Iressa (Gefitinib) – NSCLC | HongKong DengYue Medicine

  • Generic Name/Brand Name: ​Gefitinib / Iressa®
  • Indications: NSCLC
  • Dosage Form: ​Tablet
  • Specification: 250 mg × 10, 30 tablets/box

Gefitinib Application Scope

It is indicated for the first-line treatment of adult 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.

iressa gefitinib
iressa gefitinib

Gefitinib Characteristics

  • Ingredients: Gefitinib 250 mg per tablet

  • Properties:​ Selective EGFR tyrosine kinase inhibitor

  • Packaging Specification:​ 250 mg × 30 tablets per bottle

  • Storage:​ Store at controlled room temperature 20–25°C (68–77°F)

  • Expiry Date: 24 months from the date of manufacture

  • Executive Standard: ​In line with Chinese Pharmacopoeia standards

  • Approval Number: National Drug Approval No. H20030001 (China)

  • Date of Revision: July 2025

  • Manufacturer: AstraZeneca Pharmaceuticals LP, USA

Guidelines for the Use of Iressa

  • Dosage and Administration:

    • Recommended Dose: 250 mg once daily

    • Administration: Take with or without food

    • Missed Dose:​ Take as soon as remembered; skip if near next dose, do not double

  • Adverse Reactions:

    • Common Adverse Reactions:

      • Rash

      • diarrhea

      • nausea

    • Serious Adverse Reactions:

      • Interstitial lung disease

      • hepatotoxicity

      • gastrointestinal perforation

  • Contraindications: Hypersensitivity to it or excipients

  • Precautions: Use with caution in patients with liver dysfunction

Gefitinib Interactions

  • CYP3A4 Inhibitors:

    • Drugs that are strong inhibitors of CYP3A4 (e.g., ketoconazole and itraconazole) decrease it metabolism and increase gefitinib plasma concentrations. Monitor adverse reactions when administering strong CYP3A4 inhibitors with Iressa.

  • CYP3A4 Inducers:

    • Drugs that are strong inducers of CYP3A4 (e.g., rifampicin, phenytoin) increase the metabolism of it and decrease gefitinib plasma concentrations. Increase Iressa to 500 mg daily in patients receiving a strong CYP3A4 inducer and resume Iressa at 250 mg 7 days after discontinuation of the strong inducer.

  • Drugs Affecting Gastric pH:

    • Drugs that elevate gastric pH (e.g., proton pump inhibitors, histamine H2-receptor antagonists, and antacids) may reduce plasma concentrations of gefitinib. Avoid concurrent use of Iressa with proton pump inhibitors, if possible. If treatment with a proton-pump inhibitor is required, take Iressa 12 hours after the last dose or 12 hours before the next dose of the proton-pump inhibitor. Take Iressa 6 hours after or 6 hours before an H2-receptor antagonist or an antaci.

 

Note:

  • If there is a new packaging for the drug, the new packaging shall prevail. The above information is sourced from DengYue Medicine.
  • This content is for reference only. Prescription drugs must be used under a doctor’s guidance and purchased from authorized sources.
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