Does ALPHA.-ACETYLDIGOXIN Cause Condition aggravated? 6 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 6 reports of Condition aggravated have been filed in association with ALPHA.-ACETYLDIGOXIN. This represents 37.5% of all adverse event reports for ALPHA.-ACETYLDIGOXIN.
6
Reports of Condition aggravated with ALPHA.-ACETYLDIGOXIN
37.5%
of all ALPHA.-ACETYLDIGOXIN reports
6
Deaths
6
Hospitalizations
How Dangerous Is Condition aggravated From ALPHA.-ACETYLDIGOXIN?
Of the 6 reports, 6 (100.0%) resulted in death, 6 (100.0%) required hospitalization, and 5 (83.3%) 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 ALPHA.-ACETYLDIGOXIN. However, 6 reports have been filed with the FAERS database.
What Other Side Effects Does ALPHA.-ACETYLDIGOXIN Cause?
Blister (7)
Cholecystitis (7)
Cholelithiasis (7)
Dermatitis exfoliative (7)
Diarrhoea (7)
Electrolyte imbalance (7)
Erythema (7)
Hyperthyroidism (7)
Multiple organ dysfunction syndrome (7)
Nausea (7)
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)