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1. Comment on: "Safety of Marketed Cancer Supportive Care Biosimilars in the U.S.: A Disproportionality Analysis Using the Food and Drug Administration Adverse Event Reporting System (FAERS) Database".

Author

Putzke J, Haughie S, Zou KH, and Ranganna GM

Subjects
Adverse Drug Reaction Reporting Systems, Databases, Factual, Humans, United States, United States Food and Drug Administration, Biosimilar Pharmaceuticals adverse effects, Neoplasms drug therapy
Published
2021
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