423 reports of this reaction
1.9% of all ALTEPLASE reports
#10 most reported adverse reaction
HAEMORRHAGIC TRANSFORMATION STROKE is the #10 most commonly reported adverse reaction for ALTEPLASE, manufactured by Genentech, Inc.. There are 423 FDA adverse event reports linking ALTEPLASE to HAEMORRHAGIC TRANSFORMATION STROKE. This represents approximately 1.9% of all 22,483 adverse event reports for this drug.
Patients taking ALTEPLASE who experience haemorrhagic transformation stroke should discuss this symptom with their healthcare provider to determine whether it may be related to their medication and what alternatives may be available.
HAEMORRHAGIC TRANSFORMATION STROKE is a less commonly reported adverse event for ALTEPLASE, but still significant enough to appear in the safety profile.
In addition to haemorrhagic transformation stroke, the following adverse reactions have been reported for ALTEPLASE:
HAEMORRHAGIC TRANSFORMATION STROKE has been reported as an adverse event in 423 FDA reports for ALTEPLASE. This does not prove causation, but indicates an association observed in post-market surveillance data.
HAEMORRHAGIC TRANSFORMATION STROKE accounts for approximately 1.9% of all adverse event reports for ALTEPLASE, making it a notable side effect.
If you experience haemorrhagic transformation stroke while taking ALTEPLASE, 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.