Does INTERFERON BETA-1A Cause Complication of device removal? 37 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 37 reports of Complication of device removal have been filed in association with INTERFERON BETA-1A (Avonex). This represents 0.1% of all adverse event reports for INTERFERON BETA-1A.
37
Reports of Complication of device removal with INTERFERON BETA-1A
0.1%
of all INTERFERON BETA-1A reports
0
Deaths
1
Hospitalizations
How Dangerous Is Complication of device removal From INTERFERON BETA-1A?
Of the 37 reports, 1 (2.7%) required hospitalization.
Is Complication of device removal Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for INTERFERON BETA-1A. However, 37 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 Complication of device removal?
COPPER (7,895)
ETONOGESTREL (3,578)
LEVONORGESTREL (2,039)
MIRENA (44)
TREPROSTINIL (24)
IMPLANON (21)
ETHINYL ESTRADIOL\ETONOGESTREL (15)
UNSPECIFIED INGREDIENT (14)
BUPRENORPHINE (11)
DEVICE (11)
Which INTERFERON BETA-1A Alternatives Have Lower Complication of device removal 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