
Infrequent
Cholestasis
Rare
Jaundice
Very rare
Hepatic insufficiency
Very rare
Skin and subcutaneous tissue disorders
Bullous dermatosis including erythema multiforme
Very rare
Rare
Angioedema
Very rare
Erythema multiforme
Very rare
Alopecia
Infrequent
Infrequent
Purpura
Infrequent
Skin discoloration
Infrequent
Pruritus
Infrequent
Infrequent
Eruption
Infrequent
Infrequent
Hyperhidrosis
Infrequent
Exanthema
Infrequent
Urticaria
Very rare
Infrequent
Angioneurotic edema
Very rare
Rare
Exfoliative dermatitis
Very rare
Photosensitivity
Very rare
Stevens-Johnson syndrome
Very rare
Rare
Bullous erythroderma with epidermolysis
Rare
Musculoskeletal and connective tissue disorders
Swelling of the joints (including swelling of the ankles)
Frequent
Frequent
Arthralgia, myalgia
(see section Warnings and precautions for use )
Infrequent
Frequent
Muscle cramps, muscle spasms
Infrequent
Frequent
Back pain
Infrequent
Frequent
Neck pain
Infrequent
Pain in extremity
Frequent
Muscle fatigue
Infrequent
Myositis (see section Warnings and precautions for use )
Rare
Rhabdomyolysis, myopathy
(see section Warnings and precautions for use )
Rare
Tendinopathies, in rare cases tendon rupture
Rare
Immune-mediated necrotizing myopathy
Frequency not known
Kidney and urinary tract disorders
Urination disorder, nocturia, pollakiuria
Infrequent
Reproductive system and breast disorders
Incapacity
Infrequent
Infrequent
Gynecomastia
Infrequent
Very rare
General disorders and administration site conditions
Edema
Frequent
Infrequent
Peripheral edema
Infrequent
Tired
Frequent
Infrequent
Chest pain
Infrequent
Infrequent
Asthenia
Infrequent
Infrequent
Pain
Infrequent
Discomfort
Infrequent
Infrequent
Fever
Infrequent
Investigations
Increased liver enzymes: alanine aminotransferase, aspartate aminotransferase (mainly related to cholestasis)
Very rare
Frequent
Blood CK increased (see section 4.4 )
Frequent
Leukocyturia
Infrequent
* Diabetes: The frequency depends on the presence or absence of risk factors (fasting blood sugar ³ 5.6 mmol / l, BMI> 30 kg / m², increased triglyceride levels, history of high blood pressure).
caduet Interactions
Taking other medications
Tell your doctor or pharmacist if you are taking or have recently taken any other medicines, including medicines obtained without a prescription. Some medicines may interact with CADUET 10 mg / 10 mg film-coated tablets. This interaction may cause one or both of the medicines to be less effective, or on the contrary, this interaction may increase the risk or severity of side effects, including major muscle disorders known as rhabdomyolysis and myopathy (see section 4). .
Some medicines may interact with CADUET 10 mg / 10 mg film-coated tablets:
certain antibiotics such as rifampicin or certain “macrolide” antibiotics such as erythromycin, clarithromycin, telithromycin, fusidic acid or certain drugs used to treat infections caused by fungi such as ketoconazole, itraconazole,
medicines used to regulate lipid levels: fibrates, such as gemfibrozil or colestipol,
medicines used to regulate your heart rhythm, such as amiodarone, diltiazem and verapamil,
medicines used to treat or prevent seizures such as carbamazepine, phenobarbital, phenytoin, fosphenytoin, primidone,
medicines used to change how your immune system works, such as cyclosporin
protease inhibitors such as ritonavir, indinavir, nelfinavir used in the treatment of HIV,
medicines used to treat depression, such as nefazodone and imipramine,
medicines used to treat mental disorders, such as neuroleptics,
medicines used to treat heart failure, such as beta blockers
medicines used to treat high blood pressure, such as angiotensin II inhibitors, converting enzyme inhibitors, verapamil and diuretics,
alpha blockers used to treat high blood pressure or prostate problems
other medicines known to interact with CADUET 10 mg / 10 mg film-coated tablets such as ezetimibe (which lowers cholesterol), warfarin (which decreases blood clotting), oral contraceptives, stiripentol (an anticonvulsant used for treatment of epilepsy), cimetidine (used for heartburn and stomach ulcers), phenazone (a pain reliever), antacids (containing aluminum or magnesium, used to relieve problems stomach), and amifostine (used to treat cancer),
sildenafil (used in the treatment of erectile dysfunction, impotence),
dantrolene and baclofen (muscle relaxants),
steroids,
over-the-counter St. John’s Wort products.
CADUET may lower your blood pressure further if you are already taking other medicines to treat your high blood pressure.
If you are taking or have recently taken any other medicines, including medicines obtained without a prescription, talk to your doctor or pharmacist.
INTERACTIONS OF CADUET 10 MG / 10 MG WITH FOOD AND DRINK
Food and drinks
CADUET 10 mg / 10 mg film-coated tablets can be taken at any time of the day, with or without food.
Grapefruit juice
Do not take more than one or two glasses of grapefruit juice per day as large amounts of grapefruit juice may affect the effects of CADUET 10 mg / 10 mg film-coated tablets.
Alcohol
Avoid drinking too much alcohol while taking CADUET 10 mg / 10 mg film-coated tablets. See also section 2 “Take special care with CADUET 10 mg / 10 mg film-coated tablets” for more details.
Drive and use machines
Do not drive or use machines if you feel dizzy after taking this medicine.
Do not drive or use machines if you feel dizzy after taking this medicine.
Do not drive or use machines if you feel dizzy after taking this medicine.
Warnings and Precautions
Heart failure
Liver function monitoring
Clinical signs of hepatic dysfunction
Increased transaminases
Heavy alcohol consumption
Hepatic insufficiency
History of liver disease
Predisposing factor to the occurrence of rhabdomyolysis
Subject over 70 years of age
Unexplained muscle pain
Muscle cramp
Muscular weakness
Increase in CPK
Rhabdomyolysis
History of hemorrhagic stroke
History of lacunar infarction
Interstitial lung disease
Risk of diabetes
Woman of childbearing age
Heart failure
Patients with heart failure should be treated with caution. In a long-term placebo-controlled study in patients with severe heart failure (NYHA class III and IV), the reported incidence of pulmonary edema was higher in the amlodipine group compared to the placebo group. (see section Pharmacodynamic properties). Calcium channel blockers including amlodipine should be used with caution in patients with congestive heart failure because they may increase the risk of cardiovascular events and mortality.
Liver effects
Liver function tests should be performed before the start of treatment and then regularly after initiation of treatment, as well as in the event of signs or symptoms suggestive of liver damage. In the event of elevation of the serum transaminase level, monitoring is necessary until normalization.
A persistent increase in ALT or AST exceeding 3 times the upper limit of normal (ULN), should lead to discontinuation of treatment.
The half-life of amlodipine is increased and its AUC (Area Under the Curve) is greater in patients with hepatic impairment; dosage recommendations have not been established.
Due to the presence of atorvastatin, CADUET should be used with caution in patients who consume large amounts of alcohol, in patients with hepatic impairment and / or a history of liver disease.
Muscle effects
Like other HMG-CoA reductase inhibitors, atorvastatin can affect skeletal muscles and lead to myalgia, myositis and myopathies. These muscle damage may rarely progress to rhabdomyolysis, characterized by high levels of creatine kinase (CK) (more than 10 times the ULN), myoglobinemia and myoglobinuria which can lead to kidney failure, and in some cases be fatal.
Regular testing of CK or other muscle enzymes is not recommended in asymptomatic patients treated with statins. However, dosing of CKs is recommended before initiating statin therapy in patients with predisposing factors to rhabdomyolysis as well as in those with muscle symptoms during statin therapy (see below).
Very rare cases of autoimmune-mediated necrotizing myopathies (IMNM) have been reported during or after treatment with certain statins. IMNM is clinically characterized by proximal muscle weakness and increased serum creatine kinase, which persist despite discontinuation of statin therapy.
Before initiation of treatment
CADUET should be prescribed with caution in patients with predisposing factors to rhabdomyolysis. Before starting treatment with a statin, creatine kinase (CK) levels should be checked in the following situations:
Renal failure.
Hypothyroidism.
Personal or family history of genetic muscle diseases.
Personal history of muscle toxicity during treatment with a statin or a fibrate.
History of liver disease and / or excessive alcohol consumption.
In elderly patients (> 70 years), the need for these measures should be assessed, depending on the presence of other factors predisposing to rhabdomyolysis.
Situations in which increased plasma concentrations may occur, due to interactions (see section 4.5) and use in special populations including genetic polymorphisms (see section 5.2). ).
In these situations, a regular reassessment of the benefit / risk of the treatment, as well as regular clinical monitoring is recommended.
If the initial CK level is significantly elevated (more than 5 times the ULN) treatment should not be started.
Creatine kinase measurement
Creatine kinase (CK) should not be measured after heavy exercise or in the presence of another possible cause of increased CK, as this will make interpretation of the results difficult. In the event of a significant elevation of CK (more than 5 times the ULN) before treatment, this should be systematically checked again within 5 to 7 days to confirm the results.
During treatment
It is recommended that patients be asked to promptly report any unexplained muscle pain, muscle cramps or weakness, particularly if accompanied by malaise or fever.
· If symptoms appear when a patient is under treatment with CADUET, a CK levels should be measured; if the CK level is significantly elevated (more than 5 times the ULN), treatment should be discontinued.
· If muscular symptoms are severe and cause daily discomfort, discontinuation of treatment should be considered, even if CK levels did not exceed 5 times the ULN.
· If symptoms resolve and CK levels return to normal, the reintroduction of CADUET may be considered at the lowest dose and under close supervision.
Treatment with CADUET should be discontinued in the event of a clinically significant increase in CK level (> 10 times the ULN) or if rhabdomyolysis is diagnosed or suspected.
Amlodipine has no effect on laboratory parameters.
Combinations with other drugs
As with other statins, the risk of rhabdomyolysis is increased when CADUET is administered in combination with certain drugs which may increase the plasma concentration of atorvastatin, such as strong inhibitors of CYP3A4 or protein transporters (eg, cyclosporin, telithromycin, clarithromycin, delavirdine, stiripentol, ketoconazole, voriconazole, itraconazole, posaconazole, determovir and HIV protease inhibitors including ritonavir, lopinavir, atazanavir, indinavir, darunavir, tipranavir, etc / ritonavir). The risk of myopathy may also be increased in combination with gemfibrozil and other fibrates, antivirals used in the treatment of hepatitis C (HCV) (boceprevir, telaprevir, elbasvir / grazoprevir), erythromycin, niacin, l ‘ ezetimibe or colchicine. Therapeutic alternatives (not exhibiting these interactions) should be considered as far as possible.
In the event that the combination of these medicinal products with CADUET is necessary, the benefit / risk of concomitant treatments should be carefully assessed and appropriate clinical monitoring is recommended (see section Interactions with other medicinal products and other forms of interactions).
CADUET should not be administered simultaneously with fusidic acid in systemic form, and for up to 7 days after stopping treatment with fusidic acid. In patients where the use of systemic fusidic acid is considered essential, statin therapy should be discontinued for the duration of fusidic acid therapy. Cases of rhabdomyolysis (some fatal) have been reported in patients receiving fusidic acid and a statin in combination (see section Interactions with other medicinal products and other forms of interactions). Patients should be informed of the need to seek immediate medical attention if they experience symptoms of muscle weakness, pain, or muscle tenderness.
Statin therapy can be restarted seven days after the last dose of fusidic acid.
In exceptional circumstances, when prolonged treatment with systemic fusidic acid is required, e.g. for the treatment of severe infections, the need for co-administration of CADUET and fusidic acid should only be considered in cases of per case and under close medical supervision.
Prevention of stroke by aggressively lowering cholesterol levels (SPARCL study)
In a posteriori analysis performed in subgroups of patients with recent stroke or transient ischemic attack (TIA) but without coronary artery disease, a higher frequency of hemorrhagic stroke was observed in treated patients. per 80 mg atorvastatin compared to patients on placebo.
This high risk is particularly observed in patients who have already had a hemorrhagic stroke or a lacunar infarction at the inclusion of the study.
In patients with a history of hemorrhagic stroke or lacunar infarction, the benefit / risk balance of atorvastatin 80 mg is uncertain. Therefore, the potential risk of occurrence of haemorrhagic stroke should be carefully assessed before any initiation of treatment (see section Pharmacodynamic properties).
Interstitial lung disease
Cases of interstitial lung disease have exceptionally been reported with certain statins, particularly during long-term therapy .
Symptoms may include dyspnea, a non-productive cough, and altered general condition (fatigue, weight loss, and fever). If interstitial lung disease is suspected in a patient, statin therapy should be discontinued.
Diabetes
There is some evidence that statins, as a pharmacological class, increase blood sugar. In some patients at high risk of developing diabetes, statins may cause hyperglycaemia requiring the initiation of diabetes treatment. This risk is nevertheless compensated by the reduction in the vascular risk under statins and therefore it should not be a reason for stopping statins. Patients at risk (fasting blood glucose between 5.6 and 6.9 mmol / l, BMI> 30 kg / m², increased triglyceride levels, arterial hypertension) should be monitored clinically and biologically in accordance with national recommendations.
PREGNANCY & BREAST-FEEDING & FERTILITY
Caduet is contraindicated during pregnancy and lactation.
Women of childbearing age
Women of childbearing potential should use reliable contraceptive measures during treatment ( see Contraindications ).
Pregnancy
The safety of atorvastatin has not been established in pregnant women. No controlled clinical trials have been performed in pregnant women treated with atorvastatin. Following intrauterine exposure to HMG-CoA reductase inhibitors, birth defects have rarely been reported. Studies in animals have shown reproductive toxicity ( see Preclinical safety ).
Treatment of the mother with atorvastatin may reduce the fetal level of mevalonate, which is a precursor of cholesterol biosynthesis. Atherosclerosis is a chronic process, and stopping a lipid-lowering drug during pregnancy should generally have little effect on the long-term risk associated with primary hypercholesterolemia.
For these reasons, Caduet should not be used during pregnancy, or in a woman planning to become pregnant or in whom pregnancy is suspected. Caduet treatment should be withheld during pregnancy or until it has been determined that the woman is not pregnant ( see Contraindications ).
If pregnancy is discovered during treatment, it should be stopped immediately.
Feeding with milk
Amlodipine is excreted in breast milk. The proportion of maternal dose received by the infant has been estimated at an interquartile range of 3-7%, with a maximum of 15%. The effect of amlodipine on infants is unknown. The excretion of atorvastatin or its metabolites in human milk is not known. In rats, the plasma concentrations of atorvastatin and its metabolites are similar to those found in milk ( see Preclinical safety ). Due to the possibility of serious side effects, women treated with Caduet should not breast-feed their infants ( see Contraindications ). Atorvastatin is contraindicated during breastfeeding ( see Contraindications ).
Fertility
No effect of atorvastatin on fertility has been demonstrated in studies conducted in male or female animals ( see Preclinical Safety ).
Reversible biochemical changes in the sperm head have been reported in some patients treated with calcium channel blockers. There is insufficient clinical data regarding the potential effect of amlodipine on fertility. In a study carried out in rats, adverse effects were detected on male fertility ( see Preclinical safety ).
What happens if I overdose from Caduet?
No information is available regarding overdose of Caduet in humans.
Amlodipine:
For amlodipine, experience with intentional overdose in humans is limited. Massive overdose could cause extensive peripheral vasodilation and possibly reflex tachycardia. Marked and possibly prolonged systemic hypotension up to and including shock with fatal outcome has been reported. Any hypotension resulting from acute intoxication requires monitoring in an intensive cardiological care unit. A vasoconstrictor can be used to restore vascular tone and blood pressure. Since amlodipine is highly protein bound, dialysis is unlikely to provide any benefit.
Atorvastatin:
There is no specific treatment for atorvastatin overdose. In the event of overdose, the patient should receive symptomatic treatment and supportive measures should be implemented as needed. Liver function and serum CK concentrations should be monitored. Due to the strong binding of the drug to plasma proteins, hemodialysis is not expected to significantly increase the clearance of atorvastatin.
What should I do if I miss a dose?
If you forget to take CADUET 5/ 10 mg -5/ 10 mg film-coated tablets:
If you forget to take your dose of CADUET, take your next dose at the normal time.
Do not take a double dose to make up for the dose you forgot to take.
What is  Forms and Composition ?
SHAPES and PRESENTATIONS
5 mg / 10 mg film-coated tablet (oval, debossed with “Pfizer” on one side and “CDT 051” on the other side; white) and 10 mg / 10 mg (oval, debossed with “Pfizer “On one side and” CDT 101 “on the other side; blue):   Boxes of 30 and 90, in blisters.
COMPOSITION
  p cp Amlodipine (INN) as amlodipine besilate 5 mg or 10 mg Atorvastatin (INN) as atorvastatin calcium trihydrate 10 mg
Excipients (common): Core: calcium carbonate, croscarmellose sodium, microcrystalline cellulose, pregelatinized corn starch, polysorbate 80, hydroxypropylcellulose, colloidal anhydrous silica, magnesium stearate. Film- coating : 5 mg / 10 mg tablet: Opadry II white 85F28751 (polyvinyl alcohol, titanium dioxide E171, macrogol 3000, talc). 10 mg / 10 mg tablet: Opadry II blue 85F10919 (polyvinyl alcohol, titanium dioxide E171, macrogol 3000, talc, indigo carmine aluminum lake E132).
NOT’s
Edrug-online contains comprehensive and detailed information about drugs available in the medical field, and is divided into four sections:
general information:
Includes a general description of the drug, its use, brand names, FAQs, and relevant news and articles
Additional information:
General explanation about dealing with the medicine: how to take the medicine, the doses and times of it, the start and duration of its effectiveness, the recommended diet during the period of taking the medicine, the method of storage and storage, recommendations in cases for forgetting the dose and instructions to stop taking the drug and take additional doses.
Special warnings:
For pregnant and breastfeeding women, the elderly, boys and drivers, and use before surgery.
Side effects:
It treats possible side effects and drug interactions that require attention and its effect on continuous use.
The information contained in this medicine is based on medical literature, but it is not a substitute for consulting a doctor.
The post caduet tablets Uses, Dosage, Side Effects, Precautions & Warnings appeared first on Drug Online.
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colinfitzpatrick · 4 years ago
Text
caduet tablets Uses, Dosage, Side Effects, Precautions & Warnings
Drug Online
caduet Generic drug of the Therapeutic class: Cardiology and angiology Active ingredients: Amlodipine , Atorvastatin
what is caduet medication?
This medication is supplied as blue, oval-shaped, film-coated tablets debossed with “Pfizer” on one side and “CDT 101” on the other side.
Boxes of 7, 10, 14, 20, 28, 30, 50, 56, 60, 90, 100 or 200 tablets.
Not all presentations may be marketed.
what is caduet medication used for and   indication?
CADUET is indicated for the prevention of cardiovascular events in hypertensive patients with 3 associated cardiovascular risk factors, with normal to moderately elevated cholesterol without established coronary artery disease, and in whom, according to current recommendations, the concomitant use of amlodipine and a low dose of atorvastatin is suitable .
CADUET should be used when the response to regimen and other non-pharmacological measures is inadequate.
caduet dosage
Oral route
The usual starting dose is 5 mg / 10 mg once daily.
If tighter blood pressure control is required, a dosage of 10 mg / 10 mg once daily may be administered.
The tablets can be taken at any time of the day, with or without food.
CADUET can be used alone or in combination with other antihypertensive drugs, but it must not be used in combination with other calcium channel blockers or another statin.
The combination of CADUET and fibrates should generally be avoided (see sections 4.4 and Interactions with other medicinal products and other forms of interaction ).
Patients with renal impairment : No dosage adjustment is necessary in patients with impaired renal function (see sections 4.4 and Pharmacokinetic properties ).
Patients with hepatic impairment : CADUET is contraindicated in patients with active hepatic disease.
Children / Adolescents : The safety and efficacy of CADUET have not been established in children / adolescents. Therefore, the use of CADUET is not recommended in this population.
Elderly : It does not appear necessary to adjust the dose in the elderly (see section Pharmacokinetic properties ).
Combination with other medicinal products : In combination with ciclosporin, the dose of atorvastatin should not exceed 10 mg (see section Interactions with other medicinal products and other forms of interaction ).
Contraindications
CADUET is contraindicated in patients:
Being hypersensitive to dihydropyridines *, to amlodipine, to atorvastatin or to any of the excipients of this medicine,
have active liver disease or a persistent and unexplained increase in serum transaminases exceeding 3 times the upper limit of normal,
In women who are pregnant, breastfeeding or of childbearing potential and not using reliable contraceptive methods (see section Pregnancy and breast-feeding ),
In combination with itraconazole, ketoconazole, telithromycin (see section Interactions with other medicinal products and other forms of interactions ),
having severe hypotension,
Having shock (including cardiogenic shock),
Having an obstruction of the efferent pathway to the left ventricle (for example severe aortic stenosis),
With haemodynamically unstable heart failure after acute myocardial infarction.
* amlodipine is a calcium channel blocker derived from dihydropyridine.
HOW TO TAKE CADUET?
Always take this medicine exactly as your doctor or pharmacist has told you. Check with your doctor or pharmacist if in doubt.
Adults
The recommended starting dose of CADUET is one 5 mg / 10 mg tablet per day. Your doctor may increase the dose if necessary to 1 tablet of CADUET 10 mg / 10 mg per day.
The tablets should be swallowed whole with a glass of water. They can be taken at any time of the day, with or without food. However, it is best to take them at the same time each day.
Continue to follow your doctor’s dietary advice, especially to eat a low fat diet, avoid tobacco, and exercise regularly.
If you have the impression that the effect of CADUET tablets is too strong or too weak, talk to your doctor or pharmacist.
Use in children and adolescents
This medication is not recommended for children and adolescents.
If you take more CADUET 10 mg / 10 mg film-coated tablets than you should
If you accidentally take too many CADUET tablets (more than your usual dose), ask your doctor or the nearest hospital for advice. Take any remaining tablets, the carton or the whole carton with you so that hospital staff can quickly identify which medicine you have taken.
If you forget to take CADUET 10 mg / 10 mg film-coated tablets
If you forget to take your dose of CADUET, take your next dose at the normal time.
Do not take a double dose to make up for the dose you forgot to take.
If you stop taking CADUET 10 mg / 10 mg film-coated tablets
Do not stop taking CADUET unless your doctor tells you to.
If you have any further questions on the use of this medicine or want to stop taking your treatment, ask your doctor or pharmacist for more information.
How To Store Caduet?
Keep this medication out of the sight and reach of children.
Do not use this medicine after the expiry date which is stated on the blister, the carton and the vial after “EXP”. The expiration date refers to the last day of that month.
Store at a temperature not exceeding 30 ° C.
Do not throw away any medicines via a wastewater treatment plant or with household waste. Ask your pharmacist how to throw away the medicines you no longer use. These measures will help protect the environment.
caduet side effects
The safety of CADUET has been evaluated in double-blind, placebo-controlled studies in 1092 patients treated for concomitant hypertension and dyslipidemia. During clinical trials with CADUET, no specific adverse events specific to this combination were observed.
Adverse events were limited to those previously reported for amlodipine and / or atorvastatin (see table of adverse events below).
In controlled clinical trials, discontinuation of treatment due to clinical adverse events or laboratory abnormalities was observed in 5.1% of patients treated with amlodipine and atorvastatin versus 4.0% of patients treated with amlodipine and atorvastatin. patients taking a placebo.
The adverse events below, listed according to MedDRA system organ classification and frequency order, relate to amlodipine and atorvastatin individually.
Very common: ³ 1/10, common: ³ 1/100 and <1/10, infrequent: ³ 1/1000 and <1/100, rare: ³ 1/10000 and <1/1000, very rare: < 1 / 10,000, frequency not known (cannot be estimated from the available data).
MedDRA
System organ classes
Side effects
Frequency
Amlodipine
Atorvastatin
Infections and infestations
Nasopharyngitis
Frequent
Blood and lymphatic system disorders
Leukopenia
Very rare
Thrombocytopenia
Very rare
Rare
Immune system disorders
hypersensitivity
Very rare
Frequent
Anaphylaxis
Very rare
Metabolism and nutrition disorders
Hyperglycemia *
Very rare
Frequent
Weight gain
Infrequent
Infrequent
Weightloss
Infrequent
Hypoglycemia
Infrequent
Anorexia
Infrequent
Psychiatric disorders
Insomnia
Infrequent
Infrequent
Mood disorders (including anxiety)
Infrequent
Nightmares
Infrequent
Depression
Infrequent
Frequency not known
Confusion
Rare
Disorders of the system nervous
Drowsiness
Frequent
Dizziness
Frequent
Infrequent
Headache (especially at the start of treatment)
Frequent
Frequent
Tremors
Infrequent
Hypoesthesias, paresthesias
Infrequent
Infrequent
Syncope
Infrequent
Hypertonia
Very rare
Peripheral neuropathy
Very rare
Rare
Amnesia
Infrequent
Dysgeusia
Infrequent
Infrequent
Extrapyramidal syndrome
Frequency not known
Eye disorders
Blurred vision
Infrequent
Visual disturbances (including diplopia)
Infrequent
Rare
Ear and labyrinth disease
Tinnitus
Infrequent
Infrequent
Hearing loss
Very rare
Cardiac disorders
Palpitations
Frequent
Angina pectoris
Rare
Myocardial infarction
Very rare
Arrhythmia (including bradycardia, ventricular tachycardia and atrial fibrillation)
Very rare
Vascular disorders
Flushing
Frequent
Hypotension
Infrequent
Vasculitis
Very rare
Respiratory, thoracic and mediastinal disorders
Pharyngolaryngeal pain
Frequent
Epistaxis
Frequent
Dyspnea
Infrequent
Rhinitis
Infrequent
Cough
Very rare
Interstitial lung disease, especially during long-term treatment
Frequency not known
Gastrointestinal disorders
Gingival hyperplasia
Very rare
Nausea
Frequent
Frequent
Upper and lower abdominal pain
Frequent
Infrequent
Vomiting
Infrequent
Infrequent
Dyspepsia
Infrequent
Frequent
Changes in intestinal transit (including diarrhea and constipation)
Infrequent
Dry mouth
Infrequent
Dysgeusia
Infrequent
Diarrhea, constipation, gas
Frequent
Gastritis
Very rare
Pancreatitis
Very rare
Infrequent
Eructation
Infrequent
Hepatobiliary disorders
Hepatitis
Very rare
Infrequent
Cholestasis
Rare
Jaundice
Very rare
Hepatic insufficiency
Very rare
Skin and subcutaneous tissue disorders
Bullous dermatosis including erythema multiforme
Very rare
Rare
Angioedema
Very rare
Erythema multiforme
Very rare
Alopecia
Infrequent
Infrequent
Purpura
Infrequent
Skin discoloration
Infrequent
Pruritus
Infrequent
Infrequent
Eruption
Infrequent
Infrequent
Hyperhidrosis
Infrequent
Exanthema
Infrequent
Urticaria
Very rare
Infrequent
Angioneurotic edema
Very rare
Rare
Exfoliative dermatitis
Very rare
Photosensitivity
Very rare
Stevens-Johnson syndrome
Very rare
Rare
Bullous erythroderma with epidermolysis
Rare
Musculoskeletal and connective tissue disorders
Swelling of the joints (including swelling of the ankles)
Frequent
Frequent
Arthralgia, myalgia
(see section Warnings and precautions for use )
Infrequent
Frequent
Muscle cramps, muscle spasms
Infrequent
Frequent
Back pain
Infrequent
Frequent
Neck pain
Infrequent
Pain in extremity
Frequent
Muscle fatigue
Infrequent
Myositis (see section Warnings and precautions for use )
Rare
Rhabdomyolysis, myopathy
(see section Warnings and precautions for use )
Rare
Tendinopathies, in rare cases tendon rupture
Rare
Immune-mediated necrotizing myopathy
Frequency not known
Kidney and urinary tract disorders
Urination disorder, nocturia, pollakiuria
Infrequent
Reproductive system and breast disorders
Incapacity
Infrequent
Infrequent
Gynecomastia
Infrequent
Very rare
General disorders and administration site conditions
Edema
Frequent
Infrequent
Peripheral edema
Infrequent
Tired
Frequent
Infrequent
Chest pain
Infrequent
Infrequent
Asthenia
Infrequent
Infrequent
Pain
Infrequent
Discomfort
Infrequent
Infrequent
Fever
Infrequent
Investigations
Increased liver enzymes: alanine aminotransferase, aspartate aminotransferase (mainly related to cholestasis)
Very rare
Frequent
Blood CK increased (see section 4.4 )
Frequent
Leukocyturia
Infrequent
* Diabetes: The frequency depends on the presence or absence of risk factors (fasting blood sugar ³ 5.6 mmol / l, BMI> 30 kg / m², increased triglyceride levels, history of high blood pressure).
caduet Interactions
Taking other medications
Tell your doctor or pharmacist if you are taking or have recently taken any other medicines, including medicines obtained without a prescription. Some medicines may interact with CADUET 10 mg / 10 mg film-coated tablets. This interaction may cause one or both of the medicines to be less effective, or on the contrary, this interaction may increase the risk or severity of side effects, including major muscle disorders known as rhabdomyolysis and myopathy (see section 4). .
Some medicines may interact with CADUET 10 mg / 10 mg film-coated tablets:
certain antibiotics such as rifampicin or certain “macrolide” antibiotics such as erythromycin, clarithromycin, telithromycin, fusidic acid or certain drugs used to treat infections caused by fungi such as ketoconazole, itraconazole,
medicines used to regulate lipid levels: fibrates, such as gemfibrozil or colestipol,
medicines used to regulate your heart rhythm, such as amiodarone, diltiazem and verapamil,
medicines used to treat or prevent seizures such as carbamazepine, phenobarbital, phenytoin, fosphenytoin, primidone,
medicines used to change how your immune system works, such as cyclosporin
protease inhibitors such as ritonavir, indinavir, nelfinavir used in the treatment of HIV,
medicines used to treat depression, such as nefazodone and imipramine,
medicines used to treat mental disorders, such as neuroleptics,
medicines used to treat heart failure, such as beta blockers
medicines used to treat high blood pressure, such as angiotensin II inhibitors, converting enzyme inhibitors, verapamil and diuretics,
alpha blockers used to treat high blood pressure or prostate problems
other medicines known to interact with CADUET 10 mg / 10 mg film-coated tablets such as ezetimibe (which lowers cholesterol), warfarin (which decreases blood clotting), oral contraceptives, stiripentol (an anticonvulsant used for treatment of epilepsy), cimetidine (used for heartburn and stomach ulcers), phenazone (a pain reliever), antacids (containing aluminum or magnesium, used to relieve problems stomach), and amifostine (used to treat cancer),
sildenafil (used in the treatment of erectile dysfunction, impotence),
dantrolene and baclofen (muscle relaxants),
steroids,
over-the-counter St. John’s Wort products.
CADUET may lower your blood pressure further if you are already taking other medicines to treat your high blood pressure.
If you are taking or have recently taken any other medicines, including medicines obtained without a prescription, talk to your doctor or pharmacist.
INTERACTIONS OF CADUET 10 MG / 10 MG WITH FOOD AND DRINK
Food and drinks
CADUET 10 mg / 10 mg film-coated tablets can be taken at any time of the day, with or without food.
Grapefruit juice
Do not take more than one or two glasses of grapefruit juice per day as large amounts of grapefruit juice may affect the effects of CADUET 10 mg / 10 mg film-coated tablets.
Alcohol
Avoid drinking too much alcohol while taking CADUET 10 mg / 10 mg film-coated tablets. See also section 2 “Take special care with CADUET 10 mg / 10 mg film-coated tablets” for more details.
Drive and use machines
Do not drive or use machines if you feel dizzy after taking this medicine.
Do not drive or use machines if you feel dizzy after taking this medicine.
  Do not drive or use machines if you feel dizzy after taking this medicine.
  Warnings and Precautions
Heart failure
Liver function monitoring
Clinical signs of hepatic dysfunction
Increased transaminases
Heavy alcohol consumption
Hepatic insufficiency
History of liver disease
Predisposing factor to the occurrence of rhabdomyolysis
Subject over 70 years of age
Unexplained muscle pain
Muscle cramp
Muscular weakness
Increase in CPK
Rhabdomyolysis
History of hemorrhagic stroke
History of lacunar infarction
Interstitial lung disease
Risk of diabetes
Woman of childbearing age
Heart failure
Patients with heart failure should be treated with caution. In a long-term placebo-controlled study in patients with severe heart failure (NYHA class III and IV), the reported incidence of pulmonary edema was higher in the amlodipine group compared to the placebo group. (see section Pharmacodynamic properties). Calcium channel blockers including amlodipine should be used with caution in patients with congestive heart failure because they may increase the risk of cardiovascular events and mortality.
Liver effects
Liver function tests should be performed before the start of treatment and then regularly after initiation of treatment, as well as in the event of signs or symptoms suggestive of liver damage. In the event of elevation of the serum transaminase level, monitoring is necessary until normalization.
A persistent increase in ALT or AST exceeding 3 times the upper limit of normal (ULN), should lead to discontinuation of treatment.
The half-life of amlodipine is increased and its AUC (Area Under the Curve) is greater in patients with hepatic impairment; dosage recommendations have not been established.
Due to the presence of atorvastatin, CADUET should be used with caution in patients who consume large amounts of alcohol, in patients with hepatic impairment and / or a history of liver disease.
Muscle effects
Like other HMG-CoA reductase inhibitors, atorvastatin can affect skeletal muscles and lead to myalgia, myositis and myopathies. These muscle damage may rarely progress to rhabdomyolysis, characterized by high levels of creatine kinase (CK) (more than 10 times the ULN), myoglobinemia and myoglobinuria which can lead to kidney failure, and in some cases be fatal.
Regular testing of CK or other muscle enzymes is not recommended in asymptomatic patients treated with statins. However, dosing of CKs is recommended before initiating statin therapy in patients with predisposing factors to rhabdomyolysis as well as in those with muscle symptoms during statin therapy (see below).
Very rare cases of autoimmune-mediated necrotizing myopathies (IMNM) have been reported during or after treatment with certain statins. IMNM is clinically characterized by proximal muscle weakness and increased serum creatine kinase, which persist despite discontinuation of statin therapy.
Before initiation of treatment
CADUET should be prescribed with caution in patients with predisposing factors to rhabdomyolysis. Before starting treatment with a statin, creatine kinase (CK) levels should be checked in the following situations:
Renal failure.
Hypothyroidism.
Personal or family history of genetic muscle diseases.
Personal history of muscle toxicity during treatment with a statin or a fibrate.
History of liver disease and / or excessive alcohol consumption.
In elderly patients (> 70 years), the need for these measures should be assessed, depending on the presence of other factors predisposing to rhabdomyolysis.
Situations in which increased plasma concentrations may occur, due to interactions (see section 4.5) and use in special populations including genetic polymorphisms (see section 5.2). ).
In these situations, a regular reassessment of the benefit / risk of the treatment, as well as regular clinical monitoring is recommended.
If the initial CK level is significantly elevated (more than 5 times the ULN) treatment should not be started.
Creatine kinase measurement
Creatine kinase (CK) should not be measured after heavy exercise or in the presence of another possible cause of increased CK, as this will make interpretation of the results difficult. In the event of a significant elevation of CK (more than 5 times the ULN) before treatment, this should be systematically checked again within 5 to 7 days to confirm the results.
During treatment
It is recommended that patients be asked to promptly report any unexplained muscle pain, muscle cramps or weakness, particularly if accompanied by malaise or fever.
· If symptoms appear when a patient is under treatment with CADUET, a CK levels should be measured; if the CK level is significantly elevated (more than 5 times the ULN), treatment should be discontinued.
· If muscular symptoms are severe and cause daily discomfort, discontinuation of treatment should be considered, even if CK levels did not exceed 5 times the ULN.
· If symptoms resolve and CK levels return to normal, the reintroduction of CADUET may be considered at the lowest dose and under close supervision.
Treatment with CADUET should be discontinued in the event of a clinically significant increase in CK level (> 10 times the ULN) or if rhabdomyolysis is diagnosed or suspected.
Amlodipine has no effect on laboratory parameters.
Combinations with other drugs
As with other statins, the risk of rhabdomyolysis is increased when CADUET is administered in combination with certain drugs which may increase the plasma concentration of atorvastatin, such as strong inhibitors of CYP3A4 or protein transporters (eg, cyclosporin, telithromycin, clarithromycin, delavirdine, stiripentol, ketoconazole, voriconazole, itraconazole, posaconazole, determovir and HIV protease inhibitors including ritonavir, lopinavir, atazanavir, indinavir, darunavir, tipranavir, etc / ritonavir). The risk of myopathy may also be increased in combination with gemfibrozil and other fibrates, antivirals used in the treatment of hepatitis C (HCV) (boceprevir, telaprevir, elbasvir / grazoprevir), erythromycin, niacin, l ‘ ezetimibe or colchicine. Therapeutic alternatives (not exhibiting these interactions) should be considered as far as possible.
In the event that the combination of these medicinal products with CADUET is necessary, the benefit / risk of concomitant treatments should be carefully assessed and appropriate clinical monitoring is recommended (see section Interactions with other medicinal products and other forms of interactions).
CADUET should not be administered simultaneously with fusidic acid in systemic form, and for up to 7 days after stopping treatment with fusidic acid. In patients where the use of systemic fusidic acid is considered essential, statin therapy should be discontinued for the duration of fusidic acid therapy. Cases of rhabdomyolysis (some fatal) have been reported in patients receiving fusidic acid and a statin in combination (see section Interactions with other medicinal products and other forms of interactions). Patients should be informed of the need to seek immediate medical attention if they experience symptoms of muscle weakness, pain, or muscle tenderness.
Statin therapy can be restarted seven days after the last dose of fusidic acid.
In exceptional circumstances, when prolonged treatment with systemic fusidic acid is required, e.g. for the treatment of severe infections, the need for co-administration of CADUET and fusidic acid should only be considered in cases of per case and under close medical supervision.
Prevention of stroke by aggressively lowering cholesterol levels (SPARCL study)
In a posteriori analysis performed in subgroups of patients with recent stroke or transient ischemic attack (TIA) but without coronary artery disease, a higher frequency of hemorrhagic stroke was observed in treated patients. per 80 mg atorvastatin compared to patients on placebo.
This high risk is particularly observed in patients who have already had a hemorrhagic stroke or a lacunar infarction at the inclusion of the study.
In patients with a history of hemorrhagic stroke or lacunar infarction, the benefit / risk balance of atorvastatin 80 mg is uncertain. Therefore, the potential risk of occurrence of haemorrhagic stroke should be carefully assessed before any initiation of treatment (see section Pharmacodynamic properties).
Interstitial lung disease
Cases of interstitial lung disease have exceptionally been reported with certain statins, particularly during long-term therapy .
Symptoms may include dyspnea, a non-productive cough, and altered general condition (fatigue, weight loss, and fever). If interstitial lung disease is suspected in a patient, statin therapy should be discontinued.
Diabetes
There is some evidence that statins, as a pharmacological class, increase blood sugar. In some patients at high risk of developing diabetes, statins may cause hyperglycaemia requiring the initiation of diabetes treatment. This risk is nevertheless compensated by the reduction in the vascular risk under statins and therefore it should not be a reason for stopping statins. Patients at risk (fasting blood glucose between 5.6 and 6.9 mmol / l, BMI> 30 kg / m², increased triglyceride levels, arterial hypertension) should be monitored clinically and biologically in accordance with national recommendations.
PREGNANCY & BREAST-FEEDING & FERTILITY
Caduet is contraindicated during pregnancy and lactation.
Women of childbearing age
Women of childbearing potential should use reliable contraceptive measures during treatment ( see Contraindications ).
Pregnancy
The safety of atorvastatin has not been established in pregnant women. No controlled clinical trials have been performed in pregnant women treated with atorvastatin. Following intrauterine exposure to HMG-CoA reductase inhibitors, birth defects have rarely been reported. Studies in animals have shown reproductive toxicity ( see Preclinical safety ).
Treatment of the mother with atorvastatin may reduce the fetal level of mevalonate, which is a precursor of cholesterol biosynthesis. Atherosclerosis is a chronic process, and stopping a lipid-lowering drug during pregnancy should generally have little effect on the long-term risk associated with primary hypercholesterolemia.
For these reasons, Caduet should not be used during pregnancy, or in a woman planning to become pregnant or in whom pregnancy is suspected. Caduet treatment should be withheld during pregnancy or until it has been determined that the woman is not pregnant ( see Contraindications ).
If pregnancy is discovered during treatment, it should be stopped immediately.
Feeding with milk
Amlodipine is excreted in breast milk. The proportion of maternal dose received by the infant has been estimated at an interquartile range of 3-7%, with a maximum of 15%. The effect of amlodipine on infants is unknown. The excretion of atorvastatin or its metabolites in human milk is not known. In rats, the plasma concentrations of atorvastatin and its metabolites are similar to those found in milk ( see Preclinical safety ). Due to the possibility of serious side effects, women treated with Caduet should not breast-feed their infants ( see Contraindications ). Atorvastatin is contraindicated during breastfeeding ( see Contraindications ).
Fertility
No effect of atorvastatin on fertility has been demonstrated in studies conducted in male or female animals ( see Preclinical Safety ).
Reversible biochemical changes in the sperm head have been reported in some patients treated with calcium channel blockers. There is insufficient clinical data regarding the potential effect of amlodipine on fertility. In a study carried out in rats, adverse effects were detected on male fertility ( see Preclinical safety ).
What happens if I overdose from Caduet?
No information is available regarding overdose of Caduet in humans.
Amlodipine:
For amlodipine, experience with intentional overdose in humans is limited. Massive overdose could cause extensive peripheral vasodilation and possibly reflex tachycardia. Marked and possibly prolonged systemic hypotension up to and including shock with fatal outcome has been reported. Any hypotension resulting from acute intoxication requires monitoring in an intensive cardiological care unit. A vasoconstrictor can be used to restore vascular tone and blood pressure. Since amlodipine is highly protein bound, dialysis is unlikely to provide any benefit.
Atorvastatin:
There is no specific treatment for atorvastatin overdose. In the event of overdose, the patient should receive symptomatic treatment and supportive measures should be implemented as needed. Liver function and serum CK concentrations should be monitored. Due to the strong binding of the drug to plasma proteins, hemodialysis is not expected to significantly increase the clearance of atorvastatin.
What should I do if I miss a dose?
If you forget to take CADUET 5/ 10 mg -5/ 10 mg film-coated tablets:
If you forget to take your dose of CADUET, take your next dose at the normal time.
Do not take a double dose to make up for the dose you forgot to take.
What is  Forms and Composition ?
SHAPES and PRESENTATIONS
5 mg / 10 mg film-coated tablet (oval, debossed with “Pfizer” on one side and “CDT 051” on the other side; white) and 10 mg / 10 mg (oval, debossed with “Pfizer “On one side and” CDT 101 “on the other side; blue):   Boxes of 30 and 90, in blisters.
COMPOSITION
  p cp Amlodipine (INN) as amlodipine besilate 5 mg or 10 mg Atorvastatin (INN) as atorvastatin calcium trihydrate 10 mg
Excipients (common): Core: calcium carbonate, croscarmellose sodium, microcrystalline cellulose, pregelatinized corn starch, polysorbate 80, hydroxypropylcellulose, colloidal anhydrous silica, magnesium stearate. Film- coating : 5 mg / 10 mg tablet: Opadry II white 85F28751 (polyvinyl alcohol, titanium dioxide E171, macrogol 3000, talc). 10 mg / 10 mg tablet: Opadry II blue 85F10919 (polyvinyl alcohol, titanium dioxide E171, macrogol 3000, talc, indigo carmine aluminum lake E132).
NOT’s
Edrug-online contains comprehensive and detailed information about drugs available in the medical field, and is divided into four sections:
general information:
Includes a general description of the drug, its use, brand names, FAQs, and relevant news and articles
Additional information:
General explanation about dealing with the medicine: how to take the medicine, the doses and times of it, the start and duration of its effectiveness, the recommended diet during the period of taking the medicine, the method of storage and storage, recommendations in cases for forgetting the dose and instructions to stop taking the drug and take additional doses.
Special warnings:
For pregnant and breastfeeding women, the elderly, boys and drivers, and use before surgery.
Side effects:
It treats possible side effects and drug interactions that require attention and its effect on continuous use.
The information contained in this medicine is based on medical literature, but it is not a substitute for consulting a doctor.
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industryupdatenews · 5 years ago
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·         Which product/service/technology segments holds game-changing potential to dramatically shape the competitive dynamic in the Dyslipidemia Therapeutics market?
·         What are the strategies adopted by top players to retain their stronghold in the Dyslipidemia Therapeutics market?
·         Which strategic moves will new entrants adopt to gain a strong foothold in the Dyslipidemia Therapeutics market?
·         What are COVID-19 implication on Dyslipidemia Therapeutics market and learn how businesses can respond, manage and mitigate the risks?
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rajputdishank-blog · 5 years ago
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Global Osteoarthritis Therapeutics Market Set To Register Robust Cagr During 2020-2026
The increasing incidence of osteoarthritis will drive the osteoarthritis therapeutics market growth in the forthcoming years. Rising incidences of aging and obesity will directly contribute to the increasing prevalence of osteoarthritis in both developing and developed regions. Furthermore, the inflammation of adipose tissue and dyslipidemia associated with obesity is further expected to contribute majorly to the osteoarthritis therapeutics market growth in the forthcoming years.
One of the growth drivers of the global osteoarthritis therapeutics market is the availability of guidelines for disease management. This will improvise the patient acceptance of drugs, which, in turn, is expected to drive the market growth.
Get a Sample Copy of this Report: https://dataintelo.com/request-sample/?reportId=113156
The global osteoarthritis therapeutics market size is anticipated to expand at a substantial CAGR during the forecast period, 2020-2026, owing to the rapid increase in the elderly and overweight population and the surge in the occurrence of osteoarthritis illness.
Read More: https://www.marketwatch.com/press-release/global-osteoarthritis-therapeutics-market-set-to-register-robust-cagr-during-2020-2026-2020-02-20
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Nonalcoholic Steatohepatitis Treatment Market Growth Factors 2018 – 2026
Nonalcoholic steatohepatitis treatment (NASH) is a syndrome which causes liver damage in non-alcoholic patients. It develops most often in patients with at least one factors such as dyslipidemia, obesity, and glucose intolerance. NASH pathogenesis is not clearly understood however is considered to be linked with insulin resistance. It is diagnosed with the help of blood tests, imaging tests, and sometimes liver biopsy. Treatment of the NASH includes elimination of causes and risk factors such as reducing fat level in the body. NASH is also considered to be one of the chief causes of cirrhosis which can lead to complete liver failure.
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Market Dynamics
Obesity, high blood pressure and cholesterol level, type 2 diabetes and metabolic syndrome are the major cause of the NASH onset. Increasing prevalence of these conditions worldwide is expected to drive the global nonalcoholic steatohepatitis treatment market growth during the forecast period. According to the International Diabetes Federation 2017 data, approximately 425 million people were suffering from diabetes in the world and 82 million cases were in the South East Asia region which is expected to reach 151 million by 2045.
However, diagnosis of the NASH can be difficult to catch in an early stage and can take years before patients show any sort of symptoms which is a major factor hampering the nonalcoholic steatohepatitis treatment market.
Nonalcoholic steatohepatitis (NASH) is a form of nonalcoholic fatty liver disease (NAFLD) in which a person have hepatitis and inflammation of the liver, and can cause liver damage. NASH can lead to complications, such as cirrhosis and liver cancer. Patients with NASH have high chance of mortality due to liver-related causes such as liver failure.
Lifestyle modification, including change in diet and exercise, is the basic therapy recommended for nonalcoholic fatty liver disease. However, in some cases lifestyle modification is difficult to achieve and to sustain, and therefore required other treatments including medicine.
Currently available drugs for the treatment of NAFLD were historically been given for other indications. For instance, Orlistat, a gut lipase inhibitor, is indicated for decrease in the dietary fats absorption. According to the National Center for Biotechnology Information (NCBI) 2017 study, Orlistat has been approved for treatment of obesity and is available over the counter in the U.S. for weight loss. Orlistat-mediated weight loss is related with reduction in hepatic steatosis.
The global nonalcoholic steatohepatitis treatment market size was valued at US$ 1,119.9 million in 2017 (based on existing approved therapies anti-diabetics, vitamins, dietary supplements, and others) and is expected to witness a CAGR of 42.7% over the forecast period (2018 – 2026).
Nonalcoholic Steatohepatitis Treatment Market - Regional Insights
On the basis of region, the global nonalcoholic steatohepatitis treatment market is segmented into North America, Latin America, Europe, Asia Pacific, Middle East, and Africa. North America and Europe nonalcoholic steatohepatitis treatment market is expected to foresee significant growth owing to increasing incidence of obesity and fatty liver.
According to the National Health and Nutrition Examination Survey, the proportion of NAFLD among chronic liver diseases increased from 47% to 75% between 1988 and 2008 in the U.S. According to the National Institutes of Health, in 2015 nearly 3 to 12% of adults in the U.S. were suffering from NASH. The major reason for this increase was an increase in metabolic risk factors. According to the Journal of Hepatology, in 2013, approximately one-third of adults exhibit a pattern of NAFLD in Europe.
Nonalcoholic Steatohepatitis Treatment Market - Competitive Landscape
Key players operating in the global nonalcoholic steatohepatitis treatment market include AstraZeneca Plc., Conatus Pharmaceuticals, Enzo Biochem, Inc., GENFIT SA, Galmed Pharmaceuticals Ltd., Gilead Science, Immuron Ltd., Intercepts Pharmaceuticals, Novo Nordisk, Raptor Pharmaceutical Corporation, and Tobira Therapeutics, Inc.
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Detailed Segmentation:
Global Nonalcoholic Steatohepatitis Treatment Market, By Drug:
Cenicriviroc
Elafibranor
Ocaliva (Obeticholic Acid)
Selonsertib
Global Nonalcoholic Steatohepatitis Treatment Market, By Distribution Channel:
Hospital Pharmacy
Retail Pharmacy
Online Pharmacy
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Hyperlipidemia Drugs Market Share, Competitive Insights, Region, Segments And Forecast By 2022
San Francisco, 28 September 2018 - The global hyperlipidemia drugs market size is expected reach USD 22.6 billion by 2022, according to a new report by Grand View Research, Inc., expanding at a CAGR of 2.3% during the forecast period. Several factors, such as increase in target population and growth in awareness about risk of cardiovascular diseases (CVD) due to persistent hypercholesterolemia, are stoking the growth of the market.
Hyperlipidemia is the most common type of dyslipidemia and is generally caused by abnormally high lipid levels in the blood. This condition can occur due to genetic factors (primary hyperlipidemia) as well as other factors such as poor diet and unhealthy lifestyle (secondary hyperlipidemia). Statins are the first line of treatment for secondary hyperlipidemia.
Target population of antihyperlipidemic drugs is broadly divided into statin users and nonstatin users. The revenue share of statin users has been declining. The nonstatin users segment consists of statin intolerant and nonresponsive population as well as familial hyperlipidemia (FH) population. Nonstatin users are seeking high-efficacy alternatives and this is anticipated to boost the revenue of this segment.
Upcoming patent expirations are expected to lead to greater genericization in the market, mostly among statins, cholesterol absorption inhibitors, and combination drugs. However, new product launches are anticipated to continue to drive the market. Several novel mechanisms of action such as ACL inhibition, DGAT2 inhibition, and anti-ANGPTL-3 are being investigated for their potential for treatment of hyperlipidemia as well as for reducing the risk of CVD.
To request a sample copy or view summary of this report, click the link below: www.grandviewresearch.com/industry-analysis/hyperlipidemia-drugs-market
Further key findings from the report suggest:
Statins dominated the drug classes in 2016 owing to their high usage as the first line of therapy
Recent launch of PCSK9 inhibitors, such as Repatha and Praluent, is likely to change the current therapeutic scenario due to their improved efficacy and safety profile
PCSK9 inhibitors are expected to displace existing expensive therapies, lomitapide, and mipomersen for the treatment of homozygous FH patients
Europe was the leading regional market in 2016. It is estimated to maintain its dominance till 2022 owing to high prevalence of hypercholesterolemia
There are fewer growth opportunities in Japan due to unavailability of key pipeline drugs such as bempedoic acid
AstraZeneca; Merck & Co., Inc.; Pfizer, Inc.; DAIICHI SANKYO COMPANY, LIMITED; Amgen, Inc.; and Sanofi are some of the key players operating in this market
Amgen, Inc.; Sanofi; and Esperion are expected to have the highest shares in this market by 2022
Browse More Reports Of Same Category: www.grandviewresearch.com/industry/pharmaceuticals
Grand View Research has segmented the global hyperlipidemia drugs market based on drug class and region:
Hyperlipidemia Drug Class Outlook (Revenue, USD Million, 2016–2022)
Statins
Bile Acid Sequestrants
Cholesterol Absorption Inhibitors
Fibric Acid Derivatives
PCSK9 Inhibitors
Combination
Miscellaneous
Hyperlipidemia Regional Outlook (Revenue, USD Million, 2016–2022)
US.
UK.
Germany
Spain
France
Italy
Japan
Browse Press Release of this Report: www.grandviewresearch.com/press-release/global-hyperlipidemia-drugs-market
About Grand View Research
Grand View Research, Inc. is a U.S. based market research and consulting company, registered in the State of California and headquartered in San Francisco. The company provides syndicated research reports, customized research reports, and consulting services. To help clients make informed business decisions, we offer market intelligence studies ensuring relevant and fact-based research across a range of industries, from technology to chemicals, materials and healthcare.
For More Information: www.grandviewresearch.com
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industryinsights-blog1 · 6 years ago
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Hyperlipidemia Drugs Market Exhibiting Growth At A CAGR of 2.3% By 2022
San Francisco, 21 Sep 2018: The global hyperlipidemia drugs market size is expected reach USD 22.6 billion by 2022, according to a new report by Grand View Research, Inc., expanding at a CAGR of 2.3% during the forecast period. Several factors, such as increase in target population and growth in awareness about risk of cardiovascular diseases (CVD) due to persistent hypercholesterolemia, are stoking the growth of the market.
Hyperlipidemia is the most common type of dyslipidemia and is generally caused by abnormally high lipid levels in the blood. This condition can occur due to genetic factors (primary hyperlipidemia) as well as other factors such as poor diet and unhealthy lifestyle (secondary hyperlipidemia). Statins are the first line of treatment for secondary hyperlipidemia.
Target population of antihyperlipidemic drugs is broadly divided into statin users and nonstatin users. The revenue share of statin users has been declining. The nonstatin users segment consists of statin intolerant and nonresponsive population as well as familial hyperlipidemia (FH) population. Nonstatin users are seeking high-efficacy alternatives and this is anticipated to boost the revenue of this segment.
Upcoming patent expirations are expected to lead to greater genericization in the market, mostly among statins, cholesterol absorption inhibitors, and combination drugs. However, new product launches are anticipated to continue to drive the market. Several novel mechanisms of action such as ACL inhibition, DGAT2 inhibition, and anti-ANGPTL-3 are being investigated for their potential for treatment of hyperlipidemia as well as for reducing the risk of CVD.
To request a sample copy or view summary of this report, click the link below:  www.grandviewresearch.com/industry-analysis/hyperlipidemia-drugs-market
Further key findings from the report suggest:
Statins dominated the drug classes in 2016 owing to their high usage as the first line of therapy
Recent launch of PCSK9 inhibitors, such as Repatha and Praluent, is likely to change the current therapeutic scenario due to their improved efficacy and safety profile
PCSK9 inhibitors are expected to displace existing expensive therapies, lomitapide, and mipomersen for the treatment of homozygous FH patients
Europe was the leading regional market in 2016. It is estimated to maintain its dominance till 2022 owing to high prevalence of hypercholesterolemia
There are fewer growth opportunities in Japan due to unavailability of key pipeline drugs such as bempedoic acid
AstraZeneca; Merck & Co., Inc.; Pfizer, Inc.; DAIICHI SANKYO COMPANY, LIMITED; Amgen, Inc.; and Sanofi are some of the key players operating in this market
Amgen, Inc.; Sanofi; and Esperion are expected to have the highest shares in this market by 2022
Browse more reports of this category by Grand View Research at: https://www.grandviewresearch.com/industry/pharmaceuticals
Grand View Research has segmented the global hyperlipidemia drugs market based on drug class and region:
Hyperlipidemia Drug Class Outlook (Revenue, USD Million, 2016 - 2022)
Statins
Bile Acid Sequestrants
Cholesterol Absorption Inhibitors
Fibric Acid Derivatives
PCSK9 Inhibitors
Combination
Miscellaneous
Hyperlipidemia Regional Outlook (Revenue, USD Million, 2016 - 2022)
U.S.
U.K.
Germany
Spain
France
Italy
Japan
Access press release of this research report by Grand View Research: www.grandviewresearch.com/press-release/global-hyperlipidemia-drugs-market
About Grand View Research:
Grand View Research, Inc. is a U.S. based market research and consulting company, registered in the State of California and headquartered in San Francisco. The company provides syndicated research reports, customized research reports, and consulting services. To help clients make informed business decisions, we offer market intelligence studies ensuring relevant and fact-based research across a range of industries, from technology to chemicals, materials and healthcare.
For More Information: www.grandviewresearch.com
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qyresearchgroups31-blog · 7 years ago
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Cardiovascular Disease Drugs Market Size, Share, Growth, Trends and Forecast 2017-2022
The Report “Global Cardiovascular Disease Drugs Market by Manufacturers, Regions, Type and Application” covers the manufacturers’ data, detailed view about regions and countries of the world; which demonstrates a regional development status, volume and value, including market size, as well as price data. Along with segment data, including: by Type and Application segment etc. On the basis of geography this report covers North America, Europe, Asia-Pacific, South America, Middle East and Africa.
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Market segment by Application, Cardiovascular Disease Drugs can be split into
Asischemic Heart Disease Dyslipidemia Stroke Thrombosis Atherosclerosis Coronary Artery Diseases Peripheral Artery Disease Others
Market segment by Type, Cardiovascular Disease Drugs can be split into
Heparin Coumadin Sectral Zebeta Lopressor Toprol XL Norvasc Lotrel Others
This report focuses on the top players in global market, like
AstraZeneca Johnson&Johnson Pfizer Sanofi Merck Daiichi Sankyo Company Limited Novartis Bayer Takeda Pharmaceutical Hoffmann-La Roche United Therapeutics Corporation Actelion Pharmaceuticals Boehringer Ingelheim Astellas Pharma
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