REMS
Absorption: IV administration results in complete bioavailability.
Distribution: Variable penetration into CSF. May concentrate in and be slowly released from bone.
Half-Life: 3 hr (normal renal function); longer half-life of 90 hr may reflect release of drug from bone.
Contraindicated in:
Use Cautiously in:
Renal impairment (dose ↓ required if CCr ≤1.4 mL/min/kg)
;CV: chest pain, edema, palpitations, QT interval prolongation, TORSADES DE POINTES
Derm: ↑sweating, pruritus, rash, skin ulceration
EENT: conjunctivitis, eye pain, vision abnormalities
F and E: hypocalcemia, hypokalemia hypomagnesemia
hypophosphatemia
GI: diarrhea, nausea, vomiting, abdominal pain, abnormal taste sensation, anorexia, constipation, dyspepsia
GU: RENAL FAILURE, albuminuria, dysuria, nocturia, polyuria, urinary retention
Hemat: anemia, leukopenia, neutropenia
Local: pain/inflammation at injection site
MS: arthralgia, myalgia, back pain, involuntary muscle contraction
Neuro: headache, anxiety, ataxia, confusion, depression, dizziness, fatigue, hypoesthesia, neuropathy, paresthesia, SEIZURES, tremor, weakness
Misc: fever, chills, flu-like syndrome, HYPERSENSITIVITY REACTIONS (INCLUDING ANAPHYLAXIS, URTICARIA, AND ANGIOEDEMA), MALIGNANCY
Drug-drug:
Cytomegalovirus Retinitis
Renal Impairment
Herpes Simplex Virus
Renal Impairment
Monitor for seizure activity. Implement seizure precautions if necessary.
Lab Test Considerations:
Monitor serum creatinine before and 23 times weekly during induction therapy and at least once every 12 wk during maintenance therapy. Monitor 24-hr CCr before and periodically throughout therapy. If CCr drops below 0.4 mL/min/kg, discontinue foscarnet.
Monitor serum calcium, magnesium, potassium, and phosphorus before and 23 times weekly during induction therapy and at least weekly during maintenance therapy. May cause hypocalcemia, hypomagnesemia, hypokalemia, and hypophosphatemia.
Adequately hydrate patient with 7501000 mL of 0.9% NaCl or D5W before 1st infusion to establish diuresis; then administer 7501000 mL with 120 mg/kg of foscarnet or 500 mL with 4060 mg/kg of foscarnet with each dose to prevent renal toxicity.
IV Administration:
NDC Code