Does PEGINTERFERON BETA-1A Cause Intentional product use issue? 13 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 13 reports of Intentional product use issue have been filed in association with PEGINTERFERON BETA-1A (Plegridy Pen). This represents 0.1% of all adverse event reports for PEGINTERFERON BETA-1A.
13
Reports of Intentional product use issue with PEGINTERFERON BETA-1A
0.1%
of all PEGINTERFERON BETA-1A reports
0
Deaths
3
Hospitalizations
How Dangerous Is Intentional product use issue From PEGINTERFERON BETA-1A?
Of the 13 reports, 3 (23.1%) required hospitalization.
Is Intentional product use issue Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for PEGINTERFERON BETA-1A. However, 13 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 Intentional product use issue?
INFLIXIMAB (11,028)
RITUXIMAB (9,602)
INFLIXIMAB-DYYB (7,549)
TOCILIZUMAB (5,078)
METHOTREXATE (4,087)
PREDNISONE (3,961)
ABATACEPT (3,693)
ADALIMUMAB (3,557)
NIVOLUMAB (3,297)
LEFLUNOMIDE (3,280)
Which PEGINTERFERON BETA-1A Alternatives Have Lower Intentional product use issue 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