Does SOTATERCEPT-CSRK Cause Condition aggravated? 12 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 12 reports of Condition aggravated have been filed in association with SOTATERCEPT-CSRK (WINREVAIR). This represents 0.8% of all adverse event reports for SOTATERCEPT-CSRK.
12
Reports of Condition aggravated with SOTATERCEPT-CSRK
0.8%
of all SOTATERCEPT-CSRK reports
1
Deaths
4
Hospitalizations
How Dangerous Is Condition aggravated From SOTATERCEPT-CSRK?
Of the 12 reports, 1 (8.3%) resulted in death, 4 (33.3%) required hospitalization.
Is Condition aggravated Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for SOTATERCEPT-CSRK. However, 12 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 Condition aggravated?
TOFACITINIB (16,925)
INFLIXIMAB (16,616)
DUPILUMAB (16,459)
ETANERCEPT (15,897)
METHOTREXATE (14,938)
ADALIMUMAB (13,527)
PREDNISONE (10,751)
INFLIXIMAB-DYYB (10,275)
HYDROXYCHLOROQUINE (8,848)
RITUXIMAB (8,627)
Which SOTATERCEPT-CSRK Alternatives Have Lower Condition aggravated Risk?
SOTATERCEPT-CSRK vs SOTORASIB
SOTATERCEPT-CSRK vs SOTROVIMAB
SOTATERCEPT-CSRK vs SOVALDI
SOTATERCEPT-CSRK vs SOYBEAN OIL
SOTATERCEPT-CSRK vs SPARSENTAN