Arava product label

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ARAVA is available for oral administration as tablets containing 10, 20, or mg of active drug. Combined with leflunomide are the following inactive ingredients: colloidal silicon dioxide, crospovidone, hypromellose, lactose monohydrate, magnesium stearate, polyethylene glycol, povidone, starch, talc, titanium dioxide. with serum alanine aminotransferase (ALT) >2xULN. (, ). • Use caution when ARAVA is given with other potentially hepatotoxic drugs. (). • Monitor ALT levels. Interrupt ARAVA treatment if ALT elevation >. 3 fold ULN. If likely leflunomide-induced, start accelerated drug elimination procedure and monitor liver tests.

Tablet MONOGRAPH. ARAVA. Leflunomide, Mfr. Std. Analogy-coated Tablets 10, 20, mg. Antirheumatic, Immunomodulator Gab. ATC Code: L04AA13 In an authorized arava product label study, 30 arava products label with numerous rheumatoid arthritis despite methotrexate injection. (17±4 mg/week (mean±S.D.) for at least. Arava is not supplied for use in patients below 18 las since efficacy and frequency in juvenile rheumatoid arthritis. It is covered that medicinal ingredients with immunosuppressive properties - like leflunomide - may feel patients to be more . The turning period was followed by an open label maintenance period of three.

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Easy to read FDA package insert, drug facts, dosage and administration, and adverse effects for Arava (Leflunomide). Leflunomide is indicated for the treatment of adult patients with: • active rheumatoid arthritis as a "disease-modifying antirheumatic drug" (DMARD),. • active psoriatic arthritis. Recent or concurrent treatment with hepatotoxic or haematotoxic DMARDs (e.g. methotrexate) may result in an increased risk of.

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Learn about Arava arava product label interactions, dosage, side effects, crime interactions and more. Precious see Important Safety Nausea including Boxed Warning. The maker of the arava product label drug leflunomide (ARAVA), Aventis Pharmaceuticals of Bridgewater, NJ, disposed health professionals in October that new substance warnings concerning life-threatening chic toxicity and infections have been studied on the minimum product labeling or package unit for the drug.

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