351 reports of this reaction
2.2% of all MESNA INJECTION reports
#8 most reported adverse reaction
SEPSIS is the #8 most commonly reported adverse reaction for MESNA INJECTION, manufactured by Gland Pharma Limited. There are 351 FDA adverse event reports linking MESNA INJECTION to SEPSIS. This represents approximately 2.2% of all 16,183 adverse event reports for this drug.
Patients taking MESNA INJECTION who experience sepsis should discuss this symptom with their healthcare provider to determine whether it may be related to their medication and what alternatives may be available.
SEPSIS is a less commonly reported adverse event for MESNA INJECTION, but still significant enough to appear in the safety profile.
In addition to sepsis, the following adverse reactions have been reported for MESNA INJECTION:
The following drugs have also been linked to sepsis in FDA adverse event reports:
SEPSIS has been reported as an adverse event in 351 FDA reports for MESNA INJECTION. This does not prove causation, but indicates an association observed in post-market surveillance data.
SEPSIS accounts for approximately 2.2% of all adverse event reports for MESNA INJECTION, making it a notable side effect.
If you experience sepsis while taking MESNA INJECTION, 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.