Does UNSPECIFIED INGREDIENT Cause Atrial fibrillation? 300 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 300 reports of Atrial fibrillation have been filed in association with UNSPECIFIED INGREDIENT. This represents 1.2% of all adverse event reports for UNSPECIFIED INGREDIENT.
300
Reports of Atrial fibrillation with UNSPECIFIED INGREDIENT
1.2%
of all UNSPECIFIED INGREDIENT reports
42
Deaths
204
Hospitalizations
How Dangerous Is Atrial fibrillation From UNSPECIFIED INGREDIENT?
Of the 300 reports, 42 (14.0%) resulted in death, 204 (68.0%) required hospitalization, and 27 (9.0%) were considered life-threatening.
Is Atrial fibrillation Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for UNSPECIFIED INGREDIENT. However, 300 reports have been filed with the FAERS database.
What Other Side Effects Does UNSPECIFIED INGREDIENT Cause?
Death (2,090)
Off label use (1,306)
Drug ineffective (1,227)
Completed suicide (1,190)
Nausea (1,041)
Fatigue (1,020)
Dyspnoea (934)
Pneumonia (903)
Asthenia (894)
Vomiting (877)
What Other Drugs Cause Atrial fibrillation?
APIXABAN (5,690)
IBRUTINIB (3,671)
LENALIDOMIDE (2,704)
RITUXIMAB (2,100)
SACUBITRIL\VALSARTAN (2,062)
RIVAROXABAN (2,027)
ADALIMUMAB (1,709)
METOPROLOL (1,462)
DEXAMETHASONE (1,461)
METHOTREXATE (1,411)
Which UNSPECIFIED INGREDIENT Alternatives Have Lower Atrial fibrillation Risk?
UNSPECIFIED INGREDIENT vs UPADACITINIB
UNSPECIFIED INGREDIENT vs URAPIDIL
UNSPECIFIED INGREDIENT vs UREA
UNSPECIFIED INGREDIENT vs URIDINE TRIACETATE
UNSPECIFIED INGREDIENT vs UROFOLLITROPIN