Does EVOLOCUMAB Cause Poor quality device used? 31 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 31 reports of Poor quality device used have been filed in association with EVOLOCUMAB (REPATHA). This represents 0.0% of all adverse event reports for EVOLOCUMAB.
31
Reports of Poor quality device used with EVOLOCUMAB
0.0%
of all EVOLOCUMAB reports
1
Deaths
1
Hospitalizations
How Dangerous Is Poor quality device used From EVOLOCUMAB?
Of the 31 reports, 1 (3.2%) resulted in death, 1 (3.2%) required hospitalization.
Is Poor quality device used Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for EVOLOCUMAB. However, 31 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 Poor quality device used?
SOMATROPIN (3,162)
MOMETASONE FUROATE (2,159)
ALBUTEROL (1,251)
FORMOTEROL\MOMETASONE FUROATE (1,091)
MEDROXYPROGESTERONE (80)
ETHINYL ESTRADIOL\ETONOGESTREL (77)
FOLLITROPIN (58)
ETONOGESTREL (55)
ETANERCEPT (46)
ESTRADIOL (41)
Which EVOLOCUMAB Alternatives Have Lower Poor quality device used Risk?
EVOLOCUMAB vs EXELON
EVOLOCUMAB vs EXEMESTANE
EVOLOCUMAB vs EXENATIDE
EVOLOCUMAB vs EXFORGE
EVOLOCUMAB vs EXJADE