Does ABACAVIR\LAMIVUDINE Cause Adverse event? 24 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 24 reports of Adverse event have been filed in association with ABACAVIR\LAMIVUDINE. This represents 0.5% of all adverse event reports for ABACAVIR\LAMIVUDINE.
24
Reports of Adverse event with ABACAVIR\LAMIVUDINE
0.5%
of all ABACAVIR\LAMIVUDINE reports
6
Deaths
17
Hospitalizations
How Dangerous Is Adverse event From ABACAVIR\LAMIVUDINE?
Of the 24 reports, 6 (25.0%) resulted in death, 17 (70.8%) required hospitalization, and 1 (4.2%) were considered life-threatening.
Is Adverse event Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for ABACAVIR\LAMIVUDINE. However, 24 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 Adverse event?
ABATACEPT (4,028)
APIXABAN (3,871)
ETANERCEPT (3,096)
LENALIDOMIDE (2,426)
INFLIXIMAB (2,269)
ADALIMUMAB (2,121)
METHOTREXATE (1,846)
LEFLUNOMIDE (1,476)
RIVAROXABAN (1,465)
ALENDRONATE (1,462)
Which ABACAVIR\LAMIVUDINE Alternatives Have Lower Adverse event 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