Does GOLIMUMAB Cause Laboratory test abnormal? 190 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 190 reports of Laboratory test abnormal have been filed in association with GOLIMUMAB (SIMPONI ARIA). This represents 0.3% of all adverse event reports for GOLIMUMAB.
190
Reports of Laboratory test abnormal with GOLIMUMAB
0.3%
of all GOLIMUMAB reports
121
Deaths
140
Hospitalizations
How Dangerous Is Laboratory test abnormal From GOLIMUMAB?
Of the 190 reports, 121 (63.7%) resulted in death, 140 (73.7%) required hospitalization, and 130 (68.4%) were considered life-threatening.
Is Laboratory test abnormal Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for GOLIMUMAB. However, 190 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 Laboratory test abnormal?
LENALIDOMIDE (4,215)
CINACALCET (4,210)
POMALIDOMIDE (1,218)
ADALIMUMAB (845)
ETANERCEPT (753)
DALFAMPRIDINE (650)
PALBOCICLIB (550)
NIRAPARIB (536)
METHOTREXATE (507)
ECULIZUMAB (441)
Which GOLIMUMAB Alternatives Have Lower Laboratory test abnormal Risk?
GOLIMUMAB vs GOLODIRSEN
GOLIMUMAB vs GONADORELIN
GOLIMUMAB vs GONADOTROPHIN, CHORIONIC
GOLIMUMAB vs GOSERELIN
GOLIMUMAB vs GRAMICIDIN