297 reports of this reaction
2.9% of all DEFLAZACORT reports
#3 most reported adverse reaction
FALL is the #3 most commonly reported adverse reaction for DEFLAZACORT, manufactured by PTC Therapeutics, Inc.. There are 297 FDA adverse event reports linking DEFLAZACORT to FALL. This represents approximately 2.9% of all 10,344 adverse event reports for this drug.
Patients taking DEFLAZACORT who experience fall should discuss this symptom with their healthcare provider to determine whether it may be related to their medication and what alternatives may be available.
FALL is a less commonly reported adverse event for DEFLAZACORT, but still significant enough to appear in the safety profile.
In addition to fall, the following adverse reactions have been reported for DEFLAZACORT:
The following drugs have also been linked to fall in FDA adverse event reports:
FALL has been reported as an adverse event in 297 FDA reports for DEFLAZACORT. This does not prove causation, but indicates an association observed in post-market surveillance data.
FALL accounts for approximately 2.9% of all adverse event reports for DEFLAZACORT, making it one of the most commonly reported side effect.
If you experience fall while taking DEFLAZACORT, 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.