DROXIDOPA
Generic: DROXIDOPA
Sun Pharmaceutical IndustriesManufacturer
ORALRoute
DROXIDOPAActive Substance
2021-02-18Original Approval
DROXIDOPA is FDA application ANDA214384, sponsored by SUN PHARM. 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
DEATH
235 reports
2
FALL
152 reports
3
DIZZINESS
91 reports
4
HALLUCINATION
85 reports
5
HYPOTENSION
72 reports
6
DRUG INEFFECTIVE
71 reports
7
LOSS OF CONSCIOUSNESS
61 reports
8
HOSPITALISATION
57 reports
9
CONFUSIONAL STATE
51 reports
10
PRODUCT DOSE OMISSION ISSUE
47 reports