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Alsartan (Valsartan)

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Alsartan is indicated for the treatment of hypertension to reduce the risk of fatal and nonfatal cardiovascular events, primarily strokes and myocardial infarctions. It is also indicated for the treatment of heart failure (NYHA class II-IV) and for left ventricular dysfunction or failure after myocardial infarction when the use of an angiotensin-converting enzyme inhibitor (ACEI) is not appropriate.

Other names for this medication:
Alpertan, Alsart, Alsartan, Arovan, Cardival, Codiovan, Cordinate, Cotareg, Diovane, Disys, Dosara, Kalpress, Nisis, Provas, Ramartan, Sarteg, Sarval, Simultan, Starval, Teval, Valaplex, Valcap, Valitazin, Valpresan, Valpress, Valsabela, Valsacor, Valsan, Valsaprex, Valsar, Valsartanum, Valtan, Valturna, Valzek, Valzide, Varexan, Vartalan, Vasaten

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Also known as: Valsartan


Hydrochlorothiazide is a diuretic (water pill). Valsartan is an angiotensin II receptor blocker (sometimes called an ARB blocker).

Alsartan HCT is a combination medicine used to treat high blood pressure (hypertension). Lowering blood pressure may lower your risk of a stroke or heart attack.

Alsartan HCT is given after other blood pressure medicines did not work or have stopped working.


To treat high blood pressure: 80 mg or 160 mg or more once a day. The maximum dosage is 320 mg a day. To treat heart failure: 40 mg twice a day. The maximum dosage is 320 mg daily. Take Alsartan tablets orally with or without food. Do not crush or chew it. Take Alsartan at the same time every day with water. If you want to achieve most effective results do not stop taking Alsartan suddenly.


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 this medicine if you are allergic to valsartan or hydrochlorothiazide, or if you have:

decreased urination or are unable to urinate; or an allergy to sulfa drugs.

If you have diabetes, do not use Alsartan HCT together with any medication that contains aliskiren (a blood pressure medicine).

You may also need to avoid taking Alsartan HCT with aliskiren if you have kidney disease.

Tell your doctor if you have ever had:

an electrolyte imbalance (such as low levels of potassium or magnesium, or high levels of calcium in your blood); liver disease; kidney disease; gallstones; lupus; congestive heart failure; gout, or high levels of uric acid in your blood; asthma or allergies; high cholesterol or triglyceride levels; an allergy to penicillin; glaucoma; or if you are on a low-salt diet.

Do not use 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.

You should not breastfeed while using this medicine.

Alsartan HCT is not approved for use by anyone younger than 18 years old.

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SF-derived exosomes significantly stimulated the release of several inflammatory cytokines and chemokines and metalloproteinases by M1 macrophages but did not influence the expression of CD80 and CD86 costimulatory molecules. However, the efficacy of a minimally invasive surgical approach for recurrent liver cancer is not yet confirmed. Hormonal regulation in insects: facts, gaps, and future directions. A new family of oligosaccharides from the xyloglucan of Hymenaea courbaril L. Access to a hybrid endovascular suite is touted as a necessity for advanced endovascular aneurysm repair (EVAR) to improve imaging accuracy and safety. Northern blot analysis of receptor mRNA revealed that MSH receptor mRNA is not expressed in B16-G4F cells.

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Preliminary results from high-resolution analyses of ultraviolet-absorbing and carbohydrate constituents in several pathologic body fluids. The objective was to assess if RBC transfusions may induce significant changes of plasma acid-base, electrolyte, and glucose status in extremely preterm infants. While most of the differences we found are probably rooted in local tradition, a standard model for the radiology report in centers sharing the same language may be a means to avoid interpretation mistakes by referring physicians, and to promote better care. The respiration rate of exogenous reduced nicotinamide adenine dinucleotide was stimulated by all three gramicidins, but the effects on malate-pyruvate and succinate respiration depended on the type of gramicidin and the reaction media. An Arg740Cys substitution in sigma(70) of OE1-1 resulted in loss of in planta growth and virulence. Marked islet amyloid polypeptide-positive amyloid deposition: a possible cause of severely insulin-deficient diabetes mellitus with atrophied exocrine pancreas. Myoepithelial cells are absent from proximal acini, but are abundant on distal acini. Can high-frequency skin ultrasound be used for the diagnosis and management of Basal cell carcinoma?.

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Kinetic and chemical modification studies of cytosine-arabinoside and uridine transport in hamster cells in culture. The results demonstrated that deviations in pelvic and hip kinematics are related to muscle weakness and improve with crutch use. These findings demonstrate that the timing of language learning may have an impact on cognitive control, with the simultaneous learning of two languages being associated with more optimal brain connectivity for cognitive control compared to sequential language learning. Importantly, we found that the antitumor efficacy of oncolytic Ads was significantly enhanced in immunosuppressed animals. This work aims to study the acute effects on mood and impulsivity of lowering serotonin levels with acute tryptophan depletion in polydrug ecstasy users and to determine whether effects were different in men and women. We compared DRG-NOG between four genetically defined, inbred mouse strains (C57BL/6J, DBA/2J, BALB/cJ, and C3H/HeJ) and one rat strain (Sprague Dawley). Spiders reared under food restriction matured slower and at a smaller size than spiders reared in ad lib conditions.

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