I Am… Liposomal Amphotericin B: Ready to take on Aspergillus infections
Liposomal Amphotericin B was chosen to help treat Rashid's Aspergillus infection because it demonstrates:
Fungicidal activity against Aspergillus fumigatus13
Liposomal Amphotericin B has improved fungicidal activity against the most clinically important yeast and moulds vs. echinocandins and azoles.13–15
Liposomal Amphotericin B has a lower potential for pharmacokinetic DDIs vs. azoles*16–18
Amphotericin B is not known to be a substrate nor an inhibitor of the CYP450 enzyme system.16–18
Liposomal Amphotericin B has a well- established tolerability and safety profile12**
Very common adverse events associated with Liposomal Amphotericin B treatment include rigors, pyrexia, hypokalaemia, nausea and vomiting.12
*Please refer to the Liposomal Amphotericin B Summary of Product Characteristics for a full list of DDIs. No specific interaction studies have been performed with Liposomal Amphotericin B. However, recommendations in the prescribing information are based on the known DDI profile of amphotericin B and interactions that may be of clinical significance.12 Drugs that are known to have pharmacodynamic interactions with amphotericin B may also interact with Liposomal Amphotericin B.16–18 DDIs for amphotericin B are mostly related to nephrotoxicity and electrolyte disturbances, which may be augmented by co-administered drugs with similar renal side effects. Resultant changes may reduce clearance or alter the efficacy/toxicity profile of co-administered drugs that undergo renal elimination12,16–18 Regular monitoring of renal function is recommended in patients receiving Liposomal Amphotericin B in conjunction with any nephrotoxic medications, and appropriate potassium supplementation may be required.12
**Please refer to the Liposomal Amphotericin B Summary of Product Characteristics for detailed information on its safety profile.
Fungicidal activity against Aspergillus fumigatus13
Liposomal Amphotericin B has a lower potential for pharmacokinetic DDIs vs. azoles*16–18
Liposomal Amphotericin B has a well- established tolerability and safety profile12**
Liposomal Amphotericin B has improved fungicidal activity against the most clinically important yeast and moulds vs. echinocandins and azoles.13–15
*Please refer to the Liposomal Amphotericin B Summary of Product Characteristics for a full list of DDIs. No specific interaction studies have been performed with Liposomal Amphotericin B. However, recommendations in the prescribing information are based on the known DDI profile of amphotericin B and interactions that may be of clinical significance.12 Drugs that are known to have pharmacodynamic interactions with amphotericin B may also interact with Liposomal Amphotericin B.16–18 DDIs for amphotericin B are mostly related to nephrotoxicity and electrolyte disturbances, which may be augmented by co-administered drugs with similar renal side effects. Resultant changes may reduce clearance or alter the efficacy/toxicity profile of co-administered drugs that undergo renal elimination12,16–18 Regular monitoring of renal function is recommended in patients receiving Liposomal Amphotericin B in conjunction with any nephrotoxic medications, and appropriate potassium supplementation may be required.12
**Please refer to the Liposomal Amphotericin B Summary of Product Characteristics for detailed information on its safety profile.
Amphotericin B is not known to be a substrate nor an inhibitor of the CYP450 enzyme system.16–18
Very common adverse events associated with Liposomal Amphotericin B treatment include rigors, pyrexia, hypokalaemia, nausea and vomiting.12