Does DIGOXIN Cause Incorrect product administration duration? 35 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 35 reports of Incorrect product administration duration have been filed in association with DIGOXIN (Digoxin). This represents 0.5% of all adverse event reports for DIGOXIN.
35
Reports of Incorrect product administration duration with DIGOXIN
0.5%
of all DIGOXIN reports
0
Deaths
24
Hospitalizations
How Dangerous Is Incorrect product administration duration From DIGOXIN?
Of the 35 reports, 24 (68.6%) required hospitalization, and 12 (34.3%) 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 DIGOXIN. However, 35 reports have been filed with the FAERS database.
What Other Side Effects Does DIGOXIN Cause?
Toxicity to various agents (1,371)
Bradycardia (896)
Dyspnoea (762)
Nausea (762)
Vomiting (715)
Acute kidney injury (708)
Fatigue (638)
Dizziness (616)
Diarrhoea (607)
Drug ineffective (568)
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 DIGOXIN Alternatives Have Lower Incorrect product administration duration Risk?
DIGOXIN vs DIHYDRALAZINE
DIGOXIN vs DIHYDROCODEINE
DIGOXIN vs DIHYDROERGOTAMINE
DIGOXIN vs DILANTIN
DIGOXIN vs DILANTIN-125