Does DEXLANSOPRAZOLE Cause Incorrect product administration duration? 207 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 207 reports of Incorrect product administration duration have been filed in association with DEXLANSOPRAZOLE (Dexlansoprazole). This represents 0.9% of all adverse event reports for DEXLANSOPRAZOLE.
207
Reports of Incorrect product administration duration with DEXLANSOPRAZOLE
0.9%
of all DEXLANSOPRAZOLE reports
2
Deaths
15
Hospitalizations
How Dangerous Is Incorrect product administration duration From DEXLANSOPRAZOLE?
Of the 207 reports, 2 (1.0%) resulted in death, 15 (7.2%) required hospitalization.
Is Incorrect product administration duration Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for DEXLANSOPRAZOLE. However, 207 reports have been filed with the FAERS database.
What Other Side Effects Does DEXLANSOPRAZOLE Cause?
Chronic kidney disease (15,973)
Acute kidney injury (7,599)
Renal failure (6,618)
End stage renal disease (4,800)
Renal injury (4,320)
Tubulointerstitial nephritis (2,177)
Death (1,417)
Rebound acid hypersecretion (1,160)
Gastrooesophageal reflux disease (1,013)
Drug ineffective (859)
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 DEXLANSOPRAZOLE Alternatives Have Lower Incorrect product administration duration Risk?
DEXLANSOPRAZOLE vs DEXMEDETOMIDINE
DEXLANSOPRAZOLE vs DEXMETHYLPHENIDATE
DEXLANSOPRAZOLE vs DEXMETHYLPHENIDATE\SERDEXMETHYLPHENIDATE
DEXLANSOPRAZOLE vs DEXPANTHENOL
DEXLANSOPRAZOLE vs DEXRAZOXANE