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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 ENBUCRILATE Cause Device dislocation? 11 Reports in FDA Database

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According to the FDA Adverse Event Reporting System (FAERS), 11 reports of Device dislocation have been filed in association with ENBUCRILATE. This represents 12.5% of all adverse event reports for ENBUCRILATE.

11
Reports of Device dislocation with ENBUCRILATE
12.5%
of all ENBUCRILATE reports
0
Deaths
1
Hospitalizations

How Dangerous Is Device dislocation From ENBUCRILATE?

Of the 11 reports, 1 (9.1%) required hospitalization.

Is Device dislocation Listed in the Official Label?

This adverse event is not currently listed in the official FDA drug label for ENBUCRILATE. However, 11 reports have been filed with the FAERS database.

What Other Side Effects Does ENBUCRILATE Cause?

Product use in unapproved indication (36) Off label use (6) Splenic infarction (6)

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

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