Does SOTROVIMAB Cause Fibrin d dimer increased? 11 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 11 reports of Fibrin d dimer increased have been filed in association with SOTROVIMAB. This represents 0.3% of all adverse event reports for SOTROVIMAB.
11
Reports of Fibrin d dimer increased with SOTROVIMAB
0.3%
of all SOTROVIMAB reports
7
Deaths
9
Hospitalizations
How Dangerous Is Fibrin d dimer increased From SOTROVIMAB?
Of the 11 reports, 7 (63.6%) resulted in death, 9 (81.8%) required hospitalization, and 6 (54.5%) were considered life-threatening.
Is Fibrin d dimer increased Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for SOTROVIMAB. However, 11 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 Fibrin d dimer increased?
ADALIMUMAB (97)
RIVAROXABAN (91)
PREDNISONE (69)
RITUXIMAB (63)
APIXABAN (59)
ASPIRIN (54)
ACETAMINOPHEN (53)
LENALIDOMIDE (53)
METHOTREXATE (52)
BAMLANIVIMAB (49)
Which SOTROVIMAB Alternatives Have Lower Fibrin d dimer increased Risk?
SOTROVIMAB vs SOVALDI
SOTROVIMAB vs SOYBEAN OIL
SOTROVIMAB vs SPARSENTAN
SOTROVIMAB vs SPARTALIZUMAB
SOTROVIMAB vs SPESOLIMAB-SBZO