Amphotericin B liposomal 50mg powder for dispersion for infusion vials
Requires a prescription from a doctor or prescriber
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Data from the MHRA Yellow Card scheme. A reported reaction does not necessarily mean the medicine caused it. Contains public sector information licensed under the Open Government Licence v3.0.
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Amphotericin B liposomal 50mg powder for dispersion for infusion vials
Amphotericin B liposomal 50mg powder for dispersion for infusion vials
WHO defined daily dose (DDD)
35 mg
Not a recommended dose. The DDD is the assumed average maintenance dose per day for a drug used for its main indication in adults. It is a statistical measure used for research and comparison purposes only.
Source: WHO Collaborating Centre for Drug Statistics Methodology, distributed via the NHS dm+d supplementary mapping files (NHSBSA). Contains public sector information licensed under the Open Government Licence v3.0.
Therapeutically similar medicines
Similarity is based on WHO Anatomical Therapeutic Chemical (ATC) classification and on a factual NHS dm+d therapeutic-grouping code prefix. Source data: NHS dm+d via TRUD (OGL v3.0), WHO ATC/DDD Index.
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Guidelines from the National Institute for Health and Care Excellence
NICE clinical guidance(1)
Source: National Institute for Health and Care Excellence (NICE). Contains public sector information licensed under the Open Government Licence v3.0.
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SNOMED CT and dm+d codes from NHS TRUD (Technology Reference data Update Distribution), licensed under the Open Government Licence v3.0. ATC codes from the WHO Collaborating Centre for Drug Statistics Methodology (whocc.no).
Active and completed clinical studies from ClinicalTrials.gov
Source: ClinicalTrials.gov, a database of the U.S. National Library of Medicine (NLM), National Institutes of Health (NIH). Data accessed via ClinicalTrials.gov API v2. Trial information is provided for research purposes and does not constitute medical advice.
Academic studies and reviews for this medicine's active substance
Showing the 50 most relevant studies.
Reviews & meta-analyses: 22 · Randomised trials: 9 · 1999–2026
Showing the 50 most relevant studies, sorted by most relevant.
O. Cornely, J. Maertens, M. Bresnik, et al.
Clinical infectious diseases : an official publication of the Infectious Diseases Society of America, 2007
E. Kuse, P. Chetchotisakd, C. A. da Cunha, et al.
Lancet, 2007
N. Stone, T. Bicanic, R. Salim, et al.
Drugs, 2016
He L, Chen L, Liu C
2026
ObjectiveTo investigate the rapid progression and key treatment strategies for invasive pulmonary mucormycosis caused by Rhizopus in patients with diabetic ketoacidosis (DKA).MethodsWe report a fatal case of severe Rhizopus pneumonia in a patient with DKA and conducted a systematic review of relevant cases from PubMed and Web of Science for descriptive analysis.ResultsA 39-year-old male with DKA developed severe lung lesions within days post-admission. Despite confirmation via pathological diagnosis and the initiation of liposomal amphotericin B therapy, the patient succumbed rapidly. Incorporating 15 cases identified from the literature, the total cohort comprised 16 patients, yielding an overall mortality rate of 25% (4/16). Cases involving DKA frequently exhibited narrow diagnostic windows and rapid progression to respiratory failure. Most cases (11/15) received amphotericin B-based therapy, and some with localized lesions (7/15) underwent surgical resection.ConclusionPulmonary mucormycosis with DKA can progress rapidly and carries high risk. Treatment typically involves amphotericin B preparations, supplemented by surgery for focal disease. Key strategies include maintaining a high index of clinical suspicion in high-risk hosts, early pathological/molecular diagnosis, prompt antifungal therapy alongside metabolic correction, and timely surgical evaluation for localized lesions.
Abstract licence: CC BY
C. Faustino, L. Pinheiro
Pharmaceutics, 2020
Marit D. Moen, Katherine A. Lyseng-Williamson, Lesley J. Scott
Drugs, 2012
H. Hebart, L. Klingspor, T. Klingebiel, et al.
Bone Marrow Transplantation, 2009
J. Jarvis, Tshepo B Leeme, M. Molefi, et al.
Clinical Infectious Diseases, 2018
J. Jarvis, David S. Lawrence, D. Meya, et al.
The New England journal of medicine, 2022
M. Balasegaram, K. Ritmeijer, M. A. Lima, et al.
Expert Opinion on Emerging Drugs, 2012
Sources: aggregated from Europe PMC (EMBL-EBI), OpenAlex, Crossref, PubMed and other open scholarly databases. Retracted articles are excluded. Study information is provided for research purposes and does not constitute medical advice.
Scientific data (pharmacology, interactions, ADME) is not yet available for this medicine. Clinical sections are sourced from the NHS dm+d database.