Does FOSCARNET Cause Intentional product use issue? 41 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 41 reports of Intentional product use issue have been filed in association with FOSCARNET (Foscarnet Sodium). This represents 2.0% of all adverse event reports for FOSCARNET.
41
Reports of Intentional product use issue with FOSCARNET
2.0%
of all FOSCARNET reports
11
Deaths
9
Hospitalizations
How Dangerous Is Intentional product use issue From FOSCARNET?
Of the 41 reports, 11 (26.8%) resulted in death, 9 (22.0%) required hospitalization, and 3 (7.3%) 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 FOSCARNET. However, 41 reports have been filed with the FAERS database.
What Other Side Effects Does FOSCARNET Cause?
Off label use (610)
Drug ineffective (368)
Drug resistance (309)
Acute kidney injury (246)
Cytomegalovirus infection (200)
Nephropathy toxic (198)
Pathogen resistance (190)
Renal impairment (184)
Pancytopenia (170)
Cytomegalovirus infection reactivation (167)
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 FOSCARNET Alternatives Have Lower Intentional product use issue Risk?
FOSCARNET vs FOSFOMYCIN
FOSCARNET vs FOSFOMYCIN TROMETHAMINE
FOSCARNET vs FOSINOPRIL
FOSCARNET vs FOSPHENYTOIN
FOSCARNET vs FOSTAMATINIB