Does ZIDOVUDINE Cause Condition aggravated? 72 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 72 reports of Condition aggravated have been filed in association with ZIDOVUDINE (RETROVIR). This represents 1.1% of all adverse event reports for ZIDOVUDINE.
72
Reports of Condition aggravated with ZIDOVUDINE
1.1%
of all ZIDOVUDINE reports
15
Deaths
35
Hospitalizations
How Dangerous Is Condition aggravated From ZIDOVUDINE?
Of the 72 reports, 15 (20.8%) resulted in death, 35 (48.6%) required hospitalization, and 6 (8.3%) were considered life-threatening.
Is Condition aggravated Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for ZIDOVUDINE. However, 72 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 Condition aggravated?
TOFACITINIB (16,925)
INFLIXIMAB (16,616)
DUPILUMAB (16,459)
ETANERCEPT (15,897)
METHOTREXATE (14,938)
ADALIMUMAB (13,527)
PREDNISONE (10,751)
INFLIXIMAB-DYYB (10,275)
HYDROXYCHLOROQUINE (8,848)
RITUXIMAB (8,627)
Which ZIDOVUDINE Alternatives Have Lower Condition aggravated Risk?
ZIDOVUDINE vs ZILEUTON
ZIDOVUDINE vs ZILUCOPLAN
ZIDOVUDINE vs ZIMBERELIMAB
ZIDOVUDINE vs ZINC
ZIDOVUDINE vs ZINC\ZINC