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tests indicates that Torsemide does not pose a genotoxic risk to humans.
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Intramuscular (i.m.) Torsemide increases gastric pH during anaesthesia similar to famotidine.
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which may affect the therapeutic response (see PRECAUTIONS - Drug Interactions). Torsemide and its metabolites are excreted primarily in he urine with observed plasma half-lives of 6.3 and 7.4 hours for Torsemide and M1, respectively.
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The analgesic activity of Torsemide is due to both parent drug and the M1 metabolite (see CLINICAL PHARMACOLOGY, Pharmacodynamics).
For Torsemide, the following should be considered:The suitability of Torsemide suppositories for inclusion in our hospital formulary for the treatment of mild to moderate post-operative pain was evaluated.
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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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