ADD/ADHD Treatments: Tips for Vyvanse

by Dr Charles Parker on August 29, 2007 · 177 comments

bored irritatedkid 150x150 ADD/ADHD Treatments: Tips for Vyvanse

Tips for Vyvanse a new, third generation stimulant:
You already know our regular CorePsych theme with ADD/ADHD and emerging brain science: the more we know the more we can have a positive impact. Not knowing can bring years of frustration, missed opportunity and unfulfilled dreams.

-And you know that ADD is one of the most misunderstood clinical conditions, as many in this world consider it a belief system not a proven medical condition.

As you also know from these pages, I advocate for what works, what works best,
and what works with the fewest problems for patients and families. Vyvanse, in the short time on the market has set some very impressive records.

From a launch date July 1, 2007, here in the States, I have written about 100 new scripts for Vyvanse treating ADD, and the results have proven quite remarkable. Simply put: almost 0 complaints to the reps, and coming back to my office after the first visit. Unusual launch. -But a few slight problems can occur – thus this post.

These easy tips will help you understand how it works here so that you can communicate easily with your medical people. [Full disclosure: I do speak for Shire, the company that makes Vyvanse, and have for years made a considerable effort to teach medical colleagues around the country how to use stimulant meds more effectively. I have presented for Adderall since its launch, Adderall XR, Focalin XR, and Daytrana as well as Vyvanse.]

Tips and Treatment Notes for Vyvanse:
It is a prodrug with a slow and forgiving delivery process: No heavy AM hit, no big drop in the PM

  1. Both studies and clinical experience show that it is more efficacious [post hoc review] than Adderall XR, and Adderall previously held highest efficacy ratings on comparison studies.
  2. The prodrug delivery system provides a longer duration of effectiveness, with no need for a PM “kicker” dose to complete homework or home chores.
  3. Methamphetamine addicts don’t like it: as measured, get this, on a “likability scale.” Because it is a prodrug you can’t snort, chew, or inject it with any buzz success [peak Cmax about 4 hrs post ingestion]. In research they injected Vyvance into a meth addicts arm: their conclusion: this is not “likable” – no fun, no buzz. This is an excellent outcome, not previously reported with any stimulant, and in the package insert. It may be abusable, but it will be nearly impossible.
  4. Always start at the lower dose: 30mg which roughly equals Adderall XR 10mg. They may be on higher doses, even 40 mg of the Adderall XR, but always go low and slow. It’s more efficacious, and if you start at 50mg which roughly equals 20mg Adderall XR, it can give them an unpleasant feeling. Been there. Go slowly.
  5. If the duration [DOE] is out at ~ 2PM the dose is one click too low. Move up to the next dose.
  6. With a medication sensitive child/adult you may want to divide the dose in 1/2 to get started: Take the capsule, pour contents into 2 oz of water in mixing cup, drink 1 oz each of the first 2 – 4 days to start slowly. I have two children perfectly dosed with only 1/2 capsule/AM in this manner.
  7. All psych meds are better tolerated and more effective with a protein breakfast,- please review my breakfast posts linked here.
  8. Always remember the ADD 3R’s, discussed in my first post, in reference to medical treatment for ADD: Right Diagnosis, Right Medication/Intervention, Right Dosage.

Please send along any comments: this is an opportunity to work closely together and let people know how this medication can be used most effectively. -Look forward to our discussions.

cp

 ADD/ADHD Treatments: Tips for Vyvanse

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  • Sarah

    I guess I wonder: do you see any indications of which types of meds might be best, given our history? Wellbutrin and Straterra (both used at least 2 months) resulted in minimal benefits to focus (compared to ritalin or adderal), and definite negative mood issues. Of the stimulants he took before developing tics, Adderal worked best on focus, but was very negative for his mood. Ritalin/metadate cd seemed the best of the remaining alternatives, causing no mood problems, and improving concentration fairly well. After several years, though, we stopped stims, due to tics (which went away completely after the stimulants were out of his system.)We did try focalin in small doses, hoping its “cleaner” profile would be better, but no. We are hoping that Vyvance, which I understand is similar to adderal will not cause his tics to resume and will not cause the mood problems we saw with adderal. I am an optimist!

  • http://www.corepsych.com Dr. Charles Parker

    Sarah,
    Yes, for years the literature suggested the use of TCAs as a primary treatment for ADD, and even now some studies use TCAs as comparators. No disrespect to anyone on this, but the tide has significantly changed regarding TCAs for reasons of safety, efficacy, and the marked improvement of the stimulant med delivery systems.

    Naturally some outliers may respond well to TCAs just as a minimal group respond well to Strattera. But if the choice was between a TCA and Strattera, I would definitely go for the Strattera for some of the reasons you mentioned in your most recent comment. Some appear to respond well/better to Norepinephrine reuptake [vs Dopamine reuptake] inhibitors… and the jury appears out at this moment as to: why?
    cp

  • http://www.corepsych.com Dr. Charles Parker

    Shannon-
    Your report does sound interesting to me – and I have been watching to see if any of this abuse material began to surface. I would love to do some investigative journalism on this report, and would welcome an anonymous call to my office,- will call back on my nickel if that person would be willing to talk to me about it. Please do ask the user to call my office with the name Anonymous for a more in depth phone review. Office number over at Contact JR under the picture.

    Thanks for the input will be watching.
    cp

  • Shannon

    All of you that are saying it can’t be snorted are falling for something you should have done more research on. They’re trying to sell it to the parents because they’ve all clearly discovered that the ADD meds they’re giving their kids are the same thing as coke. Take it from me, I work in a restaraunt-you can most certainly snort Vyvance and get high. If you don’t believe me..if you think their advertising is true…crack one open and try it for yourself. What do you have to lose if they’re right?

  • Sarah

    Thank you so much. It is encouraging to hear that the mood issues seem less pervasive with Vyvance. We have known all along that the TCAs are a very imperfect solution, but tics made the stims unsuitable for our son (and he tried all, including focalin, that were available four years ago), so we had to look elsewhere. We have him on a low dose of desipramine, per Dr. Hallowell’s interesting article titled Pharmacotherapy for ADHD in Adults, by Jonathan Ratey, Edward Hallowell, and Catherine Leveroni, in which they say, “… Research and clinical experience have shown that the antidepressants Norpramin (desipramine) and Tofranil (imipranine) effectively increase attentiveness and reduce distractibility in children and adults. Tricyclic antidepressants exert their effect by acting upon norepinephrine and dopamine, the two major neurotransmitters in the attention system. They block the re-uptake of norepinephrine and dopamine into the presynaptic neuron and indirectly modify the rate of release, thus increase the activity of these two chemicals in the brain (McCracken, 1991).

    In our clinical experience, 40% or more of ADHD adults respond to between 5 mg/day and 40 mg/day of Norpramin. This dose range is considerably lower than that reported in current research reports (Biederman et al, 1985; Biederman, 1988). We see the return to the use of low doses as a significant contribution to the practice of pharmacotherapy for ADHD because we have found the most dramatic responses at low dose levels. Furthermore, most of our patients report that the positive effect experienced at a very low dose range is often lost as the dose is increased. In the mid 1960′s, Rapoport reported that the majority of children with “behavior problems” he studied showed marked improvement on 10 mg/day of Tofranil; in fact, a number responded most dramatically to 5 mg/day, and were maintained at that dose without a waning of response (Rapoport, 1965)….”

    However, we are planning to try Vyvance soon, once his desipramine dose is lowered to a better level (we think we may have increased it too much.) We do work with a wonderful neurologist, who has helped us since 1999. He is open to new treatments, and multiple meds, when necessary. I very much appreciate your interest, and your willingness to share your knowledge.

  • http://www.corepsychblog.com Dr Charles Parker

    Sarah-
    While TCA’s are within the standard of care, I do not recommend them to anyone for ADD, as they simply don’t do the job.

    Sounds like your son very well may have a comorbid depression with his ADD, therefore the TCA will look a bit more helpful.

    See this lengthy remark about your question here:

    http://www.corepsychblog.com/2006/12/kids-and-antidepressants-why-they-dont-mix/

    Without seeing him, just from the information here: Vyvanse consistently proves less troubling from a mood dysregulation perspective. But if Vyvanse does bring moodiness, the simple and best solution is a small dose of clean-on-CYP450/2D6 antidepressant such as Effexor XR, tho off label in children, and subject of course to your doc’s approval .

    Do not use Prozac or Paxil with Vyvanse for the reasons outlined in the above link. Interaction problems occur down the line with these meds, are predictable, and avoidable.

    Hope this helps,
    cp

  • Sarah

    I’m wondering: my now 13 year old son tried Adderal years ago, and the attention benefits were huge, but it made him terribly moody , weepy, and irritable. After years on various stims, tics became a problem, and he has been on TCAs combined with guanfacine for the past three years. TCAs have been good for the behavioral aspects of ADHD, but have not helped adequately with the cognitive issues. Focus and motivation are very poor. I wonder of Vyvance is likely to cause the same mood problems as Adderal? FWIW, he also had mood issues with Straterra and Wellbutrin, which were not as effective on cognitive issues as ritalin/adderal. I very much appreciate any insight you might have. Thank you.

  • http://www.corepsychblog.com Dr Charles Parker

    Leigh,
    Not commonly appreciated: MPH products like Focalin block 2D6, and I strongly recommend against using drugs that clearly interact – as Vyvanse is an AMP that runs thru the 2D6 pipeline [Google 2D6 on this blog and you will see much about this issue].

    Likely the dose is not correct if it isn’t working in the AM – at the correct dose it works in .5 hr… and again we aren’t looking for “feeling,” but for cognitive change.

    Look at the DOE as outlined here and titrate carefully with your doc, then if you absolutely have to mix, stay with an AMP product, one that doesn’t block that AMP metabolic pathway.

    Interesting question- and a reference on this point is in Cozza and Armstrong at CorePsych Books: Drug Interactions in Clinical Practice.

    Thanks,
    cp

  • http://www.corepsychblog.com Dr Charles Parker

    Jason,
    First a simple point: You can’t get it right with whatever was in the hookah on board – highly unlikely the fall was due to Vyvanse alone, highly likely secondary to meds + hookah, or hookah alone.

    If you are in the US you are most often talking *weed/marijuana* with “hookah” use, – and weed, as other addictive substances, should be avoided if you want the true fix.

    Often unappreciated is the fact that weed may appear at first to temporarily help with ADD, but is not indicated:
    1. It’s against the law,
    2. It has a very short half life,
    3. The incidence of cancer in many reports is 5X CA in the general population,
    4. It has not been studied for the ADD application but anecdotally we often note memory diminishes and dementia-like symptoms are increased… so if you want to do well, forget it.
    5. And one final emphatic point: Weed makes you *more ADD.* SPECT scans show clear PFC deterioration with weed use. Stimulants are working to correct, weed is working to deteriorate.

    Scrap that drug as a treatment plan.

    The Adderall dose likely did not reflect the correct titration in the first place because of the “hookah,” as titration accuracy is difficult to predict categorically [without that variable], -so will pass on that one.

    Tics and such are downstream problems of all stim meds, especially stim meds with comorbid challenges such as one finds when one regularly smokes or uses weed. We always look for a variety of other contributory metabolic issues if tics persist.

    Several comorbid issues are present here, and more should be investigated.

    Hope this helps,
    cp

  • Leigh

    Since Vyvanse does not address early am/schoolday ADHD symptomes, would it be safe to add 5 mg Focalin to help?

  • Jason

    Hello,

    I have a friend who is 27 yrs old and has just been put on Vyvanase after taking 80mg of Adderall for 6 years. The Adderall was effective and she liekd it but it caused intense fidgeting and her family thinks it was affecting her personality (argumentative, insecure, agitated).

    I’m not sure the dose of Vyvanase she is taking but I know that she is now taking it twice a day b/c it was wearing off — is this ok or should the mornign dose just be higher?

    Also, she is still fidgeting a lot (although less than the adderall) and has developed a recurring tic with the side of her mouth (new with vyvanase). Is this a normal and acceptable side-effect? I can’t find anyone posting about it.

    Lastly, the other day she got up from sitting and smoking hookah (same position for awhile) and fainted and had a small seizure. Thought it was just from standing up too fast after smoking hookah but could it be related to the vyvanase?

    She is also taking effexor daily.

    Thanks for your info.

  • http://www.corepsychblog.com Dr Charles Parker

    DrMomKat-
    Your main issue seems to be with the loss of appetite, and yes, that can be a problem. I have covered that point quite frequently on other posts including the breakfast post on the front page under the Toolkit and Protein Breakfast.

    Bottom line: breakfast of protein first, then any psych med after.

    Second point: dosage may change that reaction and the post on water titration may help.

    Third point: Some people cannot take AMP meds.

    Fourth general observation: Haven’t read the post at CyberPsych, but they clearly do know what these meds do, in fact have the specific receptors broken down in some detail, and tag Dopamine receptors and watch them on functional imaging.

    On your side of the point: and, yes, we do not yet know *everything.*

    So somewhere along that path is the debate, just what is the diagnosis? Neuropsych testing and SPECT tells us much.

    What is the dosage? Watch for the therapeutic window at this post [http://www.corepsychblog.com/2008/01/tips-on-medicat.html]
    and use, as you say, much caution with any change or increase.

    I do completely agree: with significant side effects that may not be the correct med. Side effects usually diminish by 2-3 weeks, and if not, it’s gone.

    Thanks-
    cp

  • DrMomKat

    I’ve noticed a decrease in appatite since starting Vyvanse (prev on Focaline XR). It also makes me nauseated when I do try to eat sometimes. Not so much a prob for me since I’m in my late 20′s ( and could always stand to loose 5-10 pounds) but I could see how this would pose a problem for children. Since this is a medication for children wouldn’t malnutrition be of concern for most parents (among other things)? I myself would never give a stimulant to a child but then my kids and I aren’t hyper-active or out of control either.

    It seems to me that if a child develops an uncommom reaction to meds, such as the one noted prev, I would assume she was misdiagnosed and would take her for a second opinion to a neurologist. I think all natural methods of controlling ADD in children should be exhausted before being put on any kind of unnatural medication- especially a stimulant. In a lot of cases, it’s the parent’s frustration with trying to deal that’s causing most of the problems. :) Patiance isn’t something we’re born with!

    My therapist also says a lot of times Bi-Polar Disorder is misdiagnosed for ADD … it can even be a combonation of both. Besides .. I just read an article on CyberPsych that scientists aren’t even sure what these drugs they are prescribing for ADD do or how they work. What gives?

  • http://www.corepsychblog.com Dr Charles Parker

    Deborah- from Jan 24,
    Thanks for keeping us posted on these kinds of issues. My own policy is too look for weight loss as part of my adjustment parameters in finding the therapeutic window. Without an evaluation, just offering some feedback without suggesting any specific plan… sounds like what we see in my office as too much Vyvanse.

    Please take a look at this recent post which doesn’t hit your question directly but addresses the dosing/titration issue in context.

    http://www.corepsychblog.com/2008/01/tips-on-medicat.html

    Thanks-
    Chuck

  • Deborah

    I can say that i am a 42 year old woman and i was put on Vyvanse 30mg at first and then bumped up to 50mg then 70mg. I started getting a severe backache and noticed it was only when i took the Vyvanse. I also lost 45 pounds while taking this medicene over a period of 6 months. Needless to say it was somehow and my doctor still does not understand it caused my Potassium to become extremly low and I had to be put on Potassium pills. My Thyroid is also not boderline overactive. I am not on it anymore and am trying something that is stimulant free. But for those that may be new to trying this medicene i would like to make sure that people are educated to what happened to myself.

    Thank you.

  • http://www.corepsychblog.com Dr Charles Parker

    Terry,
    Never concern yourself with an “old thread” with me… if what you are doing isn’t working, it’s new thread everyday!

    Having met Joe Biederman on several occasions and reported once here about a year ago:

    http://www.corepsychblog.com/2007/01/add_update_from.html

    I can tell you he is just great clinically and will likely shed some new light on her difficult presentation.

    I strongly recommend John Ratey’s book: User’s Guide to the Brain

    http://astore.amazon.com/cpbks-20/detail/0375701079/103-7756357-1889446

    - his work is cutting edge and he also would be a great resource for your further investigations.

    Most striking for me in your brief remarks here is the consistent series of remarks that sound toxic or metabolic. -Just back from a meeting with Dr Vojdani in CA, and will be posting about the many interesting immune dysfunction resources – specific laboratory tests – available for individuals like your daughter. See my most recent post on Dr V who is moving offices to work with NeuroScience Labs.

    Basic rule, and comment on your post not clearly discussed in previous Vyvanse posts:

    If the therapeutic window seems just too narrow and either up or down dosing is insufficient – you very likely have a metabolic problem, or simply the wrong medication for that symptom complex – from a defective 2D6 metabolic pathway [to be measured by genetic testing with either Genelex [used by the Mayo Clinic and available through our office] or Detoxigenomics [also available with our office from Genova] …or other metabolic testing indicated by our questionnaires and a personal interview.

    The encouraging news: it is highly likely that she has something measurable wrong that does need attention that can improve her situation.

    In your daughter’s difficult presentation Vyvanse may be the canary in the coal mine because the therapeutic window is too small, she isn’t getting better with what appears to be good adjustments by your doc, and she has multiple apparent “neurotoxic” symptoms.

    -Difficult presentation, hope this helps a bit.

    Chuck

  • http://www.addconsults.com Terry Matlen, ACSW

    Dr. P,

    I know this is an old thread but am hoping you still monitor responses here. An update on my “Vyvanse” kid:

    We titrated up to 80mg (saw no change from 70-80) and the pDoc is unwilling to go up any further. Though I did see a longer coverage of symptom control, I don’t think it was as effective as the Adderall XR-40mg.

    So we’re back to that.

    Another question-
    She must be medicated in order to fall asleep, yet though everything we try sedates her, her body/mind fights it and she ends up staying up way too late. She walks around with eyes half shut and looks intoxicated, yet she can’t stop her body from moving. That means repeated runs (she does not walk and she’s 19 yo) up and down the stairs, grabbing food, items, cat, etc.

    I’ve just consulted with a neuropsychiatrist here at Wayne State U and his thought is to try and get a consult with Dr. Joe Biederman. Her picture is so unique and reactions to meds unusual.
    I know John Ratey, who suggested intense exercise, but she is unable to follow formal routine exercise. I do have her skating and bowling once a week via special ed groups but know that’s not enough. This is a young lady who can’t read her body; who never tires; can’t tell hunger from full, etc. Extrememly hyper/impulsive due to her brain injury as a tot.

    The only time she is able to sit is when she perseverates on the computer.

    Any tips?

    Thanks,
    Terry Matlen, ACSW

    http://www.addconsults.com

  • http://www.corepsychblog.com Dr Charles Parker::CorePsych

    DeAnna,
    Thanks for your question about your son with ADD following CA treatment. We frequently do see *ADD symptoms* following medical procedures, from bypass to chemotherapy to treatment for asthma.

    Since I have not seen your son, I would, of course encourage follow up on any comments here with definitive work with your treating physician. Having said that, your son presents a finding typical of medical or injury induced ADD symptoms: More sensitivity to stimulant medications than others.

    The decision is with you and your doc, but I always shoot for no side effects, and if your son persists with this hyper-talk for more than a couple of days, I would suggest dropping the dose.

    You have plenty of time to increase later. If your doc is OK with the decrease plan consider the half dose in this water titration strategy post:

    http://www.corepsychblog.com/2007/11/vyvanse-for-add.html

    or here at:

    http://www.squidoo.com/vyvanse

    Low and slow will often make the day better, and if he needs more you and your medical team could consider increasing later.

    Best wishes with your guy-
    Chuck

  • DeAnna

    Dr. Chuck,
    My eight year old son just started vyvanse this weekend. He developed symptoms of ADHD after many treatments for brain cancer. His cancer is in remission. He is on 30 mg and felt better within forty-eight hours of beginning the medication. However, he talked and talked and talked. He did go to bed well tonight and at his normal time. Should we wait a week to see how his body stabilizes on 30mg or should we talk to the doc about halving the dose? Thank you for your website!

  • http://www.corepsychblog.com Dr Charles Parker

    Leslie,
    Check with your doc, sounds like the pediatrician is right on, lower and slower.
    With younger children it very often happens that everyone tries hard to get it exactly right and finds the team caught in adjusting too much.

    My policy, already approved by your doc, is to stay at a suboptimal dose for 2 weeks and let the child make the internal metabolic adjustment, – then increase to the next click.

    I have often found myself changing with young children almost weekly because the therapeutic window is so small – much work and too much energy. Best to sit tight, adjust about every other week, and diminish expectations for an immediate fix.

    The teacher will have to wait, and watching the DOE at home on the weekends you will know. Your child’s metabolic rate will settle, will therefore manifest as more precisely measureable, – then adjust.
    Chuck

  • Leslie

    My son who turned five in October was diagnosed with ADHD in November. His peditrician put him on vyvanse since he is in day care all day and he can’t swallow pills. We quickly discovered that the 30mg was too high of a dose; he talked non-stop for nine hours (scary!). I found your website and cut his dose in half (thank you!). His teacher was amazed how well his focus improved, but he was still talking a lot. We cut the dose into thirds which his peditrician said was OK. His focus is still good, however his teacher has noticed that controlling his hyper activity has gotten harder for him compared to when he was on the higher dose of meds. Is increased talking a common side effect? If I raise his dose will the talking eventually get better or should I just try another medication?

  • http://www.corepsychblog.com Dr Charles Parker

    LP-
    Without seeing the child it sounds at first blush like he is simply adjusting to the dose, and it is important not to take steps based upon this post, but get back with your doc.

    Most often in my practice under these circumstances [and without a full clinical picture]: I suggest patience, as these problems often occur in the first 3 days, maybe one week, then in 1.5-2 weeks you will best be able to assess the DOE, duration as outlined in this post.

    My biggest problem thru my career: too enthusiastic titration – pushing the dosage before the metabolic consistency hit a reasonable plateau – thus the most recent Vyvance post on water titration.

    Do try to see your doc in about 2 weeks,- if the problems become more urgent insist with your doc that this is an med urgency/emergency.

    Best,
    Chuck

  • LPritzker

    My 7.5 yo son was diagnosed with ADHD this summer (although, I always “knew it.”) We started him on Adderall 5mg and climbed to 15- then cut back to 10mg in the AM and 2.5 after school. After two months of playing with it, and him losing 11 pounds and rebounding in the afternoon horribly, not sleeping, etc. our doctor put him on Vynase 30 mg.

    It has been 4 days– the first was miraculous (as was the Adderall in the beginning.) But the last 2 days he was pretty nuts– very low frustration tolerance, lashing out his sibs (hard for me to tell if this is worse behavior than before we ever started medication, but I almost feel like his behavior wasn’t as outrageous before we started medication.)

    Today is okay so far…but I have noticed the meds are wearing off at about 4pm– and not working all that well to begin with.

    How long should we wait to increase the dosage? We got our free 30 day script and our dr said to wait until it runs out before increasing, but after yesterday I am thinking that I will be institutionalized before then :o )

    Will increasing the dosage even help if he isn’t showing much of a change (or even worse off with it,) when taking the vyanse?

    Any advice will be most appreciated.

    Thank you

  • http://www.corepsychblog.com Dr Charles Parker

    Irving,
    As you know I have a limited ability to offer any help not having seen you. Your doctor is right about trying this particular med as I do think for most people it is the best.

    Look for the therapeutic window, the top means it’s too much, the bottom, where you appear to be on this brief missive, is nada…it isn’t working. We look for the middle. You can’t get out the window by going thru it, or bumping against the window sill.

    Talk to your MD, he will likely increase it, likely to 50 mg, and then you can look for the cognitive, thinking changes as outlined in this post.

    It’s always a challenge in the beginning figuring out exactly what to expect. No effect is simply that: no effect.

    Best wishes,
    Chuck

  • Irving Drinkwine

    Sir,

    I have been taking 30 mg of vyvanse for a little more then a week. Should I be able to feel a difference taking this medication?

    I am naive to stimulants with the exception that up until 2 years ago I drank about a six pack of caffeinated soda a day. Now I avoid caffeinated drinks of all kinds.

    I thought that since the drug was a stimulant I might feel more alert or energetic, but my wife tells me that with ADD it would be the opposite.

    I am a 30 something white male, 5’6″ and about 190 pounds – fairly muscular. New diagnosis of ADD. I’ve never taken any ADD meds or any other Rx stimulants before with the exception being some of the nasal decongestants which I seldom use.

    Thank you sir,

    Irving

  • Sam

    Another good addiction site with an education center covering all addiction categories is http://www.myaddiction.com

  • http://www.corepsychblog.com Dr Charles Parker

    Betsy-
    Yours is also a very interesting post – and thanks for sharing your super daughter with us. You are clearly affirming the not-so-parenthetical-point that we must always listen to the patient, and if we do, they will tell us how to get it right.

    I completely agree with your psych about her start dose, and his observation with you that she is a fast burner at a previous Adderall dose of 80mg. You do already know she is fine with the AMP molecule, so she is not [as they say in research], a *virgin [innocent from previous stimulant, -and, in this case, not innocent from AMP stimulant] patient.*

    So, with that foundation, 50mg Vyvanse would be expected to have a positive effect on prefrontal cortical brain function [to coin a phrase!]. At the previous DOE [duration of effectiveness] on the IR Adderall @ 3.5 hr, she was slightly under-dosed. I have come to expect a solid 5-6 hr on the DOE with the IR.

    So, knowing that, and doing the math: 2x50mg=100mg Vyvanse = *roughly* 60 of Adderall XR she would likely, with your doc’s approval, be able to squeak up to 120mg because the DOE objective for me on Vyvanse, tho difficult to measure as precisely, is in the 14 hr range.

    But, having said all of that, my next question you will have some fun with [and I won't ask for an on line reply]: How many times a day does she go #2?

    Bowel irregularity [and subsequent liver dysfunction] very often confound the metabolic picture. She could be going either way: excess on the too frequent side, or, most often, on the Q2-3day side. Constipation in our entire adolescent/adult society is rampant.

    I would look for metabolic and nutritional components vigorously – and even though she is smart and motivated, I am an anti-carb hound. Carbs mess up the bowel, diminish effective metabolism, mess with the estrogen system [listen to my podcast on PCOS and the other on estrogen dominance] and then can create sleep problems, appetite and breakfast problems.

    All systems go into rusty shut down. We just can’t get it right with main drain working inefficiently. Scum is building in the bathtub.

    This is a big deal and must be chased down to get the metabolic question effectively answered. Once those questions are completely resolved we regularly find we don’t have the problem of chasing dosage.

    More in another post soon.

    Thanks for adding to this interesting discussion, hope this helps with your girl.
    Chuck

  • http://www.corepsychblog.com Dr Charles Parker

    Terry,
    Yep Frank is a super guy. Unpretentious, experienced, dedicated to getting-it-right with the ADD kids and adults. I always go to his presentations when he is in town as he continues to explore the process and the product.

    I have definitely gone higher with Vyvanse than recommended, and feel that about 2 weeks per next click up when you are near the top of the therapeutic window is just about right. The problem continues to be fully understanding the clinical parameters for precise titration, and the individuality of each specific metabolic process.

    Bottom line: My experience at the Vyvanse top with high dose: the person is likely a fast burner, and adding 30 will probably be no problem. Agitation may occur for 2-3 days but should settle and she should be consistently better.

    Messing with the water etc, is for me a front end solution to check metabolic rate and patent 2D6 pathways… more in the next post.

    I am still trying to find the precisely reportable top and bottom of the window. I do think I am right about using the objective criteria from the first interview – and about keeping treatment objectives predominantly cognitive, -but the bugaboo, as you know, is always comorbidity.

    In fact, I will do a post on the details of this metabolic/comorbidity matter now and set it to send on Tues next.

    Hope this helps, -thanks for sharing your personal experience with all of us, and please do keep us posted. -All this of course thru your own doc.
    Thanks
    Chuck

  • Betsy Davenport, PhD

    My daughter has recently begun Vyvanse (~2 months ago). She had been taking Adderall immediate release for the last 7-plus years. There were occasional forays to try XR (but she can’t swallow capsules, tablets, etc. and the taste was very bad), Methylin (which she declared needed to come in orange flavor, and refused), Daytrana which she never actually tried (would have needed at least 3 patches at a time),

    Her Adderall dose was 20 mgs. 4 times a day. It used to last longer, but at present only 3.5 hours, and still that had became somewhat uneven in result.

    Her psychiatrist started her right off at 50 mgs. Vyvanse and at first she seemed about the same (school was starting and who could tell what was what between that, her already severe anxiety disorder, and the new medication? She said the Vyvanse was “better,” and ventured that might have to do with not being married to her alarm watch. She has since observed (she is 15 and quite able to specify what the effect of medication is) that the Vyvanse is smoother, less “herky-jerky,” that she remembers where things are and what she has to do. I notice better planning and executing, and more initiative for chores and other things, too. She seems more relaxed, which is not a cognitive symptom, but certainly a secondary effect of cognitive problems. And, she hasn’t lost her sense of humor.

    I wholeheartedly agree that it is cognitive function that is the impairment to treat, and to monitor closely and in detail what is and is not affected at given doses. In my daughter’s case,it might have been all right to start lower, but her requirements have always been high and she’s sufficiently committed to medication and the help it gives her that she would not have agreed to a very low dose. I guess that’s a case of doing things in a highly individual way.

    For her, the Vyvanse is effective for about 8.5 hours and she notices a drop-off in concentration/orientation if she lets it go much longer. What are practitioners doing to handle the “after it’s done its job for the day” problem? Many people I work with need some stimulant on board in order to get to sleep, and my daughter is one of them. So many sleepless childhood nights — she averaged 4-6 hours all during her middle childhood — and we finally figured out what made the difference.

    She has been taking two equal doses of Vyvanse (50 mgs.) and this sees her through past go-to-sleep time. Covering a 16-hour day would be important for lots of people.

    I’m interested to hear more about this, and whether people think Vyvanse is going to take its place among the more-used medications for AD/HD.

    Betsy Davenport, PhD

  • http://www.adconsults.com Terry Matlen, ACSW

    Dr. Chuck,

    Thanks for the add’l information. Since she did poorly on 50mg, should I continue on it a bit before bumping up to, say, 70mg? You note that slow titration is the way to go. This is a kid who cannot be without stimulants; her impulsivity and hyperactivity are so severe, she would be in danger of getting hurt.

    The question then becomes, if 70mg doesn’t handle the above symptoms, would the next jump be to 100 (70+30), or would I have to start dissolving them to find something in between?

    I know Frank Lopez- we do projects together for Shire and I just saw him recently at the Ask The ADHD Experts. I didn’t realize he was on the Vyvanse team!

    Regards,

    Terry

  • http://www.corepsychblog.com Dr. Charles Parker

    Terry,
    Your daughter presents one of the typical/atypical problems we so often see that make this practice so interesting. On the one hand she apparently has some concommitant organic challenge with the cog impairment – which would likely make her *more sensitive* to changes and therefore *likely* would need less.

    The dose correlation with Adderall 40mgXR could be anywhere from a low 50mg [=20XR], to a higher 90/100mg Vyvanse.

    Here are the correlations from the *forced dose* research:
    10XR=30 Vyvanse
    20XR=50 Vyvanse
    30XR=70 Vyvanse
    But anyone working with Shire [the pharma company] including Frank Lopez MD one of the lead investigators, would tell you, just don’t think on those terms. Research is research, practice is practice. These are very vague guidelines only. Every med is different, even if it is the same AMP molecule at the *core…* -notice how I slipped in that word?

    From your brief report sounds like, as you noted, it was simply too little, and the odd/strange behaviors probably were a result of simply not being on enough Vyvanse.

    I have one patient at this moment on 120mg Vyvanse [roughly = 50-60mgXR?] This is unusual for me, and I confess that I see many second opinions with XR dosed much higher than I ultimately find they usually need to go. Vyvanse is most often more efficacious.

    Haven’t had enough time to see it with Vyvanse, but just looking at this post looks like *too much* is already underway.

    Biggest mistake with most folks is big guys – I have a post on this subject a while back – seems like folks are trying to medicate them into submission.

    Would continue slowly up with your daughter, looking for full coverage thruout the day [not a drop in the PM from 2-4], all, of course, with the full authorization of your medical team there. This note is not enough information to cover all of the multiple angles in this situation.

    Hope this helps a bit however,
    Chuck

  • http://www.corepsychblog.com Dr Charles Parker

    Gina-
    Excellent comments, and these postings do try to help with that last point. Stimulants need some attention! AMP is metabolized differently than MPH and that can make a difference in response.

    My own titration strategy for Vyvanse is simple: Don’t look for the “feel,” look for the cognitive improvement, the decrease in impulsivity, and leave it alone. If you go for the “feel,” you often go over.

    As I have said in all of these Vyvanse posts:
    Titration strategy is simple – go slower than you think, and don’t follow the exact dose equivalence stated in the literature.

    I saw a person just today that unexpectedly needed to go up to 70mg [started at 20 of Adderall, went to 25 with a duration of that 25XR about 8 hr] – they started Vyvanse at 50=20XR, and worried for a couple of weeks – I thought the Vyvanse dose would be “predictably less” – but it wasn’t working throughout the day. With time on our side, and good evidence for the duration, we then very successfully moved to 70mg Vyvanse for all day coverage.

    Take home: Pay attention, up and down.

    What do you watch? Duration, sleep, breakfast, agitation, all of the typical things we do every med check, but we learned early: don’t chase the feel.

    *Sometimes* we go unexpectedly up – higher than anticipated by the research. Most do better with less.
    Thanks,
    Chuck

  • http://www.addconsults.com Terry Matlen

    Dr. Parker,
    Thanks for these helpful tips. Have a 19 yo daughter w/ mild cog impairment following childhood vaccine reaction (MMR), with severe AD/HD, etc etc. Trying to switch from 40 mg Adderall XR to Vyvanse. Would 70 mg Vyvanse correlate with 40mg Adderall XR? She had one dose of 50/Vyvanse and was ineffective and strange behaviors were noted. She’s in the middle of projective testing to r/o thought disorder, so I d/c’d Vyvanse till testing is complete. Just wondering if there is a chart showing dosage comparisons.

    Thanks!
    Terry Matlen, MSW
    http://www.addconsults.com

  • http://www.ginapera.com Gina Pera

    Dr. Parker,

    Thanks for this information on Vyvanse.

    As a community volunteer in the area of ADHD, I am deeply concerned that MDs will be too fast to jump on this new d-amphetamine bandwagon without understanding that this class of stimulants — no matter the delivery system — affects a significant number of people with ADHD adversely.

    Not always right away. But after a few weeks or month, when the irritability sets in, sometimes increasing to mania or intense anger.

    This is a problem I’ve long seen with AMP, so why don’t docs realize this? I have my theories, the primary one being that they don’t often ask feedback of the significant other.

    Too many cases of “non-adherence” happen because patients (and their partners or parents) decide that the cure is worse than the symptoms. And, because too many docs aren’t careful or don’t ask the right questions, they stop treatment entirely.

    I am especially concerned by comments like the one above:

    “I have been hearing many complaints from patients on Vyvanse once they are at 70mg. Why is this? Headaches, severe apetite loss. When on the mph treatments they seem to not complain. Is no news good news here?”

    Why would you try to force a patient to stay with a stimulant class that is having an obvious adverse affect?

    PLEASE, PHYSICIANS: EDUCATE YOURSELF ON THE DIFFERENCES BETWEEN THESE TWO CLASSES OF STIMULANTS. It is too basic a difference to ignore. And, your ignorance is causing great harm–most of which might not even be on your radar screen.

    Thank you,
    Gina Pera

    • http://www.CorePsychBlog.com Dr Charles Parker

      Thanks Gina,
      Totally agree with your concern and share your observation that the challenge of specific titration strategies is often overlooked, – way too often overlooked.

      Your observation is the main reason for my forthcoming [just too forthcoming ;-) ] book on ADHD meds.
      cp

  • http://www.corepsychblog.com Dr Charles Parker

    Lester-
    One additional point clearly demonstrated in the research on this drug – reminded when I presented the full set of research slides at a presentation in downtown Norfolk last night – the GI side effects in the “forced titration studies” [wherein they pushed the dose higher and faster than we would in pvt practice] almost all occurred in the first week.

    By week 4 even at the higher *forced* dose [dose not based upon response but simply cranked up to 50 mg the second week and 70mg in the third and fourth week] the GI side effects were less than 5%.

    Conclusion = as reported in my post: go low and slow, keep the dose registered on the clinical response, expect some problems the first week, do give with food, and expect it to subside week two, certainly week 3/4, except for a very small number.

    Hope this clarifies it a bit more with the research stats.
    Chuck

  • http://www.corepsychblog.com Dr Charles Parker

    Lester-
    Two quick points on the 70 mg side effects-

    1. Similar problems when I have gone higher – when I really didn’t need to – and most of the time they are looking for the “hit” they felt with Adderall which is counterproductive and too stimulating. I have to reconfigure expectations: we are looking for a different, more cognitive result> Run it back down to 50 and let them sit there for awhile and reconfigure their expectations, -it has worked well that way and they do function better than previously.

    2. Shire is coming out with “between” doses sometime this late fall – early spring. I am looking forward to the additional doses because, as you likely already know, titration is the key. Yep,- exceptions to every rule.

    On this last point: not everyone can take AMP products, then an MPH like Concerta, does work well. Many have similar reactions to MPH and the Vyvanse then becomes a better choice.
    Thanks
    Chuck

  • Lester Valle

    I have been hearing many complaints from patients on Vyvanse once they are at 70mg. Why is this? Headaches, severe apetite loss. When on the mph treatments they seem to not complain. Is no news good news here?

  • http://www.corepsychblog.com Dr Charles Parker

    Howard-

    ASD folks with comorbid ADD/ADHD are some of the most challenging to work with because the titration strategy has to be slow, and the objectives need almost constant clarification as titration moves ahead.

    Again, as your doc likely already suggested: low and very slow. Too much = irritation, no appetite, not sleeping, but we just haven’t been seeing many side effects with Vyvanse if we go slowly.

    Most importantly, think of Vyvanse [and all stimulants] as cognitively directed. The target is “thinking and conceptualizing/organizing.” The secondary gain is less frustration and impulsivity, and thereby less anger – but stimulants do not have a primary “affective/emotional” objective.

    -Very general comments for a complicated situation. And, BTW, the Strattera and Vyvanse have no reported interactions, so can go up on one whilst down on the other.

    Chuck

  • Howard Law

    Have autistc young adult ( 22yrs) Dr. specializing in autism recommending
    maintaining present anti-siezure medications while shifting from 125mg streterra given in dosages over a daily period to Vyvanse starting as your articls recommends with gradual low dosage then going up.

    Patient is young autistic adult, essentially non-verbal but with demonstrated occasional outputs of fully rational in context verbal statements and single words in multiple settings. Note speech output while rare is not echolailic, but fully in context and has been demonstrated in multiple settings to at least four persons other than the parents. Some demonstrated independence in games, riding horses, and walking/bikes in neighborhood to known locations, also some independent typing with verbal prompts on computer ( not with facilitation – touch). Some imitative play with drums in music therapy.

    Any suggestions on items other than those in the article above to watch for during the transition. Any results from similar cases we should be aware of?

    • http://www.CorePsychBlog.com Dr Charles Parker

      Howard,
      This contemporary note is to keep you informed of other interesting neurotransmitter precursor interventions and evaluations now possible at CorePsych for these kind of challenging questions.
      Please do subscribe here and pass this note along to your team regarding ADD and comorbid conditions with Asperger’s and other metabolic dysfunctions that may contribute to unpredictable outcomes, and possibly to verbal challenges.
      cp

  • http://www.corepsychblog.com Dr Charles Parker

    Addiction-
    Many thanks for your linking us to the http://www.addicted.com/ site.

    -Went over there briefly, and it looks very interesting.

    I look forward to more dialog with the recovering and addicted community, and really must post more on recovery and dependency issues.

    Thanks also for reviewing this post. It will be very interesting to see how Vyvanse plays out on the streets.

    At this moment, having logged many hours with recovering individuals who suffer with a variety of undiagnosed biologic contributory issues, including ADD, this medication will likely provide some very interesting answers.
    Chuck

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