278 reports of this reaction
3.3% of all CARMUSTINE reports
#4 most reported adverse reaction
DISEASE PROGRESSION is the #4 most commonly reported adverse reaction for CARMUSTINE, manufactured by Azurity Pharmaceuticals, Inc.. There are 278 FDA adverse event reports linking CARMUSTINE to DISEASE PROGRESSION. This represents approximately 3.3% of all 8,401 adverse event reports for this drug.
Patients taking CARMUSTINE who experience disease progression should discuss this symptom with their healthcare provider to determine whether it may be related to their medication and what alternatives may be available.
DISEASE PROGRESSION is moderately reported among CARMUSTINE users, representing a notable but not dominant share of adverse events.
In addition to disease progression, the following adverse reactions have been reported for CARMUSTINE:
The following drugs have also been linked to disease progression in FDA adverse event reports:
DISEASE PROGRESSION has been reported as an adverse event in 278 FDA reports for CARMUSTINE. This does not prove causation, but indicates an association observed in post-market surveillance data.
DISEASE PROGRESSION accounts for approximately 3.3% of all adverse event reports for CARMUSTINE, making it a notable side effect.
If you experience disease progression while taking CARMUSTINE, 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.