Food and Drug Administration
Agency of the US Department of Health and Human Services
Food and Drug Administration ▸ Facts ▸ Comments ▸ News ▸ Videos
WH unveiled plans to vaccinate children. Hear from US surgeon general
Credit: Bleacher Report AOL Duration: 02:45Published
White House Rolls Out Vaccines For Kids
Credit: HuffPost NOW News Duration: 00:54Published
FDA to vote on J&J COVID-19 booster shoots; also looking into mixing and matching vaccine doses
Credit: ABC Action News Duration: 02:13Published
Credit: Bleacher Report AOL Duration: 04:15Published
FDA advisory committee endorses third dose of Moderna's COVID-19 vaccine for specific groups
Credit: ABC Action News Duration: 02:46Published
FDA to consider Moderna COVID-19 booster shots at Thursday's Advisory Committee Meeting
Credit: ABC Action News Duration: 02:14Published
Merck seeks FDA emergency use authorization for antiviral Covid-19 treatment
Credit: Bleacher Report AOL Duration: 03:06Published
Pfizer asks FDA to grant emergency use authorization for COVID-19 vaccine in kids aged 5 to 11
Credit: ABC Action News Duration: 02:11Published
'Terrible dilemma': Toobin on FDA's Alzheimer treatment approval
Credit: Bleacher Report AOL Duration: 01:48Published
Trump's FDA commissioner says Delta variant hasn't run its course
Credit: Bleacher Report AOL Duration: 02:19Published
Former FDA Commissioner: Delta variant will likely run its course by Thanksgiving
Credit: Bleacher Report AOL Duration: 09:04Published
Fauci reacts to FDA recommendation on Covid-19 booster shots
Credit: Bleacher Report AOL Duration: 02:48Published
Biden admin defends early booster push before vote by FDA advisers
Credit: Bleacher Report AOL Duration: 02:56Published
FDA vaccine panel rejects plan to offer Pfizer COVID-19 booster shots to all Americans
Credit: ABC Action News Duration: 01:28Published
Credit: FRANCE 24 English Duration: 01:35Published
FDA to discuss Pfizer booster shot
Credit: ABC Action News Duration: 01:53Published
3 new studies support arguments for a Pfizer booster - right before the FDA is set to debate a 3rd shot for fully vaccinated Ame
Credit: Bleacher Report AOL Duration: 09:12Published
Klain: FDA and CDC approval required before COVID booster shot rollout in September
Credit: Bleacher Report AOL Duration: 04:01Published
Klain: WH won't offer covid boosters without FDA, CDC sign off
Credit: Bleacher Report AOL Duration: 12:13Published
FDA urges people to stop taking Ivermectin for COVID-19
Credit: ABC Action News Duration: 02:04Published
You Might Like
Joe Rogan Has COVID, Cancels Show & Admits He's on IvermectinJoe says he's taking ivermectin -- the livestock de-wormer drug that the CDC and the FDA have specifically come out and warned against as a remedy to battle COVID. 🤷🏽♂️ Joe Rogan's..
'You are not a horse or a cow': Health officials warn against using livestock de-worming drug to treat COVID-19The US Food and Drug Agency (FDA) has issued a warning to people not to take an anti-parasitic drug designed for livestock to treat or prevent COVID-19 following multiple reports of poisonings.
Ocugen to take BLA route for Covaxin in US based on FDA recommendation; seek emergency use nod for CanadaBharat Biotech’s US partner Ocugen has dropped its plans of applying for an emergency use authorisation (EUA) for indigenously developed Covaxin and will be pursuing the biologics license application..
Covaxin's US approval delayed as FDA asks for more dataOcugen Inc said on Thursday it would no longer pursue an emergency use authorization for its Covid-19 vaccine candidate, Covaxin, and would instead aim to file for a full US approval of the shot...
DCGI waiver likely to bring foreign vaccines like Pfizer, Moderna a step closerIn a letter, DCGI Chief VG Somani letter said that this will be applicable for vaccines that have already been approved for restricted use by the US FDA, EMA, UK MHRA, PMDA Japan or listed for..
Uddhav Thackeray shunts FDA chief over Covid drug row
What is Remdesivir and is the drug really useful in treating COVID-19? All you need to knowRemdesivir was approved as the first drug to treat the virus by the US Food and Drug Administration in 2020.
Govt fast-tracks nod for Covid vaccination cleared in other countriesWith surging Covid-19 cases fuelling calls for faster vaccination, the Centre on Tuesday enabled faster access to foreign-made vaccines by doing away with bridging trial studies prior to grant of..
US recommends 'pause' to Johnson & Johnson jab rollout over blood clot fearsThe US Food and Drug Administration has recommended a "pause" to the rollout of the Johnson & Johnson COVID vaccine so it can investigate reports of blood clots.
Karnataka: KPSC FDA exam postponed after question paper leak, six heldThe dates for the test would be rescheduled and announced in due course, a press release said.
Johns Hopkins Professor Says U.S. COVID Response is Like 'Operation Turtle Speed'Operation Warp Speed is a misnomer, according to a Johns Hopkins doctor ... the frustrated doc says it's more like Operation Turtle Speed. Professor Marty Makary is angry the FDA hasn't gone the route..
USFDA may give impetus to plasma therapy in India, experts question efficacy
Zydus Cadila gets USFDA nod for drug trials to treat chemotherapy-induced anemiaIn a regulatory filing, Zydus Cadila said it has received approval from the US Food and Drug Administration (USFDA) to initiate clinical trials of Desidustat in CIA. Zydus Cadila Chairman Pankaj R..
FDA warns against combination of malaria drug and Gilead's remdesivirThe U.S. Food and Drug Administration on Monday issued a warning to healthcare providers against administering malaria drug hydroxychloroquine or chloroquine in combination with Gilead Sciences'..
India approves emergency use of remdesivir to treat Covid-19 patientsRemdesivir is the first drug to show improvement in Covid-19 patients in formal clinical trials. It was granted emergency use authorization by the US Food and Drug Administration last month and has..
NRI’s disinfectant tech gets US-FDA nod for medical useThe device — Molekule Air Pro RX — built by US firm Molekule based on technology developed by Yogi Goswami, has now been approved by the US Food and Drugs Administration (US-FDA) for medical use..
Roche wins U.S. nod for COVID-19 antibody test, aims to boost outputRoche has won emergency approval from the U.S. Food and Drug Administration (FDA) for an antibody test to determine whether people have ever been infected with the coronavirus, the Swiss drugmaker on..
US OKs remdesivir; India plans trialsThe US Food and Drug Administration has allowed emergency use of the experimental anti-viral drug remdesivir, previously used for Ebola, to treat Covid-19 patients even as India is looking to import..
'UN chief Guterres salutes countries like India for helping others in fight against Covid-19'UN Secretary-General Antonio Guterres salutes countries helping others in the global fight against the COVID-19 pandemic, his spokesman has said, days after India sent supplies of the anti-malarial..
Indian test kits may be non-starterNIV Validating Them But Govt Insists On USFDA Or EU Nod
Pvt labs with USFDA-approved kits can start testing for Covid-19The government has decided that private laboratories with Covid-19 testing kits approved by the US Food and Drug Administration (US FDA) can start testing suspected cases, significantly adding to the..
Make-in-India: Indo-US firm gets nod to test Covid-19 KitAn Indo-US firm — CoSara Diagnostics — based out of Baroda and supported by Bengaluru-based Centre for Cellular And Molecular Platforms (CCAMP) has developed a diagnostic kit for Covid-19, which..
FDA works to speed coronavirus tests with Roche, New York approvalsThe U.S. Food and Drug Administration (FDA) issued emergency authorization for a faster coronavirus test made by Swiss diagnostics maker Roche and allowed New York state to authorize certain labs to..
New Roche coronavirus test wins emergency U.S. approvalThe U.S. Food and Drug Administration (FDA) issued emergency authorization for a faster coronavirus test made by Swiss diagnostics maker Roche , a move aimed at boosting screening capacity to help..
United States approves coronavirus test in race to boost screening capacityThe U.S. Food and Drug Administration issued emergency authorization for a coronavirus test made by Swiss diagnostics maker Roche , a move aimed at boosting screening capacity to help contain the..
U.S. FDA official warns of possibility of coronavirus pandemicA U.S. Food and Drug Administration official on Wednesday pointed to the spread of the new coronavirus to six of the world's seven continents as he warned of the potential for a global pandemic.
U.S. expands use of coronavirus diagnostic testThe U.S. Food and Drug Administration on Tuesday granted emergency use approval for state public health laboratories to start testing for the new flu-like coronavirus from China using kits developed by..
U.S. health officials seek emergency approval to use diagnostic test for new coronavirusThe U.S. Centers for Disease Control and Prevention said on Thursday it is seeking special emergency authorization from the Food and Drug Administration to allow U.S. states to use a CDC-developed..
Maha CM rejigs some portfolios of NCP's Patil and BhujbalOn December 12, Patil was allocated Finance and Planning, Housing, Public Health, Co-operation, Food & Civil Supplies, Labour and Minority Welfare ministries. Bhujbal was entrusted with Irrigation,..
USFDA designates Indian invention a ‘breakthrough device’ for cancerThe Centre for Devices and Radiological Health (CDRH) of the US Food and Drug Administration (USFDA) has designated Cytotron—a device invented in India by a Bengaluru scientist—as a “Breakthrough..
Maharashtra: State FDA cautions people on dubious ayurvedic medicinesIn the inspection drive conducted across the state, medicines with false claims worth Rs 20 lakh were seized by the authority.
FDA raids across Maharashtra to nab e-cigarettes & hookah sellersEarlier this year, Maharashtra banned ENDS, but this week, the FDA officials started inspections to check the illegal sales of e-cigarette near schools, colleges and various educational institutes in..
Dabbawalas vouch for 'eating right' initiative in schoolsFOOD FOR THOUGHT: They will write a letter to FDA to start Tiffin services in schools
Food and Drug Administration destroys 18,000 kg of contaminated ice in MumbaiAs per the data shared by the FDA Mumbai food commissioner, inspections were conducted in around 38 locations across the wards.
Video of Mumbai idli vendor using toilet water goes viral, FDA orders enquiryShailesh Adhav, Food and Drug Administration (FDA), Mumbai, said, "The video has come to our knowledge. We will conduct an enquiry against him as well as others who use such methods to do business."