Adalimumab-aaty 40mg/80mg SC
YUFLYMA is a tumor necrosis factor (TNF) blocker indicated for:
•Rheumatoid Arthritis (RA)
•Juvenile Idiopathic Arthritis (JIA)
•Psoriatic Arthritis (PsA)
•Ankylosing Spondylitis (AS)
•Crohn’s Disease (CD)
•Ulcerative Colitis (UC)
•Plaque Psoriasis (Ps)
•Hidradenitis Suppurativa (HS) See package insert for complete information
Injection:
• Single-dose prefilled auto-injector (YUFLYMA AI): 40 mg/0.4 mL
• Single-dose prefilled syringe with safety guard : 40 mg/0.4 mL
• Single-dose prefilled syringe: 40 mg/0.4 mL
• Serious infections: Do not start YUFLYMA during an active infection. If an infection develops, monitor carefully, and stop YUFLYMA if infection becomes serious.
• Invasive fungal infections: For patients who develop a systemic illness on YUFLYMA, consider empiric antifungal therapy for those who reside or travel to regions where mycoses are endemic.
• Malignancies: Incidence of malignancies was greater in adalimumab-treated patients than in controls.
• Anaphylaxis or serious hypersensitivity reactions may occur.
• Hepatitis B virus reactivation: Monitor HBV carriers during and several months after therapy. If reactivation occurs, stop YUFLYMA and begin anti-viral therapy.
• Demyelinating disease: Exacerbation or new onset, may occur.
• Cytopenias, pancytopenia: Advise patients to seek immediate medical attention if symptoms develop, and consider stopping YUFLYMA.
• Heart failure: Worsening or new onset, may occur.
• Lupus-like syndrome: Stop YUFLYMA.