Does SOTATERCEPT Cause Product administration interrupted? 10 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 10 reports of Product administration interrupted have been filed in association with SOTATERCEPT. This represents 1.0% of all adverse event reports for SOTATERCEPT.
10
Reports of Product administration interrupted with SOTATERCEPT
1.0%
of all SOTATERCEPT reports
2
Deaths
7
Hospitalizations
How Dangerous Is Product administration interrupted From SOTATERCEPT?
Of the 10 reports, 2 (20.0%) resulted in death, 7 (70.0%) required hospitalization, and 1 (10.0%) were considered life-threatening.
Is Product administration interrupted Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for SOTATERCEPT. However, 10 reports have been filed with the FAERS database.
What Other Side Effects Does SOTATERCEPT Cause?
Headache (214)
Haemoglobin increased (151)
Nausea (131)
Diarrhoea (130)
Epistaxis (130)
Fatigue (125)
Dizziness (109)
Dyspnoea (84)
Pericardial effusion (65)
Vomiting (61)
What Other Drugs Cause Product administration interrupted?
CALCIUM OXYBATE\MAGNESIUM OXYBATE\POTASSIUM OXYBATE\SODIUM OXYBATE (1,446)
SODIUM OXYBATE (1,272)
CANNABIDIOL (511)
ISOTRETINOIN (503)
APREMILAST (314)
TREPROSTINIL (295)
EPOPROSTENOL (205)
LENALIDOMIDE (146)
ETANERCEPT (142)
INTERFERON BETA-1A (115)
Which SOTATERCEPT Alternatives Have Lower Product administration interrupted Risk?
SOTATERCEPT vs SOTATERCEPT-CSRK
SOTATERCEPT vs SOTORASIB
SOTATERCEPT vs SOTROVIMAB
SOTATERCEPT vs SOVALDI
SOTATERCEPT vs SOYBEAN OIL