#Chronic Spontaneous Urticaria Market size
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Chronic Spontaneous Urticaria Market Size, Share and Forecast by 2025-2033
The Reports and Insights, a leading market research company, has recently releases report titled “Chronic Spontaneous Urticaria Market: Global Industry Trends, Share, Size, Growth, Opportunity and Forecast 2025-2033.” The study provides a detailed analysis of the industry, including the global Chronic Spontaneous Urticaria Market share, size, trends, and growth forecasts. The report also includes competitor and regional analysis and highlights the latest advancements in the market.
Report Highlights:
How big is the Chronic Spontaneous Urticaria Market?
The global chronic spontaneous urticaria market was valued at US$ 2,105.6 million in 2024 and is expected to register a CAGR of 7.8% over the forecast period, reaching US$ 4,139.5 million in 2033.
What are Chronic Spontaneous Urticaria?
Chronic Spontaneous Urticaria (CSU) is a skin condition characterized by the spontaneous appearance of hives (urticaria), swelling (angioedema), or both for more than six weeks without an identifiable trigger. It is believed to result from immune system dysfunction, leading to the release of histamine and other inflammatory mediators from mast cells. Symptoms include itchy, red, or swollen wheals that can vary in size and location. CSU significantly impacts quality of life and is managed with antihistamines, corticosteroids, or advanced therapies like biologics in refractory cases.
Request for a sample copy with detail analysis: https://www.reportsandinsights.com/sample-request/2641
What are the growth prospects and trends in the Chronic Spontaneous Urticaria industry?
The Chronic Spontaneous Urticaria (CSU) market growth is driven by various factors and trends. The Chronic Spontaneous Urticaria (CSU) market is driven by the rising prevalence of the condition, increasing awareness, and advancements in targeted biologic therapies. The market includes antihistamines, corticosteroids, and novel biologics like omalizumab, and emerging pipeline drugs aimed at long-term symptom control. Growth is fueled by expanding healthcare access, ongoing clinical research, and regulatory approvals for innovative treatments. North America and Europe dominate due to high diagnosis rates and advanced healthcare infrastructure, while Asia-Pacific presents lucrative opportunities with increasing patient awareness. Challenges include high treatment costs and the need for more effective long-term solutions. Hence, all these factors contribute to Chronic Spontaneous Urticaria (CSU) market growth.
What is included in market segmentation?
The report has segmented the market into the following categories:
By Treatment
Medication
Phototherapy
Others
By Diagnosis
Physical Examination
Blood Test
Allergy Test
Others
By Route of Administration
Oral
Topical
Parenteral
By End User
Hospitals
Specialty Clinics
Homecare
Others
North America
United States
Canada
Europe
Germany
United Kingdom
France
Italy
Spain
Russia
Poland
Benelux
Nordic
Rest of Europe
Asia Pacific
China
Japan
India
South Korea
ASEAN
Australia & New Zealand
Rest of Asia Pacific
Latin America
Brazil
Mexico
Argentina
Middle East & Africa
Saudi Arabia
South Africa
United Arab Emirates
Israel
Rest of MEA
Who are the key players operating in the industry?
The report covers the major market players including:
Hoffmann-La Roche Ltd.
Mylan N.V.
Teva Pharmaceutical Industries Ltd.
Sanofi
Pfizer Inc.
GlaxoSmithKline plc
Novartis AG
Bayer AG
Eli Lilly and Compan
Merck & Co., Inc.
Allergan
View Full Report: https://www.reportsandinsights.com/report/Chronic Spontaneous Urticaria-market
If you require any specific information that is not covered currently within the scope of the report, we will provide the same as a part of the customization.
About Us:
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Our offerings include comprehensive market intelligence in the form of research reports, production cost reports, feasibility studies, and consulting services. Our team, which includes experienced researchers and analysts from various industries, is dedicated to providing high-quality data and insights to our clientele, ranging from small and medium businesses to Fortune 1000 corporations.
Contact Us:
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#Chronic Spontaneous Urticaria Market share#Chronic Spontaneous Urticaria Market size#Chronic Spontaneous Urticaria Market trends
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Chronic Spontaneous Urticaria Market Size in the 7MM was ~USD 2100 Million in 2022 | DelveInsight
http://dlvr.it/T5sKZq
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Chronic Spontaneous Urticaria (CSU) Market Size and Share, Market Research Report 2030
DelveInsight’s ‘Chronic Spontaneous Urticaria (CSU) Market Insights, Epidemiology, and Market Forecast 2030’ report delivers an in-depth understanding of the Chronic Spontaneous Urticaria (CSU), historical and forecasted epidemiology as well as the market trends in the United States, EU5 (Germany, Spain, Italy, France, and United Kingdom), and Japan.
Geographies covered are:
The United States, EU5 (Germany, France, Italy, Spain, and the United Kingdom), and Japan
Click here and get access to a free sample copy of the report.
Chronic Spontaneous Urticaria (CSU) Disease Overview
Chronic urticaria is a debilitating disease that is characterized by itching and hives with or without angioedema, lasting for more than 6 weeks. Chronic urticaria might be triggered due to stimuli such as stroking or scratching the skin, exercise, emotional upset (cholinergic urticaria), cold, heat, pressure, sunlight (solar urticaria), contact with water or various chemicals (contact urticaria), or vibration.
Urticaria induced, thus, is known as chronic induced urticaria (CIndU). However, more commonly chronic urticaria is endogenous and independent of any external causes. This urticaria is known as Chronic Spontaneous Urticaria (CSU).
Chronic Spontaneous Urticaria (CSU) Epidemiology
The Chronic Spontaneous Urticaria (CSU) epidemiology division provides insights about the historical and current patient pool along with the forecasted trend for every seven major countries. It helps to recognize the causes of current and forecasted trends by exploring numerous studies and views of key opinion leaders. This part of the DelveInsight report also provides the diagnosed patient pool and their trends along with assumptions undertaken.
Key Findings
· The diagnosed prevalent cases of Chronic Spontaneous Urticaria (CSU) is increasing in 7MM during the study period, i.e., 2017–2030.
· The total Chronic Spontaneous Urticaria (CSU) prevalent cases associated in 7MM countries was 1,169,632 in 2017.
Chronic Spontaneous Urticaria (CSU) Drug Chapters
· Dupilumab: Sanofi/Regeneron
· Ligelizumab: Novartis Pharmaceuticals
Chronic Spontaneous Urticaria (CSU) Market Outlook
The Chronic Spontaneous Urticaria (CSU) market outlook of the report helps to build the detailed comprehension of the historic, current and forecasted Chronic Spontaneous Urticaria (CSU) market trends by analyzing the impact of current therapies on the market, unmet needs, drivers and barriers and demand of better technology.
According to DelveInsight, Chronic Spontaneous Urticaria market in 7MM is expected to grow in the study period 2017–2030.
Key Findings
· The Chronic Spontaneous Urticaria market size in the seven major markets was found to be USD 1,073.3 million in 2017.
Request for sample pages of the report: https://www.delveinsight.com/sample-request/chronic-spontaneous-urticaria-market
Chronic Spontaneous Urticaria (CSU) Drugs Uptake
Chronic Spontaneous Urticaria (CSU) Pipeline Development Activities
The report provides insights into the therapeutic candidate in Phase I, II and III stage. It also analyses Chronic Spontaneous Urticaria (CSU) key players involved in developing targeted therapeutics.
Major players include Sanofi/Regenron, Novartis, AstraZeneca, and others.
Pipeline Development Activities
The report covers the detailed information of collaborations, acquisition, and merger, licensing and patent details for Chronic Spontaneous Urticaria (CSU) emerging therapies.
Visit our repository of report: https://www.delveinsight.com/report-store.php
About DelveInsight:
DelveInsight is a leading Business Consultant, and Market Research Firm focused exclusively on life sciences. It supports pharma companies by providing end to end comprehensive solutions to improve their performance.
#Chronic Spontaneous Urticaria market#Chronic Spontaneous Urticaria market share#Chronic Spontaneous Urticaria market size#Chronic Spontaneous Urticaria market trends#Chronic Spontaneous Urticaria market research reports
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Stablon Tablets Reviews Uses, Dosage, Side Effects,Warnings and Precautions
Drug Online
stablon drug >> Generic drug of the therapeutic class: Neurology – psychiatry active ingredients: Tianeptine
what is stablon ?
This drug is recommended in depressive states of mild, moderate or severe intensity.
Stablon Tablets indication and Uses
Major depressive episodes (ie characterized).
stablon drug Dosage
The recommended dosage is 1 tablet at 12.5 mg three times a day, morning, noon and night, at the beginning of the main meals.
In chronic alcoholic, cirrhotic or non-cirrhotic, no dosage modification is necessary.
In patients over 70 years of age and in case of renal insufficiency, limit the dosage to 2 tablets per day.
Contraindications
Tianeptine hypersensitivity
Child under 15
Teenager aged 15 to 18
Fructose intolerance
Glucose malabsorption syndrome
Galactose malabsorption syndrome
Sucrase-isomaltase deficiency
Hypersensitivity to the active substance or to any of the excipients listed in section composition.
Children and adolescents under 15 years old.
How it works Stablon Tablets
Pharmacotherapeutic group: OTHER ANTIDEPRESSANTS.
ATC Code: N06AX14.
Tianeptine is an antidepressant:
In animals, tianeptine has the following characteristics:
Tianeptine increases the spontaneous activity of pyramidal cells of the hippocampus and accelerates their recovery after functional inhibition,
Tianeptine increases serotonin reuptake speed by neurons of the cortex and hippocampus.
In humans, tianeptine is characterized by:
A clear activity on somatic complaints, in particular digestive complaints related to anxiety and mood disorders.
Tianeptine also has no effect:
On sleep and vigilance,
On the cholinergic system (absence of anticholinergic manifestation)
Stablon Side Effects
Stablon Tablets Side Effects
Summary of the security profile:
The adverse effects seen with tianeptine in clinical trials are of moderate intensity. They consist mainly of nausea, constipation, abdominal pain, drowsiness, headache, dry mouth and dizziness.
Table of adverse effects
The following adverse reactions have been observed in clinical trials and / or the post-marketing use of tianeptine and are classified according to their frequency:
Very common ( ³ 1/10); frequent ( ³ 1/100, <1/10); uncommon ( ³ 1/1000, <1/100); rare ( ³ 1/10000, <1/1000); very rare (<1/10000), undetermined (can not be estimated from the available data).
Organ-Class System (SOC)
Frequency
Side effects
Metabolism and nutrition disorders
Frequent
Anorexia
indeterminate *
hyponatremia
Psychiatric disorders
Frequent
nightmares
Rare
Abuse, addiction, especially in subjects under 50 years of age with a history of drug dependence or alcohol dependence
indeterminate *
Idiosyncratic cases and suicidal behavior have been reported during treatment with tianeptine or shortly after discontinuation (see section 4.4).
Confusional state, hallucinations
Nervous system disorders
Frequent
Insomnia
Drowsiness
Dizzying sensations
headaches
presyncope
tremors
indeterminate *
Extrapyramidal disorders
dyskinesia
Heart conditions
Frequent
tachycardia
premature
Chest pain
Vascular disorders
Frequent
Hot flashes
Respiratory, thoracic and mediastinal disorders
Frequent
Dyspnea
Gastrointestinal disorders
Frequent
Gastralgias
Abdominal pain
Dry mouth
nausea
vomiting
Constipation
flatulence
Skin and subcutaneous tissue disorders
Rare
Maculopapular or erythematous rash
itching
Urticaria
indeterminate *
Acne
Exceptional bullous reactions
Musculoskeletal and systemic disorders
Frequent
myalgia
Low back pain
General disorders and administration site abnormalities
Frequent
Asthenia
Sensation of discomfort in the throat
Hepatobiliary disorders
indeterminate *
Increased liver enzymes
Hepatitis can be exceptionally severe
* Post-market data
Stablon Tablets Interactions
Associations advised against
Irreversible MAOIs (iproniazid): because of the risk of collapse or paroxysmal hypertension, hyperthermia, convulsions, death.
Stablon Tablets Warnings and Precautions
Special warnings
Prolonged use and high doses can lead to a state of dependence.
Do not exceed the recommended dosage.
Suicidal ideation and worsening of your depression or anxiety disorder
If you suffer from depression and / or anxiety disorders, you may sometimes have ideas of self-aggression (aggression towards yourself) or suicide. These events may be increased at the beginning of antidepressant treatment, as this type of medication does not act immediately but only after 2 weeks or more of treatment.
You are more likely to exhibit such events in the following cases:
if you have ever had suicidal thoughts or self-aggression in the past.
if you are a young adult. Clinical studies have shown that the risk of suicidal behavior is increased in adults under 25 with psychiatric illness and treated with antidepressants.
If you have suicidal thoughts or self-aggression, contact your doctor immediately or go directly to the hospital.
You can get help from a friend or relative, tell them you’re depressed or have an anxiety disorder, and ask them to read this leaflet. You can ask him to tell you if he thinks your depression or anxiety is getting worse, or if he’s worried about a change in your behavior.
Due to the presence of sucrose, this drug should not be used in cases of fructose intolerance, glucose-galactose malabsorption syndrome or sucrase-isomaltase deficiency (rare metabolic diseases).
Precautions for use
Do not stop treatment abruptly, but decrease dosage for 7 to 14 days.
If you have to have a general anesthesia, you should tell the resuscitator anesthesiologist who will be able to stop the treatment 24 or 48 hours before the procedure.
Tell your doctor in case of kidney failure.
IF IN DOUBT, DO NOT HESITATE TO ASK YOUR DOCTOR OR PHARMACIST FOR ADVICE.
Drive and use machines
In some patients, a decrease in alertness is likely to occur. Attention is therefore drawn to the risk of drowsiness associated with the use of this drug, especially for vehicle drivers and machine users.
stablon drug and PREGNANCY / BREAST FEEDING / FERTILITY
stablon in Pregnancy
Maintaining a good maternal psychic balance is desirable throughout pregnancy. If medication management is necessary to ensure this balance, it should be instituted or continued in an effective dose throughout pregnancy and if possible in monotherapy.
The animal data are reassuring, but the clinical data are still insufficient.
Given these data, it is best to avoid using tianeptine during pregnancy, regardless of the term. If it is essential to initiate or maintain treatment with tianeptine during pregnancy, consider the pharmacological profile of the drug for monitoring the newborn.
Breastfeeding
Tricyclic antidepressants are excreted in breast milk, so breastfeeding is not recommended for the duration of treatment.
Fertility
In rats, one study showed a decrease in reproductive performance in females (increased preimplantation losses) at maternotoxic dose.
The clinical impact is not known.
What happens if I overdose from Stablon Tablets ?
sYMPTOMS
Experience with cases of acute tianeptine intoxication (maximum quantity: 2250mg, ingested in a single dose) mainly highlights vigilance disorders that can go as far as coma, particularly in cases of multiple intoxications.
To behave
Tianeptine has no known specific antidote. In cases of acute intoxication, symptomatic treatment and routine surveillance should be established. Specialized medical monitoring is recommended.
What is Forms and Composition?
FORMS and PRESENTATIONS
12.5 mg coated tablet (white): Box of 28, in blister packs.
Hospital model: Box of 100, in blister packs.
COMPOSITION
p cp Tianeptine (INN) sodium salt 12.5 mg
Excipients: D-mannitol, corn starch, talc, magnesium stearate. Coating:ethylcellulose, glycerol oleate, Sepifilm SE 700 white (povidone, carmellose sodium, anhydrous colloidal silica, talc, sucrose, polysorbate 80, titanium dioxide, sodium bicarbonate), white beeswax.
Excipient with known effect: sucrose.
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 Stablon Tablets Reviews Uses, Dosage, Side Effects,Warnings and Precautions appeared first on Drug Online.
from Drug Online https://bit.ly/32XeKrM via Edrug Online from faculty of medicine https://bit.ly/3grjo41 via Faculty of Medicine
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Text
Stablon Tablets Reviews Uses, Dosage, Side Effects,Warnings and Precautions
Drug Online
stablon drug >> Generic drug of the therapeutic class: Neurology – psychiatry active ingredients: Tianeptine
what is stablon ?
This drug is recommended in depressive states of mild, moderate or severe intensity.
Stablon Tablets indication and Uses
Major depressive episodes (ie characterized).
stablon drug Dosage
The recommended dosage is 1 tablet at 12.5 mg three times a day, morning, noon and night, at the beginning of the main meals.
In chronic alcoholic, cirrhotic or non-cirrhotic, no dosage modification is necessary.
In patients over 70 years of age and in case of renal insufficiency, limit the dosage to 2 tablets per day.
Contraindications
Tianeptine hypersensitivity
Child under 15
Teenager aged 15 to 18
Fructose intolerance
Glucose malabsorption syndrome
Galactose malabsorption syndrome
Sucrase-isomaltase deficiency
Hypersensitivity to the active substance or to any of the excipients listed in section composition.
Children and adolescents under 15 years old.
How it works Stablon Tablets
Pharmacotherapeutic group: OTHER ANTIDEPRESSANTS.
ATC Code: N06AX14.
Tianeptine is an antidepressant:
In animals, tianeptine has the following characteristics:
Tianeptine increases the spontaneous activity of pyramidal cells of the hippocampus and accelerates their recovery after functional inhibition,
Tianeptine increases serotonin reuptake speed by neurons of the cortex and hippocampus.
In humans, tianeptine is characterized by:
A clear activity on somatic complaints, in particular digestive complaints related to anxiety and mood disorders.
Tianeptine also has no effect:
On sleep and vigilance,
On the cholinergic system (absence of anticholinergic manifestation)
Stablon Side Effects
Stablon Tablets Side Effects
Summary of the security profile:
The adverse effects seen with tianeptine in clinical trials are of moderate intensity. They consist mainly of nausea, constipation, abdominal pain, drowsiness, headache, dry mouth and dizziness.
Table of adverse effects
The following adverse reactions have been observed in clinical trials and / or the post-marketing use of tianeptine and are classified according to their frequency:
Very common ( ³ 1/10); frequent ( ³ 1/100, <1/10); uncommon ( ³ 1/1000, <1/100); rare ( ³ 1/10000, <1/1000); very rare (<1/10000), undetermined (can not be estimated from the available data).
Organ-Class System (SOC)
Frequency
Side effects
Metabolism and nutrition disorders
Frequent
Anorexia
indeterminate *
hyponatremia
Psychiatric disorders
Frequent
nightmares
Rare
Abuse, addiction, especially in subjects under 50 years of age with a history of drug dependence or alcohol dependence
indeterminate *
Idiosyncratic cases and suicidal behavior have been reported during treatment with tianeptine or shortly after discontinuation (see section 4.4).
Confusional state, hallucinations
Nervous system disorders
Frequent
Insomnia
Drowsiness
Dizzying sensations
headaches
presyncope
tremors
indeterminate *
Extrapyramidal disorders
dyskinesia
Heart conditions
Frequent
tachycardia
premature
Chest pain
Vascular disorders
Frequent
Hot flashes
Respiratory, thoracic and mediastinal disorders
Frequent
Dyspnea
Gastrointestinal disorders
Frequent
Gastralgias
Abdominal pain
Dry mouth
nausea
vomiting
Constipation
flatulence
Skin and subcutaneous tissue disorders
Rare
Maculopapular or erythematous rash
itching
Urticaria
indeterminate *
Acne
Exceptional bullous reactions
Musculoskeletal and systemic disorders
Frequent
myalgia
Low back pain
General disorders and administration site abnormalities
Frequent
Asthenia
Sensation of discomfort in the throat
Hepatobiliary disorders
indeterminate *
Increased liver enzymes
Hepatitis can be exceptionally severe
* Post-market data
Stablon Tablets Interactions
Associations advised against
Irreversible MAOIs (iproniazid): because of the risk of collapse or paroxysmal hypertension, hyperthermia, convulsions, death.
Stablon Tablets Warnings and Precautions
Special warnings
Prolonged use and high doses can lead to a state of dependence.
Do not exceed the recommended dosage.
Suicidal ideation and worsening of your depression or anxiety disorder
If you suffer from depression and / or anxiety disorders, you may sometimes have ideas of self-aggression (aggression towards yourself) or suicide. These events may be increased at the beginning of antidepressant treatment, as this type of medication does not act immediately but only after 2 weeks or more of treatment.
You are more likely to exhibit such events in the following cases:
if you have ever had suicidal thoughts or self-aggression in the past.
if you are a young adult. Clinical studies have shown that the risk of suicidal behavior is increased in adults under 25 with psychiatric illness and treated with antidepressants.
If you have suicidal thoughts or self-aggression, contact your doctor immediately or go directly to the hospital.
You can get help from a friend or relative, tell them you’re depressed or have an anxiety disorder, and ask them to read this leaflet. You can ask him to tell you if he thinks your depression or anxiety is getting worse, or if he’s worried about a change in your behavior.
Due to the presence of sucrose, this drug should not be used in cases of fructose intolerance, glucose-galactose malabsorption syndrome or sucrase-isomaltase deficiency (rare metabolic diseases).
Precautions for use
Do not stop treatment abruptly, but decrease dosage for 7 to 14 days.
If you have to have a general anesthesia, you should tell the resuscitator anesthesiologist who will be able to stop the treatment 24 or 48 hours before the procedure.
Tell your doctor in case of kidney failure.
IF IN DOUBT, DO NOT HESITATE TO ASK YOUR DOCTOR OR PHARMACIST FOR ADVICE.
Drive and use machines
In some patients, a decrease in alertness is likely to occur. Attention is therefore drawn to the risk of drowsiness associated with the use of this drug, especially for vehicle drivers and machine users.
stablon drug and PREGNANCY / BREAST FEEDING / FERTILITY
stablon in Pregnancy
Maintaining a good maternal psychic balance is desirable throughout pregnancy. If medication management is necessary to ensure this balance, it should be instituted or continued in an effective dose throughout pregnancy and if possible in monotherapy.
The animal data are reassuring, but the clinical data are still insufficient.
Given these data, it is best to avoid using tianeptine during pregnancy, regardless of the term. If it is essential to initiate or maintain treatment with tianeptine during pregnancy, consider the pharmacological profile of the drug for monitoring the newborn.
Breastfeeding
Tricyclic antidepressants are excreted in breast milk, so breastfeeding is not recommended for the duration of treatment.
Fertility
In rats, one study showed a decrease in reproductive performance in females (increased preimplantation losses) at maternotoxic dose.
The clinical impact is not known.
What happens if I overdose from Stablon Tablets ?
sYMPTOMS
Experience with cases of acute tianeptine intoxication (maximum quantity: 2250mg, ingested in a single dose) mainly highlights vigilance disorders that can go as far as coma, particularly in cases of multiple intoxications.
To behave
Tianeptine has no known specific antidote. In cases of acute intoxication, symptomatic treatment and routine surveillance should be established. Specialized medical monitoring is recommended.
What is Forms and Composition?
FORMS and PRESENTATIONS
12.5 mg coated tablet (white): Box of 28, in blister packs.
Hospital model: Box of 100, in blister packs.
COMPOSITION
p cp Tianeptine (INN) sodium salt 12.5 mg
Excipients: D-mannitol, corn starch, talc, magnesium stearate. Coating:ethylcellulose, glycerol oleate, Sepifilm SE 700 white (povidone, carmellose sodium, anhydrous colloidal silica, talc, sucrose, polysorbate 80, titanium dioxide, sodium bicarbonate), white beeswax.
Excipient with known effect: sucrose.
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 Stablon Tablets Reviews Uses, Dosage, Side Effects,Warnings and Precautions appeared first on Drug Online.
from Drug Online https://bit.ly/32XeKrM via Edrug Online
0 notes
Text
Ventolin inhaler Uses, Dosage, Side Effects, Precautions &Warnings
Drug Online
ventolin inhaler Generic drug of the therapeutic class: Pulmonology active ingredients: Salbutamol
Important to know about Ventolin ?
It is a bronchodilator (it increases the size of the bronchi) fast acting and short duration.
It is administered by inhalation with the help of a nebuliser (nebuliser).
The use of this drug in this mode of administration should be reserved for the treatment of severe asthma attacks in children and infants, when these situations require the inhalation of high doses of salbutamol.
ventolin used for and indication
Dosage 1.25 mg / 2.5 ml: Symptomatic treatment of severe acute asthma in children and infants.
Dosages at 2.5 mg / 2.5 ml and at 5 mg / 2.5 ml:
Symptomatic treatment of severe acute asthma.
Treatment of acute attacks of chronic obstructive pulmonary disease in adults.
Note:
Severe acute asthma requires hospitalization in the intensive care unit.
Oxygen therapy and systemic corticosteroids should be combined with bronchodilator therapy.
ventolin dosage
Dosage :
This low dose presentation is not suitable for the treatment of adults, but for that of children and infants.
children and infants :
50 to 150 μg of salbutamol / kg (ie 0.1 to 0.3 ml / kg of this solution) without generally exceeding 5 mg (4 single doses of 2.5 ml) of nebulized salbutamol.
Nebulization can be repeated every 20 to 30 minutes depending on the clinical outcome and the tolerance of the treatment.
Method of administration :
– Inhaled route exclusively.This salbutamol solution should be administered by inhalation using a nebulizer (nebulizer). DO NOT INJECT – DO NOT AVALER.
– For the use and maintenance of the nebuliser, follow the instructions given by the manufacturer of the device used.
– The solution is ready for use, however if dilution is necessary, it must be performed in sterile saline.
Remove a single-dose container from the blister.
Open the container by twisting its upper end vigorously.
Squeeze the container to empty it into the nebulizer reservoir.
Assemble the nebulizer for administration according to the manufacturer’s instructions.
Eye contact should be avoided by aerosol generated by the nebulizer.
– With pneumatic nebulizers, the flow of air or oxygen to pulse the solution will be adapted according to the patient’s condition and the recommendations of the manufacturer of the nebuliser.
– Nebulization should generally not exceed 10 to 20 minutes.
– The technique of use by the patient must be checked regularly.
– After the nebulization, the unused solution remaining in the tank of the device must be discarded. Cleaning and maintenance of the equipment will be done according to the manufacturer’s recommendations.
– Single-dose containers do not contain preservatives, they should be used immediately after opening. For each nebulization a new container must be used. The contents of partially open or damaged single-dose containers should not be administered.
ventolin how it works
ATC Code: R03AC02.
BETA2 MIMETIC BRONCHODILATOR WITH RAPID ACTION AND SHORT-TERM INHALATION.
Salbutamol is a selective beta2 receptor agonist.
After inhalation, salbutamol exerts a stimulating action on the beta2 receptors of the bronchial smooth muscle thus ensuring rapid bronchodilatation, significant in minutes, persisting for 4 to 6 hours.
What are the side effects of Ventolin inhaler?
The side effects are listed below, listed by organ class and frequency. Frequencies are defined as very common (≥1 / 10), frequent (≥1 / 100 and <1/10), uncommon (≥1 / 1000 and <1/100), rare (≥1 / 10000 and <1) / 1000) and very rare (<1/10000) including isolated cases. Very frequent and frequent effects have generally been described in clinical trials. Rare and very rare side effects are usually from spontaneous post-marketing reports.
Class organ
Side effects
Frequency
Immune system disorders
Very rare hypersensitivity reactions including: angioneurotic edema, urticaria, pruritus, bronchospasm, hypotension, collapse
Very rare
Metabolism and nutrition disorders
hypokalemia *
Very rare
Nervous system disorders
Headaches, tremors
Frequent
Psychiatric disorders
Behavioral disorders: nervousness, agitation
Very rare
Heart conditions
Tachycardia Palpitations Cardiac arrhythmias (including atrial fibrillation, supraventricular tachycardia and extrasystoles)
Frequent Uncommon Very rare
Vascular disorders
Peripheral vasodilatation Very rare
Very rare
Respiratory, thoracic and mediastinal disorders
Paradoxical bronchospasm ** Very rare
Very rare
Gastrointestinal disorders
Irritation of the mouth and throat
Rare
Musculoskeletal and systemic disorders
Muscle cramps
Rare
* Beta-2 mimetics administered at very high doses may lead to hypokalaemias.
** As with other inhaled products, possibility of coughing and rarely paradoxical bronchospasm following inhalation. Do not restart this drug and use another fast-acting bronchodilator to relieve bronchospasm. The treatment should then be reassessed to consider, if necessary, the prescription of a therapeutic alternative.
High dose beta-2 mimetics may result in reversible hyperglycaemia upon discontinuation of therapy.
ventolin drug (inhaler) interactions
Not applicable.
Ventolin Warnings and Precautions
WARNINGS:
– Administration of salbutamol with a nebulizer should be restricted to acute, severe situations requiring inhalation of a high inhaled dose.
These situations require medical surveillance with the possibility of setting up resuscitation (venous access and respiratory assistance); systemic oxygen therapy and corticosteroids usually need to be combined.
– The attention of athletes will be drawn to the fact that this specialty contains an active ingredient that can induce a positive reaction of the tests performed during doping controls.
PRECAUTIONS FOR EMPLOYMENT:
– This low dose presentation is not adapted to the treatment of the adult, but to that of the child and the infant (see posology).
– In case of bronchial infection or bronchorrhea abundant, appropriate treatment is necessary to promote the optimal diffusion of the product in the respiratory tract.
– This medication should be used with caution in hyperthyroidism, cardiovascular disease, including obstructive cardiomyopathy, coronary heart disease, arrhythmias, high blood pressure, and diabetes mellitus.
– High dose beta2 mimetics may cause hypokalemia that may lead to the occurrence of cardiac arrhythmias. Monitoring of serum potassium is recommended whenever possible, particularly when concomitant use of hypokalaemic therapies, hypoxia or in subjects with increased risk of torsades de pointes (long QT or treatments likely to increase QTc).
– Pregnancy: in case of administration before delivery take into account the peripheral vasodilator effect of beta2 mimetics.
– Breast-feeding: beta2 mimetics pass into breast milk.
Drive and use machines:
Not applicable.
Ventolin and PREGNANCY / BREAST FEEDING / FERTILITY
Pregnancy :
Clinically, there is a significant decline, with a sufficient number of documented pregnancies, so that we can conclude on the safety of salbutamol during pregnancy.
As a result, inhaled salbutamol can be administered during pregnancy.
When administered during pregnancy, an acceleration of the fetal heart rate may be observed in parallel with maternal tachycardia. It is exceptional to see her persist at birth.
Similarly, postnatal blood glucose values are only exceptionally disturbed.
When administered before delivery, consider the peripheral vasodilator effect of beta-2-mimetics.
Breastfeeding:
Beta-2-mimetics pass into breast milk.
Immediately consult your doctor or pharmacist.
What is Forms and Composition Ventolin?
FORMS and PRESENTATIONS
1.25 mg / 2.5 ml Nebulizer Inhalation Solution : 2.5 ml single-dose containers, box of 20. 2.5 mg / 2.5 ml and 5 mg / 2.5 Nebulizer Inhalation Solution ml: Single-dose containers of 2.5 ml, box of 60.
COMPOSITION
p single doseSalbutamol (DCI)1.25 mgor2.5 mgor5 mg(as sulphate: 1.5 mg, 3 mg or 6 mg per dose)
Excipients (common): sodium chloride, dilute sulfuric acid, purified water (1.25 mg / 2.5 mL sol), water ppi (2.5 mg sol and 5 mg / 2.5 mL).
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 Ventolin inhaler Uses, Dosage, Side Effects, Precautions &Warnings appeared first on Drug Online.
from Drug Online https://bit.ly/3fz3XXO via Edrug Online from Faculty of Medicine https://bit.ly/37FcSnu via Internal Medicine
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Global Chronic Spontaneous Urticaria Market Significant Trends and Factors Driving the Market Development Forecast to 2027
Global chronic spontaneous urticaria market is expected to gain market growth in the forecast period of 2020 to 2027. Data Bridge Market Research analyses the market is growing at a healthy CAGR in the above-mentioned research forecast period. Emerging markets and huge investment in research and development are the factors responsible for the growth of this market.
The major players covered in the global chronic spontaneous urticaria market are Novartis AG, F. Hoffmann-La Roche Ltd, Pfizer, Inc., Allergan, AbbVie Inc, Sun Pharmaceutical Industries Ltd, Wockhardt Bio AG, Hikma Pharmaceuticals PLC, Mylan N.V., Horizon Therapeutics plc and others.
Get Sample Copy + All Related Graphs@ https://www.databridgemarketresearch.com/request-a-sample/?dbmr=global-chronic-spontaneous-urticaria-market
Key Questions Answered in This Report
– What will the market size be in 2027?
– What are the key factors driving the global marine scrubber system market?
– What are the challenges to market growth?
– Who are the key players in the marine scrubber system market?
– What are the market opportunities and threats faced by the key players?
Global Chronic Spontaneous Urticaria Market: Segmentation
Chronic spontaneous urticaria market is segmented on the basis of treatment, diagnosis, route of administration, end-users and distribution channel.
On the basis of treatment, the global chronic spontaneous urticaria market is segmented into medication, phototherapy and others. Medication can be further segmented into H2 blockers, corticosteroids, antidepressants, monoclonal antibodies and others
Based on diagnosis, the global chronic spontaneous urticaria market is segmented into physical examination, blood test, allergy test and others Route of administration segment of global chronic spontaneous urticaria market is segmented into oral, topical and parenteral
On the basis of end-users, the global chronic spontaneous urticaria market is segmented into hospitals, homecare, specialty clinics and others
On the basis of distribution channel, the global chronic spontaneous urticaria market has been bifurcated into hospital pharmacy, online pharmacy and retail pharmacy
Table of Contents
1. Introduction 2. Market Segmentation 3. Market Overview 4. Executive Summary 5. Premium Insights 6. Global, By Component 7. Product Type 8. Delivery 9. Industry Type 10. Geography 10.1. Overview 10.2. North America 10.3. Europe 10.4. Asia-Pacific 10.5. South America 10.6. Middle East & Africa 11. Company Landscape 12. Company Profiles 13. Related Reports
Get Detailed TOC @ https://www.databridgemarketresearch.com/toc/?dbmr=global-chronic-spontaneous-urticaria-market
Contact:
Data Bridge Market Research US: +1 888 387 2818 UK: +44 208 089 1725 Hong Kong: +852 8192 7475 Email: [email protected]
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Chronic Spontaneous Urticaria (CSU) Epidemiology Insights
· Total diagnosed prevalent population of Chronic Spontaneous Urticaria (CSU) in 7MM in 2020 was 1,182,486 cases.
· Germany was accounted for the highest prevalent population with 122,708 cases.
· Prevalent population of France in 2020 was 103,819 cases.
· Spain accounted for the lowest prevalent population in 2020 with 76,343 cases
Source: https://www.delveinsight.com/report-store/chronic-spontaneous-urticaria-market
#Chronic Spontaneous Urticaria market#Chronic Spontaneous Urticaria market share#Chronic Spontaneous Urticaria market size#Chronic Spontaneous Urticaria market trends#Chronic Spontaneous Urticaria market research reports#Chronic Spontaneous Urticaria market outlook
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Stablon Tablets Reviews Uses, Dosage, Side Effects,Warnings and Precautions
Drug Online
stablon drug >> Generic drug of the therapeutic class: Neurology – psychiatry active ingredients: Tianeptine
Important to know about stablon drug ?
This drug is recommended in depressive states of mild, moderate or severe intensity.
Stablon Tablets indication and Uses
Major depressive episodes (ie characterized).
stablon drug Dosage
The recommended dosage is 1 tablet at 12.5 mg three times a day, morning, noon and night, at the beginning of the main meals.
In chronic alcoholic, cirrhotic or non-cirrhotic, no dosage modification is necessary.
In patients over 70 years of age and in case of renal insufficiency, limit the dosage to 2 tablets per day.
How it works Stablon Tablets
Pharmacotherapeutic group: OTHER ANTIDEPRESSANTS.
ATC Code: N06AX14.
Tianeptine is an antidepressant:
In animals, tianeptine has the following characteristics:
Tianeptine increases the spontaneous activity of pyramidal cells of the hippocampus and accelerates their recovery after functional inhibition,
Tianeptine increases serotonin reuptake speed by neurons of the cortex and hippocampus.
In humans, tianeptine is characterized by:
A clear activity on somatic complaints, in particular digestive complaints related to anxiety and mood disorders.
Tianeptine also has no effect:
On sleep and vigilance,
On the cholinergic system (absence of anticholinergic manifestation)
Stablon Side Effects
Stablon Tablets Side Effects
Summary of the security profile:
The adverse effects seen with tianeptine in clinical trials are of moderate intensity. They consist mainly of nausea, constipation, abdominal pain, drowsiness, headache, dry mouth and dizziness.
Table of adverse effects
The following adverse reactions have been observed in clinical trials and / or the post-marketing use of tianeptine and are classified according to their frequency:
Very common ( ³ 1/10); frequent ( ³ 1/100, <1/10); uncommon ( ³ 1/1000, <1/100); rare ( ³ 1/10000, <1/1000); very rare (<1/10000), undetermined (can not be estimated from the available data).
Organ-Class System (SOC)
Frequency
Side effects
Metabolism and nutrition disorders
Frequent
Anorexia
indeterminate *
hyponatremia
Psychiatric disorders
Frequent
nightmares
Rare
Abuse, addiction, especially in subjects under 50 years of age with a history of drug dependence or alcohol dependence
indeterminate *
Idiosyncratic cases and suicidal behavior have been reported during treatment with tianeptine or shortly after discontinuation (see section 4.4).
Confusional state, hallucinations
Nervous system disorders
Frequent
Insomnia
Drowsiness
Dizzying sensations
headaches
presyncope
tremors
indeterminate *
Extrapyramidal disorders
dyskinesia
Heart conditions
Frequent
tachycardia
premature
Chest pain
Vascular disorders
Frequent
Hot flashes
Respiratory, thoracic and mediastinal disorders
Frequent
Dyspnea
Gastrointestinal disorders
Frequent
Gastralgias
Abdominal pain
Dry mouth
nausea
vomiting
Constipation
flatulence
Skin and subcutaneous tissue disorders
Rare
Maculopapular or erythematous rash
itching
Urticaria
indeterminate *
Acne
Exceptional bullous reactions
Musculoskeletal and systemic disorders
Frequent
myalgia
Low back pain
General disorders and administration site abnormalities
Frequent
Asthenia
Sensation of discomfort in the throat
Hepatobiliary disorders
indeterminate *
Increased liver enzymes
Hepatitis can be exceptionally severe
* Post-market data
Stablon Tablets Interactions
Associations advised against
Irreversible MAOIs (iproniazid): because of the risk of collapse or paroxysmal hypertension, hyperthermia, convulsions, death.
Stablon Tablets Warnings and Precautions
Special warnings
Prolonged use and high doses can lead to a state of dependence.
Do not exceed the recommended dosage.
Suicidal ideation and worsening of your depression or anxiety disorder
If you suffer from depression and / or anxiety disorders, you may sometimes have ideas of self-aggression (aggression towards yourself) or suicide. These events may be increased at the beginning of antidepressant treatment, as this type of medication does not act immediately but only after 2 weeks or more of treatment.
You are more likely to exhibit such events in the following cases:
if you have ever had suicidal thoughts or self-aggression in the past.
if you are a young adult. Clinical studies have shown that the risk of suicidal behavior is increased in adults under 25 with psychiatric illness and treated with antidepressants.
If you have suicidal thoughts or self-aggression, contact your doctor immediately or go directly to the hospital.
You can get help from a friend or relative, tell them you’re depressed or have an anxiety disorder, and ask them to read this leaflet. You can ask him to tell you if he thinks your depression or anxiety is getting worse, or if he’s worried about a change in your behavior.
Due to the presence of sucrose, this drug should not be used in cases of fructose intolerance, glucose-galactose malabsorption syndrome or sucrase-isomaltase deficiency (rare metabolic diseases).
Precautions for use
Do not stop treatment abruptly, but decrease dosage for 7 to 14 days.
If you have to have a general anesthesia, you should tell the resuscitator anesthesiologist who will be able to stop the treatment 24 or 48 hours before the procedure.
Tell your doctor in case of kidney failure.
IF IN DOUBT, DO NOT HESITATE TO ASK YOUR DOCTOR OR PHARMACIST FOR ADVICE.
Drive and use machines
In some patients, a decrease in alertness is likely to occur. Attention is therefore drawn to the risk of drowsiness associated with the use of this drug, especially for vehicle drivers and machine users.
stablon drug and PREGNANCY / BREAST FEEDING / FERTILITY
stablon in Pregnancy
Maintaining a good maternal psychic balance is desirable throughout pregnancy. If medication management is necessary to ensure this balance, it should be instituted or continued in an effective dose throughout pregnancy and if possible in monotherapy.
The animal data are reassuring, but the clinical data are still insufficient.
Given these data, it is best to avoid using tianeptine during pregnancy, regardless of the term. If it is essential to initiate or maintain treatment with tianeptine during pregnancy, consider the pharmacological profile of the drug for monitoring the newborn.
Breastfeeding
Tricyclic antidepressants are excreted in breast milk, so breastfeeding is not recommended for the duration of treatment.
Fertility
In rats, one study showed a decrease in reproductive performance in females (increased preimplantation losses) at maternotoxic dose.
The clinical impact is not known.
What happens if I overdose from Stablon Tablets ?
sYMPTOMS
Experience with cases of acute tianeptine intoxication (maximum quantity: 2250mg, ingested in a single dose) mainly highlights vigilance disorders that can go as far as coma, particularly in cases of multiple intoxications.
To behave
Tianeptine has no known specific antidote. In cases of acute intoxication, symptomatic treatment and routine surveillance should be established. Specialized medical monitoring is recommended.
What is Forms and Composition?
FORMS and PRESENTATIONS
12.5 mg coated tablet (white): Box of 28, in blister packs.
Hospital model: Box of 100, in blister packs.
COMPOSITION
p cp Tianeptine (INN) sodium salt 12.5 mg
Excipients: D-mannitol, corn starch, talc, magnesium stearate. Coating:ethylcellulose, glycerol oleate, Sepifilm SE 700 white (povidone, carmellose sodium, anhydrous colloidal silica, talc, sucrose, polysorbate 80, titanium dioxide, sodium bicarbonate), white beeswax.
Excipient with known effect: sucrose.
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.
Related POSt’s
Betadine (Povidone-iodine) Uses, Dosage, Side Effects, Precautions
MEDIATOR Uses, Dosage, Side Effects, Precautions & Warnings
Paracetamol Teva Uses, Dosage, Side Effects, Precautions
Dacryoserum Eyewash Uses, Dosage, Side Effects, Precautions
Celebrex (Celecoxib) Capsule Uses, Dosage, Side Effects, Precautions
Related Keyword’s
stablon 12.5 mg 60 tablet stablon tablet use stablon tablet stablon 12.5 mg tablet stablon tablet dosage stablon tablet price stablon tablet uses stablon tablets side effects stablon tianeptine tablets
The post Stablon Tablets Reviews Uses, Dosage, Side Effects,Warnings and Precautions appeared first on Drug Online.
from Drug Online https://bit.ly/32XeKrM via Edrug Online from faculty of medicine https://bit.ly/331LSP7 via Faculty of Medicine
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Stablon Tablets Reviews Uses, Dosage, Side Effects,Warnings and Precautions
Drug Online
stablon drug >> Generic drug of the therapeutic class: Neurology – psychiatry active ingredients: Tianeptine
Important to know about stablon drug ?
This drug is recommended in depressive states of mild, moderate or severe intensity.
Stablon Tablets indication and Uses
Major depressive episodes (ie characterized).
stablon drug Dosage
The recommended dosage is 1 tablet at 12.5 mg three times a day, morning, noon and night, at the beginning of the main meals.
In chronic alcoholic, cirrhotic or non-cirrhotic, no dosage modification is necessary.
In patients over 70 years of age and in case of renal insufficiency, limit the dosage to 2 tablets per day.
How it works Stablon Tablets
Pharmacotherapeutic group: OTHER ANTIDEPRESSANTS.
ATC Code: N06AX14.
Tianeptine is an antidepressant:
In animals, tianeptine has the following characteristics:
Tianeptine increases the spontaneous activity of pyramidal cells of the hippocampus and accelerates their recovery after functional inhibition,
Tianeptine increases serotonin reuptake speed by neurons of the cortex and hippocampus.
In humans, tianeptine is characterized by:
A clear activity on somatic complaints, in particular digestive complaints related to anxiety and mood disorders.
Tianeptine also has no effect:
On sleep and vigilance,
On the cholinergic system (absence of anticholinergic manifestation)
Stablon Side Effects
Stablon Tablets Side Effects
Summary of the security profile:
The adverse effects seen with tianeptine in clinical trials are of moderate intensity. They consist mainly of nausea, constipation, abdominal pain, drowsiness, headache, dry mouth and dizziness.
Table of adverse effects
The following adverse reactions have been observed in clinical trials and / or the post-marketing use of tianeptine and are classified according to their frequency:
Very common ( ³ 1/10); frequent ( ³ 1/100, <1/10); uncommon ( ³ 1/1000, <1/100); rare ( ³ 1/10000, <1/1000); very rare (<1/10000), undetermined (can not be estimated from the available data).
Organ-Class System (SOC)
Frequency
Side effects
Metabolism and nutrition disorders
Frequent
Anorexia
indeterminate *
hyponatremia
Psychiatric disorders
Frequent
nightmares
Rare
Abuse, addiction, especially in subjects under 50 years of age with a history of drug dependence or alcohol dependence
indeterminate *
Idiosyncratic cases and suicidal behavior have been reported during treatment with tianeptine or shortly after discontinuation (see section 4.4).
Confusional state, hallucinations
Nervous system disorders
Frequent
Insomnia
Drowsiness
Dizzying sensations
headaches
presyncope
tremors
indeterminate *
Extrapyramidal disorders
dyskinesia
Heart conditions
Frequent
tachycardia
premature
Chest pain
Vascular disorders
Frequent
Hot flashes
Respiratory, thoracic and mediastinal disorders
Frequent
Dyspnea
Gastrointestinal disorders
Frequent
Gastralgias
Abdominal pain
Dry mouth
nausea
vomiting
Constipation
flatulence
Skin and subcutaneous tissue disorders
Rare
Maculopapular or erythematous rash
itching
Urticaria
indeterminate *
Acne
Exceptional bullous reactions
Musculoskeletal and systemic disorders
Frequent
myalgia
Low back pain
General disorders and administration site abnormalities
Frequent
Asthenia
Sensation of discomfort in the throat
Hepatobiliary disorders
indeterminate *
Increased liver enzymes
Hepatitis can be exceptionally severe
* Post-market data
Stablon Tablets Interactions
Associations advised against
Irreversible MAOIs (iproniazid): because of the risk of collapse or paroxysmal hypertension, hyperthermia, convulsions, death.
Stablon Tablets Warnings and Precautions
Special warnings
Prolonged use and high doses can lead to a state of dependence.
Do not exceed the recommended dosage.
Suicidal ideation and worsening of your depression or anxiety disorder
If you suffer from depression and / or anxiety disorders, you may sometimes have ideas of self-aggression (aggression towards yourself) or suicide. These events may be increased at the beginning of antidepressant treatment, as this type of medication does not act immediately but only after 2 weeks or more of treatment.
You are more likely to exhibit such events in the following cases:
if you have ever had suicidal thoughts or self-aggression in the past.
if you are a young adult. Clinical studies have shown that the risk of suicidal behavior is increased in adults under 25 with psychiatric illness and treated with antidepressants.
If you have suicidal thoughts or self-aggression, contact your doctor immediately or go directly to the hospital.
You can get help from a friend or relative, tell them you’re depressed or have an anxiety disorder, and ask them to read this leaflet. You can ask him to tell you if he thinks your depression or anxiety is getting worse, or if he’s worried about a change in your behavior.
Due to the presence of sucrose, this drug should not be used in cases of fructose intolerance, glucose-galactose malabsorption syndrome or sucrase-isomaltase deficiency (rare metabolic diseases).
Precautions for use
Do not stop treatment abruptly, but decrease dosage for 7 to 14 days.
If you have to have a general anesthesia, you should tell the resuscitator anesthesiologist who will be able to stop the treatment 24 or 48 hours before the procedure.
Tell your doctor in case of kidney failure.
IF IN DOUBT, DO NOT HESITATE TO ASK YOUR DOCTOR OR PHARMACIST FOR ADVICE.
Drive and use machines
In some patients, a decrease in alertness is likely to occur. Attention is therefore drawn to the risk of drowsiness associated with the use of this drug, especially for vehicle drivers and machine users.
stablon drug and PREGNANCY / BREAST FEEDING / FERTILITY
stablon in Pregnancy
Maintaining a good maternal psychic balance is desirable throughout pregnancy. If medication management is necessary to ensure this balance, it should be instituted or continued in an effective dose throughout pregnancy and if possible in monotherapy.
The animal data are reassuring, but the clinical data are still insufficient.
Given these data, it is best to avoid using tianeptine during pregnancy, regardless of the term. If it is essential to initiate or maintain treatment with tianeptine during pregnancy, consider the pharmacological profile of the drug for monitoring the newborn.
Breastfeeding
Tricyclic antidepressants are excreted in breast milk, so breastfeeding is not recommended for the duration of treatment.
Fertility
In rats, one study showed a decrease in reproductive performance in females (increased preimplantation losses) at maternotoxic dose.
The clinical impact is not known.
What happens if I overdose from Stablon Tablets ?
sYMPTOMS
Experience with cases of acute tianeptine intoxication (maximum quantity: 2250mg, ingested in a single dose) mainly highlights vigilance disorders that can go as far as coma, particularly in cases of multiple intoxications.
To behave
Tianeptine has no known specific antidote. In cases of acute intoxication, symptomatic treatment and routine surveillance should be established. Specialized medical monitoring is recommended.
What is Forms and Composition?
FORMS and PRESENTATIONS
12.5 mg coated tablet (white): Box of 28, in blister packs.
Hospital model: Box of 100, in blister packs.
COMPOSITION
p cp Tianeptine (INN) sodium salt 12.5 mg
Excipients: D-mannitol, corn starch, talc, magnesium stearate. Coating:ethylcellulose, glycerol oleate, Sepifilm SE 700 white (povidone, carmellose sodium, anhydrous colloidal silica, talc, sucrose, polysorbate 80, titanium dioxide, sodium bicarbonate), white beeswax.
Excipient with known effect: sucrose.
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.
Related POSt’s
Betadine (Povidone-iodine) Uses, Dosage, Side Effects, Precautions
MEDIATOR Uses, Dosage, Side Effects, Precautions & Warnings
Paracetamol Teva Uses, Dosage, Side Effects, Precautions
Dacryoserum Eyewash Uses, Dosage, Side Effects, Precautions
Celebrex (Celecoxib) Capsule Uses, Dosage, Side Effects, Precautions
Related Keyword’s
stablon 12.5 mg 60 tablet stablon tablet use stablon tablet stablon 12.5 mg tablet stablon tablet dosage stablon tablet price stablon tablet uses stablon tablets side effects stablon tianeptine tablets
The post Stablon Tablets Reviews Uses, Dosage, Side Effects,Warnings and Precautions appeared first on Drug Online.
from Drug Online https://bit.ly/32XeKrM via Edrug Online
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Ventolin inhaler Uses, Dosage, Side Effects, Precautions &Warnings
Drug Online
ventolin inhaler Generic drug of the therapeutic class: Pulmonology active ingredients: Salbutamol
Important to know about Ventolin ?
It is a bronchodilator (it increases the size of the bronchi) fast acting and short duration.
It is administered by inhalation with the help of a nebuliser (nebuliser).
The use of this drug in this mode of administration should be reserved for the treatment of severe asthma attacks in children and infants, when these situations require the inhalation of high doses of salbutamol.
ventolin used for and indication
Dosage 1.25 mg / 2.5 ml: Symptomatic treatment of severe acute asthma in children and infants.
Dosages at 2.5 mg / 2.5 ml and at 5 mg / 2.5 ml:
Symptomatic treatment of severe acute asthma.
Treatment of acute attacks of chronic obstructive pulmonary disease in adults.
Note:
Severe acute asthma requires hospitalization in the intensive care unit.
Oxygen therapy and systemic corticosteroids should be combined with bronchodilator therapy.
ventolin dosage
Dosage :
This low dose presentation is not suitable for the treatment of adults, but for that of children and infants.
children and infants :
50 to 150 μg of salbutamol / kg (ie 0.1 to 0.3 ml / kg of this solution) without generally exceeding 5 mg (4 single doses of 2.5 ml) of nebulized salbutamol.
Nebulization can be repeated every 20 to 30 minutes depending on the clinical outcome and the tolerance of the treatment.
Method of administration :
– Inhaled route exclusively.This salbutamol solution should be administered by inhalation using a nebulizer (nebulizer). DO NOT INJECT – DO NOT AVALER.
– For the use and maintenance of the nebuliser, follow the instructions given by the manufacturer of the device used.
– The solution is ready for use, however if dilution is necessary, it must be performed in sterile saline.
Remove a single-dose container from the blister.
Open the container by twisting its upper end vigorously.
Squeeze the container to empty it into the nebulizer reservoir.
Assemble the nebulizer for administration according to the manufacturer’s instructions.
Eye contact should be avoided by aerosol generated by the nebulizer.
– With pneumatic nebulizers, the flow of air or oxygen to pulse the solution will be adapted according to the patient’s condition and the recommendations of the manufacturer of the nebuliser.
– Nebulization should generally not exceed 10 to 20 minutes.
– The technique of use by the patient must be checked regularly.
– After the nebulization, the unused solution remaining in the tank of the device must be discarded. Cleaning and maintenance of the equipment will be done according to the manufacturer’s recommendations.
– Single-dose containers do not contain preservatives, they should be used immediately after opening. For each nebulization a new container must be used. The contents of partially open or damaged single-dose containers should not be administered.
ventolin how it works
ATC Code: R03AC02.
BETA2 MIMETIC BRONCHODILATOR WITH RAPID ACTION AND SHORT-TERM INHALATION.
Salbutamol is a selective beta2 receptor agonist.
After inhalation, salbutamol exerts a stimulating action on the beta2 receptors of the bronchial smooth muscle thus ensuring rapid bronchodilatation, significant in minutes, persisting for 4 to 6 hours.
What are the side effects of Ventolin inhaler?
The side effects are listed below, listed by organ class and frequency. Frequencies are defined as very common (≥1 / 10), frequent (≥1 / 100 and <1/10), uncommon (≥1 / 1000 and <1/100), rare (≥1 / 10000 and <1) / 1000) and very rare (<1/10000) including isolated cases. Very frequent and frequent effects have generally been described in clinical trials. Rare and very rare side effects are usually from spontaneous post-marketing reports.
Class organ
Side effects
Frequency
Immune system disorders
Very rare hypersensitivity reactions including: angioneurotic edema, urticaria, pruritus, bronchospasm, hypotension, collapse
Very rare
Metabolism and nutrition disorders
hypokalemia *
Very rare
Nervous system disorders
Headaches, tremors
Frequent
Psychiatric disorders
Behavioral disorders: nervousness, agitation
Very rare
Heart conditions
Tachycardia Palpitations Cardiac arrhythmias (including atrial fibrillation, supraventricular tachycardia and extrasystoles)
Frequent Uncommon Very rare
Vascular disorders
Peripheral vasodilatation Very rare
Very rare
Respiratory, thoracic and mediastinal disorders
Paradoxical bronchospasm ** Very rare
Very rare
Gastrointestinal disorders
Irritation of the mouth and throat
Rare
Musculoskeletal and systemic disorders
Muscle cramps
Rare
* Beta-2 mimetics administered at very high doses may lead to hypokalaemias.
** As with other inhaled products, possibility of coughing and rarely paradoxical bronchospasm following inhalation. Do not restart this drug and use another fast-acting bronchodilator to relieve bronchospasm. The treatment should then be reassessed to consider, if necessary, the prescription of a therapeutic alternative.
High dose beta-2 mimetics may result in reversible hyperglycaemia upon discontinuation of therapy.
ventolin drug (inhaler) interactions
Not applicable.
Ventolin Warnings and Precautions
WARNINGS:
– Administration of salbutamol with a nebulizer should be restricted to acute, severe situations requiring inhalation of a high inhaled dose.
These situations require medical surveillance with the possibility of setting up resuscitation (venous access and respiratory assistance); systemic oxygen therapy and corticosteroids usually need to be combined.
– The attention of athletes will be drawn to the fact that this specialty contains an active ingredient that can induce a positive reaction of the tests performed during doping controls.
PRECAUTIONS FOR EMPLOYMENT:
– This low dose presentation is not adapted to the treatment of the adult, but to that of the child and the infant (see posology).
– In case of bronchial infection or bronchorrhea abundant, appropriate treatment is necessary to promote the optimal diffusion of the product in the respiratory tract.
– This medication should be used with caution in hyperthyroidism, cardiovascular disease, including obstructive cardiomyopathy, coronary heart disease, arrhythmias, high blood pressure, and diabetes mellitus.
– High dose beta2 mimetics may cause hypokalemia that may lead to the occurrence of cardiac arrhythmias. Monitoring of serum potassium is recommended whenever possible, particularly when concomitant use of hypokalaemic therapies, hypoxia or in subjects with increased risk of torsades de pointes (long QT or treatments likely to increase QTc).
– Pregnancy: in case of administration before delivery take into account the peripheral vasodilator effect of beta2 mimetics.
– Breast-feeding: beta2 mimetics pass into breast milk.
Drive and use machines:
Not applicable.
Ventolin and PREGNANCY / BREAST FEEDING / FERTILITY
Pregnancy :
Clinically, there is a significant decline, with a sufficient number of documented pregnancies, so that we can conclude on the safety of salbutamol during pregnancy.
As a result, inhaled salbutamol can be administered during pregnancy.
When administered during pregnancy, an acceleration of the fetal heart rate may be observed in parallel with maternal tachycardia. It is exceptional to see her persist at birth.
Similarly, postnatal blood glucose values are only exceptionally disturbed.
When administered before delivery, consider the peripheral vasodilator effect of beta-2-mimetics.
Breastfeeding:
Beta-2-mimetics pass into breast milk.
Immediately consult your doctor or pharmacist.
What is Forms and Composition Ventolin?
FORMS and PRESENTATIONS
1.25 mg / 2.5 ml Nebulizer Inhalation Solution : 2.5 ml single-dose containers, box of 20. 2.5 mg / 2.5 ml and 5 mg / 2.5 Nebulizer Inhalation Solution ml: Single-dose containers of 2.5 ml, box of 60.
COMPOSITION
p single dose Salbutamol (DCI) 1.25 mg or 2.5 mg or 5 mg (as sulphate: 1.5 mg, 3 mg or 6 mg per dose)
Excipients (common): sodium chloride, dilute sulfuric acid, purified water (1.25 mg / 2.5 mL sol), water ppi (2.5 mg sol and 5 mg / 2.5 mL).
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 Ventolin inhaler Uses, Dosage, Side Effects, Precautions &Warnings appeared first on Drug Online.
from Drug Online https://bit.ly/3fz3XXO via Edrug Online from faculty of medicine https://bit.ly/3efrZ9S via Faculty of Medicine
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Text
Ventolin inhaler Uses, Dosage, Side Effects, Precautions &Warnings
Drug Online
ventolin inhaler Generic drug of the therapeutic class: Pulmonology active ingredients: Salbutamol
Important to know about Ventolin ?
It is a bronchodilator (it increases the size of the bronchi) fast acting and short duration.
It is administered by inhalation with the help of a nebuliser (nebuliser).
The use of this drug in this mode of administration should be reserved for the treatment of severe asthma attacks in children and infants, when these situations require the inhalation of high doses of salbutamol.
ventolin used for and indication
Dosage 1.25 mg / 2.5 ml: Symptomatic treatment of severe acute asthma in children and infants.
Dosages at 2.5 mg / 2.5 ml and at 5 mg / 2.5 ml:
Symptomatic treatment of severe acute asthma.
Treatment of acute attacks of chronic obstructive pulmonary disease in adults.
Note:
Severe acute asthma requires hospitalization in the intensive care unit.
Oxygen therapy and systemic corticosteroids should be combined with bronchodilator therapy.
ventolin dosage
Dosage :
This low dose presentation is not suitable for the treatment of adults, but for that of children and infants.
children and infants :
50 to 150 μg of salbutamol / kg (ie 0.1 to 0.3 ml / kg of this solution) without generally exceeding 5 mg (4 single doses of 2.5 ml) of nebulized salbutamol.
Nebulization can be repeated every 20 to 30 minutes depending on the clinical outcome and the tolerance of the treatment.
Method of administration :
– Inhaled route exclusively.This salbutamol solution should be administered by inhalation using a nebulizer (nebulizer). DO NOT INJECT – DO NOT AVALER.
– For the use and maintenance of the nebuliser, follow the instructions given by the manufacturer of the device used.
– The solution is ready for use, however if dilution is necessary, it must be performed in sterile saline.
Remove a single-dose container from the blister.
Open the container by twisting its upper end vigorously.
Squeeze the container to empty it into the nebulizer reservoir.
Assemble the nebulizer for administration according to the manufacturer’s instructions.
Eye contact should be avoided by aerosol generated by the nebulizer.
– With pneumatic nebulizers, the flow of air or oxygen to pulse the solution will be adapted according to the patient’s condition and the recommendations of the manufacturer of the nebuliser.
– Nebulization should generally not exceed 10 to 20 minutes.
– The technique of use by the patient must be checked regularly.
– After the nebulization, the unused solution remaining in the tank of the device must be discarded. Cleaning and maintenance of the equipment will be done according to the manufacturer’s recommendations.
– Single-dose containers do not contain preservatives, they should be used immediately after opening. For each nebulization a new container must be used. The contents of partially open or damaged single-dose containers should not be administered.
ventolin how it works
ATC Code: R03AC02.
BETA2 MIMETIC BRONCHODILATOR WITH RAPID ACTION AND SHORT-TERM INHALATION.
Salbutamol is a selective beta2 receptor agonist.
After inhalation, salbutamol exerts a stimulating action on the beta2 receptors of the bronchial smooth muscle thus ensuring rapid bronchodilatation, significant in minutes, persisting for 4 to 6 hours.
What are the side effects of Ventolin inhaler?
The side effects are listed below, listed by organ class and frequency. Frequencies are defined as very common (≥1 / 10), frequent (≥1 / 100 and <1/10), uncommon (≥1 / 1000 and <1/100), rare (≥1 / 10000 and <1) / 1000) and very rare (<1/10000) including isolated cases. Very frequent and frequent effects have generally been described in clinical trials. Rare and very rare side effects are usually from spontaneous post-marketing reports.
Class organ
Side effects
Frequency
Immune system disorders
Very rare hypersensitivity reactions including: angioneurotic edema, urticaria, pruritus, bronchospasm, hypotension, collapse
Very rare
Metabolism and nutrition disorders
hypokalemia *
Very rare
Nervous system disorders
Headaches, tremors
Frequent
Psychiatric disorders
Behavioral disorders: nervousness, agitation
Very rare
Heart conditions
Tachycardia Palpitations Cardiac arrhythmias (including atrial fibrillation, supraventricular tachycardia and extrasystoles)
Frequent Uncommon Very rare
Vascular disorders
Peripheral vasodilatation Very rare
Very rare
Respiratory, thoracic and mediastinal disorders
Paradoxical bronchospasm ** Very rare
Very rare
Gastrointestinal disorders
Irritation of the mouth and throat
Rare
Musculoskeletal and systemic disorders
Muscle cramps
Rare
* Beta-2 mimetics administered at very high doses may lead to hypokalaemias.
** As with other inhaled products, possibility of coughing and rarely paradoxical bronchospasm following inhalation. Do not restart this drug and use another fast-acting bronchodilator to relieve bronchospasm. The treatment should then be reassessed to consider, if necessary, the prescription of a therapeutic alternative.
High dose beta-2 mimetics may result in reversible hyperglycaemia upon discontinuation of therapy.
ventolin drug (inhaler) interactions
Not applicable.
Ventolin Warnings and Precautions
WARNINGS:
– Administration of salbutamol with a nebulizer should be restricted to acute, severe situations requiring inhalation of a high inhaled dose.
These situations require medical surveillance with the possibility of setting up resuscitation (venous access and respiratory assistance); systemic oxygen therapy and corticosteroids usually need to be combined.
– The attention of athletes will be drawn to the fact that this specialty contains an active ingredient that can induce a positive reaction of the tests performed during doping controls.
PRECAUTIONS FOR EMPLOYMENT:
– This low dose presentation is not adapted to the treatment of the adult, but to that of the child and the infant (see posology).
– In case of bronchial infection or bronchorrhea abundant, appropriate treatment is necessary to promote the optimal diffusion of the product in the respiratory tract.
– This medication should be used with caution in hyperthyroidism, cardiovascular disease, including obstructive cardiomyopathy, coronary heart disease, arrhythmias, high blood pressure, and diabetes mellitus.
– High dose beta2 mimetics may cause hypokalemia that may lead to the occurrence of cardiac arrhythmias. Monitoring of serum potassium is recommended whenever possible, particularly when concomitant use of hypokalaemic therapies, hypoxia or in subjects with increased risk of torsades de pointes (long QT or treatments likely to increase QTc).
– Pregnancy: in case of administration before delivery take into account the peripheral vasodilator effect of beta2 mimetics.
– Breast-feeding: beta2 mimetics pass into breast milk.
Drive and use machines:
Not applicable.
Ventolin and PREGNANCY / BREAST FEEDING / FERTILITY
Pregnancy :
Clinically, there is a significant decline, with a sufficient number of documented pregnancies, so that we can conclude on the safety of salbutamol during pregnancy.
As a result, inhaled salbutamol can be administered during pregnancy.
When administered during pregnancy, an acceleration of the fetal heart rate may be observed in parallel with maternal tachycardia. It is exceptional to see her persist at birth.
Similarly, postnatal blood glucose values are only exceptionally disturbed.
When administered before delivery, consider the peripheral vasodilator effect of beta-2-mimetics.
Breastfeeding:
Beta-2-mimetics pass into breast milk.
Immediately consult your doctor or pharmacist.
What is Forms and Composition Ventolin?
FORMS and PRESENTATIONS
1.25 mg / 2.5 ml Nebulizer Inhalation Solution : 2.5 ml single-dose containers, box of 20. 2.5 mg / 2.5 ml and 5 mg / 2.5 Nebulizer Inhalation Solution ml: Single-dose containers of 2.5 ml, box of 60.
COMPOSITION
p single dose Salbutamol (DCI) 1.25 mg or 2.5 mg or 5 mg (as sulphate: 1.5 mg, 3 mg or 6 mg per dose)
Excipients (common): sodium chloride, dilute sulfuric acid, purified water (1.25 mg / 2.5 mL sol), water ppi (2.5 mg sol and 5 mg / 2.5 mL).
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 Ventolin inhaler Uses, Dosage, Side Effects, Precautions &Warnings appeared first on Drug Online.
from Drug Online https://bit.ly/3fz3XXO via Edrug Online
0 notes