Does INTERFERON BETA-1B Cause Product dose omission? 218 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 218 reports of Product dose omission have been filed in association with INTERFERON BETA-1B (Betaseron). This represents 1.8% of all adverse event reports for INTERFERON BETA-1B.
218
Reports of Product dose omission with INTERFERON BETA-1B
1.8%
of all INTERFERON BETA-1B reports
3
Deaths
32
Hospitalizations
How Dangerous Is Product dose omission From INTERFERON BETA-1B?
Of the 218 reports, 3 (1.4%) resulted in death, 32 (14.7%) required hospitalization.
Is Product dose omission Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for INTERFERON BETA-1B. However, 218 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 Product dose omission?
APREMILAST (4,567)
DUPILUMAB (2,729)
ALBUTEROL (1,742)
USTEKINUMAB (1,653)
INSULIN GLARGINE (1,500)
ETANERCEPT (1,400)
LENALIDOMIDE (1,400)
RUXOLITINIB (1,376)
ALIROCUMAB (1,354)
DIMETHYL (1,248)
Which INTERFERON BETA-1B Alternatives Have Lower Product dose omission 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