erdosteine: prescribing and clinical use
Focused clinical detail for use alongside current product information, local policy and patient-specific assessment.
erdosteine: clinical details
Prescribing considerations
- Licensed for symptomatic treatment of acute exacerbations of chronic bronchitis in adults and as an expectorant.
- Establish renal and hepatic status and check for active peptic ulcer before prescribing.
- Review carefully in mild hepatic impairment and follow product-specific restrictions.
Contraindications and cautions
- Hypersensitivity to erdosteine or an excipient
- Active peptic ulcer
- Use is not recommended where creatinine clearance is below 25 mL/min because data are unavailable
- Use is not recommended in severe hepatic failure because data are unavailable
Monitoring
- No routine laboratory-monitoring schedule is specified.
- Assess clinical response and watch for gastrointestinal intolerance, hypersensitivity, angioedema or new breathing difficulty.
Clinical pharmacology
Erdosteine is rapidly absorbed and undergoes first-pass conversion to the active metabolite M1. Its free thiol group reduces mucus viscosity by opening disulfide bonds in bronchial mucoproteins. Metabolites are eliminated mainly in urine, and absorption is not affected by food.
Formulation and product differences
- The selected product is a prescription-only hard capsule with a green cap and yellow body.
- The capsule shell contains gelatin, titanium dioxide, yellow iron oxide and indigotine.
- The capsule must be swallowed whole with water.
erdosteine preparations and strengths
Capsule
Route: Oral
Strengths: 300 mg
erdosteine interactions
No adverse medicine interactions are reported in the selected UK product information. Tell your doctor or pharmacist about prescription, non-prescription and herbal products you use.
Sources
These sources were used to prepare and review this medicine page.
Prepared and reviewed by the iatroX editorial team.