3 reports of this reaction
2.0% of all ALUMINUM CHLOROHYDRATE reports
#13 most reported adverse reaction
RECALLED PRODUCT ADMINISTERED is the #13 most commonly reported adverse reaction for ALUMINUM CHLOROHYDRATE, manufactured by The Procter & Gamble Manufacturing Company. There are 3 FDA adverse event reports linking ALUMINUM CHLOROHYDRATE to RECALLED PRODUCT ADMINISTERED. This represents approximately 2.0% of all 148 adverse event reports for this drug.
Patients taking ALUMINUM CHLOROHYDRATE who experience recalled product administered should discuss this symptom with their healthcare provider to determine whether it may be related to their medication and what alternatives may be available.
RECALLED PRODUCT ADMINISTERED is a less commonly reported adverse event for ALUMINUM CHLOROHYDRATE, but still significant enough to appear in the safety profile.
In addition to recalled product administered, the following adverse reactions have been reported for ALUMINUM CHLOROHYDRATE:
The following drugs have also been linked to recalled product administered in FDA adverse event reports:
RECALLED PRODUCT ADMINISTERED has been reported as an adverse event in 3 FDA reports for ALUMINUM CHLOROHYDRATE. This does not prove causation, but indicates an association observed in post-market surveillance data.
RECALLED PRODUCT ADMINISTERED accounts for approximately 2.0% of all adverse event reports for ALUMINUM CHLOROHYDRATE, making it a notable side effect.
If you experience recalled product administered while taking ALUMINUM CHLOROHYDRATE, 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.