Sandbox g12: Difference between revisions

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::* [[Ciprofloxacin|Ciprofloxacin (Cipro®, Cipro-XR®, Neofloxin®)]]
::* [[Ciprofloxacin|Ciprofloxacin (Cipro®, Cipro-XR®, Neofloxin®)]]
::* [[Clarithromycin|Clarithromycin (Biaxin®, Prevpac®)]]
::* [[Clarithromycin|Clarithromycin (Biaxin®, Prevpac®)]]
::* [[Erythromycin|Erythromycin (E.E.S.®, Robimycin®, EMycin®, Erymax®, Ery-Tab®, Eryc Ranbaxy®, Erypar®, Eryped®, Erythrocin Stearate Filmtab®, Erythrocot®, E-Base®, Erythroped®, Ilosone®, MY-E®, Pediamycin®, Zineryt®, Abboticin®, Abboticin-ES®, Erycin®, PCE Dispertab®, Stiemycine®, Acnasol®, Tiloryth®)]]
::* [[Erythromycin|Erythromycin (A/T/S®, Akne-Mycin®, Emgel®, Ery-Tab®, Eryc®, Erycette®, Eryderm®, Erygel®)]]
::* [[Fluconazole|Fluconazole (Diflucan®, Trican®)]]
::* [[Fluconazole|Fluconazole (Diflucan®, Trican®)]]
::* [[Halofantrine|Halofantrine (Halfan®)]]
::* [[Halofantrine|Halofantrine (Halfan®)]]

Revision as of 21:49, 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/minimal risk for QT interval prolongation/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.