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Lopressor is a centrally acting synthetic opioid analgesic.


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The mean absolute bioavailability of a 100 mg oral dose is approximately 75%. The mean peak plasma concentration of racemic Lopressor and M1 occurs at two and three hours, respectively, after administration in healthy adults.
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When used for long periods of time or at high doses,
Lopressor is administered as a racemate and both [-] and [+] forms of both Lopressor and M1 are detected in the circulation.
clinical trial was performed to assess the analgesic efficacy and reported side effects of Lopressor 100 mg, Lopressor 50 mg,
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Lopressor has not been shown to cause histamine release. At therapeutic doses, Lopressor has no effect on heart rate,
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The product information for Lopressor states that convulsions have been reported in patients using Lopressor at the recommended dose levels and that the risk
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Check the label on the medicine for exact dosing instructions.Lopressor may cause drowsiness and dizziness.
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Intramuscular (i.m.) Lopressor increases gastric pH during anaesthesia similar to famotidine.
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