were still collecting data when first shots in arms were being injected under the EUA. https://www.fda.gov/emergency-preparedness-and-response/mcm-legal-regulatory-and-policy-framework/emergency-use-authorization >Under section 564 of the Federal Food, Drug, and Cosmetic Act (FD&C Act), when ... Vaccines were still in phase 3, or wide scale clinical trials looking at safety and efficacy: https://www.fda.gov/vaccines-blood-biologics/vaccines/emergency-use-authorization-vaccines-explained I'm 100% with the FDA on this, the benefits outweighed the risks

www.fda.gov/food/environmental-contaminants-food/lead-food-foodwares-and-dietary-supplements#:\~:text=While%20it%20is%20not%20possible,to%20chemical%20hazards%E2%80%94including%20lead](https://www.fda.gov/food/environmental-contaminants-food/lead-food-foodwares-and-dietary-supplements#:~:text=While%20it%20is%20not%20possible,to%20chemical%20hazards%E2%80%94including%20lead). "While it is not possible to prevent or remove lead entirely from foods, the levels in food

clinical approval to sell/deploy ML systems in healthcare settings, and has greenlit a number of products: https://www.fda.gov/medical-devices/software-medical-device-samd/artificial-intelligence-and-machine-learning-aiml-enabled-medical-devices

their criteria for clinical decision support devices for AI last month. This is [the summary version](https://www.fda.gov/medical-devices/software-medical-device-samd/your-clinical-decision-support-software-it-medical-device) and the full version has more detail. It's not hard to have a highly accurate

false negative. There’s a large margin of error regarding incubation times and low viral load. https://www.fda.gov/medical-devices/safety-communications/home-covid-19-antigen-tests-take-steps-reduce-your-risk-false-negative-fda-safety-communication#:~:text=However%2C%20if%20you%20perform%20an,t%20have%20COVID-19%20symptoms.

There's a nationwide shortage: https://www.fda.gov/drugs/drug-safety-and-availability/fda-announces-shortage-adderall

held to the same standard as self medicating copping based addiction. (FDA Advisory link: https://www.fda.gov/drugs/drug-safety-and-availability/fda-drug-safety-communication-fda-warns-about-serious-risks-and-death-when-combining-opioid-pain-or

months surely Edit: downvote all you want, they were approved for emergancy use Dec 2020 https://www.fda.gov/news-events/press-announcements/fda-takes-key-action-fight-against-covid-19-issuing-emergency-use-authorization-first-covid-19

months (assuming you take the start of the pandemic as roughly mid feb) https://www.fda.gov/news-events/press-announcements/fda-takes-key-action-fight-against-covid-19-issuing-emergency-use-authorization-first-covid-19 That the delivery platform had been under research for decades doesn't mean that every vaccine using that platform

similar issue with prenatal screens: [https://www.nytimes.com/2022/01/01/upshot/pregnancy-birth-genetic-testing.html](https://www.nytimes.com/2022/01/01/upshot/pregnancy-birth-genetic-testing.html) FDA issued a warning to parents: https://www.fda.gov/medical-devices/safety-communications/genetic-non-invasive-prenatal-screening-tests-may-have-false-results-fda-safety-communication This is a different type of testing than the newborn screen (blood spot cards) you are talking about

assume they go through more scrutiny than only safety. A variation can be found [here](https://www.fda.gov/medical-devices/recently-approved-devices/accelstim-bone-growth-stimulator-p210035) which also has a link to the Exogen system

protein. I’m hesitant to recommend the Flowflex just because they had a massive counterfeit problem: https://www.fda.gov/medical-devices/coronavirus-covid-19-and-medical-devices/counterfeit-home-otc-covid-19-diagnostic-tests#diagnostic

confusion but sheds some light into the FDA's thought process on the matter: https://www.fda.gov/regulatory-information/search-fda-guidance-documents/draft-guidance-industry-and-fda-staff-whole-grain-label-statements Note: Link is the opposite of ELI5

www.fda.gov/drugs/disposal-unused-medicines-what-you-should-know/drug-disposal-drug-take-back-locations

Adderall/Ritalin (same class of med): https://www.fda.gov/drugs/drug-safety-and-availability/fda-announces-shortage-adderall

Relevant, not sure how helpful though https://www.fda.gov/drugs/drug-safety-and-availability/fda-announces-shortage-adderall

pharmacist received 8 years in prison: https://www.fda.gov/inspections-compliance-enforcement-and-criminal-investigations/press-releases/january-31-2018-new-england-compounding-center-pharmacist-sentenced-role-nationwide-fungal

anyone thinking of picking up some kohl, do look out for lead content; see https://www.fda.gov/cosmetics/cosmetic-products/kohl-kajal-al-kahal-surma-tiro-tozali-or-kwalli-any-name-beware-lead-poisoning

order of magnitude. [Per the FDA](https://www.fda.gov/radiation-emitting-products/medical-x-ray-imaging/what-are-radiation-risks-ct): "A CT examination with an effective dose of 10 millisieverts [an abdominal CT averages 8] [...] may be associated with an increase in the possibility of fatal

avoid raw milk, the threat in things like deli meat and hot dogs too is real. https://www.fda.gov/food/foodborne-pathogens/listeria-listeriosis#:~:text=Foods%20Linked%20to%20U.S.%20Outbreaks,L. Want to see how the smart folks in Food Science use viruses to actually combat

allowed up to 45](https://www.fda.gov/news-events/press-announcements/fda-approves-expanded-use-gardasil-9-include-individuals-27-through-45-years-old).

then shutting down a facility that killed babies due to unsafe food standards? [Timeline here.](https://www.fda.gov/media/158737/download) Pdf of the intitial complaints. They had gotten a warning several months prior, and then sicknesses started

From [the FDA's timeline](https://www.fda.gov/media/158737/download) someone posted above, they made their first consumer advisory 4 days after confirming bacterial contamination, 10 days after the first test showing possible contamination, and they pressed

Food and Drug and Anything Medical Administration? Always has been. (well since 1976 anyway) https://www.fda.gov/medical-devices/overview-device-regulation/history-medical-device-regulation-oversight-united-states

what we’re dealing with in the US. Just ask the [company president Xianmin Guan](https://www.fda.gov/inspections-compliance-enforcement-and-criminal-investigations/warning-letters/california-terra-garden-inc-616499-11102021)

List of skin products containing mercury or hydroquinone](https://www.fda.gov/consumers/health-fraud-scams/skin-products-containing-mercury-andor-hydroquinone) Article says it's mostly skin lighteners and hair relaxers

many questions asked. Why is this bill going against clear FDA guidance??? https://www.fda.gov/media/142766/download

were enrolled from November 27, 2021 to June 30, 2022. The bivalent booster was not [authorized](https://www.fda.gov/news-events/press-announcements/coronavirus-covid-19-update-fda-authorizes-moderna-pfizer-biontech-bivalent-covid-19-vaccines-use) until August 31, 2022. That being said, vaccination was still **highly effective** at preventing several maternal

theorized to be caused by shortened telomeres in the clones This link explains it https://www.fda.gov/animal-veterinary/animal-cloning/myths-about-cloning#Myth6

www.fda.gov/drugs/drug-safety-and-availability/fda-announces-shortage-adderall

contains about 95mg of caffeine. [The FDA also says 8oz but 80-100mg caffeine.](https://www.fda.gov/consumers/consumer-updates/spilling-beans-how-much-caffeine-too-much)

price will drop considerably. But in the past ~10 years, generic prices have risen sharply. https://www.fda.gov/drugs/cder-small-business-industry-assistance-sbia/small-business-assistance-180-day-generic-drug-exclusivity

integration sites. In fact, The FDA had a CTGTAC meeting in 2021 to discuss these issues: https://www.fda.gov/advisory-committees/cellular-tissue-and-gene-therapies-advisory-committee/2021-meeting-materials-cellular-tissue-and-gene-therapies-advisory-committee

www.fda.gov/food/agricultural-biotechnology/types-genetic-modification-methods-crops As per the government

term to refer specifically to genetic engineering. Seems like that's where the difference comes from. https://www.fda.gov/food/agricultural-biotechnology/types-genetic-modification-methods-crops These all are considered genetic modification

hydrolyzed yeast, yeast extract, soy extracts, and protein isolate, as well as in tomatoes and cheeses." https://www.fda.gov/food/food-additives-petitions/questions-and-answers-monosodium-glutamate-msg#:~:text=MSG%20occurs%20naturally%20in%20many,glutamate%2Drich%20foods%20throughout%20history.

False, [ice](https://www.fda.gov/food/buy-store-serve-safe-food/fda-regulates-safety-packaged-ice) falls more

again: https://www.fda.gov/news-events/press-announcements/fda-approves-first-covid-19-vaccine

magnesium levels can be associated with long-term use of Proton Pump Inhibitor drugs (PPIs)](https://www.fda.gov/drugs/drug-safety-and-availability/fda-drug-safety-communication-low-magnesium-levels-can-be-associated-long-term-use-proton-pump) Proper diet is inadequate if intestinal disease or age impairs nutrient absorption. The diagnostic failure rate

again: https://www.fda.gov/news-events/press-announcements/fda-approves-first-covid-19-vaccine FTA: >For Immediate Release: August 23, 2021 considering [the mandate was announced on august 16, 2021](https://www.boston.gov/news/vaccination-mandate-announced-city-boston-employees), he was right that the mandate preceded the approval. no amount

past, [the CDC is limiting the use of the Janssen (J&J) vaccine.](https://www.fda.gov/news-events/press-announcements/coronavirus-covid-19-update-fda-limits-use-janssen-covid-19-vaccine-certain-individuals)