Does INTERFERON BETA-1B Cause Expired device used? 24 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 24 reports of Expired device used have been filed in association with INTERFERON BETA-1B (Betaseron). This represents 0.2% of all adverse event reports for INTERFERON BETA-1B.
24
Reports of Expired device used with INTERFERON BETA-1B
0.2%
of all INTERFERON BETA-1B reports
0
Deaths
3
Hospitalizations
How Dangerous Is Expired device used From INTERFERON BETA-1B?
Of the 24 reports, 3 (12.5%) required hospitalization.
Is Expired device used Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for INTERFERON BETA-1B. However, 24 reports have been filed with the FAERS database.
What Other Side Effects Does INTERFERON BETA-1B Cause?
Multiple sclerosis relapse (1,229)
Influenza like illness (1,042)
Injection site pain (1,014)
Fatigue (783)
Drug ineffective (767)
Injection site erythema (724)
Injection site reaction (707)
Pain (597)
Headache (596)
Multiple sclerosis (589)
What Other Drugs Cause Expired device used?
SOMATROPIN (1,432)
LEVONORGESTREL (722)
ETANERCEPT (198)
ALBUTEROL (109)
INSULIN GLARGINE (69)
COPPER (66)
DEVICE (34)
PARATHYROID HORMONE (33)
EPINEPHRINE (31)
SUMATRIPTAN (29)
Which INTERFERON BETA-1B Alternatives Have Lower Expired device used Risk?
INTERFERON BETA-1B vs INTERFERON GAMMA
INTERFERON BETA-1B vs INTERFERON GAMMA-1B
INTERFERON BETA-1B vs INVEGA
INTERFERON BETA-1B vs INVEGA SUSTENNA
INTERFERON BETA-1B vs INVESTIGATIONAL BIOSIMILARS