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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 breakage? 6 Reports in FDA Database

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According to the FDA Adverse Event Reporting System (FAERS), 6 reports of Device breakage have been filed in association with CERLIPONASE ALFA (Brineura). This represents 1.3% of all adverse event reports for CERLIPONASE ALFA.

6
Reports of Device breakage with CERLIPONASE ALFA
1.3%
of all CERLIPONASE ALFA reports
0
Deaths
2
Hospitalizations

How Dangerous Is Device breakage From CERLIPONASE ALFA?

Of the 6 reports, 2 (33.3%) required hospitalization, and 1 (16.7%) were considered life-threatening.

Is Device breakage Listed in the Official Label?

Yes, Device breakage is listed as a known adverse reaction in the official FDA drug label for CERLIPONASE ALFA.

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 breakage?

COPPER (9,201) SOMATROPIN (7,761) ETONOGESTREL (4,140) LEVONORGESTREL (2,726) ETHINYL ESTRADIOL\ETONOGESTREL (741) CARBIDOPA\LEVODOPA (634) TREPROSTINIL (396) ADALIMUMAB (375) ALBUTEROL (256) EPOPROSTENOL (240)

Which CERLIPONASE ALFA Alternatives Have Lower Device breakage 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 breakage Reports All Drugs Causing Device breakage CERLIPONASE ALFA Demographics