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Atnol (Atenolol)
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Atnol

Atnol is used with or without other medications to treat high blood pressure (hypertension). Lowering high blood pressure helps prevent strokes, heart attacks, and kidney problems.

Other names for this medication:
Adopin, Altoma, Amchek, Amlibon, Amlica, Amlocal, Amlocard, Amloheart, Amlonol, Amlopin, Amlopres, Amlosure, Amlotest, Amlothens, Amnest, Amnorm, Amzen, Andinx, Atark, Atedine, Atemos, Atenova, Atoli, Atpartc, Biduten, Calock, Carden, Cardipin, Catenol, Cemalo, Coronol, Corvadil, Depten, Dibeta, Exlodep, Hipres, Licopin, Lodip, Pertenol, Quinoten, Syten, Telol, Tenlol, Tenoclor, Tenopress, Winten

Similar Products:
Micardis, Cymbalta, Motilium, Levaquin, Lioresal

Also known as: Atenolol

Description

Atenolol injection is used to reduce the risk of death from an acute heart attack. It is given to people who have already had a heart attack .

This medicine is a beta-blocker. It works by affecting the response to nerve impulses in certain parts of the body, like the heart. As a result, the heart beats slower and decreases the blood pressure. When the blood pressure is lowered, the amount of blood and oxygen is increased to the heart .

This medicine is available only with your doctor's prescription .

Dosage

Usual Adult Dose of Atnol for Hypertension:

Initial dose: 50 mg orally once a day Maintenance dose: 50 to 100 mg orally once a day Maximum dose: 100 mg per day Comments: -If desired response not achieved after 1 to 2 weeks, increase to 100 mg may be beneficial. -Doses greater than 100 mg once a day did not result in significant additional antihypertensive effects. Use: For the treatment of hypertension alone or in combination with other antihypertensive agents.

Usual Adult Dose of Atnol for Angina Pectoris Prophylaxis:

Initial dose: 50 mg orally once a day -Increase to 100 mg orally once a day after 1 week if optimal response not achieved Maintenance dose: 50 to 200 mg orally once a day Maximum dose: 200 mg per day Comments: -Some patients may require 200 mg per day to attain optimal effect. Use: For the long-term management of angina pectoris due to coronary atherosclerosis.

Usual Adult Dose for Angina Pectoris:

Initial dose: 50 mg orally once a day -Increase to 100 mg orally once a day after 1 week if optimal response not achieved Maintenance dose: 50 to 200 mg orally once a day Maximum dose: 200 mg per day Comments: -Some patients may require 200 mg per day to attain optimal effect. Use: For the long-term management of angina pectoris due to coronary atherosclerosis.

Usual Adult Dose of Atnol for Myocardial Infarction:

50 mg orally twice a day or 100 mg orally once a day Comments: -If IV beta blockers are contraindicated or inappropriate, oral therapy should continue for at least 7 days post-myocardial infarction (MI). -Treatment with beta blockers post MI should generally continue for 1 to 3 years if there are no contraindications. Use: For the management of hemodynamically stable patients with definite or suspected acute myocardial infarction to reduce cardiovascular mortality.

Usual Geriatric Dose for Hypertension:

Initial dose: Consider reducing the starting dose to 25 mg orally once a day

Detailed Atnol dosage information

Overdose

If you overdose Atnol and you don't feel good you should visit your doctor or health care provider immediately. Symptoms of Atnol are low blood sugar, slow heartbeat, heart failure, slowness, low blood pressure, wheezing.

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 Atnol 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.

Contraindications

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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Tuning Toehold Length and Temperature to Achieve Rapid, Colorimetric Detection of DNA from the Disassembly of DNA-Gold Nanoparticle Aggregates. This study evaluated whether receiving developmentally appropriate feedback in the form of individualized fables would affect how children and their parents reported experiencing a neuropsychological assessment. Treatment with the chemotherapeutic agent oxaliplatin produces a robust painful neuropathy similar to various other neuropathic conditions which result in loss of nerve fibers innervating the skin. Changes in the morphology of these structures are associated with long-lasting modulation of synaptic strength thought to underlie learning and memory, and can be abnormal in neuropsychiatric disease. Further prospective and intervention studies will be required to fully understand this phenomenon. Cost control at the unit level: decentralization cultivates economy at Johns Hopkins Hospital.

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Effects of butylated hydroxyanisole on ornithine decarboxylase activity induced by ultraviolet-B and PUVA in mouse skin. Any hospital within an area which becomes economically healthier through increase in the number of hospital beds filled, does so only at the expense of another. Prognostic biomarkers for acute graft-versus-host disease risk after cyclophosphamide-fludarabine nonmyeloablative allotransplantation. Recombinant viruses with mutation(s) demonstrated lower viral growth in B95a cells. Circulating lipocalin 2 is neither related to liver steatosis in patients with non-alcoholic fatty liver disease nor to residual liver function in cirrhosis. Bio monitoring was applied for detection of drug intake revealing a lack of information about bactrim antibiotic alternative OTC products and their health risks. Proactive, but Not Reactive, Distractor Filtering Relies on Local Modulation of Alpha Oscillatory Activity. The obstacles hindering more widespread use of PLGA for producing sustained-release formulations for clinical use include low drug loading, particularly of hydrophilic small molecules, high initial burst release and/or poor formulation stability.

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