KIGALI | Xinhua | The Rwanda Food and Drugs Authority (Rwanda FDA) announced Sunday that it has shut down eight liquor factories “in the interest of public health,” as the government intensifies efforts to curb alcohol abuse, particularly among young people. In a notice addressed to manufacturers, distributors, retailers and …
Read More »UNAIDS urges Gilead to cut price of new HIV prevention drug
GENEVA, Switzerland | THE INDEPENDENT | The United States Food and Drug Administration (FDA) has approved long-acting injectable lenacapavir for HIV prevention. The new medicine is administered by injection once every 6 months and is a significant step in improving prevention options for people at risk of HIV infection around the …
Read More »Tunisia announces to stop using Johnson & Johnson COVID-19 vaccine
Tunis, Tunisia | Xinhua | Tunisian Health Ministry decided to suspend using the Johnson & Johnson COVID-19 vaccine (Janssen), the official Tunis Afrique Presse reported on Monday. The Health Minister Ali Mrabet said at a press conference on Monday that Tunisian government made this decision after the U.S. Food and Drug …
Read More »Moderna to request FDA’s approval for vaccinating children aged under 6
Los Angeles, U.S. | Xinhua | American biotechnology company Moderna said Wednesday it will request the U.S. Food and Drug Administration (FDA) to grant emergency use authorization for its COVID-19 vaccine for children aged under 6. The company will submit the request to the FDA, as well as the European Medicines …
Read More »U.S. FDA okays emergency use of molnupiravir pill for COVID-19
Washington, U.S. | Xinhua | The U.S. Food and Drug Administration (FDA) on Thursday authorized American pharmaceutical company Merck’s oral antiviral for the treatment of mild-to-moderate COVID-19, the second pill approved for treating COVID-19 following the one from Pfizer. Merck’s pill, called molnupiravir, is authorized to use in adults with positive …
Read More »U.S. FDA authorizes first oral antiviral for COVID-19 treatment
Washington, U.S. | Xinhua | The U.S. Food and Drug Administration on Wednesday authorized Pfizer’s oral antiviral tablets for the treatment of mild-to-moderate COVID-19, the first pill approved for COVID-19 treatment in the country. The pill, called Paxlovid, is authorized for use in adults and pediatric patients 12 years of age …
Read More »U.S. authorizes Pfizer/BioNTech, Moderna COVID-19 vaccine boosters for all adults
New York, U.S. | Xinhua | The U.S. Food and Drug Administration (FDA) on Friday authorized boosters of the Pfizer/BioNTech and Moderna COVID-19 vaccines for all adults. The agency expanded emergency use authorization for booster doses of both the mRNA vaccines beyond who was previously eligible — boosters had been authorized …
Read More »Pfizer asks U.S. FDA to authorize COVID-19 booster for all 18 and up
New York, U.S. | Xinhua | Drugmakers Pfizer and BioNTech said on Tuesday that they had asked the U.S. Food and Drug Administration (FDA) to authorize booster shots of their COVID-19 vaccine for all adults 18 years old and over, seeking to broaden who is eligible for a third shot. The …
Read More »White House unveils plan to roll out COVID-19 vaccines for children ages 5 to 11
Washington, U.S. | Xinhua | The White House on Wednesday unveiled its plan to roll out COVID-19 vaccines for children ages 5 to 11, pending the vaccine’s approval by the U.S. Food and Drug Administration (FDA). “In anticipation of the FDA’s independent advisory committee meeting on October 26 and the CDC’s …
Read More »U.S. FDA approves Moderna, J&J COVID-19 boosters, allows ‘mix and match’ shots
Washington, U.S. | Xinhua | The U.S. Food and Drug Administration (FDA) on Wednesday authorized COVID-19 booster doses of Moderna and Johnson & Johnson, and approved “mix and match” booster dose for currently available approved COVID-19 vaccines. The agency authorized the use of a single booster dose of the Moderna COVID-19 …
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