Does UNSPECIFIED INGREDIENT Cause Dizziness? 692 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 692 reports of Dizziness have been filed in association with UNSPECIFIED INGREDIENT. This represents 2.6% of all adverse event reports for UNSPECIFIED INGREDIENT.
692
Reports of Dizziness with UNSPECIFIED INGREDIENT
2.6%
of all UNSPECIFIED INGREDIENT reports
88
Deaths
283
Hospitalizations
How Dangerous Is Dizziness From UNSPECIFIED INGREDIENT?
Of the 692 reports, 88 (12.7%) resulted in death, 283 (40.9%) required hospitalization, and 78 (11.3%) were considered life-threatening.
Is Dizziness Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for UNSPECIFIED INGREDIENT. However, 692 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 Dizziness?
ADALIMUMAB (10,324)
SACUBITRIL\VALSARTAN (8,548)
TREPROSTINIL (7,405)
DULOXETINE (6,983)
LENALIDOMIDE (6,138)
ETANERCEPT (5,928)
METHOTREXATE (5,895)
PREGABALIN (5,878)
TERIPARATIDE (5,539)
AMBRISENTAN (4,561)
Which UNSPECIFIED INGREDIENT Alternatives Have Lower Dizziness Risk?
UNSPECIFIED INGREDIENT vs UPADACITINIB
UNSPECIFIED INGREDIENT vs URAPIDIL
UNSPECIFIED INGREDIENT vs UREA
UNSPECIFIED INGREDIENT vs URIDINE TRIACETATE
UNSPECIFIED INGREDIENT vs UROFOLLITROPIN