CARBOPROST TROMETHAMINE
Generic: CARBOPROST TROMETHAMINE
Eugia US LLCManufacturer
INTRAMUSCULARRoute
CARBOPROST TROMETHAMINEActive Substance
2023-05-25Original Approval
CARBOPROST TROMETHAMINE is FDA application ANDA216939, sponsored by EUGIA PHARMA. 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
VOMITING
110 reports
2
NAUSEA
87 reports
3
DIARRHOEA
78 reports
4
OFF LABEL USE
63 reports
5
ABDOMINAL PAIN UPPER
46 reports
6
CHEST DISCOMFORT
37 reports
7
ABDOMINAL PAIN
36 reports
8
ABDOMINAL DISCOMFORT
28 reports
9
HYPERHIDROSIS
22 reports
10
PRURITUS
22 reports