|
 |
 |
| |
Composition:
Each capsule contains
Lansoprazole..30 mg
Description: - Lansoprazole is
the prototype member of a new class of substituted
benzimidazoles, which inhibit the final common
step in gastric acid secretion. The only significant
pharmacological action of Lansoprazole is dose
dependent suppression of gastric acid secretion;
without anticholinergic or H2 blocking action.
It is a powerful inhibitor of gastric acid: can
totally abolish HCl secretion, both resting as
well as that stimulated by any of the secretagogues,
without much effect on pepsin, intrinsic factor,
juice volume and gastric motility.
Lansoprazole is inactive at neutral pH, but at
pH<5 rearranges to two charged cationic forms
(a sulphenic acid and a sulphenamide configurations)
that react covalently with the SH groups of the
H+K+ATPase enzyme and inactivate it irreversibly,
specially when two molecules of Omeprazole react
with one molecule of the enzyme. After diffusing
into the parietal cell from blood it gets concentrated
in the acidic pH are unable to diffuse back. Moreover
it gets tightly bound to the enzyme. These features
and the specific localization of H+K+ATPase to
apical membrane of the parietal cells confer high
degree of selectivity of action to Lansprazole.
Acid secretion resumes only when new H+K+ATPase
molecules are synthesized. It has higher oral
bioavilability then omeprazole.
Indications: - Use in peptic
ulcer and hyperacidity problems. Reflux or ulcerative
oesophagitis. Zollinger-Ellison syndrome. NSAIDS-induced
ulcers.
Dosage: - Gastric ulcer; 20 mg
once daily for 8 weeks.
Reflux oesophagitis; 20 mg once daily for 4 weeks
Duodenal ulcer; 20 mg once daily for 4 weeks
Zollinger-Ellison syndrome 60 ml once a day with
maintenance dosage
80 mg in divided doses.
Contra indications: - Hypersensitivity
and neonates.
Pediatrics: Not recommended
Pregnancy: Safety not established.
Lactation: Safety not established.
Presentation: - 10x10 capsules
in a Multicarton. |
|
|
 |
|
|
|
|
|
|