Does EVOLOCUMAB Cause Incorrect dose administered by device? 2,840 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 2,840 reports of Incorrect dose administered by device have been filed in association with EVOLOCUMAB (REPATHA). This represents 1.9% of all adverse event reports for EVOLOCUMAB.
2,840
Reports of Incorrect dose administered by device with EVOLOCUMAB
1.9%
of all EVOLOCUMAB reports
0
Deaths
39
Hospitalizations
How Dangerous Is Incorrect dose administered by device From EVOLOCUMAB?
Of the 2,840 reports, 39 (1.4%) required hospitalization, and 3 (0.1%) were considered life-threatening.
Is Incorrect dose administered by device Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for EVOLOCUMAB. However, 2,840 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 Incorrect dose administered by device?
EXENATIDE (3,332)
SOMATROPIN (2,486)
ALBUTEROL (1,236)
ETANERCEPT (1,032)
SECUKINUMAB (996)
ERENUMAB-AOOE (973)
BUDESONIDE\FORMOTEROL (753)
INSULIN GLARGINE (753)
BUDESONIDE\FORMOTEROL\GLYCOPYRROLATE (674)
PEGFILGRASTIM (487)
Which EVOLOCUMAB Alternatives Have Lower Incorrect dose administered by device Risk?
EVOLOCUMAB vs EXELON
EVOLOCUMAB vs EXEMESTANE
EVOLOCUMAB vs EXENATIDE
EVOLOCUMAB vs EXFORGE
EVOLOCUMAB vs EXJADE