Cintapro Od

Cintapro Od Uses, Dosage, Side Effects, Food Interaction and all others data.

Cintapro Od is a gastroprokinetic agent and antiulcer benzamide with agonist activity at 5-HT1 and 5-HT4 receptors and antagonist activity at 5-HT2 receptors. It is marketed in Spain and Mexico.

Table Of contents

• Cintapro Od
• Uses
• Dosage
• Side Effect
• Precautions
• Interactions
• Uses during Pregnancy
• Uses during Breastfeeding
• Accute Overdose
• Food Interaction
• Half Life
• Volume of Distribution
• Clearance
• Interaction With other Medicine
• Contradiction
• Storage

Trade Name	Cintapro Od
Generic	Cinitapride
Cinitapride Other Names	Cinitaprida, Cinitapride, Cinitapridum
Weight	3mg
Type	Tablet
Formula	C21H30N4O4
Weight	Average: 402.4873 Monoisotopic: 402.226705468
Groups	Investigational
Therapeutic Class
Manufacturer	Zydus Cadila Healthcare Ltd
Available Country	India
Last Updated:	September 19, 2023 at 7:00 am

Uses

Cintapro Od is a benzamide with gastroprokinetic and antiemetic properties typically used for the treatment of gastrointestinal motility disorders such as gastroesophageal reflux disease (GERD), non-ulcer dyspepsia, and delayed gastric emptying.

It is indicated to treat gastrointestinal disorders associated with motility disturbances like gastroesophageal reflux disease (GERD), non-ulcer dyspepsia and delayed gastric emptying.

Cintapro Od is also used to associated treatment for these conditions: Dyspepsia, Flatulence, Gastro-esophageal Reflux Disease (GERD), Gastroesophageal Reflux, Decreased gastrointestinal motility, Meteorism, Mild Dyspepsia, Moderate Dyspepsia

How Cintapro Od works

Cintapro Od is a substituted benzamide with 5-HT receptor antagonist and agonist activity.

Toxicity

The symptoms of overdose include drowsiness, confusion and extrapyramidal effects.

Elimination Route

The absorption of cinitapride (12mg) following oral administration was rapid, with peak levels being achieved 2 h after dosing; absorption following intramuscular administration (4mg) was even more rapid, with peak levels (50% more that oral levels) being achieved 1 h after dosing.

Half Life

3-5 h during the first 8 h and a residual half-life greater than 15 h thereafter.

Innovators Monograph

You find simplified version here Cintapro Od