112 reports of this reaction
3.3% of all BENZALKONIUM CHLORIDE reports
#4 most reported adverse reaction
CONDITION AGGRAVATED is the #4 most commonly reported adverse reaction for BENZALKONIUM CHLORIDE, manufactured by Meijer, Inc.. There are 112 FDA adverse event reports linking BENZALKONIUM CHLORIDE to CONDITION AGGRAVATED. This represents approximately 3.3% of all 3,413 adverse event reports for this drug.
Patients taking BENZALKONIUM CHLORIDE who experience condition aggravated should discuss this symptom with their healthcare provider to determine whether it may be related to their medication and what alternatives may be available.
CONDITION AGGRAVATED is moderately reported among BENZALKONIUM CHLORIDE users, representing a notable but not dominant share of adverse events.
In addition to condition aggravated, the following adverse reactions have been reported for BENZALKONIUM CHLORIDE:
The following drugs have also been linked to condition aggravated in FDA adverse event reports:
CONDITION AGGRAVATED has been reported as an adverse event in 112 FDA reports for BENZALKONIUM CHLORIDE. This does not prove causation, but indicates an association observed in post-market surveillance data.
CONDITION AGGRAVATED accounts for approximately 3.3% of all adverse event reports for BENZALKONIUM CHLORIDE, making it a notable side effect.
If you experience condition aggravated 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.