Does SOLIRIS Cause Condition aggravated? 34 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 34 reports of Condition aggravated have been filed in association with SOLIRIS. This represents 1.4% of all adverse event reports for SOLIRIS.
34
Reports of Condition aggravated with SOLIRIS
1.4%
of all SOLIRIS reports
3
Deaths
23
Hospitalizations
How Dangerous Is Condition aggravated From SOLIRIS?
Of the 34 reports, 3 (8.8%) resulted in death, 23 (67.6%) required hospitalization.
Is Condition aggravated Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for SOLIRIS. However, 34 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)
Unevaluable event (140)
Dyspnoea (129)
Headache (126)
Aplastic anaemia (120)
Death (118)
Platelet count decreased (106)
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 SOLIRIS Alternatives Have Lower Condition aggravated Risk?
SOLIRIS vs SOLOSTAR
SOLIRIS vs SOLRIAMFETOL
SOLIRIS vs SOLU-MEDROL
SOLIRIS vs SOMATREM
SOLIRIS vs SOMATROGON-GHLA