Does ABACAVIR Cause Intentional product misuse? 274 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 274 reports of Intentional product misuse have been filed in association with ABACAVIR (Abacavir Sulfate). This represents 6.4% of all adverse event reports for ABACAVIR.
274
Reports of Intentional product misuse with ABACAVIR
6.4%
of all ABACAVIR reports
111
Deaths
5
Hospitalizations
How Dangerous Is Intentional product misuse From ABACAVIR?
Of the 274 reports, 111 (40.5%) resulted in death, 5 (1.8%) required hospitalization, and 5 (1.8%) 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 ABACAVIR. However, 274 reports have been filed with the FAERS database.
What Other Side Effects Does ABACAVIR Cause?
Exposure during pregnancy (504)
Virologic failure (490)
Treatment failure (450)
Pyrexia (441)
Foetal exposure during pregnancy (418)
Viral mutation identified (378)
Pathogen resistance (367)
Rash (349)
Hypertension (336)
Hypersensitivity (329)
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 ABACAVIR Alternatives Have Lower Intentional product misuse Risk?
ABACAVIR vs ABACAVIR\DOLUTEGRAVIR\LAMIVUDINE
ABACAVIR vs ABACAVIR\LAMIVUDINE
ABACAVIR vs ABACAVIR\LAMIVUDINE\ZIDOVUDINE
ABACAVIR vs ABALOPARATIDE
ABACAVIR vs ABATACEPT