Does MEGLUMINE Cause Intentional product use issue? 236 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 236 reports of Intentional product use issue have been filed in association with MEGLUMINE. This represents 40.3% of all adverse event reports for MEGLUMINE.
236
Reports of Intentional product use issue with MEGLUMINE
40.3%
of all MEGLUMINE reports
233
Deaths
229
Hospitalizations
How Dangerous Is Intentional product use issue From MEGLUMINE?
Of the 236 reports, 233 (98.7%) resulted in death, 229 (97.0%) required hospitalization, and 235 (99.6%) were considered life-threatening.
Is Intentional product use issue Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for MEGLUMINE. However, 236 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 Intentional product use issue?
INFLIXIMAB (11,028)
RITUXIMAB (9,602)
INFLIXIMAB-DYYB (7,549)
TOCILIZUMAB (5,078)
METHOTREXATE (4,087)
PREDNISONE (3,961)
ABATACEPT (3,693)
ADALIMUMAB (3,557)
NIVOLUMAB (3,297)
LEFLUNOMIDE (3,280)
Which MEGLUMINE Alternatives Have Lower Intentional product use issue Risk?
MEGLUMINE vs MELATONIN
MEGLUMINE vs MELOXICAM
MEGLUMINE vs MELPERONE
MEGLUMINE vs MELPHALAN
MEGLUMINE vs MEMANTINE