1 reports of this reaction
3.1% of all POLYETHYLENE GLYCOL 400, PROPYLENE GLYCOL reports
#15 most reported adverse reaction
PRODUCT LOT NUMBER ISSUE is the #15 most commonly reported adverse reaction for POLYETHYLENE GLYCOL 400, PROPYLENE GLYCOL, manufactured by Wal-Mart Stores, Inc.. There are 1 FDA adverse event reports linking POLYETHYLENE GLYCOL 400, PROPYLENE GLYCOL to PRODUCT LOT NUMBER ISSUE. This represents approximately 3.1% of all 32 adverse event reports for this drug.
Patients taking POLYETHYLENE GLYCOL 400, PROPYLENE GLYCOL who experience product lot number issue should discuss this symptom with their healthcare provider to determine whether it may be related to their medication and what alternatives may be available.
PRODUCT LOT NUMBER ISSUE is moderately reported among POLYETHYLENE GLYCOL 400, PROPYLENE GLYCOL users, representing a notable but not dominant share of adverse events.
In addition to product lot number issue, the following adverse reactions have been reported for POLYETHYLENE GLYCOL 400, PROPYLENE GLYCOL:
The following drugs have also been linked to product lot number issue in FDA adverse event reports:
PRODUCT LOT NUMBER ISSUE has been reported as an adverse event in 1 FDA reports for POLYETHYLENE GLYCOL 400, PROPYLENE GLYCOL. This does not prove causation, but indicates an association observed in post-market surveillance data.
PRODUCT LOT NUMBER ISSUE accounts for approximately 3.1% of all adverse event reports for POLYETHYLENE GLYCOL 400, PROPYLENE GLYCOL, making it a notable side effect.
If you experience product lot number issue while taking POLYETHYLENE GLYCOL 400, PROPYLENE GLYCOL, 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.