Product image of Inopem (Pemetrexed) supplied by GNH India

Inopem

Active Ingredient:
Pemetrexed
Origin:
EU

Inopem (Pemetrexed)

Pemetrexed, the active ingredient in Inopem, is an antifolate presented as an intravenous solution for injection use. It is employed in the treatment of malignant pleural mesothelioma and non‑small cell lung cancer (non‑squamous) in adult patients.

GNH India supplies Inopem as a licensed, GDP‑compliant international pharmaceutical supplier serving hospitals, oncology centres and pharmacies worldwide.

Manufacturer / TM Owner

Innovis Pharma

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Indications & Clinical Uses

Inopem is an antifolate chemotherapy agent indicated for specific thoracic malignancies.

  • Malignant pleural mesothelioma: improves overall survival when used in combination with cisplatin.
  • Non‑small cell lung cancer (non‑squamous): provides disease control as first‑line therapy with cisplatin.
  • Combination therapy with cisplatin: enhances antitumor efficacy in the above indications.

How It Works

  • Pemetrexed inhibits multiple folate‑dependent enzymes, including thymidylate synthase, dihydrofolate reductase, and glycinamide ribonucleotide formyltransferase, disrupting purine and pyrimidine synthesis. This blockade impairs DNA and RNA production, leading to cell cycle arrest and apoptosis in rapidly dividing tumor cells.

Side Effects

Adverse reactions may occur with Inopem therapy.

Common Side Effects

  • Fatigue: persistent tiredness during treatment.
  • Nausea: feeling of sickness often requiring antiemetics.
  • Vomiting: episodes of expulsion of stomach contents.
  • Anemia: reduced red blood cell count causing weakness.
  • Neutropenia: lowered neutrophil levels increasing infection risk.
  • Rash: skin irritation or redness.

Serious or Rare Side Effects

  • Severe allergic reaction: anaphylaxis requiring immediate medical attention.
  • Pulmonary toxicity: breathing difficulties or interstitial lung disease.
  • Renal failure: impaired kidney function needing monitoring.
  • Cardiac toxicity: arrhythmias or reduced cardiac output.
  • Febrile neutropenia: fever with low neutrophil count, a medical emergency.
  • Thromboembolic events: blood clots in veins or arteries.

Precautions & Warnings

Prior to initiating Inopem, several safety considerations are recommended.

  • Renal function: assess creatinine clearance before and during therapy.
  • Hepatic function: monitor liver enzymes for potential toxicity.
  • Hematologic status: perform regular complete blood counts.
  • Folate supplementation: consider vitamin B12 and folic acid to reduce toxicity.
  • Pregnancy: avoid use in pregnant women; discuss contraception with women of childbearing potential.
  • Store at 2-8°C: keep refrigerated, protect from light, do not freeze.

Avoid Interactions

Pemetrexed may interact with other medicines, requiring vigilance.

Major Interactions (Avoid)

  • Cisplatin: concurrent use increases risk of renal and hematologic toxicity.
  • NSAIDs: may exacerbate renal impairment when combined.
  • Folate antagonists (e.g., methotrexate): additive inhibition of folate pathways.

Moderate Interactions (Monitor Closely)

  • Warfarin: monitor INR as pemetrexed can affect coagulation.
  • Live vaccines: avoid administration during treatment due to immunosuppression.
  • Certain antibiotics (e.g., penicillins): may influence blood count changes.

Frequently Asked Questions

Inopem contains the antifolate pemetrexed and is used as a chemotherapy agent for malignant pleural mesothelioma and non‑small cell lung cancer (non‑squamous) in adult patients, typically in combination with cisplatin.

Pemetrexed blocks several folate‑dependent enzymes needed for purine and pyrimidine synthesis, which stops DNA and RNA production in rapidly dividing cancer cells, leading to cell death.

The prescribed dose of Inopem is determined by the treating oncologist based on the patient’s weight, renal function, and treatment protocol. Exact dosing regimens are individualized and not disclosed here.

The safety of Inopem in pregnancy and lactation has not been established. It is generally avoided in pregnant women, and breastfeeding is not recommended during treatment due to potential drug exposure to the infant.

To request Inopem, submit an enquiry on the product page at gnhindia.com with the required quantity. GNH India works with hospitals, pharmacies and procurement teams worldwide, verifies trade or institutional credentials, and then provides pricing, availability, shipping details (including cold‑chain if needed) and import documentation.

Inopem (pemetrexed) differs from older antifolates such as methotrexate by targeting multiple enzymes in the folate pathway, offering broader antitumor activity in mesothelioma and non‑squamous NSCLC, and often requiring folate supplementation to mitigate toxicity.

Inopem should be stored at 2‑8 °C in a refrigerator, protected from light, and must not be frozen or shaken. Keep the vial in its original packaging until use.

Inopem is given by intravenous infusion, usually over a period of 10 minutes to 1 hour, under the supervision of qualified healthcare professionals in a clinical setting.

Serious risks include severe allergic reactions, pulmonary toxicity, renal failure, cardiac toxicity, and febrile neutropenia. Patients should be monitored closely for signs of these conditions throughout treatment.

Inopem is contraindicated in patients with known hypersensitivity to pemetrexed or any component of the formulation, in those with severe renal impairment, and in pregnant women unless the benefits outweigh the risks.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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