Afatinib
Afatinib is a tyrosine kinase inhibitor which is a 4-anilinoquinazoline. Afatinib is presented as the dimaleate salt, with the chemical name 2-butenamide, N-[4-[(3-chloro-4-fluorophenyl)amino]7-[[(3S)-tetrahydro-3-furanyl]oxy]-6-quinazolinyl]-4-(dimethylamino)-,(2E)-, (2Z)-2-butenedioate (1:2). It is indicated for the first-line treatment of patients with metastatic non-small cell lung cancer (NSCLC) whose tumors have epidermal growth factor receptor (EGFR) exon 19 deletions or exon 21 (L858R) substitution mutations as detected by an FDA-approved test.
Primary Characteristics
It is of Synthetic origin and belongs to quinazolinamines.
It belongs to Tyrosine kinase inhibitor pharmacological group on the basis of mechanism of action.
Molecular Weight: 718.1 · Solubility in Water: souble · Non-proprietary name: afatinib.

Pharmacokinetics
Absorption: Afatinib has an oral bioavailability is 92%.
Distribution: Afatinib has a plasma protein binding is 95%.
Elimination: plasma half-life is 37hrs, renal excretion is 85% by feces4% by urinr.
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Indications
Afatinib is primarily indicated in conditions like Non small cell lung cancer.
Contraindications
None recorded.
Dosage
Afatinib's dosage details are as follows:
| Dose | Single Dose | Frequency | Route | Instructions |
|---|---|---|---|---|
| Adult Dosage | ||||
| 40 mg | 40 mg | — | PO | Instruct patients to take medication at least 1 hour before or 2 hours after a meal |
| 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
Afatinib is known to cause more or less tolerable side effects which are usually transient. These include Acneform, Dermatitis, Diarrhea, Dry skin, Loss of appetite, Paronychia, Pruritis, Rash, Stomatitis.
Warnings / Precautions
Available Brands
None recorded.
Storage Conditions
Drug Classification
- 1.8.2 — Cytotoxic (anti-neoplastic) drugs