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Anakinra

Monoclonal Antibody · Immunosuppressant

Monoclonal AntibodyImmunosuppressant
CDSCO approved
EXCRETION
not curated
INTERACTIONS
12 major
SEVERE in our sources
PREGNANCY
Manufacturer advises avoid.
FDA category + note
Top interactionssee all 12
  • AdalimumabSevereDatabaseKimi deep-research + Cla
  • BaricitinibSevereDatabaseDDInter
  • CertolizumabSevereDatabaseDDInter
  • CladribineSevereDatabaseDDInter

Mechanism

Anakinra inhibits the activity of interleukin-1 (IL-1). It antagonizes IL-1 action at its receptor, blocking IL-1 activity in vitro and in vivo. This thereby inhibits the progression of structural damage associated with active rheumatoid arthritis and other inflammatory conditions.

Indications

Rheumatoid arthritis (in combination with methotrexate) which has not responded to methotrexate alone (specialist use only)Cryopyrin-associated periodic syndromes (specialist use only)Still’s disease (specialist use only)rheumatoid arthritis (management of joint disease)cryopyrin-associated periodic syndromesfamilial cold autoinflammatory syndromesmuckle-wells syndromesneonatal-onset multisystem inflammatory disease

Dosing

Adult
Rheumatoid arthritis: 100 mg once daily by subcutaneous injection. Cryopyrin-associated periodic syndromes: 1–2 mg/kg daily by subcutaneous injection; for severe cases, usual maintenance is 3–4 mg/kg daily by subcutaneous injection. Still’s disease: For body-weight up to 49 kg, 1–2 mg/kg daily by subcutaneous injection; for body-weight 50 kg and above, 100 mg daily by subcutaneous injection.
Hepatic adjustment
Manufacturer advises caution in severe impairment.
Max dose
8 mg/kg daily (for severe cryopyrin-associated periodic syndromes)

Contraindications

  • Active infection
  • Neutropenia (absolute neutrophil count less than 1.5 x 10^9/litre)—do not initiate
  • Pre-existing malignancy
  • live vaccines

Side effects

Common
HeadacheInfectionNeutropeniaThrombocytopenia
Serious
  • Neutropenia (discontinue if neutropenia develops)
  • Hepatitis
  • increased risk of serious opportunistic infections

Pregnancy & lactation

Pregnancy

Manufacturer advises avoid.

Lactation

Manufacturer advises avoid—no information available.

Drug interactions

Adalimumab
Severe
Database

Markedly increased serious infection, no added benefit

Do not combine biologic DMARDs

Source: Kimi deep-research + Cla

Baricitinib
Severe
Database

Drug interaction classified as: others

Source: DDInter

Certolizumab
Severe
Database

Drug interaction classified as: synergy

Source: DDInter

Cladribine
Severe
Database

Drug interaction classified as: synergy

Source: DDInter

Deferiprone
Severe
Database

Drug interaction classified as: synergy

Source: DDInter

Etanercept
Severe
Database

Additive immunosuppression

Do not combine biologic DMARDs

Source: Kimi deep-research + Cla

Fingolimod
Severe
Database

Drug interaction classified as: synergy

Source: DDInter

Golimumab
Severe
Database

Drug interaction classified as: synergy

Source: DDInter

Infliximab
Severe
Database

Drug interaction classified as: synergy

Source: DDInter

Leflunomide
Severe
Database

Drug interaction classified as: others

Source: DDInter

Measles Virus Vaccine Live Attenuated
Severe
Database

Drug interaction classified as: others

Source: DDInter

Mumps Virus Strain B Level Jeryl Lynn Live Antigen
Severe
Database

Drug interaction classified as: others

Source: DDInter

Related guidelines

Other Monoclonal Antibody drugs

Ask House about Anakinra

Continue into a citation-backed clinical answer with the drug context already attached.

Sources: KD Tripathi 7e, Goodman & Gilman 14e, Harrison 22e, Katzung·Verified: 2026-05-10 · House clinical team