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Raloxifene may rarely be habit forming. Raloxifene should be avoided in patients with a history.

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Raloxifene has not been shown to cause histamine release.
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which may affect the therapeutic response (see PRECAUTIONS - Drug Interactions). Raloxifene and its metabolites are excreted primarily in he urine with observed plasma half-lives of 6.3 and 7.4 hours for Raloxifene and M1, respectively.
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Forty patients were treated with either Raloxifene suppositories 100 mg 6 hourly (qds) or acetaminophen/codeine suppositories 1000/20 mg qds.
The relative risk of experiencing an episode of nausea under treatment,
It is slightly soluble in water and freely soluble in alcohol,
Intramuscular (i.m.) Raloxifene increases gastric pH during anaesthesia similar to famotidine.
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Forty patients were treated with either Raloxifene suppositories 100 mg 6 hourly (qds) or acetaminophen/codeine suppositories 1000/20 mg qds.
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clinical trial was performed to assess the analgesic efficacy and reported side effects of Raloxifene 100 mg, Raloxifene 50 mg,
Raloxifene is well absorbed orally with an absolute bioavailability of 75%. Raloxifene has a volume of distribution of approximately 2.7 L/kg and is only 20% bound to plasma proteins.
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Raloxifene is administered as a racemate and both [-] and [+] forms of both Raloxifene and M1 are detected in the circulation.
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Raloxifene increases the risk of CNS and respiratory depression in these patients.
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adjustment of the dosing regimen is recommended (see DOSAGE AND ADMINISTRATION).
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