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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 CERLIPONASE ALFA Cause Device dislocation? 5 Reports in FDA Database

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According to the FDA Adverse Event Reporting System (FAERS), 5 reports of Device dislocation have been filed in association with CERLIPONASE ALFA (Brineura). This represents 1.1% of all adverse event reports for CERLIPONASE ALFA.

5
Reports of Device dislocation with CERLIPONASE ALFA
1.1%
of all CERLIPONASE ALFA reports
0
Deaths
1
Hospitalizations

How Dangerous Is Device dislocation From CERLIPONASE ALFA?

Of the 5 reports, 1 (20.0%) required hospitalization.

Is Device dislocation Listed in the Official Label?

This adverse event is not currently listed in the official FDA drug label for CERLIPONASE ALFA. However, 5 reports have been filed with the FAERS database.

What Other Side Effects Does CERLIPONASE ALFA Cause?

Pyrexia (83) Seizure (65) Vomiting (35) Device related infection (27) Device leakage (26) Csf culture positive (23) Pneumonia (20) Headache (19) Drug ineffective (17) Off label use (17)

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 CERLIPONASE ALFA Alternatives Have Lower Device dislocation Risk?

CERLIPONASE ALFA vs CERTICAN CERLIPONASE ALFA vs CERTOLIZUMAB CERLIPONASE ALFA vs CERTOLIZUMAB PEGOL CERLIPONASE ALFA vs CERTOPARIN CERLIPONASE ALFA vs CETIRIZINE

Related Pages

CERLIPONASE ALFA Full Profile All Device dislocation Reports All Drugs Causing Device dislocation CERLIPONASE ALFA Demographics