Does UMIFENOVIR Cause Condition aggravated? 5 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 5 reports of Condition aggravated have been filed in association with UMIFENOVIR. This represents 2.6% of all adverse event reports for UMIFENOVIR.
5
Reports of Condition aggravated with UMIFENOVIR
2.6%
of all UMIFENOVIR reports
1
Deaths
1
Hospitalizations
How Dangerous Is Condition aggravated From UMIFENOVIR?
Of the 5 reports, 1 (20.0%) resulted in death, 1 (20.0%) required hospitalization, and 1 (20.0%) 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 UMIFENOVIR. However, 5 reports have been filed with the FAERS database.
What Other Side Effects Does UMIFENOVIR Cause?
Off label use (119)
Product use in unapproved indication (29)
Diarrhoea (18)
Product use issue (18)
Vomiting (13)
Respiratory failure (12)
Dyspnoea (9)
Multiple organ dysfunction syndrome (9)
Acute respiratory distress syndrome (8)
Nausea (8)
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 UMIFENOVIR Alternatives Have Lower Condition aggravated Risk?
UMIFENOVIR vs UNSPECIFIED INGREDIENT
UMIFENOVIR vs UPADACITINIB
UMIFENOVIR vs URAPIDIL
UMIFENOVIR vs UREA
UMIFENOVIR vs URIDINE TRIACETATE