Does ABACAVIR\LAMIVUDINE Cause Product use issue? 235 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 235 reports of Product use issue have been filed in association with ABACAVIR\LAMIVUDINE. This represents 4.4% of all adverse event reports for ABACAVIR\LAMIVUDINE.
235
Reports of Product use issue with ABACAVIR\LAMIVUDINE
4.4%
of all ABACAVIR\LAMIVUDINE reports
87
Deaths
8
Hospitalizations
How Dangerous Is Product use issue From ABACAVIR\LAMIVUDINE?
Of the 235 reports, 87 (37.0%) resulted in death, 8 (3.4%) required hospitalization, and 5 (2.1%) 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\LAMIVUDINE. However, 235 reports have been filed with the FAERS database.
What Other Side Effects Does ABACAVIR\LAMIVUDINE Cause?
Exposure during pregnancy (593)
Pyrexia (450)
Rash (390)
Foetal exposure during pregnancy (373)
Hypertension (325)
Headache (316)
Hypersensitivity (289)
Pain (271)
Thrombocytopenia (271)
Off label use (267)
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\LAMIVUDINE Alternatives Have Lower Product use issue Risk?
ABACAVIR\LAMIVUDINE vs ABACAVIR\LAMIVUDINE\ZIDOVUDINE
ABACAVIR\LAMIVUDINE vs ABALOPARATIDE
ABACAVIR\LAMIVUDINE vs ABATACEPT
ABACAVIR\LAMIVUDINE vs ABATACEPT SUBQ /ML
ABACAVIR\LAMIVUDINE vs ABCIXIMAB