3,272 reports of this reaction
2.2% of all PEGFILGRASTIM reports
#10 most reported adverse reaction
DEVICE OCCLUSION is the #10 most commonly reported adverse reaction for PEGFILGRASTIM, manufactured by Amgen, Inc. There are 3,272 FDA adverse event reports linking PEGFILGRASTIM to DEVICE OCCLUSION. This represents approximately 2.2% of all 146,341 adverse event reports for this drug.
Patients taking PEGFILGRASTIM who experience device occlusion should discuss this symptom with their healthcare provider to determine whether it may be related to their medication and what alternatives may be available.
DEVICE OCCLUSION is a less commonly reported adverse event for PEGFILGRASTIM, but still significant enough to appear in the safety profile.
In addition to device occlusion, the following adverse reactions have been reported for PEGFILGRASTIM:
The following drugs have also been linked to device occlusion in FDA adverse event reports:
DEVICE OCCLUSION has been reported as an adverse event in 3,272 FDA reports for PEGFILGRASTIM. This does not prove causation, but indicates an association observed in post-market surveillance data.
DEVICE OCCLUSION accounts for approximately 2.2% of all adverse event reports for PEGFILGRASTIM, making it a notable side effect.
If you experience device occlusion 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.