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Title : Shocking Secrets about Clinical Trials: 2,061 Trial-Related Deaths. Yet Only 22 Were Compensated
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Shocking Secrets about Clinical Trials: 2,061 Trial-Related Deaths. Yet Only 22 Were Compensated

Clinical research in humans is considered as an essential component of the research and drug development.

is only after successfully being tested in people who are supposed to drugs to be released, but how can it be ethical to use people as guinea pigs in drug trials without accurate data on the consequences they may face?

Typically, such tests are carried out only after there evidence from animal experiments that drugs are "safe and effective" ... but this is far from a foolproof method to assess safety.

Unfortunately, many die or suffer serious injury after participating in drug trials, and worse, only a fraction increasingly compensated.

Thousands of people in India died during drug trials

India is a popular spot for clinical drug trials; the pool is huge and voluntary for drug companies, the cost is low. In many cases, pharmaceutical companies persuade poor members, illiterate, uneducated or tribal to be his "willing" participants. But what is the price of trial participants entering the test?

activist medical rights Anand Rai filed a right to information query to obtain data on deaths related to drugs trial-and events adverse drug Controller General of India. It was revealed that more than 2,000 people in India died as a result of serious adverse events (SAEs) occurring during drug trials from 2008-2011.

Only 22 of cases, a 1 percent received any compensation - which was a paltry average of about $ 4,800 per family. Pharmaceutical companies often blame the deaths occurring during tests on pre-existing medical condition of a person. But experts say the weak regulations that allow clinical trials are carried out virtually anywhere "medical supervision" is present is to blame (and drug companies often pay doctors large sums of money to carry out . this type of test)

as the Hindu reported

"the reason for such a small number of cases receiving compensation is simple: companies pharmaceutical conducting clinical trials pay compensation only in cases where it is determined that the death was caused as a result of the tests, not only during the trial.

"But it is the companies who decide whether a death was caused due to testing or not. So there is a conflict of interest there as companies want to pay compensation in the smallest possible number of cases, "says Dr. Rai, who founded the Association of Victims of Madhya Pradesh Clinical test.

" we believe that all cases of deaths related SAE should receive compensation. We filed a petition before the Supreme Court in the matter, "says Dr. Rai."

"desperately poor recruits" enroll despite possible risks

What could drive someone to voluntarily enroll in a trial of a drug of questionable safety? Poverty, of course. Drug and Cosmetic Act of India Acts says that money can not be used to be attracted to people in the trials, though a small compensation is allowed.

However, according to a report by Dateline NBC, participants can actually earn up to $ 400 by study ; in an area where the average worker earns 50 cents a day, and many are unemployed, this is a strong incentive. Not surprisingly, many of these volunteers were enrolled in multiple studies at once or join another study before the period of "wash", designed to allow your body to clean drug test has passed. This not only increases their health risks, which commits the results of the study.

And while pharmaceutical companies have some security measures to prevent these events, such as the use of a fingerprint reader to enroll volunteers, an insider India to NBC that "if companies desperately need the items, will overlook these things."

Furthermore, there is little participation by the government of India to investigate the deaths related to the study or injury, or reports of violations, such as not receiving the proper consent of participants or unauthorized trials in children and patients with mental disabilities. And although many of these tests are carried out by Western pharmaceutical companies such as Pfizer and AstraZeneca, seeking approval of drugs the Food and Drug Administration US (FDA), the FDA has no authority to access confidential records under international law.

Study Gardasil Detained in India After 6 children died

In 2010, the Indian government put a halt to trials of the HPV vaccines (HPV) Gardasil. This occurred due to an investigation led by civil society, which highlighted serious ethical violations for clinical research and the rights of informed study participants or their legal guardians consent - and followed reports that six of the young participants had killed and more than 120 girls suffered serious adverse reactions, including:

• stomach disorders
• epilepsy
• headaches
• menarche early

Unfortunately, the reports suggested that the deaths occurred either because the girls committed suicide (by poisoning) or drowned - although parental reports to the contrary ; This is, unfortunately, just one example of the deaths during drug trials.

Earlier this year, the Argentina Federation of Health Professionals accused of misleading GlaxoSmithKline participants and pressuring poor families, disadvantaged in enrolling their children in clinical trials of the vaccine experimental pediatric Synflorix pneumonia .

Fourteen of the participants in the trial of the experimental vaccine children died.

the Nuremberg Code provides ethical guidelines for doctors to protect human test subjects in scientific experiments injury, disability or death investigators. The first principle of the Nuremberg Code - that doctors must obtain voluntary informed consent person about to be experienced - seems to be often overlooked, especially when it comes to clinical trials of experimental vaccines.

for example, according to authorities in Nigeria, Pfizer illegally tested a unapproved drug on children with brain infections in a hospital in 1996. Eleven children died and dozens were defused before it was exposed illegal activity.

time and again we see how the major pharmaceutical companies plan to recruit people who do not have complete information about vaccines or experimental drugs and the risks effectively become the human guinea pigs in experiments scientists. In fact, it almost seems to be more rather than the exception rule.

Outrageously an article published by Mentor Virtual of the American Medical Association is concerned that the current enrollment in trials US vaccine is extremely low . As a solution, the authors propose a federal law requiring all Americans to "opt-out" if they do not want to participate in vaccine trials or let their children be used in vaccine trials ...

drug trials plagued with "ethical dilemmas" Even in the US

India, in particular, has seen an increase in clinical pharmaceutical studies, questionable practices and employees are increasingly evident. But there are problems in the development of other developed countries, as well as in the United States.

In a study recently published in The New England Journal of Medicine essay, the authors note "critical weaknesses" in the national system to ensure the safety of the drug that not only let dangerous drugs like Avandia, Vioxx and Celebrex reach the market, but volunteers are also part of subsequent clinical trials to marketing without revealing the true extent of the risks.

When signing up for a trial of the drug after marketing, patients should understand that they can be exposed to an exceptionally dangerous drug - which normally is testing due to suspicions that may cause serious side effects. However, volunteers are typically not say why exactly you are performing the test.

The debate was heated in 2010 when the FDA restricted the use of the diabetes drug Avandia in subsequent trials to marketing showed patients using had an increased risk of heart attack and stroke -. a risk that the drug's manufacturer, GlaxoSmithKline, knew but did not tell patients

you are your own best advocate

the main message here is that even if a drug or treatment is "backed by science" or through clinical trials, this in no way guaranteed to be safe or effective. Similarly, if an alternative treatment has not been published in a medical journal, that does not mean it is unsafe or ineffective.

must use all the resources available to you, including your own common sense and reason, expert advice on natural medicine "to determine what medical treatment or approach will be best for you in any given situation I encourage you to remain skeptical but open -. including anything I say, you have to realize that it is responsible for your health and your family, not me, and certainly not the pharmaceutical companies trying to sell their products and convince you to take dangerous suppressors "symptom" disguised as science-based solutions.

is always wise try to better understand and address the real problem behind your health, instead of covering it with a Band-Aid drug. There are hundreds of thousands of pages of free information on this site designed to help you achieve that goal, and site search is ready to help you find the information that can shed some light on your health questions

by Dr. Mercola

Source:. mercola.com

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