QUETIAPINE FUMARATE
Generic: QUETIAPINE FUMARATE
Macleods Pharmaceuticals LimitedManufacturer
ORALRoute
QUETIAPINE FUMARATEActive Substance
2016-05-17Original Approval
QUETIAPINE FUMARATE is FDA application ANDA203359, sponsored by MACLEODS PHARMS. 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
TOXICITY TO VARIOUS AGENTS
9,490 reports
2
DRUG INEFFECTIVE
8,685 reports
3
OFF LABEL USE
7,829 reports
4
DRUG INTERACTION
6,723 reports
5
COMPLETED SUICIDE
6,654 reports
6
FATIGUE
5,733 reports
7
NAUSEA
4,868 reports
8
CONDITION AGGRAVATED
4,851 reports
9
PAIN
4,753 reports
10
SOMNOLENCE
4,700 reports