Esomperazole
Brand names,
Esomperazole
Analogs
Esomperazole
Brand Names Mixture
Esomperazole
Chemical_Formula
C17H19N3O3S
Esomperazole
RX_link
http://www.rxlist.com/cgi/generic3/esomeprazole.htm
Esomperazole
fda sheet
Esomperazole
msds (material safety sheet)
Esomperazole
Synthesis Reference
No information avaliable
Esomperazole
Molecular Weight
345.417 g/mol
Esomperazole
Melting Point
155 oC
Esomperazole
H2O Solubility
Very slightly soluble in water
Esomperazole
State
Solid
Esomperazole
LogP
1.078
Esomperazole
Dosage Forms
Tablet (delayed-release); Delayed-release capsules; IV injection solution; IV iufusion solution
Esomperazole
Indication
For the treatment of acid-reflux disorders (GERD) and peptic ulcer disease
Esomperazole
Pharmacology
Esomeprazole is a compound that inhibits gastric acid secretion and is indicated in the treatment of gastroesophageal reflux disease (GERD), the healing of erosive esophagitis, and H. pylori eradication to reduce the risk of duodenal ulcer recurrence. Esomeprazole belongs to a new class of antisecretory compounds, the substituted benzimidazoles, that do not exhibit anticholinergic or H2 histamine antagonistic properties, but that suppress gastric acid secretion by specific inhibition of the H+/K+ ATPase enzyme system at the secretory surface of the gastric parietal cell. Because this enzyme system is regarded as the acid (proton) pump within the gastric mucosa, Esomeprazole has been characterized as a gastric acid-pump inhibitor, in that it blocks the final step of acid production. This effect is dose-related and leads to inhibition of both basal and stimulated acid secretion irrespective of the stimulus.
Esomperazole
Absorption
90%
Esomperazole
side effects and Toxicity
Blurred vision, confusion, drowsiness, dry mouthflushingheadache, nausea, rapid heartbeat, sweating
Esomperazole
Patient Information
No information avaliable
Esomperazole
Organisms Affected
Humans and other mammals