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Important: This site presents data from the FDA Adverse Event Reporting System (FAERS). A report does not mean the drug caused the event. Full disclaimer.

Does UNSPECIFIED INGREDIENT Cause Aortic stenosis? 34 Reports in FDA Database

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According to the FDA Adverse Event Reporting System (FAERS), 34 reports of Aortic stenosis have been filed in association with UNSPECIFIED INGREDIENT. This represents 0.1% of all adverse event reports for UNSPECIFIED INGREDIENT.

34
Reports of Aortic stenosis with UNSPECIFIED INGREDIENT
0.1%
of all UNSPECIFIED INGREDIENT reports
29
Deaths
30
Hospitalizations

How Dangerous Is Aortic stenosis From UNSPECIFIED INGREDIENT?

Of the 34 reports, 29 (85.3%) resulted in death, 30 (88.2%) required hospitalization, and 24 (70.6%) were considered life-threatening.

Is Aortic stenosis Listed in the Official Label?

This adverse event is not currently listed in the official FDA drug label for UNSPECIFIED INGREDIENT. However, 34 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 Aortic stenosis?

WARFARIN (111) ADALIMUMAB (102) ALBUTEROL (95) IPRATROPIUM (82) ONDANSETRON (82) POTASSIUM (81) AMLODIPINE (80) ROSIGLITAZONE (79) FUROSEMIDE (75) LANSOPRAZOLE (75)

Which UNSPECIFIED INGREDIENT Alternatives Have Lower Aortic stenosis Risk?

UNSPECIFIED INGREDIENT vs UPADACITINIB UNSPECIFIED INGREDIENT vs URAPIDIL UNSPECIFIED INGREDIENT vs UREA UNSPECIFIED INGREDIENT vs URIDINE TRIACETATE UNSPECIFIED INGREDIENT vs UROFOLLITROPIN

Related Pages

UNSPECIFIED INGREDIENT Full Profile All Aortic stenosis Reports All Drugs Causing Aortic stenosis UNSPECIFIED INGREDIENT Demographics