4 reports of this reaction
2.7% of all ALUMINUM CHLOROHYDRATE reports
#9 most reported adverse reaction
SKIN EROSION is the #9 most commonly reported adverse reaction for ALUMINUM CHLOROHYDRATE, manufactured by The Procter & Gamble Manufacturing Company. There are 4 FDA adverse event reports linking ALUMINUM CHLOROHYDRATE to SKIN EROSION. This represents approximately 2.7% of all 148 adverse event reports for this drug.
Patients taking ALUMINUM CHLOROHYDRATE who experience skin erosion should discuss this symptom with their healthcare provider to determine whether it may be related to their medication and what alternatives may be available.
SKIN EROSION is a less commonly reported adverse event for ALUMINUM CHLOROHYDRATE, but still significant enough to appear in the safety profile.
In addition to skin erosion, the following adverse reactions have been reported for ALUMINUM CHLOROHYDRATE:
SKIN EROSION has been reported as an adverse event in 4 FDA reports for ALUMINUM CHLOROHYDRATE. This does not prove causation, but indicates an association observed in post-market surveillance data.
SKIN EROSION accounts for approximately 2.7% of all adverse event reports for ALUMINUM CHLOROHYDRATE, making it a notable side effect.
If you experience skin erosion 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.