Does VONOPRAZAN Cause Incorrect product administration duration? 38 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 38 reports of Incorrect product administration duration have been filed in association with VONOPRAZAN (VOQUEZNA). This represents 1.9% of all adverse event reports for VONOPRAZAN.
38
Reports of Incorrect product administration duration with VONOPRAZAN
1.9%
of all VONOPRAZAN reports
0
Deaths
5
Hospitalizations
How Dangerous Is Incorrect product administration duration From VONOPRAZAN?
Of the 38 reports, 5 (13.2%) 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 VONOPRAZAN. However, 38 reports have been filed with the FAERS database.
What Other Side Effects Does VONOPRAZAN Cause?
Drug ineffective (305)
Off label use (188)
Gastrooesophageal reflux disease (162)
Nausea (138)
Diarrhoea (115)
Abdominal pain upper (107)
Dyspepsia (90)
Headache (80)
Abdominal distension (68)
Dizziness (68)
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 VONOPRAZAN Alternatives Have Lower Incorrect product administration duration Risk?
VONOPRAZAN vs VONOPRAZAN FUMURATE
VONOPRAZAN vs VORAPAXAR
VONOPRAZAN vs VORASIDENIB
VONOPRAZAN vs VORETIGENE NEPARVOVEC-RZYL
VONOPRAZAN vs VORICONAZOLE