HYDROCORTISONE BUTYRATE
Generic: HYDROCORTISONE BUTYRATE
Sun Pharmaceutical IndustriesManufacturer
TOPICALRoute
HYDROCORTISONE BUTYRATEActive Substance
2004-01-14Original Approval
HYDROCORTISONE BUTYRATE is FDA application ANDA076364, sponsored by TARO PHARM INDS. 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
OFF LABEL USE
591 reports
2
DRUG INEFFECTIVE
537 reports
3
RASH
527 reports
4
INFUSION RELATED REACTION
523 reports
5
FATIGUE
519 reports
6
GLOSSODYNIA
510 reports
7
SYSTEMIC LUPUS ERYTHEMATOSUS
506 reports
8
DUODENAL ULCER PERFORATION
503 reports
9
HAND DEFORMITY
498 reports
10
RHEUMATOID ARTHRITIS
493 reports