462 reports of this reaction
2.0% of all PEGASPARGASE reports
#8 most reported adverse reaction
HYPOTENSION is the #8 most commonly reported adverse reaction for PEGASPARGASE, manufactured by Servier Pharmaceuticals LLC. There are 462 FDA adverse event reports linking PEGASPARGASE to HYPOTENSION. This represents approximately 2.0% of all 23,600 adverse event reports for this drug.
Patients taking PEGASPARGASE who experience hypotension should discuss this symptom with their healthcare provider to determine whether it may be related to their medication and what alternatives may be available.
HYPOTENSION is a less commonly reported adverse event for PEGASPARGASE, but still significant enough to appear in the safety profile.
In addition to hypotension, the following adverse reactions have been reported for PEGASPARGASE:
The following drugs have also been linked to hypotension in FDA adverse event reports:
HYPOTENSION has been reported as an adverse event in 462 FDA reports for PEGASPARGASE. This does not prove causation, but indicates an association observed in post-market surveillance data.
HYPOTENSION accounts for approximately 2.0% of all adverse event reports for PEGASPARGASE, making it a notable side effect.
If you experience hypotension while taking PEGASPARGASE, 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.