Does EVOLOCUMAB Cause Drug dose omission by device? 23,957 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 23,957 reports of Drug dose omission by device have been filed in association with EVOLOCUMAB (REPATHA). This represents 16.0% of all adverse event reports for EVOLOCUMAB.
23,957
Reports of Drug dose omission by device with EVOLOCUMAB
16.0%
of all EVOLOCUMAB reports
7
Deaths
327
Hospitalizations
How Dangerous Is Drug dose omission by device From EVOLOCUMAB?
Of the 23,957 reports, 7 (0.0%) resulted in death, 327 (1.4%) required hospitalization, and 9 (0.0%) were considered life-threatening.
Is Drug dose omission by device Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for EVOLOCUMAB. However, 23,957 reports have been filed with the FAERS database.
What Other Side Effects Does EVOLOCUMAB Cause?
Device difficult to use (31,807)
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)
Device use error (4,002)
What Other Drugs Cause Drug dose omission by device?
SOMATROPIN (15,921)
ALBUTEROL (8,162)
ERENUMAB-AOOE (6,340)
ETANERCEPT (2,420)
PEGFILGRASTIM (2,051)
EXENATIDE (983)
SECUKINUMAB (621)
BUDESONIDE\FORMOTEROL (521)
MEDROXYPROGESTERONE (510)
BUDESONIDE\FORMOTEROL\GLYCOPYRROLATE (427)
Which EVOLOCUMAB Alternatives Have Lower Drug dose omission by device Risk?
EVOLOCUMAB vs EXELON
EVOLOCUMAB vs EXEMESTANE
EVOLOCUMAB vs EXENATIDE
EVOLOCUMAB vs EXFORGE
EVOLOCUMAB vs EXJADE