Adverse Drug Reaction Classification System

ADR Ontology
ADR Term Liver function test increased
ADR ID BADD_A06835
ADR Hierarchy
13      Investigations
13.03      Hepatobiliary investigations
13.03.01      Liver function analyses
13.03.01.044      Liver function test increased
Description Not Available
MedDRA Code 10077692
MeSH ID Not Available
ADR Severity Grade (FAERS)
ADR Severity Grade (CTCAE) Not Available
Synonym
ICG increased | LFTs raised | Raised LFTs | Liver function tests raised | Raised liver function tests | Liver function test increased
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_D01629Osimertinib0.001598%
BADD_D01653Paclitaxel--
BADD_D01654Palbociclib0.010656%
BADD_D01656Paliperidone--
BADD_D01679Paroxetine--
BADD_D01680Paroxetine hydrochloride--
BADD_D01681Paroxetine hydrochloride hemihydrate--
BADD_D01682Paroxetine impurity a--
BADD_D01683Paroxetine mesylate--
BADD_D01687Pazopanib0.011456%
BADD_D01717Pentamidine--
BADD_D01718Pentamidine isethionate--
BADD_D01728Pentosan polysulfate--
BADD_D01730Pentostatin--
BADD_D01765Phenytoin--
BADD_D01783Pirfenidone0.011001%
BADD_D01798Pomalidomide--
BADD_D01799Ponatinib0.000799%
BADD_D01804Posaconazole--
BADD_D01824Pravastatin0.000072%
BADD_D01834Prednisone--
BADD_D01835Pregabalin--
BADD_D01846Procarbazine0.000533%
BADD_D01852Progesterone--
BADD_D01922Regorafenib0.004263%
BADD_D01933Ribavirin--
BADD_D01937Rifapentine--
BADD_D01954Rivaroxaban--
BADD_D01956Rivastigmine tartrate--
BADD_D01978Ruxolitinib--
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