
Mes-D400 mg/4 m
Drug International Ltd.

IV Injection
Ifomes 400 mg/4 ml is used to prevent urothelial toxicity associated with oxazaphosphorine, ifosfamide or cyclophosphamide.
acrolein) of ifosfamide and cyclophosphamide.
It is used as a mucolytic in the management of some respiratory tract conditions e.
It acts in the kidney; reacting with thiol groups of urotoxic metabolites (e.
It acts by reducing the viscosity of pulmonary secretions; the drug's free sulfhydryl group is thought to reduce disulfide linkages of mucoproteins.
| Condition | Dosage | Notes |
|---|---|---|
| Intravenous-Prophylaxis against urothelial toxicity | Adult: Refer to individual and local protocol | Dose calculated according to cytotoxic dose. Normally given at a dose ≥cytotoxic dose. Duration of treatment should be as long as cytotoxic treatment; plus the time it takes for concentration of antineoplastic metabolites in urine to fall. Administered either by short (15-30 minutes) or continuous (24 hr) infusion |
| Child | Refer to individual and local protocol | Has been used in children >4 mth |
| Oral-Prophylaxis against urothelial toxicity | Adult: Refer to individual and local protocol | Dose calculated according to cytotoxic dose. Normally given at a dose ≥cytotoxic dose. Duration of treatment should be as long as cytotoxic treatment; plus the time it takes for concentration of antineoplastic metabolites in urine to fall |
| Child | Refer to individual and local protocol |
| Condition | Dosage | Notes |
|---|---|---|
| Intravenous-Prophylaxis against urothelial toxicity | Adult: Refer to individual and local protocol | Dose calculated according to cytotoxic dose. Normally given at a dose ≥cytotoxic dose. Duration of treatment should be as long as cytotoxic treatment; plus the time it takes for concentration of antineoplastic metabolites in urine to fall. Administered either by short (15-30 minutes) or continuous (24 hr) infusion |
| Child | Refer to individual and local protocol | Has been used in children >4 mth |
| Oral-Prophylaxis against urothelial toxicity | Adult: Refer to individual and local protocol | Dose calculated according to cytotoxic dose. Normally given at a dose ≥cytotoxic dose. Duration of treatment should be as long as cytotoxic treatment; plus the time it takes for concentration of antineoplastic metabolites in urine to fall |
| Child | Refer to individual and local protocol |
What is Ifomes 400 mg/4 ml used for?
Mesna is a cytoprotective agent indicated as a prophylactic agent in reducing the incidence of ifosfamide-induced hemorrhagic cystitis.
What is the dosage of Ifomes 400 mg/4 ml?
Intravenous-Prophylaxis against urothelial toxicity: Adult: Refer to individual and local protocol. Dose calculated according to cytotoxic dose. Normally given at a dose ≥cytotoxic dose. Duration of treatment should be as long as cytotoxic treatment; plus the time it takes for concentration of antineoplastic metabolites in urine to fall. Administered either by short (15-30 minutes) or continuous (…
What are the side effects of Ifomes 400 mg/4 ml?
Nausea, vomiting, colic, diarrhoea, anorexia, dyspepsia, unpleasant taste, constipation; headache, malaise, fatigue, depression, irritability, somnolence, hyperaesthesia, dizziness, confusion; rash, pruritus, generalised urticaria, alopecia, inj site reactions, flushing; leucopenia, thrombocytopenia, anaemia, granulocytopenia, chest pain, oedema (peripheral, facial and periorbital), hypotension, t…
Who should not take Ifomes 400 mg/4 ml?
Hypersensitivity to thiol-containing compounds.
What precautions should be taken with Ifomes 400 mg/4 ml?
Protective effect applies only to the urinary tract; pregnancy, lactation. Patients with auto-immune disorders. IV formulation may contain benzyl alcohol as a preservative; avoid in neonates or infants. Instruct patients to seek medical attention if discolouration of urine occurs. During treatment, monitor urine for erythrocytes and haematuria. Maintain adequate hydration in all patients. Patients…
Is Ifomes 400 mg/4 ml safe during pregnancy and breastfeeding?
Pregnancy Category B. Either animal-reproduction studies have not demonstrated a foetal risk but there are no controlled studies in pregnant women or animal-reproduction studies have shown an adverse effect (other than a decrease in fertility) that was not confirmed in controlled studies in women in the 1st trimester (and there is no evidence of a risk in later trimesters).
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