2019
DOI: 10.12890/2019_001131
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Interstitial Lung Disease in a Patient Treated with Denosumab

Abstract: Denosumab is an antiresorptive agent widely used for treating osteoporosis. Atypical femur fractures, osteonecrosis of the jaw and hypocalcaemia are well-known possible adverse effects of this drug. We present, to our knowledge, the first case report in the English literature of clinically significant interstitial lung disease likely related to denosumab.

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Cited by 4 publications
(3 citation statements)
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“…This is widely used in clinical research and pharmacovigilance to determine the probability that an adverse effect is related to a specific drug, according to a pre-established questionnaire [ 16 ] . The score for this case report was calculated: (a) we cited two previous conclusive reports of this reaction (YES=+1), respectively, Ruis et al [ 7 ] and Mori et al [ 8 ] ; (b) the clinical event appeared 48 hours after the third injection of denosumab (YES=+2); (c) the clinical event improved with denosumab withdrawal and corticosteroid therapy (YES=+1); (d) re-administration of denosumab was not done (=0), because of ethical aspects and the severity of the ADR; (e) there are no alternative causes (e.g. infection, immunological or post radiation origin) explaining this ADR (YES=+2).…”
Section: Discussionmentioning
confidence: 99%
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“…This is widely used in clinical research and pharmacovigilance to determine the probability that an adverse effect is related to a specific drug, according to a pre-established questionnaire [ 16 ] . The score for this case report was calculated: (a) we cited two previous conclusive reports of this reaction (YES=+1), respectively, Ruis et al [ 7 ] and Mori et al [ 8 ] ; (b) the clinical event appeared 48 hours after the third injection of denosumab (YES=+2); (c) the clinical event improved with denosumab withdrawal and corticosteroid therapy (YES=+1); (d) re-administration of denosumab was not done (=0), because of ethical aspects and the severity of the ADR; (e) there are no alternative causes (e.g. infection, immunological or post radiation origin) explaining this ADR (YES=+2).…”
Section: Discussionmentioning
confidence: 99%
“…More than 2% of women treated with denosumab experienced the adverse effects [6] . Denosumab is also responsible for different aspects of pulmonary toxicity reported in the literature; two cases of diffuse interstitial lung diseases [7,8] , one case of c-ANCA vasculitis and one case of diffuse intra-alveolar haemorrhage due to p-ANCA have been described [9,1] . Descriptions of the clinical presentations for these reported cases are provided in Table 1.…”
Section: Discussionmentioning
confidence: 99%
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