PebHmong Discussion Forum
Life & Living => Money & Investment => Topic started by: w1s3m0n on January 13, 2020, 07:48:42 PM
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For all of us traders. NK just announce on Bloomberg they have a full response (pretty much cure) many types of cancer using antigen and immunotherapy.
NOTE: This is a time-sensitive announcement. Do not be a fish and chase.
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no thankz
pump and dump
where is the FDA drug treatment approval???
just whisper in the wind
plus BERNIE SANDER single payer healthcare will bankrupty lots of healthcare companies TO THE GROUND
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I'm not talking to you HR. You like ETF. I get it that you like to value invest and that's great. Some of us take on significantly more risk than you.
FDA BLA coming 2021. By then it'll be priced in at a 3B company.
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I'm not talking to you HR. You like ETF. I get it that you like to value invest and that's great. Some of us take on significantly more risk than you.
FDA BLA coming 2021. By then it'll be priced in at a 3B company.
bro,
you know FDA APPROVAL takes YEEEARRRRSSSS
there are many stages to get drug approved
i don't even know where you get your 2021 from
we are talking about at least 5-10 years out
this is just classic PUMP AND DUMP
ride the way and get out
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you know FDA APPROVAL takes YEEEARRRRSSSS
there are many stages to get drug approved
i don't even know where you get your 2021 from
we are talking about at least 5-10 years out
"YEEEARRRRSSSS"??
"at least 5-10 years out??
The company then submits an application (usually about 100,000 pages) to the FDA for approval, a process that can take up to two and a half years. After final approval, the drug becomes available for physicians to prescribe.
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"YEEEARRRRSSSS"??
"at least 5-10 years out??
LMAO
get outta here, NOOB
real man are talking here
we know you bank with CHASE 0.01% interest rate
SOOOOO YOU ALREADY LOSING
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wiseman is just blowing smoke
i wouldn't even trust this dude
2021....yea righttttttt
FDA process.....re ad if you want to
but it's takes a freaking long time
5-10 years....maybe even 20-30 years....
long ass time
FDA Approval Process
It’s hard to watch a half-hour television show these days without being inundated with advertisement after advertisement about the latest prescription drugs or medical devices and their abilities. But how can the average consumer be sure the drugs flashing across the screen in fact do what’s promised in their labels? That’s where the U.S. Food and Drug Administration — or FDA — comes in. The government regulatory agency within the U.S. Department of Health and Human Services controls the drug-approval process and is tasked with reviewing new drugs and medical devices before companies can sell them.
The FDA’s approval process has garnered many criticisms over the years. For one, drugs and devices often make it to market simply because the manufacturers can demonstrate they are similar to products that were approved in the past — even if those products have since been recalled or have known problems.
Contrary to what most people think, just because a drug or device is FDA-approved, it does not mean the product is guaranteed to be safe. In fact, manufacturers recall about 4,500 drugs and medical devices annually. Many blame the approval process and the way pharmaceutical companies use the system to rush products onto the market.
Sarah Salem-Robinson, OB/GYN PA | 1:38
Sarah Salem-Robinson speaks with Drugwatch.com about the FDA’s role in approving drugs and devices
Sarah Salem-Robinson, OB/GYN PA
Physician Assistant Sarah Salem-Robinson discusses the FDA's role in the drug & device approval process
FDA Drug-Approval Process
A pharmaceutical company seeking FDA approval to sell a new prescription drug must complete a five-step process: discovery/concept, preclinical research, clinical research, FDA review and FDA post-market safety monitoring.
First, the company must conduct laboratory tests and try the drug on animals and then people to make sure it works and is safe.
After testing the drug, the company then sends the FDA a new drug application (NDA), which must include:
The drug’s test results
Manufacturing information to demonstrate the company can properly manufacture the drug
Data gathered during the animal studies and human clinical trials
The company’s proposed label for the drug, which includes uses for which it has been shown to be effective, possible risks and how to use it
FDA physicians and scientists then review the drug research and the labeling information on how to use the drug. If the findings show the drug’s benefits outweigh its known risks — and that the drug can be manufactured in a way that ensures a quality product — the drug is approved and can be marketed in the U.S. The FDA will continue to monitor the drug post-approval.
The FDA doesn’t actually test the drug itself before making a decision. The agency does, however, inspect the facilities where the drug will be manufactured as part of the approval process.
Vaccines and biologics follow the same general pathway as for drugs.
Researchers testing drugs in laboratory
Pharmaceutical companies, not the FDA, must complete a five-step testing process
Generic Drugs
Generic-drug makers also must gain FDA approval, though they do not need to repeat the clinical trials of the brand-name drug they copy. The application for generic drugs is the Abbreviated New Drug Application (ANDA). It’s called “abbreviated” because drug companies don’t need to include animal and human data to establish safety and effectiveness.
Generic Drug Approval
Generic-drug companies must prove that the ingredient in the drug that is effective against the illness or condition it’s treating is the same as that of the brand-name drug.
The companies also must show that the same amount of drug gets to the bloodstream and that it gets there in about the same time as with the brand-name drug.
In other words, generic-drug makers have to prove the generic drug is doing the same thing in the body as the brand-name drug. But there is a barrier for generic-drug makers once they gain FDA approval, and that’s the brand-name companies’ patents.
Drug Patents
Federal law allows generic-drug companies to work on drugs to gain FDA approval before the patents held by the brand-name companies expire. However, when a generic-drug maker files an application with the FDA, it must notify the patent holder if it’s challenging the patent that exists, meaning if the company is claiming the drug doesn’t infringe on the patent or the patent isn’t valid.
Fact
Currently, a new patent is good for 20 years from the date the application is filed in the U.S.
At that point, the brand-name company has 45 days to sue the generic-drug maker, and if there is a suit, the FDA cannot approve the generic drug for 30 months – unless the patent expires or is judged to be invalid or not infringed before that time – or until that generic-drug maker wins in court.
In essence, it’s created a legal battlefield of sorts in which companies are basically fighting over the patent. If a generic-drug maker markets a product and violates a patent, it could end up having to pay the brand-name company damages.
To encourage more generic competition, critics say there should be a limit on the amount of money a generic-drug company is responsible for paying to a brand-name company. A majority of drugs being used are generic drugs, yet most of the money is going to brand-name companies. Part of it is the patent, part of it is marketing.
Pay-for-Delay
There’s no shortage of controversy in the prescription-drug business, with current practices employed by drug companies garnering both support and criticism. Perhaps the biggest controversy today is a concept called “pay-for-delay.”
Fact
A brand-name manufacturer will contact a generic-drug maker who is close to approval and negotiate an agreement. Often times, the generic-drug company is paid not to bring or delay bringing the drug to the marketplace.
Opponents of pay-for-delay say it stifles competition and should not be legal. Proponents of the practice, however, argue it’s the brand-name company’s patent that’s protecting the brand’s market.
The court system has given the Federal Trade Commission more leeway in challenging such agreements as being anticompetitiv e and in violation of antitrust laws.
Over-the–Counter Drugs
Manufacturers of over-the-counter (OTC) drugs can choose to seek FDA approval through the NDA process or under what’s known as an OTC monograph. A monograph is described as a “recipe book” because it specifies the acceptable ingredients, formulations, labeling and testing parameters for more than 80 therapeutic classes of drugs. OTC drugs that follow an existing monograph can be sold without further FDA review. Those that do not conform to a monograph must undergo the NDA process. The FDA continually updates OTC drug monographs to include additional ingredients and labeling as needed.
Faster Approvals
In 1992, the U.S. passed the Prescription Drug User Fee Act (PDUFA), which allows the FDA to collect fees from companies to expedite the drug-approval process.
“PDUFA has allowed the Food and Drug Administration to bring access to new drugs as fast or faster than anywhere in the world. Since PDUFA was passed in 1992, more than 1,000 drugs and biologics have come to the market.”
According to the FDA
The act establishes two avenues for gaining approval: Standard Review and Priority Review.
The goal for standard review is to get a drug through the approval process in 10 months. This type of review is applied to a drug that offers little to no improvement over other therapies already on the market.
Priority review is a designation reserved for drugs that offer major advances in treatments or that provide treatment where none existed. It is an accelerated approval process in which the FDA aims to get a drug through the entire process in six months.
The problem with priority review is that it allows an NDA to be approved before means are available to measure the drug’s effectiveness — a step that would usually be required.
“Instead, less traditional measures called surrogate endpoints are used to evaluate effectiveness,” according to the FDA. “These are laboratory findings or signs that may not be a direct measurement of how a patient feels, functions, or survives, but are considered likely to predict benefit.”
The time goals set by PDUFA apply to new drug and biological applications as well as resubmissions of original applications and supplements to approved applications.
Reasons Approval may be Delayed or Denied
When the FDA denies a drug approval, it outlines its reasoning in a response letter to the pharmaceutical company that submitted the application. The agency provides the drug company with the opportunity to meet with FDA officials to discuss the issues. The company can then ask for a hearing, correct any issues and submit new information, or withdraw the application.
Fact
Unexpected safety issues, manufacturing issues or a failure to prove a drug’s effectiveness are reasons the FDA may deny a new drug application.
Common problems that may lead to denial include unexpected safety issues or failure to show a drug’s effectiveness. A drug company may need to conduct studies in more people or in different types of people, or studies that span longer periods of time.
Manufacturing issues are also among the reasons that approval may be delayed or denied. The FDA inspects manufacturing facilities before a drug can be approved to make sure the manufacturing practices meet agency standards. If the FDA identifies problems with the manufacturing, the drug company must fix them in order for a drug to be approved.
FDA Medical Device Approval Process
The FDA is also charged with evaluating medical devices. Research for medical devices begins in the lab. Most devices undergo laboratory and animal testing to answer basic questions about safety, and then they are tested on people to make sure they are safe and effective.
Researcher testing on mouse
Most devices undergo animal testing first to answer basic questions about safety
Next, the FDA thoroughly reviews the submitted data and makes a decision whether to approve it. The FDA classifies medical devices based on the risk they pose.
Class I devices are the least risky and include oxygen masks and surgical tools, whereas Class III devices support or sustain life, are implanted in the body or have the potential for unreasonable risk of illness or injury. These include pacemakers, breast implants and HIV diagnostic tests.
Medical devices can change classification s depending on the results of scientific data.
Types of Medical Device Applications
Like with the prescription-drug approval process, there are different types of applications for medical devices, too, depending on the level of risk a device poses.
Did You Know?
No evidence from clinical studies is needed to file a Premarket Notification.
Low- to moderate-risk devices are typically subjected to what’s called premarket notification — also called PMN or 510(k). Federal law requires new device manufacturers to register with the FDA and notify the agency at least 90 days before they start selling their devices. This premarket notification must prove the device is as safe and effective and substantially equivalent to a similar, legally marketed device. No evidence from clinical studies is needed.
High-risk devices undergo premarket approval, the most stringent type of device application required by the FDA. This application is for Class III devices that were found not substantially equivalent to a Class I or II marketed device. In this case, in order to gain FDA approval, there must be enough scientific evidence to prove the device is safe and effective for its intended use.
Another type of application is for a Humanitarian Use Device, which is a device that is intended to benefit patients by treating or diagnosing a disease or condition that affects fewer than 4,000 people in the U.S. annually. This application is similar to a premarket approval application, but pharmaceutical companies are not required to demonstrate effectiveness.
Medical Device Critiques
The FDA has come under fire from critics who say it’s not keeping up with evolving technology. That’s because there have been many recalls of medical devices that turned out to be dangerous once already in use.
Critics Challenge Trials
Many high-risk medical devices are approved based on the results of just one clinical trial; new medications usually require two.
“And only a small minority of clinical studies of medical devices are randomized, controlled and blinded — the gold standard for reliable evidence (and the benchmark to which studies of drugs are held),” cardiologists Rita F. Redberg and Sanket S. Dhruva wrote in The New York Times.
Critics have also raised concerns about the FDA’s monitoring of medical devices once they are on the market. They fear weak oversight could mean problems remain undetected.
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LMAO
get outta here, NOOB
real man are talking here
we know you bank with CHASE 0.01% interest rate
SOOOOO YOU ALREADY LOSING
Well a "NOOB" is still better than a FAKE/FRAUD and NOPE, nothing "real" about the FRAUD "fat 40 virgin that still lives in his mommy's basement"..No wonder he's always "LOSING"...
"YEEEARRRRSSSS"??
"at least 5-10 years out??"
The process pharmaceutical companies must go through in order to achieve FDA approval, and in turn start selling their drugs, is long and structured. It can take up to two and a half years for the FDA to approve a new dru
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The good news is that five years started 4 years ago. Check out their slide deck and come back to me.
https://ir.nantkwest.com/static-files/77614f06-5c1f-4c42-8761-b4d2f382425c
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Well a "NOOB" is still better than a FAKE/FRAUD and NOPE, nothing "real" about the FRAUD "fat 40 virgin that still lives in his mommy's basement"..No wonder he's always "LOSING"...
The process pharmaceutical companies must go through in order to achieve FDA approval, and in turn start selling their drugs, is long and structured. It can take up to two and a half years for the FDA to approve a new dru
The good news is that five years started 4 years ago. Check out their slide deck and come back to me.
https://ir.nantkwest.com/static-files/77614f06-5c1f-4c42-8761-b4d2f382425c
you need to tell that brother THEKING above
he just google and thats the answer he got
soooooo it must be 2.5 years
LMAO
i just look at the PDF
this drug has been in the works since the 90s
i don't know man
im all for finding cure
but it's too long
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you need to tell that brother THEKING above
he just google and thats the answer he got
soooooo it must be 2.5 years
LMAO
i just look at the PDF
this drug has been in the works since the 90s
i don't know man
im all for finding cure
but it's too long
You still can't tell the difference between drug R&D time and FDA approval time, "FDA Approval is at least 10-15 years out"... ;D ;D ;D:
bro,
you know FDA APPROVAL takes YEEEARRRRSSSS
there are many stages to get drug approved
i don't even know where you get your 2021 from
we are talking about at least 5-10 years out
this is just classic PUMP AND DUMP
ride the way and get out
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You read it and you didn't understand that there is going to be an FDA approval in 2021? ??? I'm starting to doubt your ability to comprehend complex information.
you need to tell that brother THEKING above
he just google and thats the answer he got
soooooo it must be 2.5 years
LMAO
i just look at the PDF
this drug has been in the works since the 90s
i don't know man
im all for finding cure
but it's too long
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Funny, you're not the first PH member to call him out for his reading comp issues..just like his basic decimal skills and overall math skills it's a FAIL ;D ;D ;D!
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You read it and you didn't understand that there is going to be an FDA approval in 2021? ??? I'm starting to doubt your ability to comprehend complex information.
too long, didn't read
i only scan
drug been in developed since the 90s
(tell our 2.5 years friend above) kekeke
work on some patient
don't work on some
50/50
i don't know about the 2021 approval
shyt can't change
gamble only what you want to lose
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To help our brothers out, I made it easier for yall.
Page 9, 35, and 43 have a timeline of FDA approvals forecasted.
Page 36 has the IND and clinical trials they are working on.
Page 42 has the cancer breakthrough they are going to make that year.
Page 44 has a SUPER high-level summary of how the TRIANGLEOFFENS E work to cure cancer. It's better than CAR-T and DAR-T.
This isn't a gamble. It's an investment based upon medical science that has been tested for 10 years coming to fruition to the market in the coming years.
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(tell our 2.5 years friend above) kekeke
"kekeke" ..
(https://i.imgur.com/CFysamf.png)
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NK
not looking too good man
you sure you are pro day trader???
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Can't be any worst than claiming to lose "$100k" but when challenged directly to prove it, just tuck and ran...Therefor e, just another lie...
Not surprised though as he doesn't even know basic common money and investment knowledge such as places like E-Trade have "inside information"... :idiot2: ;D
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wisemon don't go committing suicide now
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I love my life too much and the world is too beautiful. How’s your ETF doing? Got shaved again today. Down 20% again?
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"kekeke" ..
(https://i.imgur.com/CFysamf.png)
click on the article and read it fool
kekeke
i just stop there
YOUR RESEARCH AT DRUG.COM not mine
https://www.drugs.com/fda-approval-process.html (https://www.drugs.com/fda-approval-process.html)
FDA Approval Process
It takes on average 12 years and over US$350 million to get a new drug
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I love my life too much and the world is too beautiful. How’s your ETF doing? Got shaved again today. Down 20% again?
pretty happy man
i am a communist
this is exactly what i want
what i dream of
everything coming crashing down
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click on the article and read it fool
kekeke
i just stop there
YOUR RESEARCH AT DRUG.COM not mine
https://www.drugs.com/fda-approval-process.html (https://www.drugs.com/fda-approval-process.html)
FDA Approval Process
It takes on average 12 years and over US$350 million to get a new drug
I did and those experts count the R&D phases plus the "FDA Approval" phase...plus the prescription phase to the pharmacy phase...(from lab to pharmacy)
But if you're only talking about the "FDA Approval" phase which you WRONGLY claimed to take "at least 10-15 years out"...those same experts from "drugs.com" have said, it takes up to two and a half years after the application from the drug developers is submitted...
I mean if you can't even comprehend what they say with visual aide, no hope for you so you should "stop"...here's what those experts say in a visual aide form again .."PIC OR DIDNT HAPPEN".. ;D:
(https://i.imgur.com/CFysamf.png)
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pretty happy man
Doubt it based what you say about yourself here as well as the your well established fraudulent rep and behaviors here and being caught red handed and called out by others..
I mean crying about "help" each other, "no bash", and not even a day later, already "bash" others is just one misery examples of many...
"pretty happy" and "biggest troll" don't fly..
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lol
go back to ESL/ELL and learn to read
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You can "go back to ESL/ELL and learn to read" but doubt that's gonna do anything now as you're too deep in your hole..
"lol"
hmgFRAUD's lies:
bro,
you know FDA APPROVAL takes YEEEARRRRSSSS
there are many stages to get drug approved
i don't even know where you get your 2021 from
we are talking about at least 5-10 years out
this is just classic PUMP AND DUMP
ride the way and get out
Versus the experts in the field's words:
(https://i.imgur.com/CFysamf.png)
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And also look at the "FDA" column with the words "Review and approval process" under it:
(https://i.imgur.com/8aKIzPk.png)
Even with visual aides to show what the experts in the field say, hmgFRAUD still contradict himself by counting all the phases/stages from lab all the way to pharmacy shelf ready for sell.. even though he originally claimed: "you know FDA APPROVAL takes YEEEARRRRSSSS".."at least 5-10 years out"..:idiot2: ;D
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pretty happy man
i am a communist
this is exactly what i want
what i dream of
everything coming crashing down
You mean you are a bitter man.
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your map
not mine
i even circle it for you
you need to tilt your head sideway so you can see
remember graph chart in math class????? i know you suck at math
(https://i.imgur.com/DdJX1U4.jpg)
And also look at the "FDA" column with the words "Review and approval process" under it:
(https://i.imgur.com/8aKIzPk.png)
Even with visual aides to show what the experts in the field say, hmgFRAUD still contradict himself by counting all the phases/stages from lab all the way to pharmacy shelf ready for sell.. even though he originally claimed: "you know FDA APPROVAL takes YEEEARRRRSSSS".."at least 5-10 years out"..:idiot2: ;D
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You mean you are a bitter man.
im a communist bro
this is good for me
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im a communist bro
this is good for me
Don’t be bitter man. Remember it was capitalism that lifted China out of poverty and not communism. People are too vain to practice communism. The idea is so powerful but the practice is so pathetic. It’s like Christians who want to deport immigrants and break families apart. What happen to love thy brother and enemies you know...
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Don’t be bitter man. Remember it was capitalism that lifted China out of poverty and not communism. People are too vain to practice communism. The idea is so powerful but the practice is so pathetic. It’s like Christians who want to deport immigrants and break families apart. What happen to love thy brother and enemies you know...
I don't know
last i check
china say they were a socialism/communism state
deeply misform, need to check your fact first before you spew nonsense
that NBA dude, they almost didn't let him come home because he talk shyt about them
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your map
not mine
i even circle it for you
you need to tilt your head sideway so you can see
remember graph chart in math class????? i know you suck at math
(https://i.imgur.com/DdJX1U4.jpg)
It's not a "map" but NOT surprised the FRAUD doesn't know the difference...y our lies, not mine:
You can "go back to ESL/ELL and learn to read" but doubt that's gonna do anything now as you're too deep in your hole..
"lol"
hmgFRAUD's lies:
bro,
you know FDA APPROVAL takes YEEEARRRRSSSS
there are many stages to get drug approved
i don't even know where you get your 2021 from
we are talking about at least 5-10 years out
this is just classic PUMP AND DUMP
ride the way and get out
Versus the experts in the field's words:
(https://i.imgur.com/CFysamf.png)
And also look at the "FDA" column with the words "Review and approval process" under it:
(https://i.imgur.com/8aKIzPk.png)
Even with visual aides to show what the experts in the field say, hmgFRAUD still contradict himself by counting all the phases/stages from lab all the way to pharmacy shelf ready for sell.. even though he originally claimed: "you know FDA APPROVAL takes YEEEARRRRSSSS".."at least 5-10 years out"..:idiot2: ;D
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Dumb as a rock
Top left corner
It takes 12-15 years
YOUR PIC
NOT MINE
PIC OR IT DIDN’T HAPPEN
YOU PROOF YOURSELF WRONG
hahahahha
What a dumbass
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"Dumb as a"..hmg.."rock"
The column that says "FDA" with the words "Approval and review" under it...
It takes up to 2 and a half years just for the "Approval" phase.
YOUR LIES
NOT MINE
"PIC OR IT DIDN’T HAPPEN
YOU PROOF YOURSELF WRONG
hahahahha
What a dumbass"
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Thats your PIC
Learn to read your own PIC
Before you open your mouth and spew nonsense
Too funny
Why you mad bro?
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NOPE, NOT my "PIC" ...it belongs to the experts at drugs.com...so there's another FAIL..
I "read" those experts' "PIC" just fine and again, NOPE, NOT MY "PIC"...so there goes another FAIL...
That's what happens when EPIC FAIL FRAUD.."open" his "mouth and spew nonsense"...CAUGHT RED HANDED...
"Too funny
Why you mad bro?"
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PLZZZ STOP MAKING A FOOL OUT OF YOURSELF
top left corner
It say right there in Youuurrrrr PIC
seeing is believing
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If you wrong
You wrong
No need to keep continue with the lies
LMAO
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"PLZZZ STOP MAKING A FOOL OUT OF YOURSELF
top left corner
It say right there in Youuurrrrr PIC
seeing is believing" ....SEE what the experts said:
(https://i.imgur.com/CFysamf.png)
"If you wrong
You wrong
No need to keep continue with the lies
LMAO"
Most of us with common sense know the common knowledge fact of no one is perfect, we all make mistakes...the difference is we're able to take ownership of our mistakes and learn from it..
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Am i blind
Top left corner
12-15 years
Need to get your eyes check
DAMN SOOO SATLY
I LOVED IT!!!!!!
I wonnnnn
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You got money in NK ????
Or something
I told you not to trust wisemon
This company is going back to $1
Hahahah
SORRY FOR YOUR LOSS
DONT BE MAD AT ME
BE MAD AT WISEMON
He con you
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You're NOT "blind" ...JUST TOO MUCH OF A "retard" (YOUR WORD TO DESCRIBE YOU, NOT MINE)..TO COMPREHEND WHAT THE EXPERTS AT DRUGS.COM SAY..
FDA column with the words "Approval and review process" under it..
Don't ..."Need to get your eyes check
DAMN SOOO SATLY
I LOVED IT!!!!!!"
No wonder you got labeled as the most "bitter"...
You Lose
"SORRY FOR YOUR LOSS
DONT BE MAD AT ME" ...because you only have yourself to blame..
You're a "con"...
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NK is a long term hold but due to market liquidity crisis caused by demand shock and supply shock, I sold early this week. Had I sold last week, I would be in the profit zone...I took one to the chin just like everyone. I will buy it back soon...waiting for a bottom. This is the cancer vaccine. In two years, I'm going to let HR know. ;)
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damn this dude
he comes after the market drop
and claim to 'sold everything'
where them PIC OR IT DIDN"T HAPPEN at
hahaha
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damn this dude
he comes after the market drop
and claim to 'sold everything'
where them PIC OR IT DIDN"T HAPPEN at
hahaha
Monday was a 7% drop. You didn't sell after that? Dark Helmet has been out of the market for 2-3 weeks... He's the smart one here. I was hopeful and had profit to lose. You kept adding like a sucker because Cramer said so. ducking Cramer is why I didn't sell last week.
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since this is one of your stock
no money invovle
just bragging right
NO HARM NO FOUL NO MONEY INVOVLE
i'mma short this to $1
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Monday was a 7% drop. You didn't sell after that? Dark Helmet has been out of the market for 2-3 weeks... He's the smart one here. I was hopeful and had profit to lose.
pic or it didn't happen
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since this is one of your stock
no money invovle
just bragging right
NO HARM NO FOUL NO MONEY INVOVLE
i'mma short this to $1
SHORT IT! Nobody cares...if you don't get gains from it.
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SHORT IT! Nobody cares...if you don't get gains from it.
there's a saying in texas
"all hat, no cattle"
aka..... your just wearing a cowboy hat.....you don't even have any cattle $$
lol that you
(https://i.imgur.com/ranL27s.jpg)
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You just jealous because you think I got a bigger d1ck than you. :2funny: :2funny:
there's a saying in texas
"all hat, no cattle"
aka..... your just wearing a cowboy hat.....you don't even have any cattle $$
lol that you
(https://i.imgur.com/ranL27s.jpg)
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pic or it didn't happen
"$100k"? "$50k"?
"pic or it didn't happen"
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i like to thank you
for your donation to $NK
to help find a cure for the corona virus and all that other diease
THANK YOU
sorry for your loss
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I am a very generous person. So it's ok to donate. Just so you know, NK is working on cancer vaccine and not the coronavirus vaccine. Helps to understand the details of what you are investing in. ;)
Sadly, your donation to the total market went into nothing.
i like to thank you
for your donation to $NK
to help find a cure for the corona virus and all that other diease
THANK YOU
sorry for your loss
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I am a very generous person. So it's ok to donate. Just so you know, NK is working on cancer vaccine and not the coronavirus vaccine. Helps to understand the details of what you are investing in. ;)
Sadly, your donation to the total market went into nothing.
yeah that what's i say "to help find a cure for the corona virus and all that other diease"
thank you for your donation to science
don't think it as a lost
but to fund those scientist
O0 O0 O0
that's how you should look at it
who know if it's going recovery or not