Diacetolol
Diacetolol is a pharmacological agent that belongs to the class of beta blockers. It is a metabolite of acebutolol, a cardioselective beta blocker used in the treatment of hypertension and arrhythmia.
Pharmacodynamics[edit | edit source]
Diacetolol acts as a beta-adrenergic antagonist, blocking the action of epinephrine and norepinephrine on beta receptors. This results in a decrease in heart rate, cardiac output, and blood pressure. It is a non-selective beta blocker, meaning it blocks both beta-1 and beta-2 receptors.
Pharmacokinetics[edit | edit source]
Diacetolol is primarily excreted in the urine, with a half-life of approximately 10-12 hours. It is metabolized in the liver by the cytochrome P450 enzyme system.
Clinical Use[edit | edit source]
Diacetolol is used in the treatment of hypertension and arrhythmia. It may also be used in the management of angina pectoris, myocardial infarction, and heart failure.
Side Effects[edit | edit source]
Common side effects of Diacetolol include fatigue, dizziness, and bradycardia. Less common side effects may include gastrointestinal disturbances, sleep disturbances, and depression.
Contraindications[edit | edit source]
Diacetolol is contraindicated in patients with asthma, bradycardia, and heart block. It should be used with caution in patients with diabetes and peripheral vascular disease.
Interactions[edit | edit source]
Diacetolol may interact with other medications, including other beta blockers, calcium channel blockers, and digoxin.
See Also[edit | edit source]
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Contributors: Prab R. Tumpati, MD