Does EVOLOCUMAB Cause Intercepted product storage error? 40 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 40 reports of Intercepted product storage error have been filed in association with EVOLOCUMAB (REPATHA). This represents 0.0% of all adverse event reports for EVOLOCUMAB.
40
Reports of Intercepted product storage error with EVOLOCUMAB
0.0%
of all EVOLOCUMAB reports
0
Deaths
4
Hospitalizations
How Dangerous Is Intercepted product storage error From EVOLOCUMAB?
Of the 40 reports, 4 (10.0%) required hospitalization.
Is Intercepted product storage error Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for EVOLOCUMAB. However, 40 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 Intercepted product storage error?
TOCILIZUMAB (381)
DUPILUMAB (325)
OMALIZUMAB (256)
ALTEPLASE (227)
INSULIN GLARGINE (129)
DORNASE ALFA (115)
BEVACIZUMAB (113)
RITUXIMAB (105)
OCRELIZUMAB (88)
PERTUZUMAB (84)
Which EVOLOCUMAB Alternatives Have Lower Intercepted product storage error Risk?
EVOLOCUMAB vs EXELON
EVOLOCUMAB vs EXEMESTANE
EVOLOCUMAB vs EXENATIDE
EVOLOCUMAB vs EXFORGE
EVOLOCUMAB vs EXJADE