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JAK inhibitor (JAK1/JAK2) — systemic immunosuppressant Pregnancy: Contraindicated in pregnancy — teratogenic in rats and rabbits; no adequate data in pregnant women. Women of childbearing potential must use effective contraception during and for at least 1 week after treatment. Should not be used during breast-feeding.

Baricitinib 2–4mg (Atopic Dermatitis / Alopecia Areata)

Brand names: Olumiant (2 mg and 4 mg tablets)

Baricitinib is an oral Janus kinase (JAK) inhibitor used in dermatology for moderate-to-severe atopic dermatitis and for severe alopecia areata in adults.

Auto-extracted from the source labelling — not yet independently clinician-verified. These values were distilled from the UK SPC (or the US label where noted) but have not had a clinician sign-off. Confirm against the current SmPC before prescribing.

Adult dose

Dose: 4 mg
Route: Oral
Frequency: Once daily
Atopic dermatitis (adults) and alopecia areata: recommended dose 4 mg once daily. A dose of 2 mg once daily is recommended for patients at higher risk of VTE, MACE and malignancy, for patients aged >= 65 years and for patients with a history of chronic or recurrent infections. 4 mg once daily may be considered for patients not adequately controlled on 2 mg once daily; 2 mg once daily should be considered for patients with sustained control on 4 mg who are eligible for dose tapering. Atopic dermatitis: may be used with or without topical corticosteroids (efficacy may be enhanced with topical corticosteroids); topical calcineurin inhibitors reserved for sensitive areas (face, neck, intertriginous, genital); consider discontinuing if no evidence of therapeutic benefit after 8 weeks. Alopecia areata: once stable response achieved, continue for at least several months to avoid relapse; re-assess benefit-risk at regular intervals; consider discontinuing if no evidence of benefit after 36 weeks. Treatment initiation: do not initiate if absolute lymphocyte count < 0.5 x 10^9 cells/L, absolute neutrophil count < 1 x 10^9 cells/L, or haemoglobin < 8 g/dL. Dose reduction: in adults taking strong OAT3 inhibitors such as probenecid the recommended dose is 2 mg (paediatric dose reduced by half). Paediatric atopic dermatitis (children and adolescents 2 years and older, weight-band dosing, NOT per kg): 4 mg once daily if weighing 30 kg or more; 2 mg once daily if weighing 10 kg to less than 30 kg; consider halving the dose in those with sustained control eligible for tapering; safety and efficacy not established under 2 years, and not established in children under 18 years with alopecia areata. Hepatic impairment: no dose adjustment in mild or moderate; not recommended in severe. Clinical experience in patients aged >= 75 years is very limited. Take once daily with or without food, at any time of day; tablets may be dispersed in water only for paediatric patients unable to swallow them whole. Baricitinib should only be used if no suitable treatment alternatives are available in patients 65 years and older, those with a history of atherosclerotic cardiovascular disease or other cardiovascular risk factors, and those with malignancy risk factors. SPC also states a rheumatoid arthritis regimen (4 mg once daily, 2 mg once daily in higher-risk groups) and a juvenile idiopathic arthritis regimen (2 to <18 years: 4 mg once daily if >= 30 kg, 2 mg once daily if 10 kg to <30 kg).

Dose adjustments

Renal

Adults: 2 mg once daily if creatinine clearance 30–60 mL/min. Paediatric patients with creatinine clearance 30–60 mL/min: reduce the recommended dose by half. Not recommended for use if creatinine clearance < 30 mL/min.

Dose auto-extracted from UK Summary of Product Characteristics (SPC) via the eMC — 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
  • Pregnancy

Side effects

  • Increased LDL cholesterol / hypercholesterolaemia (26.0%)
  • Upper respiratory tract infections (16.9%)
  • Headache (5.2%)
  • Herpes simplex (3.2%); herpes zoster
  • Urinary tract infections (2.9%)
  • Nausea, abdominal pain; ALT/AST increased >= 3 x ULN; rash, acne
  • Uncommon: pneumonia, deep vein thrombosis, pulmonary embolism, neutropaenia < 1 x 10^9 cells/L, diverticulitis

Interactions

  • Strong Organic Anion Transporter 3 (OAT3) inhibitors such as probenecid — reduce dose (adults: 2 mg once daily; paediatric: reduce recommended dose by half)

Clinical monograph

How it works

It selectively inhibits JAK1 and JAK2, interrupting cytokine signalling that drives the inflammation underlying atopic dermatitis and alopecia areata.

Prescribing in practice

  • JAK inhibitors carry MHRA-highlighted risks of serious infection, venous thromboembolism, major cardiovascular events and malignancy, so use cautiously in those over 65, smokers, and patients with cardiovascular or thrombotic risk factors.
  • Screen for and exclude active and latent infection, including tuberculosis and viral hepatitis, before starting.
  • Ensure vaccinations are up to date and avoid live vaccines during treatment.

Monitoring

Monitor full blood count, lipids, liver function and for signs of infection or thromboembolism during treatment.

Counselling the patient

  • Report signs of infection, chest pain, breathlessness or leg swelling promptly.
  • Keep up to date with recommended vaccinations and avoid live vaccines while treated.
  • Attend for the blood tests arranged to monitor treatment.

Evidence & guidelines

NICE recommends baricitinib for moderate-to-severe atopic dermatitis and for severe alopecia areata within its authorised indications, subject to MHRA safety advice on JAK inhibitors.

Reference: NICE TA878 (2023); BRAVE-AA1/AA2 Trials (King et al, NEJM 2022); MHRA JAK Inhibitor Safety Review; BAD Atopic Eczema Guidelines; 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.