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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 AFLIBERCEPT 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 AFLIBERCEPT (EYLEA). This represents 0.0% of all adverse event reports for AFLIBERCEPT.

7
Reports of Device dislocation with AFLIBERCEPT
0.0%
of all AFLIBERCEPT reports
0
Deaths
5
Hospitalizations

How Dangerous Is Device dislocation From AFLIBERCEPT?

Of the 7 reports, 5 (71.4%) required hospitalization.

Is Device dislocation Listed in the Official Label?

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

What Other Side Effects Does AFLIBERCEPT Cause?

Death (7,669) Visual impairment (1,836) Blindness (1,337) Endophthalmitis (1,289) Off label use (1,156) Eye pain (1,057) Product dose omission issue (1,051) Blindness unilateral (1,012) Vision blurred (1,012) Visual acuity reduced (993)

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 AFLIBERCEPT Alternatives Have Lower Device dislocation Risk?

AFLIBERCEPT vs AGALSIDASE ALFA AFLIBERCEPT vs AGALSIDASE BETA AFLIBERCEPT vs AGOMELATINE AFLIBERCEPT vs ALAWAY AFLIBERCEPT vs ALBENDAZOLE

Related Pages

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