HYDROMORPHONE HYDROCHLORIDE
Generic: HYDROMORPHONE HYDROCHLORIDE
Fresenius Kabi USAManufacturer
INTRAMUSCULAR, INTRAVENOUS, SUBCUTANEOUSRoute
HYDROMORPHONE HYDROCHLORIDEActive Substance
1984-01-11Original Approval
HYDROMORPHONE HYDROCHLORIDE is FDA application NDA019034, sponsored by FRESENIUS KABI USA. 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 DEPENDENCE
35,112 reports
2
OVERDOSE
23,059 reports
3
PAIN
22,287 reports
4
EMOTIONAL DISTRESS
17,705 reports
5
DEATH
14,911 reports
6
DRUG WITHDRAWAL SYNDROME
14,329 reports
7
TOXICITY TO VARIOUS AGENTS
10,081 reports
8
NAUSEA
4,759 reports
9
DRUG INEFFECTIVE
4,474 reports
10
FATIGUE
3,620 reports