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Afatinib is a generic form of brand name Xovoltib 20mg, an orally bioavailable anilino-quinazoline derivative and inhibitor of the receptor tyrosine kinase (RTK) epidermal growth factor receptor (ErbB; EGFR) family, with antineoplastic activity.
Xovoltib 20mg is a targeted therapy drug. Xovoltib 20mg is a prescription drugs which is used under the supervision of medical practioners.
Xovoltib 20mg is indicated for the first-line treatment for patients with metastatic non-small cell lung cancer (NSCLC)
The recommended dose for adult patients with metastatic non-small cell lung cancer is 40mg taken once per day.
Dosages of 0-17 years is not being studied in children.
The drug should not be used age under 18 years of age
For renal impairment: prescribed dose is 30mg taken once per day
Administer the drug Xovoltib on an empty stomach. Consume the drug 1 hour before or 2 hours after a meal
Avoid cutting or crushing the tablet
overdose is resulted in patients whom ingested 360mg of Xovoltib which resulted in nausea, vomiting, asthenia, abdominal pain and hence provided supportive measurement for recovery.
Afatinib is a kind of cancer growth blocker called a protein tyrosine kinase inhibitor (TKI). Tyrosine kinases are proteins whichtrigger cells to grow. Afatinib inhibits tyrosine kinases and blocks epidermal growth factor receptor proteins in cancer cells. So Afatinib is also called an EGFR-TK inhibitor.
Absorption: High plasma time is 2-5 hr and bioavailability are 92 %
Distribution: Human plasma protein bound is 95%
Metabolism: The major circulating metabolites are covalent adducts to proteins.
Elimination: The drug excretion through feces is 85% and urine 4%
Half-life is 37 hr.
Xovoltib 20mg concomitant use with P-gp inhibitors (cyclosporine A, ketoconazole verapamil) with Xovoltib 20mg will have high exposure to Afatinib
When combination of Xovoltib 20mg with P-gp inducers (carbamazepine, phenytoin, phenobarbital) with Xovoltib 20mg will reduces the exposure to Afatinib
The drug may cause diarrhea whichleads in dehydration with or without renal impairment; some stated cases were fatal; withhold treatment for serious and extended diarrhea not responsive to antidiarrheal agents
Hepatotoxicity resulted; monitor with periodic liver testing; withhold or stoptreatment for serious or worsening liver tests
The drug may result in Interstitial lung disease (ILD)
Embryo-fetal toxicity: Xovoltib 20mg will have risk to the foetus when administrated to pregnant women
Keratitis: if patients confirm with suspected keratitis or ulcerative keratitis then stop or discontinue the drug
May have high risk for sunburn/phototoxicity; may aggravate rash or acne; patients use with caution to limit sun exposure and where sunscreen and protective clothing
While on treatment with Xovoltib 20mg Pregnancy should avoid because the drug Xovoltib 20mg is administrated to a pregnant woman will harm the foetus.
Xovoltib 20mg Excretion into human milk is unknown or will have adverse reaction in a child who is breastfed. Therefore, decision should take whether to stop breastfeeding or discontinuation of medicine.
Xovoltib 20mg Store at 250C
Keep Xovoltib 20mg away from children
Protect away free from moisture and light
If patient forget to take the dose of Xovoltib 20mg, then the missed dose must be skipped and follow the regular dosing schedule. Do not have double the dose
Must consult with medical oncologist and follow the suggestions