754 reports of this reaction
5.0% of all EMICIZUMAB reports
#2 most reported adverse reaction
NO ADVERSE EVENT is the #2 most commonly reported adverse reaction for EMICIZUMAB, manufactured by Genentech, Inc.. There are 754 FDA adverse event reports linking EMICIZUMAB to NO ADVERSE EVENT. This represents approximately 5.0% of all 15,224 adverse event reports for this drug.
Patients taking EMICIZUMAB who experience no adverse event should discuss this symptom with their healthcare provider to determine whether it may be related to their medication and what alternatives may be available.
NO ADVERSE EVENT is moderately reported among EMICIZUMAB users, representing a notable but not dominant share of adverse events.
In addition to no adverse event, the following adverse reactions have been reported for EMICIZUMAB:
The following drugs have also been linked to no adverse event in FDA adverse event reports:
NO ADVERSE EVENT has been reported as an adverse event in 754 FDA reports for EMICIZUMAB. This does not prove causation, but indicates an association observed in post-market surveillance data.
NO ADVERSE EVENT accounts for approximately 5.0% of all adverse event reports for EMICIZUMAB, making it one of the most commonly reported side effect.
If you experience no adverse event while taking EMICIZUMAB, 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.