Does ALIROCUMAB Cause Device use issue? 471 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 471 reports of Device use issue have been filed in association with ALIROCUMAB (Praluent). This represents 2.1% of all adverse event reports for ALIROCUMAB.
471
Reports of Device use issue with ALIROCUMAB
2.1%
of all ALIROCUMAB reports
0
Deaths
12
Hospitalizations
How Dangerous Is Device use issue From ALIROCUMAB?
Of the 471 reports, 12 (2.5%) required hospitalization.
Is Device use issue Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for ALIROCUMAB. However, 471 reports have been filed with the FAERS database.
What Other Side Effects Does ALIROCUMAB Cause?
Myalgia (1,571)
Product dose omission (1,354)
Injection site pain (1,220)
Muscle spasms (1,113)
Arthralgia (993)
Fatigue (922)
Pain (892)
Pain in extremity (888)
Product dose omission issue (864)
Injection site bruising (821)
What Other Drugs Cause Device use issue?
SOMATROPIN (2,571)
LEVONORGESTREL (2,489)
COPPER (1,318)
BUDESONIDE\FORMOTEROL (1,236)
EXENATIDE (992)
BUDESONIDE\FORMOTEROL\GLYCOPYRROLATE (976)
DUPILUMAB (528)
INSULIN GLARGINE (469)
BUDESONIDE\FORMOTEROL\GLYCOPYRRONIUM (459)
LEVODOPA (443)
Which ALIROCUMAB Alternatives Have Lower Device use issue Risk?
ALIROCUMAB vs ALISKIREN
ALIROCUMAB vs ALISKIREN HEMIFUMARATE
ALIROCUMAB vs ALISKIREN\HYDROCHLOROTHIAZIDE
ALIROCUMAB vs ALIZAPRIDE
ALIROCUMAB vs ALLANTOIN