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Alsartan (Valsartan)

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Alsartan is a type of blood pressure-lowering medicine called an angiotensin receptor blocker. Like other angiotensin receptor blockers, Alsartan relaxes and widens your blood vessels. This lowers your blood pressure and makes it easier for your heart to pump blood around your body.

Other names for this medication:
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Also known as: Valsartan


Alsartan is an effective remedy against hypertension. Its target is to treat heart failure and to reduce the risk of death after a heart attack. It is working by preventing the hormone angiotensin II from narrowing the blood vessels, which tends to raise blood pressure. It is angiotensin II receptor antagonist. Alsartan is also known as Valsartan, Valtan, Valzaar. Generic name of Alsartan is Valsartan. Brand name of Alsartan is Alsartan.


Usual Adult Dose for Congestive Heart Failure:

Initial dose: 40 mg orally twice a day Maintenance dose: 80 to 160 mg twice a day. The dose should be increased to the highest dose tolerated by the patient.

Usual Adult Dose for Hypertension:

Initial dose: 80 to 160 mg orally once a day. Maintenance dose: 80 to 320 mg orally once a day

Usual Adult Dose for Myocardial Infarction:

Initial dose: 20 mg orally twice a day Maintenance dose: The initial dosage may be titrated upward within 7 days to 40 mg twice daily, with subsequent titrations to a target maintenance dose of 160 mg twice a day as tolerated by the patient. If symptomatic hypotension or renal dysfunction occurs, consideration should be given to a dosage reduction. Comment: Valsartan may be initiated as early as 12 hours after a myocardial infarction, and may be given with other standard postmyocardial infarction treatment, including thrombolytics, aspirin, beta blockers, and statins.

Usual Pediatric Dose for Hypertension:

6 to 16 years: Initial dose: 1.3 mg/kg once a day (up to 40 mg) Maintenance dose: up to 2.7 mg/kg (up to 160 mg) once a day titrated according to patient response Comments: If the calculated dosage does not correspond to the available tablet strengths, or if children are unable to swallow tablets, the use of a suspension (which can be prepared from the tablets) is recommended. The valsartan dose may need to be increased if the suspension is replaced by a tablet. No data are available in pediatric patients either undergoing dialysis or with a glomerular filtration rate less than 30 mL/min.

Detailed Alsartan dosage information


Seek emergency medical attention or call the Poison Help line at 1-800-222-1222.


Store at room temperature between 15 and 30 degrees C (59 and 86 degrees F) away from moisture and heat. Keep your medicine container tightly closed. Throw away any unused medicine after the expiration date. Keep out of the reach of children.

Side effects

The most common side effects associated with Alsartan 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.


You should not use Alsartan if you are allergic to valsartan.

To make sure Alsartan is safe for you, tell your doctor if you have:

a heart condition other than one being treated with Alsartan; kidney disease (or if you are on dialysis); or if you are on a low-salt diet.

Do not use Alsartan if you are pregnant. Stop using the medicine and tell your doctor right away if you become pregnant. Valsartan can cause injury or death to the unborn baby if you take the medicine during your second or third trimester.

If you plan to get pregnant, ask your doctor for a safer medicine to use before and during pregnancy. Having high blood pressure during pregnancy may cause complications in the mother and the baby.

You should not breastfeed while using this medicine.

Alsartan is not approved for use by anyone younger than 1 year old.

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Complete response to CPT-11 and UFT/LV combination therapy in a case with simultaneous multiple lung metastases from colon cancer. The study aimed to investigate factors influencing nutritional status and to explore the pattern of snack consumption. We report a case of endoscopic ultrasound-guided cystogastrostomy with a fully covered 15-mm-diameter self-expandable metal stent and staged endoscopic necrosectomy through the stent. Using ancestry-informative markers to define populations and detect population stratification. The malaria story in Palestine/Israel and the experience of the Tennessee Valley Authority are analyzed in some detail. How to explore the patient with a rising PSA after radical prostatectomy: defining local versus systemic failure. However, patients who presented with acute urinary retention had a higher incidence of postoperative urinary retention. Immunohistochemical analysis of thymic carcinoma focusing on the possibility of molecular targeted and hormonal therapies. However, the studies addressing this issue in MS present conflicting results.

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Effects of transdermal testosterone administration on insulin sensitivity, fat mass and distribution, and markers of inflammation and thrombolysis in human immunodeficiency virus-infected women with mild to moderate weight loss. Effect of copper dosing on sulfide inhibited reduction of nitric and nitrous oxide. Herein, we report an elderly CML patient who received treatment with hydroxyurea, allopurinol, hydration and splenic irradiation. The method is shown to be highly sensitive and to fulfil the first essential criteria for exploitation in the field, namely, that it can be operated in the open air under tropical conditions, and that an adequate number of subjects can be examined in a normal working day at an acceptable cost. However, networks that have less transcriptome data points than the number of regulators are of interest. The meaning of a novel word can be acquired by extracting it from linguistic context. Immigration from outside Europe and social adversity are associated with mental health problems in young adults, especially females. In population studies and nationwide surveys, pregnant smokers report more illicit drug use than pregnant nonsmokers. In this paper, we review the available literature on these effects and emphasize the current obstacles for the therapeutic application of peptides to the problem of obesity.

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