Cisplatin Ebewe (Cisplatin)

Platinum-based chemotherapy for testicular, ovarian, lung, and head & neck cancers

Rx – Prescription Only Platinum-based Antineoplastic ATC: L01XA01
Active Ingredient
Cisplatin
Available Form
Solution for infusion (1 mg/ml)
Vial Sizes
10 ml, 20 ml, 50 ml, 100 ml
Manufacturer
Ebewe Pharma / Sandoz
Medically reviewed | Last reviewed: | Evidence level: 1A
Cisplatin Ebewe is a platinum-based chemotherapy medication containing cisplatin at a concentration of 1 mg/ml. It is used to treat several types of cancer, including testicular cancer, ovarian cancer, non-small cell lung cancer, and squamous cell carcinoma of the head and neck. Cisplatin works by forming platinum-DNA cross-links that prevent cancer cells from dividing and ultimately cause cell death. It is administered exclusively by intravenous infusion under the supervision of a specialist oncologist.
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Written and reviewed by iMedic Medical Editorial Team | Specialists in oncology

Quick Facts About Cisplatin Ebewe

Active Ingredient
Cisplatin
Platinum compound
Drug Class
Platinum
Antineoplastic agent
ATC Code
L01XA01
Platinum compounds
Common Uses
Cancer
Testicular, ovarian, lung, H&N
Available Form
IV Infusion
1 mg/ml concentrate
Prescription Status
Rx Only
Hospital-administered

Key Takeaways About Cisplatin Ebewe

  • WHO Essential Medicine: Cisplatin is on the WHO Model List of Essential Medicines, recognized as one of the most effective and important cancer treatments worldwide
  • Kidney protection is critical: Adequate hydration before, during, and after infusion is mandatory to prevent potentially severe kidney damage (nephrotoxicity)
  • Hearing must be monitored: Cisplatin can cause irreversible hearing loss (ototoxicity), so audiometric testing is performed before and during treatment
  • Highly effective in testicular cancer: Cisplatin-based chemotherapy has transformed testicular cancer into one of the most curable solid tumors, with cure rates exceeding 90%
  • No aluminum contact: Cisplatin reacts with aluminum, forming a black precipitate; all infusion equipment must be aluminum-free

What Is Cisplatin Ebewe and What Is It Used For?

Cisplatin Ebewe is a platinum-based cytotoxic (anticancer) medication used to treat several types of cancer. It belongs to a class of drugs called alkylating-like agents that work by damaging cancer cell DNA, preventing the cells from dividing and ultimately leading to their death. Cisplatin can be used alone but is most commonly given in combination with other chemotherapy drugs.

Cisplatin was one of the first platinum-based compounds discovered to have anticancer properties, and its introduction in the 1970s revolutionized the treatment of several solid tumors. Today, cisplatin remains one of the most widely used and effective chemotherapy agents in the world. It is included on the World Health Organization (WHO) Model List of Essential Medicines, reflecting its fundamental importance in cancer care globally.

The active substance in Cisplatin Ebewe is cisplatin (also known as cis-diamminedichloroplatinum(II) or CDDP), a planar inorganic complex containing a central platinum atom. Each milliliter of the solution contains 1 mg of cisplatin. The product is supplied as a clear, colorless to slightly yellowish concentrate for solution for infusion in glass vials containing 10 ml (10 mg), 20 ml (20 mg), 50 ml (50 mg), or 100 ml (100 mg) of cisplatin.

Cisplatin Ebewe is approved for the treatment of the following cancers, either as monotherapy or in combination with other anticancer agents:

  • Testicular cancer: Both seminoma and non-seminomatous germ cell tumors. Cisplatin-based regimens such as BEP (bleomycin, etoposide, cisplatin) have transformed testicular cancer into one of the most curable solid tumors, achieving overall cure rates exceeding 90% in early-stage disease
  • Ovarian cancer: Epithelial ovarian carcinoma, typically used in combination with paclitaxel or cyclophosphamide as first-line treatment following surgical debulking. According to ESMO guidelines, platinum-based chemotherapy remains the standard of care
  • Non-small cell lung cancer (NSCLC): Used in combination regimens for advanced or metastatic NSCLC. The NCCN Clinical Practice Guidelines recommend cisplatin-based doublets as a standard first-line chemotherapy option
  • Head and neck squamous cell carcinoma: Used both as induction chemotherapy and concurrently with radiotherapy for locally advanced disease. Concurrent cisplatin-radiation is considered a standard-of-care approach according to international guidelines

Your treating oncologist may also prescribe cisplatin for other cancer types not listed above, as it has demonstrated activity against a wide range of malignancies including bladder cancer, cervical cancer, esophageal cancer, and mesothelioma. The decision to use cisplatin depends on the specific type and stage of cancer, your overall health status, and the treatment goals.

How Cisplatin Works

Cisplatin exerts its anticancer effect primarily through the formation of platinum-DNA adducts. Once cisplatin enters the bloodstream and reaches cancer cells, it undergoes a chemical activation process inside the cell where chloride ligands are replaced by water molecules. This activated form of cisplatin then reacts with DNA, forming cross-links primarily between adjacent guanine bases on the same DNA strand (intrastrand cross-links) and, to a lesser extent, between the two complementary DNA strands (interstrand cross-links).

These platinum-DNA adducts distort the three-dimensional structure of the DNA helix, preventing normal DNA replication and transcription. The cell's DNA repair mechanisms attempt to fix this damage, but when the damage is too extensive, the cell activates programmed cell death pathways (apoptosis). Because cancer cells typically divide more rapidly than most normal cells, they are generally more susceptible to the DNA-damaging effects of cisplatin. However, this mechanism also explains why cisplatin affects rapidly dividing normal cells, particularly in the bone marrow, gastrointestinal tract, and hair follicles.

Historical significance:

The anticancer properties of cisplatin were discovered serendipitously by Barnett Rosenberg in the 1960s during experiments on the effects of electric fields on bacterial growth. The compound received FDA approval in 1978 and has since saved countless lives, particularly in the treatment of testicular cancer where it transformed a once-fatal disease into a highly curable condition.

What Should You Know Before Taking Cisplatin Ebewe?

Before receiving cisplatin, your doctor will perform comprehensive blood tests, kidney function assessments, and hearing tests. Cisplatin must not be used if you have significant kidney impairment, dehydration, severe bone marrow suppression, hearing loss, or if you are breastfeeding. Several medications can interact dangerously with cisplatin, and effective contraception is required during and after treatment.

Cisplatin is a potent chemotherapy agent with a well-characterized toxicity profile. Your oncologist and healthcare team will carefully evaluate whether cisplatin is appropriate for you, taking into account your overall health, kidney function, hearing status, blood counts, and any other medications you may be taking. Understanding the contraindications, warnings, and potential interactions is essential for safe treatment.

Contraindications

You must not receive Cisplatin Ebewe if any of the following apply:

  • Allergy to cisplatin or platinum compounds: If you are allergic to cisplatin, any other platinum-containing drug (such as carboplatin or oxaliplatin), or any of the other ingredients in the formulation
  • Kidney problems: If you have significant renal impairment, as cisplatin is primarily eliminated through the kidneys and can cause further kidney damage
  • Dehydration: Adequate hydration is essential for safe cisplatin administration; the drug must not be given to dehydrated patients
  • Low blood cell counts: If you have pre-existing bone marrow suppression with critically low levels of white blood cells, red blood cells, or platelets
  • Hearing impairment: If you already have significant hearing loss, as cisplatin can cause further irreversible damage to hearing
  • Breastfeeding: Cisplatin must not be used during breastfeeding, as it may pass into breast milk and harm the nursing infant
  • Yellow fever vaccine: Vaccination with yellow fever vaccine is contraindicated during cisplatin treatment due to the risk of fatal systemic vaccine disease
  • Concurrent phenytoin use for prophylaxis: The combination with phenytoin is contraindicated; cisplatin reduces the effectiveness of phenytoin

Warnings and Precautions

Talk to your doctor or nurse before receiving Cisplatin Ebewe. Your healthcare team will implement several monitoring measures and precautions during your treatment:

  • Blood tests: Your doctor will regularly check levels of calcium, sodium, potassium, and magnesium in your blood, as well as your complete blood count and liver and kidney function, before each treatment cycle
  • Specialist supervision: Cisplatin must only be administered under the strict supervision of a physician experienced in cancer chemotherapy, in a hospital or clinical setting equipped to manage potential complications
  • Hearing tests: Audiometric testing will be performed before each treatment cycle to monitor for early signs of hearing damage
  • Pre-existing nerve disease: If you have peripheral neuropathy not caused by cisplatin, inform your doctor as the drug may worsen nerve symptoms
  • Infection: If you have an active infection, consult your doctor before treatment, as cisplatin suppresses the immune system
  • Nausea and vomiting: If you experience vomiting or diarrhea after treatment, the fluid loss must be compensated to protect your kidneys
  • Skin contact: If cisplatin solution spills on your skin, wash the area immediately with soap and water, as it can cause local tissue irritation
  • Extravasation: If cisplatin is accidentally injected outside the vein during infusion, the infusion must be stopped immediately, as leakage into surrounding tissue can cause severe damage including cellulitis, fibrosis, and tissue necrosis
Critical Warning: Kidney Protection

Nephrotoxicity (kidney damage) is one of the most significant risks of cisplatin therapy. You will receive intravenous fluids before, during, and after each cisplatin infusion, and you should drink large amounts of water during the 24 hours following treatment. Your kidney function will be closely monitored with blood tests before each cycle. Do not hesitate to report any changes in urination or signs of fluid retention to your healthcare team immediately.

Pregnancy, Breastfeeding, and Fertility

Cisplatin poses significant risks to reproductive health and fetal development. If you are pregnant or think you may be pregnant, or if you are planning to have children, speak to your doctor before starting treatment.

  • Pregnancy: Cisplatin must not be used during pregnancy unless clearly necessary for the mother, as it can cause serious harm to the developing baby. Animal studies have shown that cisplatin is teratogenic (can cause birth defects) and embryotoxic
  • Contraception: Women of childbearing potential must use effective contraception during treatment and for at least 7 months after the last dose of cisplatin
  • Breastfeeding: Cisplatin is contraindicated during breastfeeding. You must not breastfeed while receiving cisplatin treatment
  • Male fertility: Men should not father children during treatment and for at least 4 months after the last dose. Cisplatin can significantly reduce or eliminate sperm production, which may be permanent. Men are strongly advised to seek sperm banking before beginning treatment
  • Female fertility: Cisplatin may affect ovulation and menstrual function. Discuss fertility preservation options with your oncologist before starting treatment

Driving and Operating Machinery

Do not drive or operate machinery that requires your full attention during cisplatin treatment, as the drug may cause drowsiness and nausea. You are responsible for assessing whether you are fit to drive or perform work requiring alertness. The side effects described in this article may affect your ability to do so safely.

Sodium Content

Cisplatin Ebewe contains sodium chloride as an excipient. The sodium content varies by vial size:

  • 10 ml vial: 35 mg sodium (1.75% of the WHO recommended maximum daily intake for adults)
  • 20 ml vial: 71 mg sodium (3.55% of maximum daily intake)
  • 50 ml vial: 177 mg sodium (8.85% of maximum daily intake)
  • 100 ml vial: 354 mg sodium (17.7% of maximum daily intake)

This should be taken into consideration for patients on a sodium-restricted diet, particularly when larger vial sizes or multiple vials are used.

How Does Cisplatin Ebewe Interact with Other Drugs?

Cisplatin has clinically significant interactions with many medications. Drugs that are toxic to the kidneys or ears can have their harmful effects amplified when combined with cisplatin. Tell your doctor about all medications you are taking, including prescription drugs, over-the-counter medicines, and herbal supplements, before starting cisplatin therapy.

Drug interactions with cisplatin can result in increased toxicity, reduced treatment efficacy, or both. Your oncologist will carefully review your medication list before each treatment cycle. Some medications may need to be adjusted, substituted, or temporarily discontinued during cisplatin therapy. The following sections detail the most clinically important interactions.

Major Interactions

These interactions can have serious or life-threatening consequences and typically require dose adjustments, enhanced monitoring, or avoidance of the combination:

Major Drug Interactions with Cisplatin
Drug / Class Interaction Clinical Significance
Aminoglycoside antibiotics (gentamicin, tobramycin, amikacin) Additive nephrotoxicity and ototoxicity Can cause severe, potentially irreversible kidney damage and hearing loss; avoid combination if possible
Loop diuretics (furosemide, bumetanide) Increased renal and ototoxic effects, especially at cisplatin doses >60 mg/m² If urine output is below 1,000 ml per day, the combination significantly increases risk of kidney and hearing damage
Amphotericin B Additive nephrotoxicity Close monitoring of kidney function required; consider alternative antifungal agents
Phenytoin Cisplatin reduces phenytoin absorption and effectiveness Contraindicated for seizure prophylaxis; phenytoin levels must be monitored if used therapeutically
Live vaccines (including yellow fever) Risk of fatal systemic vaccine disease Live vaccines are contraindicated during treatment and for at least 3 months after the last cisplatin dose
Paclitaxel / Docetaxel Severe peripheral neuropathy Enhanced neurotoxicity when combined; careful neurological monitoring required

Other Notable Interactions

The following interactions are clinically relevant and may require monitoring or dose adjustments:

  • Myelosuppressive drugs or radiation therapy: Concurrent bone marrow-suppressing medications or radiotherapy can worsen cisplatin's effects on the bone marrow, increasing the risk of severe infection, bleeding, and anemia
  • Bleomycin and methotrexate: The toxic effects of cisplatin may be enhanced when combined with other cytotoxic agents
  • Antihypertensive medications (furosemid, hydralazine, diazoxide, propranolol): May increase the nephrotoxic effect of cisplatin
  • Ifosfamide: The combination may result in increased hearing loss or additional kidney damage
  • Bleomycin and vinblastine: This combination can lead to pale or bluish discoloration of fingers and toes (Raynaud's phenomenon), indicating impaired circulation
  • Gout medications (allopurinol, colchicine, probenecid, sulfinpyrazone): Dosage adjustments of these medications may be required during cisplatin treatment, as cisplatin can increase uric acid levels
  • Antihistamines (buclizine, cyclizine, meclizine, phenothiazines): These may mask the early signs of hearing damage (dizziness, tinnitus) during cisplatin treatment
  • Pyridoxine and hexamethylmelamine: May reduce the effectiveness of cisplatin treatment
  • Bleomycin and etoposide: This combination may decrease lithium levels in the blood; lithium levels should be monitored regularly
  • Anticoagulants (warfarin, heparin): Cisplatin may affect the efficacy of blood-thinning medications; coagulation parameters should be monitored more frequently
  • Cyclosporine: Cisplatin and cyclosporine together may suppress the immune system excessively and increase the risk of abnormal lymphocyte proliferation
  • Penicillamine: May reduce the therapeutic effect of cisplatin

What Is the Correct Dosage of Cisplatin Ebewe?

Cisplatin dosage is calculated based on body surface area (BSA) in mg/m² and varies depending on the type of cancer being treated and whether cisplatin is used alone or in combination with other drugs. Typical doses range from 20 to 120 mg/m² per cycle, administered every 3–4 weeks. Cisplatin is given exclusively as an intravenous infusion in a hospital setting.

Cisplatin must only be prescribed and administered by specialist physicians experienced in cancer chemotherapy. The concentrate is diluted with sodium chloride solution, or a sodium chloride solution containing glucose or mannitol, before administration. The recommended dose depends on the patient's general condition, the expected treatment response, and whether cisplatin is being used as a single agent or in combination with other anticancer drugs.

Standard Dosing Regimens

Cisplatin as Single Agent

  • Single high-dose: 50–120 mg/m² body surface area as a single intravenous infusion, repeated every 3–4 weeks
  • Daily fractionated dose: 15–20 mg/m² per day for 5 consecutive days, repeated every 3–4 weeks

Cisplatin in Combination Therapy

  • Standard combination dose: 20 mg/m² or more, repeated every 3–4 weeks
  • Lung cancer regimens: Typically 80 mg/m² per cycle in combination regimens
Common Cisplatin-Based Chemotherapy Regimens
Cancer Type Regimen Cisplatin Dose Cycle Length
Testicular (BEP) Bleomycin + Etoposide + Cisplatin 20 mg/m² days 1–5 Every 21 days × 3–4 cycles
Ovarian Cisplatin + Paclitaxel 75–100 mg/m² day 1 Every 21 days × 6 cycles
NSCLC Cisplatin + Gemcitabine or Pemetrexed 75–80 mg/m² day 1 Every 21 days × 4–6 cycles
Head & Neck Concurrent chemoradiation 100 mg/m² day 1 Every 21 days × 3 cycles

Hydration Protocol

To prevent or minimize kidney damage, an extensive hydration protocol is followed for every cisplatin infusion. Before treatment, patients receive 1–2 liters of intravenous saline over 2–4 hours. During and after the infusion, additional fluids are administered, and patients are encouraged to drink large amounts of water during the 24 hours following treatment. Mannitol or furosemide may be used to maintain adequate urine output. The target urine output is typically at least 100 ml per hour during and for several hours after the infusion.

Administration

Cisplatin is administered exclusively by intravenous infusion. The concentrate must never be injected undiluted. It is diluted with 0.9% sodium chloride solution or appropriate mixtures containing sodium chloride. The prepared infusion is given through an intravenous line over a period determined by the specific regimen, typically 30 minutes to several hours depending on the dose.

No Aluminum Contact

Cisplatin reacts with metallic aluminum, forming a black platinum precipitate. Therefore, all equipment that comes into contact with cisplatin—including infusion sets, needles, catheters, and syringes—must not contain any aluminum components. Use only aluminum-free administration equipment.

Overdose

Your treating physician will ensure that you receive the correct dose for your condition. In the event of an accidental overdose, side effects may be amplified, particularly kidney damage, liver damage, hearing loss, severe bone marrow suppression, nausea and vomiting, and visual disturbances. There is no specific antidote for cisplatin overdose; treatment is supportive and symptomatic. Immediate measures include aggressive hydration and close monitoring of organ function. If you suspect that you have received too much cisplatin, contact your healthcare team immediately.

What Are the Side Effects of Cisplatin Ebewe?

Like all chemotherapy drugs, cisplatin can cause side effects, although not everyone experiences all of them. The most common side effects include nausea and vomiting, bone marrow suppression (causing low blood counts), kidney damage, and hearing changes. Many side effects can be prevented or managed with appropriate supportive care. Contact your doctor immediately if you experience severe or unexpected symptoms.

The side effects of cisplatin are dose-dependent and cumulative, meaning they may become more pronounced with repeated treatment cycles. Your healthcare team will implement a comprehensive supportive care plan including anti-nausea medications, intravenous hydration, and regular monitoring to minimize the impact of these effects. Below is a detailed overview of reported side effects, organized by frequency.

Seek Immediate Medical Attention If You Experience:
  • Persistent or severe diarrhea or vomiting
  • Mouth sores or inflammation of the mouth lining
  • Swelling of the face, lips, mouth, or throat
  • Unexplained respiratory symptoms such as dry cough, breathing difficulty, or wheezing
  • Difficulty swallowing
  • Numbness or tingling in fingers or toes
  • Extreme fatigue or unusual bruising or bleeding
  • Signs of infection such as sore throat and fever
  • Discomfort at or near the injection site during infusion
  • Severe pain or swelling in a leg, chest pain, or breathing difficulty (which may indicate blood clots)

Very Common (affects more than 1 in 10 patients)

May occur in the majority of patients
  • Decreased white blood cell count (leukopenia) – increased risk of infections
  • Decreased platelet count (thrombocytopenia) – increased risk of bruising and bleeding
  • Decreased red blood cell count (anemia) – may cause pale skin, weakness, and breathlessness
  • Bone marrow failure (inability to produce adequate blood cells)
  • Low sodium levels in the blood (hyponatremia)
  • Fever
  • Nausea and vomiting (occurs in over 90% of patients without adequate antiemetic therapy)

Common (affects 1 to 10 in 100 patients)

Reported in a significant number of patients
  • Sepsis (blood poisoning)
  • Heart rhythm disturbances including slow heart rate (bradycardia) and fast heart rate (tachycardia)
  • Shortness of breath (dyspnea)
  • Pneumonia and respiratory failure
  • Blood clots in the veins (venous thromboembolism)

Uncommon (affects 1 to 10 in 1,000 patients)

Less frequently reported
  • Reduced sperm production (dysfunctional spermatogenesis) and disrupted ovulation
  • Painful breast enlargement in men (gynecomastia)
  • Acute leukemia (secondary malignancy)
  • Low magnesium levels in the blood (hypomagnesemia)
  • Hearing damage (ototoxicity) – may be irreversible
  • Metal deposits on the gums

Rare (affects 1 to 10 in 10,000 patients)

Infrequently reported
  • Brain disorders (leukoencephalopathy)
  • Elevated cholesterol levels (hypercholesterolemia)
  • Seizures
  • Peripheral neuropathy (numbness, tingling, burning sensations in extremities)
  • Reversible posterior leukoencephalopathy syndrome (RPLS) – headache, confusion, seizures, visual loss with brain changes visible on MRI
  • Heart attack (myocardial infarction)
  • Mouth inflammation (stomatitis)

Very Rare (affects fewer than 1 in 10,000 patients)

Extremely rare reports
  • Elevated iron levels in the blood
  • Cardiac arrest (heart stops pumping)

Not Known (frequency cannot be estimated from available data)

Reported from post-marketing surveillance
  • Infection
  • Hemolytic anemia (Coombs-positive – breakdown of red blood cells)
  • Elevated amylase enzyme levels
  • Syndrome of inappropriate antidiuretic hormone secretion (SIADH) – causing fluid retention and dangerously low sodium
  • Dehydration
  • Low potassium, phosphate, and calcium levels in the blood
  • Elevated uric acid levels (hyperuricemia)
  • Muscle cramps (tetany)
  • Stroke (cerebrovascular accident)
  • Loss of taste
  • Lhermitte's sign (sudden pain radiating from neck down the spine when bending forward)
  • Spinal cord compression (myelopathy)
  • Autonomic neuropathy (affecting blood pressure, temperature control, digestion, bladder function)
  • Blurred vision, color blindness, visual loss (cortical blindness)
  • Optic neuritis, papilledema, retinal pigmentation
  • Tinnitus (ringing, buzzing, or clicking sounds in the ears), deafness
  • Heart problems, hemolytic uremic syndrome
  • Raynaud's phenomenon (pale and bluish fingers and toes)
  • Loss of appetite, hiccups, diarrhea
  • Elevated liver enzymes
  • Pulmonary embolism (blood clots in the lungs)
  • Skin rash, hair loss (alopecia)
  • Muscle twitching
  • Impaired or lost kidney function
  • Weakness, malaise
  • Injection site reactions (redness, inflammation, swelling, pain from extravasation)
Reporting Side Effects

If you experience any side effects, including those not listed above, talk to your doctor, pharmacist, or nurse. You can also report side effects directly to your national pharmacovigilance authority. Reporting helps to provide more information on the safety of this medicine.

How Should You Store Cisplatin Ebewe?

Cisplatin Ebewe is stored and handled by healthcare professionals in hospital settings. The unopened product should be stored below 25°C, protected from cold (do not freeze), and kept in the outer carton to protect from light. Patients do not typically need to store this medication at home.

As Cisplatin Ebewe is a hospital-administered medication, storage is managed by pharmacy and nursing staff. However, understanding proper storage conditions is important for ensuring the medication's effectiveness and safety. The following storage requirements apply:

  • Temperature: Store at or below 25°C (77°F)
  • Cold protection: Do not refrigerate or freeze. Cold temperatures can cause precipitation of the active ingredient
  • Light protection: Keep the vials in the outer carton to protect from light, as cisplatin is light-sensitive
  • Shelf life: Do not use after the expiration date printed on the carton and vial label (EXP). The expiration date refers to the last day of that month
  • Visual inspection: Do not use if you notice any visible deterioration, discoloration, or particles in the solution. Only clear, colorless to slightly yellowish solutions should be used
  • Keep out of reach of children

After Opening

Storage requirements after the vial has been opened depend on the vial size:

  • 10 ml and 20 ml vials: Single-use only. Discard any unused contents immediately. Withdraw the solution from the vial immediately before use
  • 50 ml and 100 ml vials: Chemical and physical in-use stability has been demonstrated for 28 days when stored at room temperature protected from light. From a microbiological standpoint, the product should be used immediately unless the method of opening excludes the risk of microbial contamination

After Dilution

The diluted infusion solution (at a final concentration of 0.1 mg/ml cisplatin) has demonstrated chemical and physical stability for 48 hours when stored at 2–8°C protected from sunlight, when prepared with the approved diluents (0.9% sodium chloride, sodium chloride/glucose mixture, or sodium chloride/mannitol mixture). From a microbiological standpoint, the diluted product should ideally be used immediately.

Environmental Protection

Cisplatin is a cytotoxic substance that can be harmful to the environment. Unused medicine and waste material must be disposed of in accordance with local requirements for hazardous pharmaceutical waste. Do not throw away any medicines via wastewater or household waste.

What Does Cisplatin Ebewe Contain?

Each milliliter of Cisplatin Ebewe contains 1 mg of cisplatin as the active substance. The other ingredients are sodium chloride, dilute hydrochloric acid, and water for injections. The product is available in 10 ml, 20 ml, 50 ml, and 100 ml glass vials.

Cisplatin Ebewe has a simple formulation designed to maintain the stability and solubility of the active ingredient:

Composition of Cisplatin Ebewe
Component Role Details
Cisplatin Active substance 1 mg per ml
Sodium chloride Stabilizer / tonicity agent Maintains cisplatin in solution and prevents degradation; the chloride ions are essential to keep the drug in its stable, non-reactive form until it enters cells
Dilute hydrochloric acid pH adjustment Adjusts and maintains the solution pH within the required range for stability
Water for injections Solvent Pharmaceutical-grade sterile water

Available Pack Sizes

Cisplatin Ebewe is available in the following presentations:

  • Packs of 1, 5, or 10 vials of 10 ml (containing 10 mg cisplatin each)
  • Packs of 1, 5, or 10 vials of 20 ml (containing 20 mg cisplatin each)
  • Packs of 1, 5, or 10 vials of 50 ml (containing 50 mg cisplatin each)
  • Packs of 1, 5, or 10 vials of 100 ml (containing 100 mg cisplatin each)

Not all pack sizes may be marketed in all countries. The vials are packaged with or without protective sleeves (Onco-Safe or protective film), which provide additional safety for pharmacy and healthcare staff during transport. These protective covers do not come into contact with the medicine itself.

Incompatibilities

Important preparation notes for healthcare professionals:

  • Cisplatin must not be diluted with glucose 5% solution alone or mannitol 5% solution alone; sodium chloride must always be present in the diluent
  • Antioxidants (such as sodium bisulfite), bicarbonate (sodium bicarbonate), sulfates, fluorouracil, and paclitaxel can inactivate cisplatin in the infusion set
  • All equipment must be aluminum-free, as cisplatin reacts with aluminum to form a black platinum precipitate

Frequently Asked Questions About Cisplatin Ebewe

Cisplatin is a platinum-based chemotherapy drug used to treat several types of cancer, including testicular cancer, ovarian cancer, head and neck squamous cell carcinoma, and non-small cell lung cancer. It is most commonly used in combination with other chemotherapy agents. Cisplatin is recognized by the World Health Organization as an essential medicine and has been a cornerstone of cancer treatment since its approval in 1978.

The most serious side effects include kidney damage (nephrotoxicity), hearing loss (ototoxicity), severe bone marrow suppression leading to low blood counts, and peripheral neuropathy. Kidney damage can be significantly reduced with proper hydration before and after treatment. Hearing loss may be irreversible and is monitored with regular audiometric testing. Your healthcare team will closely monitor all these parameters throughout your treatment.

Cisplatin is given exclusively as an intravenous infusion in a hospital or clinic. The concentrated solution is first diluted with sodium chloride-containing fluids. Patients receive extensive intravenous hydration before, during, and after the infusion to protect the kidneys. Anti-nausea medications are administered before treatment. The infusion duration varies depending on the specific regimen but typically ranges from 30 minutes to several hours.

Yes, cisplatin can significantly impact fertility in both men and women. In men, it may cause reduced or absent sperm production, which can be temporary or permanent. Sperm banking before treatment is strongly recommended. In women, it may disrupt ovulation. Effective contraception is required during treatment and for at least 7 months afterward for women, and 4 months for men. Discuss fertility preservation options with your oncologist before starting treatment.

Hydration is critical because cisplatin is primarily eliminated through the kidneys and can cause severe kidney damage. Adequate intravenous and oral fluid intake before, during, and for 24 hours after the infusion helps flush the drug through the kidneys more rapidly, reducing the concentration of toxic platinum compounds in the renal tubules. Without proper hydration, cisplatin can cause acute kidney injury and potentially permanent kidney failure.

Cisplatin-based chemotherapy has made testicular cancer one of the most curable solid tumors. Cure rates exceed 90% for early-stage disease and reach approximately 70–80% even for advanced metastatic disease. The standard BEP regimen (bleomycin, etoposide, and cisplatin) is typically given for 3–4 cycles. The introduction of cisplatin in the late 1970s transformed testicular cancer from a frequently fatal disease to a highly treatable condition.

References

  1. European Medicines Agency (EMA). Cisplatin – Summary of Product Characteristics. EMA EPAR. Available at: www.ema.europa.eu
  2. World Health Organization. WHO Model List of Essential Medicines – 23rd List (2023). WHO Technical Report. Available at: www.who.int
  3. Dasari S, Tchounwou PB. Cisplatin in cancer therapy: molecular mechanisms of action. European Journal of Pharmacology. 2014;740:364–378. doi:10.1016/j.ejphar.2014.07.025
  4. National Comprehensive Cancer Network (NCCN). NCCN Clinical Practice Guidelines in Oncology: Testicular Cancer, Version 1.2025. Available at: www.nccn.org
  5. ESMO Clinical Practice Guidelines. Management of Ovarian Cancer. Annals of Oncology. 2023. doi:10.1016/j.annonc.2023.01.014
  6. Galluzzi L, Senovilla L, Vitale I, et al. Molecular mechanisms of cisplatin resistance. Oncogene. 2012;31(15):1869–1883. doi:10.1038/onc.2011.384
  7. Kelland L. The resurgence of platinum-based cancer chemotherapy. Nature Reviews Cancer. 2007;7(8):573–584. doi:10.1038/nrc2167
  8. British National Formulary (BNF). Cisplatin – Drug Monograph. NICE. Available at: bnf.nice.org.uk
  9. U.S. Food and Drug Administration (FDA). Cisplatin – Prescribing Information. FDA Drug Label. Available at: www.accessdata.fda.gov
  10. Rosenberg B. Platinum complexes for the treatment of cancer: why the search goes on. In: Cisplatin: Chemistry and Biochemistry of a Leading Anticancer Drug. Wiley-VCH; 1999:3–27.

About the Medical Editorial Team

This article has been written and medically reviewed by the iMedic Medical Editorial Team, consisting of licensed physicians specializing in oncology, hematology, and clinical pharmacology. Our editorial process follows the GRADE evidence framework and adheres to international medical guidelines from WHO, EMA, FDA, NCCN, and ESMO.

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