An International Publisher for Academic and Scientific Journals
Author Login
Scholars Academic Journal of Pharmacy | Volume-6 | Issue-09
Cumulative Dose Reaction of Ambisome Infusion after Small Bowel Transplantation: A Description of 3 Cases and Review of Literature
Sumairanawaz Syed
Published: Sept. 30, 2017 |
225
127
DOI: 10.21276/sajp.2017.6.9.6
Pages: 410-412
Downloads
Abstract
AmBisome [Injection] is a non-pyrogenic lyophilized product for intravenous
infusion and each vial contains amphotericin B [50 mg], intercalated into a liposomal
membrane. The safety of Ambisome as prophylactic antifungal has been assessed in bone
marrow transplant recepients, liver transplant recepients, renal transplant recepients and
combined organ trans plant recepients. AmBisome was discontinued due to side-effects in
3% of the cases. In the current study involving small bowel transplant [SBT] patients it
can be noted that all SBT patients tolerated the amBisome test dose well. However when
intravenous infusion of amBisome was administered especially in neutropenic patients, it
was noted that 3 patients (11%) developed a severe drug reaction and the drug had to be
discontinued. The small bowel transplant patients in whom ambisome was discontinued
there was a drug reaction which can be considered as a cumulative dose related reaction.
It can be concluded that Ambisome is generally a safe drug for antifungal prophylaxis in
small bowel transplant patients. The use of ambisome in neutropenic patients may
amplify the cumulative dose reaction and may contribute to the picture that we have seen.