68 reports of this reaction
5.0% of all METHYLERGONOVINE MALEATE reports
#1 most reported adverse reaction
WRONG DRUG ADMINISTERED is the #1 most commonly reported adverse reaction for METHYLERGONOVINE MALEATE, manufactured by Lupin Pharmaceuticals,Inc.. There are 68 FDA adverse event reports linking METHYLERGONOVINE MALEATE to WRONG DRUG ADMINISTERED. This represents approximately 5.0% of all 1,362 adverse event reports for this drug.
Patients taking METHYLERGONOVINE MALEATE who experience wrong drug 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.
WRONG DRUG ADMINISTERED is moderately reported among METHYLERGONOVINE MALEATE users, representing a notable but not dominant share of adverse events.
In addition to wrong drug administered, the following adverse reactions have been reported for METHYLERGONOVINE MALEATE:
WRONG DRUG ADMINISTERED has been reported as an adverse event in 68 FDA reports for METHYLERGONOVINE MALEATE. This does not prove causation, but indicates an association observed in post-market surveillance data.
WRONG DRUG ADMINISTERED accounts for approximately 5.0% of all adverse event reports for METHYLERGONOVINE MALEATE, making it one of the most commonly reported side effect.
If you experience wrong drug administered while taking METHYLERGONOVINE MALEATE, 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.