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Angilock (Losartan)

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Angilock slows the decrease of kidney function in patients with high blood pressure and type 2 diabetes. to treat patients with high blood pressure (hypertension) in adults and in children and adolescents 6 - 18 years of age.

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Also known as: Losartan


Angilock (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.

Angilock 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.

Angilock 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.

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


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


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


Do not take Angilock if you are allergic to Angilock components. Do not take Angilock if you're pregnant or you plan to have a baby, or you are a nursing mother. Angilock can harm your baby. Do not use Angilock if you are taking salt substitutes or potassium supplements, other blood pressure medicine, diuretic (water pill). It can be dangerous to use Angilock if you suffer from or have a history of liver disease, kidney disease, heart failure. If you want to achieve most effective results without any side effects it is better to avoid alcohol. Avoid machine driving. Do not stop taking Angilock suddenly.

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Drinking, smoking, and illicit drug use among 15 and 16 year olds in the United Kingdom. BDNF levels were measured by ELISA at 3 or 7 d after birth in different regions of the brains of rats exposed to propylthiouracil (PTU) in the drinking water. Face off--the interplay between activating and inhibitory immune receptors. However, the rate of fluid and electrolyte resorption close to term is markedly different between strains. We evaluated the specificity of this increase and attempted to correlate it with the severity of coronary lesions. The perioperative management of human immunodeficiency virus (HIV) infected patients undergoing neurosurgery is challenging due to the presence of HIV-related multi-system derangements, opportunistic infections and malignancies, history of substance abuse, and adverse effects of anti-retroviral therapy (ART), together with the inherent risks of neurosurgery. GRADE is, in general, a suitable method para que se usa bisoprolol fumarate 5 mg to convey uncertainties for systematic review producers to users. In recent years, development of various 3D models has improved the study of host-tumor interaction and use of high-throughput screening platforms for anti-cancer drug discovery and development.

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