Drug lookup
Drug reference

Vincristine

Vinca alkaloid mitotic inhibitor · Antineoplastic

Also known as vincristine sulfate

START
1.4 mg/m² IV weekly (cap ~2 mg absolute) per regimen — IV ONLY, label syringe 'fatal if given intrathecally'
TYPICAL MAX
Commonly capped at 2 mg absolute per dose
STOP IF
Severe motor neuropathy/ileus, severe hyponatraemia (SIADH); never intrathecal
WATCH
Neuro exam (deep tendon reflexes) each dose, bowel regimen prophylaxis, sodium, extravasation precautions
CDSCO approvedSchedule HATC L01CA02
Dose laddermg/d
1start1.5titrate2ceiling
Renal dose adjustmenteGFR mL/min/1.73m²
FULLNo dose adjustment at any eGFR (hepatic/biliary elimination)90

KDIGO 2024 + manufacturer label

Pharmacokineticsplasma · t hours
8minONSET30minPEAK3.5d1wDURATION
ONSET
8min · absorption onset
PEAK
30min · plasma Cmax
3.5d · terminal t½
DURATION
1w · weekly cycle
EXCRETION
Hepatic CYP3A4; ~80% biliary/faecal
route + CYP
INTERACTIONS
12 major
incl. contraindicated
PREGNANCY
Avoid — teratogenic/fetotoxic; effective contraception
FDA category + note
Top interactionssee all 12
  • Intrathecal RouteContraindicatedDatabaseKimi deep-research + Cla
  • Live VaccinesContraindicatedDatabaseKimi deep-research + Cla
  • AdalimumabSevereDatabaseDDInter
  • AmprenavirSevereDatabaseDDInter
Available in India

15 branded formulations. Look up specific brands in the Drugs workspace.

Mechanism

Binds tubulin, inhibiting microtubule polymerisation and arresting cells in metaphase (M-phase) → apoptosis; the neuronal microtubule effect underlies dose-limiting peripheral neuropathy.

Indications

Acute lymphoblastic leukaemia; Hodgkin and non-Hodgkin lymphomaMany paediatric/solid tumour combination regimens (Wilms, neuroblastoma, rhabdomyosarcoma)Idiopathic thrombocytopenic purpura (off-label)

Dosing

Adult
1.4 mg/m² IV (commonly capped at 2 mg absolute dose) once weekly per regimen.
Pediatric
1.5–2 mg/m² IV weekly (or weight-based <10 kg), per protocol.
Renal adjustment
No specific adjustment (hepatic/biliary elimination).
Hepatic adjustment
Bilirubin >3 mg/dL: reduce dose ~50%; significant hepatic dysfunction — dose-reduce.
Geriatric
Greater neuropathy/constipation; monitor/reduce.
Max dose
Commonly capped at 2 mg absolute per dose

Pharmacokinetics

Onset
Cytotoxic over days; neuropathy cumulative
Peak effect
Plasma rapid (IV)
Duration
Weekly cycle
Half-life
Triphasic; terminal ~85 h
Bioavailability
IV only
Protein binding
~75%
Metabolism
Hepatic CYP3A4
Excretion
Biliary/faecal (~80%); minor renal

Contraindications

  • INTRATHECAL administration — uniformly FATAL (IV use only)
  • Demyelinating Charcot–Marie–Tooth syndrome
  • Severe hypersensitivity to vincristine
  • Caution: significant hepatic impairment, pre-existing neuropathy

Side effects

Common
Peripheral neuropathy (sensory then motor; areflexia)Constipation/ileus, abdominal painAlopeciaJaw/limb pain
Serious
  • Severe/irreversible peripheral and autonomic neuropathy
  • Paralytic ileus/severe constipation
  • SIADH/hyponatraemia
  • Fatal if given intrathecally; severe extravasation tissue necrosis (vesicant)
  • Bronchospasm (with mitomycin); seizures/encephalopathy

Pregnancy & lactation

Pregnancy

Avoid — teratogenic/fetotoxic; effective contraception

Lactation

Contraindicated — discontinue breastfeeding

Drug interactions

Intrathecal Route
Contraindicated
Database

Intrathecal vincristine causes ascending paralysis and death

NEVER intrathecal — strict labelling/handling protocols (give in minibag)

Source: Kimi deep-research + Cla

Live Vaccines
Contraindicated
Database

Immunosuppression

Avoid live vaccines

Source: Kimi deep-research + Cla

Adalimumab
Severe
Database

Drug interaction classified as: synergy

Source: DDInter

Amprenavir
Severe
Database

Drug interaction classified as: metabolism

Source: DDInter

Atazanavir
Severe
Database

Drug interaction classified as: metabolism

Source: DDInter

Baricitinib
Severe
Database

Drug interaction classified as: synergy

Source: DDInter

Boceprevir
Severe
Database

Drug interaction classified as: metabolism

Source: DDInter

Ceritinib
Severe
Database

Drug interaction classified as: metabolism

Source: DDInter

Certolizumab
Severe
Database

Drug interaction classified as: synergy

Source: DDInter

Cladribine
Severe
Database

Drug interaction classified as: synergy.

Source: DDInter

Clarithromycin
Severe
Database

Drug interaction classified as: metabolism.

Source: DDInter

Clozapine
Severe
Database

Drug interaction classified as: synergy.

Source: DDInter

Related guidelines

Ask House about Vincristine

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

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