Does LEFLUNOMIDE Cause Product quality issue? 584 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 584 reports of Product quality issue have been filed in association with LEFLUNOMIDE (Leflunomide). This represents 1.0% of all adverse event reports for LEFLUNOMIDE.
584
Reports of Product quality issue with LEFLUNOMIDE
1.0%
of all LEFLUNOMIDE reports
530
Deaths
465
Hospitalizations
How Dangerous Is Product quality issue From LEFLUNOMIDE?
Of the 584 reports, 530 (90.8%) resulted in death, 465 (79.6%) required hospitalization, and 483 (82.7%) were considered life-threatening.
Is Product quality issue Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for LEFLUNOMIDE. However, 584 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 quality issue?
ETONOGESTREL (4,651)
ALBUTEROL (4,466)
TIOTROPIUM (3,821)
MOMETASONE FUROATE (3,406)
LIDOCAINE (3,126)
FLUTICASONE\SALMETEROL (2,986)
FORMOTEROL\MOMETASONE FUROATE (2,458)
FENTANYL (2,450)
NICOTINE (1,987)
EXENATIDE (1,839)
Which LEFLUNOMIDE Alternatives Have Lower Product quality issue Risk?
LEFLUNOMIDE vs LEMBOREXANT
LEFLUNOMIDE vs LENACAPAVIR
LEFLUNOMIDE vs LENALIDOMIDE
LEFLUNOMIDE vs LENIOLISIB
LEFLUNOMIDE vs LENOGRASTIM