BICALUTAMIDE- bicalutamide tablet, film coated United States - English - NLM (National Library of Medicine)

bicalutamide- bicalutamide tablet, film coated

northstar rxllc - bicalutamide (unii: a0z3nau9dp) (bicalutamide - unii:a0z3nau9dp) - bicalutamide 50 mg - bicalutamide 50 mg daily is indicated for use in combination therapy with a luteinizing hormone-releasing hormone (lhrh) analog for the treatment of stage d2 metastatic carcinoma of the prostate. bicalutamide 150 mg daily is not  approved for use alone or with other treatments [see clinical studies (14.2)] . bicalutamide is contraindicated in: -   hypersensitivity bicalutamide is contraindicated in any patient who has shown a hypersensitivity reaction to the drug or any of the tablet’s components. hypersensitivity reactions including angioneurotic edema and urticaria have been reported. - women bicalutamide has no indication for women, and should not be used in this population. - pregnancy bicalutamide can cause fetal harm when administered to a pregnant woman [see use in specific populations (8.1)] . risk summary bicalutamide is contraindicated for use in pregnant women because it can cause fetal harm. bicalutamide is not indicated for use in females. there are no human data on the use of bicalutamide

Bicalutamide 50mg tablets United Kingdom - English - MHRA (Medicines & Healthcare Products Regulatory Agency)

bicalutamide 50mg tablets

sun pharmaceutical industries europe b.v. - bicalutamide - oral tablet - 50mg