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Kineret — Description, Dosage, Side Effects | PillsCard
OTC
Kineret
INN: anakinra
Data updated: 2026-05-02
Available in:
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About This Product
Manufacturer
User Reviews
Reviews reflect personal experiences and are not medical advice. Always consult your doctor.
Swedish Orphan Biovitrum AB (publ)
ATC Code
L04AC03
Source
EMA · EMEA/H/C/000363
(
ARTG
)
KINERET (anakinra) is indicated: -for the treatment of active adult rheumatoid arthritis (RA) in patients who have had inadequate response to one or more other Disease Modifying Anti Rheumatic Drugs (DMARDs). KINERET should be given in combination with methotrexate. - in adult and paediatric patients aged 8 months and older with a body weight of 10 kg or above for the treatment of Cryopyrin-Associated Periodic Syndromes (CAPS) including Neonatal-Onset Multisystem Inflammatory Disease (NOMID) / Chronic Infantile Neurological, Cutaneous, Articular Syndrome (CINCA), Muckle-Wells Syndrome (MWS), and Familial Cold Autoinflammatory Syndrome (FCAS). - for the treatment of active Systemic Juvenile Idiopathic Arthritis (SJIA) in patients 2 years and above who have failed to respond adequately to non-biological DMARDs
⚠️ Warnings
•Avoid vaccination while taking this medication.
Swelling or bruising at the injection site occurs; apply a cold pack on the injection site immediately after injection.
It should not be used in children.
Caution needed for patients with history of infection, asthma, HIV infection or AIDS, or kidney disease, during pregnancy and breast feeding.
Do not reuse needles, syringes, or other materials.