Adverse Drug Reaction Classification System

Pharmaceutical Information
Drug Name Acitretin
Drug ID BADD_D00036
Description An oral retinoid effective in the treatment of psoriasis. It is the major metabolite of etretinate with the advantage of a much shorter half-life when compared with etretinate.
Indications and Usage For the treatment of severe psoriasis in adults.
Marketing Status approved
ATC Code D05BB02
DrugBank ID DB00459
KEGG ID D02754
MeSH ID D017255
PubChem ID 5284513
TTD Drug ID D05QDC
NDC Product Code 17337-0003; 59981-011; 0093-1136; 0115-1752; 42291-087; 62147-0145; 0115-1751; 42794-081; 0378-7020; 71214-0698; 42291-088; 58159-058; 71052-692; 0115-1753; 17337-0004; 71214-0667; 0115-1750; 71214-0668; 71214-0669; 42291-086; 42794-080; 0093-1135; 0093-1138; 62147-0146; 76055-0001; 42794-083; 0378-7023
UNII LCH760E9T7
Synonyms Acitretin | Etretin | Isoacitretin | Isoetretin | Ro 10-1670 | Ro 101670 | Ro-10-1670 | Ro101670 | 13-cis-Acitretin | Neotigason | Soriatane | Acitretin, (Z,E,E,E)-Isomer | Ro-13-7652 | Ro137652 | Ro 13-7652 | Ro 137652
Chemical Information
Molecular Formula C21H26O3
CAS Registry Number 55079-83-9
SMILES CC1=CC(=C(C(=C1C=CC(=CC=CC(=CC(=O)O)C)C)C)C)OC
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)
Thirst08.01.09.021; 14.03.02.007---
Tinnitus04.04.01.002; 17.04.07.004--
Tongue disorder07.14.01.002---
Tongue ulceration07.14.01.003---
Urinary tract infection11.01.14.004; 20.08.02.001--
Urine abnormality20.02.01.013---
Urticaria10.01.06.001; 23.04.02.001--
Vaginal discharge21.08.02.002--
Vascular purpura01.01.04.007; 23.06.01.008; 24.07.06.011---
Vasculitis10.02.02.006; 24.12.04.027--
Vision blurred06.02.06.007; 17.17.01.0100.001250%
Visual acuity reduced06.02.10.012; 17.17.01.011--
Visual field defect06.02.07.003; 17.17.01.001---
Visual impairment06.02.10.0130.001250%-
Vitamin D deficiency14.12.03.0030.001250%-
VIth nerve paralysis06.05.02.009; 17.04.02.0020.001875%-
Vomiting07.01.07.003--
Vulvovaginitis11.01.10.003; 21.14.02.005---
Weight decreased13.15.01.005--
Weight increased13.15.01.006--
White blood cell count decreased13.01.06.012--
White blood cell count increased13.01.06.013---
White blood cells urine positive13.13.02.004---
Xerophthalmia06.06.03.008; 14.12.03.002---
Xerosis08.01.03.016---
Vasculitis gastrointestinal07.08.03.013; 10.02.02.022; 24.12.04.0280.001250%-
Joint range of motion decreased15.01.02.0060.001875%
Onychoclasis23.02.05.005---
Peripheral swelling02.05.04.015; 08.01.03.053---
Osteopenia14.04.04.004; 15.02.03.0030.001875%-
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ADReCS-Target
Drug Name ADR Term Target
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