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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 Adverse reaction? 8 Reports in FDA Database

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According to the FDA Adverse Event Reporting System (FAERS), 8 reports of Adverse reaction have been filed in association with DEVICE. This represents 0.1% of all adverse event reports for DEVICE.

8
Reports of Adverse reaction with DEVICE
0.1%
of all DEVICE reports
1
Deaths
1
Hospitalizations

How Dangerous Is Adverse reaction From DEVICE?

Of the 8 reports, 1 (12.5%) resulted in death, 1 (12.5%) required hospitalization, and 1 (12.5%) were considered life-threatening.

Is Adverse reaction Listed in the Official Label?

This adverse event is not currently listed in the official FDA drug label for DEVICE. However, 8 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 Adverse reaction?

ETANERCEPT (1,316) ADALIMUMAB (987) METHOTREXATE (808) LEFLUNOMIDE (696) DIMETHYL (577) HYDROXYCHLOROQUINE (566) RITUXIMAB (537) APREMILAST (524) ERENUMAB-AOOE (518) CERTOLIZUMAB PEGOL (511)

Which DEVICE Alternatives Have Lower Adverse reaction 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 Adverse reaction Reports All Drugs Causing Adverse reaction DEVICE Demographics