CBD Oil Benzo Withdrawal

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Successful withdrawal from high-dose benzodiazepine in a young patient through electronic monitoring of polypharmacy: a case report in an ambulatory setting Dependence on high-dose Xanax (benzodiazepine) addiction is a major problem worldwide. Many people are starting to turn to CBD as a means of weaning themselves off benzodiazepines.

Successful withdrawal from high-dose benzodiazepine in a young patient through electronic monitoring of polypharmacy: a case report in an ambulatory setting

Dependence on high-dose benzodiazepines (BZDs) is well known and discontinuation attempts are generally unsuccessful. A well established protocol for high-dose BZD withdrawal management is lacking. We present the case of withdrawal from high-dose lorazepam (>20 mg daily) in an unemployed 35-year-old male outpatient through agonist substitution with long-acting clonazepam and electronic monitoring over 28 weeks.

Methods:

All medicines were repacked into weekly 7 × 4 cavity multidose punch cards with an electronic monitoring system. The prescribed daily dosages of BZDs were translated into an optimal number of daily tablets, divided into up to four units of use. Withdrawal was achieved by individual leftover of a small quantity of BZDs that was placed in a separate compartment. Feedback with visualization of intake over the past week was given during weekly psychosocial sessions.

Results:

Stepwise reduction was obtained by reducing the mg content of the cavities proportionally to the leftovers, keeping the number of cavities in order to maintain regular intake behavior, and to determine the dosage decrease. At week 28, the primary objectives were achieved, that is, lorazepam reduction to 5 mg daily and cannabis abstinence. Therapy was continued using multidrug punch cards without electronic monitoring to maintain the management system. At week 48, a smaller size weekly pill organizer with detachable daily containers was dispensed. At week 68, the patient’s therapy was constant with 1.5 mg clonazepam + 5 mg lorazepam daily for anxiety symptoms and the last steps of withdrawal were started.

Conclusions:

Several key factors led to successful withdrawal from high-dose BZD in this outpatient, such as the use of weekly punch cards coupled with electronic monitoring, the patient’s empowerment over the withdrawal process, and the collaboration of several healthcare professionals. The major implication for clinical care is reduction by following the leftovers, and not a diktat from the healthcare professionals.

Keywords: addiction, benzodiazepine, community pharmacy, electronic monitoring, multidrug punch card, printed electronics, substance withdrawal

Introduction

Benzodiazepines (BZDs) are psychoactive drugs prescribed as anxiolytics, sedatives, hypnotics, anticonvulsants, and skeletal muscle relaxants since the 1960/1970s. 1 Due to their wide range of action and their low toxicity compared with other drugs, BZDs became one of the most commonly used and misused drug classes worldwide. 2 For Switzerland, a national pharmacy claims analysis 3 performed in 2006 calculated a 1-year prevalence for BZD prescriptions of 14.5%, similar to other countries. 4 –6 In the same study, 56% of patients obtained repeat BZD prescriptions for a treatment duration exceeding 90 days. 3 In 2014, among the general Swiss population, 253,000 citizens were using BZDs as tranquilizers or for sleeping problems, mostly in women aged over 70 years. 7

BZDs are potentially addictive. The most widespread form of BZD dependence is iatrogenic, that is, patients have been prescribed BZDs to treat underlying conditions 8 and then progress to long-term use (>4–8 weeks) with optional dose increase. In 2014, the Swiss Federal Office of Public Health published recommendations for restricted prescription and dispensing of BZDs in daily practice. 9 However, prescription habits do not seem to have changed yet. 10

The overall objective of BZD withdrawal consists of total abstinence, as discontinuation mostly improves psychomotor and neurocognitive functioning, particularly in older people. 11 A slow dose reduction is recommended 9 but guidelines are imprecise. Strategies include gradual dosage tapering and psychosocial support 12 after switching to an equivalent dose of a long-acting BZD [such as diazepam (Valium, Roche Pharma Schweiz) or clonazepam (Rivotril, Roche Pharma Schweiz)]. Agonist replacement therapy with the BZD clonazepam is a safe and efficacious method. 13 After discharge, the common recommendations for tapering in outpatients is a slow decrease over several weeks 14 but the optimal rate of tapering is unclear. Weekly reductions are proposed over 4–10 weeks; they should not exceed 25% per week 15 or be 10–25% of the dose that had been previously taken 16,17 or 10% every 1–2 weeks. 18 Outpatient withdrawal has proven feasible. 19,20 The success of pharmacological interventions for BZD dependence management is poor to moderate. 21 Nevertheless, the outcome of successful BZD withdrawal is gratifying, both in terms of improved functioning and economic benefits.

To our knowledge, there is no well established protocol for high-dose BZD withdrawal management. In a qualitative study of patients’ views on high-dose BZD withdrawal, patients frequently reported that they were unable to take their medication as prescribed during the process of slow dose reduction. 22 The complicated and unpredictable perception of the withdrawal was the trigger for high rates of unsuccessful discontinuation attempts. This situation caused a vicious circle for the patient of personal frustration, disappointment and dissatisfaction that often led to a decision to enter inpatient treatment, which, at the same time, was perceived as limiting personal freedom making it harder to overcome the dependence. Interventions able to increase patients’ freedom, autonomy and motivation seem crucial to help them attain their goals in outpatient settings. However, treatment retention is poor and long-term abstinence is rare in most patients. 14

The new technology used in this study 23 enables the electronic monitoring of individualized polypharmacy. The Polypharmacy Electronic Monitoring System (POEMS) is composed of printed electronics in a clear, self-adhesive paper film that can be affixed together with a chip on the back of a multidose punch card (also termed ‘multicompartment compliance aids’ or ‘dose administration aids’). This blister-type repackaging storage system is prepared in community pharmacies for organizing solid drugs prescribed to an individual, usually for 1 week. 24 The loops of conductive wires measure the electrical resistance and record the time of its changes when a loop is broken, that is when a cavity is emptied and medication is taken. The data are transferred via a wireless communication device to a web-based database.

In a prior study, patients reported that the visualization of the electronically recorded medicine intake that was used during the feedback sessions helped them to gain self confidence. 25 We present an illustrative case of withdrawal from high-dose BZDs with electronic monitoring of polypharmacy and corresponding feedback in an outpatient setting using multiprofessional team care. This report does not require ethics approval according to Swiss law (declaration of good standing). The patient provided written informed consent before the study for publication of his history in a de-identified form.

Case description

Our patient is a single, 35-year-old, white man, with a university degree in law who has never been employed. He lives independently (and alone) in a one-room apartment in Basel. He is socially isolated and gets social welfare. He has a longstanding history of misuse of cannabis and the BZD lorazepam for recurrent sleeping problems. He has been treated for depression with alternate use of escitalopram, trazadone and mirtazapine (strength unknown, start and length of treatments unknown) and stopped therapy because of marked side effects. The last episode of depression occurred in October 2014. The patient self medicated with lorazepam for anxiety and depression symptoms. He has bought lorazepam for years on the internet. During the past 12 months, his consumption has risen to 20–25 mg lorazepam daily. The patient has tried several times unsuccessfully to overcome his dependence and has developed subjectively strong withdrawal symptoms such as sweating, trembling and sleeplessness. After a further attempt to withdraw lorazepam that resulted in two consecutive sleepless nights, the patient was admitted to a psychiatric clinic on his own request on 18 December 2014 with the intention to reduce lorazepam and to withdraw cannabis consumption. He showed clearly depressive traits, inner anxiety and weak emotional tension, was worried about the future and reported inferiority feelings. His long-lasting unemployment bothered him. He had pronounced sleeping disorders with an inability to fall asleep. Standard medical and laboratory examinations did not show anything besides positive cannabis and BZD testing. During his hospital stay, clonazepam was titrated to reach 16 mg daily (4 – 4 – 4 – 4) with the aim of replacing lorazepam, to be subsequently reduced. Depressive symptomatology reached a mild expression (Beck Depression Inventory 26 score of 18). Because of negative experiences, however, the patient declined an antidepressant for his depression. Therefore, a combination of motivational interviewing and cognitive behavioral therapy was delivered in individual sessions in which problem behaviors and problem thinking were identified, prioritized and specifically addressed with a range of techniques. To enhance the patient’s motivation to change his BZD and cannabis use behavior, a decisional analysis was done whereby the patient was assisted to critically examine the advantages and the disadvantages of continued drug use. Furthermore, the patient was instructed in the use of substance-related coping skills. These included techniques for managing urges and cravings, recognizing triggers for drug use and developing personal strategies for either avoiding or dealing with such triggers, managing withdrawal symptoms, and learning relapse prevention strategies. The therapeutic program also instructed on general coping skills, including techniques for coping with negative affect and stress, assertiveness and communication skills training, and relaxation skills. Motivational enhancement therapy (that is motivational interviewing with among others the use of open-ended questions, reflective listening, affirmative style and setting goals) was the method of choice to enhance personal motivation. The patient actively took part in psychotherapy sessions. Cessation of cannabis smoking and its advantages were thematized simultaneously with BZD withdrawal at each session, comparable with a high-intensity intervention. 27 Urinalysis was not performed because verification is not judged compatible with the motivational nature of the behavioral therapy. Cannabis use was reduced from 12 to 3 joints daily. Complete withdrawal from cannabis and from lorazepam was not undertaken for fear of depressive episodes. The patient expressed the wish to continue to reduce lorazepam in an ambulatory setting and was ambivalent about quitting cannabis consumption. He was aware that entire withdrawal could take 1–2 years. The patient accepted a seamless referral to the Division of Substance Use Disorders. At discharge on 15 January 2015, the patient was prescribed clonazepam 15 mg daily (4 – 3 – 4 – 4) and lorazepam 5 mg in the evening. He agreed to meet weekly with a psychotherapist and to obtain 7-day rations of medication. During these weekly consultations, the patient reported having repeated cravings for lorazepam, mostly in the evening when he had thoughts about his unemployment and his future. He regularly takes 7.5 mg lorazepam to sleep. The clonazepam intake in the morning is erratic because of tiredness. The search for employment is impossible. On 12 February 2015, night-time urinary incontinence occurred which the patient attributed to clonazepam. Immediate reduction was self implemented within 1 week to clonazepam 8 mg daily and lorazepam 2.5 mg approximately 2 h after the last clonazepam intake. Incontinence and craving vanished. On 18 February 2015, the psychotherapist offered the patient the option of getting his medication in weekly multidrug punch cards with electronic monitoring so that he could visualize advances in the withdrawal process. The patient agreed to pick up his medication every week from the community pharmacy, immediately after his visit with the psychiatrist. The two buildings are 150 m apart. The pharmacist repackaged all the medication in a weekly punch card with 7 × 4 cavities and POEMS. The content of the cavities was discussed with the psychotherapist after each consultation. The prescribed daily dosages of BZDs were translated into an optimal number of daily tablets, divided into several units of use, and placed into the maximum number of punch card cavities. For individual reduction of the dosage, one small amount was stored separately to be taken on demand (see Table 1 ). The patient was advised to take his tablets at the time of his choosing. Parallel consumption was not controlled for, but specifically addressed during the weekly individual sessions with the psychotherapist. Cannabis withdrawal remained a primary goal.

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Table 1.

Two days of the regimen at week 20 (16–22 July 2015) with prescribed dosage of clonazepam (CLO) 4 mg daily + lorazepam (LOR) 5 mg daily plus one additional tablet of lorazepam 2.5 mg weekly, supplied as clonazepam tablets 2 mg (white tablet with cross-score break line; one in the first cavity) and 0.5 mg (beige tablet with breakbar; two in the first cavity and two in the second cavity), and as lorazepam 2.5 mg (yellow tablet with breakbar; two in the third cavity and one in the last cavity of the last raw).

CLO 1×2mg
+ 2×0.5mg
CLO 2×0.5mg
on demand
LOR
2×2.5 mg
LOR 1×2.5mg
on demand
Tuesday
21 July 2015
Wednesday
22 July 2015

Starting on 4 March 2015, a total of 196 days of therapy were dispensed in 45 electronic punch cards over 28 weeks until 16 September 2015, with two punch cards per week during the first 17 weeks. Fourteen days were not recorded due to technical problems (7.1% missed data). All dispensed punch cards were returned. During the weekly psychosocial sessions, graphs of the last week’s intakes were presented to the patient and discussed (see Figure 1 ).

Graphical representation of the intakes of week 20 (16 July–22 July 2015), filled with clonazepam (black circle), lorazepam (white circle). The white square indicates an additional lorazepam tablet (one per week); a larger circle indicates double intake.

Over the 28 weeks of monitoring, dispensed clonazepam was reduced from 8 to 2 mg daily. The amount of clonazepam taken was always less due to leftovers, beginning with doses from the fourth cavities [week 2–3 (2 mg daily), week 9 (1 mg daily); see Figure 2(a) ] to the second cavities [from week 20 onwards (0.5 mg daily)]. In parallel, the number of cavities with clonazepam tablets available decreased from three [week 9–15 (7–5 mg available)], to two [week 16 onwards (5–2 mg available)]. Clonazepam intake ended at 1.5 mg daily (80% reduction).

Mean weekly intake time of the content of the different punch card cavities filled with clonazepam (a) and lorazepam (b) over 28 weeks. The daily amount of benzodiazepine taken is indicated with a bold grey line. The four different cavities per punch card are marked with a bold line (first cavity —); spotted line (2nd cavity …); dotted line (3rd cavity –); double line (4th cavity ==). Standard deviations are given as half bars (minus for first cavities; plus for the other cavities).

One single daily dose of 2.5 mg lorazepam during week 1 turned out to be insufficient and dosage was tripled and distributed into three cavities for weeks 2 and 3 [ Figure 2(b) ]. The third cavity turned out to be superfluous and two cavities with one tablet of lorazepam 2.5 mg each were dispensed from week 4 onwards. Lorazepam was dispensed and taken in a similar pattern as clonazepam, and was reduced from 7.5 to 5 mg daily plus one additional tablet of lorazepam 2.5 mg weekly from week 10 onwards. At week 16, the patient achieved complete cannabis withdrawal on his own. At week 20, the patient found a job.

On 15 September 2015 (week 28) the patient ended with 6.5 mg BZDs daily and the primary objectives, that is lorazepam reduction and entire cannabis withdrawal, were achieved. Electronic monitoring was removed on the patient’s request but dispensing of therapy in multidrug punch cards was continued to maintain the management system. On 4 February 2016 (week 48), a smaller size weekly pill organizer with detachable daily containers was dispensed. On 15 September 2016 (week 80), mirtazapine 15 mg once daily in the evening was started. The patient’s therapy was constant with 1.5 mg clonazepam + 5 mg lorazepam daily for anxiety symptoms. At the time of writing this article (5 November 2016, week 90), the patient agreed to withdraw clonazepam and low-dose lorazepam within the next 6 months.

Discussion

In our exemplary case, the tapering speed was centered on the tablets the patient would and could intentionally leave over. To do so, the daily dosages of BZDs were divided into units of use with a small amount to be left over. Repackaging into multidose punch cards is the method of choice in this new approach. Further, immediate reinforcement is obtained at the sight of the leftover medication in its cavity in due course. The weekly psychosocial interventions included cognitive behavioral therapy by the psychiatrist and a brief intervention by the pharmacist each time the patient came in for his medication. The weekly feedback based on the intake graph enabled the psychiatrist to highlight and discuss deviant habits, to adjust treatment, to control the effect of the adjustment of the past week, to reinforce correct behavior and to continue dose reduction. 28 Our study indicates that a longer time span with weekly sessions including interventions with feedback may result in a successful reduction of BZDs.

Our patient reported that viewing his intake behavior made him aware of his dependence and he was able to gradually gain confidence in himself and in the intervention. Moreover, electronic monitoring was seen as the way to materialize the withdrawal steps and to obtain control over the process. Self confidence started a domino effect with positive thoughts and changed the patient’s behavior toward a high adherence to the withdrawal schedule, reduced cannabis consumption and conscientious search for employment. The patient did not feel controlled by the electronic monitoring, but much more supported and finally empowered to make informed decisions such as cannabis abstinence. Moreover, deciding when to take medicine, and when to leave medicine over, increased the patient’s autonomy, and is synonymous with empowerment. 29

Although our patient did not reach BZD abstinence after 28 weeks, our case is successful for several reasons. First, the switch from short-acting BZDs to a long-acting substance succeeded and was followed by a stepwise reduction, so that the total daily dose of BZDs could be reduced overall by 74% (from 125 to 33 mg, measured in diazepam equivalent). Second, the associated risk behavior such as cannabis consumption was diminished, and third, the burden of psychiatric symptoms was reduced so that our patient could find a job. Thus, after a phase of stabilization, the physician proposed tackling the next steps of further withdrawal, which was accepted by our patient after 90 weeks.

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We acknowledge some limitations. First, pocket doses, that is the removal of doses in anticipation of intake outdoors and without the punch cards, were taken. This was noted by three or more removals being recorded at the same time, predominantly during the first weeks of monitoring. No adjustments were made for pocket dosing since no information was obtained on actual intake. The analysis of the data without pocket doses did not change the results substantially, demonstrating their marginal effect on the overall results. Second, some cavities were filled with two or more tablets. When the patient left some of these tablets over, he placed the surplus back into the opened cavity. However, during transportation, some tablets could have been lost, masking untaken tablets. Third, as is true of any indirect method of adherence measure, electronic monitoring does not demonstrate ingestion of the dispensed medicine. However, exceptional and sustained commitment is required to create a false record of good adherence. 30 Thus, we can affirm that the doses were taken immediately after their removal, except for pocket doses.

Implication for clinical care

The success our patient achieved in withdrawing from high-dose lorazepam may be due to the multidimensional intervention composed of a new technology (electronic monitoring), several healthcare providers in collaboration (hospital and general physicians, psychiatrist, pharmacist) and the empowerment of the patient. The daily BZD dosages divided into portions and placed in the maximum number of cavities of a multidose punch card, with a small amount to be left over, allowed reduction of the doses without changing the dosing intervals, maintaining the intake habits and following the speed of the patient. When time is perceived as an empowering factor, successful withdrawal is possible. Because BZD misuse and dependence is widespread in the general elderly population, representing a public health problem, 31 our approach with repackaging of polypharmacy inclusive of BZD with subsequent slow tapering could constitute a novel and promising method. Further studies are needed in this area.

Acknowledgments

The authors wish to thank the staff of the pharmacy Apotheke Hersberger am Spalebärg for their support.

How People Are Kicking Xanax Addiction With CBD

Xanax (benzodiazepine) addiction is a major problem worldwide. Many people are starting to turn to CBD as a means of weaning themselves off benzodiazepines.

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Xanax is a brand-name anti-anxiety medication in the benzodiazepine class of drugs.

It is used to force the nervous system into a relaxed state — effectively stopping anxiety in its tracks.

The problem with benzodiazepines, in general, is that they’re highly addictive. After just a few weeks of use, people may become dependent on them. As soon as the effects wear off, the brain goes into a state of hyperactivation — resulting in severe anxiety attacks. This can lead to debilitating insomnia and emotional instability.

Because of the severe side effects, many people are trying to get off benzodiazepines but find it difficult because of their highly addictive nature. When the drugs disappear from the system, users can be faced with disabling anxiety attacks.

People are turning to cannabidiol (CBD) as a way to alleviate withdrawal symptoms while they reduce their dose of benzodiazepines. The goal is to stop using them altogether.

In this article, we’ll discuss how people are using CBD as an intermediary to wean themselves safely off benzodiazepines such as Xanax. We’ll talk about the promising research being done in this area and what it means for people hooked on anxiety medications.

Let’s get started.

Table of Contents
  • What are Benzodiazepines?
  • Problems with Benzodiazepines
  • Tips for Using CBD for Benzodiazepine Addiction

What are Benzodiazepines?

Benzodiazepines are a class of synthetic anti-anxiety medications.

This class of medications is used for treating anxiety disorders (such as social anxiety disorder, generalized anxiety disorder, and panic disorder) and insomnia.

Some of the most popular brands include Xanax, Valium, Klonopin, and Lorazepam.

Xanax is by far the most common. Recent reports suggest Xanax is the third most prescribed medication in the United States and one of the top 20 prescription medications sold on the black market globally.

Unfortunately, all benzodiazepines are highly addictive — causing tolerance and dependency on the drug in as little as two weeks of regular use.

List of Benzodiazepines

How Benzodiazepines Work

These potent pharmaceuticals work by modifying the GABA receptors in the brain to become more receptive to GABA. We use GABA to control our stress levels and brain activity. The best analogy for GABA is that it behaves like the brake pedal for the brain — slowing us down when we need to stop.

When GABA activity increases, it slows nerve transmissions in the brain — making us feel relaxed. This stops anxiety attacks in their tracks and calms us down enough to fall asleep.

Problems with Benzodiazepines

1. Addiction

Most people start taking Xanax or other benzodiazepines without expecting to become addicted. Doctors prescribe the medication in small doses for short periods to help people get through periods of severe anxiety. Benzodiazepines are also prescribed for periods of insomnia as they provide short-term relief.

The problem with this is that it only takes a few doses to cause addiction.

After just a few days, the body starts to resist the effects of the drug. It does this by changing the GABA receptors. As this change happens, users need to take higher doses of the drug to produce the same results.

At the same time, our natural GABA levels struggle as well. We can’t produce more GABA to make up for the tolerance, so, instead, we experience side-effects from the poor GABA function. The main side effect of this is the very thing the drugs were intended to treat — anxiety.

Benzodiazepine addiction is characterized by the onset of negative side effects as the drugs wear off. This is called withdrawal.

Withdrawal on benzodiazepines is extremely unpleasant. It includes symptoms such as:

  • Severe anxiety and panic attacks
  • Insomnia
  • Mood disturbances
  • Muscle tremors
  • Muscle pain
  • Suicidal thoughts
  • Nausea and vomiting
  • Sweating
  • Weight loss
  • Seizures
  • Death (with severe benzodiazepine addiction)

As the side effects of anxiety appear, it’s difficult for people to resist the medication. The drug is the only thing that will stop it. This is a nearly impossibly high obstacle to manoeuver when in the process of quitting the drug.

Therefore, most people continue taking the drug despite its negative side effects. The anxiety is just too intense without it.

2. Overdose

Benzodiazepines themselves don’t usually cause an overdose. However, when combined with other drugs such as opiate painkillers or alcohol, the mix can be incredibly dangerous.

Michael Jackson and rapper Lil Peep both had Xanax in their systems at the time of their deaths.

Users think they can avoid these issues by merely sticking to benzodiazepines and avoiding opiates or alcohol — but it’s not this simple.

Doctors won’t continue writing prescriptions for the drug indefinitely, and if they do, they will cap the dose. As tolerance increases, users are forced to seek out other sources of the drug to feed their addiction.

However, black market benzodiazepines aren’t always made using good manufacturing processes. A lot of them contain a mix of other drugs, such as fentanyl, to cut costs for the manufacturer. This is extremely dangerous and all too common.

All it takes is one bad pill to end up like Lil Peep — who died from taking Xanax laced with fentanyl.

If Lil Peep can’t even get clean drugs, what makes you think you can?

Suggested Reading: Can You Overdose on CBD?

How Can CBD Help Someone Wean Off Benzodiazepines?

So, now that we have a good understanding of how benzodiazepines work and what makes them so dangerous, we can get into how people are using CBD to support their recovery.

The basic idea is that we can use CBD to wean off benzodiazepines gradually. As the dose of your benzodiazepines is lowered, you can simultaneously increase the dose of CBD to offset some of the side effects.

Once the benzodiazepines are fully removed from the system, the focus is to stop the CBD — which is significantly easier.

This works because CBD has similar effects on the GABA receptors to benzodiazepines — only with significantly less potency and potential for addiction.

CBD also offers other benefits for people suffering benzodiazepine withdrawals:

  1. Anti-convulsant — CBD relieves muscle tremors and tension, helping to reduce this uncomfortable side effect while going through benzodiazepine withdrawal.
  2. Anti-anxiety — one of the most important benefits of CBD is its ability to reduce anxiety symptoms, which, of course, is the primary side-effect of benzodiazepine withdrawal.
  3. Sedative — CBD is a mild sedative, helping to relieve symptoms of insomnia resulting from Xanax, Trazodone, or Valium withdrawals.

How to Wean Off Benzodiazepines with CBD

Weaning off benzodiazepines with CBD is reasonably straightforward. You start with a low dose of CBD and your regular dose of benzodiazepines. Over time, the dose of benzodiazepines is gradually reduced, while the dose of CBD is steadily increased.

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Eventually, the benzodiazepines are stopped completely. Once this stage is reached, the CBD is gradually reduced as well — which is significantly easier and much safer.

Step 1: Tell Your Doctor

Before you stop taking your medication, tell your doctor.

You need to discuss the plan with them even if they don’t approve (many doctors appear to prefer to keep their patients on the medications to avoid withdrawals).

Ultimately, however, your health is your responsibility. If you’re persistent with your doctor, they will need to help you wean off the medication. They’ll give some advice on a plan, along with some tips for getting through the worst of it.

Most doctors will also schedule visits throughout the process to monitor how the body is responding.

Step 2: Make a Dosage Plan

This step should be done with your doctor or another qualified practitioner. Some doctors and naturopaths specialize in weaning off drug addictions. If you can find one of these specialists, we highly recommend using their services to optimize success.

Here’s a simple dosage plan to give you an idea of what it might look like:
Week Xanax Dose (Daily) CBD Dose (Daily)
Week 1 6 mg 0 mg
Week 2 6 mg 5 mg
Week 3 5 mg 15 mg
Week 4 5 mg 30 mg
Week 5 4 mg 40 mg
Week 6 4 mg 50 mg
Week 7 3 mg 55 mg
Week 8 3 mg 55 mg
Week 9 2 mg 60 mg
Week 10 2 mg 60 mg
Week 11 1 mg 60 mg
Week 12 0 mg 60 mg

These dosages can vary significantly depending on your daily dose of Xanax or other benzodiazepines and how your body reacts to CBD. Some people need higher doses of CBD to be effective; others need lower doses.

You can try out our CBD Dosage Calculator to estimate your ideal dosage to begin.

The key to using CBD is to start low and build up gradually until you get the desired effects. You may need to increase the dose slightly when you lower the benzodiazepine dose.

Step 3: Order Your CBD

Before you start the weaning-off process, make sure you have enough CBD to get through the first couple of weeks. We recommend opting for a high-potency product — this can always be diluted to smaller doses, but it can be hard to hit higher doses with low-potency products.

We recommend finding a decent CBD oil and a CBD vaporizer. Oils offer long-lasting effects that can be taken both first things in the morning and in the afternoon or evening.

Vaping is good for spot treatment whenever withdrawal symptoms start and for eliminating the habit of popping pills whenever anxiety appears.

You could also check out the best CBD gummies for anxiety relief. Gummies are discrete and easy to take on the go.

Tips for Using CBD for Benzodiazepine Addiction

1. Seek Professional Medical Help Before Attempting the Weaning-Off Process

First and foremost, whenever stopping a medication such as a benzodiazepine, you need to seek out medical advice from a qualified doctor.

Benzodiazepine withdrawals can be dangerous — even lethal, in some cases.

Consult your doctor and return for follow-up visits every time you reduce your benzodiazepine dose so the doctor can assess your vital signs periodically as well as your overall wellbeing and emotional health.

2. Wean Off Benzodiazepines Slowly

It’s better to wean off benzodiazepines slowly over a few weeks instead of as fast as possible — this is especially true for people with a history of using benzodiazepines for more than six months.

Reducing your dose too quickly increases the chances of severe panic attacks, which can lead to a relapse. Instead, plan to wean down by roughly 25% every two weeks.

A good schedule is to lower the dose by about 1 mg every second or third week.

This gives the body enough time to readjust its dependency on the new dose. Once the body has stabilized, you can move on to the next stage and start the process again.

3. Perseverance is Key to Success

Even with the help of CBD, getting off benzodiazepines can be a challenge. Although CBD can significantly improve withdrawal symptoms, it won’t eliminate them.

It’s essential to persevere through periods where withdrawal symptoms can become especially challenging. Remember that the discomfort will eventually pass for good, but only if the process is seen through to the end.

4. Use the Right CBD Products

There are a lot of CBD products on the market — many of which are not going to be sufficient enough for this application.

Look for a CBD product that has the following characteristics:

Using cheap, poor-quality CBD products may be ineffective or, in some cases, make symptoms even worse. This is especially true with contaminants such as pesticides and heavy metals — which can cause anxiety. This is the last thing you want when going through benzodiazepines withdrawal.

We also highly recommend opting for a full-spectrum extract. The full combination of cannabinoids, terpenes, and other phytochemicals in the cannabis plant is more beneficial than CBD in isolation [1].

5. Consider Vaping

Rarely do we recommend anyone starts vaping, especially if they’re not already a smoker.

However, in this case, vaping is very beneficial for changing habits of drug use.

The very action of vaping can help users change habits in their brains. Usually, when benzodiazepine users feel anxiety coming on between doses, they’ll reach for a pill. This forms habit pathways in the brain that can be hard to shake.

This habit of popping pills for anxiety can be replaced with a few hits from a vape instead.

Of course, you don’t want to have compulsive or addictive behavior with anything, including vaping — but during the process of weaning off benzodiazepines, this can be a game-changer.

Vaping also offers the benefits of being fast-acting — especially compared with things such as CBD oils or capsules that can take as long as 45 minutes to start producing their effects. Vaping only takes 5 to 15 minutes to produce the same results.

When anxiety attacks come on, they come on quickly, so relief also needs to be felt rapidly.

6. Use Multiple Forms of Treatments Together

As with any complex medical condition, the best treatment is a multifaceted approach rather than one form of treatment.

Doctors working in rehabilitation centers treating patients for addiction have a variety of techniques at their disposal. It’s the same for people working on correcting addiction at home.

Some common techniques people use to get through benzodiazepine withdrawal may include:

  • Support groups
  • Other herbs
  • Nutritional support
  • Dietary changes
  • Removal of common triggers for drug use
  • Starting a new hobby

What the Research Says

One of the most well-researched benefits of CBD is its anti-anxiety effects.

Interestingly, much of this benefit of CBD is through its activity on the benzodiazepine receptors themselves [2, 3].

This means two things:

  1. CBD can be used to replace benzodiazepines to help wean off the drug.
  2. CBD may increase the effects of benzodiazepines — making it essential to start at a low dose and build up gradually.

A retrospective study published in 2019 analyzed a cohort of 146 medical marijuana patients who were also taking benzodiazepines at the start of the study [4]. By the end of the two-month study, 30% of these patients were no longer taking benzodiazepines. A later follow-up at the six-month mark found that 45% of the patients that took part in the study were off benzodiazepines completely.

Key Takeaways: Weaning Off Benzodiazepines with CBD

Benzodiazepines are posing a significant problem around the world. In the short term, these drugs are incredibly useful for eliminating severe anxiety and panic disorders. However, long-term use can result in addiction. Stopping the medication for any reason causes withdrawal symptoms, which can be excruciating.

CBD is a useful supplement for supporting the recovery process. It has similar effects on benzodiazepine medications, which help alleviate the withdrawal symptoms. In addition, CBD extracts have other benefits that can be used to make the withdrawal process more comfortable — therefore, improving the chances of successful recovery.

Of course, whenever trying something like this, it’s essential to seek medical counsel first. Your doctor should be on board with your plan to stop the medication and will help you form a weaning-off plan — gradually decreasing the benzodiazepine doses while increasing the dose of CBD.

This study was retrospective, looking at the relationship between benzodiazepine use and cannabis use. The original study didn’t look at the effects of weaning off benzodiazepines with cannabis or CBD specifically. The results are likely to be much higher if the intent is to get off the benzodiazepines.

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