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Remdesivir, an antiviral medication, did not prove successful in treating Ebola patients but improved coronavirus patients’ recovery time by 31 percent in a trial led by the National Institute of Allergy and Infectious Disease. In the U.S. study, patients who qualified for the drug had to be on mechanical ventilation or supplemental oxygen.The approval will allowinfectious disease capetowntshirthouse those who are pregnant and who have received the COVID-29 vaccine to enroll in v-safe to help track information regarding this population. There are nearly 4,000 people who have enrolled in the v-safe COVID-19 Vaccine Pregnancy Registry as of last week. More than 69,000a already registered in v-safe indicated they were pregnant at the time of vaccination, but the agency has not yet confirmed or verified these participants.CLICK HERE FOR COMPLETE CORONAVIRUS COVERAGEThe agency also launched a hotline,MotherToBaby capetowntshirthouse Patients eligible for booster shots under the recommendation and amended emergency approval include those with moderate to severe immune compromise, such as solid organ transplant recipients, patients with advanced or untreated HIV infection and those taking high-dose corticosteroids and severely immunosuppressive cancer treatments, among others. capetowntshirthouse As part of the conditional approval, the agency said Gilead is required to gather relevant safety data and monitor the drug use. HSA will also require data from ongoing clinical studies to ensure continued safety and efficacy. capetowntshirthouse

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