Does ALIROCUMAB Cause Wrong schedule? 31 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 31 reports of Wrong schedule have been filed in association with ALIROCUMAB (Praluent). This represents 0.1% of all adverse event reports for ALIROCUMAB.
31
Reports of Wrong schedule with ALIROCUMAB
0.1%
of all ALIROCUMAB reports
0
Deaths
0
Hospitalizations
How Dangerous Is Wrong schedule From ALIROCUMAB?
Of the 31 reports, and 1 (3.2%) were considered life-threatening.
Is Wrong schedule Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for ALIROCUMAB. However, 31 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 Wrong schedule?
SECUKINUMAB (36)
GALCANEZUMAB-GNLM (30)
IXEKIZUMAB (27)
LAMOTRIGINE (27)
METHOTREXATE (27)
ETANERCEPT (26)
GLECAPREVIR\PIBRENTASVIR (21)
ADALIMUMAB (20)
DUPILUMAB (18)
INSULIN GLARGINE (17)
Which ALIROCUMAB Alternatives Have Lower Wrong schedule Risk?
ALIROCUMAB vs ALISKIREN
ALIROCUMAB vs ALISKIREN HEMIFUMARATE
ALIROCUMAB vs ALISKIREN\HYDROCHLOROTHIAZIDE
ALIROCUMAB vs ALIZAPRIDE
ALIROCUMAB vs ALLANTOIN