Does SOTATERCEPT-CSRK Cause Haemoglobin increased? 100 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 100 reports of Haemoglobin increased have been filed in association with SOTATERCEPT-CSRK (WINREVAIR). This represents 6.3% of all adverse event reports for SOTATERCEPT-CSRK.
100
Reports of Haemoglobin increased with SOTATERCEPT-CSRK
6.3%
of all SOTATERCEPT-CSRK reports
3
Deaths
18
Hospitalizations
How Dangerous Is Haemoglobin increased From SOTATERCEPT-CSRK?
Of the 100 reports, 3 (3.0%) resulted in death, 18 (18.0%) required hospitalization.
Is Haemoglobin increased Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for SOTATERCEPT-CSRK. However, 100 reports have been filed with the FAERS database.
What Other Side Effects Does SOTATERCEPT-CSRK Cause?
Headache (187)
Epistaxis (151)
Diarrhoea (132)
Dyspnoea (93)
Fatigue (93)
No adverse event (93)
Dizziness (90)
Nausea (88)
Dyspnoea exertional (61)
Pericardial effusion (60)
What Other Drugs Cause Haemoglobin increased?
RUXOLITINIB (332)
TREPROSTINIL (245)
SOTATERCEPT (151)
CLOZAPINE (142)
DARBEPOETIN ALFA (99)
TESTOSTERONE (96)
METFORMIN (93)
VOXELOTOR (86)
ROSUVASTATIN (85)
ADALIMUMAB (81)
Which SOTATERCEPT-CSRK Alternatives Have Lower Haemoglobin increased Risk?
SOTATERCEPT-CSRK vs SOTORASIB
SOTATERCEPT-CSRK vs SOTROVIMAB
SOTATERCEPT-CSRK vs SOVALDI
SOTATERCEPT-CSRK vs SOYBEAN OIL
SOTATERCEPT-CSRK vs SPARSENTAN