Does MEPERIDINE Cause Product dose omission? 12 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 12 reports of Product dose omission have been filed in association with MEPERIDINE (MEPERIDINE HYDROCHLORIDE). This represents 0.2% of all adverse event reports for MEPERIDINE.
12
Reports of Product dose omission with MEPERIDINE
0.2%
of all MEPERIDINE reports
0
Deaths
8
Hospitalizations
How Dangerous Is Product dose omission From MEPERIDINE?
Of the 12 reports, 8 (66.7%) required hospitalization.
Is Product dose omission Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for MEPERIDINE. However, 12 reports have been filed with the FAERS database.
What Other Side Effects Does MEPERIDINE Cause?
Drug hypersensitivity (3,278)
Drug ineffective (1,033)
Pain (828)
Nausea (798)
Drug intolerance (757)
Overdose (675)
Hyperhidrosis (654)
Off label use (640)
Rash (640)
Drug dependence (522)
What Other Drugs Cause Product dose omission?
APREMILAST (4,567)
DUPILUMAB (2,729)
ALBUTEROL (1,742)
USTEKINUMAB (1,653)
INSULIN GLARGINE (1,500)
ETANERCEPT (1,400)
LENALIDOMIDE (1,400)
RUXOLITINIB (1,376)
ALIROCUMAB (1,354)
DIMETHYL (1,248)
Which MEPERIDINE Alternatives Have Lower Product dose omission Risk?
MEPERIDINE vs MEPIVACAINE
MEPERIDINE vs MEPIVACAINE\MEPIVACAINE
MEPERIDINE vs MEPOLIZUMAB
MEPERIDINE vs MEPROBAMATE
MEPERIDINE vs MERCAPTOPURINE