Diazoxide clinical pharmacology: Difference between revisions

Jump to navigation Jump to search
(Created page with "__NOTOC__ {{Diazoxide}} {{CMG}}; {{AE}} {{SS}} ==Clinical Pharmacology== Diazoxide administered orally produces a prompt dose-related increase in blood glucose level, due pr...")
 
(Redirected page to Diazoxide#Pharmacology)
 
(One intermediate revision by one other user not shown)
Line 1: Line 1:
__NOTOC__
#REDIRECT [[Diazoxide#Pharmacology]]
{{Diazoxide}}
{{CMG}}; {{AE}} {{SS}}
 
==Clinical Pharmacology==
 
Diazoxide administered orally produces a prompt dose-related increase in blood glucose level, due primarily to an inhibition of insulin release from the pancreas, and also to an extrapancreatic effect.
 
The hyperglycemic effect begins within an hour and generally lasts no more than eight hours in the presence of normal renal function.
 
PROGLYCEM® decreases the excretion of sodium and water, resulting in fluid retention which may be clinically significant.
 
The hypotensive effect of diazoxide on blood pressure is usually not marked with the oral preparation. This contrasts with the intravenous preparation of diazoxide (seeADVERSE REACTIONS).
 
Other pharmacologic actions of PROGLYCEM® include increased pulse rate; increased serum uric acid levels due to decreased excretion; increased serum levels of free fatty acids' decreased chloride excretion; decreased para-aminohippuric acid; (PAH) clearance with no appreciable effect on glomerular filtration rate.
 
The concomitant administration of a benzothiazide [[diuretic]] may intensify the hyperglycemic and hyperuricemic effects of PROGLYCEM®. In the presence of [[hypokalemia]], hyperglycemic effects are also potentiated.
 
PROGLYCEM®-induced [[hyperglycemia]] is reversed by the administration of insulin or tolbutamide. The inhibition of insulin release by PROGLYCEM® is antagonized by alpha-adrenergic blocking agents.
 
PROGLYCEM® is extensively bound (more than 90%) to serum proteins, and is excreted in the kidneys. The plasma half-life following I.V. administration is 28 ± 8.3 hours. Limited data on oral administration revealed a half-life of 24 and 36 hours in two adults. In four children aged four months to six years, the plasma half-life varied from 9.5 to 24 hours on long-term oral administration. The half-life may be prolonged following overdosage, and in patients with impaired renal function.<ref name="dailymed.nlm.nih.gov">{{Cite web  | last =  | first =  | title = PROGLYCEM (DIAZOXIDE) SUSPENSION [TEVA GLOBAL RESPIRATORY RESEARCH LLC] | url = http://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=b16c7832-2fd9-49af-b923-1dc0d91fd6e2 | publisher =  | date =  | accessdate = 26 February 2014 }}</ref>
 
==References==
{{reflist|2}}
 
{{Nonsympatholytic vasodilatory antihypertensives}}
{{Other therapeutic products}}
{{Channel openers}}
 
[[Category:Sulfonamides]]
[[Category:Vasodilators]]
[[Category:Potassium channel openers]]
[[Category:Benzothiadiazines]]
[[Category:Organochlorides]]
[[Category:Cardiovascular Drugs]]
[[Category:Drugs]]

Latest revision as of 02:06, 22 July 2014