Does LAMIVUDINE Cause Product use issue? 144 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 144 reports of Product use issue have been filed in association with LAMIVUDINE (Lamivudine and Zidovudine). This represents 0.9% of all adverse event reports for LAMIVUDINE.
144
Reports of Product use issue with LAMIVUDINE
0.9%
of all LAMIVUDINE reports
60
Deaths
29
Hospitalizations
How Dangerous Is Product use issue From LAMIVUDINE?
Of the 144 reports, 60 (41.7%) resulted in death, 29 (20.1%) required hospitalization, and 2 (1.4%) 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 LAMIVUDINE. However, 144 reports have been filed with the FAERS database.
What Other Side Effects Does LAMIVUDINE Cause?
Foetal exposure during pregnancy (1,905)
Virologic failure (1,894)
Drug resistance (1,889)
Pathogen resistance (1,733)
Viral mutation identified (1,631)
Treatment failure (933)
Exposure during pregnancy (846)
Drug interaction (744)
Drug ineffective (726)
Immune reconstitution inflammatory syndrome (625)
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 LAMIVUDINE Alternatives Have Lower Product use issue Risk?
LAMIVUDINE vs LAMIVUDINE\NEVIRAPINE\ZIDOVUDINE
LAMIVUDINE vs LAMIVUDINE\TENOFOVIR
LAMIVUDINE vs LAMIVUDINE\TENOFOVIR DISOPROXIL
LAMIVUDINE vs LAMIVUDINE\ZIDOVUDINE
LAMIVUDINE vs LAMOTRIGINE