Sandbox g12: Difference between revisions

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::* [[Clarithromycin|Clarithromycin (Biaxin®, Prevpac®)]]
::* [[Clarithromycin|Clarithromycin (Biaxin®, Prevpac®)]]
::* [[Erythromycin|Erythromycin (A/T/S®, Akne-Mycin®, Emgel®, Ery-Tab®, Eryc®, Erycette®, Eryderm®, Erygel®)]]
::* [[Erythromycin|Erythromycin (A/T/S®, Akne-Mycin®, Emgel®, Ery-Tab®, Eryc®, Erycette®, Eryderm®, Erygel®)]]
::* [[Itraconazole]]
::* [[Itraconazole|Itraconazole (Sporanox®, Onmel®)]]
::* [[Ketoconazole]]
::* [[Ketoconazole|Ketoconazole (Nizoral®, Sebizole®, Ketomed®, Keton®)]]
::* [[Pentamidine|Pentamidine (Pentam®)]]
::* [[Pentamidine|Pentamidine (Pentam®)]]
::* [[Sparfloxacin|Sparfloxacin (Zagam®)]]
::* [[Sparfloxacin|Sparfloxacin (Zagam®)]]

Revision as of 21:52, 31 May 2015

  • Risk categories for antimicrobial agents known to have an association with TdP[1]
  • Drugs with known TdP risk
  • Drugs with possible TdP risk
  • Drugs with conditional TdP risk
  • Drugs to be avoided by congenital Long QT
  • Torsades de pointes risk stratification schedules for antimicrobial agents[2]
  • Schedule I (Highest TdP risk, potent IKr blockers, TdP risk >1%)
  • Not available
  • Schedule II (Significant risk for TdP, particularly when coadministered with CYP inhibitors, relatively potent IKr blockade)
  • Not available
  • Schedule III (Risk for TdP is described, IKr blockade, particularly when coadministered with CYP inhibitors)
  • Schedule IV (Minimal risk for TdP, case reports of TdP, mild IKr blockade, may have CYP interactions)
  • Schedule V (Questionable or minimal risk for QT interval prolongation or TdP)

References

  1. "Arizona Center for Education and Research on Therapeutics".
  2. Owens, Robert C. (2004). "QT prolongation with antimicrobial agents: understanding the significance". Drugs. 64 (10): 1091–1124. ISSN 0012-6667. PMID 15139788.