PRUCALOPRIDE
Generic: PRUCALOPRIDE
Sandoz Inc.Manufacturer
ORALRoute
PRUCALOPRIDE SUCCINATEActive Substance
2025-06-24Original Approval
PRUCALOPRIDE is FDA application ANDA218963, sponsored by APPCO. 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
HEADACHE
109 reports
2
OFF LABEL USE
95 reports
3
NAUSEA
93 reports
4
FATIGUE
80 reports
5
DRUG INEFFECTIVE
77 reports
6
DIZZINESS
65 reports
7
FALL
61 reports
8
ABDOMINAL PAIN
58 reports
9
CONSTIPATION
55 reports
10
VOMITING
52 reports