| Ημερομηνία | barcode | code | περιεχομενο | τιμή παραγωγός | χονδρική | λιανική |
|---|---|---|---|---|---|---|
| 05/2018 | 2802900102017 | 290010201 | NOVOPRAZ GR.CAP 30MG/CAP BTx14 (BLIST 1x14) | 3.37 | 3.53 | 4.87 |
| 05/2018 | 2802900102024 | 290010202 | NOVOPRAZ GR.CAP 30MG/CAP BTx28 (BLIST 2x14) | 05.02 | 5.27 | 7.26 |
For the treatment of acid-reflux disorders (GERD), peptic ulcer disease, H. pylori eradication, and prevention of gastroinetestinal bleeds with NSAID use.
Lansoprazole belongs to a class of antisecretory compounds, the substituted benzimidazoles, that do not exhibit anticholinergic or histamine H<sub>2</sub>-receptor antagonist properties, but rather suppress gastric acid secretion by specific inhibition of the (H<sup>+</sup>,K<sup>+</sup>)-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 parietal cell, Lansoprazole 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 gastric acid secretion irrespective of the stimulus.
Symptoms of overdose include abdominal pain, nausea and diarrhea.
The absorption of lansoprazole is rapid, with mean C<sub>max</sub> occurring approximately 1.7 hours after oral dosing, and relatively complete with absolute bioavailability over 80%.
1.5 (&plusmn; 1.0) hours
Following single-dose oral administration of PREVACID, virtually no unchanged lansoprazole was excreted in the urine. In one study, after a single oral dose of 14C-lansoprazole, approximately one-third of the administered radiation was excreted in the urine and two-thirds was recovered in the feces. This implies a significant biliary excretion of the lansoprazole metabolites.