Kaneva 150 mg (Tablet)

Unit Price: ৳ 1,000.00 (3 x 10: ৳ 30,000.00)
Strip Price: ৳ 10,000.00

Medicine Details

Category Details
Generic Erlotinib
Company Beximco pharmaceuticals ltd
Also available as

Indications

  • First-line treatment of patients with metastatic Non-Small Cell Lung cancer (NSCLC)
  • Maintenance treatment of patients with locally advanced or metastatic NSCLC
  • Treatment of locally advanced or metastatic NSCLC after failure of at least one prior chemotherapy regimen
  • First-line treatment of patients with locally advanced, unresectable or metastatic pancreatic cancer

Description

  • Quinazolinamine chemical composition
  • Reversibly inhibits the kinase activity of EGFR
  • Binds with higher affinity to EGFR exon 19 deletion or exon 21 (L858R) mutations
  • Inhibition of other tyrosine kinase receptors not fully characterized

Dosage & Administration

  • Recommended daily dose of Erlotinib for NSCLC is 150 mg taken on an empty stomach
  • Recommended daily dose of Erlotinib for pancreatic cancer is 100 mg taken once daily in combination with gemcitabine
  • Dose reduction and increment under specific conditions
  • Special dosing considerations for concurrent cigarette smoking

Interaction

  • Interaction with coumarin-derived anticoagulants, including warfarin
  • Metabolized predominantly by CYP3A4
  • Pre-treatment with the CYP3A4 inducer Rifampicin
  • Co-administration of Kaneva with drugs affecting gastric pH

Side Effects

  • Common adverse reactions such as rash, diarrhea, anorexia, fatigue, dyspnea, cough, nausea, and vomiting
  • Serious adverse reactions including Interstitial Lung Disease (ILD), Renal Failure, and Hepatotoxicity

Pregnancy & Lactation

  • Pregnancy category D
  • Potential for serious adverse reactions in nursing infants
  • Consideration for discontinuation of nursing or drug

Precautions & Warnings

  • Occurrence and management of Interstitial Lung Disease (ILD)
  • Monitoring for renal function and electrolytes
  • Periodic liver testing and monitoring hepatic impairment
  • Discontinuation of Kaneva for specific conditions

Use in Special Populations

  • Safety and effectiveness in pediatric patients not established
  • No significant differences in safety or efficacy observed between elderly and younger subjects

Overdose Effects

  • Tolerance of single and weekly doses up to a certain level
  • Unacceptable incidence of severe adverse reactions above the recommended dose
  • Management of suspected overdose

Therapeutic Class

  • Targeted Cancer Therapy

Storage Conditions

  • Store at a temperature not exceeding 30°C
  • Store in a dry place
  • Protection from light and moisture

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