Does DAPAGLIFLOZIN Cause Incorrect product administration duration? 21 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 21 reports of Incorrect product administration duration have been filed in association with DAPAGLIFLOZIN (QTERN). This represents 0.1% of all adverse event reports for DAPAGLIFLOZIN.
21
Reports of Incorrect product administration duration with DAPAGLIFLOZIN
0.1%
of all DAPAGLIFLOZIN reports
0
Deaths
21
Hospitalizations
How Dangerous Is Incorrect product administration duration From DAPAGLIFLOZIN?
Of the 21 reports, 21 (100.0%) required hospitalization, and 1 (4.8%) 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 DAPAGLIFLOZIN. However, 21 reports have been filed with the FAERS database.
What Other Side Effects Does DAPAGLIFLOZIN Cause?
Death (2,775)
Diabetic ketoacidosis (1,773)
Acute kidney injury (982)
Off label use (891)
Nausea (884)
Dehydration (860)
Vomiting (838)
Dizziness (817)
Ketoacidosis (803)
Fatigue (785)
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 DAPAGLIFLOZIN Alternatives Have Lower Incorrect product administration duration Risk?
DAPAGLIFLOZIN vs DAPAGLIFLOZIN PROPANEDIOL
DAPAGLIFLOZIN vs DAPAGLIFLOZIN PROPANEDIOL\METFORMIN
DAPAGLIFLOZIN vs DAPRODUSTAT
DAPAGLIFLOZIN vs DAPSONE
DAPAGLIFLOZIN vs DAPTOMYCIN