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GEFITINIB TABLETS IP 250 MG (GEFTICIP)
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What is Gefitinib 250mg (GEFTICIP) Used For?
- First-line targeted therapy for metastatic non-small cell lung cancer (NSCLC) with confirmed EGFR mutations (exon 19 deletion or exon 21 L858R)
- Precision oncology: only effective in EGFR-mutant NSCLC β EGFR mutation testing is mandatory before starting
- Second-line treatment for previously treated EGFR-mutant NSCLC after progression
- Used in HIV/immunocompromised patients with co-existing EGFR-mutant lung cancer requiring targeted oncology care
How Does Gefitinib Work?
- Selective EGFR (Epidermal Growth Factor Receptor) tyrosine kinase inhibitor β blocks the intracellular kinase domain of EGFR
- In EGFR-mutant NSCLC, mutated EGFR constitutively drives tumor cell proliferation; Gefitinib blocks this oncogenic signal
- Blocks downstream RAS/MAPK and PI3K/AKT pathways β inhibits tumor cell proliferation and promotes apoptosis
- EGFR inhibition also mediates acneiform rash (a marker of adequate EGFR pathway inhibition)
How to Use Gefitinib 250mg
Dosage: 250mg once daily
Timing: Can be taken with or without food; if missed and next dose is <12 hours away, skip the missed dose
Precaution: Monitor liver function (LFTs) at baseline and periodically; report new or worsening respiratory symptoms immediately (possible interstitial lung disease)
Side Effects of Gefitinib 250mg
Common Side Effects: Acneiform rash (~60%, often indicates efficacy), Diarrhea (~50%), Dry skin, Paronychia (nail inflammation), Nausea
Serious Side Effects (seek medical help): Interstitial lung disease/pneumonitis (~1β3%, can be fatal), Severe hepatotoxicity, GI perforation (rare), Stevens-Johnson syndrome
Benefits
- Targeted therapy: active specifically against EGFR-mutant NSCLC, sparing normal tissue compared to conventional chemotherapy
- Once-daily oral dosing β significantly better quality of life vs IV chemotherapy
- Acneiform rash correlates with treatment response β higher rash severity often predicts better outcomes
- Well-studied first-generation EGFR TKI with established efficacy and tolerability data
- Manageable side effect profile in most patients
Warnings and Precautions
- EGFR mutation testing mandatory before starting β ineffective without EGFR exon 19 del or L858R mutation
- Interstitial lung disease (ILD): any new dyspnea, cough, or fever requires immediate hold and evaluation
- Hepatotoxicity: monitor LFTs; dose interruption or discontinuation if severe elevation
- Pregnancy contraindicated β effective contraception required during and for β₯1 month after treatment
- Breastfeeding contraindicated during and after treatment
- CYP3A4 inducers from HIV regimens (Efavirenz, Rifampicin) can significantly reduce Gefitinib levels
Drug Interactions
- Strong CYP3A4 inducers (Rifampicin, Efavirenz, Carbamazepine, Phenytoin): reduce Gefitinib levels β risk of treatment failure; avoid if possible
- Strong CYP3A4 inhibitors (Ritonavir, Ketoconazole): increase Gefitinib levels β monitor for increased toxicity
- Warfarin: Gefitinib increases INR β close monitoring required with dose adjustments
- Antacids/PPIs: reduce Gefitinib absorption; take antacids at least 6 hours before/after
- HIV antiretrovirals: require careful review with oncology and HIV pharmacist before starting
Storage Information
- Store at room temperature (below 30Β°C), away from direct light and moisture
- Keep in original packaging out of reach of children
- Do not use after the expiry date
Frequently Asked Questions
Q1: What is Gefitinib 250mg (Gefticip) used for?
Gefitinib is an EGFR tyrosine kinase inhibitor (TKI) approved for first-line treatment of metastatic non-small cell lung cancer (NSCLC) with EGFR mutations (exon 19 deletions or exon 21 L858R substitution). In HIV patients, it manages co-existing lung cancer.
Q2: How does Gefitinib work against lung cancer?
Gefitinib selectively inhibits the EGFR (Epidermal Growth Factor Receptor) tyrosine kinase. In EGFR-mutant NSCLC, EGFR drives uncontrolled cell proliferation. Blocking EGFR signaling halts tumor cell growth and promotes apoptosis in EGFR-dependent cancer cells.
Q3: What EGFR test is required before starting Gefitinib?
Tumor tissue testing (or liquid biopsy) for EGFR mutations is mandatory before starting Gefitinib. It is only effective in EGFR-mutant NSCLC β specifically exon 19 deletion or exon 21 L858R mutation. Patients without these mutations should not receive Gefitinib.
Q4: How is Gefitinib 250mg taken?
Take 250mg once daily, with or without food. If a dose is missed and the next dose is less than 12 hours away, skip the missed dose. Swallow tablets whole.
Q5: What are the most common side effects?
Diarrhea (most common, affects ~50β60%), acneiform rash (paronychia, skin reactions β occurs in ~60%, often indicates efficacy), nausea, dry skin, and decreased appetite are most common.
Q6: What serious side effects require immediate medical attention?
Seek immediate care for: new or worsening respiratory symptoms (possible interstitial lung disease/pneumonitis β occurs in ~1β3% and can be fatal), severe or bloody diarrhea, severe skin blistering, or sudden vision changes (dry eye syndrome may also occur).
Q7: What is the relationship between skin rash and Gefitinib efficacy?
Interestingly, patients who develop acneiform rash on EGFR inhibitors tend to have better anti-tumor responses. The rash severity can indicate adequate drug levels and EGFR pathway inhibition.
Q8: What drug interactions affect Gefitinib?
Gefitinib is metabolised by CYP3A4. Strong CYP3A4 inducers (rifampicin, carbamazepine, phenytoin) reduce efficacy. Strong CYP3A4 inhibitors increase levels and toxicity. Gefitinib also raises warfarin INR β close monitoring needed.
Q9: How does Gefitinib interact with HIV medications?
Some HIV protease inhibitors (ritonavir, cobicistat-boosted drugs) are strong CYP3A4 inhibitors that can significantly raise Gefitinib levels and increase toxicity. Discuss HIV/cancer combination management with a team including both HIV and oncology specialists.
Q10: Is Gefitinib safe during pregnancy?
Gefitinib can cause fetal harm. It is contraindicated in pregnancy. Effective contraception is required during and for at least 1 month after treatment. Breastfeeding should be avoided during and after treatment.
Q11: How should Gefitinib 250mg be stored?
Store at room temperature away from light and moisture. Keep in original packaging out of reach of children.
Q12: Do I need a prescription for Geficip?
Yes. Gefitinib is a prescription-only oncology drug requiring confirmed EGFR mutation status, specialist prescribing, and regular monitoring of liver function and respiratory symptoms.
Customer Reviews
Riley C.
Germany Β· 1 month ago
βSensitive medication handled with complete professionalism. Discreet packaging, no personal health information on the label.β
Blair F.
Australia Β· 2 months ago
βPrivacy and quality are both paramount when ordering ARV medication. Medionix delivers on both counts every time.β
Alex M.
USA Β· 1 week ago
βPrivacy handled perfectly. Plain packaging, no labels hinting at contents. Antiretroviral therapy maintained without interruption.β
Riley C.
Germany Β· 1 month ago
βSensitive medication handled with complete professionalism. Discreet packaging, no personal health information on the label.β
Blair F.
Australia Β· 2 months ago
βPrivacy and quality are both paramount when ordering ARV medication. Medionix delivers on both counts every time.β
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The information provided on Medionix Pharma is intended for general informational purposes only. It should not be considered as medical advice, diagnosis, or treatment. Always consult a qualified healthcare professional before using any medication or starting any treatment.
Medionix Pharma does not encourage self-medication. Customers are responsible for ensuring that purchases comply with local laws and prescription requirements in their country. If you have any questions or concerns regarding the content on our website, please contact us at sales@medionixpharma.com.







