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Traceability of biologicals: present challenges in pharmacovigilance

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Dragica Edrovska, Aleksandra Grozdanova, Katerina Ancevska Netkovska & Zorica Naumovska. (2022) Traceability of biologicals: challenges in pharmacovigilance. Macedonian Pharmaceutical Bulletin 68:03, pages 481-482.
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J. O’Callaghan, B. T. Griffin, J. M. Morris & Margaret Bermingham. (2018) Knowledge of Adverse Drug Reaction Reporting and the Pharmacovigilance of Biological Medicines: A Survey of Healthcare Professionals in Ireland. BioDrugs 32:3, pages 267-280.
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Till Uhlig & Guro L. Goll. (2017) Reviewing the evidence for biosimilars: key insights, lessons learned and future horizons. Rheumatology 56:suppl_4, pages iv49-iv62.
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Stella Stergiopoulos, Carrie A. Brown, Thomas Felix, Gustavo Grampp & Kenneth A. Getz. (2016) A Survey of Adverse Event Reporting Practices Among US Healthcare Professionals. Drug Safety 39:11, pages 1117-1127.
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Hans C. Ebbers, Nina Fuentes de Tienda, Marcel C. Hoefnagel, Ria Nibbeling & Aukje K. Mantel-Teeuwisse. (2016) Characteristics of product recalls of biopharmaceuticals and small-molecule drugs in the USA. Drug Discovery Today 21:4, pages 536-539.
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Niels S. Vermeer, Hans C. Ebbers, Sabine M. J. M. Straus, Hubert G. M. Leufkens, Toine C. G. Egberts & Marie L. De Bruin. (2016) The effect of exposure misclassification in spontaneous ADR reports on the time to detection of product-specific risks for biologicals: a simulation study. Pharmacoepidemiology and Drug Safety 25:3, pages 297-306.
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