Pridesia en es it fr

Pridesia Brand names, Pridesia Analogs

Pridesia Brand Names Mixture

  • No information avaliable

Pridesia Chemical_Formula


Pridesia RX_link

Pridesia fda sheet

Pridesia msds (material safety sheet)

Pridesia MSDS

Pridesia Synthesis Reference

No information avaliable

Pridesia Molecular Weight

465.945 g/mol

Pridesia Melting Point

110 oC

Pridesia H2O Solubility

2.71 mg/L

Pridesia State


Pridesia LogP


Pridesia Dosage Forms

Suspension; Tablet

Pridesia Indication

For the symptomatic treatment of adult patients with nocturnal heartburn due to gastroesophageal reflux disease.

Pridesia Pharmacology

Cisapride is a parasympathomimetic which acts as a serotonin 5-HT4 agonist. Stimulation of the serotonin receptors increases acetylcholine release in the enteric nervous system. Cisapride stimulates motility of the upper gastrointestinal tract without stimulating gastric, biliary, or pancreatic secretions. Cisapride increases the tone and amplitude of gastric (especially antral) contractions, relaxes the pyloric sphincter and the duodenal bulb, and increases peristalsis of the duodenum and jejunum resulting in accelerated gastric emptying and intestinal transit. It increases the resting tone of the lower esophageal sphincter. It has little, if any, effect on the motility of the colon or gallbladder. Cisapride does not induce muscarinic or nicotinic receptor stimulation, nor does it inhibit acetylcholinesterase activity.

Pridesia Absorption

Cisapride is rapidly absorbed after oral administration, with an absolute bioavailability of 35-40%.

Pridesia side effects and Toxicity

No information avaliable

Pridesia Patient Information

No information avaliable

Pridesia Organisms Affected

Humans and other mammals