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Angitol (Atenolol)

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Angitol belongs to a class of drugs known as beta blockers. It works by blocking the action of certain natural chemicals in your body, such as epinephrine, on the heart and blood vessels. Angitol is used alone or in combination with other medications.

Other names for this medication:
Adipin, Aglodepin, Alinor, Amcard, Amlibon, Amlocom, Amlokos, Amloray, Amlothens, Amlotin, Amlovas, Amlovik, Amodin, Ampilife, Atcom, Atecard, Atemarc, Atenij, Atenova, Cadpres, Camcard, Cardiking, Cardipin, Catenol, Cheerten, Coronol, Dilcare, Etotan, Gericard, Glipin, Lakten, Lonol, Losar, Lotensyl, Malodip, Nifetex, Opime, Otenol, Repalol, Systonorm, Tefifin, Tenlol, Tenochek, Tenopress, Tenorex, Windep, Winten, Zodipin

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Avodart, Effexor, Flomax, Allegra, Caverta, Protonix, Adalat, Cycloran, Ometab, Mebasap, Linid, Zerofat, Metrofur, Onotrex, Sanprima, Atekind,

Also known as: Atenolol


Angitol (atenolol) is a beta-blocker that affects the heart and circulation (blood flow through arteries and veins).

Angitol is used to treat angina (chest pain) and hypertension (high blood pressure).

Angitol is also used to lower the risk of death after a heart attack.


You should take it by mouth with meals or without it. Take Angitol every day at the same time and remember that its dosage depends on patient's health state. Elderly people: Starting normal dosage is 25-50 mg a day. Adults: For angina treatment: normal starting dosage is 50 mg a day. Max dosage is 100 mg a day. For heart attack treatment: normal starting dose is 25 mg a day. Max dosage is 50 mg a day. For hypertension treatment: normal starting dose is 50 mg a day. Max dose is 100 mg a day. If you want to achieve most effective results do not stop taking Angitol suddenly.


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

Overdose symptoms may include extreme weakness or lack of energy, very slow heart rate, shortness of breath, or fainting.


Store at room temperature between 20 and 25 degrees C (68 and 77 degrees F) away from moisture and heat. Keep 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 Angitol are:

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Graded doses of 16-diMe-PGE2 were administered intravenously (0.1, 0.3, 0.5, and 1.0 mug per kilogram, intraduodenally, or intragastrically (15, 30, 50, 100 mug per kilogram) with the pancreas in the resting state or in response to (1) secretin and (2) secretin with cholecystokinin-pancreozymin. Automatic analysis of EMG (T/A analysis) and invasive muscle fiber conduction velocity in situ (MFCV) were performed in 15 patients after traumatic lesions of the knee and immobilization with quadriceps atrophy. A boy, 2 years 5 months of age, was admitted for examination and was found to be mentally retarded. The transgenic plant with cyp2e1 can metabolize various low molecular weight organic pollutants. However, there is a correlation with increased grades of ANH being associated with increased severity of urinary tract pathology. Increased physical activity and exercise have been found to reduce falls and decrease mortality and age-related morbidity in older adults.

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Evaluation of quantitative criteria for glioma grading with static and dynamic 18F-FDopa PET/CT. DHEA-sulfate causes a phase-dependent increase in melatonin secretion: a study of perifused rat pineal glands. We examined the expression of steroid receptor coactivators in fetal membranes obtained prior to and following labor at term. We generated the DUC18 T cell receptor transgenic mouse expressing an H-2Kd -restricted transgenic T cell receptor specific for the syngeneic CMS5 fibrosarcoma rejection antigen mutated ERK2(136-144). Here, we show that the binding of MCAK to chromosome arms is also regulated by Aurora B and that Aurora B-dependent chromosome arm and centromere localization is regulated by distinct two-site phosphoregulatory mechanisms. Results obtained with the different modifications of rat HDC containing all three PEST regions (full version, 1-656 HDC), only the N-terminal PEST region (1-512 HDC), or no PEST region (69-512 HDC), indicate that the N-terminal (1-69) fragment, but not the C-terminal fragment, determines that the HDC protein is a proteasome substrate in vitro. We offer as examples, from our experience as an ethics committee in a major European technical university, ways in which such a committee provides needed services and can help ensure more ethical studies involving humans outside the standard medical context.

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Most of the TRE-bound complexes in both unstimulated and angiotensin II-treated cells consist of c-jun/c-fos heterodimers. Headache data were collected from 75 patient diaries from the University of Calgary Headache Research Clinic. Reaction chemistry/nanocrystal property relations in the hot injection synthesis, the role of the solute solubility. We conclude that the Gly16 beta(2)AR polymorphism imparts attenuated vasodilatory responses to catecholamines in normal human beings and is an important genetic component in the regulation of peripheral blood flow and systemic arterial pressure. Small-particle aerosol-immunized mice were resistant to subsequent challenge with 10(2.0) respiratory median lethal doses of virulent virus, whereas large-particle aerosol-immunized mice were not protected. In 1 case where treatment was started late, small osteolytic zones persisted but with no clinical consequences. Yersinia infection tools-characterization of structure and function of adhesins. The technique uses small-phase-shift approximation, with the assumption that blood flow in the voxels at the boundary of the vessel is slow.

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