Does DOLUTEGRAVIR Cause Intentional product misuse? 190 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 190 reports of Intentional product misuse have been filed in association with DOLUTEGRAVIR (Juluca). This represents 1.8% of all adverse event reports for DOLUTEGRAVIR.
190
Reports of Intentional product misuse with DOLUTEGRAVIR
1.8%
of all DOLUTEGRAVIR reports
101
Deaths
5
Hospitalizations
How Dangerous Is Intentional product misuse From DOLUTEGRAVIR?
Of the 190 reports, 101 (53.2%) resulted in death, 5 (2.6%) required hospitalization, and 2 (1.1%) 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 DOLUTEGRAVIR. However, 190 reports have been filed with the FAERS database.
What Other Side Effects Does DOLUTEGRAVIR Cause?
Foetal exposure during pregnancy (1,036)
Exposure during pregnancy (776)
Virologic failure (770)
Pathogen resistance (586)
Maternal exposure during pregnancy (517)
Viral mutation identified (510)
Treatment failure (453)
Drug ineffective (447)
Off label use (413)
Blood hiv rna increased (410)
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 DOLUTEGRAVIR Alternatives Have Lower Intentional product misuse Risk?
DOLUTEGRAVIR vs DOLUTEGRAVIR\LAMIVUDINE
DOLUTEGRAVIR vs DOLUTEGRAVIR\LAMIVUDINE\TENOFOVIR DISOPROXIL
DOLUTEGRAVIR vs DOLUTEGRAVIR\RILPIVIRINE
DOLUTEGRAVIR vs DOMPERIDONE
DOLUTEGRAVIR vs DOMPERIDONE\PANTOPRAZOLE