Does EVOLOCUMAB Cause Product dispensing error? 209 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 209 reports of Product dispensing error have been filed in association with EVOLOCUMAB (REPATHA). This represents 0.1% of all adverse event reports for EVOLOCUMAB.
209
Reports of Product dispensing error with EVOLOCUMAB
0.1%
of all EVOLOCUMAB reports
0
Deaths
5
Hospitalizations
How Dangerous Is Product dispensing error From EVOLOCUMAB?
Of the 209 reports, 5 (2.4%) required hospitalization, and 1 (0.5%) were considered life-threatening.
Is Product dispensing error Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for EVOLOCUMAB. However, 209 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 Product dispensing error?
INSULIN GLARGINE (1,048)
FLUTICASONE FUROATE\UMECLIDINIUM\VILANTEROL TRIFENATATE (692)
ADALIMUMAB (386)
SEMAGLUTIDE (379)
PREGABALIN (323)
NIRMATRELVIR\RITONAVIR (310)
ETANERCEPT (305)
SECUKINUMAB (300)
APIXABAN (299)
PALBOCICLIB (299)
Which EVOLOCUMAB Alternatives Have Lower Product dispensing error Risk?
EVOLOCUMAB vs EXELON
EVOLOCUMAB vs EXEMESTANE
EVOLOCUMAB vs EXENATIDE
EVOLOCUMAB vs EXFORGE
EVOLOCUMAB vs EXJADE