Drug lookup
Drug reference

Vandetanib

Multikinase inhibitor (VEGFR, EGFR, RET, BRK) · Antineoplastic

START
300 mg PO once daily; ECG/electrolytes at baseline
TYPICAL MAX
300 mg/day (200 mg if CrCl 30–50)
STOP IF
QTc >500 ms, severe ILD, or severe skin/PRES events
WATCH
ECG/QTc, electrolytes (K/Mg/Ca), TSH, BP, skin/photosensitivity
CDSCO approvedSchedule HATC L01EX04
Dose laddermg/d
100reduced200renal/reduced300standard/day
Renal dose adjustmenteGFR mL/min/1.73m²
FULLStandard 300 mg/day50REDUCEStart 200 mg/day; monit…30AVOIDNot recommended90

KDIGO 2024 + manufacturer label

Pharmacokineticsplasma · t hours
2hONSET6hPEAK2.7w1dDURATION
ONSET
2h · absorption
PEAK
6h · Tmax
2.7w · t½ ~19 d
DURATION
1d · once-daily
EXCRETION
~25% renal, ~44% faecal
route + CYP
INTERACTIONS
12 major
SEVERE in our sources
PREGNANCY
Can cause fetal harm — avoid; effective contraception during and 4 months after.
FDA category + note
Top interactionssee all 12
  • AbarelixSevereDatabaseDDInter
  • AbirateroneSevereDatabaseDDInter
  • AdenosineSevereDatabaseDDInter
  • AlfuzosinSevereDatabaseDDInter

Mechanism

Inhibits VEGFR-2, EGFR, RET (including mutant forms), Src and BRK tyrosine kinases, blocking tumour angiogenesis and proliferation signalling — designed for RET-driven medullary thyroid cancer.

Indications

Symptomatic / progressive medullary thyroid cancer (unresectable, locally advanced or metastatic)

Dosing

Adult
300 mg PO once daily; reduce to 200 mg or 100 mg for toxicity / QT prolongation.
Pediatric
Body-weight–based (specialist).
Renal adjustment
CrCl 30–50: starting dose 200 mg; CrCl <30: not recommended.
Hepatic adjustment
Not recommended in moderate–severe (limited data).
Geriatric
No specific adjustment; monitor QT/electrolytes.
Max dose
300 mg/day

Pharmacokinetics

Onset
Tumour response over weeks–months
Peak effect
~6 h (Tmax)
Duration
~24 h (once-daily)
Half-life
~19 days (very long)
Bioavailability
Variable (~38%); not food-dependent
Protein binding
~90%
Metabolism
Hepatic CYP3A4 + FMO; renal excretion of unchanged drug
Excretion
~25% renal, ~44% faecal

Contraindications

  • Congenital long-QT syndrome / baseline QTc >480 ms
  • Severe hypersensitivity
  • Caution: cardiac failure, severe hepatic impairment, electrolyte disturbance

Side effects

Common
DiarrhoeaRash / photosensitivityAcneHypertensionNauseaFatigueHeadache
Serious
  • QT prolongation / torsades / sudden death (boxed)
  • Severe skin reactions (SJS/TEN, photosensitivity)
  • Interstitial lung disease
  • Heart failure
  • Posterior reversible encephalopathy
  • Ischaemic cerebrovascular events

Pregnancy & lactation

Pregnancy

Can cause fetal harm — avoid; effective contraception during and 4 months after.

Lactation

Avoid breastfeeding during and 4 months after therapy.

Drug interactions

Abarelix
Severe
Database

Drug interaction classified as: synergy

Source: DDInter

Abiraterone
Severe
Database

Drug interaction classified as: synergy

Source: DDInter

Adenosine
Severe
Database

Drug interaction classified as: synergy

Source: DDInter

Alfuzosin
Severe
Database

Drug interaction classified as: synergy

Source: DDInter

Alimemazine
Severe
Database

Drug interaction classified as: synergy

Source: DDInter

Aminolevulinic Acid
Severe
Database

Drug interaction classified as: synergy

Source: DDInter

Amiodarone
Severe
Database

Drug interaction classified as: synergy

Source: DDInter

Amisulpride
Severe
Database

Drug interaction classified as: synergy

Source: DDInter

Amitriptyline
Severe
Database

Drug interaction classified as: synergy

Source: DDInter

Amoxapine
Severe
Database

Drug interaction classified as: synergy

Source: DDInter

Anagrelide
Severe
Database

Drug interaction classified as: synergy

Source: DDInter

Apalutamide
Severe
Database

Drug interaction classified as: synergy

Source: DDInter

Related guidelines

Ask House about Vandetanib

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

Sources: Goodman & Gilman 14e, Katzung, BNF·Verified: 2026-05-20 · House clinical team·Cockpit curated: 2026-05-20