Etopor 100 mg (Etoposide) Injection

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Overview of Etopor 100 mg (Etoposide) Injection

Etopor 100 mg, containing the active ingredient Etoposide, is a potent cytotoxic chemotherapy drug used for the treatment of small cell lung cancer (SCLC). Developed by Eskayef Pharmaceuticals Ltd. and distributed globally by Saif Pharma, Etopor plays a vital role in cancer therapy due to its proven effectiveness and precision in targeting malignant cells.

This injectable formulation is designed to be used in combination with other chemotherapy agents as part of a first-line treatment regimen, offering patients a chance for improved survival and quality of life.

Indications

Etopor 100 mg is indicated for the treatment of small cell lung cancer, particularly in conjunction with other approved chemotherapeutic agents. It serves as a first-line treatment for patients diagnosed with this aggressive form of lung cancer.

Pharmacology 

Etoposide belongs to the podophyllotoxin derivatives class. It works by inhibiting mitosis, specifically by blocking the assembly of microtubules and interfering with cell cycle progression during the late S and G2 phases. This disruption prevents cancer cell replication and promotes apoptosis (programmed cell death), making it an effective agent in cancer control.

Pha rmacokinetics

When administered intravenously, Etoposide displays a biphasic distribution:

  • Distribution Half-Life: ~1.5 hours

  • Elimination Half-Life: 4 to 11 hours

  • Clearance: Ranges from 33 to 48 ml/min

  • Volume of Distribution: 18 to 29 liters

The plasma concentration of Etopor increases linearly with dose and shows no accumulation with repeated daily dosing.

Dosage & Administration

Recommended Dosage for SCLC

  • 35 mg/m²/day for 4 days, or

  • 50 mg/m²/day for 5 days, in combination with other chemotherapeutic drugs.
    Dosage may vary based on physician direction.

Dosage Adjustment for Renal Impairment
  • Creatinine clearance > 50 mL/min: 100% of dose

  • 15–50 mL/min: Reduce dose to 75%

  • <15 mL/min: Caution advised, further reduction needed

Etopor should always be administered under strict medical supervision, preferably through slow intravenous infusion over 30–60 minutes to avoid hypotension.

Drug Interactions

Concomitant administration with high-dose Cyclosporine A (>2000 ng/ml) can:

  • Increase Etoposide exposure by 80%

  • Decrease its clearance by 38%

Close monitoring and dosage adjustment may be necessary when combined with other chemotherapeutic agents or immunosuppressants.

Laboratory Monitoring

Patients undergoing treatment should have:

  • Regular complete blood counts (CBC)

  • Monitoring before and after each cycle

  • Baseline and follow-up platelet, WBC, and hemoglobin levels

These measures help manage toxicity risks and guide therapy adjustments.

Contraindications

Etopor is contraindicated in:

  • Patients with known hypersensitivity to Etoposide

  • Patients allergic to any of the formulation components

Side Effects

Etopor may cause a variety of adverse reactions, categorized below:

Hematologic Toxicity

  • Myelosuppression (dose-limiting)

  • Granulocyte & platelet nadirs

  • Fever, infection, and rare death due to neutropenia

Gastrointestinal Effects

  • Nausea, vomiting, mucositis

  • Mild to moderate severity

  • More common with oral than IV administration

Hypotension

  • Transient episodes post-infusion

  • Prevented by slow administration

Allergic Reactions

  • Anaphylactic-like responses (0.7–2%)

  • Symptoms: chills, fever, dyspnea, hypotension

  • Management: Stop infusion and administer corticosteroids or antihistamines

Other Adverse Reactions

  • Alopecia (up to 66% of patients, reversible)

  • Rash, urticaria, pruritus

  • Neurological and pulmonary symptoms (rare)

  • Severe skin reactions (e.g., Stevens-Johnson syndrome, TEN)

Pregnancy & Lactation

  • Category D: May cause fetal harm

  • Breastfeeding: Not recommended as Etoposide may be excreted in human milk

Precautions & Warnings

  • Myelosuppression risk: Frequent monitoring is essential

  • Patients with low albumin levels: Higher toxicity risk

  • Slow infusion necessary: To prevent hypotension and allergic reactions

  • Avoid rapid IV injection

Therapy should only continue if benefits outweigh the potential risks. In the case of severe reactions, discontinue use and initiate corrective measures.

Therapeutic Class

  • Cytotoxic Chemotherapy (Antineoplastic agent)

Storage Conditions
  • Store under refrigeration (2°–8°C)

  • Protect from light and moisture

  • Keep out of children’s reach

  • Follow proper handling and disposal procedures for cytotoxic drugs

Manufacturer Information

Eskayef Pharmaceuticals Ltd.
A leading pharmaceutical manufacturer in Bangladesh, Eskayef has a legacy of producing world-class medicines since 1990. Originally the Bangladesh operation of SK&F (USA), Eskayef is now part of Transcom Group and is globally respected for its premium quality pharmaceutical products.

🔗 Visit Manufacturer’s Website: www.skfbd.com

Supplier Information

Saif Pharma
Founded in 2014, Saif Pharma is a top oncology medicine supplier and distributor with a global footprint across 60+ countries, including the USA, Canada, Saudi Arabia, UAE, China, India, and Pakistan. Known for its dependable, affordable, and high-quality cancer medicines, Saif Pharma is committed to reducing the burden of cancer globally.

Conclusion

Etopor 100 mg (Etoposide) Injection stands as a cornerstone in the treatment of small cell lung cancer. Its strong efficacy profile, flexible dosing, and consistent quality make it a preferred choice among oncologists worldwide. Manufactured by Eskayef Pharmaceuticals Ltd. and distributed by Saif Pharma, Etopor ensures accessibility to life-saving cancer therapy at an affordable price. With careful patient monitoring and professional administration, Etopor continues to bring hope to thousands battling cancer.

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