METHIMAZOLE

Generic: METHIMAZOLE

Bionpharma Inc.Manufacturer
ORALRoute
METHIMAZOLEActive Substance
2023-09-25Original Approval

METHIMAZOLE is FDA application ANDA218149, sponsored by BIONPHARMA. 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
644 reports
2
OFF LABEL USE
487 reports
3
FATIGUE
445 reports
4
HYPERTHYROIDISM
407 reports
5
NAUSEA
381 reports
6
DIARRHOEA
335 reports
7
HEADACHE
330 reports
8
PAIN
310 reports
9
DIZZINESS
306 reports
10
DYSPNOEA
277 reports