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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 Intentional device misuse? 7 Reports in FDA Database

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According to the FDA Adverse Event Reporting System (FAERS), 7 reports of Intentional device misuse have been filed in association with DEVICE. This represents 0.1% of all adverse event reports for DEVICE.

7
Reports of Intentional device misuse with DEVICE
0.1%
of all DEVICE reports
0
Deaths
2
Hospitalizations

How Dangerous Is Intentional device misuse From DEVICE?

Of the 7 reports, 2 (28.6%) required hospitalization, and 1 (14.3%) were considered life-threatening.

Is Intentional device misuse Listed in the Official Label?

This adverse event is not currently listed in the official FDA drug label for DEVICE. However, 7 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 Intentional device misuse?

BUDESONIDE\FORMOTEROL (1,318) EXENATIDE (1,254) ACLIDINIUM (346) BUDESONIDE (292) BUDESONIDE\FORMOTEROL\GLYCOPYRRONIUM (182) SOMATROPIN (128) TERIPARATIDE (117) FORMOTEROL\GLYCOPYRROLATE (103) BUDESONIDE\FORMOTEROL\GLYCOPYRROLATE (102) CARBIDOPA\LEVODOPA (100)

Which DEVICE Alternatives Have Lower Intentional device misuse 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 Intentional device misuse Reports All Drugs Causing Intentional device misuse DEVICE Demographics