China Discount Price Doxycycline Hyclate Tooth Infection - Chlorothiazide – CPF manufacturers and suppliers

Discount Price Doxycycline Hyclate Tooth Infection - Chlorothiazide – CPF

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Discount Price Doxycycline Hyclate Tooth Infection - Chlorothiazide – CPF Detail:

Background

Chlorothiazide is an inhibitor of carbonic anhydrase and is slightly less potent than acetazolamide. This compound has been shown to block reabsorption of sodium and chloride ions.

Description

Chlorothiazide is a diuretic and antihypertensive. (IC50=3.8 mM) Target: Others Chlorothiazide sodium (Diuril) is a diuretic used within the hospital setting or for personal use to manage excess fluid associated with congestive heart failure. It is also used as an antihypertensive. Most often taken in pill form, it is usually taken orally once or twice a day. In the ICU setting, chlorothiazide is given to diurese a patient in addition to furosemide (Lasix). Working in a separate mechanism than furosemide, and absorbed enterically as a reconstituted suspension administered through a nasogastric tube (NG tube), the two drugs potentiate one another.

Clinical Trial

NCT Number	Sponsor	Condition	Start Date	Phase
NCT03574857	University of Virginia	Heart Failure\|Heart Failure With Reduced Ejection Fraction\|Heart Failure Acute\|Cardiovascular Diseases	June 2018	Phase 4
NCT02546583	Yale University\|National Heart, Lung, and Blood Institute (NHLBI)	Heart Failure	August 2015	Not Applicable
NCT02606253	Vanderbilt University\|Vanderbilt University Medical Center	Heart Failure	February 2016	Phase 4
NCT00004360	National Center for Research Resources (NCRR)\|Northwestern University\|Office of Rare Diseases (ORD)	Diabetes Insipidus, Nephrogenic	September 1995
NCT00000484	National Heart, Lung, and Blood Institute (NHLBI)	Cardiovascular Diseases\|Heart Diseases\|Hypertension\|Vascular Diseases	April 1966	Phase 3

Chemical structure

Chlorothiazide

2018 GMP-2
原料药GMP证书201811（captopril ,thalidomide etc）
GMP-of-PMDA-in-Chanyoo-平成28年08月03日　Nantong-Chanyoo-Pharmatech-Co
FDA-EIR-Letter-201901

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