137 reports of this reaction
1.3% of all ISTRADEFYLLINE reports
#18 most reported adverse reaction
ADVERSE DRUG REACTION is the #18 most commonly reported adverse reaction for ISTRADEFYLLINE, manufactured by Kyowa Kirin, Inc.. There are 137 FDA adverse event reports linking ISTRADEFYLLINE to ADVERSE DRUG REACTION. This represents approximately 1.3% of all 10,328 adverse event reports for this drug.
Patients taking ISTRADEFYLLINE who experience adverse drug reaction should discuss this symptom with their healthcare provider to determine whether it may be related to their medication and what alternatives may be available.
ADVERSE DRUG REACTION is a less commonly reported adverse event for ISTRADEFYLLINE, but still significant enough to appear in the safety profile.
In addition to adverse drug reaction, the following adverse reactions have been reported for ISTRADEFYLLINE:
The following drugs have also been linked to adverse drug reaction in FDA adverse event reports:
ADVERSE DRUG REACTION has been reported as an adverse event in 137 FDA reports for ISTRADEFYLLINE. This does not prove causation, but indicates an association observed in post-market surveillance data.
ADVERSE DRUG REACTION accounts for approximately 1.3% of all adverse event reports for ISTRADEFYLLINE, making it a notable side effect.
If you experience adverse drug reaction while taking ISTRADEFYLLINE, 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.