Does SOLIRIS Cause Haemoglobin decreased? 254 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 254 reports of Haemoglobin decreased have been filed in association with SOLIRIS. This represents 10.6% of all adverse event reports for SOLIRIS.
254
Reports of Haemoglobin decreased with SOLIRIS
10.6%
of all SOLIRIS reports
12
Deaths
122
Hospitalizations
How Dangerous Is Haemoglobin decreased From SOLIRIS?
Of the 254 reports, 12 (4.7%) resulted in death, 122 (48.0%) required hospitalization, and 2 (0.8%) were considered life-threatening.
Is Haemoglobin decreased Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for SOLIRIS. However, 254 reports have been filed with the FAERS database.
What Other Side Effects Does SOLIRIS Cause?
Fatigue (341)
Transfusion (183)
Abdominal pain (141)
Unevaluable event (140)
Dyspnoea (129)
Headache (126)
Aplastic anaemia (120)
Death (118)
Platelet count decreased (106)
Haemolysis (103)
What Other Drugs Cause Haemoglobin decreased?
LENALIDOMIDE (4,031)
RUXOLITINIB (3,297)
ECULIZUMAB (3,028)
ADALIMUMAB (2,459)
CLOZAPINE (2,396)
RITUXIMAB (1,803)
APIXABAN (1,779)
NIRAPARIB (1,759)
METHOTREXATE (1,754)
RIBAVIRIN (1,753)
Which SOLIRIS Alternatives Have Lower Haemoglobin decreased Risk?
SOLIRIS vs SOLOSTAR
SOLIRIS vs SOLRIAMFETOL
SOLIRIS vs SOLU-MEDROL
SOLIRIS vs SOMATREM
SOLIRIS vs SOMATROGON-GHLA