Does ESOMEPRAZOLE\NAPROXEN Cause Product administration error? 7 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 7 reports of Product administration error have been filed in association with ESOMEPRAZOLE\NAPROXEN. This represents 0.1% of all adverse event reports for ESOMEPRAZOLE\NAPROXEN.
7
Reports of Product administration error with ESOMEPRAZOLE\NAPROXEN
0.1%
of all ESOMEPRAZOLE\NAPROXEN reports
0
Deaths
0
Hospitalizations
How Dangerous Is Product administration error From ESOMEPRAZOLE\NAPROXEN?
Of the 7 reports.
Is Product administration error Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for ESOMEPRAZOLE\NAPROXEN. However, 7 reports have been filed with the FAERS database.
What Other Side Effects Does ESOMEPRAZOLE\NAPROXEN Cause?
Chronic kidney disease (2,714)
Renal failure (2,374)
Acute kidney injury (1,120)
Death (705)
Drug ineffective (459)
Off label use (440)
Nausea (431)
End stage renal disease (349)
Tubulointerstitial nephritis (315)
Hyperhidrosis (308)
What Other Drugs Cause Product administration error?
HYDROXYPROGESTERONE CAPROATE (972)
ACETAMINOPHEN (666)
CENEGERMIN-BKBJ (613)
LEUPROLIDE (595)
EVOLOCUMAB (565)
ADALIMUMAB (543)
METHYLPHENIDATE (414)
OLMESARTAN MEDOXOMIL (314)
ASPIRIN (241)
SECUKINUMAB (225)
Which ESOMEPRAZOLE\NAPROXEN Alternatives Have Lower Product administration error Risk?
ESOMEPRAZOLE\NAPROXEN vs ESTAZOLAM
ESOMEPRAZOLE\NAPROXEN vs ESTRADIOL
ESOMEPRAZOLE\NAPROXEN vs ESTRADIOL CYPIONATE
ESOMEPRAZOLE\NAPROXEN vs ESTRADIOL\LEVONORGESTREL
ESOMEPRAZOLE\NAPROXEN vs ESTRADIOL\NORETHINDRONE