ChAdOx1-S[recombinant] (COVID-19 Vaccine AstraZeneca)

ChAdOx1-S[recombinant] VAXZEVRIA (COVID-19 Vaccine AstraZeneca) On 28 January 2021, the Food and Drug Administration (FDA) issued authorization (amended on 10 March 2022) granting AstraZeneca Pharmaceuticals (Phils.) Inc. the emergency use approval […]

FDA Advisory No.2021-2380 || Public Health Warning Against the Purchase of COVID-19 Vaccines from Online Selling Platforms and Social Media Market Places

According to the Interpol “You cannot find legitimate, approved COVID-19 vaccines for sale on the internet; legitimate vaccines are not for sale, they are strictly administered and distributed by national […]

FDA Advisory No.2021-1165-A || Babala sa Publiko Tungkol sa Pagbili at Paggamit ng mga Sumusunod na Hindi Rehistradong Gamot:

Pinapayuhan ng Food and Drug Administration (FDA) ang publiko laban sa pagbili at paggamit ng mga sumusunod na hindi rehistradong gamot: 1. Candesartan Cilexetil Tablets 4mg 2. SHI HUI DA® […]

FDA Advisory No.2021-1165 || Public Health Warning Against the Purchase and Use of the Following Unregistered Drug Products:

The Food and Drug Administration (FDA) advises the public against the purchase and use of the following unregistered drug products: 1. Candesartan Cilexetil Tablets 4mg 2. SHI HUI DA® Levamlodipine […]

FDA Advisory No.2021-1191-A || Babala sa Publiko Tungkol sa Pagbili at Paggamit ng mga Sumusunod na Hindi Rehistradong Gamot:

Pinapayuhan ng Food and Drug Administration (FDA) ang publiko laban sa pagbili at paggamit ng mga sumusunod na hindi rehistradong gamot: 1. AstraZeneca Betaloc Metoprolol Tartrate Tablets – Jiushisuan Meituoluo’er […]

FDA Advisory No.2021-1191 || Public Health Warning Against the Purchase and Use of the Following Unregistered Drug Products:

The Food and Drug Administration (FDA) advises the public against the purchase and use of the following unregistered drug products: 1. AstraZeneca Betaloc Metoprolol Tartrate Tablets – Jiushisuan Meituoluo’er Pian […]

List of FDA issued Emergency Use Authorization

Emergency Use Authorization Emergency Use Authorization (EUA) is an authorization issued for unregistered drugs and vaccines in a public health emergency. The FDA Director General, by virtue of the Executive […]

FDA Advisory No. 2019-169 || Safety Information: SGLT2 inhibitors and risk of necrotizing fasciitis of the perineum (Fournier’s gangrene)

Introduction The US FDA has released safety announcement on rare occurrences of a serious infection of the genitals with sodium-glucose cotransporter-2 (SGLT2) inhibitors. The serious rare infection, called necrotizing fasciitis […]