Does MEGLUMINE Cause Product quality issue? 206 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 206 reports of Product quality issue have been filed in association with MEGLUMINE. This represents 35.2% of all adverse event reports for MEGLUMINE.
206
Reports of Product quality issue with MEGLUMINE
35.2%
of all MEGLUMINE reports
206
Deaths
199
Hospitalizations
How Dangerous Is Product quality issue From MEGLUMINE?
Of the 206 reports, 206 (100.0%) resulted in death, 199 (96.6%) required hospitalization, and 204 (99.0%) were considered life-threatening.
Is Product quality issue Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for MEGLUMINE. However, 206 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 quality issue?
ETONOGESTREL (4,651)
ALBUTEROL (4,466)
TIOTROPIUM (3,821)
MOMETASONE FUROATE (3,406)
LIDOCAINE (3,126)
FLUTICASONE\SALMETEROL (2,986)
FORMOTEROL\MOMETASONE FUROATE (2,458)
FENTANYL (2,450)
NICOTINE (1,987)
EXENATIDE (1,839)
Which MEGLUMINE Alternatives Have Lower Product quality issue Risk?
MEGLUMINE vs MELATONIN
MEGLUMINE vs MELOXICAM
MEGLUMINE vs MELPERONE
MEGLUMINE vs MELPHALAN
MEGLUMINE vs MEMANTINE