8,931 reports of this reaction
6.1% of all PEGFILGRASTIM reports
#3 most reported adverse reaction
UNINTENTIONAL MEDICAL DEVICE REMOVAL is the #3 most commonly reported adverse reaction for PEGFILGRASTIM, manufactured by Amgen, Inc. There are 8,931 FDA adverse event reports linking PEGFILGRASTIM to UNINTENTIONAL MEDICAL DEVICE REMOVAL. This represents approximately 6.1% of all 146,341 adverse event reports for this drug.
Patients taking PEGFILGRASTIM who experience unintentional medical device removal should discuss this symptom with their healthcare provider to determine whether it may be related to their medication and what alternatives may be available.
UNINTENTIONAL MEDICAL DEVICE REMOVAL is moderately reported among PEGFILGRASTIM users, representing a notable but not dominant share of adverse events.
In addition to unintentional medical device removal, the following adverse reactions have been reported for PEGFILGRASTIM:
UNINTENTIONAL MEDICAL DEVICE REMOVAL has been reported as an adverse event in 8,931 FDA reports for PEGFILGRASTIM. This does not prove causation, but indicates an association observed in post-market surveillance data.
UNINTENTIONAL MEDICAL DEVICE REMOVAL accounts for approximately 6.1% of all adverse event reports for PEGFILGRASTIM, making it one of the most commonly reported side effect.
If you experience unintentional medical device removal while taking PEGFILGRASTIM, contact your healthcare provider. They can evaluate whether the symptom is related to your medication and discuss potential adjustments to your treatment plan. Do not stop taking prescribed medication without consulting your doctor.