Does SOTATERCEPT-CSRK Cause Complication associated with device? 16 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 16 reports of Complication associated with device have been filed in association with SOTATERCEPT-CSRK (WINREVAIR). This represents 1.0% of all adverse event reports for SOTATERCEPT-CSRK.
16
Reports of Complication associated with device with SOTATERCEPT-CSRK
1.0%
of all SOTATERCEPT-CSRK reports
1
Deaths
14
Hospitalizations
How Dangerous Is Complication associated with device From SOTATERCEPT-CSRK?
Of the 16 reports, 1 (6.3%) resulted in death, 14 (87.5%) required hospitalization.
Is Complication associated with device Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for SOTATERCEPT-CSRK. However, 16 reports have been filed with the FAERS database.
What Other Side Effects Does SOTATERCEPT-CSRK Cause?
Headache (187)
Epistaxis (151)
Diarrhoea (132)
Haemoglobin increased (100)
Dyspnoea (93)
Fatigue (93)
No adverse event (93)
Dizziness (90)
Nausea (88)
Dyspnoea exertional (61)
What Other Drugs Cause Complication associated with device?
ETONOGESTREL (6,047)
COPPER (1,083)
BACLOFEN (525)
TREPROSTINIL (422)
EPOPROSTENOL (399)
LEVONORGESTREL (344)
ADALIMUMAB (269)
CARBIDOPA\LEVODOPA (169)
MACITENTAN (169)
TEDUGLUTIDE (133)
Which SOTATERCEPT-CSRK Alternatives Have Lower Complication associated with device Risk?
SOTATERCEPT-CSRK vs SOTORASIB
SOTATERCEPT-CSRK vs SOTROVIMAB
SOTATERCEPT-CSRK vs SOVALDI
SOTATERCEPT-CSRK vs SOYBEAN OIL
SOTATERCEPT-CSRK vs SPARSENTAN