LOFEXIDINE
Generic: LOFEXIDINE
Florida Pharmaceutical ProductsManufacturer
ORALRoute
LOFEXIDINE HYDROCHLORIDEActive Substance
2024-08-20Original Approval
LOFEXIDINE is FDA application ANDA218613, sponsored by REGCON HOLDINGS. 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
DYSPNOEA
5 reports
2
DRUG INTERACTION
3 reports
3
DERMATITIS BULLOUS
2 reports
4
DRUG ERUPTION
2 reports
5
ELECTROCARDIOGRAM QT PROLONGED
2 reports
6
GINGIVAL DISORDER
2 reports
7
LIP HAEMORRHAGE
2 reports
8
OEDEMA
2 reports
9
SCROTAL ULCER
2 reports
10
ABDOMINAL PAIN UPPER
1 reports