Foscarnet: Difference between revisions
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*Active against all [[human herpesviruses]] |
*Active against all [[human herpesviruses]] |
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| + | === Mechanism of Action === |
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| + | |||
| + | * Acts as a pyrophosphate analogue that competitively and reversibly inhibits herpesvirus DNA polymerase, causing premature chain termination of DNA |
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===Pharmacokinetics and Pharmacodynamics=== |
===Pharmacokinetics and Pharmacodynamics=== |
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==Safety== |
==Safety== |
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| + | === Adverse Events === |
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| − | *Nephrotoxicity, usually reversible |
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| + | |||
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| + | *Most common AEs include infusion-related [[nausea]], electrolyte abnormalities, and [[acute kidney injury]] |
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| − | *Seizures |
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| + | **Renal tubular nephrotoxicity is common, dose-dependent, and usually reversible if drug is stopped early |
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| + | **Crystal glomerular nephropathy also occurs |
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| − | *Nausea |
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| + | **Nausea is very common, and can be debilitating |
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| + | ***Minimize with concurrent IV and oral hydration, antiemetics, and slowing the infusion rate[[CiteRef::jayaweera1997mi]] |
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| + | *Other AEs include: |
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| + | **[[Seizure]] |
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| + | **[[Nephrogenic diabetes insipidus]] |
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| + | |||
| + | === Monitoring === |
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| + | |||
| + | * Close monitoring of electrolytes and creatinine is required |
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[[Category:Antivirals]] |
[[Category:Antivirals]] |
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Revision as of 10:36, 5 December 2020
Background
- Inhibits DNA polymerase in human herpesviruses
- Indications: CMV after hematopoietic stem cell transplantation, CMV after solid organ transplantation, Cytomegalovirus, Herpes simplex virus, Herpesviridae, Post-transplant acute limbic encephalitis
Spectrum of Activity
- Active against all human herpesviruses
Mechanism of Action
- Acts as a pyrophosphate analogue that competitively and reversibly inhibits herpesvirus DNA polymerase, causing premature chain termination of DNA
Pharmacokinetics and Pharmacodynamics
- CSF penetration 66% of serum levels
Dosing
Pediatric Dosing
- Induction: foscarnet 60 mg/kg IV q8h or 90 mg/kg IV q12h
- Maintenance: foscarnet 90 to 120 mg/kg IV q24h
Safety
Adverse Events
- Most common AEs include infusion-related nausea, electrolyte abnormalities, and acute kidney injury
- Renal tubular nephrotoxicity is common, dose-dependent, and usually reversible if drug is stopped early
- Crystal glomerular nephropathy also occurs
- Electrolyte abnormalities, including hypocalcemia, hypophosphatemia, hyperphosphatemia, hypomagnesemia, and hypokalemia
- Nausea is very common, and can be debilitating
- Minimize with concurrent IV and oral hydration, antiemetics, and slowing the infusion rate1
- Other AEs include:
Monitoring
- Close monitoring of electrolytes and creatinine is required
References
- ^ Dushyantha T. Jayaweera. Minimising the Dosage-Limiting Toxicities of Foscarnet Induction Therapy. Drug Safety. 1997;16(4):258-266. doi:10.2165/00002018-199716040-00003.
