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Bicalutamide is a non-steroidal androgen receptor inhibitor used to treat metastatic prostate cancer in combination with LHRH. Learn about its dosage, side effects, interactions, pregnancy and breastfeeding warnings, and more.
Bicalutamide is a prescription drug used to treat prostate cancer by blocking hormones that stimulate tumor growth. Learn about its common and serious side effects, warnings, interactions, and...
Bicalutamide is an antiandrogen medicine used with LHRH analogs to treat metastatic prostate cancer in men. It blocks the effects of testosterone and may cause side effects such as liver problems, bleeding, and breast swelling.
Bicalutamide is a drug approved to treat metastatic prostate cancer with a luteinizing hormone-releasing hormone agonist. It works by blocking the action of male hormones on prostate cancer cells. Learn more about bicalutamide, its definition, warnings, interactions, and ongoing clinical trials.
Casodex (bicalutamide) is a medicine that prevents male hormones from acting on prostate cancer cells. It is used with LHRH injections and has side effects, warnings, and interactions.
Bicalutamide blocks testosterone from reaching prostate cancer cells and may shrink or stop the cancer. Learn about how it works, possible side effects, and how to take it safely.
Bicalutamide is an antiandrogen drug for prostate cancer treatment. Learn about its dosages, side effects, drug interactions, warnings, and precautions from RxList.
Bicalutamide tablets 50 mg is an androgen receptor inhibitor indicated for use in combination therapy with a luteinizing hormone-releasing hormone (LHRH) analog for the treatment of Stage D 2 metastatic carcinoma of the prostate.
CASODEX 50 mg daily is indicated for use in combination therapy with a luteinizing hormone-releasing hormone (LHRH) analog for the treatment of Stage D 2 metastatic carcinoma of the prostate. CASODEX 150 mg daily is not approved for use alone or with other treatments [see Clinical Studies ].
Generic: 50 mg. Bicalutamide is a pure nonsteroidal androgen receptor inhibitor, specifically a competitive inhibitor for the binding of dihydrotestosterone and testosterone; prevents testosterone stimulation of cell growth in prostate cancer. Well absorbed; unaffected by food.