Authors' Reply to Michael Auerbach's Comment on: "Frequency and Associated Costs of Anaphylaxis- and Hypersensitivity-Related Adverse Events for Intravenous Iron Products in the USA: An Analysis Using the US Food and Drug Administration Adverse Event Reporting System"
- PMID: 33835350
- PMCID: PMC8053176
- DOI: 10.1007/s40264-021-01059-x
Authors' Reply to Michael Auerbach's Comment on: "Frequency and Associated Costs of Anaphylaxis- and Hypersensitivity-Related Adverse Events for Intravenous Iron Products in the USA: An Analysis Using the US Food and Drug Administration Adverse Event Reporting System"
Conflict of interest statement
Henry Trumbo is a consultant for American Regent, Daiichi Sankyo, and Allergan. Lawrence T. Goodnough is a consultant for American Regent. Karolina Kaluza and Syed Numan are employees of American Regent, the manufacturers of ferric carboxymaltose.
Comment on
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Frequency and Associated Costs of Anaphylaxis- and Hypersensitivity-Related Adverse Events for Intravenous Iron Products in the USA: An Analysis Using the US Food and Drug Administration Adverse Event Reporting System.Drug Saf. 2021 Jan;44(1):107-119. doi: 10.1007/s40264-020-01022-2. Epub 2020 Nov 25. Drug Saf. 2021. PMID: 33237523 Free PMC article.
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Comment on: Frequency and Associated Costs of Anaphylaxis- and Hypersensitivity-Related Adverse Events for Intravenous Iron Products in the USA: An Analysis Using the US Food and Drug Administration Adverse Event Reporting System.Drug Saf. 2021 May;44(5):609-610. doi: 10.1007/s40264-021-01058-y. Epub 2021 Apr 9. Drug Saf. 2021. PMID: 33835349 No abstract available.
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Comment on: Frequency and Associated Costs of Anaphylaxis- and Hypersensitivity-Related Adverse Events for Intravenous Iron Products in the USA: An Analysis Using the US Food and Drug Administration Adverse Event Reporting System.Drug Saf. 2021 May;44(5):609-610. doi: 10.1007/s40264-021-01058-y. Epub 2021 Apr 9. Drug Saf. 2021. PMID: 33835349 No abstract available.
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Frequency and Associated Costs of Anaphylaxis- and Hypersensitivity-Related Adverse Events for Intravenous Iron Products in the USA: An Analysis Using the US Food and Drug Administration Adverse Event Reporting System.Drug Saf. 2021 Jan;44(1):107-119. doi: 10.1007/s40264-020-01022-2. Epub 2020 Nov 25. Drug Saf. 2021. PMID: 33237523 Free PMC article.
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References
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- Trumbo H, Kaluza K, Numan S, Goodnough LT. Frequency and associated costs of anaphylaxis- and hypersensitivity-related adverse events for intravenous iron products in the USA: an analysis using the US Food and Drug Administration Adverse Event Reporting System. Drug Saf. 2020 doi: 10.1007/s40264-020-01022-2. - DOI - PMC - PubMed
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- Auerbach M. Comment on: “Frequency and Associated Costs of Anaphylaxis- and Hypersensitivity-Related Adverse Events for Intravenous Iron Products in the USA: An Analysis Using the US Food and Drug Administration Adverse Event Reporting System”. Drug Saf. 2021. 10.1007/s40264-021-01058-y. - PubMed
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