new-logo25kohlsGary G. Kohls, MD

 

 

Over the years, I have formally taught my patients (as well as many participants in my lectures and seminars) about the un-advertised dangers of psychiatric medications – especially the long-term brain alterations and drug-dependencies that drug companies don’t test for before the FDA grants them marketing approval.

Since my retirement from my holistic, non-drug, mental healthcare practice, I have continued to issue written warnings about the multitude of serious, sometimes even lethal, albeit unintended (and untested for), adverse consequences of taking psychiatric drugs, especially over the long-term.

My warnings have usually been directed at my fellow healthcare practitioners, nurses, social workers, clergypersons, journalists, legislators, various industry groups, and the public in general, but there seems to have been no audible response from most of them concerning the dangers to the very people that these professions are supposed to be caring for.

The information that I have relied on to treat my (subtly or overtly) drug-intoxicated patients came from many sources. Among those sources were 1) various peer-reviewed (albeit obscure) neuroscience journals, 2) whistle-blowing (and therefore often ostracized) psychiatrists, physicians, neuroscientists and medical journalists, and 3) my own extensive research into the basic neuroscience literature (which I had never had time to read as a busy family practitioner – barely having time to read the drug-industry-approved and subsidized mainstream medical journals).

In my Duty to Warn columns, I have often written about my concerns for the victims of brain-altering drugs, who, in my professional experience, had become dependent on (addicted to) any number of neurotoxic and psychotoxic drugs that Big Pharma had falsely assured me were not addictive.

Ignoring the essential reality about drug dependency and toxicity has caused many psychiatric patients (and their prescribing practitioners) to miss the fact that when the patients ran out of their meds or attempted to quit the drugs that were sickening them, they often became ill with entirely new symptoms that were the reasons for starting the drugs. (Quitting a psych drug can be as medically hazardous as starting one.)

The withdrawal symptoms that my patients experienced were always different from the symptoms that prompted the initial prescriptions, and they had been uniformly mis-diagnosed as a “recurrence” of the so-called “mental illness”, and therefore the offending drugs had usually been restarted, usually at higher doses, often with additional new drugs being added to counteract the new withdrawal symptoms.

I have also tried to alert the public, especially the media, about the epidemic of mass shootings that have been perpetrated by shooters whose brains, cognition and behaviors had been altered by psychiatric drugs. The mainstream media, not wanting to implicate the drug companies that advertise with them, prefer to demonize the folks that had been made “mentally ill” by the toxic culture rather than to the toxic drugs that can cause normal stressed-out, sleep-deprived and brain-malnourished folks, including the scores of male adolescent school shooters, to act like they are mentally ill.

Nevertheless, even medical journalists, especially those writing for major media outlets, have refused to even hint at (or been forbidden to write about by their editors or publishers) the strong connections between psychiatric drug intoxication and the epidemic of mass murder/suicide that continue to (intentionally?) confuse everybody. And so the shootings continue and the drug-marketers, drug-prescribers and other drug-profiteers continue risking the public health; and they continue getting off scot-free, never being charged as accomplices to the crimes. Just witness the pathetic failure of the defense attorneys for the Zoloft-intoxicated (150 mg per day!!) and Klonopin-intoxicated Batman Shooter from mounting a logical defense that could easily have convinced any intelligent jury to declare James Holmes of being “guilty” but temporarily insane because of his psychiatric drug-intoxication.

I attach below an important document from the Citizens Commission for Human Rights (www.cchrint.org) that contains vitally important information for readers who may be justifiably concerned about the potential consequences of the long-term use of psych drugs by their loved ones. It is highly likely that many psychiatrists, family practitioners, internists, pediatricians and nurse practitioners are not yet fully aware of the prescription drug dangers listed below and therefore will not have issued adequate warnings about the drugs.

Even though the incidence of the most dramatic dangers of psych drug-induced aberrant behaviors (including murder, suicide, psychotic behavior, criminality, aggression) are not necessarily frequent, the less serious adverse effects of drug-induced “mental illnesses” are common.

Those common adverse effects of psych drugs that can mimic mental illnesses are listed below and include increased depression, increased anxiety, mania, akathisia, suicidality, agitation, lack of empathy, fatigue and tiredness, insomnia (or somnolence), memory loss, diabetes, weight gain (or weight loss), loss of IQ points, etc.

If the readers of this warning recognize the validity of the statements below (or in the various Duty to Warn columns I have written in the past – please draw the attention of prescribing practitioners to the information. Perhaps he or she will become more aware of the serious dangers of the chronic use of brain-altering drugs. Perhaps such actions will prevent the next suicide attempt or the next mass shooting incident. (Warning: Patients who are already on such drugs are warned to not suddenly quit their drugs cold-turkey and to consult with their prescribing physicians to discuss the information above and below. There are compassionate practitioners who understand the neuroscience of addiction, drug withdrawal and brain nutrition that might be willing to help patients get through the inevitable withdrawal symptoms that commonly occur during what is ideally a slow tapering process.

Here is the article which is excerpted, with permission, from CCHR’s website. It details 22 regulatory warnings about drug dangers from various agencies around the world. We physicians were supposed to officially receive such warnings. (The documentation of each of the warnings can be found at the CCHR website or at the Duluth Reader website at (http://duluthreader.com/articles/categories/200_Duty_to_Warn)

Psychiatric Drugs—

Regulatory Warnings on Violence, Mania, Psychosis, Homicide

Fact: Despite 22 international drug regulatory warnings on psychiatric drugs citing effects of mania, hostility, violence and even homicidal ideation, and dozens of high profile shootings/killings tied to psychiatric drug use, there has yet to be a federal investigation on the link between psychiatric drugs and acts of senseless violence.

FACT: Between 2004 and 2012, there have been 14,773 reports to the U.S. FDA’s MedWatch system on psychiatric drugs causing violent side effects including: 1,531 cases of homicidal ideation/homicide, 3,287 cases of mania & 8,219 cases of aggression. Note: The FDA estimates that less than 1% of all serious events are ever reported to it, so the actual number of side effects occurring are most certainly higher.

School-related acts of violence aren’t the only cases commonly found to be under the influence of psychiatric drugs. There are 18 other recent acts of senseless violence committed by individuals taking or withdrawing from psychiatric drugs resulting in an additional 76 dead and 61 wounded.

To read all drug regulatory agency warnings & studies on psychiatric drugs, visit CCHR’s Psychiatric Drug Side Effects Search Engine.

The Drug Regulatory Agency Warnings on Psychiatric drugs and Violence

United States, November 2005:  The FDA’s Safety Information and Adverse Event Reporting Program reported “homicidal ideation“ as an adverse event of Pfizer’s Effexor ER (extended release).

(Source: “Detailed View: Safety Labeling Changes Approved By FDA Center for Drug Evaluation and Research (CDER) — November 2005,” FDA MedWatch, November 2005.)

United States, March 22, 2004:  The FDA Public Health Advisory was issued, on antidepressants stating: “Anxiety, agitation, panic attacks, insomnia, irritability, hostility, impulsivity, akathisia [severe restlessness], hypomania [abnormal excitement, mild mania] and mania [psychosis characterized by exalted feelings, delusions of grandeur and overproduction of ideas], have been reported in adult and pediatric patients being treated with antidepressants.”

(Source: “WORSENING DEPRESSION AND SUICIDALITY IN PATIENTS BEING TREATED WITH ANTIDEPRESSANT MEDICATIONS,” FDA Public Health Advisory, 22 Mar. 2004.)

United States, October 1995:  The U.S. Drug Enforcement Administration (DEA) said Novartis’s Ritalin use could lead to addiction and that “psychotic episodes, violent behavior and bizarre mannerisms had been reported” with its abuse.

(Source: “Methylphenidate,” U.S. Drug Enforcement Administration (DEA), October 1995. McNeil’s Concerta and other methylphenidate (Novartis’s Ritalin) products (stimulants) to include, “psychiatric events such as visual hallucinations, suicidal ideation, psychotic behavior, as well as aggression or violent behavior.” The FDA announced its intention to also investigate possible cardiac concerns with these drugs.

(Source: “Statement on Concerta and Methylphenidate for the June 30 PAC”, Food and Drug Administration (FDA), June 2005.)

Canada, February 2006:  Health Canada approved a new warning label for GlaxoSmithKline’s Paxil that read, in part: “A small number of patients taking drugs of this type may feel worse instead of better. For example, they may experience unusual feelings of agitation, hostility or anxiety, or have impulsive or disturbing thoughts, such as thoughts of self-harm or harm to others.  Health Canada required Paxil’s product information to detail a list of “rare” side effects, affecting fewer than one in 1,000 patients. These include delusions, hostility, psychosis, and psychotic depression.

(Source: Kate Jaimet, “’I’ve learned a lesson in the worst way possible’: What drove a loving father to kill his son?” Ottawa Citizen, 27 Aug. 2006.)

Canada, June 03, 2004:  Health Canada issued an advisory to the public that stated that stronger warnings have been placed on antidepressants. These warnings indicate that people taking these drugs at any age are at greater risk of behavioral or emotional changes including self-harm or harm to others. The advisory said, “A small number of patients taking drugs of this type may feel worse instead of better…. For example, they may experience unusual feelings of agitation, hostility or anxiety, or have impulsive or disturbing thoughts that could involve self-harm or harm to others.”

(Source: Jirina Vlk, “Health Canada advises Canadians of stronger warnings for SSRIs and other newer anti-depressants,” Health Canada, 2004-31, June 3, 2004.)

Japan, May 2009:  The Japanese Ministry of Health, Labor and Welfare investigated news reports of antidepressant users “who developed increased feelings of hostility or anxiety, and have even committed sudden acts of violence against others.” After its investigation, the Ministry decided to revise the label warnings on newer antidepressants stating, “There are cases where we cannot rule out a causal relationship [of hostility, anxiety, and sudden acts of violence] with the medication.”

(Source: “Japan Revises SSRI Warnings–Hostility, Violence,” Medical News Today, May 28, 2009.)

European Union, August 19, 2005:  The Commission of the European Communities, representing 25 European countries, endorsed and issued the strongest warning yet against child antidepressant use as recommended by Europe’s Committee for Medicinal Products for Human Use (CHMP). Clinical trials had shown that the drugs caused suicidal behavior including suicide attempts and suicidal ideation, aggression, hostility (predominantly aggression, oppositional behavior and anger) and/or related behaviors.

(Source: Commission of the European Communities Commission Decision concerning the placement on the market, under Article 21 of the Directive 2001/83/EC of the European Parliament and of the Council, Brussels 19-VIII-2005, C (2205) 3256.)

Australia, February 2009:  The Australian Therapeutic Goods Administration reported that a boxed warning (the strongest warning) was placed onto the ADHD psychostimulant drug methylphenidate (Concerta and Ritalin) for drug dependence. It warns that chronic abuse of methylphenidate can lead to a marked tolerance and psychological dependence with varying degrees of abnormal behavior and frank psychotic episodes can also occur.

(Source: “Boxed Warning, Contraindications and strengthened Precautions for Methylphenidate,” Janssen-Cilag, February 2009.)

Australia, December 2004:  The Australian Therapeutic Goods Administration published an Adverse Drug Reactions Bulletin recommending that any use of SSRI antidepressants in children and adolescents should be carefully monitored for the emergence of suicidal ideation. In a recent study involving Eli Lilly’s Prozac, it said, there was an increase in adverse psychiatric events of suicide, self-harm, aggression and violence.

(Source: “Use of antidepressants in children and adolescents,” The Australian Therapeutic Goods Administration (TGA) published an Adverse Drug Reactions Bulletin, Vol 23, No. 6, Dec. 2004, p. 22.)

United States, July 01, 2009:  The FDA has required the manufacturers of the smoking cessation aids varenicline (Pfizer’s Chantix) and bupropion (GlaxoSmithKline’s Zyban, aka the antidepressant GlaxoSmithKline’s Wellbutrin) to add new Boxed Warnings and develop patient Medication Guides highlighting the risk of serious neuropsychiatric symptoms in patients using these products. These symptoms include changes in behavior, hostility, agitation, depressed mood, suicidal thoughts and behavior, and attempted suicide.

(Source: “Information for Healthcare Professionals: Varenicline (marketed as Chantix) and Bupropion (marketed as Zyban, Wellbutrin, and generics),” FDA, July 1, 2009.)

United Kingdom, March 2009:  Medicines and Healthcare products Regulatory Agency (UK) published in their Drug Safety Update newsletter new information about Atomoxetine (Eli Lilly’s Strattera, a [alleged] “non-stimulant” ADHD drug). They warned that Strattera is associated with treatment-emergent psychotic or manic symptoms in children without a history of such disorders.

(Source: Medicines and Healthcare products Regulatory Agency, Drug Safety Update newsletter, Vol. 2, March 8, 2009.)

Australia, December 2008:  The Australian Adverse Drug Reactions Bulletin published an article about the (Cephalon’s psychostimulant Provigil (modafinil). The bulletin advised that this drug has been reported to cause serious adverse skin and psychiatric reactions including anxiety, hallucination, aggression, and mania.

(Source: Adverse Drug Reactions Advisory Committee, Australian Adverse Drug Reactions Bulletin, Vol. 27, No. 6, December 2008.)

European Union, November 20, 2008:  Eli Lilly included in their Strattera label in Europe warnings that Strattera causes “hallucinations, delusional thinking, mania or agitation in children and adolescents without a prior history of psychotic illness or mania…” Strattera is an “antidepressant” prescribed as a “non-stimulant” drug to treat ADHD.

(Source: “Official warnings issued: The ADHD drug Strattera CAUSES psychosis, hallucinations, mania and agitation” TransWorldNews, November 20, 2008.)

United States, September 2007:  The Vice President of Medical Services at the drug company Cephalon sent out a letter to health care professionals informing them of new warnings for the company’s psychostimulant Provigil. “Updated Safety Information: Warnings regarding serious rash, including Stevens Johnson Syndrome [a life-threatening condition affecting the skin] and hypersensitivity reactions, and psychiatric symptoms (including anxiety, mania, hallucinations, and suicidal ideation). 1. Provigil can cause life-threatening skin and other serious hypersensitivity reactions… 2. Provigil is not approved for use in pediatric patients for any indication. 3. Provigil can cause psychiatric symptoms.”

(Source: Jeffrey M. Dayno, M.D., “Dear Healthcare Professional,” Cephalon, September 2007.)

United States, February 21, 2007:  The FDA directed ADHD drug manufacturers to distribute “patient friendly” guides to consumers warning about serious psychiatric and cardiovascular problems, including stroke, heart attack, sudden death and psychotic reactions caused by ADHD drugs.   The psychiatric adverse events included hearing voices, becoming suspicious for no reason, or becoming manic, even in patients who did not have previous psychiatric problems.

(Source: “FDA Directs ADHD Drug Manufacturers to Notify Patients about Cardiovascular Adverse Events and Psychiatric Adverse Events,” FDA News, February 21, 2007.)

United States, August 21, 2006:  The FDA said that ADHD drug manufacturers have to strengthen their warning labels to warn that the drugs can cause suppression of growth, psychosis, bipolar illness, aggression, and ‘serious’ cardiovascular side effects, including misuse possibly leading to sudden death from heart attacks and strokes. Psychostimulant drug companies GlaxoSmithKline and Shire (makers of Adderall and Vyvanase) posted a letter to doctors about the revised prescribing information.

(Source: “UPDATE 2-US FDA calls for new warnings on ADHD drugs”, Reuters, August 21, 2006.)

European Union, April 25, 2005:  The European Medicines Agency’s scientific committee, the Committee for Medicinal Products for Human Use, concluded that Prozac-type antidepressants were associated with increased suicide-related behavior and hostility in young people. The London-based watchdog said it recommended the inclusion of strong warnings across the whole of the European Union to doctors and parents about these risks and that the drugs should not be used in children and adolescents in off label situations.

(Source: “EU calls for tougher warnings on antidepressants for kids” News-Medical.net April 25, 2005.)

United Kingdom, September 21, 2004:  The British Healthcare Products Regulatory Authority advised that it had issued guidelines that children should not be given most SSRI antidepressants because of clinical trial data showing an increase rate of harmful outcomes, including hostility.

(Source: “Antidepressant aggression concern,” BBC News, 21 Sept. 2004.)

European Union, April 22, 2004:  The European Agency for the Evaluation of Medicinal Products issued a press release to the press and public. In this press release, they reported that, according to clinical trials, GlaxoSmithKline’s paroxetine (Paxil in the U.S.) containing medicines could cause suicidal behavior and hostility in children. It recommended that paroxetine not be used in children and recommended that young adults be observed carefully for signs and symptoms of suicidal behavior or hostility. Paroxetine was shown to have little effectiveness in children according to clinical trials. The committee also recommended strengthened warnings on the withdrawal symptoms of paroxetine, which are common.

(Source: “European Agency for the Evaluation of Medicinal Products: Committee for Proprietary Medicinal Products 20-22 April 2004″ EMEA, The European Agency for the Evaluation of Medicinal Products, Press Release April 2004.)

Canada, August 22, 2003:  Wyeth Pharmaceuticals, the makers of the antidepressant Effexor, issued a warning to U.S. and Canadian doctors that use of this drug could cause hostility, suicidal ideation and self-harm in patients under the age of 18.

(Source: Wyeth Pharmaceuticals, “Dear Health Care Professional…” Health Canada, Health Products and Food Branch, August 22, 2003.)

United States, May 2007:  The FDA’s MedWatch system published a warning on the psychostimulant Desoxyn which is used for ADHD stating that the drug could cause: sudden death with pre-existing structural cardiac abnormalities or other serious heart problems, psychiatric adverse events including aggression and the emergence of new psychotic or manic symptoms, long-term suppression of growth, seizures, visual disturbance, as well as serious cardiovascular adverse events.

(Source: Food and Drug Administration (FDA), “Detailed View: Safety Labeling Changes Approved By FDA Center for Drug Evaluation and Research (CDER)”, MedWatch, May 2007.)

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Dr Kohls is a retired physician who practiced holistic mental health care for the last decade of his career. He writes a weekly column for the Reader Weekly, an alternative newsweekly published in Duluth, Minnesota, USA. Many of Dr Kohls’ columns are archived at http://duluthreader.com/articles/categories/200_Duty_to_Warn.

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