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Covid-19 vaccines: Investigate adverse events and make reports public, say public health professionals March 17, 2021 EMA report on AstraZeneca-Oxford vaccine and blood clot reports expected tomorrow Even as the European Medicines Agency (EMA) reviews the AstraZeneca-Oxford University vaccine after more than 10 countries temporarily suspended its use, a group of public health professionals have called for an investigation of deaths and serious adverse events in India as well. “AEFIs (adverse events following immunisation) are to be investigated through well-defined procedures for vaccine pharmacovigilance, and the reports made available in the public domain, for trust-building and transparency,” the public health representatives said in a letter to Health Minister Dr Harsh Vardhan and others involved with the vaccines programme.

Anand groverYogesh jainT jacob johnAmar jesaniVeena johariAstrazeneca oxford universityRight to healthEuropean medicines agencyHealth minister dr harsh vardhanSandhya srinivasanConsulting editorIndian journalMedical ethicsSenior advocateAstrazeneca oxford university vaccineCo vid