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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 SOTATERCEPT-CSRK Cause Epistaxis? 151 Reports in FDA Database

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According to the FDA Adverse Event Reporting System (FAERS), 151 reports of Epistaxis have been filed in association with SOTATERCEPT-CSRK (WINREVAIR). This represents 9.5% of all adverse event reports for SOTATERCEPT-CSRK.

151
Reports of Epistaxis with SOTATERCEPT-CSRK
9.5%
of all SOTATERCEPT-CSRK reports
0
Deaths
38
Hospitalizations

How Dangerous Is Epistaxis From SOTATERCEPT-CSRK?

Of the 151 reports, 38 (25.2%) required hospitalization, and 2 (1.3%) were considered life-threatening.

Is Epistaxis Listed in the Official Label?

Yes, Epistaxis is listed as a known adverse reaction in the official FDA drug label for SOTATERCEPT-CSRK.

What Other Side Effects Does SOTATERCEPT-CSRK Cause?

Headache (187) Diarrhoea (132) Haemoglobin increased (100) Dyspnoea (93) Fatigue (93) No adverse event (93) Dizziness (90) Nausea (88) Dyspnoea exertional (61) Pericardial effusion (60)

What Other Drugs Cause Epistaxis?

RIVAROXABAN (5,629) ASPIRIN (3,214) APIXABAN (2,831) FLUTICASONE (1,745) TREPROSTINIL (1,726) CLOPIDOGREL BISULFATE (1,560) BEVACIZUMAB (1,542) WARFARIN (1,498) PALBOCICLIB (1,280) ADALIMUMAB (1,243)

Which SOTATERCEPT-CSRK Alternatives Have Lower Epistaxis Risk?

SOTATERCEPT-CSRK vs SOTORASIB SOTATERCEPT-CSRK vs SOTROVIMAB SOTATERCEPT-CSRK vs SOVALDI SOTATERCEPT-CSRK vs SOYBEAN OIL SOTATERCEPT-CSRK vs SPARSENTAN

Related Pages

SOTATERCEPT-CSRK Full Profile All Epistaxis Reports All Drugs Causing Epistaxis SOTATERCEPT-CSRK Demographics