- European Medicines Agency (EMA) recommended adding transverse myelitis, a rare type of spinal inflammation, as a side-effect of the Johnson & Johnson's JNJ COVID-19 vaccine.
- Giving updates on the safety of all coronavirus shots, the EMA said it was assessing reports of capillary leak syndrome, a rare blood condition after Moderna Inc's MRNA vaccine.
- The EMA said it had recorded six cases of capillary leak syndrome and was assessing all data, but it was not yet clear if there was a causal association between the reports and the vaccine.
- The EMA said there was insufficient evidence of a possible link between rare cases of the multisystem inflammatory syndrome and mRNA-based vaccines from Moderna and Pfizer Inc PFE - BioNTech SE BNTX vaccine.
- Price Action: JNJ shares traded lower by 0.83 at $162.90 on the last check Thursday.
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Posted In: BiotechNewsHealth CareFDAGeneralBriefsCOVID-19 CoronavirusCOVID-19 VaccineEuropean Medicines Agency
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