Valsts: Lielbritānija
Valoda: angļu
Klimata pārmaiņas: MHRA (Medicines & Healthcare Products Regulatory Agency)
Mannitol
15%) infusion Viaflo bags (Baxter Healthcare Ltd
Mannitol
150mg/1ml
Infusion
Intravenous
No Controlled Drug Status
Valid as a prescribable product
BNF: ; GTIN: 5413760373096
OBJECT 1 MANNITOL 15% W/V SOLUTION FOR INFUSION Summary of Product Characteristics Updated 08-Feb-2018 | Baxter Healthcare Ltd 1. Name of the medicinal product Mannitol 15% w/v Solution for infusion 2. Qualitative and quantitative composition Mannitol: 150 g/l Each ml contains 150 mg mannitol. For the full list of excipients, see section 6.1. 3. Pharmaceutical form Solution for Infusion Clear, colourless solution, free from visible particles. Osmolarity: 823 mOsm/l (approx) pH: 4.5- 7.0 4. Clinical particulars 4.1 Therapeutic indications Mannitol 15% w/v Solution for infusion is indicated for use as an osmotic diuretic in the following situations: • Promotion of diuresis in the prevention and/or treatment of the oliguric phase of acute renal failure before irreversible oliguric renal failure becomes established. • Reduction of intracranial pressure and cerebral oedema, when the blood-barrier is intact. • Reduction of elevated intraocular pressure when it cannot be lowered by other means. • Promotion of elimination of renally excreted toxic substances in poisoning. 4.2 Posology and method of administration Posology: The choice of the specific mannitol concentration, dosage and rate of administration depends on the age, weight and clinical condition of the patient and concomitant therapy. Adults and adolescents: Acute renal failure The general dose range for adults is 50 to 200 g mannitol (330 to 1320 ml) in a 24-hour period, with a dosage limit of 50 g mannitol (330 ml) on any one occasion. In most instances adequate response will be achieved at a dosage of 50 to 100 g mannitol/day (330 to 660 ml). The rate of administration is usually adjusted to maintain a urine flow of at least 30-50 ml per hour. Only in emergency situations, the maximum infusion rate can be as high as 200 mg/kg infused over 5 minutes (see also test dose). After 5 minutes, the infusion rate should be readjusted to maintain a urine flow of at least 30-50 ml per hour, with a maximum dose of 200 g/24h. _Use in patients with oliguria or ren Izlasiet visu dokumentu