|
(June 2001) Drugs
firm withheld key results of vaccine test
PHARMACEUTICAL
giant Wellcome withheld damaging information about
highly reactive batches of the 3-in-1 infant vaccine from the Irish
health authorities.
The
multinational company, which has since
merged to become Glaxo Smith Kline, is at the centre of the controversy
surrounding the inadvertent injection of some children in Dublin with
the veterinary vaccine, Tribovax T rather than the 3-in-1 vaccine,
Trivax in 1973.
The late
1960s and early 70s were a period of greatly increased numbers of
adverse reactions in both Ireland and Britain.
In August
1973 the Eastern Health Board expressed its serious concern
directly to Wellcome. The EHB drew specific attention to five lots of
vaccine from which reactions were appearing most regularly.
The
information was sent to the Head of Wellcome's Clinical Immunology
Department, Dr AH Griffith who forwarded it to a senior colleague
seeking precise details.
A couple of
weeks later the results of tests carried out on the lots were relayed
to Dr Griffith.
In a memo,
thanking his colleague for the results, Dr Griffith said: "I
am not sure whether they imply that these batches are abnormally
reactogenic or whether, on intensive study, all batches are highly
reactogenic.
"There seems
to be no point in forwarding information to Dublin at this stage ... "
(July 2001) Irish
children may have been given animal vaccine for whooping cough
The Irish
authorities are again investigating reports related to the
bungled administration of child vaccines more than 30 years ago.
The
drug company involved has promised its full cooperation.
It is becoming clear, however, that not only were Irish, and some
British, children injected with highly toxic batches of whooping cough
vaccine (Trivax), but also some Irish children were injected with an
animal drug with a similar name (Tribovax T).
It seems that
some health experts in the Republic Ireland and
the United Kingdom were highly critical of the use of Trivax, but their
concerns, and those of parents, were brushed aside. Among the experts
was Gordon Stewart, emeritus professor of public health at Glasgow
University, who advised the UK Department of Health in an unpublished
1989 report that he believed the vaccine to have been "too toxic."
Vac's
comments:
Sure mistakes
happen, but all too often many years later we hear about something from
the past, from my research it is clear that all these manufacturers
seem to care about is money and profits and that is sad, so can you
honestly hand on heart say you trust them 100%.
Especially in
light of the recent events concerning Gardasil and Cervarix which I
believe triggered the death of Natalie Morton.
(Aug 2001) Health officials
supply suspect baby vaccine
THE Department of
Health has told doctors they must use stocks of a
mercury-based vaccine for infants even though it is being phased out
for
safety reasons.
The
department is issuing the brand which contains mercury despite fears
that it could be a cause of autism and other disorders. The decision
flies
in the face of European guidelines that warn it would be prudent to
avoid
such vaccines for children.
Mercury-free
vaccines are available to the health department but last month
all GPs and clinics, which inoculate more than 600,000 babies a year,
were
told all orders for the combined diphtheria, tetanus and pertussis
(DTP) and
Hib vaccine (which protects against a form of meningitis) would be met
with
a product containing thiomersal, which is almost 50% mercury. This was
"in
order to make good use of the current and future stocks available".
The previous
policy was to supply a DTP Hib vaccine, Infanrix Hib, which
does not contain mercury.
Two years ago
medicine regulators in America and Europe recommended the
mercury-containing preservative thiomersal should be phased out of
vaccines
"within the shortest possible time frame".
This followed an announcement by the United States Food and Drug
Administration (FDA) that accumulated mercury in vaccines given to
babies
under six months in America exceeded safety limits set by the
Environmental
Protection Agency.
In a related
US study, researchers from the Centres for Disease Control and
Prevention found a "statistically significant" association between
thiomersal in vaccines and children with problems such as attention
deficit
disorder and speech and language learning delays.
Last year the
European Agency for the Evaluation of Medicinal Products said:
"For vaccination in infants and toddlers, as a precautionary measure it
would be prudent to promote the general use of vaccines without
thiomersal
and other mercurial preservatives. Moreover, the use of the available
thiomersal-free vaccines should be recommended for vaccination of
newborns."
The health department's decision will outrage parents already concerned
that
vaccines may damage their children. "It beggars belief," said Isabella
Thomas, from Brighton, whose son Michael is autistic.
"To replace a
vaccine which contains no mercury, which must be safer, with
one which contains a toxic substance to use up stocks is disgraceful
and
irresponsible."
(Sep
2001) The
Risk of Seizures after Receipt of Whole-Cell Pertussis or Measles,
Mumps, and Rubella Vaccine
ABSTRACT
Background The administration of the diphtheria and tetanus toxoids and
whole-cell pertussis (DTP) vaccine and measles, mumps, and rubella
(MMR) vaccine has been associated with seizures. We studied the
relation between these vaccinations and the risk of a first seizure,
subsequent seizures, and neurodevelopmental disability in children.
Methods This cohort study was conducted at four large health
maintenance organizations and included reviews of the medical records
of children with seizures. We calculated the relative risks of febrile
and nonfebrile seizures among 679,942 children after 340,386
vaccinations with DTP vaccine, 137,457 vaccinations with MMR vaccine,
or no recent vaccination. Children who had febrile seizures after
vaccination were followed to identify the risk of subsequent seizures
and other neurologic disabilities.
Results Receipt of DTP vaccine was associated with an increased risk of
febrile seizures only on the day of vaccination (adjusted relative
risk, 5.70; 95 percent confidence interval, 1.98 to 16.42). Receipt of
MMR vaccine was associated with an increased risk of febrile seizures 8
to 14 days after vaccination (relative risk, 2.83; 95 percent
confidence interval, 1.44 to 5.55). Neither vaccination was associated
with an increased risk of nonfebrile seizures. The number of febrile
seizures attributable to the administration of DTP and MMR vaccines was
estimated to be 6 to 9 and 25 to 34 per 100,000 children, respectively.
As compared with other children with febrile seizures that were not
associated with vaccination, the children who had febrile seizures
after vaccination were not found to be at higher risk for subsequent
seizures or neurodevelopmental disabilities.
Conclusions There are significantly elevated risks of febrile seizures
after receipt of DTP vaccine or MMR vaccine, but these risks do not
appear to be associated with any long-term, adverse consequences.
(Sep 2001) Follow
the money on vaccines
It isn't often
that a governor vetoes a bill that was passed
unanimously by both Houses of the State Legislature. It reminds us of
the old saying of the mother, watching her son drill for the first time
with the troops: "Everybody's out of step except my son Jim." This time
the one who is out of step is George, as in Gov. George Ryan of
Illinois. He vetoed Senate Bill 1304, entitled "An Act Concerning
Immunizations." This bill would have provided that a person is
ineligible to serve on the Illinois Immunization Advisory Committee if
the person or his spouse is an officer, employee, or agent of, or has
any ownership or other financial interest in a pharmaceutical company
that manufactures vaccines. It also would have prohibited committee
members or their spouses from soliciting or accepting anything of value
or any other economic benefit from a pharmaceutical company that
manufacturers or produces vaccines unless it is offered and available
generally to licensed physicians or the public. That sounds like an
excellent rule and we wonder why it hasn't always been the law.
(Sep 2001) Drugs firms'
pressure 'risks lives'
Drug companies
are warned to take a back seat in clinical trials
Patient safety is
under threat because commercial interests are skewing the results of
drug trials, say the editors of some of the world's top medical
journals.
Eleven
publications say that in some cases the benefits of drugs have been
hyped in research papers, and side effects disguised.
This could lead
to doctors prescribing unsuitable drugs for their patients, they claim.
The influential
journals have threatened that unless trials can be proved to be
independent, the results will not be published in their journals to
protect patients.
(Dec 2001) Riots
in Algeria as vaccine kills seven babies
RIOTS swept
through the Algerian town of Oued el Abtal after the deaths of seven
babies who had received measles vaccinations.
Residents fought
police and set fire to government buildings when the town's prefect
arrived to attend the children's funerals.
Police fired
warning shots in an attempt to disperse the crowd in the town near
Mascara, about 225 miles west of Algiers.
The seven victims
were between three and 18 months old. Three died immediately after
receiving the injections last week as part of a vaccination campaign
and four others died within an hour, witnesses said.
Dozens more were
taken to hospital in a serious condition.
Local doctors
claimed that the vaccine had passed its expiry date, but health
authorities later denied this and said the vaccination had been
administered incorrectly.
(Original source the
Telegraph, now gone, so provide the one from above, genuine cause was
on http://www.jabs.org.uk/pages/other/other.html where I'm getting all
these from, just that articles over a few years old have gone.)
|