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INN monograph

Miconazole, skin

Antifungal · POM

POM Source-linked Grade A-

Source-linked · Updated 03 Aug 2026 · Source: Local active-ingredient clinical extract; RxNorm (NLM RxNav); PubChem; Professional class pharmacology (Antifungal)

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Risk first

Contraindications

  • Hypersensitivity.
  • Many systemic azoles contraindicated with certain CYP3A4 substrates (e.g. some statins, quinidine) — check labels.
  • Terfenadine/astemizole historical QT combinations.

Precautions

  • Hepatotoxicity monitoring for systemic azoles.
  • QT prolongation (some azoles).
  • Voriconazole: visual disturbances, photosensitivity, skin cancer risk long-term.
  • Confirm species for invasive disease.

Point of care

Dosing

Adult

Adult and children: Skin: Apply OD or BD until 10days after lesions have disappeared. Nails: Apply thinly OD covering with non-perforated bandage until new nail growth is established.

Paediatric

See label paediatric section if present; otherwise use paediatric formulary — do not extrapolate adult doses.

Renal

Fluconazole dose-adjust in CKD; amphotericin nephrotoxicity high-alert.

  • CrCl 0–120: Confirm renal dosing in product SmPC / primary label.

Hepatic

Monitor LFTs for courses >14 days or higher-risk patients.

Safety

Drug interactions

Open checker →
  • Match agent to site and species.
  • For tinea, continue topical beyond clearance.
  • Invasive fungal disease needs ID/specialist input and source control.

Safety

Adverse effects

  • GI upset, rash, raised LFTs.
  • Serious: hepatitis, severe skin reactions, arrhythmias, infusion reactions (amphotericin).

Use

Indications

  • Therapeutic use is agent- and indication-specific within the class (Antifungal).
  • Use according to culture results, national guidelines (Kenya STG/EML where applicable) and the current product SmPC.
  • Fungal skin infections.

Pharmacology

Mode of action

Azoles inhibit fungal CYP51 (lanosterol 14α-demethylase), depleting ergosterol and disrupting membrane integrity.

Azoles inhibit fungal CYP51 (lanosterol 14… Terbinafine inhibits squalene epoxidase. Polyenes bind ergosterol creating membrane…
Full mechanism text

Azoles inhibit fungal CYP51 (lanosterol 14α-demethylase), depleting ergosterol and disrupting membrane integrity. Terbinafine inhibits squalene epoxidase. Polyenes bind ergosterol creating membrane pores. Echinocandins inhibit β-glucan synthase (cell wall).

ADME

Pharmacokinetics & PD

Onset Days for clinical response (varies)
Duration Days–weeks per indication
Route ORAL / TOPICAL / IV
Metabolism with major interactions. Topicals: minimal systemic
Full PK/PD text

Fluconazole: excellent bioavailability, renal excretion, CSF penetration. Itraconazole/voriconazole: complex absorption and CYP metabolism with major interactions. Topicals: minimal systemic absorption when intact skin.

Kenya

Brands & prices

0 listed
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No brands linked yet.

Special populations

Pregnancy & lactation

Pregnancy

Systemic azoles often avoided in pregnancy (fluconazole high-dose teratogenicity signal); topical clotrimazole commonly used for VVC.

Lactation

Topicals usually fine; systemic — agent-specific.

Diet

Food & alcohol

  • Food
  • Food

Trust

Sources & disclaimer

Source: Local active-ingredient clinical extract; RxNorm (NLM RxNav); PubChem; Professional class pharmacology (Antifungal)

Open source link

Clinical review date not recorded.

Decision support only — not a substitute for clinical judgment, product SmPC, or Kenya STG/EML.

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