Luprac
Brand names,
Luprac
Analogs
Luprac
Brand Names Mixture
Luprac
Chemical_Formula
C16H20N4O3S
Luprac
RX_link
http://www.rxlist.com/cgi/generic/demadex.htm
Luprac
fda sheet
Luprac
msds (material safety sheet)
Luprac
Synthesis Reference
No information avaliable
Luprac
Molecular Weight
348.421 g/mol
Luprac
Melting Point
163-164 oC (decomposition)
Luprac
H2O Solubility
Soluble
Luprac
State
Solid
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LogP
2.404
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Dosage Forms
Liquid; Tablet
Luprac
Indication
For the treatment of hypertension, edema induced by congestive heart failure or renal disease, and ascites associated with hepatic disease.
Luprac
Pharmacology
Torasemide, a monosulfonamyl loop diuretic, differs form other thiazide diuretics in that a double ring system is incorporated into its structure. Torasemide is used alone or with atenolol in the management of hypertension and edema. Micropuncture studies in animals have shown that torsemide acts from within the lumen of the thick ascending portion of the loop of Henle, where it inhibits the Na+/K+/2Cl--carrier system.
Luprac
Absorption
Bioavailability is approximately 80%. Serum concentration peaks after approximately 1 hour.
Luprac
side effects and Toxicity
LD50 = 5 g/kg (rat, oral), 500 mg/kg (rat, intravenous). Side effects include dizziness, headache, nausea and vomiting.
Luprac
Patient Information
No information avaliable
Luprac
Organisms Affected
Humans and other mammals