Does GANCICLOVIR Cause Intentional product use issue? 145 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 145 reports of Intentional product use issue have been filed in association with GANCICLOVIR (Ganciclovir). This represents 2.9% of all adverse event reports for GANCICLOVIR.
145
Reports of Intentional product use issue with GANCICLOVIR
2.9%
of all GANCICLOVIR reports
44
Deaths
37
Hospitalizations
How Dangerous Is Intentional product use issue From GANCICLOVIR?
Of the 145 reports, 44 (30.3%) resulted in death, 37 (25.5%) required hospitalization, and 11 (7.6%) were considered life-threatening.
Is Intentional product use issue Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for GANCICLOVIR. However, 145 reports have been filed with the FAERS database.
What Other Side Effects Does GANCICLOVIR Cause?
Off label use (1,104)
Drug ineffective (924)
Cytomegalovirus infection (668)
Drug resistance (594)
Pancytopenia (403)
Product use in unapproved indication (400)
Neutropenia (396)
Cytomegalovirus infection reactivation (301)
Cytomegalovirus viraemia (294)
Product use issue (279)
What Other Drugs Cause Intentional product use issue?
INFLIXIMAB (11,028)
RITUXIMAB (9,602)
INFLIXIMAB-DYYB (7,549)
TOCILIZUMAB (5,078)
METHOTREXATE (4,087)
PREDNISONE (3,961)
ABATACEPT (3,693)
ADALIMUMAB (3,557)
NIVOLUMAB (3,297)
LEFLUNOMIDE (3,280)
Which GANCICLOVIR Alternatives Have Lower Intentional product use issue Risk?
GANCICLOVIR vs GANIRELIX
GANCICLOVIR vs GATIFLOXACIN
GANCICLOVIR vs GEFITINIB
GANCICLOVIR vs GELATIN
GANCICLOVIR vs GEMCITABINE