153 reports of this reaction
1.8% of all LOXAPINE reports
#10 most reported adverse reaction
AKATHISIA is the #10 most commonly reported adverse reaction for LOXAPINE, manufactured by Actavis Pharma, Inc.. There are 153 FDA adverse event reports linking LOXAPINE to AKATHISIA. This represents approximately 1.8% of all 8,319 adverse event reports for this drug.
Patients taking LOXAPINE who experience akathisia should discuss this symptom with their healthcare provider to determine whether it may be related to their medication and what alternatives may be available.
AKATHISIA is a less commonly reported adverse event for LOXAPINE, but still significant enough to appear in the safety profile.
In addition to akathisia, the following adverse reactions have been reported for LOXAPINE:
The following drugs have also been linked to akathisia in FDA adverse event reports:
AKATHISIA has been reported as an adverse event in 153 FDA reports for LOXAPINE. This does not prove causation, but indicates an association observed in post-market surveillance data.
AKATHISIA accounts for approximately 1.8% of all adverse event reports for LOXAPINE, making it a notable side effect.
If you experience akathisia while taking LOXAPINE, 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.