Does LEFLUNOMIDE Cause Intentional product use issue? 3,280 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 3,280 reports of Intentional product use issue have been filed in association with LEFLUNOMIDE (Leflunomide). This represents 5.8% of all adverse event reports for LEFLUNOMIDE.
3,280
Reports of Intentional product use issue with LEFLUNOMIDE
5.8%
of all LEFLUNOMIDE reports
1,468
Deaths
1,840
Hospitalizations
How Dangerous Is Intentional product use issue From LEFLUNOMIDE?
Of the 3,280 reports, 1,468 (44.8%) resulted in death, 1,840 (56.1%) required hospitalization, and 1,707 (52.0%) were considered life-threatening.
Is Intentional product use issue Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for LEFLUNOMIDE. However, 3,280 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 Intentional product use issue?
INFLIXIMAB (11,028)
RITUXIMAB (9,602)
INFLIXIMAB-DYYB (7,549)
TOCILIZUMAB (5,078)
METHOTREXATE (4,087)
PREDNISONE (3,961)
ABATACEPT (3,693)
ADALIMUMAB (3,557)
NIVOLUMAB (3,297)
HYDROXYCHLOROQUINE (3,059)
Which LEFLUNOMIDE Alternatives Have Lower Intentional product use issue Risk?
LEFLUNOMIDE vs LEMBOREXANT
LEFLUNOMIDE vs LENACAPAVIR
LEFLUNOMIDE vs LENALIDOMIDE
LEFLUNOMIDE vs LENIOLISIB
LEFLUNOMIDE vs LENOGRASTIM