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Amlom (Atenolol)
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Amlom

Amlom is in a class of medications called beta blockers. It works by relaxing blood vessels and slowing heart rate to improve blood flow and decrease blood pressure. Amlom is used alone or in combination with other medications.

Other names for this medication:
Adopin, Adpine, Amdepin, Amloheart, Amlokath, Amlom, Amlotin, Amone, Amozen, Angizaar, Atbeta, Atcardil, Atcom, Atemide, Atpark, Axynol, Betanol, Bibidip, Cadpres, Cyplol, Depten, Espin, Intalol, Niftene, Nipidol, Presolar, Stressban, Tenlol, Tenocheck, Tentoric

Similar Products:
Dulcolax, Benicar, Mellaril, Desyrel, Deltasone

Also known as: Atenolol

Description

{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.

Dosage

A nurse or other trained health professional will give you this medicine. This medicine is given through a needle placed in one of your veins .

Detailed Amlom dosage information

Overdose

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.

Storage

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 Amlom are:

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Contraindications

Appropriate studies performed to date have not demonstrated geriatrics-specific problems that would limit the usefulness of atenolol injection in the elderly. However, elderly patients are more likely to have age-related liver, kidney, or heart disease, which may require caution and an adjustment of dosage in patients receiving atenolol injection .

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Differential signal transduction via T-cell receptor CD3 zeta 2, CD3 zeta-eta, and CD3 eta 2 isoforms. Here we show that mechanically sensitive chemical groups make it possible to harness the mechanical forces generated when exposing polymer solutions to ultrasound, and that this allows us to accelerate rearrangement reactions and bias reaction pathways to yield products not obtainable from purely thermal or light-induced reactions. In conclusion, this study highlights the importance of medium components for cell interaction triggering the formation of angiogenic structures. FI cleaves its in vivo substrates C3b and C4b only in the presence of cofactors, it shows poor enzymatic activity towards synthetic substrates tested so far and it has no natural inhibitor. Toxicity of selected symmetrical hexachlorobiphenyl isomers in the mouse. In addition, the total prilosec max dose cellular protein phosphotyrosine content, measured by immunoblotting and flow cytometric analysis with anti-phosphotyrosine antibodies, did not increase in accord with the elevation of tyrosine kinase activity.

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High prevalence and early onset of cardiac autonomic neuropathy among South Indian type 2 diabetic patients with nephropathy. We tested whether early onset and late onset bipolar illness represent two different forms of bipolar illness in terms of clinical features, comorbidity and familial risk. A new approach to surface activation of porous nanomaterials using non-thermal helium atmospheric pressure plasma jet treatment. Under these circumstances, Lep mRNA and plasma leptin concentrations also remained low. The 100 A fibrils stain with both uranyl acetate and lead, whereas the central regions of the elastic fibers stain only with phosphotungstic acid. The importance of scatter correction for the assessment of lung shunting prior to yttrium-90 radioembolization therapy. Peripheral T and B cells were decreased in patients chronically infected with Trypanosome cruzi. Spleen stroma developed more complicated networks of fibroblasts, endothelial cells, macrophages, and DC. It was found that antacids such as aluminium silicate and magnesium trisilicate decreased the dissolution of minocycline and demethyl-chlortetracycline.

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