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Solute carrier family 12 member 4

2

Histamine H1 receptor

315

Dopamine D2 receptor

297

DNA

278

Bacterial penicillin-binding protein

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US Approved Rx

2

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Highest Phase

Approved

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Approval Year

1983

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Condition

Edema

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Primary

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CNS Activity

CNS Active

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Originator

Leo Pharma

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ECHA (EC/EINECS)

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EPA CompTox

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FDA UNII

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DIURETICS AND POTASSIUM-SPARING AGENTS IN COMBINATION

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HIGH-CEILING DIURETICS

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ATC Level 4

High-ceiling diuretics and potassium-sparing agents

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Sulfonamides and potassium in combination

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Sulfonamides, plain

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BUMETANIDE

0Y2S3XUQ5H

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Status:

US Approved Rx (2008)

First approved in 1983

Class (Stereo):

CHEMICAL (ACHIRAL)

Targets:

Solute carrier family 12 member 4

Solute carrier family 12 member 2

Solute carrier family 12 member 1

Solute carrier family 12 member 5

Conditions:

Bumetanide is indicated for the treatment of edema associated with congestive heart failure, hepatic and renal disease, including the nephrotic syndrome. It blocks the reabsorption of sodium and fluid from the kidney's tubules. The most frequent clin...

ical adverse reactions considered probably or possibly related to bumetanide are muscle cramps (seen in 1.1% of treated patients), dizziness (1.1%), hypotension (0.8%), headache (0.6%), nausea (0.6%) and encephalopathy (in patients with preexisting liver disease) (0.6%). One or more of these adverse reactions have been reported in approximately 4.1% of patients treated with Bumex (bumetanide). Lithium should generally not be given with diuretics (such as Bumex (bumetanide)) because they reduce its renal clearance and add a high risk of lithium toxicity. Bumex (bumetanide) may potentiate the effect of various antihypertensive drugs, necessitating a reduction in the dosage of these drugs.

BUMETANIDE SODIUM

1QC8KM52D1

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Search for Structure

Status:

US Approved Rx (2008)

First approved in 1983

Class (Stereo):

CHEMICAL (ACHIRAL)

Targets:

Solute carrier family 12 member 4

Solute carrier family 12 member 2

Solute carrier family 12 member 1

Solute carrier family 12 member 5

Conditions:

Bumetanide is indicated for the treatment of edema associated with congestive heart failure, hepatic and renal disease, including the nephrotic syndrome. It blocks the reabsorption of sodium and fluid from the kidney's tubules. The most frequent clin...

ical adverse reactions considered probably or possibly related to bumetanide are muscle cramps (seen in 1.1% of treated patients), dizziness (1.1%), hypotension (0.8%), headache (0.6%), nausea (0.6%) and encephalopathy (in patients with preexisting liver disease) (0.6%). One or more of these adverse reactions have been reported in approximately 4.1% of patients treated with Bumex (bumetanide). Lithium should generally not be given with diuretics (such as Bumex (bumetanide)) because they reduce its renal clearance and add a high risk of lithium toxicity. Bumex (bumetanide) may potentiate the effect of various antihypertensive drugs, necessitating a reduction in the dosage of these drugs.

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