
Acitretin, a synthetic retinoid, is the pharmacologically active metabolite of etretinate. It is currently approved by the US Food and Drug Administration for the treatment of severe psoriasis in adults and has been established as a second-line therapy for the treatment of psoriasis resistant to the use of topical therapy. It is also an option for generalized pustular psoriasis, palmoplantar pustulosis, exfoliative erythrodermic psoriasis, and severe psoriasis in the setting of acitretin. It also has been shown to have chemo-preventative characteristics. Acitretin is limited by its teratogenicity and therefore considered inappropriate in most female patients of childbearing age. Common side effects include mucocutaneous dryness and elevated triglycerides.
Adult, United States Food and Drug Administration, Drug Resistance, Severity of Illness Index, Acitretin, United States, Keratolytic Agents, Teratogens, Etretinate, Humans, Psoriasis, Female, Drug Approval
Adult, United States Food and Drug Administration, Drug Resistance, Severity of Illness Index, Acitretin, United States, Keratolytic Agents, Teratogens, Etretinate, Humans, Psoriasis, Female, Drug Approval
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| influence This indicator reflects the overall/total impact of an article in the research community at large, based on the underlying citation network (diachronically). | Top 10% | |
| impulse This indicator reflects the initial momentum of an article directly after its publication, based on the underlying citation network. | Top 10% |
