Does ALIROCUMAB Cause Device issue? 785 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 785 reports of Device issue have been filed in association with ALIROCUMAB (Praluent). This represents 3.4% of all adverse event reports for ALIROCUMAB.
785
Reports of Device issue with ALIROCUMAB
3.4%
of all ALIROCUMAB reports
0
Deaths
23
Hospitalizations
How Dangerous Is Device issue From ALIROCUMAB?
Of the 785 reports, 23 (2.9%) required hospitalization.
Is Device issue Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for ALIROCUMAB. However, 785 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 issue?
ADALIMUMAB (17,630)
SOMATROPIN (5,131)
PEGFILGRASTIM (5,071)
ETANERCEPT (4,143)
INSULIN GLARGINE (3,175)
EXENATIDE (2,862)
LEVONORGESTREL (2,623)
CARBIDOPA\LEVODOPA (2,574)
GOLIMUMAB (1,827)
USTEKINUMAB (1,716)
Which ALIROCUMAB Alternatives Have Lower Device issue Risk?
ALIROCUMAB vs ALISKIREN
ALIROCUMAB vs ALISKIREN HEMIFUMARATE
ALIROCUMAB vs ALISKIREN\HYDROCHLOROTHIAZIDE
ALIROCUMAB vs ALIZAPRIDE
ALIROCUMAB vs ALLANTOIN