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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 DEVICE Cause Dizziness? 268 Reports in FDA Database

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According to the FDA Adverse Event Reporting System (FAERS), 268 reports of Dizziness have been filed in association with DEVICE. This represents 2.1% of all adverse event reports for DEVICE.

268
Reports of Dizziness with DEVICE
2.1%
of all DEVICE reports
5
Deaths
62
Hospitalizations

How Dangerous Is Dizziness From DEVICE?

Of the 268 reports, 5 (1.9%) resulted in death, 62 (23.1%) required hospitalization, and 9 (3.4%) 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 DEVICE. However, 268 reports have been filed with the FAERS database.

What Other Side Effects Does DEVICE Cause?

Blood glucose increased (2,114) Device issue (1,417) Product use issue (1,076) Intercepted product preparation error (1,033) Wrong technique in product usage process (935) Device leakage (795) Injection site pain (751) Syringe issue (634) Product quality issue (567) Drug ineffective (488)

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 DEVICE Alternatives Have Lower Dizziness Risk?

DEVICE vs DEXAMETHASONE DEVICE vs DEXAMETHASONE\DEXAMETHASONE DEVICE vs DEXAMETHASONE\NEOMYCIN DEVICE vs DEXAMETHASONE\NEOMYCIN\POLYMYXIN B DEVICE vs DEXAMETHASONE\TOBRAMYCIN

Related Pages

DEVICE Full Profile All Dizziness Reports All Drugs Causing Dizziness DEVICE Demographics