Does MEGLUMINE Cause Product administration error? 6 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 6 reports of Product administration error have been filed in association with MEGLUMINE. This represents 1.0% of all adverse event reports for MEGLUMINE.
6
Reports of Product administration error with MEGLUMINE
1.0%
of all MEGLUMINE reports
0
Deaths
0
Hospitalizations
How Dangerous Is Product administration error From MEGLUMINE?
Of the 6 reports.
Is Product administration error Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for MEGLUMINE. However, 6 reports have been filed with the FAERS database.
What Other Side Effects Does MEGLUMINE Cause?
Off label use (389)
Maternal exposure during pregnancy (300)
Joint swelling (294)
Pemphigus (289)
Glossodynia (288)
Inflammation (285)
Pain (284)
General physical health deterioration (283)
Folliculitis (282)
Hypertension (282)
What Other Drugs Cause Product administration error?
HYDROXYPROGESTERONE CAPROATE (972)
ACETAMINOPHEN (666)
CENEGERMIN-BKBJ (613)
LEUPROLIDE (595)
EVOLOCUMAB (565)
ADALIMUMAB (543)
METHYLPHENIDATE (414)
OLMESARTAN MEDOXOMIL (314)
ASPIRIN (241)
SECUKINUMAB (225)
Which MEGLUMINE Alternatives Have Lower Product administration error Risk?
MEGLUMINE vs MELATONIN
MEGLUMINE vs MELOXICAM
MEGLUMINE vs MELPERONE
MEGLUMINE vs MELPHALAN
MEGLUMINE vs MEMANTINE