Does SOLIRIS Cause Investigation? 11 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 11 reports of Investigation have been filed in association with SOLIRIS. This represents 0.5% of all adverse event reports for SOLIRIS.
11
Reports of Investigation with SOLIRIS
0.5%
of all SOLIRIS reports
1
Deaths
10
Hospitalizations
How Dangerous Is Investigation From SOLIRIS?
Of the 11 reports, 1 (9.1%) resulted in death, 10 (90.9%) required hospitalization.
Is Investigation Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for SOLIRIS. However, 11 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 Investigation?
ARANESP (403)
NEULASTA (371)
XGEVA (115)
FLUTICASONE\SALMETEROL (96)
DARBEPOETIN ALFA (86)
ADVAIR (77)
DENOSUMAB (65)
ADVAIR HFA (51)
ALBUTEROL (51)
VENTOLIN (47)
Which SOLIRIS Alternatives Have Lower Investigation Risk?
SOLIRIS vs SOLOSTAR
SOLIRIS vs SOLRIAMFETOL
SOLIRIS vs SOLU-MEDROL
SOLIRIS vs SOMATREM
SOLIRIS vs SOMATROGON-GHLA