110 reports of this reaction
3.2% of all BENZALKONIUM CHLORIDE reports
#6 most reported adverse reaction
THERAPY NON RESPONDER is the #6 most commonly reported adverse reaction for BENZALKONIUM CHLORIDE, manufactured by Meijer, Inc.. There are 110 FDA adverse event reports linking BENZALKONIUM CHLORIDE to THERAPY NON RESPONDER. This represents approximately 3.2% of all 3,413 adverse event reports for this drug.
Patients taking BENZALKONIUM CHLORIDE who experience therapy non responder should discuss this symptom with their healthcare provider to determine whether it may be related to their medication and what alternatives may be available.
THERAPY NON RESPONDER is moderately reported among BENZALKONIUM CHLORIDE users, representing a notable but not dominant share of adverse events.
In addition to therapy non responder, the following adverse reactions have been reported for BENZALKONIUM CHLORIDE:
The following drugs have also been linked to therapy non responder in FDA adverse event reports:
THERAPY NON RESPONDER has been reported as an adverse event in 110 FDA reports for BENZALKONIUM CHLORIDE. This does not prove causation, but indicates an association observed in post-market surveillance data.
THERAPY NON RESPONDER accounts for approximately 3.2% of all adverse event reports for BENZALKONIUM CHLORIDE, making it a notable side effect.
If you experience therapy non responder while taking BENZALKONIUM CHLORIDE, 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.