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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 Haemoglobinuria? 100 Reports in FDA Database

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According to the FDA Adverse Event Reporting System (FAERS), 100 reports of Haemoglobinuria have been filed in association with SOLIRIS. This represents 4.2% of all adverse event reports for SOLIRIS.

100
Reports of Haemoglobinuria with SOLIRIS
4.2%
of all SOLIRIS reports
5
Deaths
34
Hospitalizations

How Dangerous Is Haemoglobinuria From SOLIRIS?

Of the 100 reports, 5 (5.0%) resulted in death, 34 (34.0%) required hospitalization.

Is Haemoglobinuria Listed in the Official Label?

This adverse event is not currently listed in the official FDA drug label for SOLIRIS. However, 100 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 Haemoglobinuria?

ECULIZUMAB (521) OXALIPLATIN (23) HUMAN IMMUNOGLOBULIN G (18) ASPIRIN (13) IBUPROFEN (11) RAVULIZUMAB-CWVZ (9) METFORMIN (8) METHYLPREDNISOLONE (8) PEGCETACOPLAN (8) QUETIAPINE (8)

Which SOLIRIS Alternatives Have Lower Haemoglobinuria Risk?

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

Related Pages

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