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Potency (pharmacology)

Measure of drug activity From Wikipedia, the free encyclopedia

Potency (pharmacology)
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In pharmacology, potency or biological potency[1] is a measure of a drug's biological activity expressed in terms of the dose required to produce a pharmacological effect of given intensity.[2] A highly potent drug (e.g., fentanyl, clonazepam, risperidone, benperidol, bumetanide) evokes a given response at low concentrations, while a drug of lower potency (e.g. morphine, alprazolam, ziprasidone, haloperidol, furosemide) evokes the same response only at higher concentrations. Higher potency does not necessarily mean greater effectiveness nor more side effects nor less side effects.

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Concentration-response curves illustrating the concept of potency. For a response of 0.25a.u., Drug B is more potent, as it generates this response at a lower concentration. For a response of 0.75a.u., Drug A is more potent. a.u. refers to "arbitrary units".
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Types of potency

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The International Union of Basic and Clinical Pharmacology (IUPHAR) has stated that "potency is an imprecise term that should always be further defined",[2] and lists of types of potency as follows:

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Miscellaneous

Lysergic acid diethylamide (LSD) is one of the most potent psychoactive drugs known, with effects occurring at doses of as low as 20 μg.[4]

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