
Kineret (Anakinra)
Brand Name: KINERETActive Ingredient: Anakinra
Dosage Form: 100 mg/0.67 mL solution for subcutaneous injection
Manufacturer Name: Swedish Orphan Biovitrum AB
For the treatment of Still’s disease, including Systemic Juvenile Idiopathic Arthritis (SJIA) and Adult-Onset Still’s Disease (AOSD), with active systemic features of moderate to high disease activity, or in patients with ongoing disease activity after treatment with non-steroidal anti-inflammatory drugs (NSAIDs) or glucocorticoids, Kineret is indicated in adults, adolescents, children, and infants aged eight months and older with a body weight of 10.
It is possible to administer Kineret alone or in combination with other anti-inflammatory medications and disease-modifying antirheumatic medications (DMARDs). The FDA-approved treatment for the neonatal-onset multisystem inflammatory disease (NOMID), a type of cryopyrin-associated periodic syndromes, in both children and adults is Kineret.


Why is Kineret injection prescribed?
- Reduce the signs and symptoms of moderate to severe active rheumatoid arthritis (RA) and slow the damage it causes.
- To treat people with a form of Cryopyrin-Associated Periodic Syndromes (CAPS) called Neonatal-Onset Multisystem Inflammatory Disease (NOMID)
- To treat people with Deficiency of Interleukin-1 Receptor Antagonist (DIRA)
To administer Kineret, a subcutaneous injection is used.
Kineret is provided in a graduated prefilled syringe and is ready for use. Using the graduated prefilled syringe, doses between 20 and 100 mg are possible. The syringe is inappropriate for pediatric patients with a body weight below 10 kg because the minimum dose is 20 mg.
Who should not take KINERET?
- Individuals with allergies to proteins produced by the E. coli bacteria.
- Individuals with allergies to any component of KINERET, including anakinra. A complete list of KINERET's ingredients can be seen at the end of the patient information sheet.
- Women who are pregnant or breastfeeding.
If you’re unsure, speak with your doctor.
What are the possible side effects of KINERET?
Severe possible side effects of KINERET include:
- Allergic reactions
- Fever or chills
- Headache
- Nausea and Vomiting
- Diarrhea
- Joint pain
- Fever
- Feeling like you have the flu
- Sore throat or runny nose
- Sinus infection
- Redness, Bruising, Swelling, and Pain
- Urinary tract infection
- Pain in your stomach area
What documents are required to import KINERET to Dubai?
The following paperwork is necessary to import:
- An authentic prescription from a licensed physician.
- Diagnostic reports for patients
- Patients id proof (Certificate of Origin)
Special Precautions For Kineret
- Anakinra is sold in graduated prefilled syringes at a reasonable injection cost.
- Kineret is a sterile, unpreserved fluid. For one use only.
- Keep in the refrigerator at 2 to 8 degrees Celsius.
- Avoid freezing.
- To protect against light, keep it in the original container.
- The prefilled syringe shouldn't be shaken.
- For ambulatory use, Kineret may be left out of the fridge for up to 12 hours at a temperature no higher than 25 °C without going past the expiration date.
- The product must be thrown off once this time has passed instead of returning it to the refrigerator.
- Before using the solution, visually inspect it for contaminants and discolouration.
- It is only advised to inject transparent, colourless to white solutions that may contain a few translucent to white amorphous particles from the substance itself.
- The existence of these particles has no impact on the product's quality.
- Following local legislation, waste and unneeded pharmaceuticals should be disposed of.
Shelf life of anakinra injection: Three years.
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Please schedule a consultation with us by calling us at +971 54 777 1238 or +971 55 223 1090 or email us at [email protected] to know how much anakinra injection costs in Dubai. Our helpful team would be happy to assist you and provide any general or medical information.
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