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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 Extravascular haemolysis? 11 Reports in FDA Database

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According to the FDA Adverse Event Reporting System (FAERS), 11 reports of Extravascular haemolysis have been filed in association with SOLIRIS. This represents 0.5% of all adverse event reports for SOLIRIS.

11
Reports of Extravascular haemolysis with SOLIRIS
0.5%
of all SOLIRIS reports
0
Deaths
1
Hospitalizations

How Dangerous Is Extravascular haemolysis From SOLIRIS?

Of the 11 reports, 1 (9.1%) required hospitalization.

Is Extravascular haemolysis 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 Extravascular haemolysis?

ECULIZUMAB (182) RAVULIZUMAB-CWVZ (99) HUMAN IMMUNOGLOBULIN G (13) DANICOPAN (9) OXALIPLATIN (7) DICLOFENAC (5)

Which SOLIRIS Alternatives Have Lower Extravascular 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 Extravascular haemolysis Reports All Drugs Causing Extravascular haemolysis SOLIRIS Demographics