| Drug name | Adverse effects | Monitoring parameters/caveats |
---|---|---|---|
First line | Amphotericin B lipid complex or liposomal amphotericin B | Infusion-related reactions, nephrotoxicity, electrolyte imbalance (hypomagnesemia, hypophosphatemia, hypokalemia, hypocalcemia), transaminitis | Renal function (SCr, BUN, urine output/input), electrolytes (potassium, magnesium, phosphorus), LFT, CBC, temperature |
Salvage therapy | Posaconazole 300 mg IV/PO DR tablet every 12 h for the first day, then 300 mg IV/PO daily. IR oral suspensiona Posaconazole 200 mg PO q6h or 400 mg PO q12h | Diarrhea, nausea, vomiting, QTc prolongation, transaminitis | LFT, QTc, CBC, Posaconazole trough concentrations DR tablet can be taken with or without food; do not chew, divide, crush, or dissolve DR tablet aIR suspension should be taken with a full meal and should be avoided with concurrent proton pump inhibitors |
Isavuconazonium sulfate 372 mg (isavuconazole 200 mg) IV/PO q8h Ă— 6 doses, followed by 372 mg IV/PO or PO q24h thereafter | Nausea, vomiting, diarrhea, transaminitis, peripheral edema, back pain, QTc shortening | LFTs, QTc, isavuconazole trough concentration monitoring is not recommended except when concerned for impaired drug absorption, therapeutic failure, and toxicity |