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All the authors participated in data analysis and reviewed and approved the final manuscript

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The FDA authorized Eli Lillys drug as part of a new program aimed at cutting drug approval times, reviewing the application in in 50 days

(5.1) Malignancies: Incidence of malignancies was greater in HUMIRA-treated patients than in controls (5.2) Anaphylaxis or serious hypersensitivity reactions may occur (5.3) Hepatitis B virus reactivation: Monitor HBV carriers during and several months after therapy