Adverse Drug Reaction Classification System

ADR Ontology
ADR Term Adverse event
ADR ID BADD_A05744
ADR Hierarchy
08      General disorders and administration site conditions
08.06      Therapeutic and nontherapeutic effects (excl toxicity)
08.06.01      Therapeutic and nontherapeutic responses
08.06.01.010      Adverse event
Description Not Available
MedDRA Code 10060933
MeSH ID Not Available
ADR Severity Grade (FAERS)
ADR Severity Grade (CTCAE) Not Available
Synonym
Certain adverse effects not elsewhere classified | Late effect of adverse effect of drug, medicinal or biological substance | Other specified adverse effect, not elsewhere classified | Other specified adverse effects, not elsewhere classified | Adverse event NOS | Adverse event
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_D00012Abatacept--
BADD_D00049Agalsidase beta--
BADD_D00065Alendronate sodium--
BADD_D00100Ambrisentan--
BADD_D00290Botulinum toxin type a--
BADD_D00472Ciprofloxacin hydrochloride--
BADD_D00529Copper--
BADD_D00774Entecavir--
BADD_D01132Idursulfase--
BADD_D01178Iodixanol--
BADD_D01586Norethindrone acetate--
BADD_D01814Pralatrexate--
BADD_D01967Ropinirole hydrochloride--
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