Sedipam

Sedipam Brand names, Sedipam Analogs

Sedipam Brand Names Mixture

No information avaliable

Sedipam Chemical_Formula

C₁₆H₁₃ClN₂O

Sedipam RX_link

http://www.rxlist.com/cgi/generic/diazepam.htm

Sedipam fda sheet

Sedipam msds (material safety sheet)

Sedipam MSDS

Sedipam Synthesis Reference

Reeder, Sternbach; U.S. Pat. 3,371,085 (1968)

Sedipam Molecular Weight

284.74 g/mol

Sedipam Melting Point

125-126^oC

Sedipam H₂O Solubility

Slightly soluble (50 mg/L)

Sedipam State

solid

Sedipam LogP

2.988

Sedipam Dosage Forms

Tablets; Injectable solution

Sedipam Indication

Used in the treatment of severe anxiety disorders, as a hypnotic in the short-term management of insomnia, as a sedative and premedicant, as an anticonvulsant, and in the management of alcohol withdrawal syndrome.

Sedipam Pharmacology

Diazepam, a benzodiazepine, generates the same active metabolite as chlordiazepoxide and clorazepate. In animals, diazepam appears to act on parts of the limbic system, the thalamus and hypothalamus, and induces calming effects. Diazepam, unlike chlorpromazine and reserpine, has no demonstrable peripheral autonomic blocking action, nor does it produce extrapyramidal side effects; however, animals treated with diazepam do have a transient ataxia at higher doses. Diazepam was found to have transient cardiovascular depressor effects in dogs. Long-term experiments in rats revealed no disturbances of endocrine function. Injections into animals have produced localized irritation of tissue surrounding injection sites and some thickening of veins after intravenous use.

Sedipam Absorption

Essentially complete, with a bioavailability of 93%.

Sedipam side effects and Toxicity

Symptoms of overdose include somnolence, confusion, coma, and diminished reflexes. Respiration, pulse and blood pressure should be monitored.

Sedipam Patient Information

Sedipam Organisms Affected

Humans and other mammals