Vandetanib
Vandetanib is an antineoplastic agent. It is a protein kinase inhibitor which inhibits the VEGFR-2, EGFR and RET tyrosine kinase. It is indicated in the treatment of medullary thyroid cancer.
Primary Characteristics
It is of Synthetic origin.
It belongs to Protein kinase inhibitor pharmacological group on the basis of mechanism of action.
Non-proprietary name: Vandetanib.

Pharmacokinetics
Distribution: Vandetanib has a volume of distribution is 7450 L. plasma protein binding is 93.7%.
Elimination: it is metabolised via hepatic, plasma half-life is 19 days, renal excretion is 25%, 44% in feces.
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Indications
Vandetanib is primarily indicated in conditions like Thyroid cancer.
Vandetanib is also indicated for secondary conditions like Tumor induced angiogenesis.
Contraindications
Vandetanib is contraindicated in conditions like Renal impairment, Hepatic impairment, Hypersensitivity, Lactation, QTc prolongation.
Dosage
Vandetanib's dosage details are as follows:
| Dose | Single Dose | Frequency | Route | Instructions |
|---|---|---|---|---|
| Adult Dosage | ||||
| 300 mg | 300 mg | Every 24h | PO | Take with or without food at about the same time each day. Starting dose is 200 mg in patients with renal impairment. |
| Paediatric Dosage (20kg) | ||||
| No data. | ||||
| Neonatal Dosage (3kg) | ||||
| No data. | ||||
Drug Interactions
Always consult your physician for the change of dose regimen or an alternative drug of choice that may strictly be required.
Side Effects
The signs and symptoms that are produced after acute overdosage of Vandetanib are Diarrhea, Hypertension, QT prolongation, Rashes .
Vandetanib is known to cause more or less tolerable side effects which are usually transient. These include Blurred vision, Diarrhea, Hypertension , Nausea, QT prolongation, Rashes .
Warnings / Precautions
Available Brands
None recorded.