Food and Drug Administration
United States federal agency
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The United States Food and Drug Administration is a federal agency of the Department of Health and Human Services. The FDA is responsible for protecting and promoting public health through the control and supervision of food safety, tobacco products, caffeine products, dietary supplements, prescription and over-the-counter pharmaceutical drugs (medications), vaccines, biopharmaceuticals, blood transfusions, medical devices, electromagnetic radiation emitting devices (ERED), cosmetics, animal foods & feed and veterinary products.
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![Supreme Court Upholds FDA Regulation on Popular Abortion Drug Mifepristone [Video]](https://video.newsserve.net/300/v/20240613/1378501354-Supreme-Court-Upholds-FDA-Regulation-on-Popular-Abortion.jpg) Supreme Court Upholds FDA Regulation on Popular Abortion Drug Mifepristone Credit: Wibbitz Top Stories Duration: 01:30Published | |
![Microdose Chocolate May Cause Seizures, FDA Warns [Video]](https://video.newsserve.net/300/v/20240610/1378141328-Microdose-Chocolate-May-Cause-Seizures-FDA-Warns.jpg) Microdose Chocolate May Cause Seizures, FDA Warns Credit: Wibbitz Top Stories Duration: 01:30Published | |
![FDA Reverses Ban on Juul E-Cigarettes [Video]](https://video.newsserve.net/300/v/20240606/1377709014-FDA-Reverses-Ban-on-Juul-Cigarettes.jpg) FDA Reverses Ban on Juul E-Cigarettes Credit: Wibbitz Top Stories Duration: 01:31Published | |
![FDA Reviewing Data on MDMA for Potential Approval of Groundbreaking PTSD Treatment [Video]](https://video.newsserve.net/300/v/20240605/1377517498-FDA-Reviewing-Data-on-MDMA-for-Potential-Approval.jpg) FDA Reviewing Data on MDMA for Potential Approval of Groundbreaking PTSD Treatment Credit: Wibbitz Top Stories Duration: 01:30Published | |
![Cucumbers Are Recalled in 14 States [Video]](https://video.newsserve.net/300/v/20240603/1377326326-Cucumbers-Are-Recalled-in-14-States.jpg) Cucumbers Are Recalled in 14 States Credit: Wibbitz Top Stories Duration: 01:31Published | |
![Hims and Hers to Offer Weight Loss Injections [Video]](https://video.newsserve.net/300/v/20240520/1376000346-Hims-and-Hers-to-Offer-Weight-Loss-Injections.jpg) Hims and Hers to Offer Weight Loss Injections Credit: Wibbitz Top Stories Duration: 01:31Published | |
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US lawmakers questions FDAs drug inspection programme in India and ChinaThree US lawmakers have raised concerns about the FDA's foreign drug inspection program in India and China, citing inconsistent inspection outcomes. They noted significant variability in findings,..IndiaTimes - Published | |
Over 100 fall ill after eating panipuris, all stable nowOver 100 individuals in Chopda taluka, Jalgaon district fell ill after consuming panipuris at Kamalgaon weekly market. Symptoms included vomiting and loose motions, leading to hospital admissions. FDA..IndiaTimes - Published | |
MDMA Treatment for PTSD Being Considered by FDA AdvisersA pharmaceutical version of MDMA, also known as midomafetamine, could become a new treatment for PTSD ... as advisers for the U.S. Food and Drug Administration are considering whether to recommend it..TMZ.com - Published | |
US FDA gathering information on MDH and Everest spice products amidst carcinogenic pesticide concernsUS Food and Drug Administration (FDA) is currently investigating products from spice manufacturers MDH and Everest following Hong Kong's decision to halt sales of certain items due to the alleged..IndiaTimes - Published | |
Aurobindo gets USFDA nod for generic version of Nasonex nasal sprayIndiaTimes - Published | |
Zydus gets USFDA nod for generic medicationThe drug maker is the first company to receive final approval for generic Gabapentin tablets (300 mg and 600 mg), it added. The product will be launched immediately in the US market, the drug firm..IndiaTimes - Published | |
Natco's Kothur facility gets 8 USFDA observationsIndiaTimes - Published | |
USFDA accepts Dr Reddy's rituximab biosimilar candidate DRL_RI for substantive reviewIndiaTimes - Published | |
First drug to slow progression of Alzheimer's disease approved in USThe US Food and Drug Administration (FDA) has fully approved a drug that slows the progression of Alzheimer's disease for the first time.Sky News - Published | |
USFDA approves world's first oral antiviral for Covid-19IndiaTimes - Published | |
Laurus gets tentative USFDA nod for paediatric HIV drugIndiaTimes - Published | |
Covid jab Covovax as heterologous booster to be available on CoWIN soon; to cost Rs 225 per doseCovovax can be administered to those who have already vaccinated with Covishield or Covaxin. The Drugs Controller General of India (DCGI) on January 16 had approved the market authorisation for Covovax..IndiaTimes - Published | |
HC quashes J&J baby powder manufacture ban over FDA test delayIndiaTimes - Published | Zydus’ US arm gets final nod from USFDA for anti-seizure drugIndiaTimes - Published |
FDA Warns TikTokers to Stop Cooking NyQuil-Marinated ChickenThe FDA is warning TikTokers who are jumping on the latest craze to beware ... because NyQuil-marinated chicken is a dangerous thing. It sounds as disgusting as it is dangerous ... "sleepy chicken" is..TMZ.com - Published | Juul E-Cigarettes To Be Banned In the U.S., WSJ ReportJuul e-cigarettes will soon be off the shelves, at least according to a report, that states the FDA is planning to ban the product from being sold in the U.S. The Wall Street Journal reports the Food..TMZ.com - Published |
FDA lifts hold on Covaxin's clinical trials in USThe US Food and Drug Administration which has put on hold the phase 2/ 3 clinical trials of Bharat Biotech's Covid-19 vaccine Covaxin, in USA, has lifted the pause, according to a statement issued by..IndiaTimes - Published | Covaxin Phase 2&3 trials to resume in US after USFDA lifts clinical holdThe US Food and Drug Administration (USFDA) has lifted the clinical hold on the Phase 2 and 3 immuno-bridging clinical trials of Bharat Biotech’s Covid-19 vaccine Covaxin that were being conducted in..IndiaTimes - Published |
FDA Investigating Lucky Charms, People Think Cereal Made Them SickScores of people say they've fallen ill after eating a bowl of Lucky Charms ... and now the feds are investigating the popular cereal. The U.S. Food and Drug Administration announced Monday the agency..TMZ.com - Published | Fallout of WHO observations: Covaxin's Phase 2/3 trials in US put on holdThe US Food and Drug Administration has put on hold the phase 2/3 clinical trials of Bharat Biotech's Covid-19 vaccine Covaxin, in USA. Bharat Biotech's partner for US and Canada for Covaxin, the FDA's..IndiaTimes - Published |
USFDA paves way for Covaxin trials in USIndiaTimes - Published | USFDA lifts clinical hold on Ocugen's IND application for Covaxin paving way for its evaluation for US marketIndiaTimes - Published |
USFDA nod to clear way for Molnupiravir use in IndiaIndiaTimes - Published | Zydus Cadila gets USFDA nod to market generic cancer drug in USIndiaTimes - Published |
Biden picks former FDA chief Califf to again lead agencyIndiaTimes - Published | Bharat Biotech partner Ocugen seeks USFDA nod for Covaxin EUA for kidsIndiaTimes - Published |
Bharat Biotech's US partner Ocugen files EUA request with FDA for paediatric use of CovaxinIndiaTimes - Published | Covid-19: Travellers vaccinated with Covaxin can enter USCDC press officer, Scott Pauley said, "CDC's travel guidance applies to FDA approved or authorized and WHO Emergency Use Listing vaccines and encompasses any new vaccines that may be added to either of..IndiaTimes - Published |
Ocugen files Covaxin IND application with USFDA, seeks nod for Phase-3 trial in USIndiaTimes - Published | 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..TMZ.com - Published |
'You are not a horse or a cow': Health officials warn against using livestock de-worming drug to treat COVID-19 The 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.Sky News - Published | |
