Secukinumab
Brand names: Cosentyx
Secukinumab is a subcutaneously administered anti-interleukin-17A monoclonal antibody used in rheumatology for psoriatic arthritis, axial spondyloarthritis (including ankylosing spondylitis) and, in dermatology, plaque psoriasis.
Adult dose
Dose adjustments
Not studied in renal or hepatic impairment - no dose recommendations can be made.
Dose auto-extracted from UK Summary of Product Characteristics (SPC) via the eMC; US FDA prescribing information (openFDA / DailyMed) — cross-check; US labelling may differ from UK — not yet clinician-verified. Always confirm against the product SmPC and your local formulary before prescribing.
Contraindications
- Hypersensitivity to the active substance or to any of the excipients
- Clinically important, active infection, e.g. active tuberculosis
Side effects
- Upper respiratory tract infections (very common, 17.1%; most frequently nasopharyngitis and rhinitis)
- Oral herpes (common)
- Headache (common)
- Diarrhoea and nausea (common)
- Eczema and fatigue (common)
- Rare: anaphylactic reactions and angioedema; uncommon: neutropenia, oral candidiasis, inflammatory bowel disease
Interactions
- Certain CYP450 substrates: increased cytokine concentrations during chronic inflammation may suppress CYP enzyme formation - on initiation or discontinuation of secukinumab in patients receiving CYP450 substrates, consider monitoring the therapeutic effect or concentration of the substrate and adjusting its dose (US label section 7; UK SPC section 4.5 not retrieved in this bundle)
Clinical monograph
How it works
It binds and neutralises interleukin-17A, a key pro-inflammatory cytokine of the Th17 pathway involved in the joint and skin inflammation of spondyloarthritides and psoriasis.
Prescribing in practice
- Screen for and treat latent tuberculosis and exclude active infection before starting, as with other biologics.
- Use with caution in inflammatory bowel disease because IL-17 inhibition can trigger new onset or exacerbations of Crohn's disease and ulcerative colitis.
- Candida and other mucocutaneous infections are more frequent, and live vaccines should be avoided during treatment.
Monitoring
Monitor clinically for infection, for new or worsening inflammatory bowel symptoms, and for treatment response throughout therapy.
Counselling the patient
- Report signs of infection, including persistent oral or genital thrush.
- Tell us about any new or worsening abdominal pain or diarrhoea.
- It is a subcutaneous injection that can be self-administered after training.
Evidence & guidelines
Its rheumatology indications are supported by randomised controlled trials demonstrating improved joint, spinal and skin outcomes in spondyloarthritis and psoriatic arthritis.
Reference: NICE TA415/TA408; FUTURE trials; Drug verified in RxNorm (NLM); confirm dosing against the manufacturer SPC (eMC). Verify against your local formulary and current prescribing references before prescribing. The structured dose values shown have been reviewed by a clinician. Monograph status: clinician-reviewed (2026-07-04).
Related
Curated clinical cross-links plus same-class fallbacks.
- Revised Original International Autoimmune Hepatitis Score (IAIHG) · Autoimmune Liver Disease
- Ho Index for Predicting Response to Medical Therapy in IBD · Inflammatory Bowel Disease
- Rh(D) Immune Globulin Dosage for Maternal-Fetal Haemorrhage · Haematology in Pregnancy
- AREDS Classification of Age-related Macular Degeneration · Macular Degeneration
- Diabetic Macular Oedema (DMO) Classification · Diabetic Retinopathy
- Retinopathy of Prematurity — International Classification (ICROP3) · Paediatric Retina
- Cutaneous Lupus Erythematosus · BAD; EULAR
- Osteoporosis / Fragility Fracture · NOGG 2021; NICE NG147; NG224
- Arteritic AION (Giant Cell Arteritis) · RCOphth; BSR
- Osteoarthritis Hip / Knee Management · NICE NG226 (2022)
- Lupus Nephritis · EULAR/ERA-EDTA 2019; KDIGO 2024
- Rheumatoid Arthritis Management · NICE CG79 2018 / EULAR 2022