The most commonly reported side effects of pegfilgrastim include device adhesion issue, wrong technique in product usage process, and unintentional medical device removal, based on 99,995 FDA adverse event reports from 2004 to 2025.
Percentages show how often each reaction appears relative to total reports for pegfilgrastim.
These are voluntary reports and do not establish that pegfilgrastim caused these reactions.
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Other drugs that appear in adverse event reports alongside pegfilgrastim. Drugs flagged as a suspected cause appear in the first column. Drugs taken at the same time but not suspected appear in the second.
Also suspected
Taken alongside
Co-occurrence in adverse event reports does not establish a drug interaction. Patients often take multiple medications, and these lists reflect prescribing patterns rather than causal relationships. Consult a healthcare provider about potential drug interactions.
53.4% of pegfilgrastim adverse event reports involve female patients and 28.1% involve male patients. The largest age group is adult at 56%. These figures reflect who reports side effects, not underlying risk.
Sex
Age group
Conditions and purposes for which patients were taking pegfilgrastim when the adverse event was reported.
Showing 15 of 931 indications
Pegfilgrastim is sold under several brand names including Neulasta, Fulphila, Udenyca.
An upward trend reflects increased FAERS reporting overall, not necessarily increased risk.
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