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137 vaccine recipients experienced 'serious' adverse reactions - FDA

Philippines | National

137 vaccine recipients experienced 'serious' adverse reactions - FDA

By Analou de Vera

The Food and Drug Administration (FDA) said that 137 out of 240,297 coronavirus disease (COVID-19) vaccine recipients have experienced “serious” adverse reactions.

FDA Director-General Rolando Enrique Domingo on Thursday, March 18, said that 83 recipients suffered serious side effects after receiving Sinovac Biotech’s vaccine while 54 people who were administered with AstraZeneca vaccine also experienced serious adverse reactions.

Among the common serious reactions noted by the FDA include allergic reactions, chest pain, nasal congestion, palpitations among others.

Meanwhile, 3,616 individuals vaccinated with the Sinovac vaccine had “non-serious” side effects while for AstraZeneca, there were 3,715 recipients who experienced the same level of adverse reaction.

“Every single report of AEFI (adverse events following immunization) reported in the Philippines is treated with utmost seriousness. There is a thorough examination of every step of the vaccination process and it is done with great care,” said National Adverse Events Following Immunization Vice Chairman Dr. Rommel Lobo.

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