22 reports of this reaction
2.0% of all TRIFLURIDINE reports
#9 most reported adverse reaction
THERAPY PARTIAL RESPONDER is the #9 most commonly reported adverse reaction for TRIFLURIDINE, manufactured by Sandoz Inc. There are 22 FDA adverse event reports linking TRIFLURIDINE to THERAPY PARTIAL RESPONDER. This represents approximately 2.0% of all 1,094 adverse event reports for this drug.
Patients taking TRIFLURIDINE who experience therapy partial responder should discuss this symptom with their healthcare provider to determine whether it may be related to their medication and what alternatives may be available.
THERAPY PARTIAL RESPONDER is a less commonly reported adverse event for TRIFLURIDINE, but still significant enough to appear in the safety profile.
In addition to therapy partial responder, the following adverse reactions have been reported for TRIFLURIDINE:
THERAPY PARTIAL RESPONDER has been reported as an adverse event in 22 FDA reports for TRIFLURIDINE. This does not prove causation, but indicates an association observed in post-market surveillance data.
THERAPY PARTIAL RESPONDER accounts for approximately 2.0% of all adverse event reports for TRIFLURIDINE, making it a notable side effect.
If you experience therapy partial responder while taking TRIFLURIDINE, 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.