for oral use Initial U.S. Approval: 1998
THALOMID in combination with dexamethasone is indicated for the treatment of patients with newly diagnosed multiple myeloma (MM). • THALOMID is indicated for the acute treatment of the cutaneous manifestations of moderate to severe erythema nodosum leprosum (ENL). THALOMID is not indicated as monotherapy for such ENL treatment in the presence of moderate to severe neuritis. THALOMID is also indicated as maintenance therapy for prevention and suppression of the cutaneous manifestations of ENL recurrence.
Facts about thalidomide capsules
Approval Date: 1998
Proprietary Name: On Request
Active Ingredient(s): thalidomide capsules
Dosage Forms And Strengths: Capsules: 50 mg, 100 mg, 150 mg and 200 mg
Current indications: multiple myeloma
Medicine Approved By: – European Medical Agency (EMA), Food and Drug Administration (FDA), Health Canada, Therapeutic Goods Administration (TGA), Medsafe (NZ)
Summary of FDA approved use on approval date: Click Here
(see Drugs@FDA for complete indication)
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Query For thalidomide capsules
Approved accessible "thalidomide capsules"
THALOMID is a prescription medicine used: to treat people who have been newly diagnosed with multiple myeloma (MM), and take along with the medicine dexamethasone. to treat people who have moderate to severe new lesions of leprosy. THALOMID is not used by itself to treat the skin lesions when there is moderate to severe nerve pain. to prevent and keep the skin lesions of leprosy from coming back (recurring). It is not known if THALOMID is safe and effective in children under 12 years of age. Active ingredient: thalidomide Inactive ingredients: pregelatinized starch and magnesium stearate.
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