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Sagisal Brand names, Sagisal Analogs

Sagisal Brand Names Mixture

  • No information avaliable

Sagisal Chemical_Formula


Sagisal RX_link

Sagisal fda sheet

Sagisal FDA

Sagisal msds (material safety sheet)

Sagisal MSDS

Sagisal Synthesis Reference

No information avaliable

Sagisal Molecular Weight

514.617 g/mol

Sagisal Melting Point


Sagisal H2O Solubility

Practically insoluble

Sagisal State


Sagisal LogP


Sagisal Dosage Forms


Sagisal Indication

For the treatment of hypertension.

Sagisal Pharmacology

Telmisartan is an orally active nonpeptide angiotensin II antagonist that acts on the AT1 receptor subtype. New studies suggest that telmisartan may also have PPARγ agonistic properties that could potentially confer beneficial metabolic effects. This observation is currently being explored in clinical trials. Angiotensin II is formed from angiotensin I in a reaction catalyzed by angiotensin-converting enzyme (ACE, kininase II). Angiotensin II is the principal pressor agent of the renin-angiotensin system, with effects that include vasoconstriction, stimulation of synthesis and release of aldosterone, cardiac stimulation, and renal reabsorption of sodium. Telmisartan works by blocking the vasoconstrictor and aldosterone secretory effects of angiotensin II.

Sagisal Absorption

Absolute bioavailability depends on dosage. Food slightly decreases the bioavailability (a decrease of about 6% is seen when the 40-mg dose is administered with food).

Sagisal side effects and Toxicity

Intravenous LD50 in rats is 150-200 mg/kg in males and 200 to 250 mg/kg in females. Acute oral toxicity is low: no deaths and no changes occurred in rats or dogs at 2000 mg/kg, the highest dose tested. Limited data are available with regard to overdosage in humans. The most likely manifestations of overdosage with telmisartan would be hypotension, dizziness and tachycardia; bradycardia could occur from parasympathetic (vagal) stimulation.

Sagisal Patient Information

Sagisal Organisms Affected

Humans and other mammals