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Cleocin may rarely be habit forming. Cleocin should be avoided in patients with a history.
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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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The analgesic activity of Cleocin is due to both parent drug and the M1 metabolite (see CLINICAL PHARMACOLOGY, Pharmacodynamics).

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This is known as physical DEPENDENCE. If you suddenly stop taking Cleocin , you may experience WITHDRAWAL symptoms including anxiety;
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alcohol or use medicines that may cause drowsiness (eg, sleep aids, muscle relaxers) while you are using Cleocin ; it may add to their effects.
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How does Cleocin work? What will it do for me?Cleocin can cause side effects that may impair your thinking or reactions.
adjustment of the dosing regimen is recommended (see DOSAGE AND ADMINISTRATION).
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Linear pharmacokinetics have been observed following multiple doses of 50 and 100 mg to steady-state.Racemic Cleocin is rapidly and almost completely absorbed after oral administration.
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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.
Cleocin may not work as well and may require higher doses to obtain.
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The 6-hour TOTPAR scores for the Cleocin groups and ASA/,
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The mean absolute bioavailability of a 100 mg oral dose is approximately 75%. The mean peak plasma concentration of racemic Cleocin and M1 occurs at two and three hours, respectively, after administration in healthy adults.
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