Does MEGLUMINE Cause Incorrect product administration duration? 38 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 38 reports of Incorrect product administration duration have been filed in association with MEGLUMINE. This represents 6.5% of all adverse event reports for MEGLUMINE.
38
Reports of Incorrect product administration duration with MEGLUMINE
6.5%
of all MEGLUMINE reports
38
Deaths
37
Hospitalizations
How Dangerous Is Incorrect product administration duration From MEGLUMINE?
Of the 38 reports, 38 (100.0%) resulted in death, 37 (97.4%) required hospitalization, and 37 (97.4%) were considered life-threatening.
Is Incorrect product administration duration Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for MEGLUMINE. However, 38 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 Incorrect product administration duration?
ETONOGESTREL (3,974)
POLYETHYLENE GLYCOL 3350 (2,129)
NIRMATRELVIR\RITONAVIR (744)
DOCOSANOL (634)
LANSOPRAZOLE (564)
LOPERAMIDE (543)
NAPROXEN (499)
INSULIN LISPRO (479)
DICLOFENAC (362)
OMEPRAZOLE (302)
Which MEGLUMINE Alternatives Have Lower Incorrect product administration duration Risk?
MEGLUMINE vs MELATONIN
MEGLUMINE vs MELOXICAM
MEGLUMINE vs MELPERONE
MEGLUMINE vs MELPHALAN
MEGLUMINE vs MEMANTINE