HIV, AZT, big science & clinical failure
By MARTIN J. WALKER
Martin
J. Walker was chairman of the Steering Committee on AZT Malpractice (SCAM)
and the AZT on Trial Conference, London 1993.
INTRODUCTION
In April
1984, Robert Gallo told America that he had found the 'probable' cause of
AIDS in 'a virus' later called the Human Immunodeficiency Virus (HIV). Since
that time, those who have dissented from orthodoxy have been trying to understand
how within two years the general consensual acceptance of Gallo's hypothesis
- which came to be that an HIV was the sole cause of a number of AIDS-defining
illnesses - was transformed into a universal scientific tenet . Gallo's
idea, which has never been scientifically proven, even survived the opinions
of Luc Montagnier, one of France's most eminent virologists who is now credited
with having discovered HIV in 1983 and who in l991 stated that HIV alone
was insufficient to cause AIDS.
AZT specifically, and ongoing work by scientists on attempts at anti-viral
therapies generally, confirmed in both the public and scientific mind, that
a HIV was the sole cause of AIDS. AZT was marketed as the cure for a viral
condition and, lay thinking went, scientists would not have invented an
anti-viral cure if the illness was not caused by a virus. AZT may well have
been the first drug in history which defined the illness it was meant to
treat, rather than the other way around.
In the process of producing and marketing AZT, the Wellcome Foundation set in chain a powerfully persuasive machine which created information, culture and social relations with one purpose, to sell the drug. This network had a life force which would have continued to drive it forward, even if it had occurred that the drug quickly killed everyone who took it.
TRADING PLACES
The production and marketing of AZT can best be viewed within the context of the global pharmaceutical industry in general and the Wellcome Foundation in particular*. The world pharmaceutical industry is worth £130 billion. Over the last ten years the industry has been characterised by high growth and high profits.
Throughout the eighties and nineties, the pharmaceutical industry has been in a state of transition. Mergers, takeovers, the buying up of smaller companies and the divestment of unprofitable productive sections, has left a few large companies jostling for position.
Takeovers and mergers represent one response to a crisis of profitability in the industry, a crisis which has been brought about by cut backs in public health spending in Europe and America and spiralling research and development budgets. This integration into larger global corporations has occurred also because many pharmaceutical companies have been extending their reach into different levels of health care, into hospital management, corporate employee health schemes and cradle to grave health care planning.
AZT ORPHANED AT A YOUNG AGE
AZT was not designed as a drug to combat an HIV. It was developed, from a herring and salmon sperm extract, by Jerome Horowitz in 1964 for the National Cancer Institute (NCI). As cancer chemotherapy, it was designed to destroy dividing cells which were producing tumours. AZT was, however, indiscriminately cytotoxic. It could kill any dividing cells by interfering with the reproduction of DNA.
After development of AZT was dropped it became an 'orphan drug', one with no pharmaceutical company parent to rear it and it languished, on the shelves of the National Institutes of Health. The decision to test AZT in 1985 for anti-viral properties was not due to farsightedness or any sixth sense - in 1985 and 1986, inside NIH research establishments everything which came to hand was being tested for antiviral qualities.
THE TRIALS OF AZT
The traditional form of evaluating research has been peer review, followed by publication in a few established and meritorious journals. This system of gate-keeping clearly had its drawbacks because it meant that orthodoxy retained control not only over standards of research, but inevitably over content. The peer review system attempted to act as a centralised clearing house for research while keeping a continuous if nominal check on standards.
Today, there are no universal standards for the evaluation of non- license application drug trials. Commercial and industrial interests have helped launch a large number of vested interest journals which print the research work which they have funded. Drug trials are overseen primarily by research staff working for the producer company and even the investigators are often supported by the company or work in units which rely for future funding from the company concerned.
For the first five years of AZT's life, Wellcome controlled almost all the known AIDS cases in Europe and America by drawing them into trials. In November 1987, eight months after licensing in the US, Dr Trevor Jones declared in a press release that they soon anticipated clinical studies to involve 6,000 patients, aside from 5,000 patients who were already using the treatment. Nussbaum (1990) reported that in 1988, practically 80% of the patient slots in the NIAID's AIDS clinical trial group were for AZT trials.
By 1992, Dr Jones was able to tell the press that 4,000 separate studies had now been carried out which demonstrated the benefits of AZT.
THE MEDICAL PROFESSION
Since the middle of the last century, first serving the new industrial bourgeoisie and later the working class as well, the general practitioner became the mainstay of the National Health Service. Until the 1960s, many general practitioners had a reputation for independence of mind. Over the last thirty years this independence has been eroded on the one hand by the drug marketing and the introduction of centralised high technology centres of scientific medical excellence and on the other hand by ongoing fiscal crisis.
From the beginning, Wellcome marketed AZT as a complex, high flying and very expensive drug. One of the advantages of this was that Wellcome did not have to depend upon general practitioners to dispense the drug. The ordinary doctor was, in fact, a serious problem for Wellcome as they entered the field of AIDS. What if general practitioners were to find other ways of treating HIV antibody positive patients? Wellcome set out to educate general practitioners to the enormous dangers of HIV and AIDS, ensuring that most general practitioners were so afraid of the highly contagious nature of the 'disease', that they quickly passed patients on to the hospitals. To reinforce this and strike further discipline into doctors, the General Medical Council ruled that it would be a disciplinary offence for general doctors to treat AIDS patients.
In 1987, the year that AZT was licensed, the British Medical Association (BMA), the professional trade union for doctors and an organisation which had substantial links with Wellcome, set up the BMA Foundation for AIDS. In March 1988, Wellcome gave a covenant to the Foundation, a sum of £36,000 annually for four years, totalling £144,000. This meant that at the very heart of the British medical profession, Wellcome had control of the information flow on AIDS.
THE VOLUNTARY SECTOR ORGANISATIONS
The 1968 Medicines Act makes it a criminal offence to advertise medical treatments directly to patients (vulnerably ill people). However, the sale of AZT directly to individuals who had tested 'HIV antibody' positive - using a Wellcome-produced testing kit - was from the beginning the cornerstone of Wellcome's marketing strategy.
Those who suffered AIDS-associated illnesses or who had been diagnosed 'HIV antibody' positive, mainly gay men, were an unknown factor. Pharmaceutical companies had no real experience of dealing with large, youthful, cultural identity groups.
The greatest potential for drug pushing was to be found in the plethora of self-help organisations which were springing up throughout the country.
Here at these focal locations, not only gay men gathered but specifically those who had tested 'HIV antibody' positive.
Wellcome set out to buy up all the self-help groups which had contact with gay men who tested 'HIV antibody' positive in Britain and America. Where they were unable to fund them directly, they gave grants for journals, papers and magazines or for specific projects. There were no overt strings attached to such money but recipients had to adhere to the medical model of AIDS and act as conduits by which off-the-street gay men concerned about their health could be funnelled into the charnel houses of chemotherapy.
The grant funding of self-help groups in the field of AIDS, by vested interest organisations, is perhaps one of the greatest scandals of AIDS medicine. By bombarding newly tested gay men with partial information about AZT and other so-called anti-viral drugs, Wellcome had found a way round the Medicines Act and the perfect way to construct a drugs market. Wellcome adopted a strategy which has been known within politics for hundreds of years. Wellcome didn't need General Practitioners to sell AZT, they mounted their beach heads in the bourgeois sectors of the gay community and developed a colonial class which administered the medical model for them.
The use of self-help organisations was and still is a systematic marketing strategy, and while it is important to list the groups which received drug company money, it is more important to understand the strategy which Wellcome used.
Sally joined an organisation called Positive Life (PL) which had been set up by people who were HIV antibody positive. PL had been set up for five years by the time Sally joined in 1991.
Soon after starting work, Sally was asked to write a number of articles about AZT. Sally was nervous about writing the articles because she felt the need to be critical but responsible and she was worried she might upset people by suggesting AZT was toxic.
Not long after her first article came out she was contacted by the head of the Health Education Authority AIDS programme who suggested that her article might contain inaccuracies. She was insistent that Sally should have lunch with her. When Sally went to lunch she found that a media relations manager from Wellcome's Public Relations Department was also there.
The conversation over lunch centred upon Wellcome's relationship with voluntary sector organisations and the problems of marketing AZT. Not long after the lunch, the coordinator of PL received a phone call from a public relations company informing them that Wellcome wanted to fund their organisation. PL did not accept the money.
Wellcome did not always have to make such direct advances to groups. From an early stage they managed to gain influence on the committees and boards of the major fund-dispensing bodies which acted as gate-keepers for voluntary sector funding. These strategically placed individuals, on the board, for example, of CRUSAID, an organisation which in the early nineteen nineties was controlling in excess of £4 million in funding, made sure that funds were channelled only to organisations which believed in the use of anti-viral drugs.
BIG SCIENCE RIDING OFF INTO THE BLACK HOLE
Much dissent especially in politics is based upon an intuitive and heart-felt sense of right and wrong; arguments take place around moral or ethical issues which are often impossible to prove. In AIDS, the principal orthodox proposition - that a Human Immunodeficiency Virus is the cause of AIDS - appeared to be based upon a scientific truth.
While it appears at first that only the idea of Gallo's retrovirus and its transmission has shaped our perception of AIDS and its social relations, it is more complex than this. Gallo and Gallo's idea are themselves a product of the social and commercial relations which exist inside science and the production of scientific knowledge.
Had Gallo presented his theory thirty years ago in a reputable scientific journal, rather than at a fin de sciècle press conference in Washington, his proposal would have been tested by his peers. A focused and centralised authority which had responsibility for evaluating scientific knowledge would have made a judgment, its clinical basis would have been replicated and a dialectical process would hopefully have forged the truth. As it was, there was no proving, no dialectical process, no clinical proof and no biological proof, no peer review, no open public critique. Gallo's idea was passed down in tablets of stone and 'HIV' was found guilty without any kind of trial or search for the truth. Science by absolute decree of the idea.
This is not how science has been practiced nor how truth has been arrived at over the last two centuries.
The fact that people were ill with greater frequency and died more quickly when they took AZT, did not affect the the public perception that users of AZT got better, or lived longer lives of better quality than people who unfortunately did not have access to the drug. From a very early stage, the great, mysterious and very male-oriented adventure of science began to depart from the real record of absolute clinical failure of so-called antiviral remedies. This total failure was in part disguised by the increasing understanding of doctors, and their ability to treat the individual infections and other illnesses which made up the spectrum of AIDS.
Wellcome's strategy of hegemony, brilliantly orchestrated, was highly successful. In 1992, five years after AZT was licensed, the 44.7 tonnes of AZT produced that year returned Wellcome over £250 million profit. The profits for the following year were even higher.
Over the last few years, AIDS science, which has as its only aim the production of magic-bullet drugs, has moved further and further away from the conditions of people's living illnesses. The mad scramble of science to understand the intricacies of 'HIV' has given new meaning to the old axiom, 'The operation was successful but the patient died'. AIDS scientists are now openly declaring that clinical end-points are no measure of the success of their work. To protect their authority, they have created an impenetrable wall around themselves, and within this wall its practitioners discuss mutual ideas which over the years have come to develop their own inner logic.
To people knowledgeable about AIDS but beyond the pale of orthodoxy, it appears as if AIDS scientists are slipping deeper into some kind of group psychosis. Apparently considered statements by scientists take on the meaning and form of mantras or cultish utterances which are nonsensical to those outside AIDS science. Such statements as: 'If antivirals don't work it's because the virus is very intelligent and keeps mutating'; or 'Non-infectious HIV is pathogenic' or 'Protease inhibitors mean AIDS is over'.
At some point early on in the bang of big AIDS science and its widening galaxy of abstract theorising it became impossible to readdress fundamental ideas. At issue in this reluctance was not only the plausibility of science and the authority of individual scientists but the continuing production and the profitability of anti-viral drugs. AZT was undoubtedly one of the factors which pushed the handcart of early AIDS speculation over the hill, and transformed it into the juggernaut of premature consensus.
If any doubt did begin to creep like cracks through the cultural hegemony created around AZT, at the end of the Concorde trials, these cracks were quickly filled by the culture of pharmaceutical influence which stood ready with the cocktail of combination therapy. The 'combo' approach which after all still had AZT as its central support, quickly came to be reflected upon with gothic disbelief but even then, science and medicine was saved at the last minute by protease inhibitors. These miracle drugs, despite the fact that they had been trialed for only two years will, it was said, give all those who are 'HIV antibody' positive, a happy and contented old age. The grim deception of that view is already apparent.
We are all in awe of science, especially medical science for it appears inarguable. What science does, is, and what science says can happen, scientists make happen. Like the stone masons and architects of the seventeenth century, scientists are constructing the everyday reality within which contemporary society lives.
When we look closely at the science of AIDS, and particularly at Gallo's hypothesis, we realise quite quickly that we are not dealing with scientific truth in the normal sense of the expression. The idea that an HIV is the cause of AIDS-associated illnesses, is just that - an idea - there is, even now, no evidence but only supposition to support it.
This idea, however, has achieved a materiality of considerable proportion, and it has spurned an industry. An understanding of how this happened is important - important because in understanding it, we understand not only how knowledge is reproduced in our society, but also how power is mediated.
Without this information we can not know how to dissent. We have to have this intimate understanding of the way in which the power relations of orthodoxy shape the world in order that we can resist it.
We do not believe power resides in slogans and our dissent does not become real when we say 'HIV is not the cause of AIDS'. Nor does our dissent become real if we simply argue the opposing scientific perspective. We have to dissent with who we are, with our acts; this is why the intimate knowledge of the orthodoxy's power is important to us. To oppose them we must behave differently, resist their social and institutional relations and the way in which they produce and make material knowledge.
People have to empower themselves, in every area where industry and capitalist production have taken over the basic functions and interchanges of everyday life. People have to fight back by finding themselves and a better way of treating themselves.
BIBLIOGRAPHY
(Parts I & II) Burkett, E. (1995) The Gravest Show on Earth. Houghton Miflin, New York.
Duesberg, P. (1996) Inventing the AIDS Virus. Regnery, Washington.
Hodgkinson, N. (1996) AIDS: The Failure of Contemporary Science. Fourth Estate, London.
Kennedy, I. (1983) The Unmasking of Medicine. Sutton, Surrey: Paladin.
Schiff, M. (1996) The Memory of Water. Thorsons, London.
Lauritsen, J. (1993) The AIDS War. Asklepios, New York.
Lauritsen, J. & Young, I. (1997) The AIDS Cult : Essays on the Gay Health Crisis. Asklepios, Provincetown.
Marks, K. and Engls, F. (1942) The German Ideology. Laurence and Wishart edition, London.
Miller, J. (1994) The Passion of Michel Foucault. Flamingo, London.
Nussbaum, B. (1990) Good Intentions. Atlantic Monthly Press, New York.
Papadopulos-Eleopulos, E. (1993) Is a positive Western blot proof of HIV infection? Bio/technology vol. 11.
Root-Bernstein, R. (1993) Rethinking AIDS. Free Press, New York.
Walker, M.J. (1993) Dirty Medicine: Science, Big Business and the Assault on Natural Health Care. Slingshot, London.
Url for this page:
http://www.aidsmyth.com/azt.htm
21st Nov 2000
AidsMyth.com
Today's
Aids News
& Views

click
Glaxo Wellcome's
sham informed consent
on drugs for HIV+ babies.
By
Fintan Dunne
Editor, AidsMyth.com

Side-effects
and limitations
of Aids medications are not being
disclosed to Irish mothers who undergo treatment to prevent the transmission
of HIV infection to their babies.
Ethical
issues regarding informed consent are focused on Glaxo Wellcome's multi-billion
dollar revenue anti-HIV drug, AZT (Zidovudine, azidothymidine). Glaxo
Wellcome was recently embroiled in controversy over similar consent issues
in vaccine tests on children in Irish orphanages in the 1970's. Now new
research shows AZT may worsen Aids, can produce birth defects such as webbed
hands and may cause infants to develop cancers later in life. But the company
stanuchly defends AZT's effectiveness.
Glaxo's defence of AZT should be viewed in this context: Tuesday, another
Glaxo drug, the bowel medication Lotronex was forced of the US market
by the Federal Drugs Administration (FDA), after eight women died of
intestinal failure and more had portions of intestine removed due to
side-effects. Despite this, Glaxo responded by expressing regret at the
FDA decision, describing their irritable bowel drug as "effective"
and claiming that "its side effects are manageable."
Given such confidence, it is unsurprising that recent evidence indicating
that AZT may cause rather than prevent Aids is not being disclosed
to HIV+ Irish mothers considering AZT in pregnancy. Earlier this year a
study of AZT in Aids Rapid Disease Progresion (RPD) incidence among over
400 infants born to HIV+ mothers in Miami-Dade, Florida, USA concluded that
rapid progression to 'full-blown' Aids was "three times
more likely to occur in infants born to [AZT] treated compared with findings
in [AZT] untreated mothers." In fact, Figure 1 of the
paper clearly shows a dose response curve. The earlier the mother began
AZT treatment while pregnant, the sooner her HIV positive child got sick
and died compared with the HIV positive children born to HIV positive mothers
who did not take AZT during pregnancy.
Does
AZT Cause AIDS?
AZT was originally developed as a cancer
chemotherapy, but never marketed for that purpose prior to it's application
in the treatment of Aids and the prevention of mother to child transmission
of HIV, on it's own or in combination with other anti-HIV drugs. Toxic effects
and fatalities associated with AZT have been observed internationally in
many studies, but modern practice is to place these concerns secondary to
fighting the HIV virus to the point of elimination.
Glaxo is well aware of concerns over AZT that date back years. Another
material fact not being disclosed is that the study which secured US FDA
approval for AZT, was conducted using a derived metabolized form, AZT-TP
(tri-phosphate) and not AZT as medicated. Scientific controversy now
surrounds the question of whether mothers and babies can, in practice,
phosphorylate AZT to the proper form for anti-HIV effectiveness. Some studies
have shown that the drug is instead mostly metabolized to AZT-MP (mono-phosphate).
According to a 1999 critical review of AZT by Eleni Papadopulos-Eleopulos
et al., this would mean AZT would interfere with all DNA replication
in the body instead of just that of the HI virus. That would cause toxic,
carcinogenic and mutagenic side-effects --including immune suppression indistinguishable
from Aids.
AZT causes dementia (AIDS defining), certain lymphomas (AIDS defining) muscle
wasting (AIDS defining), severe immune definciency (AIDS defining), diarhea
(AIDS defining), life-threatening anemia, abortions, birth defects and the
list goes on.
Indeed, Glaxo's Retrovir (AZT) drug packaging carries this warning:
"PROLONGED USE
OF RETROVIR HAS BEEN ASSOCIATED WITH SYMPTOMATIC MYOPATHY SIMILAR TO THAT
PRODUCED BY HUMAN IMMUNODEFICIENCY VIRUS."
Side Effects
In September, 1998, Principal researcher on a transmission study, Dr.
Ellen Cooper, told US Mothering magazine "We don't know
what the long term effects of AZT use during pregnancy might be, but so
far we have seen no adverse effects in the short term...Not one single tumor.
Not one... I mean [the children] have cancers, lymphomas, and other problems
like that... but there is no reason to link those cancers to AZT."
Another keen HIV warrior, Nurse-practitioner Mary Caffrey, University of
San Diego Medical Center, seemed equally unaware of the import of her words
when she admitted late last year to Zenger's magazine that there had been
birth defects among AZT-treated infants: "I know we have
seen some webbed fingers....but these birth defects are cosmetic and don't
interfere with life."
But not all the birth defects are as obvious as are webbed fingers. AZT
mimics thymidine -one of the four building blocks of DNA, and interferes
with DNA replication. This can destroy the effectiveness of gut bacteria
and also the primitive mitochondria inside human cells that harness
our food energy. One study found eight HIV-negative infants treated with
AZT had extremely rare mitochondrial toxicity, which led to the death
of two and severe abnormalities in three more.
Many practitioners discount these worrying findings about AZT, and
the newer anti-HIV medications with which it is used in combination. The
alternative to aggressive therapy, they say, is to allow HIV a foothold
in the child that will lead to eventual death. The Irish aim is to decrease
transmission rates to only 1%, based on post-natal HIV testing of infants.
But is a 1% transmission rate to be achieved regardless of clinical
outcome over the course of a child's entire life?
Drug Dependent
Because if AZT is, as now claimed, only partially metabolized, its
toxic effects slow DNA replication in the infant's immune system.
A lowered immune system would not trigger the HIV test -despite the presence
of the virus. This could explain the low observed rate of HIV positivity
in treated infants. Why then do the infants immune compromised by AZT not
get sick? The partially metabolised AZT also acts as a toxic antibiotic
that inhibits the replication of any pathogen trying to take advantage
of the lowered immune function.
In summary, AZT may be more an anti-biotic than anti-HIV. It may work
after a fashion, but ordains for the child an impossible-to-sustain
lifetime dependency on medication to hold infection at bay.
Why so impossible to sustain? Pay special attention to the caveat that Dr.
Karina Butler, a leading Irish consultant in paediatric infectious diseases
placed on record in an interview with the Irish Times about her work. She
warned that the "honeymoon period,"
could end if the HI virus adapts to the drugs which are used to combat it's
spread. This misleads us by implying this outcome is only a possibility.
In fact, in the USA, where these drugs have been pioneered, they are already
failing in clinical practice. Doctors are reporting a recent surge in 'full-blown'
Aids among those on long term treatment, due to a phenomenon they
dub "viral rebound." Even if the drugs were not
failing, heart disease, liver failure and other serious side-effects are
anyhow forcing patients to abandon Aids medications. The honeymoon
is already over, despite any coyness in admitting it. The new concern is
that we have all-the-while merely accelerated Aids progression by attacking
sickness instead of boosting health.
Ireland is now ready to apply this type of treatment to any Irish mother
who tests HIV positive. Yet the accuracy of the HIV test falls dramatically
when applied to general populations rather than to just those in known Aids
risk groups. But once tested positive, mothers who are aware of these issues
and are reluctant to follow current medical advice could find a court
mandating medication for their baby. Legal precedent is already established
by a court-ordered blood transfusion for a child in an Irish Jehovah's
Witness congregation.
Conclusion
If we engage in widespread use of drugs like AZT, unacknowledged
side-effects may come back to haunt us. They did when the widely-promoted
DES anti-miscarriage drug of the 1950's proved carcinogenic. Our informed
consent must be fully informed by both doctors and the media. The goal of
treatment must be improved morbidity and mortality in all HIV+ infants and
this must not be made subservient to achieving low rates of transmission
in some.
Recent international controversy following questions about Aids diagnosis
and AZT phosphorylation raised by South African president Thabo Mbeki; the
current failure of yet another generation of Aids drugs in the USA, and
the news that prescription drug effects and doctor error are the fourth-leading
cause of death in US hospitals, all herald that for the Aids industry
too, the honeymoon period is over.
In an unprecedented development, the US television network ABC, will
soon air a prime-time 20/20 documentary on Christine Maggiore, who
campaigns to save babies from Aids drugs. The half hour segment will feature
once HIV positive Christine and her drug-free and disease-free son
Charlie, and will interview scientists who for years have questioned
all aspects of the current Aids paradigm.
A more questioning journalistic and scientific eye must and will be
trained on Aids -one that goes beyond mere jingoistic repetition of the
safe sex public health message, and insists on safe and informed medical
practices too.
Research:
Kathy Mc Mahon, News Editor, AidsMyth.com
Thanks to Anita Allen, South Africa
-------------------------------------------------------------------------------
"AZT kills any bit of DNA that tries to replicate.
It is a crazy way to attempt to kill the HIV virus because so few Lymphocytes
are carrying a copy of HIV (1/10,000) and the viral copy is only about 1/100,000
of the size of the host cell DNA......Yet Burroughs-Welcome's figures indicate
that 200,000 people world-wide receive AZT every day at the cost of $2,300
per year."
- Dr Charles Thomas
-------------------------------------------------------------------------------
REFERENCES
& SOURCES
Miami-Dade Study
Ricardo S. de Souza et al., (2000) Effect
of prenatal zidovudine on disease progression in perinatally HIV-1-infected
infants, Journal of Acquired Immune Deficiency Syndromes
24: 154-161.
RETROVIR (zidovudine)
March 4, 1998: Glaxo Wellcome
PRECAUTIONS:
Information for Patients: Fifth paragraph, second sentence revised
(new text in italics) - "The long-term consequences of in utero and
infant exposure to Retrovir are unknown, including the possible risk
of cancer.
AZT
(SIDE) EFFECTS
Body as a whole: abdominal pain, back pain, body odor, chest
pain, chills, edema of the lip, fever, flu syndrome, hyperalgesia.
Cardiovascular: syncope, vasodilation.
Gastrointestinal: bleeding gums, constipation, diarrhea, dysphagia,
edema of the tongue, eructation, flatulence, mouth ulcer, rectal hemorrhage.
Hemic and Lymphatic: lymphadenopathy.
Musculoskeletal: arthralgia, muscle spasm, tremor, twitch.
Nervous: anxiety, confusion, depression, dizziness, emotional lability,
loss of mental acuity, nervousness, paresthesia, somnolence, vertigo.
(partial list)
A Critical Analysis of the Pharmacology of AZT and its Use
in AIDS
Eleni Papadopulos-Eleopulos (1), Valendar F. Turner (2), John M. Papadimitriou (3), David Causer (4), Helman Alphonso (5) and Todd Miller (6)
(1)
Corresponding author, Biophysicist, Department of Medical Physics, Royal
Perth Hospital, Wellington Street, Perth 6001, Western Australia (2) Consultant
Emergency Physician, Department of Emergency Medicine, Royal Perth Hospital
(3) Professor of Pathology, University of Western Australia (4) Senior Physicist,
Department of Medical Physics, Royal Perth Hospital (5) Head, Department
of Research, Universidad Metropolitana Barranquilla, Colombia (6) Assistant
Scientist,Department of Molecular and Cellular Pharmacology, University
of Miami School of Medicine, Florida, USA
http://www.virusmyth.com/aids/data/epazt2.htm
Physician Data on AZT Retrovir
http://www.virusmyth.com/aids/data/pdrazt.htm
Modifications to AZT pharmacological datasheet.
http://www.virusmyth.com/aids/data/fdaaztadd.htm
see also www.debating-azt.co.za