821 reports of this reaction
2.3% of all MEPERIDINE HYDROCHLORIDE reports
#6 most reported adverse reaction
HYPERHIDROSIS is the #6 most commonly reported adverse reaction for MEPERIDINE HYDROCHLORIDE, manufactured by Hospira, Inc.. There are 821 FDA adverse event reports linking MEPERIDINE HYDROCHLORIDE to HYPERHIDROSIS. This represents approximately 2.3% of all 36,000 adverse event reports for this drug.
Patients taking MEPERIDINE HYDROCHLORIDE who experience hyperhidrosis should discuss this symptom with their healthcare provider to determine whether it may be related to their medication and what alternatives may be available.
HYPERHIDROSIS is a less commonly reported adverse event for MEPERIDINE HYDROCHLORIDE, but still significant enough to appear in the safety profile.
In addition to hyperhidrosis, the following adverse reactions have been reported for MEPERIDINE HYDROCHLORIDE:
The following drugs have also been linked to hyperhidrosis in FDA adverse event reports:
HYPERHIDROSIS has been reported as an adverse event in 821 FDA reports for MEPERIDINE HYDROCHLORIDE. This does not prove causation, but indicates an association observed in post-market surveillance data.
HYPERHIDROSIS accounts for approximately 2.3% of all adverse event reports for MEPERIDINE HYDROCHLORIDE, making it a notable side effect.
If you experience hyperhidrosis 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.