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Tag Archives: anaphylaxis

COVID-19 UK Advises People With Serious Allergies To Avoid Pfizer COVID-19 Vaccine – Canada issues advisory

9th December, 2020 · admin

Scroll down for Anaphylaxis/COVID 19 news stories and reports

See the Science page for medical journal articles re: COVID-19 vaccines and anaphylaxis.


Access to Information emails describing anaphylaxis to COVID-19 vaccines in British Columbia (pdf)


Hypertensive Anaphylaxis After Moderna COVID-19 Vaccination: A Case Report


 

COVID-19 Vaccination Results in Wide Array of Skin Disorders – Rashes Are More Common in People with Baseline Medical Problems – Peter A. McCullough, MD, MPH™

 

UK warns people with serious allergies to avoid Pfizer vaccine after two adverse reactions

https://www.reuters.com/article/health-coronavirus-britain-vaccine/uk-warns-people-with-serious-allergies-to-avoid-pfizer-vaccine-idUSKBN28J1DX
LONDON (Reuters) – “Britain’s medicine regulator has advised that people with a history of significant allergies do not get Pfizer-BioNTech’s COVID-19 vaccine after two people reported severe adverse reactions on the first day of rollout.

…

Pfizer has said people with a history of severe adverse allergic reactions to vaccines or the candidate’s ingredients were excluded from their late stage trials, which is reflected in the MHRA’s emergency approval protocol.

The new MHRA guidance, sent out to health professionals, said a much broader segment should not take the vaccine.

“Any person with a history of a significant allergic reaction to a vaccine, medicine or food (such as previous history of anaphylactoid reaction or those who have been advised to carry an adrenaline autoinjector) should not receive the Pfizer BioNtech vaccine,” it said.

It also said resuscitation facilities should be available for all vaccinations.”

UPDATE – UK walks back Food Allergy Warning

U.K. to refine allergy warning on Pfizer vaccine sparked by two adverse reactions – The Medicines and Healthcare Products Regulatory Agency (MHRA) initially advised anyone with “a history of a significant allergic reaction to a vaccine, medicine or food” to avoid taking the vaccine. However, by the end of Wednesday that guidance was set to be refined after discussions with experts on the nature of the reactions. ‘We’re tweaking advice to make it very clear that if you’ve got a food allergy, you’re not more at risk,’ Imperial College London’s Paul Turner, an expert in allergy and immunology who has been advising the MHRA on their revised guidance, told Reuters.”

Video from Reuters here:


#CanWeTalkAboutIt
July 21 severe systemic allergic reaction anaphylaxis 1st dose Az #vaccineinjuries pic.twitter.com/79oDlRSKk2

— Nik (@Manxie1989) June 14, 2022

RFK, Jr. Warned FDA Three Months Ago About Ingredient in Pfizer COVID Vaccine That Likely Caused Life-Threatening Reaction in Two UK Healthcare Workers – An investigation this week identified polyethylene glycol (PEG) as the likely reason two people in the UK suffered anaphylaxis after receiving Pfizer’s COVID vaccine. In September, CHD Chairman RFK, Jr. warned the FDA that PEG in COVID vaccines could lead to severe allergic reactions. By Lyn Redwood, RN, MSN

5 Questions Fauci and FDA Need to Answer on Pfizer and Moderna COVID Vaccines – As reports surfaced today of yet another healthcare worker who suffered a severe allergic reaction to Pfizer’s COVID vaccine, it’s time the FDA and Fauci explain what they plan to do about it. By Lyn Redwood, RN, MSN

FDA Investigates Allergic Reactions to Pfizer COVID Vaccine After More Healthcare Workers Hospitalized – The FDA is investigating allergic reactions in “multiple states.” The agency acknowledged the reactions may have been caused by PEG, a compound in the Pfizer vaccine that CHD previously told the FDA could put millions of people at risk. – Children’s Health Defense Team

Comment from Vinu Arumugham – Posted by the Food and Drug Administration on Dec 8, 2020
“The Pfizer COVID-19 vaccine increases risk of developing de novo asthma or exacerbation of existing asthma (and allergies, GI diseases). All vaccines are contaminated with aeroallergens thus increasing risk of developing asthma. The Pfizer vaccine is distributed in a multi-dose vial which needs to be diluted. This step along with the “pressure equalization” step further increases risk of aeroallergen contamination of the vaccine. Since it is also known that the vaccine has high reactogenicity, it will cause a strong undesirable immune response against these aeroallergens. One can expect increase in asthma and aeroallergen related allergies following this vaccine. And the two dose requirement, will boost the asthma and allergies too.
https://assets.publishing.service.gov.uk/government/uploads/system/uploads/attachment_data/file/941452/Information_for_healthcare_professionals.pdf

Aeroallergen contamination of multi-dose and reconstituted vaccine vials cause the development of asthma, gastrointestinal diseases and proves vaccine makers and vaccine safety regulators are incompetent
https://doi.org/10.5281/zenodo.2544037”


Pfizer-BioNTech COVID-19 vaccine: Health Canada recommendations for people with serious allergies – Advisory from the Government of Canada – “What to do: People with allergies to any of the ingredients in the Pfizer-BioNTech COVID 19 vaccine should not receive it. Speak with your health professional about any serious allergies or other health conditions you may have before you receive this vaccine.”

Anaphylaxis Following m-RNA COVID-19 Vaccine Receipt (pdf) – December 19, 2020 – CDC.gov


Alaska healthcare worker with no history of drug allergies suffered serious ‘anaphylactic-like’ reaction after getting Pfizer’s coronavirus vaccine – A healthcare worker in Juneau, Alaska, suffered a severe allergic reaction within 10 minutes of receiving Pfizer Inc’s coronavirus vaccine on Tuesday – She remains stable in the ICU and is expected to be discharged later on Wednesday – The woman has no known history of allergies and is said to be disappointed that she can’t receive the vaccine’s second dose – The anaphylactic-like reaction is believed to be the same one suffered by two British healthcare workers last week, both of whom have since recovered – It led the U.K.’s regulatory body to warn that anyone with severe allergic reactions to food or medicine not get the vaccine – In Pfizer’s clinical trial, 137 people who were given the vaccine suffered allergic reactions as did 111 in the placebo group – December 16, 2020


Suspicions grow that nanoparticles in Pfizer’s COVID-19 vaccine trigger rare allergic reactions – Sciencemag.org – “Severe allergy-like reactions in at least eight people who received the COVID-19 vaccine produced by Pfizer and BioNTech over the past 2 weeks may be due to a compound in the packaging of the messenger RNA (mRNA) that forms the vaccine’s main ingredient, scientists say. A similar mRNA vaccine developed by Moderna, which was authorized for emergency use in the United States on Friday, also contains the compound, polyethylene glycol (PEG).”


Hamilton PSW says allergic reaction to COVID-19 vaccine led to fainting, seizures and CPR – Deborah Tilli says she still thinks people should get the vaccine – CBC – “”I do have a severe allergy to bumblebees, and the nurse went over that with me and even questioned me about it, but … it seemed like she really didn’t know what she was doing,” Tilli said. … Tilli says when she woke up, she was told she suffered seizures and needed CPR for a brief period. She doesn’t remember much during the reaction, but says one moment sticks out — accepting the fact that she could die. ‘There was a moment where, I don’t want to say I gave up, but I was just like ‘It is what it is.’ … [Days later] when I was in bed the other night, I was thinking, ‘What if I left my two girls without a mother?’ Tilli said.”


2 North Dakotans have allergic reaction suspected from COVID-19 vaccine; infectious disease specialist says ‘don’t be alarmed’ – KXNET.com


Oregon health care worker hospitalized after severe reaction to coronavirus vaccine – KATU2.com – “An employee at a northeastern Oregon hospital had a severe allergic reaction to the Moderna vaccine and was hospitalized, the Oregon Health Authority reported Thursday. The employee works at Wallowa Memorial Hospital in Wallowa County. After taking the vaccine this week, OHA said the employee experienced anaphylaxis. OHA said the employee is recovering in the hospital.”


Boston doctor has severe allergic reaction after receiving Moderna jab – Daily Mail via MSN.com – “A doctor from Boston with an allergy to shellfish suffered a serious reaction after receiving the Moderna coronavirus vaccine. Dr. Hossein Sadrzadeh, who works as geriatric oncologist at Boston Medical Center, became dizzy and experienced an increased heart rate after he took the jab on Christmas Eve.”


Maine health care worker experienced severe allergic reaction to coronavirus vaccine, CDC reports – MSN.com – “The Maine Med employee had a history of severe allergies and past experience with anaphylaxis, which can cause a widespread rash and swelling, plummeting blood pressure, rapid heartbeat, and difficulty breathing. Hospital staff at the vaccination clinic were briefed on the employee’s medical history and observed the person after being vaccinated, as with all COVID-19 inoculations, according to the Portland Press-Herald.”


NYC health care worker has city’s first allergic reaction to COVID-19 vaccine – New York Post – “A New York City health care worker suffered a “significant allergic reaction” to a COVID-19 vaccine — the first “serious adverse event” to the jab in the Big Apple, officials said Wednesday.”


Alabama health officials verify allergic reaction to COVID vaccine – WTOK.com – “The Alabama Department of Public Health reported Wednesday that it was notified that a person who received the Pfizer BioNTech COVID-19 vaccine Tuesday experienced anaphylaxis (a severe allergic reaction) several minutes after taking the vaccine and while in required post-vaccine observation. The patient was immediately treated with anaphylaxis protocol at Decatur Morgan Hospital where the vaccine was administered.”


Mexican Doctor Taken to ICU After Experiencing Serious Reaction to Pfizer Vaccine – The female Mexican doctor experienced seizures, difficulty in breathing and developed skin rashes after she took the Pfizer-BioNTech vaccine. – “The female doctor suffered from seizures and had difficulty in breathing besides developing skin rashes. The Mexican Health Ministry said in a statement that the initial diagnosis revealed that it was encephalomyelitis, which is an inflammation of the brain and spinal cord.”


CDC says severe allergic reactions to the Covid vaccine run 10 times reactions to the flu shot but they’re still rare – CNBC – “A new CDC study published Wednesday found that people receiving Covid-19 vaccines experience anaphylaxis at a rate 10 times higher compared with the flu vaccine.” – Link to study.


Scientist Calls for Polyethylene Glycol (PEG) Sensitivity Patch Testing Prior to COVID19 Vaccine and Drug Use – James Lyons-Weiler Blog


California calls for pause of 330,000 doses, investigation after allergic reactions to Moderna vaccine batch – A cluster of allergic reactions prompted state officials to call for a pause of Moderna batch 041L20A


Tip of the Iceberg? Thousands of COVID Vaccine Injuries and 13 U.S. Deaths Reported in December Alone – In December, 3,916 COVID vaccine-related adverse events, including 13 deaths, were reported to VAERS. As more adverse events — ranging from life-threatening anaphylaxis to death — occur, it will be tougher to “sell” the experimental injections.


‘My throat started closing’: San Diego woman describes allergic reaction to COVID-19 vaccine – “Brennan was one of up to ten people who had suspected allergic reactions after getting vaccines at Petco Park, the home of Major League Baseball’s San Diego Padres, last week. … Brennan said she’s allergic to shellfish.”


Pfizer vaccine gives Queensland health care worker an anaphylactic reaction


Four Australians suffer severe allergic reaction to AstraZeneca Covid-19 vaccine in the past 48 hours – The four Queenslanders had received AstraZeneca jab within the past two days – They suffered anaphylaxis after receiving the jab, health authorities revealed – Health officials have said reactions in people with allergies are to be expected – All four patients had a history of severe allergic reactions or anaphylaxis


Japan reports 47 anaphylaxis cases after 580,000 Pfizer vaccine shots – “The figure as of last Sunday implies an anaphylactic reaction rate of around 81 cases per million doses administered, much higher than five cases in every 1 million doses administered in the United States and 20 cases per million in Britain.”


Obituary: Kansas woman dies of allergic reaction after receiving a COVID-19 vaccine – EMS dispatch states the woman was having difficulty breathing and speaking when 911 was called – “In the obituary posted with Becker Dyer-Stanton Funeral Home, family members said 68-year-old Jeanie M. Evans, of Effingham, died unexpectedly on Wednesday at the Stormont-Vail Hospital after having a reaction to a COVID-19 vaccine. Emergency dispatch records note a patient had an allergic reaction at a vaccine clinic site just after 4 p.m. on Tuesday. Dispatch identified the patient as a 68-year-old female having difficulty breathing and speaking — adding that she had been injected with an EpiPen and that there were two nurses with her on the scene.”


P.E.I. woman hospitalized over ‘extremely rare’ COVID-19 vaccine allergy shares her story – Expert says getting COVID-19 itself is much worse than very low risk from vaccination – “The 32-year-old had no known allergies, but sometimes felt slightly unwell after annual flu shots, so staff at the King’s County Memorial Hospital in Montague, P.E.I., flagged her to wait 30 minutes after her Pfizer-BioNTech shot instead of the usual 15, to make sure she would be all right.”


Mother, 25, is put into intensive care coma after ‘very rare’ reaction to second Covid Pfizer jab caused terrifying anaphylactic shocks – Kirsty Hext, 25, has suffered 14 anaphylactic shocks since having vaccine – She also had a seizure and fractured her wrist, leg and cheekbone after falling – Carer is still in hospital after suffering the most recent anaphylactic shock


RE: Urgent preliminary report of Yellow Card data up to 26th May 2021 – “The Allergic responses to the vaccines comprised 25,270 reported ADRs, with 4 fatalities occurring among 1,001 people experiencing anaphylactic reactions.”


Adverse Events Following Immunization (AEFIs) for COVID-19 in Ontario: December 13, 2020 to June 5, 2021 – EVENTS MANAGED AS ANAPHYLAXIS There were 186 reports of events managed as anaphylaxis, in which 17 met the definition of a serious AEFI. Of all 186 reports of events managed as anaphylaxis: 164 received epinephrine, 163 were seen in the emergency department and 130 were fully recovered at the time of reporting. – Public Health Ontario


Three cases of vesiculobullous non-IgE-mediated cutaneous reactions to tozinameran (Pfizer-BioNTech COVID-19 vaccine) – “The Phase III trial of tozinameran, a ribonucleic acid (RNA) vaccine, demonstrated a risk of anaphylaxis at 11.1 cases per million doses1 . Little is known regarding various non-IgE-mediated cutaneous reactions arising from the use of these vaccines. We report three cases of non-IgE-mediated cutaneous reactions following tozinameran administration, in a tertiary hospital in Singapore.”


IgE-mediated allergy to polyethylene glycol (PEG) as a cause of anaphylaxis to mRNA COVID-19 vaccines


Kansas woman Jeanie Evans died of an allergic reaction to COVID-19 vaccine, autopsy shows – Topeka Capital-Journal


Maple Ridge woman compensated for mother’s death from COVID-19 vaccine – Frustrated by Canada’s Vaccine Injury Support Program – “Her mother had received a Moderna vaccine. Ten minutes later, she was having a hard time breathing. Soon she was unconscious. A nurse administered two EpiPens – one in a leg, and one in an arm, but they couldn’t save her. “She was gone in 15 minutes.” It had been a severe anaphylactic shock, despite the fact that she had never had an allergic reaction in the past. “I was stunned,” said DuPerron. “I couldn’t wrap my head around it.” – August 2022


EU adds severe allergies as side effect of Novavax COVID vaccine – Novavax stock fell 20.3% after news of severe side effects


Posted in News | Tags: allergic reaction, anaphylaxis, COVID-19, vaccine |

PENTA Vaccine Letter

11th December, 2016 · admin

For further information on the Penta vaccine see the Penta Project page.

Rita Hoffman

rita (at) fastmail.net

 

VIA REGISTERED MAIL AND E-MAIL

December 12, 2016

The Honorable Jane Philpott
Minister of Health
House of Commons
Ottawa, Ontario K1A 0A6
Jane.Philpott@parl.gc.ca

The Honorable Eric Hoskins
Minister of Health & Long-Term Care
10th Floor, Hepburn Block
80 Grosvenor Street
Toronto, Ontario M7A 2C4
ehoskins.mpp@liberal.ola.org

Dear Ministers Dr. Philpott and Dr. Hoskins,

Re: PENTA 5 in 1 vaccine injected into babies in Canada (except Manitoba) from 1994 to 1997 and its relationship to the epidemic of anaphylaxis in children and young adults

I could not let another New Year go by without writing heads of government to ensure that the sordid history of the PENTA vaccine is recorded in your correspondence archives.

According to the SickKids Foundation, anaphylaxis to foods is affecting approximately 300,000 children and their families in Canada. It is unsure whether this estimate includes the first wave of the epidemic that included my son, who is now an adult at 23. What was the difference between his vaccination schedule and his mildly allergic sister 6 years older? While our daughter received the polysaccharide Hib – on its own – at the age of 18 months, our son was in the first wave of children to receive various conjugate Hib vaccines (adjuvanted) concurrent or combined (PENTA 5 in 1) with the DPT-IPV in infancy. The scientific literature is clear …. Vaccines can cause anaphylaxis.

Since the introduction of concurrent administration of DPT-P + haemophilus influenza B conjugate in infancy in 1993 there has been a dramatic increase in life threatening chronic children’s health conditions including anaphylaxis. In 2008, then Prime Minister Stephen Harper announced additional funding (for a total of $5 Million) for the MedicAlert Foundation’s No Child Without program including free medical bracelets for children. Stunningly, the press release states:

“In Canada, the number of children suffering from afflictions such as allergies, asthma, or childhood diabetes, is ever increasing. Critical conditions (e.g. asthma, various allergies) sometime require urgent medical attention by paramedics and/or doctors. It’s estimated that one in 10 Canadian children have severe allergies, asthma, diabetes, epilepsy and other conditions that can be life-threatening if emergencies are not treated properly and promptly.”

That was in 2008. I would hope that you and every other doctor, government and public health official in this country would find it unacceptable that 1 in 10 children in Canada live with life threatening conditions, and would leave no stone unturned to find out WHY. While a single measles case can cause pandemonium, the numbers of these affected children continue to rise without any alarm bells. What is being done by government and health officials, other than throwing money at MedicAlert bracelets, to address the epidemic of life threatening conditions in children?

Parents of children affected by food anaphylaxis and/or autism have spent numerous years and countless hours investigating why our children are affected with such severe immune system and brain malfunctions. The PENTA Project investigations have revealed that the PENTA 5 in 1 combination (1994 – 1997) did not have a DIN # or a Notice of Compliance rendering it illegal according to Health Canada. 11,000+ adverse events, including deaths, were reported to PHAC for the PENTA combination over the three years that PENTA was in use.   You may request PHAC ATIP reports A-2013-00096 and A-2013-00097 to view all of this data, which is too large to upload to a website. All subsequent 5 in 1 vaccines including Pentacel and Pediacel are based on this illegal combination, putting into question all vaccine schedules since 1994.

Access to Information requests over many years to all levels of government including requesting PENTA licensing information provided scant information, and Ontario, Canada, and local health unit ATIP responses did not acknowledge that the PENTA combination existed at all!

Parents like me have scoured the medical literature to find scientific proof of a vaccine connection to anaphylaxis. The website https://deadlyallergy.com resource and science sections outline some of that literature. The book The Peanut Allergy Epidemic, What’s Causing It and How to Stop It by Canadian Historian Heather Fraser MA, BA, B.Ed. details the history of the whole sordid mess. Mrs. Fraser’s book is fully referenced, and should be read by every doctor, nurse, politician, health official and parent.

Heather Fraser contacted her Member of Parliament, Nathaniel Erskine-Smith, on June 27, 2016 with a “Request for an investigation into the unlicensed PENTA vaccine & its long term consequences” that was sent to you, Health Minister Philpott, on Heather’s behalf.   The extensive binder of evidence, memory stick with the full file of PENTA adverse events, along with a copy of the book, The Peanut Allergy Epidemic, never received a response or even the courtesy of an acknowledgement. Minister Philpott, what happened to this material, and when are you going to respond to Heather Fraser?

I will send any recipient of this e-mail a copy of Heather Fraser’s book upon request in hopes of SOMEONE finally addressing the long term health effects experienced by the recipients of the PENTA vaccines and children continuing to be affected by the epidemic of anaphylaxis.

Surprisingly, the Canadian Medical Association Journal published my letter in 2004: http://www.cmaj.ca/content/170/4/437/reply#cmaj_el_942 which includes some information on the PENTA saga prior to our knowledge of this vaccine combination being illegal:

“After retrieving the lot numbers of the vaccines given to my anaphylactic child I sent in an Access to Information request to Health Canada for 1) the 100% composition of the vaccines my child received and 2) a list of vaccine adverse events reported for the 8 lots he received. Health Canada can’t provide me with a 100% composition because it’s proprietary information. For the adverse event information I was asked to pay $600 down and $1200 in fees. This information, from 1993-95, was not on a computerized database – why wasn’t it?

After waiting a year and paying only for photocopying, I received the data from Health Canada. I had to manually count the 975 reactions: death, seizure/convulsion, dysopnoae, speech disorder, allergic reaction, adenopathy, hypotonic-hyporesponsive episode, severe pain and/or swelling, screaming episode, hypokinesia, persistent crying, severe vomiting and/or diarrhea, lethargy, fever, cyanosis, rashes, eczema, pneumonia, lymphocytosis, sterile abcess/nodule/necrosis, infective abscess, tachycardia, gait abnormal, ataxia, bulging fontanelle, sepsis, vaso-vagal reaction, tremor, arthritis, cellulitis, bradyapnoea, delirium, reduced consciousness, shaking, somnolence, anaphylaxis, apnoae, encephalopathy, asthma, injection site reaction, shortness of breath, and confusion.

Repeated attempts to get an explanation as to why one particular lot was able to rack up 664 reactions (including 34 seizures/convulsions) without being pulled from the market have gone unanswered by local and Ontario health officials, officials with Health Canada and participants of IMPACT. Also unanswered: The National Report on Immunization, 1996 states: “If the number and type of reports for a particular vaccine lot suggested that it was associated with more serious adverse events or deaths than are expected by chance, the federal government has the responsibility and will, as well as the legal authority, to immediately recall that lot.” The U.S. Centers for Disease Control considers a vaccine “hot lot” one that generates reports of more than two deaths or two convulsions or a total of 10 adverse reports. Health Canada officials reported an investigation should be initiated after a “cluster of reports” and that means “3 or more.” This being the case the majority of vaccines my child received should have been recalled? Why weren’t they?

Another of the many unanswered questions is “How do you determine whether the adverse event is attributed to the DPT-P or the Hib when they were both given at the same time, and now in the same syringe? Could anyone provide me with safety studies relating to the DPT-P and Hib being given concurrently, and whether IgE levels were tested pre and post vaccination?”

To make matters worse, my recent Access to Information request for a product monograph, including studies that the licensure was based on, for the 5 in 1 “PENTA” (whole cell pertussis, DTPolio combined with Hib) vaccine that Health Canada supposedly licensed in 1994 and my child received in 1995 was answered with “After a thorough search for the requested information, no records were located which respond to your request.” The “PENTA” vaccine is not even listed in the Compendium of Pharmaceutical Specialties for 1993, 1994 or 1995.

Frightening………..and unacceptable.”

The United States FDA never approved the 5 in 1 PENTA, and the FDA waited until 2008 to license the acellular pertussis version of PENTA called Pentacel.   The FDA approval document for Pentacel lists “several items of concern” … this with a vaccine that had been injected in Canadian children since Pentacel was rushed in to take the place of PENTA on July 1, 1997.

As stated above, the Toronto’s SickKids Foundation reports that there are 300,000 children in Canada living with life threatening food anaphylaxis. Are they including the children who received the PENTA vaccine who are now adults? We don’t know. Clearly, anaphylaxis continues to affect children at epidemic proportions in this country.

To not mention the vaccine connection to allergy (as shown in the medical literature) prior to vaccination means that parents do not have fully informed consent to vaccination. Now that Ontario is intent on changing the legislation of the Immunization of School Pupils Act to require an “education session” prior to a parent filing an exemption, the province must ensure that fully informed consent is given. I would suggest that until such time that concrete causes of anaphylaxis are found that “vaccines are not tested for their potential to cause allergic disease” must be included in any informed consent discussions with Ontario parents and children prior to vaccination. For that matter, until such time that the cause of cancer is found, a statement such as “vaccines are not tested for their potential to be carcinogenic or mutagenic” (see Section 13) must also be included.

Informed consent, according to the Health Care Consent Act in Ontario:

Elements of consent

  1. (1) The following are the elements required for consent to treatment:
  2. The consent must relate to the treatment.
  3. The consent must be informed.
  4. The consent must be given voluntarily.
  5. The consent must not be obtained through misrepresentation or fraud.

and must include:

  1. The nature of the treatment.
  2. The expected benefits of the treatment.
  3. The material risks of the treatment.
  4. The material side effects of the treatment.
  5. Alternative courses of action.
  6. The likely consequences of not having the treatment.

Members of the National Advisory Committee on Immunization (NACI) and vaccine decision makers in upper levels of provincial and federal governments should not be allowed to have any Conflict of Interest with any pharmaceutical company.   Of the current NACI Chair and Vice Chair (voting) and the 10 voting members 11 out of 12 have indirect or direct conflict of interest. This is unacceptable. According to this Conflict of Interest report the IMPACT network, which is supposed to monitor vaccine injury in this country, is conflicted! (See Wendy Vaudry) ….. “YES …Co Primary Investigator of the IMPACT Network – which is partially supported by grants from Industry (Novartis, GlaxoSmithKline, Sanofi)”     This is an outrage!   No wonder I never heard from any of the IMPACT participants after pleading for them to look into anaphylaxis in 2002!

I request a reply with your suggestions on how to put a halt to this epidemic of anaphylaxis. At the very least, children exhibiting any form of rash or other allergy symptoms should have their vaccinations delayed or offered in individual (one at a time) vaccinations in fractioned doses to prevent the development of severe allergic disease (this was done in the past, see History section of deadlyallergy.com ). Sadly individual doses of infant/toddler vaccine are no longer available.   5 or 6 in 1 and 3 in 1 combination vaccines are the only choices for parents now. Is there any wonder parents are worried when the vaccination schedule begins at 2 months with 7 or 8 different vaccines in 5 or 6 in 1 combinations (depending on the province) at one “well baby visit”?

Respectfully yours,

Rita Hoffman

Dedicated to Pierre Morin, Penta Project parent, who died in October of 2010

CC:
Rt. Honourable Justin Trudeau, Prime Minister of Canada justin.trudeau@parl.gc.ca
Honorable Kathleen Wynne, Premier of Ontario kwynne.mpp@liberal.ola.org
Dr. Barbara Law, Chief Vaccine Safety, PHAC
Dr. Richard Schabas, MOH, HPE Public Health
Dr. Lynn Noseworthy, MOH, HKPR District Health Unit
Dr. Monica Naus
Dr. Brian Ward
Dr. Kumanan Wilson
Dr. David Williams Chief Medical Officer of Health, Ontario
Dr. Gregory Taylor
Dr. John Spika, Senior Medical Advisor to the Assistant Deputy Minister of the Infectious Disease Prevention and Control Branch
Dr. Scott Halperin
Dr. David Scheifele
Dr. Ron Gold
Dr. Philippe De Wals
Dr. Pierre Dery
Dr. William Albritton
Marie Adèle Davis, Executive Director, Canadian Paediatric Society
Dr. Allan Becker
Dr. Kelly Moher, Gateway Community Health Centre
Dr. Alex Hukowich (retired)
Dr. Granger Avery, President, Canadian Medical Association
Food Allergy Canada
Vaccine Choice Canada
#NoMandates Canada
The Penta Project

 

PDF for printing the above letter


Reply from Canadian Health Minister Jane Philpott dated February 8, 2017 (PDF format)

My reply to Minister Philpott’s letter linked above dated February 13, 2017

Subject: In response to your correspondence / 16-013578 – 522 – ss
Date: Mon, 13 Feb 2017 17:09:19 -0500
From: Rita Hoffman <rita@fastmail.net>
To: Jane.Philpott@parl.gc.ca, Minister_Ministre <Minister_Ministre@hc-sc.gc.ca>
CC: nathaniel.erskine-smith@parl.gc.ca, Heather Fraser, Vaccine Choice (Canada)

Dear Health Canada / Minister Philpott,

Thank you for the correspondence from Minister Philpott dated February 8, 2017 (attached)  16-013578 – 522 – ss regarding my letter dated December 12, 2016 regarding “PENTA 5 in 1 vaccine injected into babies in Canada (except Manitoba) from 1994 to 1997 and its relationship to the epidemic of anaphylaxis in children and young adults” which was sent to Minister Philpott via E-mail and also via Registered Mail.   This letter can be read here:  https://deadlyallergy.com/2016/12/penta/

My correspondence may have been confused with Heather Fraser’s package of information sent to Minister Philpott via Heather’s Member of Parliament, Nathaniel Erskine-Smith in the summer of 2016, who is cc’d on my correspondence (attached).    Mr. Erskine-Smith is not my Member of Parliament.   The title of Heather Fraser’s Binder of information was “Request for an investigation into the unlicensed PENTA vaccine & its long term consequences” and she included a copy of her book The Peanut Allergy Epidemic, two CDs with over 25,000 pages of AEFI reports made by doctors documenting adverse reactions and injuries in children who had been vaccinated with the PENTA vaccine.

My letter from the Minister states “enclosed copy of The Peanut Allergy Epidemic”.  I never sent a copy of The Peanut Allergy Epidemic to Minister Philpott, though I did offer to send her a copy upon request, as stated in my December 12, 2016 letter.   Can you please advise if these two different correspondences were confused as I did not send the Minister a book and my MP is not Mr. Erskine-Smith?

Also, I am very disappointed to read information in your attached letter that is contradictory to what is known as the law in Canada.  The PENTA vaccine 5 in 1 combination did NOT have a DIN #, which is required for licensing of a vaccine product in Canada.   You state, “No safety concerns were identified that warranted any action regarding the PENTA Vaccine”.   You must not have read my letter or you would have NEVER have said this, as my child’s lot # received hundreds of reported injuries and NOTHING was done.  It’s time to acknowledge that Canadian children were, in fact, guinea pigs between 1994 and 1997, and it’s time to launch an investigation as Heather Fraser requested many month ago to ensure that this travesty never happens again in this country.

I look forward to your reply at your earliest convenience.

Sincerely,

Rita Hoffman
——– Forwarded Message ——–

Subject:

In response to your correspondence / 16-013578 – 522 – ss

Date:

Wed, 8 Feb 2017 11:28:58 -0500

From:

Minister_Ministre <Minister_Ministre@hc-sc.gc.ca>

To:

Rita Hoffman

CC:

NATHANIEL.ERSKINE-SMITH@PARL.GC.CA

 

Please find attached a response to your correspondence sent to the Minister of Health.

Thank you.

Health Canada

To view this file you will need Adobe Reader – http://get.adobe.com/reader/

(See attached file: 16-013578-522 FINAL.pdf)

Posted in PENTA Project | Tags: anaphylaxis, conflict of interest, DTP-Polio, food allergy, Health Canada, Hib, informed consent, PENTA, vaccine |

Vaccines cause the development of food allergies: the latest evidence

15th July, 2016 · admin

Vaccines and the development of food allergies: the latest evidence British Medical Journal Rapid Response to Re: Non-specific immunological effects of selected routine childhood immunisations: systematic review (BMJ)

By Vinu Arumugham

Drs. Commins and Platts-Mills were the first to describe tick bites causing red meat allergy.1⁠

A case of a naturally injected allergen causing the development of allergy.

Vaccines of course are artificial injections of food allergens, causing the development of food allergies.2⁠

The same team above, now describes their findings regarding food allergy and vaccination.

Changes in IgE Levels Following One-Year Immunizations in Two Children with Food Allergy

https://wao.confex.com/wao/2015symp/webprogram/Paper9336.html

Case 1 in the above study

“Case 1: At 8 months-old, her serum IgE values (in IU/mL) were total 61.4, peanut 13.6, almond 4.04, milk 3.84, egg 2.01, soy 1.6, and wheat 0.98, compared to total 44.1, peanut 11.2, almond 1.54, milk 2, egg 1.71, soy 1.62, and wheat 2.2 at 12 months-old. After the 12 month-old labs were drawn, she received the vaccines Prevnar13, hepatitis A, MMR, and Varicella. 3 weeks later, at 12.7 months-old, her IgE values were total 75.6, peanut 16.5, almond 2.18, milk 5.06, egg 3.4, soy 3.64, and wheat 3.75.”

The vaccines caused increases in peanut, almond, milk, egg, soy and wheat IgE.

Let’s look at the food proteins contaminating the vaccines the patient received.3⁠

Prevnar 13 contains casamino acids (cow’s milk derived) and soy peptone broth.

Polysorbate 80 from EMD Millipore may contain wheat proteins.

Polysorbate 80 is present in many vaccines including Prevnar 13.

https://www.emdmillipore.com/US/en/product/Tween-80-%28Polysorbate%29,MDA_CHEM-817061#documentation

says:

“The following materials are used as raw material but are not present in the final product: Maize, Wheat

We point out that we do not perform any testing on allergens in the above-mentioned product.”

Polysorbate and other excipients derived from vegetable sources are present in many other vaccines and most suppliers do not have allergen information. So polysorbate and other excipients could also be a source of peanut and almond protein contamination of vaccines.

MMR contains chick embryo culture proteins and the vaccine package insert4⁠ has a warning for patients with egg allergy. Some egg proteins may be common to or cross react with chick embryo proteins.

 

Case 2 in the above study

“Case 2: At 12 months-old, the boy’s IgE values were total 21.1, egg 1.16, and peanut, milk, wheat, soy, cod, and shrimp <0.1. A week later, he received Prevnar13, MMR, and Varicella. 3 weeks later, at 13 months-old, his IgE values were total 23.8, egg 4.02, and peanut, milk, wheat, soy, cod, and shrimp <0.35 “

For case 2, again, MMR could have been the cause of the increase in egg IgE.

Clear evidence that food proteins in vaccines turn them into food allergy booster shots that boost the severity of food allergies. Children are taking longer to outgrow allergies.5⁠ How can they outgrow their food allergies, if we insist on giving them food allergy booster shots?

This latest evidence adds to the solid body of scientific evidence,2⁠ demonstrating a causal relationship between food protein contaminated vaccines and the development of food allergies.

References

1. Commins SP, Platts-Mills T a E. Allergenicity of carbohydrates and their role in anaphylactic events. Curr Allergy Asthma Rep. 2010;10(1):29–33.

2. Arumugham V. Evidence that Food Proteins in Vaccines Cause the Development of Food Allergies and Its Implications for Vaccine Policy. J Dev Drugs. 2015;4(137):2.

3. Vaccine Excipient & Media Summary [Internet]. 2015 [cited 2016 Jan 16]. Available from: http://www.cdc.gov/vaccines/pubs/pinkbook/downloads/appendices/B/excipient-table-2.pdf

4. MMR II Vaccine Package Insert [Internet]. [cited 2016 May 3]. Available from: http://www.fda.gov/downloads/BiologicsBloodVaccines/Vaccines/ApprovedProducts/UCM123789.pdf

5. Wang J. Management of the patient with multiple food allergies. Curr Allergy Asthma Rep. 2010;10(4):271–7.

 

 

Posted in Resources | Tags: anaphylaxis, food allergy, IgE, immunization, MMR, peanut allergy, polysorbate, vaccine excipient |

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