TIOPRONIN
Generic: TIOPRONIN
Teva PharmaceuticalsManufacturer
ORALRoute
TIOPRONINActive Substance
2024-07-22Original Approval
TIOPRONIN is FDA application ANDA216456, sponsored by TEVA PHARMS INC. 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
OFF LABEL USE
19 reports
2
PYREXIA
14 reports
3
NAUSEA
13 reports
4
NEPHROTIC SYNDROME
13 reports
5
DIARRHOEA
12 reports
6
TUBULOINTERSTITIAL NEPHRITIS
12 reports
7
VOMITING
12 reports
8
PNEUMONIA
10 reports
9
ALANINE AMINOTRANSFERASE INCREASED
9 reports
10
ASPARTATE AMINOTRANSFERASE INCREASED
9 reports