106 reports of this reaction
2.0% of all CEVIMELINE HYDROCHLORIDE reports
#9 most reported adverse reaction
FALL is the #9 most commonly reported adverse reaction for CEVIMELINE HYDROCHLORIDE, manufactured by Aurobindo Pharma Limited. There are 106 FDA adverse event reports linking CEVIMELINE HYDROCHLORIDE to FALL. This represents approximately 2.0% of all 5,260 adverse event reports for this drug.
Patients taking CEVIMELINE HYDROCHLORIDE 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 CEVIMELINE HYDROCHLORIDE, but still significant enough to appear in the safety profile.
In addition to fall, the following adverse reactions have been reported for CEVIMELINE HYDROCHLORIDE:
The following drugs have also been linked to fall in FDA adverse event reports:
FALL has been reported as an adverse event in 106 FDA reports for CEVIMELINE HYDROCHLORIDE. This does not prove causation, but indicates an association observed in post-market surveillance data.
FALL accounts for approximately 2.0% of all adverse event reports for CEVIMELINE HYDROCHLORIDE, making it a notable side effect.
If you experience fall while taking CEVIMELINE HYDROCHLORIDE, 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.