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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 Device dislocation? 23 Reports in FDA Database

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According to the FDA Adverse Event Reporting System (FAERS), 23 reports of Device dislocation have been filed in association with DEVICE. This represents 0.2% of all adverse event reports for DEVICE.

23
Reports of Device dislocation with DEVICE
0.2%
of all DEVICE reports
0
Deaths
11
Hospitalizations

How Dangerous Is Device dislocation From DEVICE?

Of the 23 reports, 11 (47.8%) required hospitalization.

Is Device dislocation Listed in the Official Label?

This adverse event is not currently listed in the official FDA drug label for DEVICE. However, 23 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 Device dislocation?

LEVONORGESTREL (13,757) COPPER (6,955) CARBIDOPA\LEVODOPA (2,937) ETONOGESTREL (2,909) TREPROSTINIL (1,626) MIRENA (677) BACLOFEN (492) PARAGARD 380A (479) ADALIMUMAB (372) EPOPROSTENOL (358)

Which DEVICE Alternatives Have Lower Device dislocation 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 Device dislocation Reports All Drugs Causing Device dislocation DEVICE Demographics