282 reports of this reaction
1.9% of all EMICIZUMAB reports
#11 most reported adverse reaction
MUSCLE HAEMORRHAGE is the #11 most commonly reported adverse reaction for EMICIZUMAB, manufactured by Genentech, Inc.. There are 282 FDA adverse event reports linking EMICIZUMAB to MUSCLE HAEMORRHAGE. This represents approximately 1.9% of all 15,224 adverse event reports for this drug.
Patients taking EMICIZUMAB who experience muscle haemorrhage should discuss this symptom with their healthcare provider to determine whether it may be related to their medication and what alternatives may be available.
MUSCLE HAEMORRHAGE is a less commonly reported adverse event for EMICIZUMAB, but still significant enough to appear in the safety profile.
In addition to muscle haemorrhage, the following adverse reactions have been reported for EMICIZUMAB:
The following drugs have also been linked to muscle haemorrhage in FDA adverse event reports:
MUSCLE HAEMORRHAGE has been reported as an adverse event in 282 FDA reports for EMICIZUMAB. This does not prove causation, but indicates an association observed in post-market surveillance data.
MUSCLE HAEMORRHAGE accounts for approximately 1.9% of all adverse event reports for EMICIZUMAB, making it a notable side effect.
If you experience muscle haemorrhage 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.