Does ABACAVIR Cause Product use issue? 297 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 297 reports of Product use issue have been filed in association with ABACAVIR (Abacavir Sulfate). This represents 6.9% of all adverse event reports for ABACAVIR.
297
Reports of Product use issue with ABACAVIR
6.9%
of all ABACAVIR reports
110
Deaths
15
Hospitalizations
How Dangerous Is Product use issue From ABACAVIR?
Of the 297 reports, 110 (37.0%) resulted in death, 15 (5.1%) required hospitalization, and 5 (1.7%) were considered life-threatening.
Is Product use issue Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for ABACAVIR. However, 297 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 Product use issue?
INFLIXIMAB (12,752)
DUPILUMAB (10,575)
POLYETHYLENE GLYCOL 3350 (9,432)
METHOTREXATE (8,185)
DICLOFENAC (8,009)
RITUXIMAB (6,948)
ADALIMUMAB (6,379)
ETANERCEPT (6,062)
TOCILIZUMAB (5,944)
ABATACEPT (5,915)
Which ABACAVIR Alternatives Have Lower Product use issue Risk?
ABACAVIR vs ABACAVIR\DOLUTEGRAVIR\LAMIVUDINE
ABACAVIR vs ABACAVIR\LAMIVUDINE
ABACAVIR vs ABACAVIR\LAMIVUDINE\ZIDOVUDINE
ABACAVIR vs ABALOPARATIDE
ABACAVIR vs ABATACEPT