Important: VAERS reports alone cannot determine if a vaccine caused an adverse event. Reports may contain incomplete, inaccurate, or unverified information. Correlation does not equal causation.
#379 most reported symptom for this vaccine
Fibrin D dimer has been reported 53 times in association with COVID-19 Bivalent (Moderna) vaccination in VAERS. This represents 0.1% of all 42,946 reports for this vaccine.
Among these reports, 0 mentioned death (0.00%) and 24 involved hospitalization (45.3%).
Fibrin D dimer is the #379 most frequently reported symptom for COVID-19 Bivalent (Moderna) out of 2434 total symptoms.
Disclaimer: VAERS reports describe events that occurred after vaccination but do not establish that the vaccine caused the event. Many reported symptoms may be coincidental or related to underlying conditions.
Seeing 53 reports of Fibrin D dimer after COVID-19 Bivalent (Moderna) vaccination may seem alarming, but context is critical.
The mortality rate among these reports is very low at 0.00%, suggesting most cases are non-fatal.
This data comes from the Vaccine Adverse Event Reporting System (VAERS), jointly managed by CDC and FDA.