129 reports of this reaction
1.6% of all LOXAPINE reports
#17 most reported adverse reaction
TACHYCARDIA is the #17 most commonly reported adverse reaction for LOXAPINE, manufactured by Actavis Pharma, Inc.. There are 129 FDA adverse event reports linking LOXAPINE to TACHYCARDIA. This represents approximately 1.6% of all 8,319 adverse event reports for this drug.
Patients taking LOXAPINE who experience tachycardia should discuss this symptom with their healthcare provider to determine whether it may be related to their medication and what alternatives may be available.
TACHYCARDIA is a less commonly reported adverse event for LOXAPINE, but still significant enough to appear in the safety profile.
In addition to tachycardia, the following adverse reactions have been reported for LOXAPINE:
The following drugs have also been linked to tachycardia in FDA adverse event reports:
TACHYCARDIA has been reported as an adverse event in 129 FDA reports for LOXAPINE. This does not prove causation, but indicates an association observed in post-market surveillance data.
TACHYCARDIA accounts for approximately 1.6% of all adverse event reports for LOXAPINE, making it a notable side effect.
If you experience tachycardia 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.