Anti-TNF-α therapy induced psoriasis in patients with rheumatoid arthritis according to FDA postmarketing surveillance data

  FDA Adverse Event Reporting System (FAERS) The United States Food and Drug Administration Adverse Event Reporting System (FAERS) is a data repository that collects voluntary drug-related reports from healthcare professionals, consumers, and legal representatives. In cases where the adverse reaction (AE) is reported to the manufacturer, the manufacturer is required to forward the report…