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Jevtana
Cabazitaxel
$4495.00
60mg/1.5ml · 60 vial
BrandBranded medicine· By Sanofi
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40mg/ml
60mg/1.5ml
60mg/6ml
FDA boxed warningNeutropenia and hypersensitivity
Neutropenic deaths have been reported. Obtain frequent blood counts to monitor for neutropenia. JEVTANA is contraindicated in patients with neutrophil counts of ≤1,500 cells/mm 3. Primary prophylaxis with G-CSF is recommended in patients with high-risk clinical features. Consider primary prophylaxis with G-CSF in all patients receiving a dose of 25 mg/m 2
Severe hypersensitivity can occur and may include generalized rash/erythema, hypotension and bronchospasm. Discontinue JEVTANA immediately if severe reactions occur and administer appropriate therapy.
Contraindicated if history of severe hypersensitivity reactions to cabazitaxel or to drugs formulated with polysorbate 80.
About Jevtana
Overview
Jevtana (cabazitaxel) is a prescription cancer medicine in the taxane family, given by intravenous infusion. It is used with prednisone to treat prostate cancer that has spread and is resistant to treatment that lowers testosterone, in patients previously treated with docetaxel. It works by stabilising structures inside cells called microtubules, disrupting cell division and other cell functions.
What it treats
Metastatic castration-resistant prostate cancer, in combination with prednisone, in patients previously treated with a docetaxel-containing regimen.
Safety information
Side effects
Common side effects of Jevtana include low white blood cell counts, anemia (low red blood cell counts), diarrhea, nausea, tiredness, weakness, vomiting, blood in the urine, constipation, reduced appetite, back pain and abdominal pain. Contact a doctor immediately for fever or signs of infection, a severe allergic reaction, severe diarrhea, bleeding from the digestive tract, severe abdominal pain, blood in the urine or breathing problems. Serious risks include bone marrow suppression, infections associated with low white blood cell counts, bowel perforation or inflammation, kidney failure, bladder inflammation and severe lung inflammation or respiratory distress. Some of these complications can be fatal. People aged 65 or older have a higher risk of certain serious side effects and fatal outcomes. Frequent blood count monitoring is needed during treatment. People who previously received pelvic radiation need monitoring for bladder inflammation.
FDA boxed warning
Neutropenia and hypersensitivity
Neutropenic deaths have been reported. Obtain frequent blood counts to monitor for neutropenia. JEVTANA is contraindicated in patients with neutrophil counts of ≤1,500 cells/mm 3. Primary prophylaxis with G-CSF is recommended in patients with high-risk clinical features. Consider primary prophylaxis with G-CSF in all patients receiving a dose of 25 mg/m 2
Severe hypersensitivity can occur and may include generalized rash/erythema, hypotension and bronchospasm. Discontinue JEVTANA immediately if severe reactions occur and administer appropriate therapy.
Contraindicated if history of severe hypersensitivity reactions to cabazitaxel or to drugs formulated with polysorbate 80.
A boxed warning is the strongest warning the US Food and Drug Administration requires on a medicine label. Text is taken from the official label, with internal section references removed.
When to call your doctor
If symptoms are severe or getting worse quickly, seek emergency care rather than waiting.
Before taking this medicine
Jevtana (cabazitaxel) must not be used in people with: • A neutrophil count of 1,500/mm³ or lower. Neutrophils are a type of white blood cell. • A history of severe allergic reactions to cabazitaxel or to other medicines formulated with polysorbate 80. • Severe liver impairment, defined as total bilirubin more than three times the upper limit of normal. Extra caution and monitoring are needed in people aged 65 or older, those with haemoglobin below 10 g/dL, and those with mild or moderate liver impairment. Blood counts must be checked frequently because Jevtana can suppress bone marrow function, causing low neutrophil counts and serious or fatal infections. Severe allergic reactions can occur. Medicines are given before treatment to reduce this risk; the infusion must be stopped immediately if a reaction occurs. Other serious risks include severe diarrhoea and dehydration, gastrointestinal bleeding or perforation, bowel inflammation associated with low neutrophil counts, kidney failure, and lung inflammation or acute respiratory distress. Some of these complications have been fatal. Bladder inflammation and blood in the urine can also occur; people who previously received pelvic radiation need monitoring for bladder symptoms. Jevtana can harm an unborn baby and cause pregnancy loss. Men with female partners who could become pregnant should use effective contraception.
Interactions
Jevtana should not be used with medicines that strongly inhibit an enzyme called CYP3A. Tell your doctor about all medicines you take so they can check for this interaction. If using a strong CYP3A inhibitor is necessary, your prescriber may adjust your Jevtana dose.
Using Jevtana
Dosing
Dosing is set by your prescriber. Each health care professional may prescribe medication differently according to a patient's medical history and condition, so follow the directions on your prescription label and speak to your doctor or pharmacist before changing anything.
Storage
Store in the original carton below 25°C, protected from light, unless the pack states refrigeration. Do not freeze. Keep all medicines out of the sight and reach of children.
Clinical information on this page is summarised from the US FDA label JEVTANA (CABAZITAXEL) KIT [SANOFI-AVENTIS U.S. LLC] (DailyMed, retrieved 19 September 2026).
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