Voriconazole: Difference between revisions

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== Adverse Effects ==
== Adverse Drug Reactions ==
* Visual
* Visual
** Floaters etc that may improve with time
** [[Adverse drug reaction::Floaters]] etc that may improve with time
** Visual hallucinations
** [[Adverse drug reaction::Visual hallucinations]]
** Colour vision loss
** [[Adverse drug reaction::Colour vision loss]]
* Photosensitivity
* [[Adverse drug reaction::Photosensitivity]]
* Hepatotoxicity
* [[Adverse drug reaction::Hepatotoxicity]]
* QTc prolongation
* [[Adverse drug reaction::QTc prolongation]]


== Further Reading ==
== Further Reading ==

Revision as of 03:14, 18 February 2020

Therapeutic Drug Monitoring

  • Measure trough within 7 days of starting, and at regular intervals or following dose adjustment
  • Target trough > 1 mg/L for prophylaxis and treatment
Trough (mcg/mL) Recommendation
0.0 to 0.6 Increase dose by 100 mg and recheck trough on day 5 of new regimen
0.7 to 0.9 Increase dose by 50 mg and recheck trough on day 5 of new regimen
1.0 to 4.0 At target, no dose adjustment needed
4.1 to 5.5 Decrease dose by 50 mg and recheck trough on day 5 of new regimen
5.6 to 7.9 Hold dose. Follow daily trough levels, then restart when trough is ≤2.5 at a dose decreased by 100 mg. Recheck trough on day 5 of new regimen.
≥8.0 Hold dose. Follow daily trough levels, then restart when trough is ≤2.5 at a dose decreased by 50%. Recheck trough level on day 5 of new regimen.

Adverse Drug Reactions

Further Reading

References

  1. ^  Romeo-Gabriel Mihăilă. Voriconazole and the liver. World Journal of Hepatology. 2015;7(13):1828. doi:10.4254/wjh.v7.i14.1828.