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Important: This site presents data from the FDA Adverse Event Reporting System (FAERS). A report does not mean the drug caused the event. Full disclaimer.

Does MEGLUMINE Cause Product use issue? 114 Reports in FDA Database

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According to the FDA Adverse Event Reporting System (FAERS), 114 reports of Product use issue have been filed in association with MEGLUMINE. This represents 19.5% of all adverse event reports for MEGLUMINE.

114
Reports of Product use issue with MEGLUMINE
19.5%
of all MEGLUMINE reports
111
Deaths
111
Hospitalizations

How Dangerous Is Product use issue From MEGLUMINE?

Of the 114 reports, 111 (97.4%) resulted in death, 111 (97.4%) required hospitalization, and 112 (98.2%) were considered life-threatening.

Is Product use issue Listed in the Official Label?

This adverse event is not currently listed in the official FDA drug label for MEGLUMINE. However, 114 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 use issue?

INFLIXIMAB (12,752) DUPILUMAB (10,575) POLYETHYLENE GLYCOL 3350 (9,432) METHOTREXATE (8,185) DICLOFENAC (8,009) RITUXIMAB (6,948) ADALIMUMAB (6,379) ETANERCEPT (6,062) TOCILIZUMAB (5,944) ABATACEPT (5,915)

Which MEGLUMINE Alternatives Have Lower Product use issue Risk?

MEGLUMINE vs MELATONIN MEGLUMINE vs MELOXICAM MEGLUMINE vs MELPERONE MEGLUMINE vs MELPHALAN MEGLUMINE vs MEMANTINE

Related Pages

MEGLUMINE Full Profile All Product use issue Reports All Drugs Causing Product use issue MEGLUMINE Demographics