NITAZOXANIDE
Generic: NITAZOXANIDE
ANI PharmaceuticalsManufacturer
ORALRoute
NITAZOXANIDEActive Substance
2025-02-03Original Approval
NITAZOXANIDE is FDA application ANDA214844, sponsored by ANI 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
DIARRHOEA
68 reports
2
DRUG INEFFECTIVE
56 reports
3
OFF LABEL USE
53 reports
4
DISEASE PROGRESSION
46 reports
5
DYSPNOEA
41 reports
6
CHEST PAIN
33 reports
7
THERAPEUTIC PRODUCT EFFECT INCOMPLETE
32 reports
8
COMA SCALE ABNORMAL
31 reports
9
MICROSPORIDIA INFECTION
31 reports
10
PNEUMOCYSTIS JIROVECII INFECTION
31 reports