Does GOLIMUMAB Cause Product quality issue? 646 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 646 reports of Product quality issue have been filed in association with GOLIMUMAB (SIMPONI ARIA). This represents 0.9% of all adverse event reports for GOLIMUMAB.
646
Reports of Product quality issue with GOLIMUMAB
0.9%
of all GOLIMUMAB reports
488
Deaths
451
Hospitalizations
How Dangerous Is Product quality issue From GOLIMUMAB?
Of the 646 reports, 488 (75.5%) resulted in death, 451 (69.8%) required hospitalization, and 474 (73.4%) 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 GOLIMUMAB. However, 646 reports have been filed with the FAERS database.
What Other Side Effects Does GOLIMUMAB Cause?
Drug ineffective (17,959)
Rheumatoid arthritis (12,272)
Pain (11,443)
Fatigue (9,626)
Off label use (8,764)
Alopecia (8,394)
Rash (8,331)
Joint swelling (8,264)
Arthralgia (7,968)
Abdominal discomfort (7,902)
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 GOLIMUMAB Alternatives Have Lower Product quality issue Risk?
GOLIMUMAB vs GOLODIRSEN
GOLIMUMAB vs GONADORELIN
GOLIMUMAB vs GONADOTROPHIN, CHORIONIC
GOLIMUMAB vs GOSERELIN
GOLIMUMAB vs GRAMICIDIN