Does PEGINTERFERON BETA-1A Cause Product dispensing error? 12 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 12 reports of Product dispensing error have been filed in association with PEGINTERFERON BETA-1A (Plegridy Pen). This represents 0.1% of all adverse event reports for PEGINTERFERON BETA-1A.
12
Reports of Product dispensing error with PEGINTERFERON BETA-1A
0.1%
of all PEGINTERFERON BETA-1A reports
0
Deaths
1
Hospitalizations
How Dangerous Is Product dispensing error From PEGINTERFERON BETA-1A?
Of the 12 reports, 1 (8.3%) required hospitalization.
Is Product dispensing error Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for PEGINTERFERON BETA-1A. However, 12 reports have been filed with the FAERS database.
What Other Side Effects Does PEGINTERFERON BETA-1A Cause?
Influenza like illness (1,431)
Injection site erythema (1,041)
Multiple sclerosis relapse (945)
Fatigue (673)
Headache (587)
Pain (580)
Injection site reaction (569)
Device malfunction (567)
Multiple sclerosis (536)
Pyrexia (503)
What Other Drugs Cause Product dispensing error?
INSULIN GLARGINE (1,048)
FLUTICASONE FUROATE\UMECLIDINIUM\VILANTEROL TRIFENATATE (692)
ADALIMUMAB (386)
SEMAGLUTIDE (379)
PREGABALIN (323)
NIRMATRELVIR\RITONAVIR (310)
ETANERCEPT (305)
SECUKINUMAB (300)
APIXABAN (299)
PALBOCICLIB (299)
Which PEGINTERFERON BETA-1A Alternatives Have Lower Product dispensing error Risk?
PEGINTERFERON BETA-1A vs PEGINTRON
PEGINTERFERON BETA-1A vs PEGLOTICASE
PEGINTERFERON BETA-1A vs PEGUNIGALSIDASE ALFA-IWXJ
PEGINTERFERON BETA-1A vs PEGVALIASE-PQPZ
PEGINTERFERON BETA-1A vs PEGVISOMANT