
Deflaxen6 mg
Everest Pharmaceuticals Ltd.
FDA-Approved Indication: Duchenne Muscular Dystrophy Deflazacort is FDA-approved (established indication) for the treatment of Duchenne muscular dystrophy (DMD) in patients 2 years of age and older.
Deflazacort is FDA-approved (established indication) for the treatment of Duchenne muscular dystrophy (DMD) in patients 2 years of age and older. Deflazacort is used to help slow the decline in muscle strength associated with this genetic muscle-wasting disease.
Outside the United States - including in Bangladesh, where Deflazacort is widely prescribed - Deflazacort is also used as a general corticosteroid for a broad range of inflammatory, allergic, and autoimmune conditions. These uses are guideline-supported or established in regional clinical practice but are not part of the US FDA-approved label for Deflazacort:
Dosing and duration for each condition should be individualized by a qualified physician.
The dose and duration of Deflazacort must be determined by a qualified healthcare professional based on the specific condition being treated, patient age, body weight, and response to therapy - there is no single dose of Deflazacort that applies to all patients. For most conditions, Deflazacort is taken once daily by mouth. If Deflazacort has been taken for more than a few days, the dose of Deflazacort must be reduced gradually (tapered) under medical supervision rather than stopped abruptly, because sudden discontinuation of Deflazacort can cause life-threatening adrenal insufficiency.
Deflazacort is contraindicated in:
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