Geficent 250 mg Tablet is an oral targeted therapy containing Gefitinib, a potent epidermal growth factor receptor (EGFR) tyrosine kinase inhibitor. It is designed for the treatment of patients with metastatic non-small cell lung cancer (NSCLC) harboring specific EGFR mutations (exon 19 deletions or exon 21 L858R substitution), providing a first-line therapy option. Geficent selectively blocks abnormal EGFR signaling in cancer cells, inhibiting tumor growth and proliferation while sparing normal cells.
রেজিস্টার্ড চিকিৎসকের পরামর্শ অনুযায়ী ঔষধ সেবন করুন
Geficent 250 mg is indicated for:
First-line treatment of metastatic NSCLC in patients whose tumors exhibit EGFR exon 19 deletions or exon 21 (L858R) substitution mutations, as confirmed by an FDA-approved test.
This therapy is particularly valuable for patients with EGFR-positive tumors who require a targeted and effective oral treatment option.
Targeted Cancer Therapy (EGFR Tyrosine Kinase Inhibitor)
Geficent 250 mg selectively binds to the ATP-binding site of the EGFR tyrosine kinase, blocking its activity. EGFR is overexpressed in many carcinoma cells, including lung and breast cancers, leading to inappropriate activation of the Ras signaling pathway, uncontrolled cell proliferation, and tumor growth. By inhibiting EGFR, Geficent interrupts this cascade, inducing apoptosis and reducing malignant cell proliferation.
As a first-generation EGFR inhibitor, Geficent targets tumor cells with activating EGFR mutations while sparing most normal tissues, which contributes to its tolerable safety profile.
Recommended dose: 250 mg orally once daily, with or without food
Continue therapy until disease progression or unacceptable toxicity occurs
If a dose is missed, do not take it within 12 hours of the next scheduled dose
Special administration for patients with difficulty swallowing:
Dissolve the tablet in 4–8 ounces of water, stir for ~15 minutes, and consume immediately.
Rinse the container with additional water and drink immediately, or administer via nasogastric tube if required.
CYP3A4 inducers (e.g., rifampicin, phenytoin, carbamazepine, barbiturates) may reduce plasma levels
CYP3A4 inhibitors (e.g., itraconazole, ketoconazole) may increase plasma levels
Can increase INR or bleeding risk with warfarin
May increase metoprolol levels
Potentially exacerbates vinorelbine-induced neutropenia
Drugs affecting gastric pH (PPIs, H2 antagonists) may reduce absorption and efficacy
Known hypersensitivity to Gefitinib or any component of the tablet
Lactation
Common adverse effects include:
Rash, pruritus, urticaria, alopecia
Diarrhea, nausea, vomiting, anorexia, stomatitis
Dry skin and mouth
Epistaxis, hematuria
Nail disorders, eye pain, corneal erosion or ulcer, aberrant eyelash growth
Laboratory abnormalities: elevated creatinine, proteinuria
Rare but severe effects:
Interstitial lung disease (ILD), pancreatitis, toxic epidermal necrolysis, ocular ischemia, ocular hemorrhage, erythema multiforme
Pregnancy category D: positive evidence of fetal risk
Use only if benefits outweigh potential risks
Effective contraception recommended during treatment
Interstitial Lung Disease (ILD): discontinue if confirmed
Hepatotoxicity: monitor liver function; discontinue for severe impairment
Gastrointestinal perforation: discontinue if it occurs
Diarrhea: withhold for Grade 3+ events
Ocular disorders: withhold for severe keratitis; discontinue for persistent ulcers
Severe skin reactions: withhold or discontinue for Grade 3+ events
Embryo-fetal toxicity: advise contraception for women of reproductive potential
Pediatric: safety and efficacy not established
Geriatric: no overall differences in safety, but efficacy data limited
Store at 20–25°C
Protect from moisture and light
Keep out of reach of children
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