Oedema

Active Ingredient: Bumetanide

Indication for Bumetanide

Population group: only adults (18 years old or older)

Bumetanide is indicated for the treatment of oedema associated with e.g. congestive heart failure, renal dysfunction including nephrotic syndrome and cirrhosis of the liver in adults.

For this indication, competent medicine agencies globally authorize below treatments:

1-2 mg in 1-2 divided doses daily

Route of admnistration

Oral

Defined daily dose

1 - 2 mg

Dosage regimen

From 1 To 2 mg once every day

Detailed description

Most patients require a daily dose of 1 mg given as a single morning or early evening dose. Depending on the patient’s response, a second dose can be given 6-8 hours later. In refractory cases, the dose can be increased until a satisfactory diuretic response is obtained, or infusions of bumetanide can be given.

0.5-1 mg

Route of admnistration

Intravenous

Defined daily dose

0.5 - 1 mg

Dosage regimen

From 0.5 To 1 mg once every day

0.5-1 mg

Route of admnistration

Intramuscular

Defined daily dose

0.5 - 1 mg

Dosage regimen

From 0.5 To 1 mg once every day

Active ingredient

Bumetanide

Bumetanide is a potent loop diuretic with a rapid onset and a short duration of action. The primary site of action is the ascending limb of the loop of Henle where it exerts inhibiting effects on electrolyte reabsorption, causing its diuretic and natriuretic action.

Read more about Bumetanide

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