ZINC SULFATE
Generic: ZINC SULFATE
Somerset TherapeuticsManufacturer
INTRAVENOUSRoute
ZINC SULFATEActive Substance
2024-07-17Original Approval
ZINC SULFATE is FDA application ANDA216135, sponsored by SOMERSET THERAPS LLC. 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
223 reports
2
FATIGUE
180 reports
3
NAUSEA
173 reports
4
DEATH
155 reports
5
OFF LABEL USE
154 reports
6
PAIN
145 reports
7
VOMITING
141 reports
8
DYSPNOEA
137 reports
9
PYREXIA
129 reports
10
HEADACHE
105 reports