Does SOTROVIMAB Cause Product administration error? 17 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 17 reports of Product administration error have been filed in association with SOTROVIMAB. This represents 0.4% of all adverse event reports for SOTROVIMAB.
17
Reports of Product administration error with SOTROVIMAB
0.4%
of all SOTROVIMAB reports
0
Deaths
1
Hospitalizations
How Dangerous Is Product administration error From SOTROVIMAB?
Of the 17 reports, 1 (5.9%) required hospitalization.
Is Product administration error Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for SOTROVIMAB. However, 17 reports have been filed with the FAERS database.
What Other Side Effects Does SOTROVIMAB Cause?
Exposure during pregnancy (1,348)
Infusion related reaction (275)
Product storage error (259)
Off label use (231)
Pyrexia (185)
Covid-19 (158)
Nausea (135)
Dyspnoea (134)
Live birth (133)
Pruritus (107)
What Other Drugs Cause Product administration error?
HYDROXYPROGESTERONE CAPROATE (972)
ACETAMINOPHEN (666)
CENEGERMIN-BKBJ (613)
LEUPROLIDE (595)
EVOLOCUMAB (565)
ADALIMUMAB (543)
METHYLPHENIDATE (414)
OLMESARTAN MEDOXOMIL (314)
ASPIRIN (241)
SECUKINUMAB (225)
Which SOTROVIMAB Alternatives Have Lower Product administration error Risk?
SOTROVIMAB vs SOVALDI
SOTROVIMAB vs SOYBEAN OIL
SOTROVIMAB vs SPARSENTAN
SOTROVIMAB vs SPARTALIZUMAB
SOTROVIMAB vs SPESOLIMAB-SBZO