Does TERIFLUNOMIDE Cause Product dose omission? 1,081 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 1,081 reports of Product dose omission have been filed in association with TERIFLUNOMIDE (Teriflunomide). This represents 2.8% of all adverse event reports for TERIFLUNOMIDE.
1,081
Reports of Product dose omission with TERIFLUNOMIDE
2.8%
of all TERIFLUNOMIDE reports
1
Deaths
157
Hospitalizations
How Dangerous Is Product dose omission From TERIFLUNOMIDE?
Of the 1,081 reports, 1 (0.1%) resulted in death, 157 (14.5%) required hospitalization, and 2 (0.2%) were considered life-threatening.
Is Product dose omission Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for TERIFLUNOMIDE. However, 1,081 reports have been filed with the FAERS database.
What Other Side Effects Does TERIFLUNOMIDE Cause?
Alopecia (5,441)
Multiple sclerosis relapse (4,745)
Fatigue (4,257)
Diarrhoea (4,175)
Fall (2,878)
Hypoaesthesia (2,851)
Headache (2,651)
Paraesthesia (2,472)
Drug ineffective (2,469)
Nausea (2,311)
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 TERIFLUNOMIDE Alternatives Have Lower Product dose omission Risk?
TERIFLUNOMIDE vs TERIPARATIDE
TERIFLUNOMIDE vs TERIZIDONE
TERIFLUNOMIDE vs TERLIPRESSIN
TERIFLUNOMIDE vs TESAMORELIN
TERIFLUNOMIDE vs TESTOSTERONE