Does SOTROVIMAB Cause Wrong product administered? 6 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 6 reports of Wrong product administered have been filed in association with SOTROVIMAB. This represents 0.2% of all adverse event reports for SOTROVIMAB.
6
Reports of Wrong product administered with SOTROVIMAB
0.2%
of all SOTROVIMAB reports
0
Deaths
0
Hospitalizations
How Dangerous Is Wrong product administered From SOTROVIMAB?
Of the 6 reports.
Is Wrong product administered Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for SOTROVIMAB. However, 6 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 Wrong product administered?
INSULIN LISPRO (337)
INSULIN GLARGINE (226)
RISPERIDONE (141)
QUETIAPINE (137)
ACETAMINOPHEN (133)
INSULIN ASPART (112)
CLOZAPINE (106)
INSULIN HUMAN (104)
TUBERCULIN PURIFIED PROTEIN DERIVATIVE (104)
IBUPROFEN (102)
Which SOTROVIMAB Alternatives Have Lower Wrong product administered Risk?
SOTROVIMAB vs SOVALDI
SOTROVIMAB vs SOYBEAN OIL
SOTROVIMAB vs SPARSENTAN
SOTROVIMAB vs SPARTALIZUMAB
SOTROVIMAB vs SPESOLIMAB-SBZO