DOH reminded the public that the Philippine government had no registered COVID-19 vaccine yet. The Department of Health (DOH) on Monday reminded the public that the Philippine government had no registered COVID-19 vaccine yet. For a vaccine to be approved in the country, the manufacturer must secure clearance from the Food and Drug Administration (FDA), … Read more
US FDA was set to make EUA data public for COVID-19 vaccines. The United States Food and Drug Administration (US FDA) on Tuesday said that it would make public reviews of all data and information about the emergency use authorization (EUA) granted to COVID-19 vaccines. In a statement, US FDA Commissioner Stephen Hahn said that … Read more
Reno Liver Spread secured FDA registration. Reno liver spread brand was already back in the Philippine market after securing a product registration certificate from the Food and Drug Administration (FDA). The said news was confirmed by FDA Director General Eric Domingo. On Friday, Domingo told GMA News Online that the Reno liver spread already have … Read more
FDA had warned consumers against buying and using “misbranded” face masks. The Food and Drug Administration (FDA) had warned consumers against purchasing and using “misbranded” face masks that have labels printed in foreign characters. This, as the Food and Drug Administration posted an advisory on its Facebook page. In its advisory, FDA Director General Dr. … Read more
FDA Philippines reminded the public about the use of the UK’s new antiviral drug. The Food and Drug Administration (FDA) Philippines recently reminded the public about the use of the UK’s new antiviral drug in the Philippines. This, as FDA Philippines on Friday released FDA Advisory No. 2020-1131 reminding the public about the use of … Read more
Japan planned to approve Remdesivir in treating patients with COVID-19, according to the Japanese government. Japan on Thursday planned to approve the antiviral drug Remdesivir in treating patients with coronavirus disease 2019 or COVID-19, according to the Japanese government. Aside from this, Japan was also targeting to approve the anti-flu drug Avigan this month. Japan … Read more
The US FDA approved the emergency use of Remdesivir in treating patients with severe COVID-19. US FDA — The Food and Drug Administration in the United States approved the emergency use of Remdesivir in treating patients with severe COVID-19. This, as US Food and Drug Administration Commissioner Stephen Hahn said that the experimental drug, Remdesivir, … Read more
The Fabunan Antiviral Injection still wasn’t registered with the FDA, according to DOH. The Fabunan Antiviral Injection still wasn’t registered with the Food and Drug Administration, according to the Department of Health. This, as Maria Rosario Vergeire, the undersecretary of the Department of Health, told reporters in a virtual briefing on Tuesday that the public … Read more
Bodysphere Inc’s COVID-19 Rapid Test Kit was approved by the United States Food and Drug Administration. The United States Food and Drug Administration (FDA) approved the COVID-19 rapid test kit from Bodysphere Inc. This, as Reuters reported that the Bodysphere Inc’s COVID-19 Rapid Test Kit can detect the COVID-19 or the coronavirus disease in “two … Read more
The Food and Drug Administration (FDA) in the United States already made an update on its guidelines for its testing procedures The Food and Drug Administration (FDA) in the United States already made an update on its guidelines for its testing procedures in order for their patients to make the process more comfortable. This would … Read more
