DESMOPRESSIN ACETATE
Generic: DESMOPRESSIN ACETATE
Sun Pharmaceutical Industries LimitedManufacturer
INTRAVENOUS, SUBCUTANEOUSRoute
DESMOPRESSIN ACETATEActive Substance
2023-03-20Original Approval
DESMOPRESSIN ACETATE is FDA application ANDA216904, sponsored by GLAND. 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.
Recalls
Top Reported Reactions
1
HYPONATRAEMIA
217 reports
2
DRUG INEFFECTIVE
131 reports
3
NAUSEA
96 reports
4
HEADACHE
90 reports
5
OFF LABEL USE
81 reports
6
VOMITING
74 reports
7
FATIGUE
72 reports
8
PAIN
56 reports
9
DIARRHOEA
53 reports
10
DIZZINESS
53 reports