Hepatic dysfunction (incidence <0.1%) and jaundice (incidence unknown), as indicated by increases in AST (GOT), ALT (GPT), γ-GTP, and alkaline phosphatase levels have been reported in patients receiving Rebamipide. If abnormal laboratory findings are observed, the drug should be discontinued and appropriate measures taken.
Other adverse reactions: See table.
Click on icon to see table/diagram/image
View ADR Reporting Link
Sign Out