Valpin 50
Valpin 50 Brand names, Valpin 50 Analogs
Valpin 50 Brand Names Mixture
- No information avaliable
Valpin 50 Chemical_Formula
C17H32BrNO2
Valpin 50 RX_link
No information avaliable
Valpin 50 fda sheet
Valpin 50 msds (material safety sheet)
Valpin 50 Synthesis Reference
No information avaliable
Valpin 50 Molecular Weight
362.346 g/mol
Valpin 50 Melting Point
329 oC
Valpin 50 H2O Solubility
1600 mg/L
Valpin 50 State
Solid
Valpin 50 LogP
0.60
Valpin 50 Dosage Forms
Tablet (oral, 50mg)
Valpin 50 Indication
For use in conjunction with antacids or histamine H2-receptor antagonists in the treatment of peptic ulcer, to reduce further gastric acid secretion and delay gastric emptying.
Valpin 50 Pharmacology
Anisotropine methylbromide is a quaternary ammonium compound. Its use as treatment adjunct in peptic ulcer has been replaced by the use of more effective agents. Depending on the dose, anisotropine methylbromide may reduce the motility and secretory activity of the gastrointestinal system, and the tone of the ureter and urinary bladder and may have a slight relaxant action on the bile ducts and gallbladder. In general, smaller doses of anisotropine methylbromide inhibit salivary and bronchial secretions, sweating, and accommodation; cause dilatation of the pupil; and increase the heart rate. Larger doses are required to decrease motility of the gastrointestinal and urinary tracts and to inhibit gastric acid secretion.
Valpin 50 Absorption
Gastrointestinal absorption is poor and irregular. Total absorption after an oral dose is about 10 to 25%.
Valpin 50 side effects and Toxicity
No information avaliable
Valpin 50 Patient Information
Valpin 50 Organisms Affected
Humans and other mammals
