Does EVOLOCUMAB Cause Product storage error? 6,606 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 6,606 reports of Product storage error have been filed in association with EVOLOCUMAB (REPATHA). This represents 4.4% of all adverse event reports for EVOLOCUMAB.
6,606
Reports of Product storage error with EVOLOCUMAB
4.4%
of all EVOLOCUMAB reports
2
Deaths
88
Hospitalizations
How Dangerous Is Product storage error From EVOLOCUMAB?
Of the 6,606 reports, 2 (0.0%) resulted in death, 88 (1.3%) required hospitalization, and 1 (0.0%) were considered life-threatening.
Is Product storage error Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for EVOLOCUMAB. However, 6,606 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)
Back pain (5,254)
Myalgia (5,061)
Drug dose omission (4,914)
Injection site bruising (4,409)
Device use error (4,002)
What Other Drugs Cause Product storage error?
INSULIN GLARGINE (7,743)
ETANERCEPT (3,653)
DENOSUMAB (3,621)
ERENUMAB-AOOE (2,958)
DUPILUMAB (2,631)
ALBUTEROL (2,474)
ABATACEPT (2,101)
DARBEPOETIN ALFA (1,619)
INSULIN LISPRO (1,448)
USTEKINUMAB (1,338)
Which EVOLOCUMAB Alternatives Have Lower Product storage error Risk?
EVOLOCUMAB vs EXELON
EVOLOCUMAB vs EXEMESTANE
EVOLOCUMAB vs EXENATIDE
EVOLOCUMAB vs EXFORGE
EVOLOCUMAB vs EXJADE