35 reports of this reaction
1.9% of all ORPHENADRINE CITRATE reports
#9 most reported adverse reaction
DIZZINESS is the #9 most commonly reported adverse reaction for ORPHENADRINE CITRATE, manufactured by Actavis Pharma, Inc.. There are 35 FDA adverse event reports linking ORPHENADRINE CITRATE to DIZZINESS. This represents approximately 1.9% of all 1,883 adverse event reports for this drug.
Patients taking ORPHENADRINE CITRATE who experience dizziness should discuss this symptom with their healthcare provider to determine whether it may be related to their medication and what alternatives may be available.
DIZZINESS is a less commonly reported adverse event for ORPHENADRINE CITRATE, but still significant enough to appear in the safety profile.
In addition to dizziness, the following adverse reactions have been reported for ORPHENADRINE CITRATE:
The following drugs have also been linked to dizziness in FDA adverse event reports:
DIZZINESS has been reported as an adverse event in 35 FDA reports for ORPHENADRINE CITRATE. This does not prove causation, but indicates an association observed in post-market surveillance data.
DIZZINESS accounts for approximately 1.9% of all adverse event reports for ORPHENADRINE CITRATE, making it a notable side effect.
If you experience dizziness while taking ORPHENADRINE CITRATE, 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.