LEVOPRAID® 25 Levosulpiride 25mg

GERD Makes Their Life Miserable
Due to Poor Lower Esophageal Sphincter Tone
When the esophageal sphincter is weak, it lacks the strength necessary to hold back stomach contents. Thus erosive stomach contents are allowed to backup (or reflux) into the esophagus.
Poor Esophageal Clearance
Normally when an episode of reflux occurs the esophagues has mechanism that quickly push the refluxed materials back into the stomach. If these mechanism malfunction the errosive stomach contents may remain in the esophagus for prolonged periods. This can result in irritation and even damage to the esophageal lining.
Levopraid ® 25 A Selective Dopamine DA2 Receptor Antagonist  
Levopraid 25 is more effective than domperidone and placebo to improve the severity of main reflux symptoms.

Levosulpiride 25mg tid
Domperidone 10mg tid
Placebo

 
 

No. of Patients: 30 duration: 12 weeks

Demonstrate better safety profile
The incidence of side effects with Levopraid 25 is significantly less than Domperidone and Metoclopramide.2  
 
Levosulpiride 25mg
Domperidone 10mg
Metoclopramide 10mg
   
Moreover...    
Recent studies showed that Cisapride but not Levosulpiride has structural properties similar to those of class III antiarrhythmic drugs, which delays repolarization and prolong QT interval.3
Hence, Levopraid 25 does not cause cardiac arrhythmias.    
Relieves GERD, Functional dyspepsia & IBS With better safety profile
Effectively Relives GERD, Functional Dyspepsia & IBS Better tolerability than metoclopramide and Domperidone. Doesnot cause cardiac arrhythmias and diarrhoea. No extrapyramidal side effects.
Indication Dosage Duration
GERD
1 Tab. TID
12 Weeks
Functional Dyspepsia
1 Tab. TID
4 Weeks
IBS
1 Tab.TID
4--6 Weeks

Ref 1: Masci et.al., current Therapeutic Research Vol-53, 1993
Ref 2: Corazza GR,Biagi F, Albano O, et al. Levosulpiride in functional dyspepsia: a multicentric, double-blind,controlled trial. Ital J. Gastroenterol 1996; 28 317-23
Ref 3: Corazza GR and Tonini M Levosulpiride for Dyspepsia and emesis, Clin drug invest 2000 Feb.19(2) 151-162


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