| Ημερομηνία | barcode | code | περιεχομενο | τιμή παραγωγός | χονδρική | λιανική |
|---|---|---|---|---|---|---|
| 05/2018 | 2802729901013 | 272990101 | NOXADIF GR.TAB 40MG/TAB BTx14 (BLIST 1x14) | 0.98 | 01.03 | 1.42 |
| 05/2018 | 2802729901020 | 272990102 | NOXADIF GR.TAB 40MG/TAB BTx28 (BLIST 2x14) | 2.19 | 2.30 | 3.17 |
| 05/2018 | 2802729901051 | 272990105 | NOXADIF GR.TAB 40MG/TAB BTx30 (BLIST 3x10) | 2.52 | 2.64 | 3.64 |
Short-term (up to 16 weeks) treatment of erosive esophagitis.
Pantoprazole is a proton pump inhibitor (PPI) that suppresses the final step in gastric acid production by forming a covalent bond to two sites of the (H<sup>+</sup>,K<sup>+</sup> )- ATPase enzyme system at the secretory surface of the gastric parietal cell. This effect is dose- related and leads to inhibition of both basal and stimulated gastric acid secretion irrespective of the stimulus.
Single intravenous doses of pantoprazole at 378, 230, and 266 mg/kg (38, 46, and 177 times the recommended human dose based on body surface area) were lethal to mice, rats and dogs, respectively. The symptoms of toxicity included hypoactivity, ataxia, hunched sitting, limb-splay, lateral position, segregation, absence of ear reflex, and tremor. There is limited experience regarding cases of human overdosage, and treatment should be symptomatic and supportive.
Pantoprazole is well absorbed. It undergoes little first-pass metabolism resulting in an absolute bioavailability of approximately 77%.
1 hour
After administration of a single intravenous dose of 14C-labeled pantoprazole to healthy, normal metabolizer subjects, approximately 71% of the dose was excreted in the urine with 18% excreted in the feces through biliary excretion.
* 11.0 to 23.6 L
* 7.6-14.0 L/h