Does ALIROCUMAB Cause Product preparation error? 402 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 402 reports of Product preparation error have been filed in association with ALIROCUMAB (Praluent). This represents 1.8% of all adverse event reports for ALIROCUMAB.
402
Reports of Product preparation error with ALIROCUMAB
1.8%
of all ALIROCUMAB reports
0
Deaths
8
Hospitalizations
How Dangerous Is Product preparation error From ALIROCUMAB?
Of the 402 reports, 8 (2.0%) required hospitalization.
Is Product preparation error Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for ALIROCUMAB. However, 402 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 Product preparation error?
ONABOTULINUMTOXINA (3,593)
EVOLOCUMAB (2,785)
DUPILUMAB (2,707)
BUPRENORPHINE\NALOXONE (777)
ABOBOTULINUMTOXINA (751)
ALBIGLUTIDE (691)
ALBUTEROL (520)
PEGFILGRASTIM (473)
LEUPROLIDE (400)
SODIUM OXYBATE (222)
Which ALIROCUMAB Alternatives Have Lower Product preparation error Risk?
ALIROCUMAB vs ALISKIREN
ALIROCUMAB vs ALISKIREN HEMIFUMARATE
ALIROCUMAB vs ALISKIREN\HYDROCHLOROTHIAZIDE
ALIROCUMAB vs ALIZAPRIDE
ALIROCUMAB vs ALLANTOIN