#janet woodcock

[killed-by-choice]

“Wanda Roe” (USA 2006)

Information from the CDC and the FDA revealed multiple deaths from the chemical abortion pill that were unknown to the general public. One of them was Wanda Roe.

Wanda, who died in the Western United States, was yet another woman killed by Planned Parenthood. She was given 200 mg of mifepristol orally, then 800 mcg of misoprostol vaginally.

Wanda died from an infection of Clostridium perfringens, the pathogen that causes gas gangrene.

Dr. Janet Woodcock, Deputy Commissioner for Operations at the FDA, confirmed multiple deaths from the dangerous drug that had been previously unknown to the general public. Most of the people killed are still unidentified.

Please note that the CDC never approved the abortion pill as a vaginal suppository, but Planned Parenthood commonly used this method on their clients anyway. A PP spokesperson even informed the New York Times that against the FDA’s warnings to strictly stick to the only approved regimen, they were going to continue instructing clients to use the abortion pill in particularly hazardous ways, such as sending it home to self-administer without medical supervision.

At a CDC event, it was noted by an OB/GYN speaker that “Mifepristone impairs innate host responses and may predispose to lethal infections” and that the estimated/reported rate of death was much higher than the reported death rate for surgical abortion. One of the recommended strategies for risk reduction that was ruled as a more effective option was to eliminate the use of the drug.

CDC archives: see slide 31, investigations, how the abortion pill causes septic shock, An OB/GYN View of Early Medical Termination and Clostridium sordellii Infection, James A. McGregor, M.D.C.M., Univ. of Southern California

https://www.nytimes.com/2006/03/18/us/after-2-more-deaths-planned-parenthood-alters-method-for-abortion-pill.html

#tw abortion #unsafe yet legal #tw murder #tw ab*rtion #abortion #abortion debate #death from legal abortion #unidentified victim #chemical abortion #the abortion pill kills

[beardedmrbean]

Feb. 1 (UPI) -- Hong Kong on Wednesday implemented a ban CBD, putting it in the same class as heroin and cocaine.

The new law prohibits CBD, or cannabidiol, under the Dangerous Drugs Ordinance and imposes a penalty of up to seven years in prison and a fine of up to $127,510 in prison for possession and consumption and life in prison and a fine of nearly $638,000 for trafficking and "illicit manufacturing."

The Hong Kong Police Force said that as of Jan. 29 it had collected more than 77,400 items including skin care products, edible oils and health supplements containing CBD in disposal boxes that were set up prior to the implementation of the law.

The government targeted CBD alleging it can't be separated from tetrahydrocannabinol, or THC, the primary psychoactive element that produces the high from cannabis, and that CBD can decompose and convert into CBD.

RELATED70% of people over 50 experience joint pain, poll shows lol "joint" pain

CBD vendors and users have argued that the amount of THC contained in the product is negligible and can't produce a similar high.

The ban also bars travelers from bringing CBD products with them.

Those traveling to Hong Kong with CBD items should declare them on arrival to prevent action against them, said Brian Chan, a divisional commander with the Hong Kong Customs and Excise Department's Air Passenger Division.

"We will investigate the cases and get legal advice from the Department of Justice and determine if there is enough evidence to conduct further actions," Chan said, according to the Hong Kong Free Press.

While CBD is unregulated in the United States, Janet Woodcock, the principal deputy commissioner of the Food and Drug Administration said last week that new regulations may be necessary given the concerns about long-term use and mistaken exposure.

#nunyas news #this is gonna go over well I bet #wnba stay away from hong kong

[newswireml]

New Way Needed to Regulate Cannabidiol, FDA Says#Needed #Regulate #Cannabidiol #FDA

The government needs to develop a better pathway for regulating cannabidiol (CBD) in food and dietary supplements, the FDA said Thursday. “After careful review, the FDA has concluded that a new regulatory pathway for CBD is needed that balances individuals’ desire for access to CBD products with the regulatory oversight needed to manage risks,” FDA Principal Deputy Commissioner Janet Woodcock,…

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[rnewspost]

FDA says no to regulating CBD products as supplements

The U.S. Food and Drug Administration said Thursday it can’t regulate CBD supplements because there isn’t enough evidence on their safety. The agency also called on Congress to create new rules for what has become a burgeoning industry. “The use of CBD raises various safety concerns, especially with long-term use,” FDA Deputy Commissioner Dr. Janet Woodcock said in a statement. “Studies have…

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[drugsinceu]

#cbd #fda #VerenigdeStaten #wetgeving

[nycannabistimes]

#Repost @nocohempexpo ・・・ "The U.S. Food and Drug Administration has begun to look into whether hemp-derived CBD is safe in food or supplements. The substance has been federally legal since 2018 but remains largely unregulated.⁠ ⁠ According to a Dec. 29, 2022, article in the Wall Street Journal, FDA officials said that in the coming months they planned to make recommendations on regulating CBD and other hemp-derived products.⁠ ⁠ FDA Principal Deputy Commissioner Janet Woodcock signaled a skeptical approach.⁠ ⁠ 'Given what we know about the safety of CBD so far, it raises concerns for FDA about whether these existing regulatory pathways for food and dietary supplements are appropriate for this substance,' she said.⁠ ⁠ Woodcock will be in charge of the agency’s review of the regulations. ⁠ ⁠ Patrick Cournoyer, who heads the FDA office that will develop the agency’s cannabis strategy, told the Wall Street Journal that the agency, concerned about possible effects on fertility, wanted to know whether CBD could be safely eaten every day during a pregnancy or for another long period.⁠ ⁠ Morris Beegle, co-founder and president of the WAFBA (We Are for Better Alternatives) family of brands, including the NoCo Hemp Expo and Let’s Talk Hemp Media, said Woodcock is a well-known pro-pharmaceutical industry ally who has pushed to relax the criteria to approve various opioid medications despite inadequate evidence of their safety."⁠ ⁠ Read more on this via our Featured Article (link in bio)! 👆⁠ ⁠ ⁠ ⁠ ⁠ ⁠ ⁠ .⁠ .⁠ .⁠ .⁠ #hemp #FDA #cbdsafety #usfda #nocohempexpo #hempeducation #hemppolicy #hemplaws #dietarysupplements #supplements #wellness #hempnews (at Thái Sơn Vietnamese restaurant) https://www.instagram.com/p/CnM6YQ7uxMt/?igshid=NGJjMDIxMWI=

#repost #hemp #fda #cbdsafety #usfda #nocohempexpo #hempeducation #hemppolicy #hemplaws #dietarysupplements #supplements #wellness #hempnews

[emk-irl]

Pink Viagra: limited effectiveness with side effects

The US Food and Drug Administration (FDA) on Tuesday approved the marketing of the first "female 비아그라" after two refusals in 2010 and 2013. This little pink pill, containing flibanserin, will be marketed under Addyi's name.

"This clearance gives women with low sexual desire a treatment option," said Janet Woodcock, director of the FDA's Center for Drug Evaluation and Research.

According to several studies, nearly 40% of premenopausal women suffer from a lack of sexual desire. A loss of libido not resulting from drug treatment, a physiological or psychiatric disorder. “It is a frequent phenomenon in humans, and in women in particular, underlines Dr. Sylvain Mimoun, gynecologist-andrologist at Cochin Hospital. Lack of desire is the hardest symptom to deal with.”

Unlike male 비아그라, which acts on the genitals to promote erection without stimulating desire, flibanserin acts on the brain , the conductor of desire. By limiting the secretion of serotonin, flibanserin is supposed to  awaken the libido in women. However, the FDA recalls that the mechanisms of action are not yet known.

This little pink pill then presents itself as a revolutionary drug capable of solving sexual dysfunctions. However, this is far from being the case. As the FDA points out, about 10% of women who took Addyi reported improved sex and desire compared to women on placebo. 

“This product is described as an aphrodisiac in the sense of a sexual stimulant when in reality it is a disinhibitorallowing certain blockages to be lifted,” explains the specialist. Thus, if these brakes are (too) numerous, it is possible that the drug will be ineffective. “If a woman repeatedly complains of having little or no sexual desire, she can tell herself that this drug is capable of solving her problems. But we must not be in all or nothing and believe in miracles. This treatment will allow a gradual return of desire,” says Dr. Mimoun.

In addition, American experts insist on the risk of interaction with alcohol and its side effects . Addyi can cause a drop in blood pressure, dizziness and loss of consciousness. Increased risks with alcohol consumption and 비아그라 drugs that inhibit CYP 3A4 such as antiretrovirals, antiepileptics or certain cardiovascular drugs. They also indicate that treatment should be discontinued if no improvement has appeared after 8 weeks.

#비아그라

[techvercy]

The FDA May Nix the Word ‘Milk’ From Your Almond Milk Carton

The FDA May Nix the Word ‘Milk’ From Your Almond Milk Carton

An official high up in the agency essentially agreed with her critique, Bottemiller Evich reports. The agency has “too many programs and not enough resources,” Janet Woodcock, FDA’s principal deputy commissioner, told her, “and the mismatch is profound.” As for the food division, it’s “really important, but it’s very under-resourced.”  And yet the FDA has apparently found time to intervene on…

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[saveself6]

Dedicated Server - So Easy Even Your Youngsters Can Do It

But it is distinguished by a selected control panel (or add-ons over the usual system) and totally custom-made server software for a selected sport (for instance, Minecraft) based on its necessities. A virtual server can be managed easily by a control panel, and it may be managed with ease. A digital dedicated server (VDS) provides a excessive stage of safety and control for hosting your website. A digital dedicated servers control panel gives the shopper complete management of the server, together with monitoring and managing the efficiency of the server. A virtual dedicated server is more expensive than a VPS, but it gives all the benefits of both. Improved Consumer Expertise: A quick site, no downtime and low latency help to create a superior person experience allowing your prospects to get pleasure from and interact along with your site extra fully. Devoted prompt servers provide a superior user expertise in comparison with shared servers which run more slowly and infrequently shouldn't have strong or dependable maintenance.

Our ARK servers provide probably the most versatile game mode types. With GTHost, our devoted immediate servers are available in as little as 5 to 15 minutes of your fee. Short Term Contracts: At GTHost, we work to ensure our clients are utterly happy with our servers and this is why we provide short contracts. Your server provider must also provide a number of security options: Monitoring Services, for instance, screens your server across the clock and informs you about malfunctions. Cloud Server Hosting with Enterprise Cloud Stack is a straightforward to make use of cloud server internet hosting which enables you to spin up hundreds of cloud servers immediately. After you click deploy, they'll orchestrate the Vultr cloud platform and allocate your instances over the chosen information heart. DirectAdmin makes using these cloud easy same as your dedicated server with full root access. Choose your very best choices for storage, bandwidth, server location and other key options then select your payment methodology and your server shall be just minutes away from helping you get one of the best in reliable webpage efficiency.

Yet, Fauci mentioned, "there's less disagreement and conflicts than seem to get out into the tweetosphere." He ticked off a variety of distinguished scientists in the sphere - together with Surgeon Common Vivek Murthy, performing FDA Commissioner Janet Woodcock and covid vaccine inventor Barney Graham - who were on board with his place. We’ve lined up an inventory of one of the best Minecraft servers, and inside you’ll discover a wide variety of options to check out and find one that matches your preferences. DoorDash rolled out a new product, DoorDash Storefront, that helps restaurants set up their very own on-line stores and prices a flat fee instead of a per-order fee. 24/7 customer service: Never be stuck with a server issue when you've got access to our 24/7 customer support which helps you get service when you need. Our server solutions present reasonably priced, dependable and fast service to your web site with 24/7 customer support, in-house maintenance, low-price trial durations, unmetered bandwidth and FREE setup in less than 15 minutes.

Along with our quick setup, GTHost offers features and customization options that make our servers inexpensive, dependable and handy. The distributed architecture of compute, community and storage provides a really stable efficiency. Write SPIDERMAN GAMING over a HDD as there aren't any moving elements. Are there any recommended companies we could use that we can contact or use to setup just a few dedicated servers remotely? If Everything There is Inexperienced But You're Still Getting Errors When Trying To Play Gta Online Or Purple Lifeless Online, It May be As a result of Your Ip Obtained Randomly Blacklisted. He may not be as popular as Federer and Nadal -- not getting as much love from followers does irk Djokovic -- however he is thrashing them often when it counts. When you've got a small sport, this might not be the way in which you wish to go. Elevated Page Ranking: Because sluggish page loading is such an important a part of the best way users perceive a site, Google makes use of site pace as part of its web page ranking system. We would not label Avatar a failure when the number of screens exhibiting it begins to decrease, and perhaps we must always view MMOs the same manner. However it does have the identical options as a dedicated one.

#Spiderman gaming #spiderman's blog about games

[cheapadulttoys]

FDA: Americans Should Treat COVID-19 Like The Flu

FDA: Americans Should Treat COVID-19 Like The Flu

FDA: Americans Should Treat COVID-19 Like The Flu Authored by Jack Phillips via The Epoch Times, Several top Food and Drug Administration (FDA) officials, including Commissioner Robert Califf, admitted that Americans will now have to accept COVID-19 as another respiratory virus, comparing it to influenza. Califf, Principal Deputy Commissioner Janet Woodcock, and top vaccine official Dr. Peter…

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[dropchin00]

Pink Viagra: limited effectiveness with side effects

Female viagra, which has just been authorized by the FDA in the United States, would only have a beneficial effect for one in ten women. The US Food and Drug Administration (FDA) on Tuesday approved the marketing of the first "female Viagra" after two rejections in 2010 and 2013. This little pink pill, containing flibanserin, will be marketed under the Addyi's name. " 비아그라 gives women with low sexual desire a treatment option," said Janet Woodcock, director of the FDA's Center for Drug Evaluation and Research. According to several studies, nearly 40% of premenopausal women suffer from a lack of sexual desire. A loss of libido not resulting from drug treatment, a physiological or psychiatric disorder. “It is a frequent phenomenon in humans, and in women in particular, underlines Dr. Sylvain Mimoun, gynecologist-andrologist at Cochin Hospital. Lack of desire is the hardest symptom to deal with.” Unlike male Viagra, which acts on the genitals to promote erection without stimulating desire, flibanserin acts on the brain , the conductor of desire. By limiting the secretion of serotonin, flibanserin is supposed to awaken the libido in women. However, the FDA recalls that the mechanisms of action are not yet known. This little pink pill then presents itself as a revolutionary drug capable of solving sexual dysfunctions. However, this is far from being the case. As the FDA points out, about 10% of women who took Addyi reported improved sex and desire compared to women on placebo. “This product is described as an aphrodisiac in the sense of a sexual stimulant when in reality it is a disinhibitorallowing certain blockages to be lifted,” explains the specialist. Thus, if these brakes are (too) numerous, it is possible that the drug will be ineffective. “If a woman repeatedly complains of having little or no sexual desire, she can tell herself that this drug is capable of solving her problems. But we must not be in all or nothing and believe in miracles. This treatment will allow a gradual return of desire,” says Dr. Mimoun. In addition, American experts insist on the risk of interaction with alcohol and its side effects . Addyi can cause a drop in blood pressure, dizziness and loss of consciousness. Increased risks with alcohol consumption and certain drugs that inhibit CYP 3A4 such as antiretrovirals, antiepileptics or certain cardiovascular drugs. They also indicate that treatment should be discontinued if no improvement has appeared after 8 weeks.

#비아그라 #비아그라 구입 #비아그라 구매 #비아그라 판매

[gettothestabbing]

One attempt to gain understanding of a problem that experts around the world are struggling to understand is being carried out by Dr. Janet Woodcock, who was acting commissioner of the FDA until Feb. 17.

Woodcock, now the FDA’s principal deputy director, has been personally evaluating neurologic side effects from the COVID-19 vaccines since at least Sept. 13, 2021, according to the emails, many of which have not been reported on previously. FDA epidemiologists are also gathering data to look into the issues, according to messages from Dr. Peter Marks, another top FDA official.

A team at the NIH’s National Institute of Neurological Disorders and Stroke (NINDS), meanwhile, started seeing patients reporting vaccine injuries for a study in early 2021 after receiving complaints shortly after the vaccines were made available. A portion of the patients was examined in person at the Bethesda, Maryland, facility.

None of the reviews or studies appear to have been announced, and health officials have said little about them publicly, despite a growing recognition among experts that at least some issues are likely linked to the vaccines.

Woodcock was aware of reports of post-vaccination issues by April 16, 2021, according to the emails.

Woodcock said she was sorry for the ordeals people were going through and that she was trying to find ways to examine what was happening. Eventually, she disclosed that she was working on an evaluation of “neurologic side effects from the COVID 19 vaccines,” according to a Sept. 16, 2021, email reviewed by The Epoch Times.

Prodded by people with diagnosed vaccine injuries, Woodcock insisted she was still working on the project.

“I am awaiting some information from the epidemiologists that I expect to get tomorrow,” she wrote on Nov. 16, 2021. “We are having difficulty pinning down these nervous system-related events that have been brought to our attention. I’ve asked for specific searches of the reports we get both from here and ex-U.S. (as these vaccines have been used in many countries) as well as from trials, where oversight of participants is greater.”

Woodcock said she was aware that people who suffer issues after getting vaccinated were looking for guidance on treatment but that there was “not a lot of certainty about what causes the symptoms.”

Woodcock confirmed to The Epoch Times in an email that the evaluation is still ongoing and has not been completed.

#FDA #National Institute of Health #Epoch Times #vaccine injuries #federal agencies #covid vaccines #neurology #Janet Woodcock #side effects #epidemiology

[sleepydrummer]

Free Range Vineyard Haven, Massachusetts Janet Woodcock

#janet woodcock #free range #rooster #chicken #farm animal #Flock 13 #fowl #cocky #massachusetts #vineyard haven #photography #photographer

[drugsinceu]

FDA wil nieuw regelgevingskader voor CBD

De Amerikaanse Food and Drug Administration zei donderdag dat het niet van plan is nieuwe richtlijnen te geven voor het gebruik van de populaire cannabisverbinding CBD in voedsel en supplementen. De FDA wil eerst in samenwerking met het Congres een heel nieuw regelgevingskader ontwikkelen.Het bureau zei dat de huidige veiligheidsnormen voor voedingssupplementen of voedseladditieven niet geschikt zijn voor cannabidiol, op basis van gegevens en onderzoeken die het heeft beoordeeld en uitgevoerd. "We hebben niet voldoende bewijs gevonden om te bepalen hoeveel cannabidiol kan worden geconsumeerd, en voor hoe lang, voordat het schade veroorzaakt", zei plaatsvervangend hoofdcommissaris Janet Woodcock van de FDA. Nieuwe regels voor cbd Cannabidiol is een niet-psychoactieve stof die is afgeleid van cannabis. Langdurig gebruik van de verbinding kan volgens de FDA zorgen voor schade aan de lever en het mannelijke voortplantingssysteem. Er is weinig handhaving op CBD. De FDA heeft zich voornamelijk gericht op voedingsmiddelen en dranken die ongefundeerde gezonheidsclaims bevatten. De FDA zei dat de huidige regels niet voldoende zijn om aan te tonen hoe CBD-producten kunnen voldoen aan de veiligheidsnorm voor stoffen in dierlijk voedsel. "Er is een nieuw regelgevend traject voor cannabidiol nodig dat de wens van individuen om toegang te krijgen tot CBD-producten in evenwicht brengt met het regelgevend toezicht dat nodig is om risico's te beheersen", aldus het bureau.Bron: Reuters.com (EN) Read the full article

[adminnewstrust24]

FDA approves vaccine for 12 to 15 years old children, Pfizer-BioNotech vaccine

Between the Corona period, the US Food and Drug Administration (FDA) on Monday made an important decision to approve the Pfizer-BioNtech vaccine for emergency use for children aged 12 to 15 years. FDA Commissioner Janet Woodcock called the move extremely important against the corona epidemic. Janet said that this decision is in the interest of the children and at the same time will help them…

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#America #American company Pfizer #BioNtech vaccine #FDA Commissioner #Janet Woodcock #Pfizer vaccine #Pfizer-BioNtech vaccine