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Amodep (Atenolol)

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Amodep is a beta-blocker that affects the heart and circulation (blood flow through arteries and veins). Amodep is used to treat angina (chest pain) and hypertension (high blood pressure).

Other names for this medication:
Aglodepin, Agloten, Altas, Amloact, Amlobid, Amlocas, Amlocom, Amloten, Amnorm, Angizaar, Aniloc, Atekind, Atpark, Atpartc, Carden, Hyten, Niftene, Nilol, Novaten, Olate, Saiten, Tecard, Telol, Tenorex, Tensicard, Topdip

Similar Products:
Cymbalta, Valium, Zanaflex, Kamagra, Differin, Maxalt, Deltasone

Also known as: Atenolol


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

{name} is used to treat angina (chest pain) and hypertension (high blood pressure).

{name} 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 Amodep 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 Amodep 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 Amodep 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.


There are no adequate studies in women for determining infant risk when using this medication during breastfeeding. Weigh the potential benefits against the potential risks before taking this medication while breastfeeding.

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Our aim was to document this little-reported type of dysfluency and to develop a possible explanation for them and how they relate to developmental stuttering. Transplanting Grem1(-/-) neonatal ovaries showed that folliculogenesis proceeded to large antral follicle stage, but Grem1(-/-) ovaries contained corpora lutea-like structures not found in control-transplanted ovaries. Subjective advantages were seen in children and adults for stereoscopic depth perception, better visualization of anatomical structures and understanding of the anatomy, as well as for complex maneuvers such as suturing. Here we introduce a group task that requires complementary actions among participants in order to reach a shared goal. In the heads of the tentacles these fibrils occur in bundles and are especially well developed in the mesoglea of the mouth tentacles. The transport activity for cystine and glutamate in cultured human diploid fibroblasts is enhanced in response to diethyl maleate treatment. There was a very high sedimentation rate and fine needle aspiration yielded bizarre cells which zebeta tabs raised the possibility of malignancy. No improvement appeared to be obtainable in such cases from postoperative peritoneal lavage.

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3D image analysis of plants using electron tomography and micro-CT. Viruses containing mutations in one or both of their late domain motifs were attenuated by one log unit. The patient had worked on a pig farm a few years before presentation. Oxidized low-density lipoprotein activates p66Shc via lectin-like oxidized low-density lipoprotein receptor-1, protein kinase C-beta, and c-Jun N-terminal kinase kinase in human endothelial cells. These results suggest that although the representation of the tactual sense in the cortical association areas has been shown to increase as a result of visual deprivation during the early sensitive period of life, increased representation does not improve the tactual discrimination ability of simple tactual stimuli.

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