BICALUTAMIDE
Generic: BICALUTAMIDE
Viona Pharmaceuticals Inc.Manufacturer
ORALRoute
BICALUTAMIDEActive Substance
2009-07-06Original Approval
BICALUTAMIDE is FDA application ANDA079089, sponsored by ADAPTIS. Any recalls listed below come from FDA drug enforcement reports, and reaction counts are the number of FAERS adverse event reports that mention the drug and that reaction; a report does not prove the drug caused it.
Top Reported Reactions
1
FATIGUE
833 reports
2
DEATH
601 reports
3
PROSTATIC SPECIFIC ANTIGEN INCREASED
566 reports
4
PROSTATE CANCER
501 reports
5
HOT FLUSH
498 reports
6
ASTHENIA
478 reports
7
DRUG INEFFECTIVE
448 reports
8
MALIGNANT NEOPLASM PROGRESSION
348 reports
9
NAUSEA
332 reports
10
DIARRHOEA
317 reports