Does EVOLOCUMAB Cause Device issue? 1,659 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 1,659 reports of Device issue have been filed in association with EVOLOCUMAB (REPATHA). This represents 1.1% of all adverse event reports for EVOLOCUMAB.
1,659
Reports of Device issue with EVOLOCUMAB
1.1%
of all EVOLOCUMAB reports
0
Deaths
34
Hospitalizations
How Dangerous Is Device issue From EVOLOCUMAB?
Of the 1,659 reports, 34 (2.0%) required hospitalization, and 4 (0.2%) were considered life-threatening.
Is Device issue Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for EVOLOCUMAB. However, 1,659 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 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 EVOLOCUMAB Alternatives Have Lower Device issue Risk?
EVOLOCUMAB vs EXELON
EVOLOCUMAB vs EXEMESTANE
EVOLOCUMAB vs EXENATIDE
EVOLOCUMAB vs EXFORGE
EVOLOCUMAB vs EXJADE