This information is for educational purposes only. It is not intended as medical advice. Always consult a qualified healthcare professional.
Simponi — Description, Dosage, Side Effects | PillsCard
OTC
Simponi
50 mg/.5mL, Injection, solution
INN: GOLIMUMAB
Data updated: 2026-05-02
Available in:
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Form
INJECTION, SOLUTION
Dosage
50 mg/.5mL
Route
SUBCUTANEOUS
Storage
—
About This Product
User Reviews
Reviews reflect personal experiences and are not medical advice. Always consult your doctor.
Manufacturer
Janssen Biotech, Inc.
ATC Code
L04AB06
Source
OPENFDA_NDC
(
ARTG
)
SIMPONI,Rheumatoid arthritis (RA),SIMPONI, in combination with methotrexate, is indicated for:,The treatment of moderate to severely active rheumatoid arthritis in adult patients when the response to disease-modifying anti-rheumatic drug therapy, including methotrexate, has been inadequate. SIMPONI has also been shown to inhibit the progression of joint damage as measured by X-ray.,Psoriatic arthritis (PsA),SIMPONI, alone or in combination with methotrexate, is indicated for:,The treatment of active and progressive psoriatic arthritis in adult patients when the response to previous disease-modifying anti-rheumatic drug therapy has been inadequate. SIMPONI has also been shown to inhibit the progression of peripheral joint damage as measured by X-ray in patients with polyarticular symmetrical subtypes of the disease, and improve physical function.,Axial Spondyloarthritis,Ankylosing spondylitis (AS),SIMPONI is indicated for:,The treatment of active ankylosing spondylitis in adult patients.
Non-radiographic axial spondyloarthritis (nr-Axial SpA),SIMPONI is indicated for the treatment of adults with active non-radiographic axial spondyloarthritis with objective signs of inflammation as indicated by elevated C-reactive protein (CRP) and/or magnetic resonance imaging (MRI) evidence, who have had an inadequate response to, or are intolerant to, nonsteroidal anti-inflammatory drugs (NSAIDs).,Ulcerative colitis (UC),SIMPONI is indicated for:
The treatment of moderately to severely active ulcerative colitis in adult patients who have had an inadequate response to conventional therapy. Patients should show a clinical response within 6 weeks of treatment to continue treatment beyond that time (see section 5.1 PHARMACODYNAMIC PROPERTIES, Clinical Trials).
⚠️ Warnings
• Caution should be exercised in patients with history of tuberculosis, jaundice, heart problem, sugar, HIV, cancer, tingling, nervousness, autoimmune disorder, blood disorder, who are taking other medication, any allergy, elderly, children, during pregnancy and breastfeeding.
• It may cause dizziness or vision problem, do not drive a car or operate machinery while taking this medication.
• Avoid excess dosage.
• Change injection sites.
• Patient may develop with increased risk of blood cancer with the following symptoms: unusual bruising, unusual lumps or swelling, unusual tiredness or weakness, weight loss. If it is so consult with your doctor.
• It may reduce platelet counts; avoid bruising or injury while taking this medication.