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Important: This site presents data from the FDA Adverse Event Reporting System (FAERS). A report does not mean the drug caused the event. Full disclaimer.

Does SOLIRIS Cause Haemolysis? 103 Reports in FDA Database

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According to the FDA Adverse Event Reporting System (FAERS), 103 reports of Haemolysis have been filed in association with SOLIRIS. This represents 4.3% of all adverse event reports for SOLIRIS.

103
Reports of Haemolysis with SOLIRIS
4.3%
of all SOLIRIS reports
2
Deaths
53
Hospitalizations

How Dangerous Is Haemolysis From SOLIRIS?

Of the 103 reports, 2 (1.9%) resulted in death, 53 (51.5%) required hospitalization, and 3 (2.9%) were considered life-threatening.

Is Haemolysis Listed in the Official Label?

This adverse event is not currently listed in the official FDA drug label for SOLIRIS. However, 103 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 Haemolysis?

ECULIZUMAB (1,476) HUMAN IMMUNOGLOBULIN G (357) RITUXIMAB (261) RAVULIZUMAB-CWVZ (242) PREDNISONE (192) CYCLOSPORINE (173) DEXAMETHASONE (167) ACETAMINOPHEN (134) VINCRISTINE (132) TACROLIMUS (116)

Which SOLIRIS Alternatives Have Lower Haemolysis Risk?

SOLIRIS vs SOLOSTAR SOLIRIS vs SOLRIAMFETOL SOLIRIS vs SOLU-MEDROL SOLIRIS vs SOMATREM SOLIRIS vs SOMATROGON-GHLA

Related Pages

SOLIRIS Full Profile All Haemolysis Reports All Drugs Causing Haemolysis SOLIRIS Demographics