Adverse Drug Reaction Classification System

Pharmaceutical Information
Drug Name Terbinafine
Drug ID BADD_D02160
Description Terbinafine hydrochloride (Lamisil) is a synthetic allylamine antifungal.[L9065,L9068] It is highly lipophilic in nature and tends to accumulate in skin, nails, and fatty tissues.[A1279] Like other allylamines, terbinafine inhibits ergosterol synthesis by inhibiting the fungal squalene monooxygenase (also called squalene epoxidase), an enzyme that is part of the fungal cell wall synthesis pathway.[A1279,A1281,L9068] Terbinafine hydrochloride was granted FDA approval on 30 December 1992.[L9064]
Indications and Usage Terbinafine hydrochloride is indicated to treat fungal skin and nail infections caused by _Trichophyton_ species, _Microsporum canis_, _Epidermophyton floccosum_,[L9068] and _Tinea_ species.[L9065] Terbinafine hydrochloride also treats yeast infections of the skin caused by _Candida_ species and _Malassezia furfur_.[L9068]
Marketing Status approved; investigational; vet_approved
ATC Code D01AE15; D01BA02
DrugBank ID DB00857
KEGG ID D02375
MeSH ID D000077291
PubChem ID 1549008
TTD Drug ID D01AYJ
NDC Product Code 71205-152; 71335-1668; 69097-859; 62135-572; 63187-213; 76282-209; 72189-243; 59349-0008; 70518-1191
UNII G7RIW8S0XP
Synonyms Terbinafine | Terbinafine, (Z)-isomer | Terbinafine, (Z)- | Lamisil | (E)-N-(6,6-Dimethyl-2-heptenynyl)-N-methyl-1-naphthalenementhamin hydrochloride | TDT-067 | TDT 067 | TDT067 | DA 5505 | SF 86-327 | SF 86 327 | SF 86327 | SF-86-327 | SF86327 | Terbinafine Hydrochloride
Chemical Information
Molecular Formula C21H25N
CAS Registry Number 91161-71-6
SMILES CC(C)(C)C#CC=CCN(C)CC1=CC=CC2=CC=CC=C21
Chemical Structure
ADRs Induced by Drug
*The priority for ADR severity classification is based on FAERS assessment, followed by the most severe level in CTCAE rating. If neither is available, it will be displayed as 'Not available'.
**The 'Not Available' level is hidden by default and can be restored by clicking on the legend twice.
ADR Term ADReCS ID ADR Frequency (FAERS) ADR Severity Grade (FAERS) ADR Severity Grade (CTCAE)
Deficiency of bile secretion09.01.01.0110.000223%-
Drug-induced liver injury09.01.07.023; 12.03.01.0440.003783%-
Drug reaction with eosinophilia and systemic symptoms10.01.01.021; 12.03.01.064; 23.03.05.0050.001489%-
Multiple organ dysfunction syndrome08.01.03.0570.000447%
Abnormal loss of weight14.03.02.0190.000298%-
Alcohol interaction08.06.03.003---
Cholangitis acute09.02.01.0060.000298%-
Concomitant disease aggravated08.01.03.0630.000223%-
Dermatitis exfoliative generalised10.01.01.029; 23.03.07.0020.000447%-
Faeces pale07.01.03.0050.000298%-
Hairy cell leukaemia01.10.06.002; 16.01.06.0020.000298%-
Nikolsky's sign23.03.07.0090.000149%-
Pityriasis rosea23.03.08.0030.000372%-
Rash papulosquamous23.03.08.0140.000223%-
Urticarial vasculitis10.01.06.012; 23.04.02.012; 24.12.04.0250.000223%-
Subacute cutaneous lupus erythematosus10.04.03.012; 15.06.02.012; 23.03.02.0200.002234%-
Onychalgia23.02.05.0260.000149%-
Skin plaque23.03.03.0440.000670%-
Herbal interaction08.06.03.0050.000223%-
Small fibre neuropathy05.07.04.007; 14.07.04.007; 17.09.03.0210.000223%-
Tongue discomfort07.14.02.019---
Drug ineffective for unapproved indication08.06.01.038; 12.09.02.002---
Hepatic cytolysis09.01.07.0360.000596%-
Intermenstrual bleeding21.01.01.0150.000477%-
Palmoplantar pustulosis10.02.01.099; 23.03.14.0110.000298%-
Pharyngeal swelling22.04.05.028---
Symmetrical drug-related intertriginous and flexural exanthema10.01.01.046; 23.03.05.0120.000149%-
Taste disorder07.14.03.004; 17.02.07.0290.000477%-
The 12th Page    First    Pre   12    Total 12 Pages