Does ALIROCUMAB Cause Product storage error? 341 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 341 reports of Product storage error have been filed in association with ALIROCUMAB (Praluent). This represents 1.5% of all adverse event reports for ALIROCUMAB.
341
Reports of Product storage error with ALIROCUMAB
1.5%
of all ALIROCUMAB reports
0
Deaths
18
Hospitalizations
How Dangerous Is Product storage error From ALIROCUMAB?
Of the 341 reports, 18 (5.3%) required hospitalization.
Is Product storage error Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for ALIROCUMAB. However, 341 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 storage error?
INSULIN GLARGINE (7,743)
EVOLOCUMAB (6,606)
ETANERCEPT (3,653)
DENOSUMAB (3,621)
ERENUMAB-AOOE (2,958)
DUPILUMAB (2,631)
ALBUTEROL (2,474)
ABATACEPT (2,101)
DARBEPOETIN ALFA (1,619)
INSULIN LISPRO (1,448)
Which ALIROCUMAB Alternatives Have Lower Product storage error Risk?
ALIROCUMAB vs ALISKIREN
ALIROCUMAB vs ALISKIREN HEMIFUMARATE
ALIROCUMAB vs ALISKIREN\HYDROCHLOROTHIAZIDE
ALIROCUMAB vs ALIZAPRIDE
ALIROCUMAB vs ALLANTOIN