Acetylcysteine sandoz

Recorded active ingredients: Acetylcysteine

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Countries

Belgium Canada Poland

Diseases

Asthma Bronchitis Pneumonia Tuberculosis Abscess Chronic Obstructive Lung Disease Lung Abscess Bronchiolitis Chronic Sinusitis Amyloidosis Atelectasis Emphysema

Drug Actions

Ophthalmologicals All other therapeutic products Antioxidant Cough and cold preparations Expectorant Hepatoprotective Mucolytic

Medicines with the same recorded active ingredients

These listings match the full ingredient set recorded for Acetylcysteine sandoz. Strength, dosage form and route may differ or be missing. This does not establish interchangeability; confirm a suitable product with a pharmacist.

Acc Acc (acetylcysteine) Acemuk Acetylcysteine Broncolium Toflux Acemuc Acetadote Dbl acetylcysteine Omegapharm acetylcysteine Nac - 1 a pharma Nac (acetylcysteine) Nac akut - 1 a pharma Nac al Nac long Nac-ct N-ace Nacecis Nacel N-acetilcisteina germed

Incompatibilities

In the absence of compatibility studies, this medicinal product must not be mixed with other medicinal products.

Preclinical safety data

Acute toxicity studies in rats and mice, by oral, intraperitoneal and intravenous administration showed Acetylcysteine Sandoz to be of low toxicity. LD50 values greater than 7 g / kg in mice and 6 g / kg in rats have been reported. Chronic toxicity studies with Acetylcysteine Sandoz in rats at doses up to 2000 mg/ kg/ day and dogs at doses up to 300 mg/ kg / day for periods up to 52 weeks demonstrate that Acetylcysteine Sandoz is well tolerated, even at higher doses. In reproductive toxicity studies in rats and rabbits, the oral administration of doses up to 2000 mg / kg / day did not show changes in reproductive capacity, teratogenic effects or peri/postnatal toxicity.

Pharmacotherapeutic group

Mycolytics, ATC code: R05CB01

Special precautions for disposal and other handling

No special requirements for disposal. Any unused product should be disposed of in accordance with local requirements.