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Mebendazole

Benzimidazole anthelmintic · Anti-parasitic

Also known as Mebex, Wormin, Mebendol

START
Pinworm 100 mg single dose, repeat in 2 weeks; STH 100 mg BID ×3 days or 500 mg single
TYPICAL MAX
Short-course/single-dose; high-dose systemic regimens specialist only
STOP IF
Severe skin reaction, marrow suppression (high-dose), hepatotoxicity
WATCH
Treat close contacts/hygiene (pinworm); high-dose: CBC + LFTs; avoid metronidazole co-use (SJS reports)
CDSCO approvedJan AushadhiNPPA price-controlledATC P02CA01
Dose laddermg/d
100start500ceiling
Renal dose adjustmenteGFR mL/min/1.73m²
FULLNo dose adjustment at any eGFR (minimal absorption)90

KDIGO 2024 + manufacturer label

Pharmacokineticsplasma · t hours
2hONSET2hPEAK4h1dDURATION
ONSET
2h · luminal action
PEAK
2h · low systemic Cmax
4h · absorbed-fraction t½
DURATION
1d · daily dosing (course)
EXCRETION
Mainly faecal (unabsorbed); minor renal
route + CYP
INTERACTIONS
1 major
SEVERE in our sources
PREGNANCY
Avoid first trimester; later trimesters only if clearly needed (WHO permits in deworming after 1st trimester)
FDA category + note
Top interactionssee all 5
  • MetronidazoleSevereDatabaseKimi deep-research + Cla
Available in India

28 branded formulations and 4 fixed-dose combinations. Look up specific brands in the Drugs workspace.

Jan Aushadhi — generic available at GoI pharmacies

Mechanism

Binds nematode beta-tubulin inhibiting microtubule polymerisation, blocking helminth glucose uptake → glycogen depletion and parasite death; poorly absorbed (acts in gut lumen).

Indications

Intestinal nematode infections: enterobiasis (pinworm), ascariasis, trichuriasis, hookwormMass deworming programmesCapillariasis, trichinellosis (higher doses)

Dosing

Adult
Pinworm: 100 mg single dose, repeat in 2 weeks. Ascaris/hookworm/whipworm: 100 mg BID ×3 days or 500 mg single dose.
Pediatric
≥1–2 years same as adult (per programme); WHO uses 500 mg single dose in deworming.
Renal adjustment
No adjustment (minimal absorption).
Hepatic adjustment
Caution/monitor in high-dose prolonged use (hepatotoxicity); systemic disease use specialist.
Geriatric
No specific adjustment.
Max dose
Single-dose/short-course regimens; high-dose systemic (e.g. echinococcosis) specialist

Pharmacokinetics

Onset
Antiparasitic over days (gut)
Peak effect
Low systemic Cmax (poorly absorbed)
Duration
Course-based; single-dose for many indications
Half-life
~3–6 h (absorbed fraction)
Bioavailability
<10% (increased with fatty meal)
Protein binding
~90–95% (absorbed fraction)
Metabolism
Hepatic (extensive first-pass to inactive metabolites)
Excretion
Mainly faecal (unabsorbed); minor renal/biliary

Contraindications

  • Hypersensitivity to mebendazole
  • First trimester of pregnancy (avoid; later only if necessary)

Side effects

Common
Generally well toleratedTransient abdominal pain/diarrhoea (heavy worm burden)Nausea
Serious
  • Bone marrow suppression/agranulocytosis (high-dose prolonged)
  • Hepatotoxicity (high-dose)
  • Severe skin reactions (SJS/TEN — rare, often with metronidazole co-use)
  • Convulsions (rare, infants)

Pregnancy & lactation

Pregnancy

Avoid first trimester; later trimesters only if clearly needed (WHO permits in deworming after 1st trimester)

Lactation

Limited absorption — generally considered compatible; short course

Drug interactions

Metronidazole
Severe
Database

Reports of Stevens-Johnson syndrome / toxic epidermal necrolysis with concurrent use

Avoid concurrent metronidazole

Source: Kimi deep-research + Cla

Cimetidine
Moderate
Database

Increased mebendazole plasma levels (relevant in high-dose systemic therapy)

Monitor in prolonged high-dose use

Source: Kimi deep-research + Cla

Strong Cyp Inducers
Moderate
Database

Reduced mebendazole levels (systemic therapy)

Higher doses may be needed for systemic indications

Source: Kimi deep-research + Cla

Fatty Meals
Mild
Database

Increased absorption (beneficial for systemic disease)

Take with fat for systemic indications

Source: Kimi deep-research + Cla

Hepatotoxic Drugs
Mild
Database

Additive hepatic effects in prolonged high-dose use

Monitor LFTs

Source: Kimi deep-research + Cla

6 additional low-confidence interactions hidden — those rows lack a documented mechanism or management plan in our sources.

Related guidelines

Ask House about Mebendazole

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

Sources: KD Tripathi 7e, Goodman & Gilman 14e, Harrison 22e, Katzung·Verified: 2026-05-19 · House clinical team·Cockpit curated: 2026-05-19