3,249 reports of this reaction
9.0% of all MEPERIDINE HYDROCHLORIDE reports
#1 most reported adverse reaction
DRUG HYPERSENSITIVITY is the #1 most commonly reported adverse reaction for MEPERIDINE HYDROCHLORIDE, manufactured by Hospira, Inc.. There are 3,249 FDA adverse event reports linking MEPERIDINE HYDROCHLORIDE to DRUG HYPERSENSITIVITY. This represents approximately 9.0% of all 36,000 adverse event reports for this drug.
Patients taking MEPERIDINE HYDROCHLORIDE who experience drug hypersensitivity should discuss this symptom with their healthcare provider to determine whether it may be related to their medication and what alternatives may be available.
DRUG HYPERSENSITIVITY is moderately reported among MEPERIDINE HYDROCHLORIDE users, representing a notable but not dominant share of adverse events.
In addition to drug hypersensitivity, the following adverse reactions have been reported for MEPERIDINE HYDROCHLORIDE:
The following drugs have also been linked to drug hypersensitivity in FDA adverse event reports:
DRUG HYPERSENSITIVITY has been reported as an adverse event in 3,249 FDA reports for MEPERIDINE HYDROCHLORIDE. This does not prove causation, but indicates an association observed in post-market surveillance data.
DRUG HYPERSENSITIVITY accounts for approximately 9.0% of all adverse event reports for MEPERIDINE HYDROCHLORIDE, making it one of the most commonly reported side effect.
If you experience drug hypersensitivity while taking MEPERIDINE HYDROCHLORIDE, 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.