Does TERIFLUNOMIDE Cause Product dose omission issue? 1,411 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 1,411 reports of Product dose omission issue have been filed in association with TERIFLUNOMIDE (Teriflunomide). This represents 3.6% of all adverse event reports for TERIFLUNOMIDE.
1,411
Reports of Product dose omission issue with TERIFLUNOMIDE
3.6%
of all TERIFLUNOMIDE reports
11
Deaths
140
Hospitalizations
How Dangerous Is Product dose omission issue From TERIFLUNOMIDE?
Of the 1,411 reports, 11 (0.8%) resulted in death, 140 (9.9%) required hospitalization.
Is Product dose omission issue Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for TERIFLUNOMIDE. However, 1,411 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 issue?
DUPILUMAB (18,189)
USTEKINUMAB (9,405)
GUSELKUMAB (9,267)
LENALIDOMIDE (8,145)
MEPOLIZUMAB (5,873)
TOFACITINIB (5,646)
VOXELOTOR (5,122)
BELIMUMAB (4,671)
SECUKINUMAB (4,572)
APREMILAST (4,460)
Which TERIFLUNOMIDE Alternatives Have Lower Product dose omission issue Risk?
TERIFLUNOMIDE vs TERIPARATIDE
TERIFLUNOMIDE vs TERIZIDONE
TERIFLUNOMIDE vs TERLIPRESSIN
TERIFLUNOMIDE vs TESAMORELIN
TERIFLUNOMIDE vs TESTOSTERONE