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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 International normalised ratio increased? 7 Reports in FDA Database

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According to the FDA Adverse Event Reporting System (FAERS), 7 reports of International normalised ratio increased have been filed in association with SOLIRIS. This represents 0.3% of all adverse event reports for SOLIRIS.

7
Reports of International normalised ratio increased with SOLIRIS
0.3%
of all SOLIRIS reports
0
Deaths
7
Hospitalizations

How Dangerous Is International normalised ratio increased From SOLIRIS?

Of the 7 reports, 7 (100.0%) required hospitalization.

Is International normalised ratio increased Listed in the Official Label?

This adverse event is not currently listed in the official FDA drug label for SOLIRIS. However, 7 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 International normalised ratio increased?

WARFARIN (5,622) RIVAROXABAN (863) ACETAMINOPHEN (533) ASPIRIN (448) APIXABAN (317) CLOPIDOGREL BISULFATE (314) FLUINDIONE (286) AMIODARONE (277) FUROSEMIDE (277) DABIGATRAN ETEXILATE (223)

Which SOLIRIS Alternatives Have Lower International normalised ratio increased Risk?

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

Related Pages

SOLIRIS Full Profile All International normalised ratio increased Reports All Drugs Causing International normalised ratio increased SOLIRIS Demographics