Fenoldopamum [Latin] en es it fr

Fenoldopamum [Latin] Brand names, Fenoldopamum [Latin] Analogs

Fenoldopamum [Latin] Brand Names Mixture

  • No information avaliable

Fenoldopamum [Latin] Chemical_Formula

C20H32F2O5

Fenoldopamum [Latin] RX_link

No information avaliable

Fenoldopamum [Latin] fda sheet

Fenoldopamum_[Latin] FDA

Fenoldopamum [Latin] msds (material safety sheet)

Fenoldopamum [Latin] Synthesis Reference

No information avaliable

Fenoldopamum [Latin] Molecular Weight

390.462 g/mol

Fenoldopamum [Latin] Melting Point

No information avaliable

Fenoldopamum [Latin] H2O Solubility

Practically insoluble

Fenoldopamum [Latin] State

Solid

Fenoldopamum [Latin] LogP

4.453

Fenoldopamum [Latin] Dosage Forms

Capsule (24 µg)

Fenoldopamum [Latin] Indication

For the treatment of chronic idiopathic constipation in the adult population.

Fenoldopamum [Latin] Pharmacology

Chronic idiopathic constipation is generally defined by infrequent or difficult passage of stool. The signs and symptoms associated with chronic idiopathic constipation (i.e., abdominal pain or discomfort, bloating, straining, and hard or lumpy stools) may be the result of abnormal colonic motility that can delay the transit of intestinal contents and impede the evacuation of rectal contents. One approach to the treatment of chronic idiopathic constipation is the secretion of fluid into the abdominal lumen through the activation of chloride channels in the apical membrane of the gastrointestinal epithelium. Lubiprostone is a locally acting chloride channel activator that enhances a chloride-rich intestinal fluid secretion without altering sodium and potassium concentrations in the serum.

Fenoldopamum [Latin] Absorption

Lubiprostone has low systemic availability following oral administration and concentrations of lubiprostone in plasma are below the level of quantitation (10 pg/mL).

Fenoldopamum [Latin] side effects and Toxicity

In a definitive Phase 1 cardiac repolarization study, 51 patients were administered a single oral dose of 144 mcg of lubiprostone, which is 6 times the normal single administration dose. Thirty-nine (39) of the 51 patients experienced an adverse event. The adverse events reported in >1% of this group included the following: nausea (45.1%), vomiting (27.5%), diarrhea (25.5%), dizziness (17.6%), loose or watery stools (13.7%), headache (11.8%), retching (7.8%), abdominal pain (5.9%), flushing or hot flush (5.9%), dyspnea (3.9%), pallor (3.9%), stomach discomfort (3.9%), syncope (3.9%), upper abdominal pain (2.0%), anorexia (2.0%), asthenia (2.0%), chest discomfort (2.0%), dry mouth (2.0%), hyperhidrosis (2.0%), skin irritation (2.0%) and vasovagal episode (2.0%).

Fenoldopamum [Latin] Patient Information

No information avaliable

Fenoldopamum [Latin] Organisms Affected

Humans and other mammals