Please use this identifier to cite or link to this item: https://ahro.austin.org.au/austinjspui/handle/1/33242
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dc.contributor.authorMuhandiramge, Jaidyn-
dc.contributor.authorLee, Vivian-
dc.contributor.authorTran, Monica-
dc.contributor.authorHo, Lannie-
dc.date2023-
dc.date.accessioned2023-07-14T02:26:48Z-
dc.date.available2023-07-14T02:26:48Z-
dc.date.issued2023-07-
dc.identifier.citationInternal Medicine Journal 2023-07; 53(7)en_US
dc.identifier.issn1445-5994-
dc.identifier.urihttps://ahro.austin.org.au/austinjspui/handle/1/33242-
dc.description.abstractCoadministration of ferric carboxymaltose and denosumab may cause hypocalcaemia and hypophosphataemia; however, this interaction is not well-described in the literature and has typically been described in patients with chronic kidney disease (CKD). We present a case of this interaction in a patient without preexisting CKD. We suggest the use of alternative iron preparations and an interval of at least 4 weeks between administrations.en_US
dc.language.isoeng-
dc.subjectdenosumaben_US
dc.subjectferric carboxymaltoseen_US
dc.subjecthypocalcaemiaen_US
dc.subjecthypophosphataemiaen_US
dc.subjectosteoporosisen_US
dc.titleInteraction between ferric carboxymaltose and denosumab causing severe hypocalcaemia and hypophosphataemia in a patient without chronic kidney disease.en_US
dc.typeJournal Articleen_US
dc.identifier.journaltitleInternal Medicine Journalen_US
dc.identifier.affiliationSchool of Public Health and Preventive Medicine, Monash University, Melbourne, Victoria, Australia.en_US
dc.identifier.affiliationAustin Healthen_US
dc.identifier.doi10.1111/imj.16156en_US
dc.type.contentTexten_US
dc.identifier.orcid0000-0002-6999-802Xen_US
dc.identifier.pubmedid37384573-
item.fulltextNo Fulltext-
item.openairecristypehttp://purl.org/coar/resource_type/c_18cf-
item.grantfulltextnone-
item.languageiso639-1en-
item.openairetypeJournal Article-
item.cerifentitytypePublications-
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