SOLIRIS for Neuromyelitis optica: Side Effects & Safety Data
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There are 17 adverse event reports in the FDA FAERS database where SOLIRIS was used for Neuromyelitis optica.
Most Reported Side Effects for SOLIRIS
| Side Effect | Reports | % | Deaths | Hosp. |
|---|---|---|---|---|
| Fatigue | 341 | 14.2% | 14 | 95 |
| Haemoglobin decreased | 254 | 10.6% | 12 | 122 |
| Transfusion | 183 | 7.6% | 8 | 67 |
| Abdominal pain | 141 | 5.9% | 8 | 69 |
| Unevaluable event | 140 | 5.8% | 17 | 129 |
| Dyspnoea | 129 | 5.4% | 10 | 57 |
| Headache | 126 | 5.3% | 3 | 49 |
| Aplastic anaemia | 120 | 5.0% | 4 | 27 |
| Death | 118 | 4.9% | 118 | 38 |
| Platelet count decreased | 106 | 4.4% | 12 | 60 |
| Haemolysis | 103 | 4.3% | 2 | 53 |
| Pyrexia | 103 | 4.3% | 11 | 78 |
| Haemoglobinuria | 100 | 4.2% | 5 | 34 |
| Off label use | 96 | 4.0% | 26 | 22 |
| Vomiting | 95 | 4.0% | 8 | 54 |
Other Indications for SOLIRIS
Paroxysmal nocturnal haemoglobinuria (1,478)
Haemolytic uraemic syndrome (811)
Off label use (102)
Product used for unknown indication (30)
Thrombotic microangiopathy (10)
Transplant rejection (8)
Glomerulonephritis membranoproliferative (5)