Does INTERFERON BETA-1A Cause Maternal exposure timing unspecified? 50 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 50 reports of Maternal exposure timing unspecified have been filed in association with INTERFERON BETA-1A (Avonex). This represents 0.1% of all adverse event reports for INTERFERON BETA-1A.
50
Reports of Maternal exposure timing unspecified with INTERFERON BETA-1A
0.1%
of all INTERFERON BETA-1A reports
0
Deaths
3
Hospitalizations
How Dangerous Is Maternal exposure timing unspecified From INTERFERON BETA-1A?
Of the 50 reports, 3 (6.0%) required hospitalization.
Is Maternal exposure timing unspecified Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for INTERFERON BETA-1A. However, 50 reports have been filed with the FAERS database.
What Other Side Effects Does INTERFERON BETA-1A Cause?
Multiple sclerosis relapse (5,931)
Influenza like illness (4,475)
Memory impairment (3,468)
Multiple sclerosis (3,412)
Fatigue (3,164)
Fall (3,128)
Gait disturbance (3,031)
Death (2,766)
Pain (2,692)
Headache (2,533)
What Other Drugs Cause Maternal exposure timing unspecified?
RITUXIMAB (402)
METHOTREXATE (350)
ADALIMUMAB (343)
DICLOFENAC (331)
TOCILIZUMAB (327)
HYDROXYCHLOROQUINE (309)
FOLIC ACID (304)
INFLIXIMAB (303)
LEFLUNOMIDE (302)
SECUKINUMAB (301)
Which INTERFERON BETA-1A Alternatives Have Lower Maternal exposure timing unspecified Risk?
INTERFERON BETA-1A vs INTERFERON BETA-1B
INTERFERON BETA-1A vs INTERFERON GAMMA
INTERFERON BETA-1A vs INTERFERON GAMMA-1B
INTERFERON BETA-1A vs INVEGA
INTERFERON BETA-1A vs INVEGA SUSTENNA