ISONIAZID
Generic: ISONIAZID
Chartwell RXManufacturer
ORALRoute
ISONIAZIDActive Substance
1988-06-13Original Approval
ISONIAZID is FDA application ANDA089776, sponsored by CHARTWELL MOLECULAR. 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 INEFFECTIVE
1,183 reports
2
PYREXIA
1,102 reports
3
DRUG INTERACTION
935 reports
4
NAUSEA
903 reports
5
DRUG-INDUCED LIVER INJURY
862 reports
6
OFF LABEL USE
860 reports
7
DRUG REACTION WITH EOSINOPHILIA AND SYSTEMIC SYMPTOMS
744 reports
8
VOMITING
636 reports
9
HEADACHE
614 reports
10
PARADOXICAL DRUG REACTION
553 reports