FDA is Mind-Numbing America: Psychotropic Drugs and Electroshock Approval Boosts $35B Industry

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READ MORE AT HEALTH IMPACT NEWS 

By CCHR International
The Mental Health Industry Watchdog

Excerpts:

The Food and Drug Administration (FDA) is considering approving Johnson & Johnson’s (J&Js) new nasal spray antidepressant, esketamine (Spravato[1]) after an FDA advisory committee voted on February 12, 2019 in its favor.[2]

The drug is a chemical mirror of ketamine, a potent “dissociative anesthetic” that is abused as the illegal “club drug,” Special K, and generates an intense high and euphoric effects, and hallucinations.

If approved, it would add to the mind-numbing of America that an FDA-psychiatric collusion is causing, says the Citizens Commission on Human Rights (CCHR). The group said the FDA’s continuing clearance of potentially addictive and dangerous psychotropic drugs and, more recently, electroshock treatment devices, fuels a lucrative $35 billion a year industry at the cost of consumers’ mental health and lives.

Astoundingly, with more than 43.6 million Americans each year now taking antidepressants once touted as “miracle pills,” psychiatrists now claim that the drugs don’t work in one out of every three people taking them.

It was known when the drugs were approved that they could cause suicidal thoughts and violence-related effects—hardly a recipe for improving depression.

Jan Eastgate, president of CCHR International, says:

“Drugs and ECT are recommended for ‘treatment-resistant depression,’ a term invented to mislead consumers into thinking the problem is theirs and not the failure of psychiatric treatments. Despite the failure, the serious and deadly risks of treatment and a history of manufacturers covering up adverse effects, the FDA keeps giving them license to profit.”

Between 1988 and 2005, the FDA approved nine new antidepressants and five new antipsychotics.[3]

At least four more antidepressants have been approved since 2010.[4] Drug companies provide 60% of the FDA’s drug review costs—a colossal conflict of interest—representing more than $712 million a year in revenue.[5] There’s another estimated $24 million for medical device clearance.[6]

This adds to a lucrative mental health market. Spending on non-institutionalized mental disorder treatment accounted for $89 billion in 2013.[7] The up to 90% prevalence of polypharmacy in psychiatry—prescribing a patient multiple drugs—would contribute to those costs.[8]

Esketamine is but another touted “hopeful” drug that will merely mask—but not cure—depression. The nasal spray would be given with an antidepressant.[9]

Several side effects of esketamine are dissociation and sedation, prompting the FDA advisory panel to recommend not allowing people to take the nasal spray at home but remain monitored in a healthcare facility for two hours until these side effects subside.[10]

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There’s been a boom in the off-label (non-FDA approved) use of ketamine as a treatment for depression and other psychiatric conditions. Dozens of for-profit ketamine clinics have opened up around the country,[11] including in Florida.[12] The clinics regularly charge $650 – $1,200 per treatment, with most people needing six – eight treatments (up to $9,600) to get started.[13]

J&J anticipates $1 billion-plus in sales from a crop of new drugs that includes esketamine. This won’t recoup the costs it has paid in settlements of lawsuits over its antipsychotic, Risperdal (risperidone) and a $2.2 billion Department of Justice fine over marketing and selling Risperdal and other drugs off-label.[14]

J&J has paid out millions of dollars to settle lawsuits about its failure to warn that Risperdal can cause gynecomastia (male breast growth). One youth was awarded $70 million in damages after alleging Risperdal caused him to grow size 42D breasts.[15] None of this appears to be of concern to FDA officials or psychiatrists advocating for yet another brain-altering drug.

Source: http://healthimpactnews.com/2019/fda-is-mind-numbing-america-psychotropic-drugs-and-electroshock-approval-boosts-35b-industry/

Read the full article at CCHRINT.com.

References:

[1] https://psychcentral.com/blog/spravato-new-ketamine-treatment-to-be-approved-by-fda/.

[2] “Esketamine Nasal Spray Gets Support from FDA Advisory Committee,” MD, 12 Feb. 2019, https://www.mdmag.com/medical-news/esketamine-nasal-spray-support-fda-advisory-committee.

[3] https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2690138/.

[4] https://www.medhealthdaily.com/new-antidepressants/.

[5] http://www.anh-usa.org/microsite-subpage/the-fda-is-in-the-pocket-of-the-drug-industry/.

[6] https://medcitynews.com/2010/11/medical-device-makers-spend-millions-to-meet-fda-rules-study-finds/

[7] https://www.healthsystemtracker.org/chart-collection/current-costs-outcomes-related-mental-health-substance-abuse-disorders/#item-cost-treating-mental-illness-grown-relatively-slowly-compared-disease-categories-price-index-mental-illness-treatment-grew-average-annual-growth-rate-3-1-fro

[8] https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3653237/

[9] https://psychcentral.com/blog/spravato-new-ketamine-treatment-to-be-approved-by-fda/

[10] https://psychcentral.com/blog/spravato-new-ketamine-treatment-to-be-approved-by-fda/

[11] https://www.statnews.com/2019/02/20/psychiatry-awaits-esketamine-with-excitement-hesitation/

[12] https://www.bing.com/search?q=Ketamine%20clinic%20Florida&qs=n&form=QBRE&sp=-1&ghc=1&pq
=ketamine%20clinic%20florida&sc=4-23&sk=&cvid=5DB62CDC17D5444CB036E7C5AEB5161F

[13] https://psychcentral.com/blog/spravato-new-ketamine-treatment-to-be-approved-by-fda/

[14] https://www.consumersafety.org/legal/risperdal-lawsuit/

[15] https://clearviewpost.com/nationwide-risperdal-lawsuits-shed-light-on-the-patchwork-of-state-laws-that-can-determine-the-value-of-your-life/

[16] https://psychcentral.com/news/2013/03/14/adding-antipsychotic-meds-to-antidepressants-shows-risk-little-benefit/52597.html

[17] Ana Jelovac, et al., “Relapse Following Successful Electroconvulsive Therapy for Major Depression: A Meta-Analysis,” Neuropsychopharmacology, Nov 2013, https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3799066/.

One thought on “FDA is Mind-Numbing America: Psychotropic Drugs and Electroshock Approval Boosts $35B Industry

  1. You do readers a disservice by making direct comparisons between Esketamine and Ketamine. They are not identical as most articles lead readers to believe. Esketamine is PART of ketamine.

    I’ve been dealing with treatment resistant major depressive disorder w/suicidal ideation for decades. There was a suicide attempt. I’ve been prescribed a dozen medications over the years. None improved my condition, at all. Nearly all caused multiple side effects, some of which were debilitating.

    In 2017 I was a participant in the clinical trial of intranasal esketamine. It did NOT numb my mind and it did NOT get me high (unlike IV Ketamine). At no time did I ever feel like my depression was being masked. It simply ceased to be the ruling factor in my life … like taking aspirin for a headache. The side effects that I experienced were minimal (sneezing, post-nasal drip, ear ringing) and lasted no more than 30-40 minutes . My overall psychological/social improvement was dramatic. There’s no other way to describe it.

    For those of us who have sought relief for many years, esketamine is not a quick fix. Besides, our concern is efficacy, not speed. I have been clinging desperately to the hope that this drug will be approved. I consider it my last chance. The alternative is suicide.

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