Does LANSOPRAZOLE Cause Incorrect product administration duration? 564 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 564 reports of Incorrect product administration duration have been filed in association with LANSOPRAZOLE (Lansoprazole). This represents 0.9% of all adverse event reports for LANSOPRAZOLE.
564
Reports of Incorrect product administration duration with LANSOPRAZOLE
0.9%
of all LANSOPRAZOLE reports
3
Deaths
25
Hospitalizations
How Dangerous Is Incorrect product administration duration From LANSOPRAZOLE?
Of the 564 reports, 3 (0.5%) resulted in death, 25 (4.4%) required hospitalization, and 4 (0.7%) were considered life-threatening.
Is Incorrect product administration duration Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for LANSOPRAZOLE. However, 564 reports have been filed with the FAERS database.
What Other Side Effects Does LANSOPRAZOLE Cause?
Chronic kidney disease (32,517)
Acute kidney injury (16,359)
Renal failure (12,509)
End stage renal disease (9,734)
Renal injury (9,383)
Tubulointerstitial nephritis (3,860)
Death (2,517)
Gastrooesophageal reflux disease (2,482)
Off label use (2,183)
Nephrogenic anaemia (2,162)
What Other Drugs Cause Incorrect product administration duration?
ETONOGESTREL (3,974)
POLYETHYLENE GLYCOL 3350 (2,129)
NIRMATRELVIR\RITONAVIR (744)
DOCOSANOL (634)
LOPERAMIDE (543)
NAPROXEN (499)
INSULIN LISPRO (479)
DICLOFENAC (362)
OMEPRAZOLE (302)
ALENDRONATE (287)
Which LANSOPRAZOLE Alternatives Have Lower Incorrect product administration duration Risk?
LANSOPRAZOLE vs LANTHANUM
LANSOPRAZOLE vs LANTUS
LANSOPRAZOLE vs LANTUS SOLOSTAR
LANSOPRAZOLE vs LAPATINIB
LANSOPRAZOLE vs LAPATINIB DITOSYLATE