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FDA informed health care professionals of changes to the ADVERSE REACTIONS and POST-MARKETING sections of prescribing information for RotaTeq after six cases of Kawasaki disease were observed during the Phase III clinical trial. Kawasaki is also upgrading its L20A gas turbon line-up, with low 150kW-20MW emission technology. Genetic evidence now suggests that a previously unknown coronavirus may account for some of the many respiratory diseases for which a causative agent is unidentified, and may have a role in Kawasaki disease, the most common cause of acquired heart disease in children in developed countries. |
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