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The analgesic activity of Cleocin is due to both parent drug and the M1 metabolite (see CLINICAL PHARMACOLOGY, Pharmacodynamics).
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The analgesic activity of Cleocin is due to both parent drug and the M1 metabolite (see CLINICAL PHARMACOLOGY, Pharmacodynamics).
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Cleocin has been shown to inhibit reuptake of norepinephrine and serotonin in vitro,
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The analgesic activity of Cleocin is due to both parent drug and the M1 metabolite (see CLINICAL PHARMACOLOGY, Pharmacodynamics).
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Some people who use Cleocin for a long time without a break may develop a physical need to continue taking it.
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Cleocin was evaluated in peri- and post-natal studies in rats.
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This may not be a complete list of all interactions that may occur. Ask your health care provider if Cleocin may interact with other medicines that you take.
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1 Dosing may be increased to 100 mg every four to six hours, but the daily dosage should not exceed 400 mg 1 and should be limited to 250 to 300 mg .
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A single i.m. dose of Cleocin is useful pre-treatment to minimize the risk of acid aspiration during operation,
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The binding of Cleocin to human plasma proteins is approximately 20%,
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Cleocin was not mutagenic in the following assays: Ames Salmonella microsomal activation test,
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The effects of Cleocin are similar to those of narcotic analgesics. Although Cleocin is not classified as a narcotic, it may become habit-forming,
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Do not use this medication if you are allergic,
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