Literary Review of Overdo$ed America
Dr. Abramson Described How the Pharmaceutical Companies Were Affecting the FDA Negatively Leading to Medications Being Approved in Less Time (New Publication)
Literary Review of Overdo$ed America
Overdo$ed America written by Dr. Abramson describes how the pharmaceutical companies had created a monopoly through compromising medical journal articles, promoting newer and more expensive dangerous medications, and affecting the doctor patient relationship negatively through false advertisements (seen in Claritin). Dr. Abramson's book is a great work on medical ethics. The book details how it is possible to be ethical in medicine despite the corruption and deceit that has increased since the 1980s and 1990s. With pharmaceutical companies and health insurance companies attempting to take autonomy from primary care physicians since the 1980s, Dr. Abramson describes how it is still possible to remain ethical and moral by choosing to not be a part of corruption and deceit.
We learn that there is always a choice to remain ethical and practice integrity. There is the choice to persevere with morality despite the temporary lies of the snake that says, "Everyone sins. Why not sin and be like everyone else?" We can choose to avoid the lies of the snake knowing that there are individuals that are good and practice integrity. We do not need to believe the temporary lies of the snake that envies when individuals worship GOD Almighty. We choose to remain ethical and speak out against corruption especially when it attempts to promote faulty "medications" and "vaccines". We can choose to avoid adverse experimental "vaccines" and expose corruption.
Exposing Deceit and Choosing Integrity
"The ideals and personal goals that had brought me to medicine and then to family practice now called me to investigate, full-time, just how the fundamental mission of American medicine was being undermined-and how we might begin to fix it."- (page 71)
Dr. Abramson described how he had left medical practice in order to describe how the medical field was being affected negatively by the pharmaceutical monopoly (socialism). Dr. Abramson described how he decided to leave a busy medical practice in order to research and expose the corruption and lies of medical journal articles, questionable medical treatments and medications based on deceitful medical journal articles, and how the pharmaceutical companies had essentially attempted to usurp power from researchers and physicians in the 2000s. Dr. Abramson left a busy practice where he had practiced primary care for many decades in order to understand just how bad the state of the medical system was in the 2000s.
Dr. Abramson discovered that medicine had been corrupted by pharmaceutical companies. He probably left practice after seeing how patients were actually demanding newer, more expensive, and brand name medication because of commercials. Despite the newer medications not being better than generics in some cases (i.e. Vioxx, Celebrex, Actonel, Fosamax, Quinoglute, and Norpace), individuals demanded newer medications instead of listening to Dr. Abramson's medical counseling. Dr. Abramson discovered that commercials for medications were using deception to make it seem that medications were the solution to disease when there are other solutions including exercise, diet counseling, inexpensive generic medications, and preventative care that are actually more effective at improving health or reducing disease. Apparently pharmaceutical companies had used commercials, ads, medical journal articles, continuing medical education classes, and marketing firms in order to sell more newer, brand name, prescribed medications. Dr. Abramson decided to write Overdo$ed America to describe the reality of primary care medicine in the 2000s. The book is impressive because it describes how the truth can allow individuals to not believe the lies of deception. Pharmaceutical companies wanted to sell newer medications that were not better than generics and could have even caused worse disease. Dr. Abramson decided to fight corruption instead of being a part of corruption. Overdo$ed America describes how there are individuals that choose integrity and genuine empathy over corruption and deceit.
Medical Advancements in the Early and Mid 1900s and Decreased Medical Care Quality in the 1980s
Dr. Abramson described how there have been substantial medical advances in the US since the 1900s. There have been great medications and treatments created since the beginning of the 20th century. Dr. Abramson offers constructive criticism concerning how medicine has been commercialized since the 1980s and resulted in the decreased quality of medical care. This is interesting because science is a tool that can be used to help individuals and patients instead of leading to poor health outcomes including heart attacks, strokes, osteoporosis, and falls. There have been great innovations in medicine such as the Polio vaccine that was created in the 1950s by the healthy competition of Dr. Salks and Dr. Sabin that resulted in the decrease of polio cases and lower limb paralysis. The cardiopulmonary bypass machine has helped with surgery in the 1950s. Coronary artery bypass graft surgeries also were successful in the 1960s to remove blocked arteries.
Dialysis machines created in the 1960s have helped individuals with chronic kidney disease. Hip and knee replacement surgeries allow for increased mobility for patients. There have been medical innovations such as Dr. Debackey's heart surgery inventions that have helped patients survive heart surgery. Izoniazid and streptomycin were antibiotic treatments that helped against bacterial infections. Tagamet was created in 1977 and helped against ulcers. Zantac was later created and approved because it caused less side effects than Tagamet. Prilosec OTC was later approved being better, cheaper, and without the need of a prescription compared to Zantac. Medical innovations and inventions have helped patients. Despite great innovations, medical care quality has decreased since the 1980s due to socialism's attempts to corrupt medical research, the medical supplies industry, and medicine. Socialism has attempted to decrease the quality of medical innovations seen most obviously with the covid experimental "vaccine" in 2019, yet even newer, expensive medications approved in the 1980s (including statins) can cause adverse health effects. Surveys and statistics have described how the quality of medical care in the US has decreased. It is most likely because of corruption and socialism (monopoly "capitalism") The quality of health care has decreased due to the decreased autonomy of physicians since the 1980s seen in how insurance companies have tried to usurp authority, and socialists have fought against H.M.O. plans that were actually suppressing the cost of medical care. H.M.O. plans were actually cost effective in the 1980s and also gave physicians autonomy to practice. Because H.M.O.s were cost effect and not allowing medical costs to balloon to double digits, socialists slandered and lied about cost saving H.M.O.s with great physicians who were preventing a rising cost of medical care while providing great medical care quality in primary care.
"Then I saw an article in the Journal of the American Medical Association, in July 2000, claiming that 'the U.S. population does not have anywhere near the best health in the world.'"- (page 44-45)
"The low ranking of Americans' health reported in this article was so disparate from what I had believed that I started to look for other sources of comparitive data to see if this was right. An extensive comparison of the health of the citizens of industrialized countries done by the Organization for Economic Co-Operation and Development (OECD) confirmed the conclusions presented in Dr. Starfield's article. The United States again ranked poorly, with 18 industrialized countries having greater life expectancy."- (page 45)
"Children born in the United States today can expect to live the equivalent of about 69.3 healthy years of life, while children born in the other 22 industrialized countries can expect an average of 2.5 additional years of healthy life."- (page 46)
Corruption in Medicine in the 1940s
"Estrogen was approved by the FDA in 1942 for the treatment of symptoms associated with menopause." -(page 59)
"Clearly, restricting the use of Estrogen to women with troublesome menopausal symptoms limited its potential market greatly. If more drugs were to be sold, new reasons to take estrogen would have to be found."- (page 60)
"Estrogen became the most frequently prescribed drug in the United States in 1966. It remained one of the most frequently prescribed drugs through 1975."- (page 62)
It is difficult to pinpoint when medicine began to be corrupted. In the 1940s, there was a case of corruption when a corrupt physician, Dr. Wilson, decided to publish a book and an article in a medical journal about how estrogen replacement therapy helped women with menopause and also prevented "breast and gential cancer" in 1962. Combined estrogen therapy was marketed as supposedly helping decrease cervical cancer (1979), heart attacks (1985), strokes, and improved overall health.
"In a 1962 article published in JAMA, Dr. Wilson, a gynecologist, reported the results of a study in which 304 women had been treated with estrogen. Though 18 cancers were predicted over the time that the women had been taking estrogen, none developed."- (page 60)
"Perhaps Wilson's own tongue had been sharpened by the support his foundation was receiving from several drug companies, including the manufacturer of estrogen. In 1965 the Wilson Research Foundation received $34,000 (the equivalent of about $175,000 in 2004 dollars) in contributions from drug companies, enough to cover Wilson's expenses while he was writing his book. In total, Wilson's foundation received $1.3 million from drug companies."- (page 60)
Dr. Wilson had financial ties with pharmaceutical companies (Wyeth-Ayerst) who paid him to promote estrogen replacement therapy. It was noted in the 2000s that estrogen replacement therapy increases cancer incidence in women 8% for every year that they take estrogen. Dr. Wilson did not describe the risk of cancer in the 1940s despite there probably being cases.
It was not until 2003 and 2004 that new studies described that taking estrogen replacement therapy causes cancer, stroke, Alzheimer's disease, and heart attacks. It is possible that estrogen replacement therapy was marketed as an amazing treatment by pharmaceutical companies since the 1940s as population control. Socialists hate that the population size keeps growing and probably falsely marketed estrogen replacement therapy as a good treatment in the 1940s without real scientific evidence. A lying journal article and a lying book were used to promote cancer causing medication to women in the 1940s. It took 60 years to find out that estrogen replacement therapy actually caused adverse health effects. (Covid experimental "vaccines" may not be good vaccinations either despite lies from socialist propaganda.)
It seems that because American industriousness and ethics allowed for innovations in medicine since the 1900s, socialists wanted to prevent such great medical care and advancements starting in 1942 with false lying information published about estrogen replacement therapy. Initially, it was stated that estrogen replacement therapy prevented cancer while actually causing different types of cancer, strokes, osteoporosis, and Alzheimer's disease. Researchers published medical journal articles in 1975 that described that estrogen replacement therapy caused cancer. Taking estrogen replacement therapy increased the risk of cancer 14 times after seven years of treatment. Yet another lying article stated that adding progestin hormone to estrogen therapy prevented cancer. This was probably to protect sales of estrogen replacement therapy in 1979.
"In December 1975, two articles published in NEJM showed that estrogen therapy increased the risk of cancer of the lining of the uterus (endometrial cancer), up to 14-fold after seven years of treatment. This fear was quashed when, four years later, in 1979, an article published in the Lancet showed that adding another hormone, progestin, for about 10 days each month to estrogen therapy prevented the changes in the lining of the uterus that predisposed to cancer. Several other studies soon confirmed that progestin protected women on estrogen therapy from developing endometrial cancer. Still, HRT had been linked with cancer in the public's mind, and sales plummeted. Only half as many prescriptions for Estrogen were filled in 1980 as had been filled in 1975."-(page 62)
"An aggressive drug rehabilitation program was needed. 'Marketing a disease is the best way to market a drug.'"- (page 62) [Osteoporosis was marketed as a disease that could be improved with estrogen replacement therapy in 1986.]
Since individuals were realizing that estrogen may have caused cancer in 1975, the socialists decided to rehabilitate the medication by marketing osteoporosis as another disease that can be treated with estrogen. Before 1985, few people had heard about osteoporosis being a deadly disease. Osteoporosis was marketed heavily in the 1980s as a dangerous disease for women that could lead to falls and fractures in order to sell estrogen since sales had plummeted in the 1970s. It is possible that the disease was heavily marketed to increase sales of estrogen.
"And osteoporosis or thinning of the bones was a perfect disease to market: there are no symptoms until you develop fractures, so no postmenopausal woman could be sure she was safe. And the criteria were set so that one quarter of all women over 65, and more than half over 75, would be diagnosed with the disease if they had bone density tests. There was, however, a lot of work to be done to turn osteoporosis from part of the normal spectrum of skeletal aging into a feared disease."- (page 62)
Osteoporosis may have been marketed in advertising by pharmaceutical companies in medical journal ads, funded medical meetings, and lectures about osteoporosis to make osteoporosis a feared disease and cause estrogen sales to increase again. The pharmaceutical industry did not care about the health of women, and instead chose to market a non-existent disease (osteoporosis is actually normal in the aging process and improves with exercise and nutrition) that caused the prescribing of estrogen therapy. This may have led to numerous cases of heart attacks, strokes, cancers, and Alzheimer's disease to women. This was while it was known in 1975 that estrogen therapy caused cancer. The pharmaceutical companies marketed a drug that was known to cause cancer in 1975.
"The next step was to 'educate' the public. In 1985, only 23 percent of women had heard of osteoporosis. But, according to US News and World Report, that changed quickly as the result of the efforts of Burson-Marsteller, the public relations firm hired by Wyeth-Ayerst. The campaign was successful at increasing public concern (some would say unnecessary fear), generating many articles in women's magazines and culminating in National Osteoporosis Week. The National Osteoporosis Foundation was started with drug company support in 1986. Doctors and patients came to fear that undiagnosed osteoporosis would lead to hip bones' suddenly snapping with minimal trauma, though in more than 20 years as a busy family doctor I never saw such a thing."
The pharmaceutical companies caused for estrogen to be seen as a good treatment to osteoporosis by helping create disinformation in ads, National Osteoporosis Week, and even the National Osteoporosis Foundation to educate women on the need to take estrogen. The pharmaceutical companies followed the disinformation about osteoporosis with additional lies that estrogen replacement therapy prevented heart attacks while actually causing heart attacks. The prescribing of estrogen increased to its 1975 high prescription levels in 1992 through lies and deceit and may be responsible for adverse health outcomes further described in randomized controlled studies in 2004.
"Coinciding with the public's "education" about osteoporosis was a 1985 report in NEJM about the positive effect of estrogen on the risk of heart disease. More than 30,000 postmenopausal women participating in the Nurse's Health Study, which followed the women for more than three years, showed that nurses who were currently using estrogen had 70 percent less risk of developing coronary heart disease than women who had not used hormones-a dramatic finding."- (page 63) [Another lying article published in a medical journal about estrogen therapy decreasing heart attack risk after sales had decreased.]
"By 1992, estrogen sales were topping their 1975 peak."
"One out of five postmenopausal women in the United States was taking hormones. The prestigious American College of Physicians issued guidelines to practicing physicians recommending that 'all women... should consider preventive hormone therapy,' and that 10 to 20 years of therapy were recommended for 'maximum benefit'. The American College of Obstetrics and Gynecology also recommended that all postmenopausal women, barring a medical contraindication like breast cancer, should take HRT for life. Bolstered by the recommendations of these professional organizations, estrogen use increased another 40 percent over the next three years. In 1995 estrogen once again became the most frequently prescribed brand-name drug in the United States. Perhaps the strongest evidence supporting routing HRT was presented in a 1997 article published in NEJM showing that 'mortality among women who use postmenopausal hormones is lower than among nonusers,' again overriding continuing concerns about the link to breast cancer."- (page 64)
After promoting estrogen as a treatment for osteoporosis and prevention of heart attacks, sales of estrogen increased. In 1992, one out of five women were taking estrogen replacement therapy even after studies in 1975 described that estrogen replacement therapy caused cancer. This was due to the advertisements placed in medical journals and lying medical journal articles published in 1979 and 1985. Not only the pharmaceutical companies created the Osteoporosis Foundation to promote estrogen as a treatment for osteoporosis, but they also told the American College of Physicians and the American College of Obstetrics and Gynecology to promote estrogen replacement therapy. In 1997, another lying article was published in the NEJM stating that women who took estrogen replacement therapy had lower mortality rates. It was not until the year 2000 that truthful journal articles described the risk of increased cancer incidence of women who took estrogen replacement therapy. Instead of helping women be healthier, estrogen replacement therapy caused increased mortality rates in postmenopausal women.
"It is amazing that before 1998, not one of the claims supporting the benefits of HRT had been substantiated by large randomized control trials."- (page 66)
"The Nurses' Health Study was the source of the data for the 1997 NEJM article showing a lower mortality rate among women taking HRT. This benefit of HRT lasted for up to five years after woman stopped taking the therapy, but after five years they had a 16 percent increase in their death rate compared with women who had never taken hormones. These contradictory findings deserved a lot more attention that they got at the time. Why did the nurses experience a lower death rate while they were taking hormones, and for five years after they stopped? And why did they go on to experience a significantly higher death rate than women who had never been on HRT?" -(page 66) [1997 NEJM article describing that estrogen replacement therapy lowered mortality rate for five years then increased mortality rate after five years.]
The reasoning to why some women had decreased mortality rates while taking estrogen replacement therapy was that the warning label of estrogen therapy described that women with heart disease, high blood pressure, and diabetes were not supposed to take estrogen therapy. This could mean that women who were healthier and had not started estrogen replacement therapy did not have chronic disease such as heart disease, high blood pressure, and diabetes.
"Dr. Elizabeth Barrett-Connor, a professor at the University of California, San Diego, points out that while the observational studies of HRT were going on, doctors across the country knew, from estrogen product labeling (included in the Physicians' Desk Reference), that woman with a history of heart disease, high blood pressure, or diabetes should not be treated with estrogen. This would contribute to the spurious findings in the observational studies that women who took hormones had less heart disease. Of course they did: Not only were they the type of women who were going to be healthier; the women taking hormones had already been screened to exclude those with heart disease, high blood pressure, and diabetes. The observational studies that found that estrogen decreased the risk of heart disease had not, according to Dr. Barrett-Connor, adequately adjusted for this." -(page 67)
After they stopped taking estrogen replacement therapy (after five years), they began to develop chronic disease and an increase incidence of mortality rates. This means that estrogen replacement therapy actually caused increased adverse health effects in healthy post-menopausal women taking estrogen replacement therapy for multiple years. However, these findings were not considered significant and estrogen kept being prescribed and sold in pharmacies in the 1990s. Also the studies were observational and not randomized controlled studies. (Observational studies are not the best type of studies because they can have significant bias compared to randomized controlled trials.) The observational studies may have been biased to make it appear that estrogen replacement therapy was beneficial to women (the women did not have chronic disease and were healthier), while not explaining the increased mortality rate after women stopped taking estrogen for multiple years (healthy women then had heart attacks and adverse heart disease).
In the 1990s, the pharmaceutical company Wyeth-Ayerst requested the FDA to approve estrogen for the prevention of heart disease in postmenopausal women. This was when there were only biased observational studies and no randomized controlled trials. The FDA did not approve estrogen treatment for the prevention of heart disease in postmenopausal women in the 1990s. This was because there were no randomized controlled trials demonstrating that estrogen therapy was effective at preventing heart disease. Pharmaceutical companies probably wanted to increase drug sales while disregarding the health risks such medication caused. Estrogen had not been completely studied and researched since the 1940s when the medication was approved for postmenopausal symptoms in postmenopausal women. (There is the need to be skeptical of untested and unresearched medication and "vaccines".)
"In 1998 the results of the first randomized controlled clinical trial of HRT were published. This manufacturer-sponsored study showed that despite significantly lowering LDL (bad) cholesterol and raising HDL (good) cholesterol, HRT increased women's risk of heart disease by 50 percent in the first year. And over the four years of the study, treatment with hormones provided no reduction in the risk of developing cardiovascular disease. In fact, this study showed that the overall death rate was not lower in the women who took hormones; it was slightly higher."
It was noted in 1998 and in the 2000s in medical journal articles that combined estrogen and progestin hormone replacement therapy caused worsening health effects such as heart attacks and strokes. It is questionable how estrogen therapy could have been promoted on medical journals, books, magazines, and commercials for so long while actually leading to cancer, heart attacks, strokes, and even dementia. Even in 2000 when a journal article published in JAMA showed an 8 percent increase in breast cancer in women every year that combined estrogen replacement therapy was taken, doctors continued to prescribe combined hormone replacement therapy. In 2001, despite a new journal article describing that combined estrogen replacement therapy causes cancer, estrogen was the third most prescribed medication in the US. That was after journal articles published in 1975, 1998, and 2000 showed significant adverse health effects in postmenopausal women taking combined estrogen replacement therapy. It was not until 2004 that estrogen and combined estrogen replacement therapy was repudiated as a treatment due to multiple scientific studies with randomized control trials. (There is the need for healthy skepticism with new medications and "vaccines".)
"The truth about HRT came out very slowly and was difficult for most doctors to accept. Even after the article appeared in JAMA in 2000 showing the 8 percent per year increase in the risk of breast cancer in women taking combined hormone therapy, most experts continued to recommend, and most doctors continued to prescribe, routine hormone replacement for postmenopausal women. In 2001, estrogen was still the third most frequently prescribed drug in the United States."- (page 68)
"[Article in July 2002] The study found a statistically significant increase (15 percent) in the overall frequency of adverse events in the women taking HRT compared with the women who took a placebo. This translated into about one adverse event for every 100 women who took hormones for five years. The data and safety monitoring board of the study determined that the increased frequency of complications in women who had taken HRT instead of a placebo had 'crossed the designated boundary... of a finding of overall harm,' and that it was no longer ethical to continue the study knowing that the women taking HRT were going to be harmed more than helped." -(page 69)
"The newspapers were full of articles about the government-sponsored Women's Health Initiative study, which had been specifically designed to determine whether routine HRT was beneficial for postmenopausal women. The 16,000 women in the study had been randomly assigned to take either (estrogen and progestin) HRT or placebo. The study had been scheduled to run through 2005, but the women received letters instructing them to stop taking the study medication because the risk (increase in breast cancer, heart attack, stroke, and blood clots) associated with combined HRT had been found to be significantly greater than the benefit (decrease in hip fractures and colon cancers). The study found a statistically significant increase (15 percent) in the overall frequency of adverse events in the women taking HRT compared with the women who took a placebo." -(page 69)
"In May 2003 more results from the Women's Health Initiative were published showing that combined HRT not only did not prevent Alzheimer's disease, but actually doubled the risk of developing dementia (primarily Alzheimer's disease) in women aged 65 and older, causing about 1 additional case of dementia for every 100 women treated with HRT for five years."
"[Another study with sample size of 1 million described increased cancer in the women taking combined estrogen replacement therapy.] The results showed that women who were currently taking hormones had a 66 percent higher chance of getting breast cancer (30 percent for those taking only estrogen, and 100 percent for those taking both estrogen and progestin) than the women who were not taking hormones. The women taking hormones were also significantly more likely to die of breast cancer than the women not taking hormones. To put the risk into perspective, the researchers calculated that there had been about 20,000 extra cases of breast cancer caused by HRT in the United Kingdom over the previous 10 years. Based on the difference of population size alone, even at the same rate of hormone use, there would have been an extra 94,000 cases of breast cancer in the United States in the previous 10 years as a result of women taking HRT. The total number of American women who developed breast cancer because of taking HRT was likely to be much higher than this, though, because women in the United States were about four times more likely to take HRT than women in the United Kingdom."- (page 70)
It was concluded through multiple research articles published in medical journals in the 2000s that women who took HRT for more than five years developed significant adverse health effects. Such adverse health effects included breast cancer, heart attack, strokes, dementia and Alzheimer's disease, blood clots, and possibly even other health complications including cardiac problems. It is stated that probably 94,000 women in the US were affected in ten years yet estrogen replacement therapy had been approved and prescribed since the 1940s. It is possible that a lot more women were affected due to the use of estrogen replacement therapy and combined replacement therapy. This describes how the pharmaceutical companies did not fully research the effects of estrogen therapy for postmenopausal women in 1940. It took 60 years later to prove that the increase of cancer cases in women was due to estrogen replacement therapy. There is the need to be skeptical of new medications and "vaccines".
"...Starting in the early 1980s, progestins where added to estrogen to reduce the risk of uterine cancer in women who had not had a hysterectomy. The risk of uterine cancer was reduced to near zero, but nobody evaluated the overall effect of adding progestin to routine HRT. The Million Women Study confirmed that taking estrogen without progestin caused 10 extra uterine cancers and 5 extra breast cancers, a total of 15 extra cancers per 1000 women over 10 years. Adding progestin did, in fact, eliminate the risk of uterine cancer but caused an extra 19 breast cancers per 1000 women over 10 years. In other words, the problem of uterine cancer was 'solved' by adding a drug that increased a woman's risk of getting other types of cancer."- (page 70)
Dr. Abramson described how progestin was added to estrogen replacement therapy in order to prevent uterine cancer in postmenopausal women. The treatment was approved yet was not completely researched. It was not until the 2000s that randomized controlled trials described that progestin did not in fact prevent cancer. Progestin prevented uterine cancer yet resulted in additional types of cancer. The pharmaceutical industry advertised combined estrogen therapy as a good treatment against cancer while actually causing different types of cancer. A study conducted in the 2000s described how progestin prevented 15 cases of uterine cancer while adding 19 cases of other types of cancer. This describes that estrogen and progestin combined hormone replacement therapy caused more cancers than estrogen therapy alone. This was after combined estrogen replacement therapy with progestin was approved in 1980. Ethical researchers told participants of the study to stop taking combined estrogen and progestin hormone replacement therapy because it caused cancer and other adverse health effects. It was not until the 2000s that the truth about estrogen and progestin replacement therapy was told and estrogen therapy was no longer favored as a treatment for menopausal symptoms.
"The estrogen-only part of the Women's Health Initiative Study was ended prematurely, in February 2004. Researchers concluded that after almost seven years, the women taking estrogen had more strokes and fewer broken hips than the women taking placebos. The most important finding was that there was no overall benefit to taking estrogen and that, therefore, it 'should not be recommended for chronic disease prevention in postmenopausal women.'"- (page 70)
The Women's Health Initiative Study was ended prematurely in February 2004 because the findings noted that estrogen therapy caused strokes to postmenopausal women. The researchers published their findings and allowed for the truth on estrogen replacement therapy to be known. The most interesting and significant finding was that taking estrogen replacement therapy showed no overall benefit and that it should not be recommended for chronic disease prevention in postmenopausal women. This was when estrogen replacement therapy was said to prevent postmenopausal symptoms in the 1940s without having significant adverse health effects. Estrogen was touted as helping combat osteoporosis and heart disease in the 1980s without randomized controlled trials. The treatment showed no overall benefit to health after randomized controlled trials were done in the 2000s. This describes the need to see science as a tool and not as a religion. Science can be used for good, yet can also be misutilized by unethical scientists. We should keep healthy skepticism against pseudo-science, lies, deceit, and bad medicine. The estrogen replacement therapy treatment was approved since the 1940s without knowing how the medication actually affected individuals until the 2000s.
"The important lessons from this chapter of American medical history will be lost if we simply attribute the debacle of routine HRT for healthy postmenopausal women to the vagaries of medical progess. Failure to understand how this mistake occurred commits us (doctors and patients alike) to being naïvely swept up by each new cycle of exaggerated claims about the effectiveness and safety of ever more expensive medical therapies- that is, until even newer 'medical knowledge' is produced that supports even costlier drugs. The fundamental lesson to be learned from the HRT debacle is that therapeutic decisions must be based on solid and unbiased scientific evidence. The trend, however, is going in exactly the opposite direction.'"- (page 71)
Dr. Abramson describes that there is a lesson to learn from the prescription of HRT since the 1940s that caused cancer, strokes, heart attacks, falls, and severe disease to women. We can learn that there is the need for healthy skepticism against newer "medication" and "vaccines" that may have been created in haste and attempted to lead to adverse health conditions. There is the need to study the effects of new "vaccines" and "medications" prior to deciding to take said newer "vaccinations" and "medications". There is the need to be skeptical of newer "medical knowledge" that may be false and written with the intention to lead to the taking of bad "medication" and "vaccines". We can persevere without covid "vaccines".
Increased Corruption in the 1980s in Medicine
It seems that the 1980s was when medicine began to be increasingly corrupted by financial ties with big pharma and researchers from medical journal articles (newer statins). Cost saving H.M.O.'s and great primary care physicians were under attack from the socialist media for preventing the rising cost of medical care while also preventing chronic disease in patients.
Great primary care and cost saving insurance H.M.O.'s were preventing medical costs from increasing substantially. Socialists despised that Americans were getting affordable quality care and began to state lies about how doctor visits were being rushed and that cost saving H.M.O.'s were not good. This led to increased medical costs with inflation of prices in the double digits. Quality of care also decreased because counseling the patient on preventative medicine was not remunerated economically while patient visit times were decreased. While lifestyle changes such as exercise, nutrition counseling, and smoking cessation have led to healthier lives without the need of newer, expensive, and brand name medication, patient counseling was not looked upon favorably by socialists (prevention of chronic diseases). This would describe why the patient doctor visit times were significantly decreased from an hour or thirty minutes prior to 1980s to fifteen minutes. (There was a psychiatrist that was let go for spending more than fifteen minutes per visit with her patients while being an amazing psychiatrist in the 2010s).
H.M.O. Plans and Managed Care Plans Caused Medical Costs to Decrease While Providing Great Medical Care
"The period of the late 1980s and early 1990s was the golden era of HMOs and managed care plans. They appeared to have solved the problem of rising health insurance costs..."-(page 78)
"Health care spending budgets that would have been unacceptable coming from the government were created by competing independent health plans, which employers choosing which to offer and employees usually (but not always) given a choice of several from which to choose... This market-based approach successfully tamed the double-digit percentage increases in health insurance premiums of the late 1980s and early 1990s, bringing the annual rate of increase down from a peak of 18 percent in 1989 to less than 2 percent by 1996."
Dr. Abramson described how competing HMO plans in the 1980s allowed for decreased medical costs and great quality of care. HMO insurance plans worked with employers to provide inexpensive health insurance plans while also providing great medical quality working with primary care physicians. Dr. Abramsondescribed how his work with HMO plans helped patients. Dr. Abramson described how preventative care allowed for better health outcomes, decreased hospitalizations and emergency room visits, and inexpensive routine check ups and vaccination visits that improved the health of communities in many cities in the United States. It is probable that because the insurance companies had to compete with other insurance companies through real capitalism, socialists were envious.
True competition allows for the better insurance companies to get more patients while expensive and ineffective insurance companies do not get customers. Because individuals were getting great healthcare at reduced costs in the 1980s, socialists began to slander and speak lies about great HMOs. A statistic stated that the annual rate of increase of health insurance premiums fell from 18 percent in 1989 to less than 2 percent in 1996. The cost of health insurance premiums fell 16 percent which may have caused envy from socialists. Since medical care costs had decreased signicantly with improved outcomes for patients and less hospitalizations with chronic disease, socialists attacked HMO cost saving plans. Socialists did not want healthier individuals and a decreased cost to great medical care. HMO plans began to be the major health care plans in the 1980s and 1990s until socialists slandered and lied about rushed doctor visits in the television (medical journal studies described how patient visits from HMO plans were not rushed and actually within average patient visit times. This is while socialists actually have caused for patient doctor visit times to decrease significantly from the early 1980s from an hour or half an hour to fifteen minutes.) Dr. Abramson described how it was probable that the pharmaceutical monopoly, medical equipment industries, and hospital industries may have had decreased financial revenues that led to negative coverage of HMO plans. Socialists probably did not care about improved health outcomes and actually cared about financial revenues. HMO plans were attacked and slandered because they prevented medical costs from increasing significantly each year.
Dr. Abramson Described How the Pharmaceutical Company Used False Advertisements to Cause Conflict Between the Doctor-Patient Relationship
"To exactly the same extent that a person is seduced by the false hopes and dreams offered by the medical industry's marketing efforts, the ability to trust his or her doctor, especially a primary care doctor, is eroded."- (page 80)
Dr. Abramson described how false advertisement led to the straining of the doctor patient relationship in the 1990s and 2000s. The pharmaceutical companies were probably looking to cause conflict between patients and physicians. Socialists do not like harmony and cooperation between patients and doctors. Socialists tried to decrease the amount of time of doctor visits since the 1980s for primary care doctor visits. Then advertisements tried to tell patients to tell their doctors to prescribe the medications on the advertisements. This was when some medications were not good and caused adverse health effects.
Dr. Abramson tried to reason and counsel patients on not believing the deceit of false advertisement especially with bad medications (Vioxx and Celebrex). Patients began demanding the medications on advertisement when they may have caused adverse health effects. Dr. Abramson decided to not prescribe such medications. Dr. Abramson described how false advertisement from pharmaceutical companies may have also contributed to the doctor patient relationship being affected in a negative manner. There were patients who were angry when their med requests were not granted and even demanded faulty medications. Dr. Abramson decided against prescribing bad medication and left practice in the 2000s.
Socialists Slandered HMOs and Managed Care Plans Because of Cost Savings
"When there were no more cost savings to be squeezed out of the fees paid to health care providers, HMOs and managed care companies had only one avenue open: they had to start to really 'manage' care, that is, control costs by eliminating unnecessary or wasteful care. (Of course, cutting down on advertising, executive salaries, and profits would have helped, too.)"- (page 81)
Dr. Abramson described how the insurance companies had lowered the cost of medical care and also allowed for the management of price inflation. This led to unnecessary and wasteful care to be eliminated. This meant that insurance companies and providers in primary care were helping contain costs of medical care. Medical care inflation was at 2% in the 1990s each year yet grew to almost 14% in 2003 each year once the slander and lies occurred against price saving insurance companies. Socialists saw that great insurance companies and great physicians were reducing the cost of medicine.
Because medical costs were decreased, socialists wanted more revenues and did not like that health care was inexpensive and effective. Since medicine was being practiced efficiently and effectively and reducing costs, socialists turned to lying and slander. Socialists instead of lowering executive salaries or decreasing advertisements decided to lie about insurance companies not being good for patients. 59% of people expressed negative feelings about HMOs and managed care in general after lying propaganda, yet 69% actually were satisfied by the medical care they were receiving by HMOs and managed care plans. It is probable that marxist socialists disdained great, low cost medical care.
Dr. Abramson Described How Increased Litigation in Medicine Caused Doctors to Leave Medicine and Increased the Cost of Medical Care
Dr. Abramson described how increased litigation in medicine caused for medical care to also increase in costs. Medical care prices were increasing due to the attacks of socialists against the HMOs and managed care plans. Socialists caused medical prices to increase substantially almost 14% in the late 1990s and early 2000s. Another cause of price increases was the increase of litigation in medical care. It is possible that the socialists were also responsible for increased medical prices due to increased litigation. The increase of litigation cases caused medical prices to increase because physicians ordered more tests to prevent a negative interaction with hostile patients that could have led to litigation. The cost of medical malpractice insurance also went up due to the increase use of litigation. This may have been due to socialists who wanted the doctor patient relationship to be adversarial instead of co-operative.
Even physicians left medical practice because of high medical malpractice insurance costs. The costs of medical malpractice insurance increased substantially in the 2000s. Primary care physicians left private practice and instead chose to change professions because of high medical malpractice costs and an adversarial doctor patient relationship in the 2000s. Physicians with multiple years of experience left private practice because of the litigation in medicine and high medical malpractice costs. Others practiced without insurance. This contributed to the high costs of medical care in the 2000s. The socialists and socialism are the reason that medicine in the US has substantially increased in pricing due to preventing HMOs and managed care plans from controlling price inflation, an adversarial doctor patient relationship fomented by pharmaceutical drug advertisement (telling patients to request newer, brand name medication) and 15 minute doctor patient visits, increased litigation in medicine, and increased costs of medical malpractice.
"Doctors are aware of the risk of a malpractice suit lurking in every patient visit. Three-fifths of doctors in the United States admit that they do more diagnostic testing than is necessary because of the threat of litigation. And why not? The risk of ordering an extra test is nil, but the threat of a lawsuit because of a test not ordered is ever present- even when the likelihood of serious disease is very low and reasonable professional judgment would say the test was not necessary. These extra tests can and often do set off a cascade effect, requiring even more tests to follow up on abnormal results, many of which then turn out to be normal. With the specter of malpractice looming, doctors feel justified in ordering almost any test, including tests in which they have a financial interest."- (page 84)
Dr. Abramson described how medical practice had changed due to the adversarial doctor patient relationship. Doctors ordered more tests, medication, and lab work because of the need to prevent a negative patient interaction. We learn that while some lab tests were unnecessary, they were ordered to prevent the threat of litigation. We learn that because more labwork was being ordered, this led to increases of medical care spending. More tests, imaging, and lab work resulted in additional tests being ordered.
This may also explain why medical care has increased in pricing since the 2000s. We have seen how socialists have attempted to prevent cost controls in medical care since the 1990s and also how decreased patient doctor visit times have led to an adversarial relationship between doctors and patients. We learn that the ordering of unnecessary labwork, imaging, and medications have led to increased costs of medicine. This also may be attributable to socialists preventing cost controls in medicine and causing decreased co-operation between doctors and patients. All of this has led to increased costs in medicine since the late 1990s and early 2000s.
Doctors Left Medical Practice Due to the Increasing Cost of Medical Malpractice Insurance
"The rising cost of malpractice insurance is causing a rebellion among doctors forced to pay the price for our litigious culture regardless of their own track record and commitment to quality care. Some, caught between the ever-present fears of litigation and the mounting costs of insurance, are shielding their assets and practicing without insurance, while others are leaving the practice of medicine altogether."- (page 84)
Dr. Abramson described how physicians were leaving the practice of medicine because of the high cost of medical malpractice insurance. We learned that medical care prices had increased in the late 1990s and early 2000s due to socialists going against the HMOs and managed care plans that decreased price inflation and contained costs. The litigious medical culture led to an increase of litigation and also increase in the price of medical malpractice insurance. The cost of medical malpractice increased and some physicians decided to leave medical practice than pay rising costs and also have to practice under adversarial and negative conditions.
Other physicians practiced without malpractice insurance. This describes how medical care prices have increased due to several factors yet the understanding is that socialism has attempted to prevent co-operation between doctors and patients and also caused increases of medical care pricing. There were physicians in the 2000s who like Dr. Abramson decided to leave medical practice and instead changed professions or wrote about the manner that medicine was being affected negatively. There were also other physicians on medical blogs that described that medicine was changing negatively and decided to leave medical practice instead. Doctors have described how the litigation culture of medicine has caused negativity and an adversarial doctor patient relationship instead of a positive and co-operative doctor patient relationship. There are stories of a few not so good doctors who practiced medicine and harmed patients and went through litigation, yet there are also stories of good physicians who went through litigation not because they had been negligent but because of a negative outcome that was not based on medical negligence (described in Philip Howards book). Medical practice had changed and physicians preferred to leave practice that practice medicine. This describes how there were physicians that preferred to practice with autonomy than to be restricted in their manner of practicing medicine. Insurances also told doctors what to order and how to practice which also caused physicians to leave the practice of medicine after the 1980s. Doctors have written how medicine has changed since the 1980s.
Dr. Abramson Described How the Pharmaceutical Companies Were Affecting the FDA
"The drug companies agreed to pay a $300,000 fee for each new drug application; in return, the FDA's Center for Drug Evaluation and Research promised to adhere to a speedier timetable for the new drug approval process. According to a 2002 GAO report, a little more than half the cost of reviewing new drug applications was funded by user fees from the drug industry."- (page 85)
Dr. Abramson described how the pharmaceutical monopolies were attempting to affect the FDA regulators by fast tracking approval of newer, more expensive, and brand name medications. The pharmaceutical monopoly decided to invest money into the drug approval process. It took close to twenty months to approve new medications for review and the pharmaceutical industry paid money to have the time shortened to six months. The pharmaceutical companies paid close to $300,000 per new medication to have the medication approved for review. This caused the pharmaceutical companies to use their funds to fast track the approval of newer medication and also have greater influence in the drug approval process. The pharmaceutical companies were essentially obtaining more influence to tell regulators that newer medications had to be approved despite the decrease of time to review the medication. This led to newer medications being approved in less time that were not completely studied for adverse effects.
This probably began happening in the early 1990s or early 2000s when pharmaceutical companies began to gain more influence. Dr. Abramson describes how this affected negatively the FDA since the FDA was approving newer medications that had less time to be reviewed. We learned that Dr. Gueriguian was on a review board for a new diabetes medication, when he was dismissed from the review board for denying the approval of the new drug that could have caused adverse health effects. Dr. Gueriguian had 19 years in the FDA reviewer position being a physician and was still dismissed from his position for preferring to safeguard patients by denying the newer medication. Despite his integrity and years of experience being a physician and FDA reviewer, the FDA dismissed him from his position and allowed the newer medication to be approved. The newer medication was less effective and safe than generic medications yet was approved. There were several newer medications that also caused adverse health effects and were approved.
"In the four years following the enactment of the Prescription Drug User Fee Act, the median length of time the FDA took to decide on priority new-drug applications dropped from 20 months down to six months. At the same time, the average number of new drugs approved doubled. Funding by drug companies may have seemed like a good idea for the cash-strapped FDA, but what about protecting the consumer from the drug companies' influence? How unbiased can the Center for Drug Evaluation and Research be when half its budget comes from the drug companies themselves?"- (page 86)
Dr. Abramson Described How the Pharmaceutical Companies Were Affecting the FDA Negatively Leading to Medications Being Approved in Less Time
Socialists removed the publication on the literary review of Overdo$ed America on 03/17/2026 after publishing about how the pharmaceutical monopolies gained more control over the approval process of newer and more expensive brand name medication. Reviewers at the FDA said that medications were being approved with too little time. This was when the approval for new reviews was changed from twenty months to six months and reviewers stated that newer medications were being approved that should not have been approved.
"An anonymous survey done by Public Citizen in 1998 revealed that the FDA review officers felt that standards had declined as pressure to approve new drugs increased. The FDA medical officers who responded to the survey identified 27 new drugs that had been approved within the previous three years that they felt should not have been."
It appears that the pharmaceutical companies had decided to gain greater control over the research and approval process of medications done by the FDA. We learn that this may have led to the approval of newer and more expensive brand name medication that was not benefecial and may have caused adverse health effects since the late 1990s.
"A similar report on CDER by the inspector general of the U.S. Department of Health and Human Services, published in March 2003, found that 58 percent of the medical officers said that the six months allotted for review of priority drugs is not adequate, and that one-third of respondents did not feel comfortable expressing their differing opinions."- (page 86)
Medical officers described that they did not feel comfortable expressing their differing opinions. We learn that there were many medications that were approved that were either not better than the generics or that even caused severe health effects. This describes how new medication research had been compromised by financial ties between the monopoly pharmaceutical companies and new research. FDA review officers described how the approval for the review of new medication, that lasted six months compared to twenty months, was not adequate.This may have led to newer and brand name medications being approved in haste while they may not have been better than generics and may have also caused adverse health effects. (And may explain covid vaccines).
Dr. Abramson described how once pharmaceutical companies began to influence the research on newer medications, FDA reviewers described that the standards for approving new medications had declined. This was because newer medications were being approved in shorter time. FDA medical officers responded to a survey that stated that 27 new drugs had been approved within three years when they felt that the newer medication should not have been approved. This means that in the late 1990s medications were being approved that were not supposed to be approved by the FDA since they caused adverse health effects. This describes how the pharmaceutical monopoly was causing for newer medications to be approved while there were adverse health effects from the newer medications. This describes how the FDA was approving newer medication that was not helpful and did not help individuals. The newer medication could have caused severe health problems in patients. Reviewers also felt that the amount of time to review the newer medication was not enough.
The FDA reviewers even stated in a report that a third did not feel comfortable expressing their differing opinions. This means that the time to review medications was not optimal leading to the approval of possibly dangerous and bad medications while also review officers were not comfortable having opposing opinions. This would also describe how the pharmaceutical monopoly began to obtain more control over the research of newer medication. This describes how the pharmaceutical companies began to attempt to gain more control over the approval of newer, more expensive, and brand name medications. This led to the approval of newer and brand name medications that were later withdrawn from the pharmacies due to adverse health effects.
The FDA Withdrew Pharmaceutical Drugs That Were Approved in Haste Between 1997 and 2000
"The most dangerous consequences of these changes was that the number of drugs approved by the FDA but later withdrawn from the market for safety reasons increased from 1.6 percent of drugs approved between 1993 and 1996 to 5.3 percent between 1997 and 2000."
Dr. Abramson described how the pharmaceutical companies were approving newer and brand name medication in shorter amounts of time than in the past. We learn that because the pharmaceutical companies began to pay money to fast track newer and brand name medication for approval, the amount of time required to approve a medication decreased substantially. This led to newer medication being approved that later was withdrawn because of serious side effects. The number of medications that were withdrawn was 1.6 percent between 1993 and 1996 but increased to 5.3 percent between 1997 and 2000. The medications withdrawn were known to cause severe health effects including death. The medications that were withdrawn were noted to have caused more than a thousand deaths although it is unknown if there were more individuals who had severe health problems and disease from taking newer medications that were approved in shorter time.
This describes how even in the 1990s there were newer and more expensive medication that were approved and caused severe health effects. A specific drug, Rezulin, caused liver toxicity in patients that may have led to severe health outcomes. This describes how newer medications were approved in haste and later withdrawn from the pharmacies for their toxic effects on a patient's health. This describes how there is the need to be skeptical about new medications and "vaccines" that are approved in haste. The newer and more expensive medications need 8-10 years of research to know if they are helpful and beneficial or if they cause severe health effects. We can persevere making sure that we have healthy skepticism about medications and "vaccines" that did not go through the four stages of clinical research development and 8-10 years of review.
"The Los Angeles Times reported that these drugs were suspected of causing more than 1000 deaths (though the number of deaths could actually be much higher because reporting of adverse drug events to the FDA is voluntary). Even though none of these seven drugs was lifesaving, according to the Los Angeles Times, 'the FDA approved each of those drugs while disregarding danger signs or blunt warnings from its own specialists.' All told, 22 million Americans, one out of every 10 adults, had taken a drug that was later withdrawn from the market between 1997 and 2000."- (page 86)
Dr. Abramson Described How Rezulin Was a Faulty Medication
"The blood sugar-lowering diabetes drug Rezulin is one of the drugs that were approved in haste by the FDA- and later withdrawn, but much too late for many Americans. The details of the story were first presented in 2000 in a Pulitzer Prize-winning series of investigative reports by David Willman of the Los Angeles Times."
"The medical officer evaluating the new drug application, Dr. John L. Gueriguian, was a 19-year veteran of the FDA. His review recommended that Rezulin not be approved: the drug appeared to offer no significant advantage over other diabetes drugs already on the market, and it had a worrisome tendency to cause inflammation of the liver."
"However, reports of fatal liver toxicity due to Rezulin soon started to appear. Notwithstanding reports of deaths in the United States as well as in Japan, and the withdrawal of the drug from the United Kingdom because of liver toxicity in December 1997, Dr. Eastman and his colleagues decided to continue treating volunteers in the Diabetes Prevention Program study with Rezulin. Only after Audrey LaRue, a 55-year-old high school teacher, died of liver failure in May 1998 did Rezulin stop being given to the volunteers in the study. Warner-Lambert maintained that Rezulin was not responsible for the liver failure that led to her death."- (page 87)
Dr. Abramson described how in 1997 the new brand name drug Rezulin was being tested in a study to treat diabetes. The drug was noted to cause severe liver toxicity by an FDA physician with 19 years experience. Despite his warnings of not approving the drug due to liver toxicity, the FDA decided to remove him from his position at the review board because he denied the approval of the new drug. The new drug caused health problems yet was approved for treatment of diabetes. Once it was noted in 1997 that Rezulin was causing severe health effects, the drug began to be recalled. Dr. Eastman kept treating volunteers in the Diabetes Prevention Program with Rezulin until 1998 due to a death from Rezulin medication. The researchers decided to remove the use of Rezulin in the study in 1998 noting the negative health outcome.
The pharmaceutical company decided to state that the new medication did not cause the negative health outcome. This describes how the pharmaceutical companies cared more about profits than the health of research participants or patients. The new brand name drug was not withdrawn until 2000 describing how faulty medications were approved in 1997 and withdrawn after causing serious adverse health effects.
Why Medical Care Quality in the US Has Decreased Despite Higher Costs?
Dr. Abramson described that since 2004 the cost of medical care in the United States has increased significantly while the quality has not improved. It has been noted that the quality of care in the US has decreased because of big pharma's influence on primary care, changes in the doctor-patient relationship (decrease of time in doctor visits), and also because of the commercialization of medicine (despite no universal healthcare). On the measure of performance on the level of health, the US was number 72 in the world.
"Despite the poor performance of the American health care system, our healthcare costs are simply staggering. In 2004, health expenditures in the United States are projected to exceed $6,100 for every man, woman, and child. How does this compare with other countries? The United States spends more than twice as much per person on health care as the other industrialized nations. Even taking into account our higher per person gross domestic product, the United States spends 42 percent more on healthcare per person than would be expected, given spending in healthcare in the other OECD nations. The excess spending on health care in the United States is like a yearly tax of more than $1,800 on every American citizen. (And still the United States is the only industrialized country that does not provide universal health insurance, leaving more than 43 million Americans uninsured.)"- (page 46)
The United States has increased spending in health care, yet the quality of the medical care has decreased according to surveys and statistics. Most of this is due to many factors dealing with envy and socialism. It is known that primary care medicine is vital and indispensible for a nation's good health. Nations with good and excellent health care have multiple primary care physicians. Almost 50% of physicians in countries with excellent healthcare are primary care physicians and not specialists (compared to less than 30% in the US). In the United States, there are more specialists than primary care doctors since socialist medical mentality has disdained primary care for its long hours, decreased pay, and the manner that primary care actually allows for preventative medicine to be practiced. Preventative medicine prevents chronic disease from becoming worse disease. (Specialists are still needed in countries with good healthcare, yet primary care physicians are actually given importance, respect, and are seen with admiration for preventing chronic disease through the patient-doctor visit.) The socialists in the US since the 1980s have attempted to portray primary care as "insignificant", low paying, too much work, and inane while giving positive support of other specialties. Younger doctors since the 1980s were discouraged from being primary care physicians while being led to high paying specialties creating a limited amount of primary care physicians. Less primary care physicians means less preventative care. Less preventative care means more chronic diseases. More chronic diseases means more spending on health care.) Do socialists prefer instructing preventative care or allowing for less preventative care and more chronic disease? Socialists prefer chronic disease and disdain preventative care. That is why primary care has been disdained by socialists in the US since the 1980s.
There is also the manner that medicine is a practice that has increased litigation also since the 1980s. This is because socialists want patients and doctors to be hostile to each other instead of being partners in the improvement of health. Socialists wanted patients and doctors to be in conflict instead of working together. This has been seen in how litigation increased in the medical field causing doctors to order unnecessary testing based on patient requests or in order to prevent a negative patient visit to prevent litigation (this makes sense of why unnecessary tests and treatments have caused for medicine to increase in costs. Can not blame the physicians for this and rather can blame socialism (monopoly "capitalism"). The socialists probably caused for litigation to be seen in medicine after causing the decreased patient visit times from 30 minute to an hour visits prior to 1980 to 15 minutes.) Instead of only ordering needed tests and treatment, doctors had to order unnecessary tests in order to prevent litigation rather than not order tests. Litigation in medicine is from socialism. (Yet at the same time in 2019, pharmaceutical companies did not want individuals to litigate against pharmacutical companies and faulty covid experimental "vaccines".)
Another cause of increased spending in medicine while causing decreased quality of care has been the manner that pharmaceutical medications have been seen as the solution to everything. Instead, preventative care is more important to preventing disease. Expensive, newer, and brand name medication has caused increased costs in medical care. Part of the high cost of medicine is due to expensive medication that is not better than generics. Medicare also helped pharmaceutical companies prescribe newer and more expensive medication instead of generics in the 2000s. Dr. Abramson described how some of the dangerous medications (Pravachol, Lipitor, Vioxx, Celebrex, Actonel, and Fosamax) were among the most prescribed to medicare recipients instead of generic medication. Even tax payers had to pitch in to pay for expensive bad meds in the 2000s. The newer and more expensive bad medications may have also caused strokes, heart attacks, osteoporosis, and falls that also increased medical costs while not increasing quality of care. This describes why medical care has decreased in quality while increasing in cost.
This is also with the understanding that there is no universal healthcare in the US. Instead there are faulty covid experimental "vaccines". Not the best of times.
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