Does BETA.-ACETYLDIGOXIN Cause Condition aggravated? 13 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 13 reports of Condition aggravated have been filed in association with BETA.-ACETYLDIGOXIN. This represents 24.1% of all adverse event reports for BETA.-ACETYLDIGOXIN.
13
Reports of Condition aggravated with BETA.-ACETYLDIGOXIN
24.1%
of all BETA.-ACETYLDIGOXIN reports
13
Deaths
13
Hospitalizations
How Dangerous Is Condition aggravated From BETA.-ACETYLDIGOXIN?
Of the 13 reports, 13 (100.0%) resulted in death, 13 (100.0%) required hospitalization, and 12 (92.3%) were considered life-threatening.
Is Condition aggravated Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for BETA.-ACETYLDIGOXIN. However, 13 reports have been filed with the FAERS database.
What Other Side Effects Does BETA.-ACETYLDIGOXIN Cause?
Toxic epidermal necrolysis (34)
Respiratory disorder (22)
Multiple organ dysfunction syndrome (21)
Diarrhoea (18)
Restlessness (18)
Cholecystitis (17)
Electrolyte imbalance (17)
Hyperthyroidism (17)
Nausea (17)
Blister (16)
What Other Drugs Cause Condition aggravated?
TOFACITINIB (16,925)
INFLIXIMAB (16,616)
DUPILUMAB (16,459)
ETANERCEPT (15,897)
METHOTREXATE (14,938)
ADALIMUMAB (13,527)
PREDNISONE (10,751)
INFLIXIMAB-DYYB (10,275)
HYDROXYCHLOROQUINE (8,848)
RITUXIMAB (8,627)