#Walgreens settles allegations of violation of federal and state anti-kickback laws with FIFTY MILLION FINE

Walgreens settles over ‘savings club’ claim

http://myjournalcourier.com/news/105609/walgreens-settles-over-savings-club-claim

Normally violating Medicare/Medicaid anti-kickback laws results in a 5 yrs in prison and $25,000 fine for EACH VIOLATION… who at Walgreens is going to JAIL ?

Illinois has joined at least 30 other states and the federal government to settle allegations that Walgreen Co. unlawfully solicited and persuaded Medicare and Medicaid recipients to enroll in its “Prescription Savings Club” to gain more profitable customers.

Such a move would be a violation of federal and state anti-kickback laws, according to Attorney General Lisa Madigan.

Walgreen Co., headquartered in Deerfield, gave Medicare and Medicaid patients savings, coupons and other offers to join the company’s prescription savings club, which amounted to an unlawful marketing scheme, Madigan contends. Walgreens will pay the states and the federal government $50 million, of which nearly $8.5 million will go to state Medicaid programs. The remaining portion of the settlement is attributed to Medicare and Tricare programs.

Illinois will receive more than $740,000 in restitution and other recoveries from the settlement.

The investigation resulted from a false claims action originally filed in January 2012 in U.S. District Court for the Southern District of New York under the federal False Claims Act and various state false claims statutes.

Deputy Bureau Chief Heather Tullio D’Orazio with Madigan’s Medicaid Fraud Bureau led a National Association of Medicaid Fraud Control Units team that participated in the investigation and conducted the settlement negotiations with Walgreen on behalf of the states.

lack of sleep is making emergency medical services personnel “stupid, slow and dangerous”

Sleep deprivation contributes to medical errors, affects health care workers’ health

http://siouxcityjournal.com/lifestyles/health-med-fit/sleep-deprivation-contributes-to-medical-errors-affects-health-care-workers/article_ccf8f3d3-0e63-5e97-b028-544a8cbd936f.html

SIOUX CITY — Even on his days off, Ricky Osorio, a registered nurse who works in UnityPoint Health — St. Luke’s emergency department, struggled to fall asleep.

He’d drink hot decaffeinated tea, read a book, meditate and picture a beach in Mexico.

“I would lay there for hours,” said the 28-year-old Sioux City man, who is a member of the Army National Guard and a student finishing up his master’s degree. “It’s just really hard to adjust from working night shift to day shift. We work night shift, but the rest of the world operates on day shift.”

 

A growing number of health care workers are suffering from sleep deprivation and fatigue, according to a survey published in the journal Sleep in 2010. Thirty-two percent of health care workers reported getting six or fewer hours of sleep per day in 2007, up from 28 percent in 1985. Seven to nine hours of sleep is recommended daily for adults.

Heather Davis said sleep deprivation is ingrained into the culture of medicine. Davis, director of UCLA’s paramedic education program, will give a presentation about how a lack of sleep is making emergency medical services personnel “stupid, slow and dangerous” at the 2017 Emergency Conference, Feb. 24-25 at the Sioux City Convention Center.

After working a 24- or 48-hour shift, Davis said health care workers wear their tiredness and fatigue like a “badge of honor,” even though it contributes to medication errors that kill more than 100,000 Americans every year.

A 2006 National Academy of Sciences study found interns who worked just three hours more per shift committed 22 percent more critical errors, which result in increased morbidity and mortality, than their counterparts.

Davis said shift work and long hours combined with the desire to do more in less time is leaving nurses fatigued. Instead of going home and sleeping for seven or eight hours after their shift, she said they’re studying for classes, taking care of their kids and running errands. They’re also likely picking up more hours at work, as there’s a national shortage of nurses.

She said EMS workers make minimum wage, so they may have a second job to make ends meet. Rural areas are served by volunteer EMTs, who are on call at night and work another job during the day.

When his 4-year-old son was younger, Osorio didn’t have a day care provider. He would sleep just two hours before returning to work for another 12-hour shift. Approaching 3 a.m., Osorio said he could either be his normal happy self or a bit crabby.

“I’m usually pretty happy all the time now because I sleep a lot more,” he said. “We’ve got day care now, thank god. But still it’s hard managing.”

Davis said losing two hours of sleep a night over the course of two weeks is equivalent to being awake for two days. She said a person could recover from such a sleep deficit if they started getting adequate amounts of sleep again.

 

“If it was just the holidays where you were so busy, you would recover from that,” she said. “The problem is, for folks who work in health care, it’s not just the holidays. It’s all the time, so they’re chronically sleep deprived.”

People who are sleep deprived feel drained and sluggish. They suffer from muscles aches, exhibit crankiness and become easily frustrated. Their decision-making and impulse control are also affected. Researchers at the University of Warwick linked sleeping for less than six hours a night to an increased risk of dying from a heart attack or stroke.

Davis said norepinephrine — the neurotransmitter most involved in “fight or flight” — is chronically being released in the bodies of the sleep deprived, raising their blood pressure and heart rate.

She said sleep deprivation also takes a toll on the endocrine system, increasing inflammation in the body and the stress hormone cortisol, which ramps up appetite and leads to weight gain.

a critical element of Humana’s strategy going forward… with 500 FEWER EMPLOYEES?

Humana to lay off 500 home-care workers in Ohio and Florida

http://www.modernhealthcare.com/article/20170209/NEWS/170209906?

Humana will lay off about 500 employees in Ohio and Florida who work in the insurer’s home healthcare division.

Employees were notified on Feb. 1, Cincinnati.com reported. The layoffs will take effect April 3.

Kate Marx, a Humana spokeswoman, said the layoffs weren’t related to the insurer’s recently blocked mega-merger with Aetna.

Louisville, Ky.-based Humana Wednesday reported significant losses for its fourth quarter of fiscal year 2016. It recorded a loss of $401 million for the quarter, and $614 million in profit for the full year 2016, down from $1.3 billion in 2015.

The insurer’s Humana at Home unit employs support staff to help customers transition from an inpatient stay to their home.

Eighty-eight of the employees laid off are based in Ohio, and the remaining work in Florida. Some of them may be eligible for new roles with Humana, Marx said.

The unit launched eight years ago, and Marx said it remains “a critical element of Humana’s strategy going forward.”

Dying patients have Pence’s backing on ‘right to try’ policy

Dying patients have Pence’s backing on ‘right to try’ policy

http://www.enewscourier.com/cnhi_network/dying-patients-have-pence-s-backing-on-right-to-try/article_2a797621-fab0-5044-a511-bd8b40068ccd.html

Just don’t expect PENCE to support the pt’s right to pain management

Vice President Mike Pence may have just picked another fight with pharmaceutical companies — one that doesn’t involve drug prices.

 Pence is pushing for legislation that would give terminally ill patients expanded access to experimental drugs that haven’t been approved yet but have made it through the first of three approval phases.

The vice president had championed the so-called right-to-try issue while governor of Indiana and later on the campaign trail. While dying patients may be willing to try anything, wider access to unproven treatments may give them no more than false hope, opponents to the proposal say. And if patients have adverse reactions, that may put a premature halt to the clinical trials necessary to show drugs’ effectiveness.

Drugmakers have resisted providing experimental medications under state right-to-try laws that have been passed in more than half of the states, including Indiana.

In a private meeting with advocates Tuesday afternoon, Pence reaffirmed his support for national legislation, said Laura McLinn, an Indiana resident whose eight-year-old son has a deadly disease known as Duchenne muscular dystrophy and was the face of right-to-try efforts in Indiana.

“He also let us know that he and President Trump have had multiple conversations about this and it’s something the president is very passionate about,” McLinn said on Wednesday in a call with reporters that was set up by the Goldwater Institute, a group advocating limited government that has pushed for right-to-try laws. The White House confirmed her account of the meeting.

Access to experimental drugs is a thorny topic that has raised ethical questions, pitting stricken families’ desperation versus the risks of hurting, or even killing patients, and having to shut down clinical studies that could have benefited others.

The Food and Drug Administration has a system in place that has authorized doctors to give experimental treatments to thousands of patients on a case-by-case basis, with the manufacturer’s approval. Existing right-to-try state laws bypass FDA scrutiny as long as the drugs have completed early safety tests. Yet drugmakers don’t like leaving the FDA out of the equation. They don’t have to provide the medication under right-to-try regulations and they often decide not to.

“Any legislation should protect the integrity of clinical trials and the FDA oversight of expanded access to maintain the best interests of patients,” the Pharmaceutical Research and Manufacturers of America, the Washington lobby group for drugmakers, said in an emailed statement. “Because investigational medicines have not been approved by the FDA and determined to be safe and effective, FDA must approve expanded access to an investigational drug before a biopharmaceutical company can provide it to a patient.”

Opponents say experimental drugs can in some cases do more harm than good, even for patients who are already terminally ill. In addition, they and their families may need to pay for the drug out of pocket because insurance wouldn’t cover an unapproved treatment.

“These drugs are not benign,” Rebecca Dresser, a biomedical ethics law professor at Washington University School of Law in St. Louis, Missouri. “We don’t hear the stories of cases where people tried drugs and experienced bad side effects so that their remaining lives were much more difficult — full of pain and suffering — than they would have been if they hadn’t tried the drug.”

Sen. Ron Johnson, a Wisconsin Republican, introduced right-to-try legislation last month that would allow patients access to experimental medications if they have a certification from their doctor and have tried or don’t qualify for all other treatment options.

Federal legislation is needed to reinforce state laws, McLinn said. Her son, Jordan, hasn’t been able to gain access to the only approved treatment for Duchenne, Sarepta Therapeutic Inc.’s Exondys 51, because he has a different mutation causing the disease.

The FDA referred right-to-try questions to the White House. Peter Lurie, FDA’s associate commissioner for public health strategy and analysis, testified last year before a Senate committee on access to experimental drugs for terminally ill patients.

“Even patients with serious or life-threatening diseases and conditions require protection from unnecessary risks, particularly as, in general, the products they are seeking through expanded access are unapproved — and may never be approved,” Lurie said at the time.

The FDA has authorized 99 percent of the 7,176 requests it received for single-patient access to experimental drugs in the fiscal years 2010 to 2015, according to Lurie’s September testimony. The FDA also attempted to make it easier for physicians to apply on behalf of their patients for experimental drug access. The process takes about 45 minutes, Lurie said.

WIS: meth epidemic amid concerns for children

State, federal officials warn lawmakers of meth epidemic amid concerns for children

wbay.com/2017/02/09/state-federal-officials-warn-lawmakers-of-meth-epidemic-amid-concerns-for-children/

MADISON, Wis. (WBAY) – Our state’s meth problem is worse than the opioid epidemic in some parts of Wisconsin.

That bold statement came from Attorney General Brad Schimel Wednesday during a hearing before lawmakers in Madison.

It’s the beginning of what may be a big shift of attention on methamphetamine, from state and federal drug agents, in the coming months.

The Department of Justice says new funding is coming to the meth fight.

It’s pictures of a nursery and other rooms in a home where children appear to live that are likely to invoke anger and sadness.

Assistant Special Agent in Charge Robert Bell, from DEA Milwaukee, shared the photos during an informational hearing before the Senate Committee on Judiciary and Public Safety and Assembly Committee on Criminal Justice and Public Safety.

“In the photo to the right you see a crib, on the dresser, you see what’s probably finished methamphetamine because you see a scale there,” explains Bell.

“In the lower left picture, you actually see a baby in the crib with substances hidden under the mattress.”

Schimel, along with agents from the FBI, DEA and the Wisconsin Department of Justice, Division of Criminal Investigation spent two and a half hours testifying before lawmakers, sharing their biggest worries about the explosion of meth.

“We’re also finding with users that smoke methamphetamine, that residue goes throughout their residences. And especially if they have children, that sticks to carpets, toys, furniture,” says FBI Special Agent in Charge Justin Tolomeo.

“So you’re seeing an uptick in children that are showing meth use.”

“Human services agencies in the state are reporting that in the meth-affected counties, they’ve seen dramatic increases of out-of-home placements of children due to neglect and abuse driven by meth abuse by a parent,” says Schimel.

While Action 2 News has been reporting on the surge in meth in this area for nearly two years, one question always comes up. Why meth? Especially seeing the physical consequences of using it.

Treatment providers told lawmakers, based on what addicts tell hem, some users turn to meth to lose weight or have more energy to get things done.

“There’s actually, in some areas, where drug dealers are getting free samples. They’re using heroin. They’re using opioids. Well here’s some meth, too” says Sheila Weix, Director of Substance Abuse Services for Family Health Center, Marshfield Clinic.

In response, Schimel says Wisconsin was just awarded a $1.5 Million dollar federal grant from the 2016 Cops Anti-Methamphetamine Initiative Task Force Program. He says Wisconsin’s grant is the largest in the country, and will be used to pay for officer overtime and equipment used in meth-lab related investigations.

Schimel also says there is money in the governor’s proposed budget for an educational campaign on meth, similar to current ones on opioids.

But half the battle is helping those currently addicted.

“We need to develop system where when people need treatment, they can get in. Right now, that doesn’t exist,” says Weix.

Lawmakers say they will look into ways to address these concerns in the coming months

Marijuana Today: Sen. Jeff Sessions confirmed

Marijuana Today: Sen. Jeff Sessions confirmed

Plus, pot slows brain cancer; and the weed gender gap is closing; …

http://www.sfgate.com/news/article/Marijuana-Today-Sen-Jeff-Sessions-confirmed-10920803.php

TOP NEWS
Sen. Jeff Sessions was confirmed in a split 52-47 vote yesterday.
 
 … Here’s what I think you can count on: Jeff Sessions is going to do his worst. But, if history is any guide, it will matter little. … Sessions has a bb gun, and he is shooting at a glacier.
 
This former DEA agent understands. It’s a resources game. Sessions has 5,500 DEA agents, and a couple billion dollars in budget. But only a fraction of that can go to cannabis. Meanwhile, 21 percent of the U.S. population is in a legalization state; about 76 million people; the industry employs 122,000 people; and is worth maybe $50 billion per year in total retail sales alone.
 
Remember — President Obama spent hundreds of millions of dollars interfering in state-legal medical cannabis systems. His DOJ attacked the best, brightest, most state-legal actors, in order to make the point that no one was safe from federal law. And what happened? The California crackdown of 2011 engendered a backlash that drew in unprecedented new allies. Cannabis will have even more this time. 
 
Mark my words — there will be raids, forfeiture threats, regulatory intimidation, propaganda, new sentencing, everything that happened under President Obama. And if the People are more upset about it than ever — then the people will win, again.
 
More on that thread: “John J. Hudak of the Brooking Institute, last weekend at the Virginia Cannabis Conference, explained how ‘you’re insane‘ if you think the marijuana industry is too big and popular to be a target of Republican wrath”.
 
Meanwhile, the MPP is “cautiously optimistic”. The NCIA said “We look forward to Attorney General Sessions maintaining …[the status quo]”… TheDCMJ is “hopeful”. … NORML said “we will never stop fighting.” … And theDPA said attacking pot will leave Trump and Co. “even less popular than they are now.”
 
OTHER BIG NEWS
Yup, pot helps treat brain cancer. … GW Pharma is almost done bottling it up.
 
Nevada is set to kick California’s butt in the race to implement recreational. … They’re going to do temporary regulations by July.
 
There might be almost 300 pot-related patents already on the books.
 
The L.A. Times endorses Measure M to catch the city up to where San Francisco was in 2005 — you know, actually regulating dispensaries.
 
Weed app data shows the gender gap closing, and cannabis replacing alcohol.
 
JUST A BILL ON CAPITOL HILL
Congressional bill HR 715 would legalize CBD.
 
Another bill would shield state-legal pot activity from federal drug laws.
 
HIGHLY DUBIOUS
There is something deeply wrong in the Personnel Review Board of Orange County, CA.
 
MEDICINE
pot for PTSD trial gets underway, via Army Times.
 
SURPRISING DISCOVERIES
Style brands Vanderpop and Tokyo Smoke merge.
 
Moxies Meds makes it into Cosmo Mag.
 
High Times out-Cosmos Cosmo with ‘How To Make Weed Lube for V-Day’.
 
The inventor of Ganga Yoga is throwing an Easter retreat to Yosemite.

And Puff, Pass, and Paint comes to San Francisco.

When you dig down “into the weeds”

Appeals Court Keeps Block on Trump Immigration Order in Place

http://abcnews.go.com/Politics/appeals-court-deliver-ruling-trump-executive-order/story?id=45386342

While this may appear way off topic for my blog… please follow the logic..  These judges would not reinstate the ban because it was determined – by them – that a certain group of people were being discriminated against because of their religion…

Could this logic be extended that the passage of the CDC opiate dosing guidelines and various states that have passed similar laws… be a discrimination AGAINST a group of HANDICAPPED PEOPLE  – covered by the ADA ?… and thus ILLEGAL..

But even though our President is the final authority on laws being enforced or not… but .. in this particular incident… a single person – a judge – in the  judicial district that has a history of having the most ruling being over turned on appeal.  So they whole issue will go back to the court system to be determined.

This is just an example of how our judicial system is not always “just” and does not always follows the letter of the law… It could also be a good example for the chronic pain community to unite … develop a “legal war chest” to challenge the constitutionality of many of the laws that are harming those in the chronic pain community.

Those who pass rules/laws/regulations/guidelines… have no mandate that what they pass … is in fact constitutional… they pass it… and it is up to those being affected/harm to take the bureaucracy to court to prove that they have exceeded their authority and their actions are unconstitutional.

A panel of federal appeals court judges ruled to keep a restraining order against Donald Trump’s controversial immigration action in place, according to court documents.

“We hold that the Government has not shown a likelihood of success on the merits of its appeal, nor has it shown that failure to enter a stay would cause irreparable injury, and we therefore deny its emergency motion for a stay,” the panel, from the 9th Circuit Court of Appeals, wrote in the decision Thursday.

The three-judge panel heard arguments from a lawyer representing the state of Washington Tuesday who argued that the executive order — which temporarily halted immigration from seven predominantly Muslim countries in the Middle East and Africa and temporarily shut down the refugee program — discriminated on the basis of religion among other claims.

Department of Justice lawyers claimed that the order was made on national security grounds and that Washington District Court Judge James Robart’s issuance of a temporary restraining order pausing the ban nationwide was “overbroad.”

Trump unleashed a series of attacks on Robart following the judge’s initial decision to interrupt his order last week. On Twitter, the president called Robart a “so-called judge,” said his decision was “ridiculous and will be overturned,” and added that “[i]f something happens blame him and court system.”

Those comments were later condemned by members of both major political parties. Trump’s Supreme Court nominee Judge Neil Gorsuch classified Trump’s criticisms of the judiciary as “demoralizing” and “disheartening” in conversations on Capitol Hill, according to a spokesman, but the White House insisted he was not referring to a specific case.

The administration has denied that the order is a Muslim ban.

Where health is EVERYTHING… RPh didn’t get that memo ?

I’m a 57 year old disabled man. I have been going to CVS STORE #2990 here in Las Vegas, NV for over 4 years with no problems what so ever. On the 8th of February I went to CVS to fill my prescriptions at which time was accepted and I was told to come back in two hours.  Express leaving a new pharmacy manager came up named jerry that I never seen stated that he doesn’t feel comfortable filling my prescriptions and to go elsewhere. This man had a smile on his face and was taking his time giving me back my prescriptions so I could leave and every time I would ask he would chuckle and say no. This man made copies of my prescriptions stopped in front of me with a smile on his face and with my prescriptions and copies of my prescriptions said no when I asked why can’t you just use the copies ? I became very upset and scared. Being disabled and on social security I didn’t know where to go because of the actions of the predigest pharmacy manager that I never had seen in my over 4 years of never having a problem with. I called the corporate office at 1800cvs pharmacy and all I got was a “we will talk with him”. This manager stated that I was never allowed in ANY CVS and that he was going to notify the state about my abuse of my medications. I informed him that my prescriptions where for the 8th of February as stated on my prescriptions at which time he stated I was always coming in early and he could refuse anyone at any time. I had gone to 6-7 other pharmacies who stated no and the only one who would I had to wait tell the 10th. As of today’s date I have been unable to take my medication and have had several seizures I feel very depressed and unable to function properly and I’m in so much pain right now that I cry and get angry that this pharmacy manager purposely caused this.

 

Here is my response to this abused/discriminated pt:

           Pharmacist Jerry … gets paid every week.. regardless if he fills your prescription or not..  and from what I have heard back from other pts.. the major chain stores.. could care less.

I would suggest that you contact a local independent pharmacy.. here is a website to help you find one by zip code http://www.ncpanet.org/home/find-your-local-pharmacy

 

I ran the zip code of 89108 and it shows 40 stores within 10 miles…

 

You will be dealing with the Pharmacist/owner… who depends on filling legal prescriptions to put bread/butter on his/her table and will not start first looking for a reason not to fill your prescription(s)… Like Pharmacist Jerry did.  I would suggest that you have a talk with the Pharmacist/owner at the independent and tell them that you are willing to transfer all your prescription business to them… presuming that they will not “play games” on your refill dates.

 

Presuming that you can fine a pharmacy… ask the pharmacist about syncing up all your refills so that you will be getting all your Rxs filled on the same day each month… will be able to save you a lot of time/trouble over the long run and most independent pharmacies are more than happy to do so.

 

http://bop.nv.gov/Services/complaint/

Here is the complaint form for the NV board of Pharmacy… file a grievance with the BOP… since you have been patronizing the pharmacy for some time.. there should be little reason for the pharmacy/Pharmacist to reject your medications to be filled. The store has a PIC ( Pharmacist in charge) who is responsible for the legal operation of the Rx dept to the BOP… if Jerry is not the PIC.. file the grievance against Jerry, the PIC, & CVS (permit holder).. your grievance should be “denial of care”, pt/senior abuse, intentionally throwing a pt into cold turkey withdrawal, medical battery

 

I presume that you are on Medicare/Medicaid/Medicare Advantage… suggest that you file a grievance with that entity against CVS for failing to honor their contract – to fill legal/medical necessary Rx – with the insurance company.  If the insurance company refuses to do anything… then you need to file a grievance with

 

www.cms.gov (800-MEDICARE)… even If the insurance company does something positive… I would still file a grievance against CVS with CMS (Center Medicare & Medicaid Services)

 

You may also want to file a grievance with https://www.ada.gov/filing_complaint.htm because it is consider a civil rights violation of the American’s with Disability Act for discriminating against disabled pts… for refusing to fill a legit/on time/medically necessary prescription.

 

Take care of yourself first, by finding a independent pharmacy to take care of ALL YOUR MEDICATIONS… because all those entities that you will be filing a grievance with… will move at the speed of cold molasses

 

Tell your story abt being harmed by CDC opiate guidelines…

Calling all chronic pain warriors who have been hurt by the CDC’s guidelines for PCP’s. Many states are making laws & our pain management practices are doing us harm. Please send your stories to Sherman.sherry224@comcast.net. I’m meeting with representatives on 2/28 & leaving 2/27 for hotel. I’m asking for personal stories from all who’ve been affected including your friends, significant other & all who have been affected. Please title it “CHRONIC PAIN STORY.” We must be heard & this is the time to have our voices heard. Thank you

Per Forrest Gump: Stupid is as stupid does

Georgia bill would require new ADHD prescriptions every 5 days

(CNN)A bill meant to curb the abuse of prescription opioids in Georgia has stirred outrage in the ADHD community because a provision requires adults and children on medications for attention deficit hyperactivity disorder to get new prescriptions every five days.

“It’s clearly a cause for concern,” said state Sen. Nan Orrock, an Atlanta Democrat who wants the provision struck from the bill. “The argument is pretty hard to debunk: that families coming in every five days for ADHD prescriptions is impossible. There’s just a panic list of questions this creates.”
News of the measure spread rapidly across social media on Tuesday after a post from a parent about the restrictions on medications for ADHD was shared on Facebook.
“What I understand is that, if this bill passes, prescribers will only be able to write 5-day prescriptions and will have to review their patients in a database every 90 days. That would require getting a new prescription weekly,” said the post, which was widely shared.
In this era of rapid-fire “fake news” posts, it seemed almost absurd.
But it is true. “Every five, days the patient would have to come back in,” said Orrock, a member of the Georgia Senate’s Health and Human Services Committee, which held a hearing last week to receive input on the bill. “That’s absolutely what would happen if that bill became law in its current form.”
Across Georgia, doctors, state senators and advocates for people with ADHD began fielding a flood of phone calls. Their inboxes filled with questions about the bill, known as SB 81 (PDF), and worried parents sent messages over social media.
The bill is meant to curb the abuse of prescription opioid painkillers, such as OxyContin and Vicodin. It was drafted by Sen. Renee Unterman, a Republican committee chairwoman from the suburbs of Atlanta, in an effort to stop the state’s growing opioid epidemic.
It would allow over-the-counter sales of an opioid blocker called naloxone, an emergency medicine that can save people from dying during an overdose. The bill also allows doctors to see whether a patient has recently received an opioid prescription, allowing them to determine that patients are going from doctor to doctor.
“What it does is prevent doctor-shopping. It prevents these legal drugs from becoming street drugs and sold at exorbitant prices,” Unterman told The Telegraph newspaper in Macon, Georgia.
Unterman has not responded to CNN’s request for comment.
The controversial provision of the bill deals with the limiting of doctors’ ability to write prescriptions on controlled substances to only five days. The main medications to treat ADHD, such as Adderall, Ritalin and Vyvanse, are listed as Schedule II drugs, and the bill makes no exclusions for those with ADHD.
Although the loudest outcry came from the ADHD community, the bill would also apply to other vital medications, including some used to treat seizures, that are listed as controlled substances. Patients have been taking many of those medications for years, and there are already strict measures for getting refills.
The bill does make exceptions for medications “necessary for palliative care or to treat a patient’s acute medical condition, chronic pain or pain associated with a cancer diagnosis.” In those cases, the prescriber must “indicate that an alternative to such controlled substance was not appropriate to treat such medical condition.”
Dr. Jennifer Shu, an Atlanta-area pediatrician, said the bill lumps ADHD medications “in with opioids, which are the main concern of the bill.”
“I would hope that the legislators focus strictly on the narcotics and not on ADHD medications if they pass such a law,” Shu wrote in an email.
Elaine Taylor-Klaus, who helps coach parents of children with ADHD and runs the counseling and education company ImpactADHD.com, had never heard of the provision until Tuesday, when the social media post made the rounds and she was hit with a deluge of people seeking guidance.
“My Facebook Messenger blew up,” she said.
Addicted? How to get help

If you’re addicted to prescription drugs, help is available. You can call the Substance Abuse Mental Health Services Administration 24/7 hotline at 1-800-662-HELP(4357) or visit their website.

Taylor-Klaus advocates across the nation to educate people about ADHD, but even she was surprised by the provision. She credited the social media post with raising awareness and rallying the community.
She said she immediately called her legislators to find out the details of the bill and was assured that there is “some awareness of the problem” of the provision and that changes will probably be made.
“I hadn’t heard about (the provision) because there’s no organization specifically focused on ADHD that’s advocating and lobbying on a local level,” she said. “Unless there’s somebody watching out very closely, this is one of those obscure pieces of legislation that could pass through quite easily without anybody realizing what the full implications are.”
She noted the irony of the measure: The bill would require new prescriptions weekly, but people with ADHD struggle with organization skills.
“Not only would it be impossible for a family to manage,” she said, “but it would be impossible for a physician’s office to manage that kind of onerous requirement.”
Orrock, the Democrat seeking changes to the bill, said she’s confident the measure will be revised. However, she hasn’t seen a new bill yet. She said she hopes a revised version is presented Thursday, when the committee meets again.
“There’s nothing close to look at yet,” she said. “The work is still going on.”
Join the conversation

See the latest news and share your comments with CNN Health on Facebook and Twitter.

Efforts to get comment from several Republicans on the Health and Human Services Committee, including Vice Chairman Dean Burke and Bill Cowsert, were unsuccessful.
Tom Krause, Cowsert’s chief of staff, said the state senator is closely “monitoring” the progress of the bill. He added that Unterman is working with two senators who are physicians and has said she “expects changes to the legislation.”
“Sen. Cowsert said it would be premature to comment on SB 81 until after he sees the changes,” Krause said.