
Holoxan1 gm/vial
Synovia Pharma PLC
Ifosfamide is an alkylating agent (oxazaphosphorine) chemotherapy medicine used in the treatment of certain cancers, always under the supervision of a physician experienced in cancer chemotherapy.
Ifosfamide is an alkylating agent (oxazaphosphorine) chemotherapy medicine used in the treatment of certain cancers, always under the supervision of a physician experienced in cancer chemotherapy.
Ifosfamide is never used as a stand-alone, first-line treatment; it is always given as part of a physician-directed combination chemotherapy protocol along with mandatory supportive care (see Dosage and Administration).
Ifosfamide dosing is individualized by the treating oncologist based on the specific regimen, body surface area, and patient tolerance. It is always given as a slow intravenous infusion (over at least 30 minutes) together with mandatory mesna and hydration to reduce bladder toxicity.
| Regimen component | Typical dose | Schedule |
|---|---|---|
| Ifosfamide | 1.2 g/m² body surface area, by IV infusion over ≥30 minutes | Once daily for 5 consecutive days, repeated every 3 weeks (or upon adequate hematologic recovery) for several cycles as directed by the oncologist |
| Mesna (mandatory) | Approximately 20% of the Ifosfamide dose | Given at the time of, and at 4 and 8 hours after, each Ifosfamide dose (or as a continuous infusion), for each of the 5 days |
| IV/oral hydration | At least 2 liters of fluid per 24 hours | Throughout each treatment day |
Dose and schedule of Ifosfamide vary considerably by indication (e.g., sarcoma or lymphoma protocols may use different total doses given over 1–5 days). The exact protocol, dose, and number of cycles must be determined and supervised by an oncologist experienced with the specific regimen.
Ifosfamide and its toxic metabolites are cleared substantially by the kidneys. In patients with renal impairment, clearance is reduced and the risk of central nervous system and kidney toxicity is increased; dose reduction, closer monitoring, or avoidance is required, and Ifosfamide should generally be avoided in severe renal impairment (see Contraindications).
Since Ifosfamide requires hepatic activation to its active form, significant hepatic impairment may alter its efficacy and toxicity profile. There are no well-established formal dose-adjustment guidelines for hepatic impairment; such patients should be monitored closely and managed by the treating oncologist.
Ifosfamide commonly causes side effects related to its cytotoxic mechanism. Patients are monitored closely by their oncology team throughout treatment.
Patients should seek urgent medical attention for fever, signs of infection, severe confusion, difficulty urinating, visible blood in urine, or unusual bleeding/bruising.
Ifosfamide is contraindicated in patients with:
Ifosfamide should not be given without concurrent mesna and adequate hydration, as these are integral, non-optional parts of safe administration rather than separate precautions.
Disclaimer
The information provided is accurate to the best of our knowledge, but it does not replace professional medical advice. We cannot guarantee its completeness or accuracy, and the absence of specific information about a drug should not be taken as an endorsement. We are not responsible for any consequences arising from this information, so please consult a healthcare professional for any concerns or questions.