OXYMORPHONE HYDROCHLORIDE
Generic: OXYMORPHONE HYDROCHLORIDE
Aurolife PharmaManufacturer
ORALRoute
OXYMORPHONE HYDROCHLORIDEActive Substance
2016-04-26Original Approval
OXYMORPHONE HYDROCHLORIDE is FDA application ANDA204459, sponsored by AUROLIFE PHARMA LLC. 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
DEPENDENCE
4,904 reports
2
DEATH
3,324 reports
3
TOXICITY TO VARIOUS AGENTS
2,759 reports
4
OVERDOSE
2,310 reports
5
DRUG DEPENDENCE
583 reports
6
DRUG ABUSE
551 reports
7
BACK PAIN
432 reports
8
DRUG WITHDRAWAL SYNDROME NEONATAL
350 reports
9
FOETAL EXPOSURE DURING PREGNANCY
331 reports
10
PAIN
307 reports