Does ESOMEPRAZOLE Cause Intentional product misuse? 2,852 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 2,852 reports of Intentional product misuse have been filed in association with ESOMEPRAZOLE (Esomeprazole Magnesium). This represents 3.8% of all adverse event reports for ESOMEPRAZOLE.
2,852
Reports of Intentional product misuse with ESOMEPRAZOLE
3.8%
of all ESOMEPRAZOLE reports
25
Deaths
494
Hospitalizations
How Dangerous Is Intentional product misuse From ESOMEPRAZOLE?
Of the 2,852 reports, 25 (0.9%) resulted in death, 494 (17.3%) required hospitalization, and 125 (4.4%) were considered life-threatening.
Is Intentional product misuse Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for ESOMEPRAZOLE. However, 2,852 reports have been filed with the FAERS database.
What Other Side Effects Does ESOMEPRAZOLE Cause?
Chronic kidney disease (35,281)
Acute kidney injury (18,678)
Renal failure (14,633)
End stage renal disease (10,231)
Renal injury (9,440)
Gastrooesophageal reflux disease (4,746)
Drug ineffective (4,420)
Tubulointerstitial nephritis (4,024)
Off label use (3,180)
Pain (2,898)
What Other Drugs Cause Intentional product misuse?
ETANERCEPT (3,992)
PREGABALIN (3,731)
BUDESONIDE\FORMOTEROL (3,399)
ACETAMINOPHEN (2,924)
MINOXIDIL (2,418)
TOFACITINIB (2,331)
CINACALCET (2,092)
QUETIAPINE (1,855)
ALPRAZOLAM (1,709)
TERIPARATIDE (1,503)
Which ESOMEPRAZOLE Alternatives Have Lower Intentional product misuse Risk?
ESOMEPRAZOLE vs ESOMEPRAZOLE\ESOMEPRAZOLE\ESOMEPRAZOLE
ESOMEPRAZOLE vs ESOMEPRAZOLE\NAPROXEN
ESOMEPRAZOLE vs ESTAZOLAM
ESOMEPRAZOLE vs ESTRADIOL
ESOMEPRAZOLE vs ESTRADIOL CYPIONATE