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Important: This site presents data from the FDA Adverse Event Reporting System (FAERS). A report does not mean the drug caused the event. Full disclaimer.

Does SOTROVIMAB Cause Product use issue? 47 Reports in FDA Database

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According to the FDA Adverse Event Reporting System (FAERS), 47 reports of Product use issue have been filed in association with SOTROVIMAB. This represents 1.1% of all adverse event reports for SOTROVIMAB.

47
Reports of Product use issue with SOTROVIMAB
1.1%
of all SOTROVIMAB reports
6
Deaths
5
Hospitalizations

How Dangerous Is Product use issue From SOTROVIMAB?

Of the 47 reports, 6 (12.8%) resulted in death, 5 (10.6%) required hospitalization.

Is Product use issue Listed in the Official Label?

This adverse event is not currently listed in the official FDA drug label for SOTROVIMAB. However, 47 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 use issue?

INFLIXIMAB (12,752) DUPILUMAB (10,575) POLYETHYLENE GLYCOL 3350 (9,432) METHOTREXATE (8,185) DICLOFENAC (8,009) RITUXIMAB (6,948) ADALIMUMAB (6,379) ETANERCEPT (6,062) TOCILIZUMAB (5,944) ABATACEPT (5,915)

Which SOTROVIMAB Alternatives Have Lower Product use issue Risk?

SOTROVIMAB vs SOVALDI SOTROVIMAB vs SOYBEAN OIL SOTROVIMAB vs SPARSENTAN SOTROVIMAB vs SPARTALIZUMAB SOTROVIMAB vs SPESOLIMAB-SBZO

Related Pages

SOTROVIMAB Full Profile All Product use issue Reports All Drugs Causing Product use issue SOTROVIMAB Demographics