Does TERIFLUNOMIDE Cause Product dose omission in error? 371 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 371 reports of Product dose omission in error have been filed in association with TERIFLUNOMIDE (Teriflunomide). This represents 0.9% of all adverse event reports for TERIFLUNOMIDE.
371
Reports of Product dose omission in error with TERIFLUNOMIDE
0.9%
of all TERIFLUNOMIDE reports
1
Deaths
25
Hospitalizations
How Dangerous Is Product dose omission in error From TERIFLUNOMIDE?
Of the 371 reports, 1 (0.3%) resulted in death, 25 (6.7%) required hospitalization.
Is Product dose omission in error Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for TERIFLUNOMIDE. However, 371 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 in error?
DUPILUMAB (7,586)
TOFACITINIB (2,461)
LENALIDOMIDE (618)
PALBOCICLIB (592)
DIROXIMEL (481)
ABALOPARATIDE (457)
NIRAPARIB (428)
RUXOLITINIB (425)
DIMETHYL (308)
RELUGOLIX (293)
Which TERIFLUNOMIDE Alternatives Have Lower Product dose omission in error Risk?
TERIFLUNOMIDE vs TERIPARATIDE
TERIFLUNOMIDE vs TERIZIDONE
TERIFLUNOMIDE vs TERLIPRESSIN
TERIFLUNOMIDE vs TESAMORELIN
TERIFLUNOMIDE vs TESTOSTERONE