Does ZIDOVUDINE Cause Unevaluable event? 5 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 5 reports of Unevaluable event have been filed in association with ZIDOVUDINE (RETROVIR). This represents 0.1% of all adverse event reports for ZIDOVUDINE.
5
Reports of Unevaluable event with ZIDOVUDINE
0.1%
of all ZIDOVUDINE reports
0
Deaths
2
Hospitalizations
How Dangerous Is Unevaluable event From ZIDOVUDINE?
Of the 5 reports, 2 (40.0%) required hospitalization.
Is Unevaluable event Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for ZIDOVUDINE. However, 5 reports have been filed with the FAERS database.
What Other Side Effects Does ZIDOVUDINE Cause?
Foetal exposure during pregnancy (1,816)
Virologic failure (741)
Exposure during pregnancy (575)
Drug resistance (568)
Pathogen resistance (552)
Viral mutation identified (531)
Treatment failure (409)
Maternal exposure during pregnancy (395)
Anaemia (380)
Premature baby (367)
What Other Drugs Cause Unevaluable event?
ADALIMUMAB (4,242)
ETANERCEPT (3,902)
LENALIDOMIDE (3,331)
OXYCODONE (3,145)
AMBRISENTAN (2,336)
SODIUM OXYBATE (2,328)
CARBIDOPA\LEVODOPA (1,632)
DUPILUMAB (1,410)
MORPHINE (1,161)
ACETAMINOPHEN\HYDROCODONE (1,118)
Which ZIDOVUDINE Alternatives Have Lower Unevaluable event Risk?
ZIDOVUDINE vs ZILEUTON
ZIDOVUDINE vs ZILUCOPLAN
ZIDOVUDINE vs ZIMBERELIMAB
ZIDOVUDINE vs ZINC
ZIDOVUDINE vs ZINC\ZINC