Does LEFLUNOMIDE Cause Product dose omission issue? 205 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 205 reports of Product dose omission issue have been filed in association with LEFLUNOMIDE (Leflunomide). This represents 0.4% of all adverse event reports for LEFLUNOMIDE.
205
Reports of Product dose omission issue with LEFLUNOMIDE
0.4%
of all LEFLUNOMIDE reports
0
Deaths
89
Hospitalizations
How Dangerous Is Product dose omission issue From LEFLUNOMIDE?
Of the 205 reports, 89 (43.4%) 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 LEFLUNOMIDE. However, 205 reports have been filed with the FAERS database.
What Other Side Effects Does LEFLUNOMIDE Cause?
Drug ineffective (31,396)
Rheumatoid arthritis (20,886)
Pain (15,594)
Drug intolerance (14,142)
Joint swelling (13,026)
Fatigue (11,959)
Arthralgia (11,880)
Rash (11,239)
Contraindicated product administered (11,206)
Abdominal discomfort (10,333)
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 LEFLUNOMIDE Alternatives Have Lower Product dose omission issue Risk?
LEFLUNOMIDE vs LEMBOREXANT
LEFLUNOMIDE vs LENACAPAVIR
LEFLUNOMIDE vs LENALIDOMIDE
LEFLUNOMIDE vs LENIOLISIB
LEFLUNOMIDE vs LENOGRASTIM