Does PEGINTERFERON BETA-1A Cause Device defective? 7 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 7 reports of Device defective have been filed in association with PEGINTERFERON BETA-1A (Plegridy Pen). This represents 0.1% of all adverse event reports for PEGINTERFERON BETA-1A.
7
Reports of Device defective with PEGINTERFERON BETA-1A
0.1%
of all PEGINTERFERON BETA-1A reports
0
Deaths
2
Hospitalizations
How Dangerous Is Device defective From PEGINTERFERON BETA-1A?
Of the 7 reports, 2 (28.6%) required hospitalization.
Is Device defective Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for PEGINTERFERON BETA-1A. However, 7 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 Device defective?
SOMATROPIN (1,719)
USTEKINUMAB (1,071)
SECUKINUMAB (666)
GUSELKUMAB (574)
GOLIMUMAB (539)
ABATACEPT (458)
ALBUTEROL (445)
TOCILIZUMAB (400)
INSULIN GLARGINE (397)
EXENATIDE (387)
Which PEGINTERFERON BETA-1A Alternatives Have Lower Device defective 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