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The Adverse Events in FDAs Review Three FAERS reports were discussed FDAs briefing describes reports in its Adverse Event Reporting System involving an injection-site reaction, shortness of breath, diffuse skin darkening, and gum darkening

[DOI] [PMC free article] [PubMed] [Google Scholar] 12.Gomes A.P., Price N.L., Ling A.J., Moslehi J.J., Montgomery M.K., Rajman L., White J.P., Teodoro J.S., Wrann C.D., Hubbard B.P., et al

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