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    The analgesic activity of Lotensin is due to both parent drug and the M1 metabolite (see CLINICAL PHARMACOLOGY, Pharmacodynamics).
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    Lotensin had only slight thermoregulatory effects. Its use is thus unlikely to provoke hypothermia or to facilitate fever.

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    The mean absolute bioavailability of a 100 mg oral dose is approximately 75%. The mean peak plasma concentration of racemic Lotensin and M1 occurs at two and three hours, respectively, after administration in healthy adults.
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