QUININE SULFATE
Generic: QUININE SULFATE
Teva Pharmaceuticals USAManufacturer
ORALRoute
QUININE SULFATEActive Substance
2012-09-28Original Approval
QUININE SULFATE is FDA application ANDA091661, sponsored by TEVA 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
DRUG ABUSE
727 reports
2
TOXICITY TO VARIOUS AGENTS
506 reports
3
DYSPNOEA
486 reports
4
FALL
454 reports
5
NAUSEA
450 reports
6
PAIN
429 reports
7
DIARRHOEA
376 reports
8
VOMITING
368 reports
9
DIZZINESS
341 reports
10
MUSCLE SPASMS
311 reports