Tag Archives: FDA

The US Food and Drug Administration on Monday gave the green light to updated Covid-19 vaccine booster shots from Moderna and Pfizer/BioNTech. The updated vaccines are each approved for people 12 and older and are authorized under emergency use for individuals 6 months through 11 years old. As part of …

Neuralink aims to solve a range of medical complaints by implanting a chip into a subject’s skull. Neuralink, Elon Musk’s brain implant company which hopes to use its technology to treat conditions such as paralysis and blindness, has been cleared to conduct human trials after it received approval from the …

The US Food and Drug Administration has approved a fast-acting nasal spray from Pfizer designed to treat migraines, the US pharmaceutical giant said Friday. Pfizer said it expected the drug, marketed under the name Zavzpret, to be available in pharmacies in July 2023. “The FDA approval of Zavzpret marks a …

Diabetes injections used for weight loss without a doctor’s prescription are far more dangerous than people think, doctors have said amid a recent diet fad that has worsened the global shortage of such medications. From TikTok videos to advertisements on Instagram, weight loss injections are being promoted as a miracle …

The U.S. Food and Drug Administration on Tuesday authorized the use of a booster shot of Pfizer and BioNTech’s COVID-19 vaccine for children aged 5 to 11, making everyone in the country over the age of 5 eligible for a third shot. The U.S. Centers for Disease Control and Prevention …

Moderna on Thursday asked U.S. regulators to authorize low doses of its COVID-19 vaccine for children younger than 6, a long-awaited move toward potentially opening shots for millions of tots by summer. Frustrated families are waiting impatiently for a chance to protect the nation’s littlest kids as all around them …

The Food and Drug Administration has granted emergency use authorization to a new COVID-19 test that can detect infections with only a sample of a patient’s breath, using a device that can yield results in less than three minutes. The agency says the InspectIR COVID-19 Breathalyzer will only be available …

U.S. health regulators on Thursday authorized the second pill against COVID-19, providing another easy-to-use medication to battle the rising tide of omicron infections. The Food and Drug Administration authorization comes one day after the agency cleared a competing drug from Pfizer. That pill is likely to become the first-choice treatment …

The new Pfizer COVID-19 pill may not see Emergency Use Authorization for another month as health officials continue to highlight the promising effects it may bring. Dr. Anthony Fauci praised the data presented by Pfizer regarding the COVID pill, which someone would take within 48 hours of showing symptoms and …

The Pfizer/BioNTech COVID-19 vaccine showed 90.7% efficacy against the coronavirus in a clinical trial of children 5 to 11 years old, the U.S. drugmaker said on Friday. Sixteen children in the trial who had received a placebo got COVID-19, compared with 3 who were vaccinated, Pfizer said in briefing documents …

The US Food and Drug Administration is expected to soon recommend that persons 40 and older receive Pfizer or Moderna COVID-19 booster shots, CNN reported on Tuesday. The US has administered 409,438,987 doses of COVID-19 vaccines in the country as of Tuesday morning and distributed 495,844,635 doses, the US Centers …

The Pfizer Inc/BioNTech SE COVID-19 vaccine was 93 percent effective in preventing hospitalizations among those aged 12 to 18, according to an analysis released by the US Centers for Disease Control and Prevention (CDC) on Tuesday. The study was conducted between June and September when the extremely contagious Delta variant …

Merck & Co Inc said on Monday it has applied for emergency use authorization in the US for its oral drug to treat mild-to-moderate patients of COVID-19. The treatment, molnupiravir, has been developed with Ridgeback Biotherapeutics. If authorized, it would be the first oral antiviral medication. Data released last week …

The United States will accept the use by international visitors of COVID-19 vaccines authorized by US regulators or the World Health Organization, the Centers for Disease Control and Prevention said late on Friday. On Sept. 20, the White House announced the United States in November would lift travel restrictions on …

Pfizer Inc and BioNTech said on Thursday they had asked US regulators to approve emergency use of their COVID-19 vaccine for children aged from five to 11, Pfizer said in a post on Twitter. “We and BioNTech Group officially submitted our request to US FDA for Emergency Use Authorization (EUA) …

Biden administration officials say a new pill that could provide an easier, effective way to treat COVID 19 is good news while adding vaccination remains the key to controlling the pandemic. Officials at drug maker Merck say they’ll soon seek regulatory approval for the experimental pill, which reduced hospitalizations and …

Booster shots to bolster immunity against the coronavirus would be free and accessible, US President Joe Biden said on Friday, one day after federal health agencies backed a booster rollout, and he pledged to get his own shot as soon as possible. “Like your first and second shot. The booster …

German company BioNTech, which in partnership with Pfizer developed one of the most widely used anti-Covid shots, says it’s preparing for the worldwide launch of its jab for younger recipients and might get approval in October. An mRNA vaccine against coronavirus for children aged between five and 11 years old …

US President Joe Biden has signed an executive order requiring all federal workers and contractors to be vaccinated against Covid-19, according to multiple reports. The order is one of several measures Biden is expected to announce. Biden signed the order on Thursday, hours before he was due to give a …

Health experts in the US are warning people against the use of Ivermectin, a drug that is often used to treat or prevent parasites in horses and other animals, as a home remedy for COVID-19. The Food and Drug Administration (FDA) said recently of a growing trend interest in using …