GNH USA

Europe — EMA

Kineret

GNH USA supplies Kineret (Anakinra), a Interleukin‑1 receptor antagonist for rheumatoid arthritis, CAPS, NOMID, systemic juvenile idiopathic arthritis

Anakinra

Request sourcing

1
Pack/s

What is Anakinra?

Anakinra, the active ingredient in Kineret, is a Interleukin-1 receptor antagonist presented as a 100 mg/mL solution for injection for subcutaneous use. It treats rheumatoid arthritis and several autoinflammatory conditions in adults and children.

GNH USA supplies Kineret as a licensed, GDP-compliant international pharmaceutical supplier serving hospitals, pharmacies and clinics worldwide.

What is Anakinra used for?

Kineret is an Interleukin‑1 receptor antagonist used in a range of inflammatory and autoinflammatory diseases. - Rheumatoid arthritis: reduces signs and symptoms of disease activity. - Cryopyrin‑Associated Periodic Syndromes (CAPS): controls recurrent fever and systemic inflammation. - Neonatal‑onset multisystem inflammatory disease (NOMID): mitigates chronic inflammatory manifestations. - Systemic juvenile idiopathic arthritis: improves joint function and reduces systemic features. - Adult‑onset Still's disease: alleviates fever, rash and joint pain. - Acute gout flares: shortens duration and severity of attacks.

What are the side effects of Anakinra?

Kineret may cause a range of adverse reactions, from mild to severe.

Common Side Effects: - Injection‑site reactions such as redness, swelling or pain. - Headache. - Nausea. - Upper respiratory tract infection. - Dizziness. - Arthralgia.

Serious or Rare Side Effects: - Neutropenia or other significant blood‑count abnormalities. - Serious infections, including sepsis. - Anaphylactic or severe allergic reactions. - Elevated liver enzymes. - Rare malignancies reported in long‑term use.

What precautions apply to Anakinra?

Before initiating Kineret, clinicians should evaluate several safety considerations. - Pregnancy: Category B – use only when the potential benefit justifies the potential risk to the fetus. - Infection risk: screen for active infections and monitor for new signs during therapy. - Neutropenia: obtain baseline and periodic complete blood counts. - Live vaccines: avoid administration while on treatment. - Renal impairment: dose adjustment may be required in severe cases. - Store at 2-8°C: keep refrigerated, protect from light, do not freeze or shake.

What does Anakinra interact with?

Kineret can interact with other agents that affect immune function.

Major Interactions (Avoid): - Live vaccines: may cause severe infection. - Concurrent use of other biologic immunosuppressants (e.g., TNF inhibitors): heightened infection risk. - Cytotoxic chemotherapy: increased immunosuppression.

Moderate Interactions (Monitor Closely): - Systemic corticosteroids: additive immunosuppressive effect. - Conventional disease‑modifying antirheumatic drugs (e.g., methotrexate, azathioprine): monitor for infection. - Antibiotics: adjust therapy if neutropenia develops.

Frequently asked questions

What conditions is Kineret used to treat?+
Kineret (anakinra) is approved for rheumatoid arthritis, Cryopyrin‑Associated Periodic Syndromes (CAPS), Neonatal‑onset multisystem inflammatory disease (NOMID), systemic juvenile idiopathic arthritis, adult‑onset Still's disease, and acute gout flares. It targets diseases driven by excess interleukin‑1 activity.
How does anakinra work?+
Anakinra is a recombinant form of the human interleukin‑1 receptor antagonist. It binds competitively to the IL‑1 type I receptor, blocking both IL‑1α and IL‑1β from initiating inflammatory signaling, which reduces downstream cytokine production and clinical inflammation.
What is the usual dose of Kineret?+
The prescribing healthcare professional determines the dose of Kineret based on the specific indication, patient weight, renal function and clinical response. Dosing is individualized and should follow the latest prescribing information or specialist guidance.
Is Kineret safe during pregnancy or breastfeeding?+
Kineret is classified as Pregnancy Category B, indicating that animal studies have not shown risk but there are limited human data. It should be used only if the potential benefit outweighs any possible risk to the fetus. Caution is also advised during breastfeeding.
How do I order Kineret from GNH USA?+
To order Kineret, submit an enquiry on the product page at gnh-usa.com with the required quantity. GNH USA supplies hospitals, pharmacies and procurement teams worldwide, verifies trade or institutional credentials, and then provides pricing, availability, cold‑chain shipping details and necessary import documentation.
How does Kineret compare with other IL‑1 inhibitors?+
Kineret (anakinra) is a short‑acting IL‑1 receptor antagonist administered daily, whereas agents like canakinumab are longer‑acting monoclonal antibodies given monthly. Anakinra offers rapid onset and flexibility in dose adjustment, but requires more frequent injections compared with longer‑acting alternatives.
What are the storage requirements for Kineret?+
Kineret should be stored refrigerated at 2‑8 °C. Keep the vial in its original packaging, protect it from light, and do not freeze or shake the solution. If temperature excursions occur, discard the product according to local regulations.
How is Kineret administered?+
Kineret is supplied as a 100 mg/mL solution for injection and is given subcutaneously, usually in the abdomen, thigh or upper arm. It is administered using a prefilled syringe or autoinjector according to the prescriber’s instructions.
What are the most serious risks to watch for while using Kineret?+
The most serious risks include severe infections such as sepsis, neutropenia or other blood‑count abnormalities, and hypersensitivity reactions including anaphylaxis. Patients should be monitored regularly for signs of infection, low white‑blood‑cell counts and any allergic symptoms.
Who should not use Kineret?+
Kineret is contraindicated in individuals with known hypersensitivity to anakinra or any component of the formulation. It should also be avoided in patients with active, serious infections until the infection is adequately treated.
Information provided on this page is for educational use by procurement and clinical professionals. Always consult a licensed healthcare provider for medical advice and prescribing decisions. GNH USA supplies this product subject to applicable regulatory and licensing requirements.

Product details

Drug
Anakinra
Route
Subcutaneous Use
Manufacturer
Swedish Orphan Biovitrum Ab (Publ)
Origin
EU

Related products