Cinitapride: Difference between revisions

From WikiMD's Wellness Encyclopedia

CSV import
Tags: mobile edit mobile web edit
 
CSV import
 
Line 30: Line 30:


{{stub}}
{{stub}}
<gallery>
File:Cinitapride.svg|Cinitapride chemical structure
File:3D_Cinitapride.png|3D model of Cinitapride
File:Cinitapride_synthesis.svg|Cinitapride synthesis pathway
</gallery>

Latest revision as of 02:11, 18 February 2025

Cinitapride is a gastroprokinetic agent and antiulcer agent of the benzamide class which is marketed in Spain and Mexico. It acts as an agonist of the 5-HT1 and 5-HT4 receptors and as an antagonist of the 5-HT2 receptors.

Mechanism of action[edit]

Cinitapride has a dual mechanism of action. It works as an agonist of the 5-HT1 and 5-HT4 receptors, and as an antagonist of the 5-HT2 receptors. This dual action makes it effective in treating certain gastrointestinal conditions.

Uses[edit]

Cinitapride is used in the treatment of gastroesophageal reflux disease (GERD), non-ulcer dyspepsia, and as a prokinetic agent in conditions such as gastroparesis and functional dyspepsia.

Side effects[edit]

The most common side effects of cinitapride include dizziness, headache, diarrhea, and abdominal pain. In rare cases, it can cause extrapyramidal symptoms.

Contraindications[edit]

Cinitapride is contraindicated in patients with known hypersensitivity to the drug, and in those with gastrointestinal hemorrhage, mechanical obstruction, or perforation.

Interactions[edit]

Cinitapride may interact with other drugs such as anticholinergic medications, antipsychotic drugs, and antiarrhythmic drugs.

Pharmacokinetics[edit]

Cinitapride is rapidly absorbed from the gastrointestinal tract and undergoes extensive first-pass metabolism in the liver. It is excreted primarily in the urine.

See also[edit]

This article is a medical stub. You can help WikiMD by expanding it!
PubMed
Wikipedia