283 reports of this reaction
1.2% of all DURVALUMAB reports
#20 most reported adverse reaction
MYELOSUPPRESSION is the #20 most commonly reported adverse reaction for DURVALUMAB, manufactured by AstraZeneca Pharmaceuticals LP. There are 283 FDA adverse event reports linking DURVALUMAB to MYELOSUPPRESSION. This represents approximately 1.2% of all 23,251 adverse event reports for this drug.
Patients taking DURVALUMAB who experience myelosuppression should discuss this symptom with their healthcare provider to determine whether it may be related to their medication and what alternatives may be available.
MYELOSUPPRESSION is a less commonly reported adverse event for DURVALUMAB, but still significant enough to appear in the safety profile.
In addition to myelosuppression, the following adverse reactions have been reported for DURVALUMAB:
The following drugs have also been linked to myelosuppression in FDA adverse event reports:
MYELOSUPPRESSION has been reported as an adverse event in 283 FDA reports for DURVALUMAB. This does not prove causation, but indicates an association observed in post-market surveillance data.
MYELOSUPPRESSION accounts for approximately 1.2% of all adverse event reports for DURVALUMAB, making it a notable side effect.
If you experience myelosuppression while taking DURVALUMAB, 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.