Does SOLIRIS Cause Unevaluable event? 140 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 140 reports of Unevaluable event have been filed in association with SOLIRIS. This represents 5.8% of all adverse event reports for SOLIRIS.
140
Reports of Unevaluable event with SOLIRIS
5.8%
of all SOLIRIS reports
17
Deaths
129
Hospitalizations
How Dangerous Is Unevaluable event From SOLIRIS?
Of the 140 reports, 17 (12.1%) resulted in death, 129 (92.1%) required hospitalization, and 2 (1.4%) were considered life-threatening.
Is Unevaluable event Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for SOLIRIS. However, 140 reports have been filed with the FAERS database.
What Other Side Effects Does SOLIRIS Cause?
Fatigue (341)
Haemoglobin decreased (254)
Transfusion (183)
Abdominal pain (141)
Dyspnoea (129)
Headache (126)
Aplastic anaemia (120)
Death (118)
Platelet count decreased (106)
Haemolysis (103)
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 SOLIRIS Alternatives Have Lower Unevaluable event Risk?
SOLIRIS vs SOLOSTAR
SOLIRIS vs SOLRIAMFETOL
SOLIRIS vs SOLU-MEDROL
SOLIRIS vs SOMATREM
SOLIRIS vs SOMATROGON-GHLA