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Myodura (Atenolol)
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Myodura

Myodura is a beta blocker that works specifically on the heart. It works by slowing down the heart rate and makes the heart more efficient at pumping blood around the body. Myodura is also used to relieve the symptoms caused by an overactive thyroid gland.

Other names for this medication:
Adbeta, Aloten, Aminol, Amlokath, Amlong, Amlopin, Amlosure, Amodep, Ampilife, Amzen, Aniloc, Atamo, Atemos, Atenex, Axynol, Betanif, Bibidip, Camcard, Carden, Cardenol, Cardipress, Catenol, Dipress, Emadine, Hypernorm, Lakten, Licopin, Neocard, Nilol, Nipidol, Nolotin, Novaten, Otenol, Pdnol, Pertenol, Primodil, Telol

Similar Products:
Panadol, Provigil, Zyloprim, Lozol, Singulair, Lexapro, Neoral, Fosamax, Imodium, Ativan

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 Myodura 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 Myodura 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 Myodura 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 Myodura dosage information

Overdose

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

Appropriate studies have not been performed on the relationship of age to the effects of atenolol injection in the pediatric population. Safety and efficacy have not been established .

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