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Araten (Losartan)

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Araten belongs to a family of medications known as angiotensin II receptor blockers. These medications are used in adults and children over the age of six to lower mild-to-moderate hypertension (high blood pressure).

Other names for this medication:
Angilock, Anreb, Arapres, Aratan, Araten, Cardon, Cormac, Corodin, Corus, Cosart, Cozzar, Fensartan, Giovax, Gitox, Hilos, Lakea, Lepitrin, Lifezar, Loctenk, Losakind, Losamet, Losan, Losaprex, Losardil, Losargamma, Losartan, Losartanum, Losartas, Losartil, Losazide, Losium, Lostad, Lostankal, Lostat, Loxibin, Maxartan, Myotan, Niten, Normatens, Ocsaar, Omnitan, Ozarium, Prosan, Psycholanz, Resilo, Sarve, Sortiva, Tensaar

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Also known as: Losartan


Araten (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.

Araten 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.

Araten 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.

Araten 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. Araten 25 mg, Araten 50 mg, and Araten 100 mg may also contain carnauba wax.


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


If you overdose Araten and you don't feel good you should visit your doctor or health care provider immediately. Symptoms of Araten 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 Araten are:

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Side effect occurrence does not only depend on medication you are taking, but also on your overall health and other factors.


Use of drugs that act on the renin-angiotensin system during the second and third trimesters of pregnancy reduces fetal renal function and increases fetal and neonatal morbidity and death. Resulting oligohydramnios can be associated with fetal lung hypoplasia and skeletal deformations. Potential neonatal adverse effects include skull hypoplasia, anuria, hypotension, renal failure, and death. When pregnancy is detected, discontinue Araten as soon as possible.

In patients with an activated renin-angiotensin system, such as volume- or salt-depleted patients (e.g., those being treated with high doses of diuretics), symptomatic hypotension may occur after initiation of treatment with Araten. Correct volume or salt depletion prior to administration of Araten.

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Localization of the gene for distal hereditary motor neuronopathy VII (dHMN-VII) to chromosome 2q14. In contrast to previous studies, these results indicate that CLL cells consistently retain the capacity to further differentiate toward plasma cells and secrete immunoglobulin. gummifera clearly indicated that the botanical source of commercially available dikamali is G. Forty-one patients with isolated coronary artery ectasia and 72 patients with normal coronary arteries were included in the study. The differential activation between OCD patients and healthy subjects might contribute to the pathophysiological understanding of obsessive compulsive disorder. Symptoms suggestive of mild recurrent erosions included sharp pains, the sensation of the eyelid sticking to the eyeball, and soreness of the eyelid to touch, a previously unrecognized symptom of this condition. However, we show here that the initial traffic of BA spores from lungs to LDLNs is largely independent of LDCs and CCR7, occurring instead in association with B cells.

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