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The Food and Drug Administration (FDA) clarifies that Remdesivir is not approved by the FDA for treatment of COVID-19. Remdesivir is use in adults and pediatric patients (12 years of age and older and weighing at least 40 kg) for the treatment of COVID-19 requiring hospitalization.
On 10 March 2022, the Food and Drug Administration (FDA) issued authorization (amended on 20 June 2022) granting Pfizer, Inc. the emergency use approval of Nirmatrelvir + Ritonavir (Paxlovid).
Overview & Facts. Types & Symptoms. Diagnosis & Medications. Cold sores are a common viral infection. They are tiny, fluid-filled blisters on and around your lips. These blisters are often grouped together in patches. After the blisters break, a crust forms over the resulting sore.
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 Order No. 121 of the President of the Philippines, authorizes the issuance of the EUA. List of COVID-19 Vaccines Authorized by the FDA.
List of antiviral drugs. Antiviral drugs are different from antibiotics. Flu antiviral drugs are different from antiviral drugs used to treat other infectious diseases such as COVID-19. Antiviral drugs prescribed to treat COVID-19 are not approved or authorized to treat flu. [1]
Nov 23, 2021 · Molnupiravir, developed by the US drug companies Merck, Sharp and Dohme and Ridgeback Biotherapeutics, is the first antiviral medication for Covid-19 that can be taken orally, rather than injected or given intravenously. Patients must take the drug within five days of symptoms, according to experts.
Dec 23, 2021 · Merck. & Co. MANILA, Philippines — The Philippines’ drug regulator has given the first emergency use authorization for an anti-COVID pill, allowing wider use of the drug that was previously...
