Does CERLIPONASE ALFA Cause Device issue? 10 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 10 reports of Device issue have been filed in association with CERLIPONASE ALFA (Brineura). This represents 2.1% of all adverse event reports for CERLIPONASE ALFA.
10
Reports of Device issue with CERLIPONASE ALFA
2.1%
of all CERLIPONASE ALFA reports
0
Deaths
2
Hospitalizations
How Dangerous Is Device issue From CERLIPONASE ALFA?
Of the 10 reports, 2 (20.0%) required hospitalization.
Is Device issue Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for CERLIPONASE ALFA. However, 10 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 issue?
ADALIMUMAB (17,630)
SOMATROPIN (5,131)
PEGFILGRASTIM (5,071)
ETANERCEPT (4,143)
INSULIN GLARGINE (3,175)
EXENATIDE (2,862)
LEVONORGESTREL (2,623)
CARBIDOPA\LEVODOPA (2,574)
GOLIMUMAB (1,827)
USTEKINUMAB (1,716)
Which CERLIPONASE ALFA Alternatives Have Lower Device issue Risk?
CERLIPONASE ALFA vs CERTICAN
CERLIPONASE ALFA vs CERTOLIZUMAB
CERLIPONASE ALFA vs CERTOLIZUMAB PEGOL
CERLIPONASE ALFA vs CERTOPARIN
CERLIPONASE ALFA vs CETIRIZINE