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Loortan (Losartan)

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Loortan belongs to a group of medicines known as angiotensin-II receptor antagonists. Angiotensin-II is a substance produced in the body which binds to receptors in blood vessels, causing them to tighten. This results in an increase in blood pressure. Loortan prevents the binding of angiotensin-II to these receptors, causing the blood vessels to relax which in turn lowers the blood pressure. Loortan slows the decrease of kidney function in patients with high blood pressure and type 2 diabetes.

Other names for this medication:
Acetensa, Angibloc, Arapres, Asart, Biortan, Cardzaar, Corodin, Cosart, Cozzar, Enromic, Faxiven, Hypozar, Lakea, Loben, Loctenk, Lopernal, Losalet, Losan, Losaprex, Losardil, Losargamma, Losartan, Losartas, Losatan, Losazid, Lostan, Lostat, Lotan, Lyosan, Myotan, Normatens, Osartan, Osartil, Portiron, Psycholanz, Ranlozar, Sartens, Sarvas, Sarvastan, Sarve, Satoren, Simperten, Sortal, Sortiva, Stadazar, Tacardia, Tanlozid, Tiasar, Xartan

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Microzide, Benicar, Lasix, Norvasc, Aceon, Lozol, Minipress

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Also known as: Losartan


Loortan (losartan potassium) is an angiotensin II receptor blocker acting on the AT1 receptor subtype. Losartan potassium, a non-peptide molecule, is chemically described as 2-butyl-4-chloro-1-[p-(o-1Htetrazol- 5-ylphenyl)benzyl]imidazole-5-methanol monopotassium salt.

Loortan is a white to off-white free-flowing crystalline powder with a molecular weight of 461.01. It is freely soluble in water, soluble in alcohols, and slightly soluble in common organic solvents, such as acetonitrile and methyl ethyl ketone. Oxidation of the 5-hydroxymethyl group on the imidazole ring results in the active metabolite of losartan.

Loortan is available as tablets for oral administration containing either 25 mg, 50 mg or 100 mg of losartan potassium and the following inactive ingredients: microcrystalline cellulose, lactose hydrous, pregelatinized starch, magnesium stearate, hydroxypropyl cellulose, hypromellose, and titanium dioxide.

Loortan 25 mg, 50 mg and 100 mg tablets contain potassium in the following amounts: 2.12 mg (0.054 mEq), 4.24 mg (0.108 mEq) and 8.48 mg (0.216 mEq), respectively. Loortan 25 mg, Loortan 50 mg, and Loortan 100 mg may also contain carnauba wax.


Take Loortan tablets orally with or without food. Do not crush or chew it. Take Loortan once or twice a day at the same time. If you want to achieve most effective results do not stop taking Loortan suddenly.


If you overdose Loortan and you don't feel good you should visit your doctor or health care provider immediately. Symptoms of Loortan overdosage: fainting, feeling lightheaded, rapid heartbeat.


Store at room temperature between 15 and 30 degrees C (59 and 86 degrees F) away from moisture, light and heat. Keep container tightly closed. Throw away any unused medicine after the expiration date. Keep out of the reach of children in a container that small children cannot open.

Side effects

The most common side effects associated with Loortan are:

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Changes in renal function including acute renal failure can be caused by drugs that inhibit the reninangiotensin system and by diuretics. Patients whose renal function may depend in part on the activity of the renin-angiotensin system (e.g., patients with renal artery stenosis, chronic kidney disease, severe congestive heart failure, or volume depletion) may be at particular risk of developing acute renal failure on COZAAR. Monitor renal function periodically in these patients. Consider withholding or discontinuing therapy in patients who develop a clinically significant decrease in renal function on Loortan.

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