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which may affect the therapeutic response (see PRECAUTIONS - Drug Interactions). Cleocin and its metabolites are excreted primarily in he urine with observed plasma half-lives of 6.3 and 7.4 hours for Cleocin and M1, respectively.
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Do not stop using this medication suddenly without first talking to your doctor.
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Cleocin has not been shown to cause histamine release. At therapeutic doses, Cleocin has no effect on heart rate, left-ventricular function or cardiac index.
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which may affect the therapeutic response (see PRECAUTIONS - Drug Interactions). Cleocin and its metabolites are excreted primarily in he urine with observed plasma half-lives of 6.3 and 7.4 hours for Cleocin and M1, respectively.
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Cleocin is administered as a racemate and both [-] and [+] forms of both Cleocin and M1 are detected in the circulation.
Cleocin had only slight thermoregulatory effects. Its use is thus unlikely to provoke hypothermia or to facilitate fever.
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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.
Cleocin was being used with selective serotonin reuptake inhibitors (10 cases),
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Cleocin is well absorbed orally with an absolute bioavailability of 75%. Cleocin has a volume of distribution of approximately 2.7 L/kg and is only 20% bound to plasma proteins.
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Cleocin increases the risk of CNS and respiratory depression in these patients.
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The 6-hour TOTPAR scores for the Cleocin groups and ASA/,
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Cleocin has a volume of distribution of approximately 2.7 L/kg and is only 20% bound to plasma proteins.
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