Does INTERFERON BETA-1A Cause Product administration interrupted? 115 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 115 reports of Product administration interrupted have been filed in association with INTERFERON BETA-1A (Avonex). This represents 0.2% of all adverse event reports for INTERFERON BETA-1A.
115
Reports of Product administration interrupted with INTERFERON BETA-1A
0.2%
of all INTERFERON BETA-1A reports
6
Deaths
62
Hospitalizations
How Dangerous Is Product administration interrupted From INTERFERON BETA-1A?
Of the 115 reports, 6 (5.2%) resulted in death, 62 (53.9%) required hospitalization, and 4 (3.5%) were considered life-threatening.
Is Product administration interrupted Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for INTERFERON BETA-1A. However, 115 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 Product administration interrupted?
CALCIUM OXYBATE\MAGNESIUM OXYBATE\POTASSIUM OXYBATE\SODIUM OXYBATE (1,446)
SODIUM OXYBATE (1,272)
CANNABIDIOL (511)
ISOTRETINOIN (503)
APREMILAST (314)
TREPROSTINIL (295)
EPOPROSTENOL (205)
LENALIDOMIDE (146)
ETANERCEPT (142)
ADALIMUMAB (86)
Which INTERFERON BETA-1A Alternatives Have Lower Product administration interrupted 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