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  • The 6 Worst Health Scandals of the Past 25 Years

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    In medicine, there’s almost no such thing as a free lunch. Just about every drug or intervention will have its side effects.

    Ideally, rigorous studies and the regulatory process will ensure that an approved drug’s benefits clearly outweigh any potential harms. But sometimes, researchers (and patients) will uncover side effects that went unnoticed during the approval process. Other times, more rarely, a drug’s maker is revealed to have buried incriminating information about their drug’s harms from the public or to have created a product that doesn’t work at all as intended. And when that happens, a bad or ineffective treatment can spark a major scandal.

    There’s no shortage of pharmaceutical scandals that have occurred over the years, but to keep things short, let’s just focus on some of the biggest ones to have happened in this quarter-century.

    1. Johnson & Johnson’s talcum powder products

    For decades, people had unsuccessfully tried to sue J&J over its consumer products containing talc, particularly baby powder, claiming that the products had contributed to their cancers.

    In 2018, however, an explosive report from Reuters found the company had hidden evidence that the talc it used could sometimes contain detectable levels of asbestos, a known carcinogen. The report helped fuel a new wave of lawsuits and growing public distrust in the company’s baby powder products. In the years since, the company has repeatedly lost civil suits over its talc products, some totaling into the billions, and its appeals continued to fail, even before the Supreme Court.

    Though J&J has maintained that its products are safe, the company eventually removed talc from all its powder brands (instead using cornstarch), tried and failed to cover its liability over these lawsuits by having a subsidiary declare bankruptcy, and even this year has continued to lose court cases tying its products to people’s cancer.

    Interestingly enough, though asbestos is known to cause cancer, past research hasn’t found a clear link between talc as a whole (including asbestos-free talc) and cancer, and there remains some disagreement over the extent of the risk posed by talcum powder products. The American Cancer Society states that if talc can raise a person’s risk of ovarian cancer (the primary type of cancer linked to talc), the “overall increase is likely to very be small” for an individual woman. The World Health Organization has stated that asbestos-containing talc should be considered carcinogenic, while talc in general is “probably carcinogenic.

    2. Biogen and the Alzheimer’s drug that wasn’t

    In June 2021, the FDA approved Biogen and Eisai’s antibody-based Alzheimer’s drug Aduhelm. At first glance, the approval should have been good news: the first drug of its kind, and one intended to actually target a key driver of the degenerative disorder, beta amyloid. But in actuality, it was anything but.

    In a rare move at the time, the FDA went against the recommendations of its expert advisory panel, who voted against approval. The outside experts rightly noted that the data supporting the drug’s effectiveness was mixed at best. The FDA also granted Aduhelm accelerated approval, a special category that requires less rigorous evidence. Media outlet STAT News later uncovered an unusually friendly relationship between top Biogen employees and FDA officials, which prompted a Congressional investigation into the matter. And to add insult to injury, Biogen initially set Aduhelm’s list price at $56,000 a year—a cost high enough to potentially devastate the pockets of patients and Medicare if the drug saw widespread use among older Americans.

    Many doctors soon rebelled against the approval, refusing to prescribe it to their patients, while Medicare decided to severely restrict its coverage of the drug. Biogen eventually gave up trying to make Aduhelm a thing, following years of poor sales, and pulled the drug from the market in early 2024.

    This saga does have a bit of a happy ending, at least. There have been other similar drugs developed and approved in recent years, and unlike Aduhelm, these drugs do seem to have a real, if still modest, effect on treating the condition.

    3. Purdue Pharma and OxyContin

    Purdue Pharma has perhaps become the most infamous poster child for the opioid crisis.

    Bottles of Oxycontin. © PureRadiancePhoto via Shutterstock

    Its blockbuster drug, OxyContin, helped fuel growing rates of opioid use disorder following its release to the public in 1996. And though there are many drivers of the crisis, including the proliferation of more potent agents like fentanyl in later years, the company did eventually admit to downplaying the addictive risk of its products, paying doctors illegal kickbacks to prescribe their drugs, and turning a blind eye to the widespread diversion of its drugs from pharmacies to the black market.

    Following a glut of civil and federal lawsuits over OxyContin, Purdue Pharma shuttered its doors, and its sole owners—the Sackler family—agreed to pay out more than $4 billion as part of a far-reaching settlement in 2021. The courts bumped this up to $6 billion in 2023. That settlement, however, also provided immunity from further civil charges against the Sacklers themselves. And though the situation has finally started to improve as of late, roughly 50,000 Americans still died from opioid overdoses last year.

    4. Martin Shkreli’s drug price surge

    Sometimes the scandals aren’t about the drugs themselves, but what they’re being sold for.

    In 2015, Martin Shkreli became public enemy number one when his company, Turing Pharmaceuticals, bought the anti-parasitic and anti-HIV drug Daraprim and raised its $13.50 price tag per pill by over 5,000 percent. Shkreli’s cocky, unrepentant attitude toward his many critics earned him the nickname of the “Pharma bro.”

    Ironically enough, his initial downfall had nothing to do with Daraprim. Soon after he became infamous, federal prosecutors in New York charged Shkreli with securities fraud, and in 2017, he was convicted and sentenced to seven years of federal prison.

    Martin Shkreli
    Martin Shkreli speaks to the press after the jury issued a verdict in his case at the U.S. District Court for the Eastern District of New York, August 4, 2017.  © Drew Angerer via Getty

    Though Shkreli was released early in 2022, his company’s management of Daraprim did later come back to bite him. In 2020, the FTC and others sued the company, now called Vyera Pharmaceuticals after Shkreli’s imprisonment, alleging that it carried out an “elaborate anticompetitive scheme” to maintain its monopoly on the drug. The company reached a settlement with the FTC a year later, and the legal battle eventually required Shkreli himself to pay out a $64 million fine and to stay away from the pharmaceutical industry entirely. In 2023, Vyera declared bankruptcy and sold the rights to Daraprim. Last year, the U.S. Supreme Court snubbed Shkreli’s attempt to dismiss his personal fine and ban.

    Don’t feel too bad for Shkreli, though. Since his release from prison, he’s been busy trying to shill crypto and AI knockoffs of WebMD.

    5. Abbott’s tainted baby formula

    Powderedbabyformula
    Baby formula powder in a measuring scoop © Strigana via Shutterstock

    In early 2022, the FDA warned families to stay away from certain powdered baby formulas produced by the company Abbott Nutrition. The products, it turns out, were contaminated by Cronobacter bacteria.

    Several children were hospitalized, and two infants who had consumed the products later died. Abbott issued a widespread recall of its products and shut down its formula production facility in Sturgis, Michigan. The FDA’s investigation concluded that Abbott had failed to maintain sanitary conditions and that the facility had at least eight recent instances of Cronobacter contamination dating back to 2019.

    It would take four months for the company’s Sturgis plant to reopen, following an agreement with the FDA to overhaul its safety practices, the length of which helped contribute to a nationwide formula shortage that year. Lawmakers on both sides also criticized the FDA for its delayed response to the crisis, since the agency first caught wind of potential issues as early as September 2021.

    Though there haven’t been similar recalls or reported outbreaks since, an extensive ProPublica report in April 2025 interviewed workers who claimed that the Sturgis plant continues to have serious safety and sanitary risks to this day. One employee reported what they found to the FDA, but it’s unclear whether the new Trump administration will take action.

    6. Elizabeth Holmes and Theranos

    Elizabeth Holmes founded the company Theranos in 2003. It centered around the development of a device intended to make blood tests easier than ever. With just a few drops of blood from a single finger prick, Holmes claimed, her company’s “Edison” device could accurately detect a litany of health conditions. By the mid-2010s, Holmes’ marketing of Theranos had allowed her to become a darling of the biotech world: a young, self-made entrepreneur styled after Steve Jobs, who at one point was worth nearly $5 billion.

    The trouble was, as the world eventually found out, it was all based on falsehoods. Starting in late 2015, Wall Street Journal reporter John Carreyrou exposed the fraudulent practices of Holmes and Theranos. Though Holmes had struck a partnership with retail chain Walgreens in 2013 to provide the Edison device to its customers, the Edison could simply never do what Holmes claimed it could. And eventually, the company secretly resorted to using other commercially available machines to perform most of its blood testing services.

    Holmes’ deception didn’t just mislead investors; several people reported that the faulty test results provided by Theranos made them fearful about having medical conditions they didn’t actually have, such as HIV, or otherwise harmed their health.

    Holmes was convicted of investor fraud and other charges over Theranos in 2022 and was sentenced to an 11-year stint in prison (later reduced by two years), while her co-executive and one-time romantic partner Ramesh “Sunny” Balwani was sentenced to nearly 13 years the next month. As of this year, she’s made her return to social media (via having someone else post her words).

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    Ed Cara

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  • PillSafe Spearheads Solutions to Opioid Crisis With Revolutionary Technology

    PillSafe Spearheads Solutions to Opioid Crisis With Revolutionary Technology

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    Government and industry have tried and failed to stem the overdose epidemic for more than two decades. Open-source PillSafe Technologies offer hope.

    About 1.2 million people will die from opioid overdoses in the United States and Canada this decade, demonstrating the urgent need for a solution to the drug epidemic. The PillSafe Bottle is the culmination of five patented feature sets that together create a “smart” pill delivery system to ensure patients take medications safely and as prescribed by their physician.

    Opioids are a class of drugs used to control pain, including oxycodone (OxyContin, Percocet), hydrocodone (Vicodin, Norco), fentanyl, morphine, and others. The illegal drug heroin also is an opioid.   

    Because of aggressive marketing of these controlled substances, ineffective regulations and a trend of physicians placing more emphasis on treating pain, U.S. opioid use has soared. Americans, just 5% of the world’s population, consume 80% of the world’s opioid supply and 90% of the hydrocodone supply. Since the late 1990s, opioid overuse has become a crisis: overdose deaths doubled from 2000 to 2010 and then tripled from 2010 to 2020. More than 80,000 Americans died from opioid overdoses in 2021.  

    Dr. John Barr created PillSafe in response to two decades of efforts by pharmaceutical companies and the U.S. Food and Drug Administration to stem the opioid epidemic. That response began with pushing for labeling changes on OxyContin as early as 2001, and as late as December 15, 2023, the FDA is still implementing labeling requirements for immediate-release and extended-release opioid painkillers. Debate over safer forms of opioids has continued for decades.  

    Barr cites, in particular, the focus of pharmaceutical companies and the FDA on developing “abuse deterrent formulations” (ADFs) of opioid painkillers. The process began in 2013 and continues today, but after more than a decade, the effectiveness of those formulations in preventing abuse is still unproven, Barr said.   

    The failed market and regulatory response left Barr determined to find a better solution.   

    “PillSafe can help protect patients and offers a safer way to deliver medication in the healthcare and drug manufacturing industries,” Barr said. “The way our technology works is that every pill stays within the confines of our system, and that has the potential to save lives from drug abuse.”  

    The PillSafe medication delivery system secures medications at the source.  

    The pharmacist inserts the medication into the PillSafe container, snaps the lid in place, and programs the bottle to deliver the proper dosage on the precise schedule set by the doctor. Each PillSafe bottle has a unique, preset three-digit access code that the patient enters to dispense the medication at the time intervals set by the physician. The patient presses down on the lid and rotates it clockwise to access the medication. Then the device is locked again, and the countdown timer restarts for the next dose.  

    An electronic net inside each PillSafe container can detect any breach attempt. PillSafe can be programmed to destroy the medication or notify the physician or the pharmacy to confirm compliance. The PillSafe container is single-use and disposable.  

    “We created PillSafe to keep patients safe, by ensuring they comply with their doctor’s orders,” Barr said. “This is an innovative technology that can battle the opioid epidemic on the front lines and provide a solution that has been elusive for more than 20 years.”  

    For more information, please visit https://pillsafeprotection.com/.  

    About PillSafe  

    PillSafe is a pioneering “smart” open technology consisting of five patented feature sets that uniquely impact compliance, the standard of care and the managed delivery of additive medications. In recognizing the potential for numerous solutions to this challenge, the PillSafe Team is offering its technology to all interested parties, from manufacturing to medical, software and product producers, to insurance and the government. PillSafe technology provides an opportunity for packaging manufacturers and pharmaceutical companies to lead the industry in designing truly child-resistant senior-friendly (CRSF) packaging for medicines.   

    PillSafe technology as a delivery tool helps the doctor manage pain effectively, identify issues, confirm compliance, and prevent misuse and abuse. PillSafe technology is a protection against counterfeit drugs, utilizing a secure tamper-proof, adult-proof bottle, that cannot be duplicated by nefarious pill-mills. Cities, counties, and states can verify that medications have arrived safely to the intended recipient, aiding in the accuracy of the required governmental reporting.   

    Now more than ever, the medical community and government must think of out-of-the-box solutions to achieve better results. PillSafe Technology offers advantages that can make a significant difference at many levels. For more detailed information and a demonstration of PillSafe Technologies, contact the PillSafe team at https://pillsafeprotection.com/.   

    Source: PillSafe

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  • Can Cannabinoids Help People Wean Off Opioids? | High Times

    Can Cannabinoids Help People Wean Off Opioids? | High Times

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    Doctors desperately need tools to battle the opioid epidemic, and they’re turning to cannabinoids for new ways to approach the problem of opioid use disorder (OUD). Recently researchers aimed to create an open-access framework designed to help people wean off and eventually replace opioids with cannabinoids as an alternative. 

    Last August, a study provided a clinical framework for cannabinoids in the battle against the opioid epidemic. The study, entitled “An answered call for aid? Cannabinoid clinical framework for the opioid epidemic,” was published in Harm Reduction Journal.

    Researchers provided an evidence-based clinical framework for the utilization of cannabinoids to treat patients with chronic pain who are dependent on opioids, seeking alternatives, and tapering off of opioids.

    “Based on a comprehensive review of the literature and epidemiological evidence to date, cannabinoids stand to be one of the most interesting, safe, and accessible tools available to attenuate the devastation resulting from the misuse and abuse of opioid narcotics,” researchers wrote. “Considering the urgency of the opioid epidemic and broadening of cannabinoid accessibility amidst absent prescribing guidelines, the authors recommend use of this clinical framework in the contexts of both clinical research continuity and patient care.”

    Recent research has shown a role for CBD in treating cannabis use disorder, and likewise, the compound could be useful in treating OUD. Researchers are also exploring the potential of THC and acidic cannabinoids as well. Cannabis is known anecdotally for the treatment of low-to-moderate amounts of pain despite working in very different ways than opiates.

    The open-access framework includes opioid tapering recommendations that are in accordance with the CDC’s latest clinical practice guidelines for managing opioids for pain. 

    “As opioid deaths continue to be a global problem, patients are increasingly self-medicating with cannabis while researchers struggle to standardize protocols and providers feel uncomfortable recommending cannabinoids amidst absent prescribing guidelines,” researchers wrote. “If we consider cannabis as a harm reduction tool that patients are already using without medical guidance, we can realign our focus to supporting researchers and providers with a clinical framework for standardizing research and recommending cannabinoids more informatively as safe, effective, accessible tools for assisting in the management of chronic pain. To our knowledge, this is one of the first comprehensive evidence-based peer-reviewed clinical frameworks for the safe use of cannabinoid products for chronic pain and OUD.”

    The researchers acknowledged that many of their patients have already begun their own self-guided journey into pain management with cannabinoids.

    The Devastating Toll of Opioid Overdoses

    Opioids continue to wreak havoc on people in America, leading to confusion about who needs powerful opioids and who doesn’t, and overdose deaths continue a steady pace of devastation.

    According to The National Center for Health Statistics (NCHS) under the U.S. Centers for Disease Control and Prevention, drug overdose deaths rose from 2019 to 2021 with over 106,000 drug overdose deaths reported in 2021. Deaths involving synthetic opioids—primarily fentanyl and excluding methadone—continued its death march with 70,601 overdose deaths reported in 2021. Fentanyl in particular kills 150 Americans per day.

    Over-prescription of opioids could be part of the problem. A 2018 longitudinal analysis showed that prescriptions for all opioids in the U.S. fell by 14.4% when medical cannabis dispensaries opened—particularly for hydrocodone and morphine, but also for benzodiazepines, stimulants, and many other medications known to be over-prescribed and addictive. 

    In some states, opioid use disorder is a qualifying condition for the use of medical cannabis. Researchers are still learning about the efficacy of cannabinoids in animal and human trials.

    Studies on Cannabis and Opioid Abuse Vary

    Opioid addiction is a complex phenomenon, and studies vary in their results of whether or not cannabinoids are effective. One study concluded that there is “no evidence that cannabis reduces opioid misuse.”

    According to research published in the American Journal of Psychiatry, researchers instead found “no evidence” showing that cannabis may not be an effective long-term strategy for reducing opioid abuse.

    “There are claims that cannabis may help decrease opioid use or help people with opioid use disorders keep up with treatment. But it’s crucial to note those studies examine short-term impact and focus on treatment of chronic pain and pain management, rather than levels of opioid use in other contexts,” Dr Jack Wilson, the lead author of the study and a postdoctoral research fellow at The Matilda Centre for Research in Mental Health and Substance Use at the University of Sydney in Australia, said in a statement.

    “Our investigation shows that cannabis use remains common among this population, but it may not be an effective long-term strategy for reducing opioid use,” he added.

    Recent studies show the vast potential of cannabis in the fight against the opioid epidemic that continues to ravage the U.S.

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    Benjamin M. Adams

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  • Access to CBD Leads to Decrease in Opioid Prescriptions, Study Shows | High Times

    Access to CBD Leads to Decrease in Opioid Prescriptions, Study Shows | High Times

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    A recent report published in the Southern Economic Journal on Oct. 26 found evidence that legal access to CBD has helped lead to a decrease in opioid prescriptions.

    A study called “CBD as a cure-all? The impacts of state-level legalization of prescription cannabidiol (CBD) on opioid prescriptions,” was authored by economists associated with South Carolina-based Wofford College, and California State University Bakersfield. “We find that the ability to purchase CBD legally leads to 6.6% to 8.1% fewer opioid prescriptions,” the authors stated.

    Researchers make it clear that it wasn’t just CBD legalization that led to opioid prescription reduction, but that of legal access to CBD products. “In general, we find that state level legalization of CBD products only leads to a statistically significant reduction in opioid prescriptions when states also allow for open and legal dispensaries, suggesting that adequate supply-side access is necessary to realize the potential benefits of legalization,” authors wrote.

    The report stated that stores selling CBD help decrease opioid prescriptions by 3.5% just two years after legalization goes into effect. It’s not the same for every state though, as this statistic varied for states with stricter regulations on CBD sales, including the requirement that people provide their ID or submit their personal info to a registry. “…(i) state legalization of prescription CBD alone does not reduce opioid usage; (ii) regulations limited purchasing, such as ID laws, negate nearly all of the benefits of demand-side legalization; and (iii) supply-side access, either via interstate purchasing or legal and open dispensaries, are vital in using pain-management substances to fully combat the opioid epidemic.”

    “Our paper provides important preliminary evidence that CBD may in fact reduce opioid prescription rates,” the authors said. “While CBD products may not necessarily be the cure-all they are marketed as, they do appear to be net substitutes for opioids.”

    The authors examined individual state laws and regulations specifically focused on CBD, such as Iowa, Tennessee, and Texas, between 2010-2019. During that window, there was a significant shift in CBD as an accepted and mainstream product. “Although the fastest growing segment of the CBD market is over-the-counter [OTC] usage, the vast majority of states that have established industrial hemp programs did not do so until 2016, meaning that OTC CBD products were largely unavailable until later in our study period.”

    They also examined Centers for Disease Control and Prevention (CDC) data for opioid prescriptions on a county level, but noted that it suggests “…that further research on the impacts of CBD is warranted.”

    The 2018 Farm Bill transformed the hemp industry in the U.S. Prior to the passage of the bill though, access was more limited. As time passed, states such as Tennessee decided to permit legal importation of CBD products from outside the state in 2016.

    The authors explained that while opioid prescriptions were reduced in those CBD-only states, the states that also allowed medical marijuana laws (MMLs) and/or recreational marijuana laws (RMLs) still made more of an impact on opioid prescription reduction. “Compared to states with no legal usage of marijuana, those who have adopted MMLs or RMLs prescribe fewer opioids per 100 population. However, these areas tend to be healthier and have more doctors, suggesting it is possible difference in opioid usage rates are not due to the presence of legal marijuana.”

    A state with a variety of CBD-only dispensaries appears to lead to the most significant drops in opioid prescriptions though. “Importantly, we see that [states with] CBD laws have lower opioid prescribing rates than states with no laws, though still higher than in states with MMLs or RMLs,” However, when we look at states that have allowed CBD dispensaries, we see that opioid prescribing rates are lower than those found in states with MMLs or RMLs, even with similar objective health measures (obesity and diabetes) to states with CBD laws.”

    Medical cannabis states experienced a 35% decrease in opioid prescriptions, but states that have not yet legalized still saw a decrease of 33%.

    Researchers concluded that their study is just a glimpse into the positive benefits of CBD and its effect on opioid prescriptions. “While further work is needed to understand the degree to which our results are generalizable to the over-the-counter market for CBD, our results suggest policy makers should consider the costs of regulation and carefully balance the tradeoffs between ensuring the quality of and restricting access to CBD,” authors said in their conclusion.

    In 2020, a former Drug Enforcement Administration (DEA) agent, Anthony Armour, who tried to swap opioids with CBD was fired from his position. Most recently in September 2023, the DEA defended its decision to fire the individual. “Mr. Armour argues that he ‘displayed negligence or poor decision-making,’ and DEA properly held him accountable for his poor decisions when they resulted in a verified positive drug test. DEA lost trust in Mr. Armour and properly removed him.”

    Separately, the DEA is currently considering recommendations from the Department of Health and Human Services. It’s uncertain if the agency will move forward to reschedule cannabis into a less restrictive category that shows medical value of the plant.

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    Nicole Potter

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  • Surprising Number Uses Marijuana To Not Get High

    Surprising Number Uses Marijuana To Not Get High

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    With Canada fully legal, 24 states in the US for recreational and 40 with medical, marijuana has gone mainstream.  A full 90% of people believe it should be legal in some form.  Is cannabis like alcohol and there for a good time, or are people truly using it for something else? The data say a surprising number uses marijuana to not get high, but to manage something medical.

    Part of the reason this number is significant is research has shown cannabis is no where near as addictive as opioids. North America is facing an unprecedented opioid crisis leaving cities big and small in a turmoil about what to do.

    According to a report from High Yield Insights, a Chicago-based consumer behavior research firm the numbers are intriguing.  States where recreational use has been legalized, nearly half (44 percent) of cannabis consumers are using cannabis for medical purposes, including for pain relief (69 percent) and sleep assistance (65 percent), and to manage anxiety (54 percent).

    In another study published in Psychopharmacology, the numbers are lower but significant. In  US legal–recreational states (34%) than US illegal states (23%), US legal–medical only states (25%), and Canada (25%). The most common physical health reasons include use to manage pain (53%), sleep (46%), headaches/migraines (35%), appetite (22%), and nausea/vomiting (21%). For mental health reasons, the most common were for anxiety (52%), depression (40%), and PTSD/trauma (17%). There were 11% who reported using cannabis for managing other drug or alcohol use and 4% for psychosis.

    Photo by Keenan Constance via Unsplash

    High Yield Insights shared medical marijuana patients are twice as likely to check CBD levels when they purchase cannabis, with 47 percent verifying CBD concentrations versus 25 percent of recreational users. Medical users also seek out more convenient and discrete ways to consume, such as edibles, topicals, oils and tinctures. Notably, medical users are twice as likely as recreational consumers to use topicals (22 percent vs 11 percent) and over three times as likely to use tinctures (17 percent vs 5 percent).

    Related: Cannabis Consumers Wean Off Of Booze, Over-The-Counter Drugs

    “The industry generally understands that the adult use consumer differs significantly from the medical user. We saw an opportunity to quantify this customer segment’s behaviors and preferences in a way to yield deeper understanding and reveal untapped market opportunities,” said Mike Luce, co-founder of High Yield Insights and a veteran in consumer and market research.

    “Flower will always play a significant role, but medical users are seeking solutions that feel familiar and accessible. With edibles, we’re seeing a demand for low- dose, fast-onset options that meet users’ needs for discretion and convenience. CBD-focused companies also have an opportunity for growth if aligned with medical cannabis users’ interest in what today are niche product forms,” Luce added.

    Several studies have demonstrated medical marijuana helps reduce the opioid dosage for patients undergoing treatment for non-cancer pain. More research can be done to legal the patients benefits.

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    Sarah Johns

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