AZATHIOPRINE
Generic: AZATHIOPRINE
Ascend LaboratoriesManufacturer
ORALRoute
AZATHIOPRINEActive Substance
2020-03-27Original Approval
AZATHIOPRINE is FDA application ANDA208687, sponsored by ALKEM LABS LTD. 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
11,054 reports
2
DRUG INEFFECTIVE
10,737 reports
3
CONDITION AGGRAVATED
5,619 reports
4
ARTHRALGIA
4,652 reports
5
DIARRHOEA
4,065 reports
6
FATIGUE
4,023 reports
7
NAUSEA
3,999 reports
8
HEADACHE
3,628 reports
9
DRUG INTOLERANCE
3,570 reports
10
PAIN
3,357 reports