HHS is implementing a strategy and framework to reduce the overprescription of psychiatric medications. The administrators of four HHS agencies penned a Dear Colleague letter encouraging health care providers to provide full, informed consent for medications while prioritizing non-pharmacological methods as the first line of defense.

“HHS encourages clinicians and provider organizations to support a treatment approach grounded in shared decision-making, patient autonomy, and fully informed consent,” the administrators wrote. “Individuals should receive clear, understandable information regarding the potential benefits and risks of psychiatric medications at initiation, during ongoing treatment, and when discontinuation is being considered. That discussion should include the purpose of the medication, expected benefits, possible adverse effects, monitoring needs, potential discontinuation symptoms, the risks of abrupt cessation when relevant, the possibility of relapse or recurrence, and the availability of evidence-based non-pharmacological interventions.”

The administrators described several medical billing pathways where providers can be reimbursed for providing non-pharmacological treatment options to patients. The administrators encourage providers to use these options when appropriate, on a case-by-case basis. These options include diet modification, nutritional therapy, psychotherapy, and family-based interventions. They emphasize nutrition, psychotherapy, and family-based services as an important part of a “comprehensive, person-centered behavioral health care” approach.

CDC data from 2020 shows that 20.3% of adults received mental health treatment. 16.5% took prescription medication for their mental health, and 10.1% received counseling or therapy from a mental health professional. One out of five American adults received mental health treatment, and only about half of them received counseling, even though 81% of them received medication.

Alongside this announcement, the MAHA Institute held a Mental Health and Overmedicalization Summit with HHS Secretary Robert F. Kennedy Jr., researchers, clinicians, and former medicalized patients to discuss problems associated with psychiatric medications.

“Millions of our young people now grow up convinced something is wrong with them,” said Laura Delano, an author and consultant who was medicalized on antidepressants as a teenager and stayed on the medications for 14 years. “They’ve been taught to take their despair and self-doubt and loneliness, their shame and obsession and alienation, their struggles in friendship and romance, their fear and angst and grief, and translate all of these experiences into symptoms of incurable brain pathology requiring lifelong pharmaceutical use. They’ve grown convinced, like I once was, that their life’s main purpose is symptom management with endless pills, therapy, and programs. They are convinced the only way the depth of their pain can be seen, understood, and validated is through medicalizing it.”

Surveys show that as much as 30-50% of antidepressant users have no evidence-based indication to continue. During the summit, several patients described serious side effects they experienced as a result of antidepressant medications from sexual dysfunction to permanent brain damage.

One speaker, identified as Dani, said she was prescribed at the age of seven after her parents were referred to a doctor for the treatment of ADHD. She said she was diagnosed with a learning disability, but the medication itself caused her to have the very learning disability it was supposed to be correcting.

“Adverse side effects were interpreted as new diagnosis, and more drugs were prescribed to treat the problems that the medications themselves had caused,” Dani said. “This spiraled into a prescription cascade of anti-depressants, benzodiazepines, mood stabilizers, and antipsychotics, all before my 10th birthday. None of it ever felt right. But I was a child, and I didn’t have the words to explain what was happening. And I didn’t have the authority to challenge it. My completely normal childhood behavior was pathologized. I wasn’t in crisis. I wasn’t struggling or acting out. I was simply a fidgety, shy, sensitive little girl who didn’t fit the mold of how a child was supposed to behave in a classroom setting.”

The administrators in the Dear Colleague letter explained that deprescribing is appropriate in multiple scenarios, including at times when the psychiatric medications are causing burdensome side effects or the treatment is not providing a meaningful benefit. The administrators also say patients can be tapered off from medication if the treatment goals have been met or the patient’s informed preferences call for a carefully monitored taper. The administrators note that deprescribing is done on an individualized basis and is not the same as “abrupt discontinuation or blanket medication reduction.”

A 2019 review explains that “most depressed patients treated with antidepressants experience fewer than the required diagnostic number (five of nine for 2 or more weeks) of Major Depressive Disorder symptoms.” The author adds that antidepressant drugs for these patients have marginal benefits from the medication, at best. The paper states that this is among the top four drugs that are overprescribed alongside opioids for the treatment of chronic pain.

The HighWire reported in March about a pervasive issue that has existed for decades involving the use of antipsychotic medications for dementia patients in nursing homes. While the practice has been a known issue, nursing homes have started falsely diagnosing patients with schizophrenia to justify the use of antipsychotics.

A 2021 review concluded that mothers with postpartum depression are being overprescribed antidepressants, especially in certain geographical locations, despite no evidence of benefit. Furthermore, the authors note that studies showing a benefit for mothers with postpartum depression contain small or underrepresented samples.

Steven Middendorp

Steven Middendorp is an investigative journalist, musician, and teacher. He has been a freelance writer and journalist for over 20 years. More recently, he has focused on issues dealing with corruption and negligence in the judicial system. He is a homesteading hobby farmer who encourages people to grow their own food, eat locally, and care for the land that provides sustenance to the community.

Other Headlines

Coronavirus

Fauci Advisor Indicted for Conspiracy, Deleting and Concealing Records; Faces 51 Years in Prison

David Morens, a former senior advisor to Dr. Anthony Fauci in the National Institute of Allergy and Infectious Diseases (NIAID), has been indicted by the Department of Justice for conspiracy against the United States, two counts of destruction, alteration, or falsification of records in federal investigations, and two counts of concealment, removal, or mutilation ofContinue reading Fauci Advisor Indicted for Conspiracy, Deleting and Concealing Records; Faces 51 Years in Prison

More news about Coronavirus

Health & Nutrition

HHS Implements Strategy To Stop Overmedicalization With Psychiatric Medications

HHS is implementing a strategy and framework to reduce the overprescription of psychiatric medications. The administrators of four HHS agencies penned a Dear Colleague letter encouraging health care providers to provide full, informed consent for medications while prioritizing non-pharmacological methods as the first line of defense. “HHS encourages clinicians and provider organizations to support aContinue reading HHS Implements Strategy To Stop Overmedicalization With Psychiatric Medications

More news about Health & Nutrition

Vaccines

No Duty of Care: Ontario Court Dismisses Lawsuit Over 17-Year-Old’s Death 33 Days After COVID Vaccine

The Ontario Court of Appeals has dismissed the case of Dan Hartman, who sued federal Canadian government officials following the death of his 17-year-old son Sean, who died 33 days after receiving the COVID-19 vaccine as a requirement to participate in hockey. The lawsuit alleged the Attorney General of Canada and the Minister of Health,Continue reading No Duty of Care: Ontario Court Dismisses Lawsuit Over 17-Year-Old’s Death 33 Days After COVID Vaccine

More news about Vaccines

Science & Tech

Anthropic Unauthorized Access Investigation Raises Questions About AI Safety Amidst Rapid Development

Anthropic is investigating a reported security breach that allowed a small group of people to gain access to Claude Mythos Preview, the company’s AI software that is too powerful to release to the public. AI models are becoming increasingly capable, and the 2026 International AI Safety Report notes that some hypothetical scenarios pose risks asContinue reading Anthropic Unauthorized Access Investigation Raises Questions About AI Safety Amidst Rapid Development

More news about Science & Tech

Environment

Supreme Court Considers Granting Bayer Protection From Pesticide ‘Failure-To-Warn’ Lawsuits

The U.S. Supreme Court heard oral arguments Monday about whether Bayer can be held liable for state-level failure to warn claims when the company followed EPA labeling guidelines after the federal agency classified glyphosate as “not likely carcinogenic to humans.” The court is not considering the underlying safety profile of glyphosate or Roundup, but theContinue reading Supreme Court Considers Granting Bayer Protection From Pesticide ‘Failure-To-Warn’ Lawsuits

More news about Environment

Policy

Supreme Court Considers Granting Bayer Protection From Pesticide ‘Failure-To-Warn’ Lawsuits

The U.S. Supreme Court heard oral arguments Monday about whether Bayer can be held liable for state-level failure to warn claims when the company followed EPA labeling guidelines after the federal agency classified glyphosate as “not likely carcinogenic to humans.” The court is not considering the underlying safety profile of glyphosate or Roundup, but theContinue reading Supreme Court Considers Granting Bayer Protection From Pesticide ‘Failure-To-Warn’ Lawsuits

More news about Policy