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clinical trial was performed to assess the analgesic efficacy and reported side effects of Pravachol 100 mg, Pravachol 50 mg,
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Pravachol may rarely be habit forming. Pravachol should be avoided in patients with a history of opiate addiction or hypersensitivity to opiate medications.

The relative risk of experiencing an episode of nausea under treatment,
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The 6-hour TOTPAR scores for the Pravachol groups and ASA/,
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Pravachol is a centrally acting synthetic opioid analgesic.
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Nalbuphine consumption in the first 24 h after operation was reduced by 35% in the Pravachol group.

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Pravachol is found in breast milk. Do not breast-feed while taking Pravachol .When used for long periods of time or at high doses,
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Nonetheless, Pravachol nearly doubled the interthreshold range at a concentration near 200 ng/mL.
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which may affect the therapeutic response (see PRECAUTIONS - Drug Interactions).
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In an open randomized trial, rectal Pravachol was compared with our standard treatment acetaminophen/codeine suppositories. We expected Pravachol to be equally effective as our current standard but with fewer side effects.
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Pravachol has not been shown to cause histamine release. At therapeutic doses, Pravachol has no effect on heart rate, left-ventricular function or cardiac index.
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Nonetheless, Pravachol nearly doubled the interthreshold range at a concentration near 200 ng/mL.
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In vitro studies indicate that Pravachol is unlikely to inhibit,
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Nonetheless, Pravachol nearly doubled the interthreshold range at a concentration near 200 ng/mL.
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Pravachol is extensively metabolized by a number of pathways, including CYP2D6 and CYP3A4,
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