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Educational draft · awaiting clinical reviewUse Rapid for revision, not patient-care decisions. Check current national and local guidance and the BNF or BNFC before acting.

Topical calcineurin inhibitors

Dermatology · UK scope · Sources checked 27 Aug 2026 · Clinical review pending

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Disseminated viral infection

Rapidly spreading painful monomorphic vesicles, punched-out erosions, fever, periocular disease or widespread varicella in a person applying a topical calcineurin inhibitor may represent eczema herpeticum or another serious viral infection rather than expected application burning.

Action: Stop application to infected skin, obtain urgent clinical and ophthalmic assessment where indicated, sample fresh lesions without delaying systemic antiviral treatment, and restart only after infection has resolved and the responsible clinician has reviewed the plan.

Synopsis

Use tacrolimus and pimecrolimus as steroid-sparing topical immunomodulators for supported indications, select age and strength correctly, counsel about burning, infection and ultraviolet exposure, and review non-response or persistent lesions safely.

  • Tacrolimus and pimecrolimus inhibit calcineurin-dependent T-cell signalling and cytokine release without causing corticosteroid skin atrophy.
  • They are not first-line treatment for ordinary atopic eczema: NICE positions them second line when appropriate topical corticosteroid control fails or serious atrophy risk is important.
  • Initiation should be by a clinician with a special interest and experience in dermatology after the diagnosis, severity, site and prior corticosteroid technique are confirmed.
  • Tacrolimus 0.03% ointment is used from age 2 years; 0.1% is an adult and age-16-and-over strength under its licensed eczema pathway.
  • Pimecrolimus 1% cream is a NICE second-line option for mild or moderate facial and neck eczema in children aged 2–16 years when steroid atrophy risk is serious.
  • Transient warmth, stinging or burning is common during the first days and usually reduces; severe pain, vesicles or deterioration is not routine adjustment.
  • Do not apply to clinically infected skin, beneath occlusion, or directly to mucosa, and use handwashing and a mapped treatment area.
  • Minimise natural and artificial ultraviolet exposure, avoid sunbeds and use clothing and broad-spectrum protection; combining treatment with phototherapy needs specialist direction.
  • Twice-weekly tacrolimus maintenance on non-consecutive days can prevent flares in selected frequent relapsers who responded to induction, with formal review rather than indefinite automatic repeats.
  • Vitiligo, genital or facial psoriasis and several other dermatoses may use calcineurin inhibitors off label; record the evidence, alternatives, consent and outcome separately from licensed eczema use.

Key red flags

Painful vesicles, punched-out erosions, fever, eye symptoms, spreading bacterial infection, persistent or unexplained lymphadenopathy, an indurated or ulcerated lesion, immune compromise outside the treatment plan, or major photosensitivity requires prompt reassessment before further application.

Focal tumour warning

A lasting indurated, ulcerated, bleeding or otherwise atypical lesion should be biopsied or referred rather than suppressed repeatedly with local immunomodulation.

Investigation priorities

01
Diagnosis and severity confirmationFirst step

Ensure a supported inflammatory diagnosis and treatment threshold before initiation.

02
Observed topical-treatment auditFirst line

Show that appropriate first-line corticosteroid and emollient care genuinely failed or carried serious risk.

Management branches

First-line eligibilityVerify the second-line indication

A topical calcineurin inhibitor is being considered for atopic eczema.

  1. Confirm diagnosis, severity and sensitive-site burden and review a correctly delivered topical corticosteroid and emollient plan.
  2. Establish inadequate control or a serious corticosteroid adverse-effect risk and have an experienced clinician select tacrolimus or pimecrolimus by age, site and severity.
  3. Discuss licence, expected burning, infection actions, ultraviolet avoidance, amount, duration and alternatives and record any off-label element.

Key medicines

Tacrolimus 0.03% ointmentFor ages 2–15 years with licensed atopic eczema, apply thinly twice daily for up to 3 weeks then once daily until clear; adults may use this strength when stepping down. Selected maintenance uses once daily on 2 non-consecutive days each week.Do not use under age 2, on clinically infected skin or beneath occlusion. Explain early burning, UV avoidance, alcohol flushing, lymph-node review and product-specific vaccination advice.
Tacrolimus 0.1% ointmentFor people aged 16 years and over, apply thinly twice daily to affected atopic-eczema skin until clear; use the product-guided step-down or twice-weekly non-consecutive maintenance schedule after response.Avoid infection, mucosa, occlusion, sunbeds and unnecessary UV exposure. Reassess failure at 2 weeks, unexplained nodes and any persistent indurated or ulcerated focus.
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Sources and review status4 sources · checked 27 Aug 2026 · clinical review pending+
Sources

Sources and review status

National guidance is shown before implementation-dependent detail. Typical adult dose examples remain subject to patient factors, contraindications and the live BNF or specialist protocol. Source check completed 27 Aug 2026; clinical approval remains outstanding.

  • NICE TA82 topical calcineurin inhibitorsSecond-line indications, ages, severity, site and specialist initiation for atopic eczema.
  • BAD topical calcineurin inhibitorsMechanism, application, early burning, infection, ultraviolet precautions and off-label contexts.
  • Protopic 0.1 percent ointment SmPCAdult induction, maintenance, contraindications, infection and ultraviolet safety.
  • NICE childhood atopic eczema recommendationsPlace in therapy, age-specific eczema care, infection recognition and review.

Editorial contact: Doctor’s Passport editorial team. Source-check date is separate from clinical approval. Report a content problem · Content changes

Authoring stateRapid draftClinical stateAwaiting reviewJurisdictionUnited Kingdom