Ulsaven
Brand names,
Ulsaven
Analogs
Ulsaven
Brand Names Mixture
- Tritec (ranitidine bismuth citrate salt)
Ulsaven
Chemical_Formula
C13H22N4O3S
Ulsaven
RX_link
http://www.rxlist.com/cgi/generic2/ranitbc.htm
Ulsaven
fda sheet
Ulsaven
msds (material safety sheet)
Ulsaven
Synthesis Reference
B. J. Price et al., U.S. Pat. 4,128,658 (1978)
Ulsaven
Molecular Weight
314.405 g/mol
Ulsaven
Melting Point
69-70 oC
Ulsaven
H2O Solubility
24.7 mg/mL
Ulsaven
State
Solid
Ulsaven
LogP
1.93
Ulsaven
Dosage Forms
Capsule; Liquid; Solution; Tablet; Syrup
Ulsaven
Indication
Used in the treatment of peptic ulcer disease (PUD), dyspepsia, stress ulcer prophylaxis, and gastroesophageal reflux disease (GERD).
Ulsaven
Pharmacology
Ranitidine is a histamine H2-receptor antagonist similar to cimetidine and famotidine. An H2-receptor antagonist, often shortened to H2 antagonist, is a drug used to block the action of histamine on parietal cells in the stomach, decreasing acid production by these cells. These drugs are used in the treatment of dyspepsia, however their use has waned since the advent of the more effective proton pump inhibitors. Like the H1-antihistamines, the H2 antagonists are inverse agonists rather than true receptor antagonists.
Ulsaven
Absorption
Approximately 50% bioavailability orally.
Ulsaven
side effects and Toxicity
LD50=77mg/kg (orally in mice). Symptoms of overdose include muscular tremors, vomiting, and rapid respiration.
Ulsaven
Patient Information
PATIENT INFORMATION
Phenylketonurics: ZANTAC 25 EFFERdose Tablets contain phenylalanine 2.81 mg per 25 mg of ranitidine. ZANTAC 150 EFFERdose Tablets
contain phenylalanine 16.84 mg per 150 mg of ranitidine. ZANTAC EFFERdose Tablets should not be chewed, swallowed whole, or dissolved
on the tongue.
Ulsaven
Organisms Affected
Humans and other mammals