Indications |
Oral Mucolytic Adult: 300 mg bid. Max duration: 10 days. |
Contraindications |
Active peptic ulcer. |
Warnings / Precautions |
Pregnancy, lactation. |
Adverse Reactions |
Epigastralgia, nausea, vomiting, loose stools, spasmodic colitis, headache. |
Mechanism of Actions |
Erdosteine contains two sulfhydryl groups, which are freed after metabolic transformation in the liver. The liberated sulfhydryl groups break the disulphide bonds, which hold the glycoprotein fibres of mucus together. This makes the bronchial secretions more fluid and enhances elimination. Absorption: Rapid absorption after oral admin. Distribution: Protein binding: 64.5%. Metabolism: Undergoes 1st-pass metabolism to form an active metabolite, N-thiodiglycolyl-homocysteine. Excretion: Elimination half-life: About 1.46 hr (erdosteine), and about 1.62 hr (metabolite). Mainly via the urine, as metabolites. |
Storage Conditions |
Oral: Store below 25°C. |
ATC Classification |
R05CB15 - erdosteine ; Belongs to the class of mucolytics. Used in the treatment of wet cough. |
Storage |
Oral: Store below 25°C. |
Available As |
|
Erdosteine
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Erdosteine Containing Brands
Erdosteine is used in following diseases
Drug - Drug Interactions of Erdosteine
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