Syria Turkish border, early 70ies, shortly after sunrise
The vaccine
Nervous and sleepy we alighted from our taxi in front of the customs border building, in the middle of nowhere. The other side, Turkey, was 9 km away, crossing the no mans land. It was better than Iran Afghanistan border, where the no mans land was over 20km.
Our escape from the Syrian secret service police seemed done, but we did not know what was expecting us inside the custom building.
The sun was slowly rising from somewhere.
There was nobody inside. Only the custom police officer was behind the glass.
He looked at our passport, smiling. The passport did miracles. It was a passport issued by a state in Balcans, now defunct and dead as its Cosmic Mind exploded like any garbage dump. WD has no regrets and nostalghia whatsoever now or then or when it happened, but the passport was even better than some diplomatic passports. No visas all over the world, except for the USA, Great Britain and France. It was the best friendly passport in any god forbidden place one visited.
The custom officer did not stamp it, instead he invited us in the room near.
Inside was sitting a military officer, by a worn table adorned with a rusty metal box and some files on it .He said he was a doctor and asked where are our international vaccine booklets.
We took them out and he put an intelligent face on and started browsing the vaccine stamps in the booklet.
Yes. Yellow fever is fine, hmm, this is fine but,
TsTsTs, no good, where is the Cholera vaccine? You know there is cholera spreading in Syria?
No, we said we do not know, but how about doing it now?
Tsts, ts, he said. Maybe I can make an exception, he said, after a while, your passports show that you are from a friendly nation.
We all vigorously nodded and guaranteed that we are all big friends.
He reached for the metal, rusty box and opened it. Inside was a huge syringe and the needle was even bigger.
The whole thing looked definitely, over any reasonable doubt poisonous and never sterilized.
We paled in the sight of this huge, dirty syringe and its terrible needle.
Yes it could have been a trick, but, one never knows.
We tentatively started to explain that we are very healthy and that there is no need to do this now, and how about some other , more practical way out of this impasse.
He looked, thinking and then said, ok, 80 German marks and I will stamp the booklets.
5 minutes of haggling and explaining that we are young and poor, the proof was the passport that we are not some colonial power members, etc, and we got the booklet stamped , all 4 of them for 40 German marks.
We were running out from the room to stamp the passports, everybody was smiling happy,officers included, the famous Balcan football player at that time,Jaitsch, whose name we by luck knew since we did not give a damn about football except when we played it, worked as the last visa and charm for exiting Syria,and we
Took the rope ladder to the Moon
Somewhere South Europe, deadly smallpox epidemics, early 70ies
The Vaccine
The deadly smallpox came fast. From one pilgrim visiting the middle east it has spread through the Balcans like a fire..
Witchdoctor went for a compulsory, mandatory vaccine shot.
Witchdoctor was already vaccinated against many things, Tuberculosis included.No problem.He is not against vaccines, even today.
He got the vaccine, it was not a syringe but the incision in form of a cross or two parallel lines
on his shoulder.
It did not work.
He, after a while, got a Second.
It did not work
And a Third.
It did not work.
His shoulder was deep red, the wounds were not healing, even some puss was coming out.
HE GOT A FOURTH vaccine incision.
IT DID NOT WORK.
He was in trouble. The doctor said that he was immune enough by his own immune system that the vaccine did not work, but not immune enough to get smallpox for real.
Now, folks, it was FOUR Times they vaccinated him, over and over again.Luckily , as it seems, there were no side effects of such wrongdoing and malpractice.. OK, maybe his IQ was boosted, but that is irrelevant in this world.
Witchlady mother , after the first shot had such adverse reaction that she almost died.
She forged by the help of his doctor the booklet, if not, she could not go to back to work , she was an expat.
Some friend had also multiple vaccinations for smallpox which did not work.
We fixed it. It was 50 years ago.
OK. NOW. Remember.
Take a case of Penicillin antibiotic.It saves millions of lives, but some people are very allergic to it. Very few but they are people, too. They get the anaphylaxis shock, the throat, the tongue suddenly swells, they can not breath and they suffocate to death.
Are you allergic to Penicillin and it derivatives?
Do you want to take penicillin mandatory, compulsory, by law?
Are you a World Leader allergic to some drug in a deadly manner?
DO YO WANT TO CALCULATE THE RISK/BENEFIT OF A TREATMENT WHICH CERTAINLY INCLUDES YOUR DEATH?
OR? You do not give a fu..k. there is a monoclonal medicine ready for you for some hundred thousand of euros.
You are a hero or a dumbass?
WORLD. 2020, end November, early December
The Vaccine
Dear Time travelers.
Lets talk. The tales of Ulixes.
If it is true that the new covid 19 vaccines are going to be registered all over the world in this way, AS THE EMERGENCY USE AUTHORIZATION?
As Wikipedia: “”Emergency Use Authorization (EUA)
Consideration of a drug for an EUA requires a finding that it is “reasonable to believe” that the drug “may be effective” “to prevent, diagnose, or treat serious or life-threatening diseases or conditions that can be caused by a [chemical, biological, radiological, and nuclear] agent(s)” or to mitigate a disease or condition caused by an FDA-regulated product … used to diagnose, treat, or prevent a disease or condition caused by” such an agent.[1]
The “may be effective” standard for EUAs provides for a lower level of evidence than the “effectiveness” standard that FDA uses for product approvals, using a risk-benefit analysis based on “the totality of the scientific evidence available”, it is “reasonable to believe” that the product may be effective for the specified use.[1] “”
Reasonable to believe? May be effective? Risk/benefit? LOWER EVIDENCE?
Because the registration of the new Covid19 vaccines goes at the speed of light, so quick that only AI automated reading of the data from the BIG PHARMA can be able to read all this tens of thousand of pages in such speed, understand them , evaluate, ask for clarifications and approve all in a few days! As for controlling them? Oh yea. They are already shipping them without a FDA or EU check and clearance. Science method is finally going down the drain.The FDA or EU agency clearance is certainly a formality. If this is so, why do not close this agencies once for all and stop pretending,sack and put this blind faith experts on a Universal Basic Income or let them plant trees.. Leave it to the Corporate health and do not bollock Witchdoctor on this Simulacra of State control and its capabilities.
Propublica.org:
“FDA Repays Industry by Rushing Risky Drugs to Market
As pharma companies underwrite three-fourths of the FDA’s budget for scientific reviews, the agency is increasingly fast-tracking expensive drugs with significant side effects and unproven health benefits.”
Waiving liability for drugmakers of vaccines?
IS THIS True?
is it true that Vaccine makers want legal immunity, want to be not responsible, no liability, no possibility that somebody can SUE them in any legal way for the side effects of vaccines?
Is this waiver, exemption from liabilities , the immunity from the law ( on which only serfs must abide) already given to the Pharma industry vaccine for covid 19?
REMEMBER. Fast track,low evidence, maybe it works, checked in a few days by some “independent” organization and even the company which makes it holds immunity from any type of prosecution and can not be sued in court for damages?
WHAT KIND of Contract is this?
WHat kind of Vaccine is this, when the maker do not wants to have any responsibility whatsoever of the product he is selling, when he is selling it ,and the rulers want it to be compulsory, mandatory to take it?
This is a contract?
Who is so stupid to sign this , take it, do not ask, there is no guarantee, you may even die if you sign but you can do nothing, just sign.
THis is not a contract, this is an order disguised. The order to take it.
What is then a social contract and the set of rule of law we live in? A compulsory bollocks like the ones above ?
Is This all true?
And Witchdoctor has to sign it, ? Why sign it if instead they will send the police or the military and give a shot.
And nobody brings a shred of a guarantee.
Karl Popper is turning in its grave, the Open Society and its enemies ended in the garbage dump?
And, then.
Lets follow this path further. The UK Government is issuing a tender, a bid, for:
Short description:
The MHRA urgently seeks an Artificial Intelligence (AI) software tool to process the expected high volume of Covid-19 vaccine Adverse Drug Reaction (ADRs) and ensure that no details from the ADRs’ reaction text are missed.
The WD screenshot, yes, make screenshots because things rapidly change or disappear:
Supplies
“”Legal Basis:
Directive 2014/24/EU
Section I: Contracting authority
I.1)Name and addresses
Official name: MHRA Buyer Organisation
Town: London
NUTS code: UK UNITED KINGDOM
Postal code: E14 4PU
Country: United Kingdom
E-mail: purchasing@mhra.gov.uk
Telephone: +44 2030806000
Internet address(es):
Main address: https://www.gov.uk/government/organisations/medicines-and-healthcare-products-regulatory-agency
I.4)Type of the contracting authority
Ministry or any other national or federal authority, including their regional or local subdivisions
I.5)Main activity
Health
Section II: Object
II.1)Scope of the procurement
II.1.1)Title:
SafetyConnect — AI
II.1.2)Main CPV code
48000000 Software package and information systems
II.1.3)Type of contract
Supplies
II.1.4)Short description:
The MHRA urgently seeks an Artificial Intelligence (AI) software tool to process the expected high volume of Covid-19 vaccine Adverse Drug Reaction (ADRs) and ensure that no details from the ADRs’ reaction text are missed.
II.1.6)Information about lots
This contract is divided into lots: no
II.1.7)Total value of the procurement (excluding VAT)
Value excluding VAT: 1 500 000.00 GBP
II.2)Description
II.2.2)Additional CPV code(s)
48000000 Software package and information systems
II.2.3)Place of performance
NUTS code: UK UNITED KINGDOM
II.2.4)Description of the procurement:
The MHRA urgently seeks an Artificial Intelligence (AI) software tool to process the expected high volume of Covid-19 vaccine Adverse Drug Reaction (ADRs) and ensure that no details from the ADRs’ reaction text are missed.
II.2.5)Award criteria
Price
II.2.11)Information about options
Options: no
II.2.13)Information about European Union funds
The procurement is related to a project and/or programme financed by European Union funds: no
II.2.14)Additional information
Section IV: Procedure
IV.1)Description
IV.1.1)Type of procedure
Award of a contract without prior publication of a call for competition in the Official Journal of the European Union in the cases listed below
The procurement falls outside the scope of application of the directive
Explanation:
For reasons of extreme urgency under Regulation 32(2)(c) related to the release of a Covid-19 vaccine MHRA have accelerated the sourcing and implementation of a vaccine specific AI tool.
Strictly necessary — it is not possible to retrofit the MHRA’s legacy systems to handle the volume of ADRs that will be generated by a Covid-19 vaccine. Therefore, if the MHRA does not implement the AI tool, it will be unable to process these ADRs effectively. This will hinder its ability to rapidly identify any potential safety issues with the Covid-19 vaccine and represents a direct threat to patient life and public health.
Reasons of extreme urgency — the MHRA recognises that its planned procurement process for the SafetyConnect programme, including the AI tool, would not have concluded by vaccine launch. Leading to a inability to effectively monitor adverse reactions to a Covid-19 vaccine.
Events unforeseeable — the Covid-19 crisis is novel and developments in the search of a Covid-19 vaccine have not followed any predictable pattern so far.
FOLKS, SINCE THERE IS NO REAL TIME FOR TESTING THE VACCINES PROPERLY AND INDEPENDENTLY, YOU ARE THE PART OF THE EXPERIMENT. YOU WILL BE THE 3RD PHASE OF TESTING IF IT WORKS.
BUT, IF SOMETHING GOES WRONG, YOU CAN NOT SUE, THEY ARE BEING GRANTED IMMUNITY, AND THE CONTROL AGENCIES ARE MAYBE COMING IN PLAY NOT NOW BUT MAYBE AFTER, WHEN THEY HAVE TESTED THE REACTION OF THE DRUG ON TENS OF MILLIONS OF PEOPLE.
YOU WILL BE THE GUINEA PIGS.
CROSSFINGERS. Read: The MHRA urgently seeks an Artificial Intelligence (AI) software tool to process the expected high volume of Covid-19 vaccine Adverse Drug Reaction (ADRs) !
Reasons of extreme urgency — the MHRA recognises that its planned procurement process for the SafetyConnect programme, including the AI tool, would not have concluded by vaccine launch. “”
IS THIS TRUE?
LINKS USED: NOT ONE CONSPIRACY SITE, ONLY :
INTERESTING LINK ON DENGUE VACCINE FAILURE AND DEATHS FROM SANOFI:
https://www.npr.org/sections/goatsandsoda/2019/05/03/719037789/botched-vaccine-launch-has-deadly-repercussions?t=1606147922123&t=1606413812092
THE OTHER LINKS, INCLUDING MODERNA STRANGE BUSINESS.
https://edition.cnn.com/2020/05/01/us/coronavirus-moderna-vaccine-invs/index.html
target=”_blank”>https://www.latimes.com/nation/la-122001fda-story.htmlhttps:
//ted.europa.eu/udl?uri=TED:NOTICE:506291-2020:TEXT:EN:HTML&src=0
https://www.propublica.org/article/fda-repays-industry-by-rushing-risky-drugs-to-market
https://en.wikipedia.org/wiki/Emergency_use_authorization
Drug Companies Continue to Shed Liability for Rushed Coronavirus Treatments:
https://theintercept.com/2020/08/28/coronavirus-vaccine-prep-act/
THE BLIND FAITH, MANIPULATION, PROFIT
You have read here, when science becomes politics, the scientists become political scientists, it ends in shatters. The political virology is not a science.When Science becomes Blind Faith, it is worse than Religion. It is manipulation and profit.
DO YOU WANT TO CONVINCE WITCHDOCTOR in the rightness of this method and in the 99,90% probability that the vaccine is OK??
THEN, SCRAP ALL THIS METHODS ABOVE.From legal immunity, to maybe it works , to ex post testing the vaccine on the people.
Try. WD is ready to be convinced.
CONCLUSION
Folks. Why is all this happening? There is one Boundary Condition and the common denominator of all you see, now. Boundary condition is Change and how nobody wants it.
The Ruling Class and it vast majority of supporters, left and right, lets say. To understand better, something of a math group supporting Biden deep down does not want any, any significant change. The other part, Lets say Trump group, by denying, by negating, also does not wants change.
We have, smoke and mirrors, two vast majority groups who from seemingly opposite reasons do not want change. The Covid 19 is the catalyzer which, in this mega experiment shows, that the heterogenesis of the ends works for a status quo.
One group,like Biden, by asserting the problem under current boundary conditions, which include the neoliberal system as the very broad definition, does not want change, they want to repair it a little.
The other group, by negating or diminishing the problem reasserts the system as it is.
When a group of Monkeys, Macacu Humans reaches an equilibrium ( a state of balance between opposing forces or actions that is either static (as in a body acted on by forces whose resultant is zero) or dynamic (as in a reversible chemical reaction when the rates of reaction in both directions are equal)of submission where the Ruling class dominance and being submissive to it, is a state of less anxiety and less stress.Biden group.
Trump group , same less stress and less anxiety goal,by negating the Covid 19 disrupting power as a game changer, makes the same conclusion. Both groups do not want any change in their lifestyle model, maybe only some adjustment of the reached equilibrium comfort zone.
Covid 19 is a nasty player, and that is why, the vast majority, to keep their achieved comfort zones, will take any measure necessary. In this case, Biden camp will take a vaccine to keep the current ruling order, and the Trump group will negate the vaccine and covid19 to keep the current ruling order.
WOW!
Monkey business,
but Witchdoctor will be released…..in this last waltz
They say everything can be replaced
They say every distance is not near
So I remember every face
Of every man who put me here
HERE IS THE NOT DEFINITIVE LIST OF DRUGS APPROVED BY THE REGULATORY AGENCIES WHICH PROVOKED DEATHS or serious illnesses:
FROM WIKIPEDIA
Significant withdrawals
Drug name Withdrawn Country Remarks
Adderall XR 2005 Canada Risk of stroke[1] The ban was later lifted because the death rate among those taking Adderall XR was determined to be no greater than those not taking Adderall.
Alatrofloxacin 2006 Worldwide Serious liver injury leading to liver transplant or death.[2]
Alclofenac 1979 UK Vasculitis[3]
Alpidem (Ananxyl) 1995 Worldwide Not approved in the US, withdrawn in France in 1994[4] and the rest of the market in 1995 because of rare but serious hepatotoxicity.[3][5]
Alosetron (Lotronex) 2000 US Serious gastrointestinal adverse events; ischemic colitis; severe constipation.[2] Reintroduced 2002 on a restricted basis [citation needed]
Althesin (=Alphaxolone amineptine + Alphadolone) 1984 France, Germany, UK Anaphylaxis.[3]
Amineptine (Survector) 1999 France, US Hepatotoxicity, dermatological side effects, and abuse potential.[6]
Aminopyrine 1999 France, Thailand risk of agranulocytosis and severe acne.[3]
Amobarbital 1980 Norway Risk of overdose.[3]
Amoproxan 1970 France Dermatologic and ophthalmic toxicity.[3]
Anagestone acetate 1969 Germany Animal carcinogenicity.[3]
Antrafenine 1984 France Unspecific experimental toxicity.[3]
Aprotinin (Trasylol) 2008 US Increased risk of death.[2]
Ardeparin (Normiflo) 2001 US Not for reasons of safety or efficacy.[7]
Astemizole (Hismanal) 1999 US, Malaysia, Multiple Nonspecified Markets Fatal arrhythmia[2][3]
Azaribine 1976 US Thromboembolism.[3]
Bendazac 1993 Spain Hepatotoxicity.[3]
Benoxaprofen 1982 Germany, Spain, UK, US Liver and kidney failure; gastrointestinal bleeding; ulcers.[2][3]
Benzarone 1992 Germany Hepatitis.[3]
Benziodarone 1964 France, UK Jaundice.[3]
Beta-ethoxy-lacetanilanide 1986 Germany Renal toxicity, animal carcinogenicity.[3]
Bezitramide 2004 Netherlands Risk of fatal overdose[8]
Bithionol 1967 US Dermatologic toxicity.[3]
Brotizolam 1989 UK Animal carcinogenicity.[3]
Bromfenac 1998 US Severe hepatitis and liver failure (requiring transplantation).[2]
Bucetin 1986 Germany Kidney damage[3]
Buformin 1978 Germany Metabolic toxicity.[3]
Bunamiodyl 1963 Canada, UK, US Nephropathy.[9]
Butamben (Efocaine)(Butoforme) 1964 US Dermatologic toxicity; psychiatric Reactions.[3]
Canrenone 1986 Germany Animal Carcinogenicity.[3]
Cerivastatin (Baycol, Lipobay) 2001 US Risk of rhabdomyolysis[2]
Chlormadinone (Chlormenadione) 1970 UK, US Animal Carcinogenicity.[3]
Chlormezanone (Trancopal) 1996 European Union, US, South Africa, Japan Hepatotoxicity & Steven-Johnson Syndrome [3]
Chlorphentermine 1969 Germany Cardiovascular Toxicity.[3]
Cianidanol 1985 France, Germany, Spain, Sweden Hemolytic Anemia.[3]
Cinepazide 1988 Spain Agranulocytosis.[10][11]
Cisapride (Propulsid) 2000 US Risk of fatal cardiac arrhythmias[2]
Clioquinol 1973 France, Germany, UK, US Neurotoxicity.[3]
Clobutinol 2007 Germany Ventricular arrhythmia, QT-prolongation.[12]
Cloforex 1969 Germany Cardiovascular toxicity.[3]
Clomacron 1982 UK Hepatotoxicity.[3]
Clometacin 1987 France Hepatotoxicity.[3]
Co-proxamol (Distalgesic) 2004 UK Risk of overdose
Cyclobarbital 1980 Norway Risk of overdose[3]
Cyclofenil 1987 France Hepatotoxicity.[3]
Dantron 1963 Canada, UK, US Mutagenic.[13] withdrawn from general use in UK but permitted in terminal patients
Dexfenfluramine 1997 European Union, UK, US Cardiotoxic[3]
Propoxyphene (Darvocet/Darvon) 2010 Worldwide Increased risk of heart attacks and stroke.[14]
Diacetoxydiphenolisatin 1971 Australia Hepatotoxicity.[3]
Diethylstilbestrol 1970s US Carcinogen
Difemerine 1986 Germany Multi-Organ toxicities.[3]
Dihydrostreptomycin 1970 US Neuropsychiatric reaction.[3]
Dilevalol 1990 UK Hepatotoxicity.[3]
Dimazole (Diamthazole) 1972 France, US Neuropsychiatric reaction.[3]
Dimethylamylamine (DMAA) 1983 US Voluntarily withdrawn from market by Lily.[15]:12 Reintroduced as a dietary supplement in 2006;[15]:13 and in 2013 the FDA started work to ban it due to cardiovascular problems[16]
Dinoprostone 1990 UK Uterine hypotonus, fetal distress.[3]
Dipyrone (Metamizole) 1975 UK, US, Others Agranulocytosis, anaphylactic reactions.[3]
Dithiazanine iodide 1964 France, US Cardiovascular and metabolic reaction.[3]
Dofetilide 2004 Germany Drug interactions, prolonged QT.[12]
Drotrecogin alfa (Xigris) 2011 Worldwide Lack of efficacy as shown by PROWESS-SHOCK study[17][18][19]
Ebrotidine 1998 Spain Hepatotoxicity.[3]
Efalizumab (Raptiva) 2009 Germany Withdrawn because of increased risk of progressive multifocal leukoencephalopathy[12]
Encainide 1991 UK, US Ventricular arrhythmias.[2][3]
Ethyl carbamate 1963 Canada, UK, US, Carcinogen.[20]
Etretinate 1989 France Teratogen.[2][3]
Exifone 1989 France Hepatotoxicity.[3]
Fen-phen (popular combination of fenfluramine and phentermine) 1997 Cardiotoxicity
Fenclofenac 1984 UK Cutaneous reactions; animal carcinogenicity.[3]
Fenclozic acid 1970 UK, US Hepatotoxicity.[3]
Fenfluramine 1997 European Union, UK, US, India, South Africa, others Cardiac valvular disease, pulmonary hypertension, cardiac fibrosis;[3][21] re-approved in June 2020 for the treatment of seizures associated with Dravet syndrome, under FDA orphan drug rules.
Fenoterol 1990 New Zealand Asthma mortality.[3]
Feprazone 1984 Germany, UK Cutaneous reaction, multiorgan toxicity.[3]
Fipexide 1991 France Hepatotoxicity.[3]
Flosequinan (Manoplax) 1993 UK, US Increased mortality at higher doses; increased hospitalizations.[2][3]
Flunitrazepam 1991 France Abuse.[3]
Flupirtine 2018 European Union Liver toxicity.[22]
Gatifloxacin 2006 US Increased risk of dysglycemia.[2]
Gemtuzumab ozogamicin (Mylotarg) 2010 US No improvement in clinical benefit; risk for death.[2] Returned to market in 2017. [23]
Glafenine 1984 France, Germany Anaphylaxis.[3]
Grepafloxacin (Raxar) 1999 Withdrawn Germany, UK, US others Cardiac repolarization; QT interval prolongation.[2]
Hydromorphone (Palladone, extended release version) 2005 High risk of accidental overdose when extended release version (Palladone) administered with alcohol. Standard hydromorphone is sold in most of the world including the US
Ibufenac 1968 UK Hepatotoxicity, jaundice.[3]
Indalpine 1985 France Agranulocytosis.[3]
Indoprofen 1983 Germany, Spain, UK Animal carcinogenicity, gastrointestinal toxicity.[3]
Ingenol mebutate gel 2020 Suspended in Europe Increased risk of skin cancers.[24][25]
Iodinated casein strophantin 1964 US Metabolic reaction.[3]
Iproniazid 1964 Canada Interactions with food products containing tyrosine.[26]
Isaxonine phosphate 1984 France Hepatotoxicity.[3]
Isoxicam 1983 France, Germany, Spain, others Stevens johnson syndrome.[3]
Kava Kava 2002 Germany Hepatotoxicity.[12]
Ketorolac 1993 France, Germany, others Hemorrhage, Kidney Failure.[3]
L-tryptophan 1989 Germany, UK Eosinophilic myalgia syndrome.[3] Still sold in the US
Levamisole (Ergamisol) 1999 US Still used as veterinary drug and as a human antihelminthic in many markets; listed on the WHO List of Essential Medicines. In humans, it was used to treat melanoma before it was withdrawn for agranulocytosis.[27][28][29]
Levomethadyl acetate 2003 US Cardiac arrhythmias and cardiac arrest.[2]
Lorcaserin (Belviq) 2020 US Increased risk of cancer. [30]
Lumiracoxib (Prexige) 2007–2008 Worldwide Liver damage
Lysergic acid diethylamide (LSD) 1950s–1960s Marketed as a psychiatric drug; withdrawn after it became widely used recreationally. Now illegal in most of the world.
Mebanazine 1975 UK Hepatotoxicity, drug intereaction.[3]
Methandrostenolone 1982 France, Germany, UK, US, others Off-label abuse.[3]
Methapyrilene 1979 Germany, UK, US Animal carcinogenicity.[3]
Methaqualone 1984 South Africa (1971), India (1984), United Nations (1971–1988) Withdrawn because of risk of addiction and overdose[31][32]
Metipranolol 1990 UK, others Uveitis.[3]
Metofoline 1965 US Unspecific experimental toxicity.[3]
Mibefradil 1998 European Union, Malaysia, US, others Fatal arrhythmia, drug interactions.[2][3]
Minaprine 1996 France Convulsions.[3]
Moxisylyte 1993 France Necrotic hepatitis.[3]
Muzolimine 1987 France, Germany, European Union Polyneuropathy.[3]
Natalizumab (Tysabri) 2005–2006 US Voluntarily withdrawn from US market because of risk of Progressive multifocal leukoencephalopathy (PML). Returned to market July, 2006.
Nefazodone 2007 US, Canada, others Branded version withdrawn by originator in several countries in 2007 for hepatotoxicity. Generic versions available.[33]
Nialamide 1974 UK, US Hepatotoxicity, drug intereaction.[3]
Nikethamide 1988 multiple markets CNS Stimulation.[3]
Nitrefazole 1984 Germany Hepatic and hematologic toxicity.[3]
Nomifensine 1981–1986 France, Germany, Spain, UK, US, others Hemolytic Anemia, hepatotoxicity, serious hypersensitive reactions.[2][3]
Oxeladin 1976 Canada, UK, US (1976) Carcinogen.[34]
Oxyphenbutazone 1984–1985 UK, US, Germany, France, Canada Bone marrow suppression, Stevens–Johnson syndrome.[3][35][36]
Oxyphenisatin (Phenisatin) Australia, France, Germany, UK, US Hepatotoxicity.[3]
Ozogamicin 2010 US No improvement in clinical benefit; risk for death; veno-occlusive disease.[2]
Pemoline (Cylert) 1997 Canada, UK Withdrawn from US in 2005. Hepatotoxicity[37] Reason:hepatotoxicity.[3]
Pentobarbital 1980 Norway Risk of fatal overdose[3]
Pentylenetetrazol 1982 US Withdrawn for inability to produce effective convulsive therapy, and for causing seizures.
Pergolide (Permax) 2007 US Risk for heart valve damage.[2]
Perhexiline 1985 UK, Spain Neurologic and hepatic toxicity.[3]
Phenacetin 1975 Canada An ingredient in “A.P.C.” tablet; withdrawn because of risk of cancer and kidney disease[38] Germany Denmark, UK, US, others Reason: nephropathy.[3]
Phenformin and Buformin 1977 France, Germany US Severe lactic acidosis[3]
Phenolphthalein 1997 US Possible carcinogen.[39]
Phenoxypropazine 1966 UK Hepatotoxicity, drug intereaction.[3]
Phenylbutazone 1985 Germany Off-label abuse, hematologic toxicity.[3]
Phenylpropanolamine (Propagest, Dexatrim) 2000 Canada, US Hemorrhagic stroke.[40][41]
Pifoxime (=Pixifenide) 1976 France Neuropsychiatric reaction.[3]
Pirprofen 1990 France, Germany, Spain Liver toxicity.[3][10]:223
Prenylamine 1988 Canada, France, Germany, UK, US, others Cardiac arrythmia[42] and death.[3]
Proglumide 1989 Germany Respiratory reaction.[3]
Pronethalol 1965 UK Animal carcinogenicity.[3]
Propanidid 1983 UK Allergy.[3]
Proxibarbal 1998 Spain, France, Italy, Portugal, Turkey Immunoallergic, thrombocytopenia.[3]
Pyrovalerone 1979 France Abuse.[3]
Rapacuronium (Raplon) 2001 US, multiple markets Withdrawn in many countries because of risk of fatal bronchospasm[2]
Remoxipride 1993 UK, others Aplastic anemia.[3]
rhesus rotavirus vaccine-tetravalent (RotaShield) 1999 US Withdrawn due to risk of intussusception[43]
Rimonabant (Acomplia) 2008 Worldwide Risk of severe depression and suicide[12]
Rofecoxib (Vioxx) 2004 Worldwide Withdrawn by Merck & Co. Risk of myocardial infarction and stroke[2]
Rosiglitazone (Avandia) 2010 Europe Risk of heart attacks and death. This drug continues to be available in the US
Secobarbital France, Norway, others. Risk of overdose[3]
Sertindole 1998 European Union Arrhythmia and sudden cardiac death[3][44]
Sibutramine (Reductil/Meridia) 2010 Australia,[45] Canada,[46] China,[47] the European Union (EU),[48] Hong Kong,[49] India,[50] Mexico, New Zealand,[51] the Philippines,[52] Thailand,[53] the United Kingdom,[54] and the United States[55] Increased risk of heart attack and stroke.[2]
Sitaxentan 2010 Germany Hepatotoxicity.[12]
Sorivudine 1993 Japan Drug interaction and deaths.[56]
Sparfloxacin 2001 US QT prolongation and phototoxicity.[2]
Sulfacarbamide 1988 Germany Dermatologic, hematologic and hepatic reactions.[3]
Sulfamethoxydiazine 1988 Germany Unknown.[3]
Sulfamethoxypyridazine 1986 UK Dermatologic and hematologic reactions.[3]
Suloctidil 1985 Germany, France, Spain Hepatotoxicity.[3]
Suprofen 1986–1987 UK, Spain, US Kidney damage.[2][3]
Tegaserod (Zelnorm) 2007 US Risk for heart attack, stroke, and unstable angina.[2] Was available through a restricted access program until April 2008; returned to market in 2019.
Temafloxacin 1992 Germany, UK, US, others Low blood sugar; hemolytic anemia; kidney, liver dysfunction; allergic reactions[2][3]
Temafloxacin 1992 US Allergic reactions and cases of hemolytic anemia, leading to three patient deaths.[1]
Temazepam (Restoril, Euhypnos, Normison, Remestan, Tenox, Norkotral) 1999 Sweden, Norway Diversion, abuse, and a relatively high rate of overdose deaths in comparison to other drugs of its group. This drug continues to be available in most of the world including the US, but under strict controls.
Terfenadine (Seldane, Triludan) 1997–1998 France, South Africa, Oman, others, US Prolonged QT interval; ventricular tachycardia[2][3]
Terodiline (Micturin) 1991 Germany, UK, Spain, others Prolonged QT interval, ventricular tachycardia and arrhythmia.[3]
Tetrazepam 2013 European Union Serious cutaneous reactions.[57]
Thalidomide 1961 Germany Withdrawn because of risk of teratogenicity;[58] returned to market for use in leprosy and multiple myeloma under FDA orphan drug rules
Thenalidine 1963 Canada, UK, US Neutropenia[3][59]
Thiobutabarbitone 1993 Germany Kidney injury.[3]
Thioridazine (Melleril) 2005 Germany, UK Withdrawn worldwide due to severe cardiac arrhythmias[60][61]
Ticrynafen (Tienilic acid) 1980 Germany, France, UK, US others Liver toxicity and death.[3]
Tolcapone (Tasmar) 1998 European Union, Canada, Australia Hepatotoxicity[3]
Tolrestat (Alredase) 1996 Argentina, Canada, Italy, others Severe hepatotoxicity[3]
Triacetyldiphenolisatin 1971 Australia Hepatotoxicity.[3]
Triazolam 1991 France, Netherlands, Finland, Argentina, UK others Psychiatric adverse drug reactions, amnesia.[3][62]
Triparanol 1962 France, US Cataracts, alopecia, ichthyosis.[3]
Troglitazone (Rezulin) 2000 US, Germany Hepatotoxicity[2]
Trovafloxacin (Trovan) 1999–2001 European Union, US Withdrawn because of risk of liver failure[2][3]
Valdecoxib (Bextra) 2004 US Risk of heart attack and stroke.[2]
Vincamine 1987 Germany Hematologic toxicity.[3]
Xenazoic acid 1965 France Hepatotoxicity.[3]
Ximelagatran (Exanta) 2006 Germany Hepatotoxicity[12]
Zimelidine 1983 Worldwide Risk of Guillain–Barré syndrome, hypersensitivity reaction, hepatotoxicity[3][63][64] banned worldwide.[65]
Zomepirac 1983 UK, Germany, Spain, US Anaphylactic reactions and non-fatal allergic reactions, kidney failure[2][3]
somewhere. end November, peace.
Witchdoctor