1 reports of this reaction
4.8% of all ALUMINUM HYDROXIDE, MAGNESIUM HYDROXIDE, DIMETHICONE reports
#7 most reported adverse reaction
DYSURIA is the #7 most commonly reported adverse reaction for ALUMINUM HYDROXIDE, MAGNESIUM HYDROXIDE, DIMETHICONE, manufactured by KROGER COMPANY. There are 1 FDA adverse event reports linking ALUMINUM HYDROXIDE, MAGNESIUM HYDROXIDE, DIMETHICONE to DYSURIA. This represents approximately 4.8% of all 21 adverse event reports for this drug.
Patients taking ALUMINUM HYDROXIDE, MAGNESIUM HYDROXIDE, DIMETHICONE who experience dysuria should discuss this symptom with their healthcare provider to determine whether it may be related to their medication and what alternatives may be available.
DYSURIA is moderately reported among ALUMINUM HYDROXIDE, MAGNESIUM HYDROXIDE, DIMETHICONE users, representing a notable but not dominant share of adverse events.
In addition to dysuria, the following adverse reactions have been reported for ALUMINUM HYDROXIDE, MAGNESIUM HYDROXIDE, DIMETHICONE:
The following drugs have also been linked to dysuria in FDA adverse event reports:
DYSURIA has been reported as an adverse event in 1 FDA reports for ALUMINUM HYDROXIDE, MAGNESIUM HYDROXIDE, DIMETHICONE. This does not prove causation, but indicates an association observed in post-market surveillance data.
DYSURIA accounts for approximately 4.8% of all adverse event reports for ALUMINUM HYDROXIDE, MAGNESIUM HYDROXIDE, DIMETHICONE, making it a notable side effect.
If you experience dysuria while taking ALUMINUM HYDROXIDE, MAGNESIUM HYDROXIDE, DIMETHICONE, 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.