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; D017093; D017093; 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
ADR Related Proteins
Protein Name UniProt AC TTD Target ID
Not AvailableNot AvailableNot Available
Drugs Leading to the ADR
Drug IDDrug NameADR Frequency (FAERS)ADR Severity Grade (FAERS)
BADD_D02442Magnesium oxide0.000152%
BADD_D02453Midostaurin0.000139%
BADD_D02461Lanreotide0.001023%
BADD_D02464Fingolimod--
BADD_D02466Levomilnacipran0.000076%
BADD_D02470Nintedanib0.000556%
BADD_D02477Tenofovir alafenamide0.000377%
BADD_D02480Alectinib0.000347%
BADD_D02483Ribociclib0.000278%
BADD_D02509Brigatinib0.000139%
BADD_D02524Ivosidenib0.000139%
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