Verified by DRAP ๐Ÿฉบ ANTINEOPLASTICS ๐Ÿท๏ธ Podophyllo toxins derivative
๐Ÿ‘จโ€โš•๏ธ Clinically Reviewed by: PakistaniBano Medical Editorial Board (Pharm.D Panel)
๐Ÿ“… Reviewed: November 2026 โ€ข ๐Ÿ” Authority: DRAP / WHO ATC
๐Ÿ“ฆ Formulations, Pack Sizes & Retail Prices Currency: Rs.
Dosage Form Reg. No Pack Size Trade Price (TP) Maximum Retail Price (MRP)
Cap 50 mg o45649 20 Rs.578.00 Rs.680.00
Inj100 mg 045603 1 Vial Rs.468.00 Rs.550.00

๐Ÿ“‹ Indications & Clinical Dosage

*Small cell carcinoma of the bronchus, the lymphomas and testicular cancer:* BY IV INF: Adults: 60-120 mg/m2slow IV INF over 1/2-1 hr daily for 3-5 days followed by treatment-free interval of 14 days.

๐Ÿ’Š Mode of Administration

Administer lower doses IVP Bolus over at least 30 min to minimize the risk of hypotensive reactions. At room temperature in D5W or NS in polyvinyl chloride, the concentration is stable as follows: 0.2 mg/ml: 96 hours; 0.4 mg/ml: 48 hours; 0.6 mg/ml: 8 hours; 1 mg/ml: 2 hours; 2 mg/ml: 1 hour; 20 mg/ml (undiluted): 24 hours. Standard IV Dilution: Lower dose regimens (<1 gm/dose): Doses may be diluted in 100-1000 ml of D5W or NS. If the concentration is >0.6 mg/ml, it is highly unstable and a syringe of undiluted etoposide accompanied with the appropriate volume of diluent will be sent to the nursing unit to be mixed at the bedside just prior to administration. High-dose regimens (>1 gm/dose): Total dose should be drawn into an empty Viaflex container and the appropriate amount of diluent (for a final concentration of 1 mg/ml) will be sent. Use the 2-Channel Pump Method: Instill all of the etoposide dose into one container (concentration equal to 20 mg/ml). Infuse this into one channel. The etoposide should be Y-sited into the port most proximal to the patient. A 0.22 micron filter should be attached to the line after the Y-site and before entry into the patient.

โ›” Contraindications

Severe hepatic dysfunction; acute infection.

โš ๏ธ Precautions & Warnings

Debilitated patients; prolonged chemotherapy. Monitor blood count; avoid contact with skin & eyes; avoid extravasation. Not to be admin-istered intrapleurally or intraperitoneally.

โš ๏ธ Adverse Reactions / Side Effects

Alopecia, bone-marrow suppression, hyperuricaemia, irritant to tissues, nausea, oral mucositis, thromboembolism, tumourlysis syndrome, vomiting

๐Ÿคฐ Pregnancy & Lactation Safety

Pregnancy Risk:
Positive evidence of risk: Avoid
Lactation / Breastfeeding:
Contraindicated. Discontinue breast-feeding.

๐Ÿงช Compatibility & Storage Stability

Compatibility: Stable in D5W, LR.

๐Ÿ“š Official Regulatory & Clinical References

  • Drug Regulatory Authority of Pakistan (DRAP): Drug Registration, S.R.O. Price Gazettes & National Essential Medicines List (NEML).
  • World Health Organization (WHO): Collaborating Centre for Drug Statistics Methodology (ATC/DDD Index).
  • Formulary Standards: British National Formulary (BNF) & Pakistan National Formulary (PNF) guidelines.
DRAP Registration Number: 045603

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