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Home / Drugs / Starting with D / Diazoxide
 
Diazoxide
 

A benzothiadiazine derivative that is a peripheral vasodilator used for hypertensive emergencies. It lacks diuretic effect, apparently because it lacks a sulfonamide group. [PubChem]
BrandsDizoxide
Eudemine
Hyperstat
Hypertonalum
Mutabase
Proglicem
Proglycem
CategoriesAntihypertensive Agents
Vasodilator Agents
Diuretics, Thiazide
ManufacturersTeva branded pharmaceutical products r&d inc
Abraxis pharmaceutical products
Schering corp sub schering plough corp
Teva global respiratory research llc
PackagersIvax Pharmaceuticals
Medisca Inc.
Teva Pharmaceutical Industries Ltd.

indication

Used parentally to treat hypertensive emergencies. Also used to treat hypoglycemia secondary to insulinoma.

pharmacology

Diazoxide is a potassium channel activator, which causes local relaxation in smooth muscle by increasing membrane permeability to potassium ions. This switches off voltage-gated calcium ion channels which inhibits the generation of an action potential.

mechanism of action

As a diuretic, diazoxide inhibits active chloride reabsorption at the early distal tubule via the Na-Cl cotransporter, resulting in an increase in the excretion of sodium, chloride, and water. Thiazides like diazoxide also inhibit sodium ion transport across the renal tubular epithelium through binding to the thiazide sensitive sodium-chloride transporter. This results in an increase in potassium excretion via the sodium-potassium exchange mechanism. The antihypertensive mechanism of diazoxide is less well understood although it may be mediated through its action on carbonic anhydrases in the smooth muscle or through its action on the large-conductance calcium-activated potassium (KCa) channel, also found in the smooth muscle. As a antihypoglycemic, diazoxide inhibits insulin release from the pancreas, probably by opening potassium channels in the beta cell membrane.

toxicity

Oral LD50 in rat and mouse: 980 mg/kg and 444 mg/kg, respectively.

biotransformation

Hepatic.

absorption

Readily absorbed following oral administration.

half life

28 ±8.3 hours in normal adults.

route of elimination

Proglycem is extensively bound (more than 90%) to serum proteins, and is excreted in the kidneys.

drug interactions

Bendroflumethiazide: Significant hyperglycemic effect

Chlorpropamide: Antagonism.

Chlorthalidone: Significant hyperglycemic effect

Fosphenytoin: Diazoxide decreases the hydantoin effect

Glyburide: Antagonism.

Hydrochlorothiazide: Significant hyperglycemic effect

Indapamide: Significant hyperglycemic effect

Phenytoin: Diazoxide decreases the efficacy of phenytoin.

Trandolapril: Diazoxide may increase the hypotensive effect of Trandolapril. Monitor for changes in blood pressure.