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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 Tremor? 167 Reports in FDA Database

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According to the FDA Adverse Event Reporting System (FAERS), 167 reports of Tremor have been filed in association with DEVICE. This represents 1.3% of all adverse event reports for DEVICE.

167
Reports of Tremor with DEVICE
1.3%
of all DEVICE reports
3
Deaths
27
Hospitalizations

How Dangerous Is Tremor From DEVICE?

Of the 167 reports, 3 (1.8%) resulted in death, 27 (16.2%) required hospitalization, and 7 (4.2%) were considered life-threatening.

Is Tremor Listed in the Official Label?

This adverse event is not currently listed in the official FDA drug label for DEVICE. However, 167 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 Tremor?

CARBIDOPA\LEVODOPA (3,689) DULOXETINE (2,493) LENALIDOMIDE (2,342) PREGABALIN (2,122) SERTRALINE (2,035) ADALIMUMAB (1,979) ARIPIPRAZOLE (1,921) QUETIAPINE (1,883) GABAPENTIN (1,553) VALBENAZINE (1,455)

Which DEVICE Alternatives Have Lower Tremor 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 Tremor Reports All Drugs Causing Tremor DEVICE Demographics