Does EVOLOCUMAB Cause Device use error? 4,002 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 4,002 reports of Device use error have been filed in association with EVOLOCUMAB (REPATHA). This represents 2.7% of all adverse event reports for EVOLOCUMAB.
4,002
Reports of Device use error with EVOLOCUMAB
2.7%
of all EVOLOCUMAB reports
0
Deaths
76
Hospitalizations
How Dangerous Is Device use error From EVOLOCUMAB?
Of the 4,002 reports, 76 (1.9%) required hospitalization.
Is Device use error Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for EVOLOCUMAB. However, 4,002 reports have been filed with the FAERS database.
What Other Side Effects Does EVOLOCUMAB Cause?
Device difficult to use (31,807)
Drug dose omission by device (23,957)
Wrong technique in product usage process (21,664)
Accidental exposure to product (16,160)
Injection site pain (9,988)
Product storage error (6,606)
Back pain (5,254)
Myalgia (5,061)
Drug dose omission (4,914)
Injection site bruising (4,409)
What Other Drugs Cause Device use error?
PEGFILGRASTIM (6,001)
ALBUTEROL (5,215)
ALBIGLUTIDE (4,056)
SOMATROPIN (2,801)
FLUTICASONE\SALMETEROL (1,749)
FLUTICASONE (783)
FLUTICASONE FUROATE\VILANTEROL TRIFENATATE (766)
ERENUMAB-AOOE (711)
ETANERCEPT (665)
TREPROSTINIL (563)
Which EVOLOCUMAB Alternatives Have Lower Device use error Risk?
EVOLOCUMAB vs EXELON
EVOLOCUMAB vs EXEMESTANE
EVOLOCUMAB vs EXENATIDE
EVOLOCUMAB vs EXFORGE
EVOLOCUMAB vs EXJADE