Does GOLIMUMAB Cause Intentional product misuse? 116 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 116 reports of Intentional product misuse have been filed in association with GOLIMUMAB (SIMPONI ARIA). This represents 0.2% of all adverse event reports for GOLIMUMAB.
116
Reports of Intentional product misuse with GOLIMUMAB
0.2%
of all GOLIMUMAB reports
58
Deaths
106
Hospitalizations
How Dangerous Is Intentional product misuse From GOLIMUMAB?
Of the 116 reports, 58 (50.0%) resulted in death, 106 (91.4%) required hospitalization, and 70 (60.3%) were considered life-threatening.
Is Intentional product misuse Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for GOLIMUMAB. However, 116 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 Intentional product misuse?
ETANERCEPT (3,992)
PREGABALIN (3,731)
BUDESONIDE\FORMOTEROL (3,399)
ACETAMINOPHEN (2,924)
ESOMEPRAZOLE (2,852)
MINOXIDIL (2,418)
TOFACITINIB (2,331)
CINACALCET (2,092)
QUETIAPINE (1,855)
ALPRAZOLAM (1,709)
Which GOLIMUMAB Alternatives Have Lower Intentional product misuse Risk?
GOLIMUMAB vs GOLODIRSEN
GOLIMUMAB vs GONADORELIN
GOLIMUMAB vs GONADOTROPHIN, CHORIONIC
GOLIMUMAB vs GOSERELIN
GOLIMUMAB vs GRAMICIDIN