Adverse Drug Reaction Classification System

ADR Ontology
ADR Term Hepatic failure
ADR ID BADD_A02001
ADR Hierarchy
09      Hepatobiliary disorders
09.01      Hepatic and hepatobiliary disorders
09.01.03      Hepatic failure and associated disorders
09.01.03.002      Hepatic failure
Description A disorder characterized by the inability of the liver to metabolize chemicals in the body. Laboratory test results reveal abnormal plasma levels of ammonia, bilirubin, lactic dehydrogenase, alkaline phosphatase, aminotransferase, and/or prolongation of prothrombin time (INR.) Drug-induced liever injury (DILI) as defined by Hy's Law. [CTCAE] Severe inability of the LIVER to perform its normal metabolic functions, as evidenced by severe JAUNDICE and abnormal serum levels of AMMONIA; BILIRUBIN; ALKALINE PHOSPHATASE; ASPARTATE AMINOTRANSFERASE; LACTATE DEHYDROGENASES; and albumin/globulin ratio. (Blakiston's Gould Medical Dictionary, 4th ed) [MeSH]
MedDRA Code 10019663
MeSH ID D017093; D048550
ADR Severity Grade (FAERS)
ADR Severity Grade (CTCAE)
Synonym
Failure liver | Hepatic failure | Liver failure | Hepatic insufficiency | Hepatobiliary insufficiency | Hepatic decompensation | Liver Failure | Hepatic Failure
Drugs Leading to the ADR
Drug IDDrug NameADR Frequency (FAERS)ADR Severity Grade (FAERS)
BADD_D02500Alpelisib0.000224%
BADD_D02505Gilteritinib0.000112%
BADD_D02509Brigatinib0.000112%
BADD_D02515Pexidartinib0.000112%
BADD_D02524Ivosidenib0.000168%
BADD_D02526Larotrectinib0.000246%
BADD_D02556Ferrous cation0.001882%
BADD_D02568Lutetium oxodotreotide lu-177-
BADD_D02577Oseltamivir acid0.000496%
BADD_D02585Pralsetinib0.000302%
BADD_D02586Radium ra-223 dichloride-
BADD_D02588Remdesivir0.000988%
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