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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 Extra dose administered? 8 Reports in FDA Database

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According to the FDA Adverse Event Reporting System (FAERS), 8 reports of Extra dose administered have been filed in association with SOTROVIMAB. This represents 0.2% of all adverse event reports for SOTROVIMAB.

8
Reports of Extra dose administered with SOTROVIMAB
0.2%
of all SOTROVIMAB reports
0
Deaths
0
Hospitalizations

How Dangerous Is Extra dose administered From SOTROVIMAB?

Of the 8 reports.

Is Extra dose administered Listed in the Official Label?

This adverse event is not currently listed in the official FDA drug label for SOTROVIMAB. However, 8 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 Extra dose administered?

TIRZEPATIDE (6,774) DULAGLUTIDE (3,047) LORATADINE (1,556) DUPILUMAB (1,422) FEXOFENADINE (1,413) NAPROXEN (908) POLYETHYLENE GLYCOL 3350 (589) ACETAMINOPHEN (552) DALFAMPRIDINE (519) FLUTICASONE\SALMETEROL (499)

Which SOTROVIMAB Alternatives Have Lower Extra dose administered Risk?

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

Related Pages

SOTROVIMAB Full Profile All Extra dose administered Reports All Drugs Causing Extra dose administered SOTROVIMAB Demographics