DANAZOL
Generic: DANAZOL
Teva Pharmaceuticals USAManufacturer
ORALRoute
DANAZOLActive Substance
1996-08-09Original Approval
DANAZOL is FDA application ANDA074582, sponsored by BARR. 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
DRUG INEFFECTIVE
463 reports
2
OFF LABEL USE
442 reports
3
HEADACHE
340 reports
4
ANGIOEDEMA
248 reports
5
HYPERSENSITIVITY
247 reports
6
DRUG INTOLERANCE
236 reports
7
DYSPHONIA
233 reports
8
SWELLING FACE
233 reports
9
SWOLLEN TONGUE
228 reports
10
HEREDITARY ANGIOEDEMA
226 reports