Osmotically acting laxatives
Mannitol 25%
The FDA lists this product in 10 strengths and forms.
Indications
For Intravenous Injection Mannitol Injection, USP is indicated for the following therapeutic uses:
- The promotion of diuresis, in the prevention and/or treatment of the oliguric phase of acute renal failure before irreversible renal failure becomes established.
- The reduction of intracranial pressure and treatment of cerebral edema by reducing brain mass.
- The reduction of elevated intraocular pressure when it cannot be lowered by other means.
- The promotion of urinary excretion of toxic substances. For Urologic Irrigation Mannitol solution, 2.5% is indicated as an irrigation solution in transurethral prostatic resection or other transurethral surgical procedures. For Intravenous Injection Mannitol Injection, USP is indicated for the following therapeutic uses:
- The promotion of diuresis, in the prevention and/or treatment of the oliguric phase of acute renal failure before irreversible renal failure becomes established.
- The reduction of intracranial pressure and treatment of cerebral edema by reducing brain mass.
- The reduction of elevated intraocular pressure when it cannot be lowered by other means.
- The promotion of urinary excretion of toxic substances. For Urologic Irrigation Mannitol solution, 2.5% is indicated as an irrigation solution in transurethral prostatic resection or other transurethral surgical procedures.
Contraindications
- Well established anuria due to severe renal disease.
- Severe pulmonary congestion or frank pulmonary edema.
- Active intracranial bleeding except during craniotomy.
- Severe dehydration.
- Progressive renal damage or dysfunction after institution of mannitol therapy, including increasing oliguria and azotemia.
- Progressive heart failure or pulmonary congestion after mannitol therapy is started.
Warnings and precautions
In severe impairment of renal function a test dose should be given (see DOSAGE AND ADMINISTRATION ). A second test dose may be given if there is an inadequate response. No more than two test doses should be attempted. Excessive loss of water and electrolytes may lead to serious imbalances. Serum sodium and potassium should be carefully monitored during mannitol therapy. The diuresis after rapid infusion of mannitol may increase preexisting hemoconcentration.



