Adalimumab-atto 40mg/80mg SC
AMJEVITA is a tumor necrosis factor (TNF) blocker indicated for treatment of:
• Rheumatoid Arthritis (RA).
• Juvenile Idiopathic Arthritis (JIA).
• Psoriatic Arthritis (PsA).
• Ankylosing Spondylitis (AS).
• Adult Crohn’s Disease (CD).
• Ulcerative Colitis (UC).
• Plaque Psoriasis (Ps) .
See package insert for complete information.
• Injection: 40 mg/0.8 mL in a single-use prefilled SureClick® autoinjector.
• Injection: 40 mg/0.8 mL in a single-use prefilled glass syringe.
• Injection: 20 mg/0.4 mL in a single-use prefilled glass syringe.
Serious infections: Do not start AMJEVITA during an active infection. If an infection develops, monitor carefully, and stop AMJEVITA if infection becomes serious.
• Invasive fungal infections: For patients who develop a systemic illness on AMJEVITA, consider empiric antifungal therapy for those who reside or travel to regions where mycoses are endemic.
• Malignancies: Incidence of malignancies was greater inadalimumab product-treated patients than in controls.
• Anaphylaxis or serious allergic reactions may occur
• Hepatitis B virus reactivation: Monitor HBV carriers during and several months after therapy. If reactivation occurs, stop AMJEVITA 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 AMJEVITA. • Heart failure: Worsening or new onset, may occur.
• Lupus-like syndrome: Stop AMJEVITA.