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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 Dyspnoea? 129 Reports in FDA Database

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According to the FDA Adverse Event Reporting System (FAERS), 129 reports of Dyspnoea have been filed in association with SOLIRIS. This represents 5.4% of all adverse event reports for SOLIRIS.

129
Reports of Dyspnoea with SOLIRIS
5.4%
of all SOLIRIS reports
10
Deaths
57
Hospitalizations

How Dangerous Is Dyspnoea From SOLIRIS?

Of the 129 reports, 10 (7.8%) resulted in death, 57 (44.2%) required hospitalization, and 1 (0.8%) were considered life-threatening.

Is Dyspnoea Listed in the Official Label?

This adverse event is not currently listed in the official FDA drug label for SOLIRIS. However, 129 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) Headache (126) Aplastic anaemia (120) Death (118) Platelet count decreased (106) Haemolysis (103)

What Other Drugs Cause Dyspnoea?

ALBUTEROL (21,856) TREPROSTINIL (16,348) AMBRISENTAN (13,367) PREDNISONE (12,830) BUDESONIDE\FORMOTEROL (11,158) TIOTROPIUM (10,863) ADALIMUMAB (10,547) DUPILUMAB (10,310) FLUTICASONE\SALMETEROL (9,783) MEPOLIZUMAB (9,192)

Which SOLIRIS Alternatives Have Lower Dyspnoea Risk?

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

Related Pages

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