Erlocent Tablet 100 mg contains Erlotinib, a targeted anticancer medicine classified as an epidermal growth factor receptor (EGFR) tyrosine kinase inhibitor. It is primarily used in the treatment of specific types of cancers where abnormal EGFR signaling plays a key role in tumor growth and progression. Erlocent Tablet helps slow down or stop the growth of cancer cells by blocking signals required for their survival and proliferation.
রেজিস্টার্ড চিকিৎসকের পরামর্শ অনুযায়ী ঔষধ সেবন করুন
Antineoplastic agent
EGFR Tyrosine Kinase Inhibitor
Erlotinib selectively inhibits the intracellular phosphorylation of EGFR tyrosine kinase, which is expressed on the surface of normal and cancer cells. EGFR activation triggers a cascade of downstream signaling pathways involved in cell proliferation, angiogenesis, metastasis, and inhibition of apoptosis. By blocking EGFR activity, Erlocent Tablet 100 mg interferes with these pathways, leading to reduced tumor cell growth and increased cancer cell death. This targeted mechanism allows Erlotinib to act more specifically on cancer cells compared to traditional chemotherapy.
Erlocent Tablet 100 mg is indicated for the treatment of:
Non-small cell lung cancer (NSCLC), particularly in patients with EGFR-activating mutations
Locally advanced or metastatic NSCLC after failure of at least one prior chemotherapy regimen
Pancreatic cancer, in combination with gemcitabine, for locally advanced, unresectable, or metastatic disease
The usual recommended dose is 100 mg to 150 mg once daily, depending on the indication and patient tolerance
Erlocent Tablet should be taken on an empty stomach, at least 1 hour before or 2 hours after food
Tablets should be swallowed whole with water and should not be crushed or chewed
Dose adjustments may be required based on adverse reactions, liver function, or drug interactions
Treatment should be continued as long as clinical benefit is observed or as directed by the physician
Erlocent Tablet 100 mg is contraindicated in:
Patients with known hypersensitivity to Erlotinib or any component of the formulation
Severe hepatic impairment, unless the potential benefit outweighs the risk
Commonly reported side effects include:
Skin rash, acneiform dermatitis, dry skin, itching
Diarrhea, nausea, vomiting, abdominal pain
Fatigue, loss of appetite
Stomatitis and mouth ulcers
Less common but serious adverse effects may include:
Interstitial lung disease-like events
Severe hepatic toxicity
Gastrointestinal perforation
Patients should seek medical attention if severe or persistent symptoms occur.
Concomitant use with strong CYP3A4 inhibitors or inducers may alter Erlotinib plasma levels
Proton pump inhibitors and H2-receptor antagonists may reduce Erlotinib absorption
Smoking can significantly reduce Erlotinib exposure and should be avoided
Monitor liver function tests periodically during therapy
Use with caution in patients with pre-existing lung disease
Severe diarrhea and dehydration should be managed promptly
Effective contraception is recommended during treatment
Pregnancy Category D
Erlocent Tablet may cause fetal harm and should not be used during pregnancy
Breastfeeding should be discontinued during Erlotinib therapy
Store below 30°C
Keep protected from light and moisture
Keep out of reach of children
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