You have to hand it to Democratic lawmakers who get triggered over anything. When collusion and impeachment failed domestically, why not call upon The Hague for charges of crimes against humanity? Hmmm.
Never mind that Speaker of the House Nancy Pelosi was encouraging San Franciscans to “come to Chinatown and join” crowds at a parade in late February. Forget the Democratic NYC Health Commissioner Oxiris Barbot downplaying the health warnings by telling the residents to immerse themselves in Lunar New Year festivities because stigmatization is a far bigger threat to people than a pesky virus.
Guess who is now telling people to stay at home? Yep, you guessed it – Oxiris Barbot. Even though she retweeted someone’s praise of her status as the first Latino female to occupy the post after it had all gone pear-shaped! If only one’s abilities were seen as more important than their identity…NYers would have been happier with an old white guy provided his medical advice kept the city from holding the highest infection rates.
Never mind that The Hill had criticized Trump’s travel ban on Feb 7th as unnecessary, parroting none other WHO, to then write on April 5th that he hadn’t done enough to block travel into the US. Which is it? The NY Times was happy to run a story on Feb 24th saying Trump’s travel ban was more an “emotional or political reaction.”
Do Democratic House representatives hold such little faith in the domestic judiciary that Trump needs to be tried in an international court over supposed domestic crimes against innocent civilians? It won’t be long before Nancy Pelosi launches another impeachment trial over coronavirus. We encourage her to do it for the sake of revealing just whether she has any ties to America.
Rep Tavia Galonski’s tweet came shortly after Trump’s media briefing in which he once again spoke of hydroxychloroquine sulfate, a drug which he has previously reported has shown promise as a means of treating COVID-19.
How is it that the mainstream media outlets backflipped on their initial criticism on hydroxychloroquine to acknowledging its potential as reported by the medical profession to flip back to “irresponsibility” again. No country has a silver bullet and in such circumstances
Rep Galonski may have a case if the state was force-feeding strapped down patients against their will. The FDA says otherwise.
“On March 28, 2020, the FDA issued an Emergency Use Authorization (EUA) to allow hydroxychloroquine sulfate and chloroquine phosphate products donated to the Strategic National Stockpile (SNS) to be distributed and used for certain hospitalized patients with COVID-19. These drugs will be distributed from the SNS to states for doctors to prescribe to adolescent and adult patients hospitalized with COVID-19, as appropriate, when a clinical trial is not available or feasible. The EUA requires that fact sheets that provide important information about using chloroquine phosphate and hydroxychloroquine sulfate in treating COVID-19 be made available to health care providers and patients, including the known risks and drug interactions. The SNS, managed by ASPR, will work with the Federal Emergency Management Agency (FEMA) to ship donated doses to states.”
The FDA’s latest fact sheet on hydroxychloroquine is here.
To be honest, who needs the FDA when we can rely on the tweets from a NY Times best-selling author with a law degree, Kurt Eichmann, who proposed 11 questions the White House press corps should ask of Trump with respect to hydroxychloroquine.
1. What dosage should people take?
2. How long should people take it?
3. What studies are you relying on for dosage and time?
3. Are you saying this is prophylactic or post-diagnosis?…(while he won’t know what the last question means if he says anything close to prophylactic)
5. How does hydroxychloroquine prevent viral infection?
6. Since hydroxychloroquine is an immunosuppressant, how isn’t there a risk that it will *increase* the risk of infection?
7. What studies have you reviewed showing it has a preventative effect because I can’t find any. (they don’t exist.)
(If he says for treatment…)
8. At what stage of infection should people take the medicine?
9. What should people with lupus and other autoimmune diseases do to find their medication, since your recommendations have led to a national shortage of hydroxychloroquine?
10. Will the government subsidize lupus & rheumatoid arthritis patients, given the price-gouging happening with these drugs?
11. Are you concerned about lupus and autoimmune patients who can’t find their medication refusing to vote for you because they’re now in pain?
As with any drug, a doctor prescribes medication based on the severity of illness and a whole range of other factors – size, age, gender. Trying to get Trump to answer a series of “gotcha” questions in the hope he bungles some of them just smacks of how little integrity there is in journalism. If Trump told journalists that drinking Drano was great for fixing stomach ulcers, would they believe him? Wouldn’t readers prefer medical opinion?
Let’s deal with the facts.
Hydroxychloroquine sulphate is an FDA approved drug dating back to April 1955. It is best known under the brand name of Plaquenil. There are generic manufacturers such as Teva and Mylan are already making the drug. In the US, it is strictly prescription-only medication. It has been approved to treat malaria
The 65-year-old Plaquenil and its 25-yo generic brothers haven’t been approved for the application of COVID19, which, as we know, in and of itself is a brand new strain of pathogen. So the “drug” has been approved but the application has not.
It is worth noting that it takes on average 12 years and over US$350 million to get a new drug from the laboratory onto the pharmacy shelf. At the company level, it undergoes around three and a half years of laboratory testing, before an application is made to the U.S. FDA to begin the testing on humans. Only 1 in 1000 compounds that enter lab testing will ever make it to the human testing stage.
Which is exactly why the FDA stated in its release late last month that there isn’t enough hard data due to a lack of clinical trials. Stands to reason that a drug we’re trying to find a cure for hasn’t a cure.
The FDA Accelerated Approval pathway was introduced in 1992 so that drugs to treat life-threatening diseases could be brought to market to make a significant impact on the course of diseases. For example, many antiretroviral drugs used to treat HIV/AIDS entered the market via accelerated approval, and subsequently altered the treatment paradigm.
Clearly, there has been no chance to conduct clinical trials on Plaquenil on COVID19 to get official FDA approval. The side effects of Plaquenil, when taken for malaria, are well known with 65 years of data. It is a question of whether the impact of the drug causes other side effects when used to treat COVID19. Hence why the FDA is trying to ensure that people are aware of the risks if they elect to take it.
Yes, the president has a habit of saying unnecessary things. He can be unpresidential at times. We have never hidden that.
However, at what point is Trump deserved of standing trial in The Hague given the timeline of events and an insane liberal media? Perhaps President Xi of China would be a more worthy respondent in the International Criminal Court for the cover-up which led to the outbreak in the first place.