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Known adverse events associated with propranolol (hypoglycemia, hypotension, bradycardia, and bronchospasm) occurred infrequently, with no significant difference in frequency between the placebo group and the groups receiving propranolol.

The related study imposed stressful circumstances on research participants and measured whether impaired thinking related to that stress could be improved by propranolol, a beta-blocker associated with treatment of a variety of disorders ranging from high blood pressure and heart arrhythmias to migraine headaches and panic attacks.

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Supportive Therapy: Hypotension and bradycardia have been reported following Propranolol overdose and should be treated appropriately.

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Therefore, when discontinuance of propranolol is planned, the dosage should be gradually reduced over at least a few weeks, and the patient should be cautioned against interruption or cessation of therapy without the physician's advice.

When this drug is chronically administered, particularly in patients with ischemic heart disease, the dose should be reduced gradually over a period of 1 to 2 weeks and patients should be monitored.

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Further studies are required to determine the optimal dose and duration of propranolol treatment for problematic hemangiomas.

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However, this bias is controlled, in principle, by the fact that in studies using the protocol from Cahill and colleagues, the propranolol and placebo groups do not differ on memory performance for the neutral material, suggesting that propranolol does not influence memory encoding more than placebo.

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It is advised to stop taking propranolol several days before you gradually reduce the dose of clonidine.

Therefore, we predicted that functional connectivity would be greater after propranolol than after nadolol, which would serve as our primary outcome measure.

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