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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 OZURDEX Cause Device dislocation? 7 Reports in FDA Database

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According to the FDA Adverse Event Reporting System (FAERS), 7 reports of Device dislocation have been filed in association with OZURDEX. This represents 14.0% of all adverse event reports for OZURDEX.

7
Reports of Device dislocation with OZURDEX
14.0%
of all OZURDEX reports
0
Deaths
0
Hospitalizations

How Dangerous Is Device dislocation From OZURDEX?

Of the 7 reports.

Is Device dislocation Listed in the Official Label?

This adverse event is not currently listed in the official FDA drug label for OZURDEX. However, 7 reports have been filed with the FAERS database.

What Other Side Effects Does OZURDEX Cause?

Complication of device insertion (14) Visual acuity reduced (8) Cataract (7) Off label use (6) Corneal oedema (5) Endophthalmitis (5) Intraocular pressure increased (5)

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)

Related Pages

OZURDEX Full Profile All Device dislocation Reports All Drugs Causing Device dislocation OZURDEX Demographics