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.
#39 most reported symptom for this vaccine
Dyspnoea has been reported 16 times in association with Rubella (Meruvax II) vaccination in VAERS. This represents 1.6% of all 1,021 reports for this vaccine.
Among these reports, 1 mentioned death (6.25%) and 4 involved hospitalization (25.0%).
Dyspnoea is the #39 most frequently reported symptom for Rubella (Meruvax II) out of 178 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 16 reports of Dyspnoea after Rubella (Meruvax II) vaccination may seem alarming, but context is critical.
The 6.25% mortality rate among these reports is elevated, but this reflects the severity of the condition itself rather than vaccine causation.
This data comes from the Vaccine Adverse Event Reporting System (VAERS), jointly managed by CDC and FDA.