Does DIGOXIN Cause Intentional product use issue? 288 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 288 reports of Intentional product use issue have been filed in association with DIGOXIN (Digoxin). This represents 3.7% of all adverse event reports for DIGOXIN.
288
Reports of Intentional product use issue with DIGOXIN
3.7%
of all DIGOXIN reports
1
Deaths
105
Hospitalizations
How Dangerous Is Intentional product use issue From DIGOXIN?
Of the 288 reports, 1 (0.3%) resulted in death, 105 (36.5%) required hospitalization, and 76 (26.4%) were considered life-threatening.
Is Intentional product use issue Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for DIGOXIN. However, 288 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 Intentional product use issue?
INFLIXIMAB (11,028)
RITUXIMAB (9,602)
INFLIXIMAB-DYYB (7,549)
TOCILIZUMAB (5,078)
METHOTREXATE (4,087)
PREDNISONE (3,961)
ABATACEPT (3,693)
ADALIMUMAB (3,557)
NIVOLUMAB (3,297)
LEFLUNOMIDE (3,280)
Which DIGOXIN Alternatives Have Lower Intentional product use issue Risk?
DIGOXIN vs DIHYDRALAZINE
DIGOXIN vs DIHYDROCODEINE
DIGOXIN vs DIHYDROERGOTAMINE
DIGOXIN vs DILANTIN
DIGOXIN vs DILANTIN-125