Posted on Leave a comment

    Front End Listing (Product) Manager

    An image or logo the article is about a simulator for learners who want to learn the basics about digital advertising and Google Ads

    Looking for assistance building a Digital Advertising Simulator for learners wanting to learn the basic of adding product ads how to create a basic product feed csv. Manage advertising campaign’s in order to manage their own ads or manage a clients ads.

    Trying to find a front-end manager that will enable users to list products not to sell (not a multi-vendor-marketplace) Trying to build a simulator for learners to Google Ads. To give learners a way to list product ads manually or via product feed csv. list product ads in real time free using real ads (sellersÔÇÖ ads) for learners to practice listing product ads, finding clients, creating product feeds, etc. Tried with a multi-vendor-marketplace while these plugins enable listing products its designed to sell more interested in how many ways a marketplace can charge a vendor, too heavy with features like shipping options, vendor sales, vendor commissions, shopping carts. While I need some shopping cart features like listing products most of them like vendor plugin with woo all aspects of product sales I don’t need as all products are sold on the sellers advertisersÔÇÖ website.?á I am trying to build a Google Ads simulator so learners can find advertisers and list their products on website not on google ads. The website I am trying to build is the advertising network. It works like Google Ads except no advertising costs or any fees or charges. To give learners in South Africa an intro to Digital Advertising. Looking for a front-end manager as multi-vendor-marketplace- plugin provides too many features for sale of products. I need the listing features not sale features for front end users.?á

    Posted on Leave a comment

    Christmas Sale | EcoFlow South Africa

    21ÔÇô26 minutes


    Free EcoFlow DELTA 2 Bag With

    EcoFlow DELTA 2 + EcoFlow DELTA 2 Smart Extra Battery

    Available on Dec 18

    Expand the capacity with plug-and-play setup

    10,698 OFF

    Smart Devices

    WAVE Portable Air Conditioner

    Available on Dec 18

    Fast cooling with 4000 BTUs

    9,000 OFF

    Free EcoFlow RIVER Bag With

    EcoFlow RIVER Pro + EcoFlow RIVER Pro Extra Battery

    Available on Dec 18

    Double the capacity from 720Wh to 1440Wh

    8,098 OFF

    Free EcoFlow DELTA Max Cover With

    EcoFlow DELTA Max (2000) + EcoFlow DELTA Max Smart Extra Battery

    Available on Dec 18

    5 years of comprehensive warranty

    30,698 OFF

    • Top Offers
    • Load-Shedding Essentials
    • For Higher-Stage Load Shedding
    • Get Freebies
    • Lucky Spin
    • Referral
    • Community Benefits

    Top Offers

    Indulge in the biggest discounts of the year.

    Load-Shedding Essentials

    Power stations: Cover your critical usage
    during load shedding.

    EcoFlow RIVER Pro

    5,000 OFF

    EcoFlow DELTA 1300

    13,999 OFF

    EcoFlow DELTA Max 2000

    15,000 OFF

    EcoFlow DELTA Pro

    14,000 OFF

    Solar generators: Combat load shedding with renewable power.

    EcoFlow DELTA 1300 + 220W Portable Solar Panel

    Solar Input: 400W
    Capacity: 1260Wh

    16,499 OFF

    EcoFlow DELTA 1300 + 400W Portable Solar Panel

    Solar Input: 400W
    Capacity: 1260Wh

    20,999 OFF

    EcoFlow DELTA Max 2000 + 400W Portable Solar Panel

    Solar Input: 800W
    Capacity: 2016Wh

    26,999 OFF

    EcoFlow DELTA Pro + 400W Portable Solar Panel

    Solar Input: 1600W
    Capacity: 3600Wh

    37,999 OFF

    For Higher-Stage Load Shedding

    Expand the capacity and whole-home protection.

    DELTA 2 Smart Extra Battery

    1,000 OFF

    RIVER Pro Extra Battery

    1,000 OFF

    DELTA Max Smart Extra Battery

    12,000 OFF

    DELTA Pro Smart Extra Battery

    10,000 OFF

    110W Portable Solar Panel

    2,200 OFF

    220W Portable Solar Panel

    1,500 OFF

    100W Rigid Solar Panel ?ù 2

    300 OFF

    400W Rigid Solar Panel ?ù 2

    1,000 OFF

    Get Chillin. Get Movin.

    EcoFlow GLACIER Coming Soon

    EcoFlow GLACIER Coming Soon

    Available on 9:00am 18th Dec (SAST)

    Free Gifts Await

    Lucky Spin

    Spin the wheel and get a great prize!

    It costs you 100 EcoCredits to do one round of Lucky Spin. You can spin the wheel 2 times in 1 day

    Refer a Friend & Get Rewarded

    Christmas Sale T&C

    Campaign Period: Christmas Sale runs from December 1, 2023, 00:00 (SAST) to December 31, 2023, 23:59 (SAST). EcoFlow reserves the right to shorten or extend the Campaign Period at its sole discretion without prior notice.

    Eligibility:The Sale is open to all users on za.ecoflow.com, who are South African citizens and 18 years old or older as of 00:00 on December 1, 2023 (SAST) (“participant(s)”).

    Campaign Mechanism:

    Lucky Spin:

    1. Each draw costs 100 EcoCredits in the participant’s EcoFlow member account. Each EcoFlow ID is subject to a maximum of two spins daily, subject to SAST.
    2. All prizes from the Lucky Spin event, including EcoCredits, coupons, and physical prizes, are non-transferable, non-exchangeable, and non-deductible for cash.
    3. If any prize is awarded to a participant who provides false or incorrect identification or information, EcoFlow reserves the right to disqualify the participant from receiving the prize.

    Free Gifts Await

    During the EcoFlow Christmas Sale promotion period (December 1 to December 31, 2023), customers who place an order with a subtotal value of over the required amount will automatically receive freebies:

    Order amount greater than R16000: Camping Light; Order amount greater than R26000: Foldable Camping Chair;Order amount greater than R36000: Folding Wagon Cart.

    1. The order amount referred to here is the subtotal price, which is the price you paid after discounts. The final subtotal price may not meet the threshold for free gifts if a discount code is used.
    2. Each order is limited to one gift.
    3. When placing an order on the official website and meeting the conditions, the gift will be automatically added to the generated order.
    4. The gifts offered during the EcoFlow Black Friday Sale are only available on the EcoFlow official website (za.ecoflow.com)
    5. The gifts offered during the EcoFlow Black Friday Sale are non-transferable, non-redeemable, and non-refundable.
    6. When applying for a refund, orders placed during the EcoFlow Black Friday Sale will be refunded based on the actual amount paid. The gift must be returned intact with packaging. Otherwise, the refund can not be processed.

    All Coupons are subject to the following usage conditions

    1. Available for all products, excluding RIVER 2 portable power station and flash sale products.
    2. Limited to one coupon per order.
    3. Only applies to customers in South Africa.

    Flash Sale

    EcoFlow will launch Flash Sale products on the Christmas sale page at 00:00 SAST on December 18.

    1. Flash Sale products are only available for 24 hours. Events will occur on December 18 from 00:00 to 23:59.
    2. All coupon codes can’t be applied to flash sale products.

    General

    1. Participants agree to release and discharge EcoFlow from any liabilities and claims, including breach of contract, tort, negligence, or any other cause of action at law or equity, arising out of or in any way connected to this campaign or the participant’s entry into the campaign.
    2. Participants further agree to release and discharge any third party related to or connected with this campaign from any liabilities and claims, including breach of contract, tort, negligence, or any other cause of action at law or equity, arising out of, or in any way connected to, this campaign or the participant’s entry into the campaign.
    3. By participating in this campaign, participants agree to indemnify and hold EcoFlow and the EcoFlow Group of Companies, their officers, directors, shareholders, predecessors, successors, employees, agents, and representatives harmless from any claims, losses, damages, liabilities, or expenses (including legal fees) arising from this campaign or related to it in any way.
    4. EcoFlow reserves the right to disqualify participants who use or have used improper means to participate in this campaign without prior notice and may initiate legal proceedings to the fullest extent permitted by applicable law.
    5. EcoFlow reserves the right to modify, adjust, or terminate this campaign, with any changes, adjustments, or terminations being announced on the online sales platform.
    6. If you have any questions, please contact customer service: support.za@ecoflow.com.
    7. This campaign and its terms and conditions are governed by the laws of South Africa
    Posted on Leave a comment

    Get started with Shopping Campaigns

    Posted on Leave a comment

    Reach New Customers

    Bassey Medical & Family Health Centres_Logo Tele-Health Repeat Scripts E-Scripts
    Posted on 1 Comment

    Welcome to Rentech on Feedonomy

    Rentech is the leading renewable energy product and service provider in Africa.

    Welcome to?áRentech?áon Feedonomy and?áRentech on BrowSearch?áon BrowSearch (Beta). Please note that this is an unofficial mock-up only, provided by Feedonomy. A few years ago, I stumbled upon an article from Investec,?áThe Fourth Industrial Revolution?áwhich piqued my interest in renewable energy, batteries, electric vehicles, solar, and wind farms. This fascination led me to explore various companies in this industry, and after nearly two years of research, I discovered a handful of exceptional companies. Although more than 95% of them turned out to be online sellers or small e-commerce concerns, two companies clearly stood out from the rest. Since then, IÔÇÖve been closely following Rentech. Please understand that this is not an advertisement but rather a testament to my genuine admiration for this company. While I acknowledge that my writing skills may not do justice to the topic, I hope you can look past that. IÔÇÖd like to emphasize the importance of the capital-lettered note: NOTE: THIS IS AN UNOFFICIAL MOCK-UP ONLY. I have not sought RentechÔÇÖs permission to include their listings on this platform. This project has been on hold for almost two years, and thereÔÇÖs a possibility that it may disappear, along with this review, or even have an impact on Rentech. I have reached out to Rentech twice in the past, once expressing my interest in becoming a reseller and later to inquire about purchasing one of their power backup products. Unfortunately, both times, I was met with a polite decline. Normally, I would delete my previous efforts and reconsider my approach, but this time is different. I genuinely believe that the Rentech brand is exceptional. I deeply admire the companyÔÇÖs values and its commitment to quality and long-term sustainability, in stark contrast to the many others solely focused on making quick profits. Additionally, I happen to know the manufacturer of their solar panels, which, while not the largest, is undeniably one of the top global manufacturers. I also want to highlight that I have first-hand experience with portable power solutions. I initially purchased two that looked promising, but they both turned out to be of low quality. However, when I got my hands on the Rentech brand, it proved to be a game-changer. I still use it daily, sometimes for up to 8 or 9 hours a day. For me, itÔÇÖs Rentech or nothing. Thanks.

    Posted on Leave a comment

    Prescription stimulants in individuals with and without attention deficit hyperactivity disorder: misuse, cognitive impact, and adverse effects

    Shaheen E. Lakhan & Annette Kirchgessner
    Global Neuroscience Initiative Foundation, Los Angeles, California

    disorder, oppositional-de´¼üant disorder, antisocial person-
    ality, substance use, and anxiety) (Faraone et al. 1997;
    Rasmussen and Gillberg 2000; Kollins et al. 2005; Bieder-
    man et al. 2006). However, early treatment may decrease
    negative outcomes of ADHD including the rate of con-
    duct disorder and adult antisocial personality disorder
    (Dopheide and Pliszka 2009).
    There are both pharmacological and nonpharmacologi-
    cal (e.g., cognitive behavioral therapy [CBT]) treatments
    of ADHD. Stimulants, such as methylphenidate (MPH;
    Ritalin and Concerta) and dextroamphetamine-AMP
    (d-AMP; Adderall) are the most common pharmacologic
    treatments (The MTA Cooperative Group 1999) and
    abundant data support the potentially positive effects of
    prescription stimulants for the majority of children, ado-
    lescents, and adults with ADHD. Experts estimate that
    approximately 60% of children with ADHD are treated
    with prescription stimulants (Center for Disease Control
    and Prevention 2005a); therefore, approximately three
    million children in this country take stimulants for prob-
    lems with focusing. At the same time, many studies have
    revealed the numerous adverse effects associated with pre-
    scription stimulants when they are used inappropriately.
    Stimulants are classi´¼üed as Schedule II drugs (i.e., pro-
    viding positive medicinal effects but also considerable
    abuse potential). The nonmedical use of prescription
    stimulants represents the second common most form of
    illicit drug use in college, second only to marijuana use
    (Johnston et al. 2004). Indeed, many consider stimulants
    ÔÇô whether obtained by prescription or illicitly ÔÇô a conve-
    nient option to improve performance or to induce
    euphoria (get ÔÇ£highÔÇØ). Major daily newspapers such as
    The New York Times have reported a trend toward grow-
    ing use of prescription stimulants, commonly called
    ÔÇ£smart pills,ÔÇØ by high school and college students for
    enhancing school or work performance (Jacobs 2005).
    Unfortunately, media reports appear to condone this
    behavior as 95% of articles mentioned at least one possi-
    ble bene´¼üt of using a prescription stimulant for neuroen-
    hancement, but only 58% mentioned any risks/side effects
    (Partridge et al. 2011). Stimulant misuse is often pre-
    dicted on individualsÔÇÖ misconceptions or simple lack of
    knowledge of associated risks.
    This review discusses recent studies regarding the use
    and misuse of stimulants among high school and college
    students, including athletes, with and without ADHD.
    Given the widespread belief that prescription stimulants
    are ÔÇ£smart pills,ÔÇØ we address if these drugs actually
    enhance cognition in a healthy individual. Athletes may
    see stimulants as a way to help maintain physical ´¼ütness
    for their competitive sport or to improve their concentra-
    tion. Finally, we elaborate on the long-term effects of
    chronic stimulant use. Addiction and tolerance are major
    concerns, as are psychosis and cardiovascular effects. Sur-
    prisingly, these associated risks of stimulant misuse are
    not frequently addressed in the media and literature.
    Clearly, the widespread misuse of prescription stimulants
    represents an important public health issue faced by stu-
    dents, school of´¼ücials, health centers, and parents.
    Methods
    This review was initiated with a PubMed search of the
    US National Library of Medicine with combinations of
    the following key words: ÔÇ£Adderall,ÔÇØ ÔÇ£amphetamine,ÔÇØ
    ÔÇ£methylphenidate,ÔÇØ ÔÇ£dexamphetamine,ÔÇØ ÔÇ£ADHD,ÔÇØ ÔÇ£mis-
    use,ÔÇØ ÔÇ£illicit use,ÔÇØ ÔÇ£non-prescription use,ÔÇØ ÔÇ£non-medical
    use,ÔÇØ ÔÇ£diversion,ÔÇØ ÔÇ£students,ÔÇØ and ÔÇ£athletes.ÔÇØ A review of
    all titles was conducted to include only pertinent publica-
    tions. A hand search of psychiatry journals was performed
    and reference lists from relevant studies were searched.
    Prescription stimulant use in ADHD
    It is estimated that about two-thirds of the children diag-
    nosed with ADHD receive pharmacological treatment
    (Centers for Disease Control and Prevention 2010) and
    the majority of medications used are stimulants (Center
    for Disease Control and Prevention 2005b). The pre-
    scribed use of stimulant medications to treat ADHD in
    children age 18 and younger rose steadily from 1996 to
    2008, from an estimated 2.4% in 1996 to an estimated
    3.5% of US children in 2008 (Zuvekas and Vitiello 2011).
    Overall, prescription stimulant use among 6- to 12-year-
    olds is highest, going from 4.2% in 1996 to 5.1% in 2008;
    however, the fastest growth rate occurred among
    13ÔÇô18 year olds, going from 2.3% in 1996 to 4% in 2008.
    Prescription stimulant use remained consistently low in
    the West than in other US regions and in lower racial/
    ethnic minorities.
    MPH and d-AMP are the most widely used prescrip-
    tion stimulants approved by the US Food and Drug
    Administration (FDA) for the treatment of ADHD. MPH
    is a short-acting stimulant drug. Generic MPH is available
    in many forms, and several versions of the long-acting
    MPH have been introduced, with Concerta getting the
    largest share of the market. According to the U.S. Drug
    Enforcement Administration (DEA), MPH has been the
    fourth most prescribed controlled substance in the United
    States since 2003, with over 58,000 Americans purchasing
    MPH in 2006 (Department of Justice: Drug Enforcement
    Administration 2008). Both the production and prescrip-
    tion of MPH has risen as the diagnosis of ADHD has
    concurrently increased. In addition, with the realization
    that ADHD is a lifelong disorder, MPH has become more
    commonly prescribed for adolescents and adults, and
    662 ?¬ 2012 The Authors. Published by Wiley Periodicals, Inc.
    Stimulants in Individuals With and Without ADHD S. E. Lakhan & A. Kirchgessnertreatment duration has increased (Horrigan 2001). Both
    MPH and d-AMP are ef´¼ücacious and well-tolerated medi-
    cations and remain the ´¼ürst choice for short duration
    management in adolescent and adult ADHD (Faraone
    and Glatt 2010). Although the precise mechanisms under-
    lying the action of these medications are not completely
    understood, they appear to increase the availability of
    dopamine, which could account for their therapeutic
    effects.
    Although ADHD is a multifactorial disorder, disrupted
    dopamine (DA) neurotransmission plays an important
    role in its pathophysiology. In addition, polymorphisms
    in the dopamine D1 receptor (DRD1) are associated with
    the disorder (Misener et al. 2004). MPH and d-AMP both
    enhance DA signaling in the brain. MPH increases DA by
    blocking dopamine transporters (DATs) and AMP by
    releasing DA from the nerve terminal using the DAT as
    carrier (Kuczenski and Segal 1997). In healthy controls
    and in adolescents and adults with ADHD (Rosa-Neto
    et al. 2005; Volkow et al. 2007), MPH signi´¼ücantly
    increased DA in the ventral striatum (VS) (Volkow et al.
    2012), a crucial brain region involved with motivation
    and reward (Wise 2002). Moreover, intravenous MPH-
    induced increases in DA in the VS were correlated with
    improvement in symptoms of inattention after long-term
    oral MPH treatment. Historically, the core feature of
    ADHD has been characterized as one of attention de´¼ücit,
    but increasing evidence suggests that a reward and moti-
    vation de´¼ücit may be of equal importance. It has been
    proposed that increasing DA in the VS would enhance
    the saliency of the task, thus improving attention in
    ADHD (Volkow et al. 2012). Intravenous MPH also sig-
    ni´¼ücantly increased DA in the prefrontal and temporal
    cortices that were associated with decreased ratings of
    inattention, which may be therapeutically relevant.
    The widespread use of prescription stimulants for
    ADHD has not been without critics. In recent months,
    we have heard speculation about whether ADHD is a real
    disease, and if it is real, whether it is being grossly over-
    diagnosed. Disorders often become widely diagnosed after
    drugs come along that can alter a set of suboptimal
    behaviors. In this way, Ritalin and Adderall helped make
    ADHD a household name. If there is a pill that can clear
    up the wavering focus of sleep-deprived youth, then those
    rather ordinary states may come to be seen as syndrome.
    A recent opinion piece entitled ÔÇ£Ritalin Gone WrongÔÇØ in
    the New York Times (Sroufe 2012) by psychology profes-
    sor L. Alan Sroufe argues that attention-de´¼ücit drugs do
    more harm than good over the long term, a conclusion
    other professionals in his ´¼üeld dispute. Studies have
    shown that children who take MPH can show reductions
    in ADHD symptomatology (inattention, hyperactivity,
    and impulsivity) and gains in social and classroom
    behaviors. Studies of adults with ADHD have con´¼ürmed
    its usefulness for this population as well. However, the
    bene´¼üts of prescription stimulants on ADHD symptom-
    atology do not appear to last long.
    The Multimodal Treatment Study of Children with
    ADHD (MTA) compared four distinct treatment strate-
    gies during childhood for children diagnosed with DSM-
    IV ADHD, Combined Type (The MTA Cooperative
    Group 1999). Children were randomly assigned to
    14 months of (a) systematic medication management
    (MedMgt), which was initial placebo-controlled titration,
    three times a day dosing, 7 days a week, and monthly
    30-min clinic visits, (b) multicomponent behavior therapy
    (Beh), which included 27-session group parent training
    supplemented with eight individual parent sessions, an
    8-week summer treatment program, 12 weeks of
    classroom administered behavior therapy with a half-time
    aide, and ten teacher consultation sessions, (c) their
    combination (Comb), or (d) usual community care (CC).
    This randomized, six-site, controlled clinical trial featured
    rigorous diagnostic criteria at study entry and compared
    the relative effectiveness of treatments of well-established
    ef´¼ücacy. The initial MTA ´¼ündings reported that all groups
    showed improvement over baseline at the end of the
    14-month treatment period; however, the Comb and
    MedMgt group participants showed signi´¼ücantly greater
    improvements in ADHD symptoms than did the Beh or
    CC participants. By the next follow-up, 3 years after
    enrollment, there were no longer signi´¼ücant treatment
    group differences in ADHD symptoms or functioning
    (Jensen et al. 2007). Molina et al. (Molina et al. 2009)
    reported the next two follow-up assessments of the MTA
    sample at 6 and 8 years after random assignment, when
    the sample ranged in age from 13 to 18 years and found
    similar ´¼ündings.
    Prevalence of prescription stimulant
    misuse
    The misuse of a stimulant medication ÔÇô taking a stimu-
    lant not prescribed by a physician or in a manner not in
    accordance with physician guidance ÔÇô has been growing
    over the past two decades. In fact, in the past 10 years
    there has been a surge in prevalence rates of non-
    prescription stimulant use among both adolescents and
    young adults. In general, nonprescription use of MPH in
    2000 was reported as 1.2% and in 2006 this number had
    risen to 2%. Breaking the sample down by age, nonpre-
    scription use among adolescents (ages 12ÔÇô17) went from
    2.2% to 1.8% between 2000 and 2006, a slight decrease.
    Among college-aged individuals (ages 18ÔÇô25), however,
    usage increased signi´¼ücantly from 3.6% in 2000 to 5.4%
    by 2006. Finally, among those 26 and older, usage is the
    ?¬ 2012 The Authors. Published by Wiley Periodicals, Inc. 663
    S. E. Lakhan & A. Kirchgessner Stimulants in Individuals With and Without ADHDlowest of any group, but rates are rising. In 2000, only
    0.7% reported any lifetime usage of MPH, but this num-
    ber had doubled to 1.5% by 2006 (Bogle and Smith
    2009).
    The majority of research on the misuse of prescription
    stimulants has focused on undergraduate college students.
    The nonprescription use of stimulants has increased in
    this population, to the extent that the misuse of prescrip-
    tion stimulants is second only to marijuana as the most
    common form of illicit drug use among college students
    (Johnston et al. 2004). A 2001 nationwide self-reported
    survey of more than 10,000 students from 4-year univer-
    sities in the United States reported a 6.9% lifetime preva-
    lence of nonprescription stimulant misuse, including a
    past-year prevalence of 4.1% and a past-month prevalence
    of 2.1% (McCabe et al. 2005). Colleges with the highest
    past-year prevalence rates were typically located in the
    northeastern United States, which is corroborated by
    other reports (McCabe et al. 2005). A study by Teter
    et al. (2005) of 9161 undergraduates reported an 8.1%
    lifetime nonprescription stimulant misuse rate among col-
    lege students, including 5.4% over the past year. Accord-
    ing to a 2002 survey of a single US college, 35.5% of
    undergraduates reported using stimulants without a pre-
    scription, with greater frequency occurring in males com-
    pared with females (Low and Gendaszek 2002).
    The majority of nonprescription stimulant users
    reported obtaining the drugs from a peer with a prescrip-
    tion ÔÇô a process termed diversion. The diversion of stim-
    ulants is very common and can begin in childhood,
    adolescence, or young adulthood. A study conducted by
    Wilens et al. (2008) reported that lifetime rates of diver-
    sion ranged from 16% to 29% of students with stimulant
    prescriptions asked to give, sell, or trade their medications
    (Wilens et al. 2008). One survey reported that 23.3% of
    middle and high school students taking prescribed stimu-
    lants had been solicited to divert their medication to oth-
    ers at a rate that increased from middle school to high
    school (McCabe et al. 2004). A review of 161 elementary
    and high school students prescribed the stimulant MPH
    revealed that they had been asked to give or sell their
    medication to others (Musser et al. 1998). Data has
    shown that the diversion continues among college stu-
    dents. McCabe et al. found 54% of college students who
    were prescribed stimulants for ADHD had been
    approached to divert their medication (McCabe and Boyd
    2005). Nearly 29% of 334 college students had sold or
    given their medication to others (Upadhyaya et al. 2005).
    McCabe et al. (2005) examined the prevalence rates
    and correlates of nonprescription use of stimulants (Rita-
    lin, Adderall, or Dexedrine) among US college students
    and found evidence that misuse is more prevalent among
    particular subgroups of US college students and types of
    colleges. The lifetime prevalence of nonprescription
    stimulant use was 6.9%, past-year prevalence was 4.1%,
    and past-month prevalence was 2.1%. Multivariate
    analysis indicated that nonprescription use was higher
    among college students who were male, white, members
    of fraternities and sororities and earned lower grade point
    averages. Wilens et al. (2008) reported similar ´¼ündings.
    Rates were higher at colleges located in the northeastern
    region of the United States and colleges with more
    competitive admission standards. Nonprescription
    stimulant users were more likely to report use of alcohol,
    cigarettes, marijuana, ecstasy, cocaine, and other risky
    behaviors. Among college students, available evidence
    suggests that individuals who misuse MPH were more
    likely to be white, male, af´¼üliated with a formally
    organized fraternity, and more likely to use other illicit
    and illegal substances (Bogle and Smith 2009).
    A descriptive, nonexperimental, cross-sectional study
    examined the nonprescription use of stimulants among
    student pharmacists (Lord et al. 2003). Lifetime preva-
    lence of stimulant misuse was 7% and was more likely in
    students who were white, older, and fraternity or sorority
    members, whereas past-year misuse was more likely in
    whites and low academic achievers. A recent survey found
    that the misuse of prescription stimulants is also rampant
    among dental and dental hygiene students (McNiel et al.
    2011). The survey, which was mailed to dental education
    institutions in the south-central region of the United
    States, found that 12.4% of these students used a stimu-
    lant without a prescription and, of those, 70% took it to
    improve attention and/or concentration. The most com-
    monly reported stimulant medication used was Adderall
    (77%). The majority (87%) of the students obtained the
    medication through friends, and 90% began using the
    drug in college. Interestingly, 17% of the students sur-
    veyed felt it was easy to obtain stimulant medication for
    use at their school, and 17% thought it was a problem
    within their institution. The use, misuse, and diversion of
    prescription stimulants among middle and high school
    students were also examined by McCabe et al. (2005). In
    this study, the odds for nonprescription stimulant use
    were lower among African American students and higher
    among those students with no plans for attending college.
    These students also had the highest rates of alcohol and
    other drug use.
    The prevalence of prescription stimulant misuse in
    medical students is also high. In fact, discussion based
    websites such as Facebook, Medical School Forum, and
    The Student Doctor Network are rife with Adderall
    ÔÇ£expertsÔÇØ and informal question-and-answer sessions on
    the drug. An anonymous survey was administered to
    388 medical students (84.0% return rate) across all
    4 years of education at a public medical college. More
    664 ?¬ 2012 The Authors. Published by Wiley Periodicals, Inc.
    Stimulants in Individuals With and Without ADHD S. E. Lakhan & A. Kirchgessnerthan 10% of medical students reported using stimulants
    to improve academic performance. ADHD was diag-
    nosed in 5.5% of students and 72.2% of those students
    were diagnosed after the age of 18 years (Tuttle et al.
    2010). This study suggests that medical students appear
    to be a relatively high-risk population for prescription
    stimulant misuse. Several of´¼ücials now say the problem
    is increasing in medical schools (Harris 2009). ÔÇ£During
    the last few years, the number of requests for ADD
    evaluations has hugely increased,ÔÇØ Paula Stoessel, Ph.D.,
    director of mental health services for physicians in
    training at the University of California, Los Angeles,
    David Geffen School of Medicine. ÔÇ£We make them
    [medical students] go through a lot before we hand out
    medication, but IÔÇÖve heard them talk about [obtaining
    Adderall prescriptions] in passing.ÔÇØ Clearly, the results
    emphasize the need for education about stimulants and
    their adverse side effects.
    Why are prescription stimulants
    misused?
    The reasons why prescription stimulants are misused are
    numerous and include achieving euphoria, and helping
    cope with stressful factors related to their educational
    environment. According to a survey of 334 ADHD-
    diagnosed college students taking prescription stimulants,
    25% misused their own prescription medications to get
    ÔÇ£highÔÇØ (Upadhyaya et al. 2005). Like cocaine, MPH
    inhibits the DAT, which increases synaptic levels of DA,
    and this is presumed to mediate MPHÔÇÖs reinforcing effects
    and abuse potential. In laboratory studies, it has been
    shown that animals will repeatedly administer MPH as
    they do cocaine (Kollins 2003), and humans receiving
    both drugs indicate a similar ÔÇ£highÔÇØ (Volkow et al. 1995).
    A frequent concern regarding the use of stimulants for
    ADHD is their mechanism of action, which increases DA
    and thus may increase the risk for overt, illicit drug use.
    However, research points to the conclusion that people of
    any age receiving a stimulant for ADHD have no greater
    risk for illicit substance abuse compared with the general
    population (Wilens 2003).
    Stimulants are especially popular at the end of a school
    term when students will often use the drugs to stay awake
    through the night to study for exams or complete aca-
    demic projects. In fact, prescription stimulants are most
    commonly misused to enhance school performance.
    According to a Web survey of 115 ADHD-diagnosed col-
    lege students, enhancing the ability to study outside of
    class was the primary motive for misuse (Rabiner et al.
    2009). Pressures such as a persistent desire to succeed
    academically, poor sleep habits due to large workloads,
    and the persistence of underlying social and ´¼ünancial
    demands may place students at an increased risk for mis-
    use of various drugs, including stimulants (Kadison 2005;
    Teter et al. 2005). Students who misused ADHD medica-
    tions generally felt that doing so was helpful. Thus, pre-
    scription stimulants developed to help children with
    ADHD improve their focus and attention are often mis-
    used by the patient, especially ADHD patients with con-
    duct disorder or comorbid substance abuse (Kollins
    2008). Moreover, students without ADHD misuse stimu-
    lants to improve performance or to induce euphoria. A
    web-based survey administered to medical and health
    profession students found that the most common reason
    for nonprescription stimulant use was to focus and con-
    centrate during studying (93.5%) (Herman et al. 2011).
    In this study, approximately 10.4% of students surveyed
    (45.2% female; 83.9% male; 83.9% Caucasian) have either
    used a stimulant or are currently using prescription stim-
    ulants, and the most commonly abused stimulant
    (71.4%) was d-AMP. A recent survey found that 70% of
    dental and dental hygiene students used a prescription
    stimulant nonmedically to improve attention and/or con-
    centration (McNiel et al. 2011). Student pharmacists
    (Lord et al. 2003) and medical students (Tuttle et al.
    2010) are also using stimulants to improve concentration
    and academic performance.
    Effects of prescription stimulants on
    cognition in ADHD
    Neuropsychological studies of ADHD children and adults
    indicate impairments in many cognitive areas including
    selective attention, memory, reaction time, information
    processing speed, and executive control function such as
    set-shifting, and working memory. The bene´¼üts of pre-
    scription stimulants for enhancing classroom manageabil-
    ity and increasing attention and academic productivity in
    children are well established. Prescription stimulants may
    increase the quality of note taking, scores on quizzes and
    worksheets, writing output, and homework completion.
    Nevertheless, they do not normalize the ability to learn
    and apply knowledge (Advokat 2010). In fact, it has been
    recognized over 30 years that there is little evidence that
    prescription stimulants such as MPH and AMP improve
    the academic achievement of ADHD-diagnosed children.
    Children with ADHD have a consistently lower full-scale
    IQ than normal controls. They score signi´¼ücantly lower
    on reading and arithmetic tests, use more remedial aca-
    demic services, and are more likely to be placed in a spe-
    cial education class, or repeat a grade compared with
    controls. They also take more years to complete high
    school and have lower rates of college attendance
    (Advokat 2010). Thus, prescription stimulants have only
    a modest impact on these outcomes.
    ?¬ 2012 The Authors. Published by Wiley Periodicals, Inc. 665
    S. E. Lakhan & A. Kirchgessner Stimulants in Individuals With and Without ADHDThe ´¼ürst review to describe the general academic func-
    tioning of adults with ADHD summarized the results
    from 23 studies (Weyandt and DuPaul 2006). ADHD-
    diagnosed college students were found to have signi´¼ü-
    cantly lower grade point averages, report more ÔÇ£academic
    problemsÔÇØ and to be less likely to graduate from college.
    Nevertheless, ADHD-diagnosed college students did not
    differ in IQ from those without ADHD, and were shown
    to be able to meet the demands of college courses. On
    psychological tests, they showed signi´¼ücant de´¼ücits in
    attention, but were not different from normal students on
    other measures, such as the ability to be ´¼éexible and to
    maintain performance, as task demands varied (Weyandt
    and DuPaul 2006). More recent reports have reached sim-
    ilar conclusions. Interestingly, like elementary and high
    school students, college students with ADHD are less
    likely to reach the same academic level as their non-
    ADHD counterparts, even when they use stimulant medi-
    cations. Thus, stimulant medications do not necessarily
    equalize academic achievement in the typical adult with
    ADHD.
    A recent controlled, cross-sectional study evaluated the
    effects of stimulants on cognition in adults with ADHD
    and found that treated ADHD subjects had signi´¼ücantly
    better scores on measures of IQ than did untreated
    patients (Biederman et al. 2012). Thus, either good cogni-
    tive functioning may be a determinant of seeking treat-
    ment or stimulant treatment may improve cognition in
    adults with ADHD. When ADHD studies address the
    issue of cognition, they usually demonstrate that treated
    patients perform better than untreated patients on neuro-
    psychological tests or measures after they are treated.
    Whether treatment normalizes neurocognitive perfor-
    mance is rarely addressed. In fact, adults with ADHD are
    less likely to attain the same educational levels as those
    without the diagnosis relative to what would be predicted
    based on their IQ, and this outcome does not appear to
    be improved by stimulant medication. In one recent
    study, for example, although 84% of ADHD-diagnosed
    adults were statistically expected to be college graduates,
    only 50% reached this level of education (Biederman
    et al. 2008a,b). Gualtieri and Johnson (2008) conducted a
    cross-sectional study of ADHD patients treated with
    different ADHD drugs (Adderall XR, atomoxetine,
    Concerta) (Adderall XR is an extended-release formu-
    lation with duration of action of approximately 10ÔÇô12 h.
    This is signi´¼ücantly longer than the duration of action of
    most methylphenidate formulations, with the exception of
    Concerta. Immediate-release methylphenidate lasts at
    most for 6 h). PatientsÔÇÖ performance on a computerized
    neurocognitive screening battery was compared with
    untreated ADHD patients and normal controls. Signi´¼ü-
    cant differences were detected between normal and
    untreated ADHD patients. Treated patients performed
    better than untreated patients but remained signi´¼ücantly
    impaired compared with normal subjects. Thus, even after
    optimal treatment, neurocognitive impairments persisted
    in the ADHD patients.
    It has never been established that the cognitive effects
    of stimulant drugs are central to their therapeutic utility.
    In fact, although ADHD medications are effective for the
    behavioral components of the disorder, little information
    exists concerning their effects on cognition. Barkley and
    Cunningham (1978) summarized 17 short-term research
    studies ranging from 2 weeks to 6 months, and found
    stimulant medications produced little improvement in the
    academic performance of hyperkinetic ADHD children.
    The drugs appeared to reduce disruptive behavior rather
    than improve academic performance. Stimulant drugs do
    improve the ability (even without ADHD) to focus and
    pay attention. One function, which is reliably improved
    by stimulant medications, is sustained attention, or vigi-
    lance. Stimulants improve sustained, focused attention,
    but ÔÇ£selective attentionÔÇØ and ÔÇ£distractibilityÔÇØ may be
    worsened, possibly because of a drug induced increase in
    impulsivity. Both AMP and MPH do not improve (and
    may even impair) short-term acquisition of information.
    In addition, AMP and MPH do not improve, and may
    impair ÔÇ£cognitive ´¼éexibilityÔÇØ as assessed with tests such as
    the Wisconsin Card Sort and Attentional Set-Shifting
    tasks. MPH has been shown to improve performance on
    an auditory arithmetic task, the Paced Auditory Serial
    Addition Task, in adults with ADHD relative to control
    subjects (Schweitzer et al. 2004). AMP and MPH might
    improve long-term retention of information, if the drugs
    are active during a period in which memory is being
    ÔÇ£consolidated.ÔÇØ However, this may only occur in situa-
    tions where retention is already suboptimal.
    Effects of stimulants on cognition in
    individuals without ADHD
    Recognition that ADHD persists into adulthood has sub-
    stantially increased the prescription stimulant treatment
    of adults with the disorder (see above). It has also
    resulted in a corresponding escalation of nonprescription
    stimulant use in many college students con´¼ürmed by
    numerous surveys. Studies consistently show that students
    report using stimulant medications, legally or illicitly, to
    improve academic performance, speci´¼ücally to increase
    concentration and the ability to stay up longer and study.
    Intuitively, it would seem logical that drugs that improve
    attention and concentration should also promote learning
    and academic achievement. Inherent in terms like ÔÇ£cogni-
    tive enhancers,ÔÇØ ÔÇ£smart drugs,ÔÇØ and ÔÇ£neuroenhancersÔÇØ is
    the assumption that MPH and d-AMP enhance cognition.
    666 ?¬ 2012 The Authors. Published by Wiley Periodicals, Inc.
    Stimulants in Individuals With and Without ADHD S. E. Lakhan & A. KirchgessnerMajor magazines such as The New Yorker have reported a
    trend toward growing use of prescription stimulants by
    college students for ÔÇ£neuroenhancementÔÇØ. In fact, some
    students are faking ADHD to gain access to prescription
    stimulant medication, which has led to a shortage of
    ADHD drugs such as Adderall (Mitchell 2012). Unfortu-
    nately, media reports appear to condone this behavior as
    95% of articles mentioned at least one possible bene´¼üt of
    using prescription drugs for neuroenhancement, but only
    58% mentioned any risks or side effects (Partridge et al.
    2011). Duke University recently enacted a new policy pro-
    hibiting the nonmedical use of prescription stimulants for
    any academic purposes (McLaughlin 2012). Students
    received an email stating policy changes including, ÔÇ£The
    unauthorized use of prescription medication to enhance
    academic performance has been added to the de´¼ünition
    of Cheating.ÔÇØ In the past, the use of such drugs without a
    prescription was only a violation under the UniversityÔÇÖs
    drug policy. Oddly, the assumption that prescription
    stimulants are truly ÔÇ£cognitive enhancersÔÇØ is not really
    questioned. Stimulants reduce hyperactivity, impulsivity,
    and inattention in children and adults with ADHD, so it
    has been assumed that these drugs enhance long-term
    intellectual performance. However, contrary to simple
    implicit assumptions found in bioethics and media dis-
    courses, there are actually only a few studies on the
    enhancement effects of ÔÇ£cognitive enhancersÔÇØ in individu-
    als without ADHD.
    Smith and Farah (2011) reviewed data on prescription
    stimulants as neuroenhancers from over forty laboratory
    studies involving healthy, nonelderly adults. Most of the
    studies looked at one of three types of cognition: learn-
    ing, working memory, and cognitive control. Effects of
    d-AMP or MPH on cognition were assessed by a variety
    of tasks (Table 1). A typical learning task asks subjects
    to memorize a list of paired words; an hour, a few days,
    or a week later, subjects are presented with the ´¼ürst
    words in the pairs and asked to come up with the sec-
    ond. In general, with single exposures of verbal material,
    the studies on learning showed that no bene´¼üts are seen
    immediately following learning, but later recall and rec-
    ognition are enhanced. Of the six articles reporting on
    memory performance (Rapoport et al. 1978; Soetens
    et al. 1993; Camp-Bruno and Herting 1994; Fleming
    et al. 1995; Unrug et al. 1997; Zeeuws and Soetens
    2007), encompassing eight separate experiments, only
    one of the experiments yielded signi´¼ücant memory
    enhancement on short delays (Rapoport et al. 1978). In
    contrast, retention was reliably enhanced by d-AMP
    when subjects were tested after longer delays, with recall
    improved after 1 h through 1 week (Soetens et al. 1993,
    1995; Zeeuws and Soetens 2007). These data suggest that
    when people are given rote-learning tasks their perfor-
    mance is improved by stimulants. The bene´¼üts were
    more apparent in studies where subjects had been asked
    to remember information for several days or longer.
    However, studies only found a correlation with rote
    memory tasks, not complex memory, which is more
    likely to appear on college exams.
    In contrast to the types of memory, which are long
    lasting and formed as a result of learning, working mem-
    ory is a temporary store of information that plays a role
    in executive function. Several studies have assessed the
    effect of MPH or d-AMP on tasks examining various
    aspects of working memory (Sahakian and Owen 1992;
    Oken et al. 1995; Elliott et al. 1997; Mehta et al. 2000;
    Barch and Carter 2005; Silber et al. 2006; Clatworthy
    et al. 2009) (see Table 1). One classic approach to the
    assessment of working memory is the span task, in which
    a series of items is presented to the subject for repetition,
    transcription, or recognition. A spatial span task, in which
    the subjects must retain and reproduce the order in which
    boxes in a scattered spatial arrangement change color was
    employed by Elliott et al. (1997) to assess the effects of
    MPH on working memory. For the subjects in the group
    who received placebo ´¼ürst, MPH increased spatial span.
    However, for the subjects who received MPH ´¼ürst, there
    was a nonsigni´¼ücant opposite trend. The authors noted
    that the subjects in the ´¼ürst group performed at an overall
    lower level, and so, this may have contributed to the lar-
    ger enhancement effect for less able subjects. Barch and
    Carter (2005) obtained similar results and Mehta et al.
    (2000) found evidence of greater accuracy with MPH. In
    the study by Mehta et al. (2000), the effect depended on
    subjectsÔÇÖ working memory ability: the lower a subjectÔÇÖs
    score on placebo, the greater the improvement on MPH.
    In contrast to the three previous studies, Bray et al.
    (2004) reported that MPH does not improve the cogni-
    tive function of sleep-deprived young adults. In sum, the
    evidence concerning stimulant effects of working memory
    is mixed, with some ´¼ündings of enhancement and some
    null results, although no ´¼ündings of overall performance
    impairment (Smith and Farah 2011). However, the small
    effects were mainly evident in subjects who had low
    cognitive performance to start with, showing that the
    drug is more effective at correcting de´¼ücits than
    ÔÇ£enhancing performance.ÔÇØ Farah et al. (2009) recently
    examined the effect of Adderall upon creativity, a
    component of cognition stimulants are suspected of sti-
    ´¼éing, in a double-blind, placebo-controlled trial. They
    found that the drug enhanced creativity on speci´¼üc tasks,
    but the amount of enhancement depended upon the
    baseline performance of individuals: lower-performing
    individuals were more enhanced than high-performers.
    Thus, the drugs do not offer as much help to people with
    greater intellectual abilities.
    ?¬ 2012 The Authors. Published by Wiley Periodicals, Inc. 667
    S. E. Lakhan & A. Kirchgessner Stimulants in Individuals With and Without ADHDTable 1. Overview of effects of prescription stimulants on cognitive performance in adults without ADHD.
    Study Tests Finding
    Barch and Carter
    (2005)
    Spatial working memory Decrease in reaction time
    Stroop test Decrease in response time
    Breitenstein et al.
    (2004)
    Probabilistic learning Steeper increase in hits and decrease in misses across learning sessions;
    increase in retention after more than 1 year
    Breitenstein et al.
    (2006)
    Probabilistic learning Steeper learning curve
    Brignell et al.
    (2007)
    Single-exposure verbal learning At 1 week improved recognition
    Brumaghim and
    Klormart (1998)
    Associative learning: word pairs No effect
    Burns et al. (1967) Associative learning: location of stimulus and
    response
    Slower rate of learning
    Callaway (1983) Item recognition No effect
    Camp-Bruno and
    Herting (1994)
    Repeated-exposure verbal learning 1 h: no effect; 2 h: borderline effect
    Camp-Bruno and
    Herting (1994)
    Single-exposure verbal learning Up to 2.5 h: no effect
    Clatworthy et al.
    (2009)
    Spatial working memory No effect
    Reversal learning No effect
    Cooper et al.
    (2005)
    Continuous performance test (double version) 5 min: decrease in reaction time; decrease in errors of omission
    de Wit et al.
    (2000)
    Stop-signal task No effect
    de Wit et al.
    (2002)
    Repeated-exposure verbal learning 25 min: no effect
    Digit span Increase in performance
    Go/no-go Decrease in number of false alarms
    Delay of grati´¼ücation No effect
    Dodds et al.
    (2008)
    Reversal learning No effect
    Elliott et al. (1997) Spatial span Decrease in errors
    Spatial working memory Decrease in errors
    Attentional set-shifting No effect
    Verbal ´¼éuency No effect
    Sequence generation No effect
    New Tower of London No effect
    Tower of London Relative decrease in accuracy
    Fillmore et al.
    (2005)
    Stop-signal task No effect
    n-back Increase in processing rate
    Fitzpatrick et al.
    (1988)
    Item recognition: stimulus evaluation/
    response selection task
    Decrease in reaction time
    Fleming et al.
    (1995)
    Single-exposure verbal learning 20 min: no effect on single-exposure verbal learning
    Continuous performance test 5 min: decrease in reaction time
    Spatial working memory No effect
    Wisconsin Card Sorting Test No effect
    Verbal ´¼éuency No effect
    Hurst et al. (1969) Associative learning: word pairs Increase in retention after 1 week delay
    Kennedy et al.
    (1990)
    Item recognition No effect
    Grammatical reasoning No effect
    Klorman et al.
    (1984)
    Continuous performance test (BX version) 45 min: decrease in reaction time; 12.5/45 min: decrease in errors of
    omission
    Koelega (1993) Vigilance performance Improves the overall level of vigilance performance and prevents the
    decrement that occurs over time under normal circumstances
    Kumari et al.
    (1997)
    Motor sequence learning No effect
    Motor sequence learning No effect
    (Continued)
    668 ?¬ 2012 The Authors. Published by Wiley Periodicals, Inc.
    Stimulants in Individuals With and Without ADHD S. E. Lakhan & A. KirchgessnerThe third type of cognition is cognitive control. Cogni-
    tive control is a broad concept that refers to guidance of
    cognitive processes in situations where the most natural,
    automatic, or available action is not necessarily the cor-
    rect one (Smith and Farah 2011). Attention and working
    memory are thought to rely on cognitive control and loss
    of cognitive control is a major component of many neu-
    ropsychiatric diseases such as schizophrenia. The effects
    of MPH and d-AMP have been determined on several
    tests used to study cognitive control, including the go/no-
    go task, the stop-signal task, and the Flanker test. In gen-
    eral, the effects of stimulants on cognitive control are not
    robust, but MPH and d-AMP appear to enhance cogni-
    tive control in some tasks for some people, especially
    those less likely to perform well on cognitive control tasks
    (Smith and Farah 2011). The results of these studies cur-
    rently provide limited support for the enthusiastic por-
    trayals of cognitive enhancement.
    The neural basis of error processing has become a key
    research interest in cognitive neuroscience. Recently, a
    single dose of MPH was shown to improve the ability of
    healthy volunteers to consciously detect performance
    errors (Hester et al. 2012). Furthermore, this behavioral
    effect was associated with a strengthening of activation
    Table 1. Continued.
    Study Tests Finding
    Makris et al.
    (2007)
    Item recognition Proportion correct sustained across multiple trials
    Mattay et al.
    (1996)
    Wisconsin Card Sorting Test No effect
    Mattay et al.
    (2000)
    n-back No effect
    Mattay et al.
    (2003)
    n-back No effect
    Wisconsin Card Sorting Test No effect
    Mehta et al.
    (2000)
    Spatial working memory Decrease in between-search errors
    Mintzer and
    Grif´¼üths (2007)
    Single-exposure verbal learning 2 h: improved recognition; no effect on recall
    n-back No effect
    Item recognition No effect
    Oken et al. (1995) Digit span No effect
    Rapoport et al.
    (1978)
    Single-exposure verbal learning; continuous
    performance test (BX version)
    10 min: improved recall; decrease in errors of omission
    Rogers et al.
    (1999)
    Attentional set-shifting Increase in intradimensional shift errors; decrease in extradimensional shift
    errors; increase in response latencies
    Schmedje et al.
    (1988)
    Digit span No effect
    Pattern memory No effect
    Schroeder et al.
    (1987)
    Strategic choice task Decrease in changeover rate
    Servan-Schreiber
    et al. (1998)
    Flanker task Decrease in response time; increase in accuracy
    Silber et al. (2006) Digit span No effect
    Trail Making Test No effect
    Soetens et al.
    (1993)
    Single-exposure verbal learning 20 min: no effect; 1 hÔÇô3 days: improved long-term retention
    Soetens et al.
    (1995)
    Single-exposure verbal learning 1 hÔÇô1 week: improved long-term retention in free recall; 1 week: improved
    recognition
    Strauss et al.
    (1984)
    Associative learning: word pairs; continuous
    performance test (double version)
    No effect; 45 min: decrease in reaction time; 45 min: decrease in errors of
    omission
    Unrug et al.
    (1997)
    Single-exposure verbal learning 20 min: no effect
    Ward et al. (1997) Motor sequence learning; item recognition No effect; decrease in reaction time
    Weitzner (1965) Associative learning: word pairs Improved performance only when pairs were uniquely semantically related
    Willett (1962) Repeated-exposure verbal learning Decrease in number of trials to reach criterion
    Zeeuws and
    Soetens (2007)
    Single-exposure verbal learning 30 min: no effect; 1 hÔÇô1 day: improved long-term retention
    Table adapted with permission from Smith and Farah (2011), Copyright 2011 by the American Psychological Association. The use of APA informa-
    tion does not imply endorsement by APA.
    ?¬ 2012 The Authors. Published by Wiley Periodicals, Inc. 669

    differences in the dorsal anterior cingulate cortex and
    inferior parietal lobe during the MPH condition for
    errors made with versus without awareness. How the
    brain monitors ongoing behavior for performance errors
    is a central question of cognitive neuroscience. Dimin-
    ished awareness of performance errors limits the extent to
    which humans engage in corrective behavior and has been
    linked to loss of insight in ADHD and drug addiction.
    As it remains unclear whether stimulant medication
    has the same effect on healthy individuals as for those
    with ADHD, it is possible that many reported effects of
    prescription stimulants in healthy individuals may stem
    from placebo effects. Looby and Earleywine (2011) exam-
    ined whether placebo effects in´¼éuence reports of subjec-
    tive mood and cognitive performance among college
    students who endorsed several risk factors for prescription
    stimulant misuse (e.g., low grade point average, frater-
    nity/sorority involvement, binge drinking). Interestingly,
    participants believed that they had better ability to focus
    and persevere, particularly for a sustained amount of
    time, when they expected to receive MPH (Looby and
    Earleywine 2011). This is similar to circumstances in
    which participants may engage in nonmedical-stimulant
    use to study or cram for extended hours. On the other
    hand, when experimental participants did not expect to
    receive MPH, their attention appeared disrupted resulting
    in inconsistent reaction times throughout the CPT. Inter-
    estingly, subjective feelings of being high and stimulated
    were produced solely by expecting to receive MPH. This
    ´¼ünding is important to consider when examining initia-
    tion and maintenance of nonmedical prescription stimu-
    lant use. As motives for nonprescription stimulant use
    include the desire to feel high (Barrett et al. 2005), it is
    likely that individuals who use a stimulant for this pur-
    pose will consequently feel high due to these demon-
    strated placebo effects, which will likely maintain misuse
    of the drug.
    Prescription stimulant misuse in
    athletes
    ADHD is a controversial problem in sport as participants
    with this disorder often require banned stimulants while
    competing. Many of the governing bodies of competitive
    sports have developed regulations that limit the use of
    stimulant medications to treat ADHD. In other cases,
    stimulant use is allowed in the setting of a documented
    diagnosis of ADHD. Most sports organizations around
    the world now follow the guidelines set forth by the
    World Anti-Doping Agency (WADA). According to this
    document, the diagnosis of ADHD is to be made by
    ÔÇ£experienced cliniciansÔÇØ and in accordance to the DSM-
    IV. Stimulant medications are considered to be a
    ÔÇ£medical best practice treatmentÔÇØ that do require the
    athlete to ´¼üle a therapeutic use exemption (TUE). A TUE
    gives athletes with medical diagnoses an exemption to
    use a drug normally prohibited by MLB, to treat a
    legitimately diagnosed medical condition. WADA
    recommends reassessments of continued treatment every
    3ÔÇô4 months. Other organizations, such as the National
    College Athletic Association (NCAA) and individual
    professional leagues, such as the National Football League
    (NFL) and Major League Baseball (MLB), have developed
    their own regulations.
    The NCAA does not require that physicians prescribe a
    trial of nonstimulant medications before prescribing stim-
    ulants, only that the prescribing physician considers non-
    stimulants ´¼ürst. The NCAA acknowledges that
    nonstimulant medication may not be as effective as stim-
    ulant medications in treating ADHD. In contrast to the
    NCAA regulations, athletes who are also participating in
    events governed by the International Olympic Committee
    (IOC) and/or WADA are not allowed to use stimulant
    medications, even with a TUE. These organizations
    require that the athlete with ADHD on stimulant medica-
    tions stop taking these medication or risk disquali´¼ücation
    (Putukian et al. 2011).
    It has been reported that MLB players are using an
    ADHD diagnosis to evade the AMP ban (Associated Press
    2009). According to records MLB of´¼ücials turned over to
    congressional investigators as part of George MitchellÔÇÖs
    probe into steroid use in baseball, the number of players
    getting ÔÇ£therapeutic use exemptionsÔÇØ from baseballÔÇÖs AMP
    ban jumped in 1 year from 28 to 103 ÔÇô which means that,
    suddenly, 7.6% of the 1354 players on major-league rosters
    have been diagnosed with ADHD. MLB banned AMP in
    2006. The prevalence of ADHD in athletes has not been
    studied, although there is no reason to believe it would dif-
    fer from the general population. Thus, 2ÔÇô3 times the usual
    adult rate of ADHD in baseball players is alarming. Ath-
    letes may see stimulants as a way to help maintain physical
    ´¼ütness for their competitive sport or to improve their con-
    centration. Certainly some of the players getting prescrip-
    tions for ADHD medications may have a legitimate
    medical need and without treatment, players manifesting
    the symptoms of untreated ADHD would be at a disadvan-
    tage to non-ADHD players. A therapeutic dose of MPH
    will bene´¼üt concentration, and may improve motor coor-
    dination. Prescription stimulants to treat ADHD could be
    used as performance enhancing drugs (PEDs); however, a
    proper diagnosis would prevent athletes from abusing the
    TUE status to ÔÇ£cheat within the rules.ÔÇØ
    Some athletes will only take medications episodically for
    school testing or for studying purposes. Others may feel
    that their sport performance is improved on stimulants,
    whereas others may temporarily stop taking them so
    670 ?¬ 2012 The Authors. Published by Wiley Periodicals, Inc.
    Stimulants in Individuals With and Without ADHD S. E. Lakhan & A. Kirchgessnerthat their sports play is more random and unfocused,
    which they feel improves their performance (Pelham et al.
    1990).
    Potential adverse affects of chronic
    stimulant use
    ADHD is now recognized as a chronic disorder that con-
    tinues into adulthood; therefore, some individuals take
    stimulants such as MPH and d-AMP for years. The medi-
    cal literature provides abundant data to support the
    potentially positive effect of stimulants for the majority of
    children, adolescents, and adults with ADHD, and stimu-
    lants have been considered to be relatively safe (Elia et al.
    1999; Brown et al. 2005). However, reports of adverse
    events in conjunction with the use of these drugs have
    raised concern about their safety.
    Large doses of stimulants can lead to psychosis, sei-
    zures, and cardiovascular events. The induction of schizo-
    phrenic-like states in AMP abusers is well documented,
    although the onset of such states in children on pre-
    scribed doses of stimulant medication is observed far less
    often (Polchert and Morse 1985; Masand et al. 1991;
    Murray 1998). Surles et al. (2002) published a case report
    of psychotic reactions to AMP (10 mg/day) in an adoles-
    cent ADHD patient. The patient displayed many of the
    characteristics of AMP-induced psychosis including visual
    hallucinations, delusions, anorexia, ´¼éattening of affect,
    and insomnia. It is thought that the mechanism of AMP-
    induced psychosis is mediated by dopaminergic excess. As
    the patientÔÇÖs symptoms disappeared when taken off the
    stimulant medication, it suggests that the psychosis was
    indeed secondary to AMP.
    The most commonly observed cardiovascular effects
    linked with ADHD stimulant medications include hyper-
    tension and tachycardia. In addition, cardiomyopathy,
    cardiac dysrhythmias, and necrotizing vasculitis have been
    described. In February 2005, the brand medication Adder-
    all XR (Shire BioChem Inc, Quebec, Canada) was with-
    drawn from the Canadian market by Health Canada. Case
    reports on serious cardiovascular adverse drug reactions
    (ADRs), sudden death, and psychiatric disorders led regu-
    latory agencies to warn against the use of MPH in the
    pediatric population in 2006 and 2007 (European Medi-
    cines Agency 2007). In 2006, warnings were also linked to
    atomoxetine use due to reports of hepatotoxicity and
    suicidal thoughts in children. These concerns received
    glaring attention in 2006 and led the US Food and Drug
    Administration advisory committee to propose placing a
    black box warning concerning sudden death on
    psychostimulants in response to ADR reports.
    Adderall use is associated with myocardial infarction
    and even sudden death (Gandhi et al. 2005; Jiao et al.
    2009). Gandhi et al. (2005) reported the case of a
    15-year-old male subject who suffered a myocardial
    infarction after taking two 20 mg tablets of Adderall. Jiao
    et al. (2009) reported a second case of a 20-year-old
    ADHD college freshman with myocardial infarction after
    taking two 15-mg tablets of Adderall XR. Recently,
    Sylvester and Agarwala (2012) reported another case of a
    15-year-old male subject who suffered a myocardial
    infarction after starting Adderall XR. The patient was
    otherwise in good health with no previous cardiac abnor-
    malities and improved with cessation of medication. The
    ´¼ündings of the case have been disputed (Rosenthal 2012).
    In addition, a recent report by Alsidawi et al. (2011)
    discusses the case of a 19-year-old female subject with
    Adderall overdose induced inverted-Takotsubo cardiomy-
    opathy, also known as stress-induced cardiomyopathy.
    The patient was brought to the emergency department
    after ingesting 30 Adderall tablets. She complained of
    pressure like chest pain and shortness of breath. Her car-
    diac enzymes were elevated, but the electrocardiogram
    was unremarkable. Echocardiography identi´¼üed a low
    ejection fraction of 25ÔÇô35% with severe hyperkinetic apex
    and akinetic base consistent with the diagnosis of
    inverted-TTC. Her symptoms resolved in 24 h. Drug-
    induced-Takotsubo cardiomyopathy has been previously
    reported and is mainly attributed to sympathetic oversti-
    mulation (Amariles 2011). In this case, the patient over-
    dosed on Adderall, which is a sympathomimetic drug.
    The mechanisms for AMP-induced cardiac injury are pos-
    tulated to be similar to those seen with cocaine, which
    include coronary spasm, prothrombotic state, accelerated
    atherosclerosis due to endothelial injury, and direct myo-
    cardial (Chen 2007). Inappropriate dosing or taking with
    alcohol increases the risk of serious cardiovascular side
    effects like myocardial infarction, even without underlying
    cardiovascular risk factors.
    Unfortunately, there are few long-term studies (i.e.,
    longer than 24 months) on the use of stimulants for the
    management of ADHD; therefore, the precise long-term
    effects ÔÇô either adverse or positive ÔÇô remain unknown.
    A recent study (Vitiello et al. 2011) suggests that the
    chronic use of stimulant medication to treat ADHD in
    children does not appear to increase the risk for high
    blood pressure in the long term, but it may have modest
    effects on heart rate. The MTA study found that stimulant
    medication does not appear to increase the risk for
    abnormal elevations in blood pressure or heart rate over a
    10-year period; however, the effect of stimulants on heart
    rate can be detected even after years of use (Vitiello et al.
    2011). The effect on heart rate may be clinically signi´¼ücant
    for individuals who have underlying heart conditions.
    A cohort study sought to determine whether use of
    MPH in adults is associated with elevated rates of serious
    ?¬ 2012 The Authors. Published by Wiley Periodicals, Inc. 671
    S. E. Lakhan & A. Kirchgessner Stimulants in Individuals With and Without ADHDcardiovascular events compared with rates in nonusers
    (Schelleman et al. 2012). All new MPH users with at least
    180 days of prior enrollment were identi´¼üed. Initiation of
    MPH was associated with a 1.8-fold increase in risk of sud-
    den death or ventricular arrhythmia; however, the lack of a
    dose response relationship suggested that this association
    might not be a causal one. A recent study by Habel and
    colleagues (Habel et al. 2011), which compared approxi-
    mately 150,000 adults prescribed ADHD medication with
    approximately 300,000 nonusers, found no evidence of a
    link between ADHD medication and cardiovascular risk
    (myocardial infarction, sudden death, or stroke). Although
    the student enrolled adults, the same group also has
    reported a similar lack of signi´¼ücant association between
    serious cardiovascular events and use of ADHD medica-
    tions in children and younger adults (Cooper et al. 2011).
    These ´¼ündings support the ´¼ünal decision of the US Food
    and Drug Administration committee to not to place a
    black box warning for all children and adults, but to
    pursue further research. However, the study by Habel et al.
    (2011) has limitations stemming from its focus on the
    most severe cardiovascular event. The databases were not
    used to examine other cardiovascular adverse effects, such
    as palpitations and dyspnea, which, although less severe,
    are nonetheless alarming to patients.
    Additional potential ADRs associated with stimulant use
    are important to note including abdominal pain, anorexia,
    constipation, dizziness, dry mouth, headache, insomnia,
    jitteriness, irritability, nausea, and palpitations (Greydanus
    and Strasburger 2006). College students with ADHD who
    misuse prescribed stimulants also reported hyperactivity
    symptoms as a common adverse event. Of particular
    signi´¼ücance to athletes, many stimulants utilized in treat-
    ing ADHD may increase core temperature (Piper et al.
    2005), possibly increasing risk of heart injury. These agents
    may also mask signs and symptoms of fatigue and allow
    for a longer duration of exercise with elevated temperature
    in excess of 40??C. Thus, in situations of increased exoge-
    nous heat stress, stimulants should be used with caution.
    Conclusion
    Although prescription stimulants have been shown to be
    relatively safe and effective in managing the symptoms of
    ADHD, there exists a signi´¼ücant potential for misuse. The
    data are clear that individuals with and without ADHD,
    including athletes misuse stimulants to enhance perfor-
    mance. Although stimulants may improve an individualÔÇÖs
    performance when given a rote-learning task, they do not
    offer as much help to people with greater intellectual abil-
    ities. Stimulants do not increase IQ (Advokat et al. 2008).
    In fact, very little is known about the effects of nonpre-
    scription stimulants on cognitive enhancement outside of
    the student population, although it is frequently reported
    in newspaper articles. Thus, the rumored effects of ÔÇ£smart
    drugsÔÇØ may be a false promise, as research suggests that
    stimulants are more effective at correcting de´¼ücits than
    ÔÇ£enhancing performance.ÔÇØ Moreover, students are taking
    unnecessary risks including the potential for harmful side
    effects, which may cause sudden death. This requires edu-
    cation on the proper use of stimulants and on the signs
    and symptoms of misuse and the health risks associated
    with misuse. It is important that students with prescription
    stimulants understand that they are the main source of
    diversion to other students, and should receive education
    in the prevention of stimulant diversion. Health centers
    should aim to recognize students who are misusing stimu-
    lants because they may present with a variety of signs
    including insisting on a larger dose, and demanding more
    drug during times within the academic year, such as dur-
    ing ´¼ünals. Students with past or active drug abuse patterns
    should not be prescribed stimulants, as they are more
    likely to divert their prescription stimulants. It is also
    important that athletes be warned that the NCAA, the US
    Olympic Committee, and the IOC ban MPH. As a result,
    education on the proper use of stimulants and on the signs
    and symptoms of misuse is an imperative.
    Acknowledgments
    The development of this work was supported by the
    Global Neuroscience Initiative Foundation (GNIF).
    Con´¼éict of Interest
    The authors declare that they have no competing interests.
    Authors contributions: All authors participated in the
    preparation of the manuscript, and read and approved
    the ´¼ünal manuscript.
    References
    Advokat, C. 2010. What are the cognitive effects of stimulant
    medications? Emphasis on adults with attention-de´¼ücit/
    hyperactivity disorder (ADHD). Neurosci. Biobehav. Rev.
    34:1256ÔÇô1266.
    Advokat, C. D., M. S. Guidry, and B. A. Martino. 2008. Licit
    and illicit use of medications for attention de´¼ücit
    hyperactivity disorder in undergraduate college students.
    J. Am. Coll. Health 56:601ÔÇô607.
    Alsidawi, S., J. Muth, and J. Wilkin. 2011. Adderall induced
    inverted-Takotsubo cardiomyopathy. Catheter. Cardiovasc.
    Interv. 78:910ÔÇô913.
    Amariles, P. 2011. A comprehensive literature search: drugs as
    possible triggers of Takotsubo cardiomyopathy. Curr. Clin.
    Pharmacol. 6:1ÔÇô11.
    672 ?¬ 2012 The Authors. Published by Wiley Periodicals, Inc.
    Stimulants in Individuals With and Without ADHD S. E. Lakhan & A. KirchgessnerAmerican Psychiatric Association. 2000. DSM-IV-TR.
    American Psychiatric Association, Washington, DC.
    Associated Press. 2009.ADHD exemptions on rise in MLB.
    ESPN, New York, NY.
    Barch, D. M., and C. S. Carter. 2005. Amphetamine improves
    cognitive function in medicated individuals with
    schizophrenia and in healthy volunteers. Schizophrenia Res.
    77:43ÔÇô58.
    Barkley, R. A., and C. E. Cunningham. 1978. Do stimulant
    drugs improve the academic performance of hyperkinetic
    children? A review of outcome studies. Clin. Pediatr.
    (Phila.) 17:85ÔÇô92.
    Barrett, S. P., C. Darredeau, L. K. Brody, and R. O. Pihl. 2005.
    Characteristics of methylphenidate misuse in a university
    student sample. Can. J. Psychiatry 50:457ÔÇô461.
    Biederman, J., M. C. Monuteaux, E. Mick, T. Spencer, T. E.
    Wilens, J. M. Silva, et al. 2006. Young adult outcome of
    attention de´¼ücit hyperactivity disorder: a controlled
    10 year prospective follow-up study. Psychol. Med.
    36:167ÔÇô179.
    Biederman, J., C. R. Petty, R. Fried, R. Kaiser, C. R. Dolan, S.
    Schoenfeld, et al. 2008a. Educational and occupational
    underattainment in adults with attention-de´¼ücit/
    hyperactivity disorder: a controlled study. J. Clin. Psychiatry
    69:1217ÔÇô1222.
    Biederman, J., L. J. Seidman, C. R. Petty, R. Fried, A. E. Doyle,
    D. R. Cohen, et al. 2008b. Effects of stimulant medication
    on neuropsychological functioning in young adults with
    attention de´¼ücit/hyperactivity disorder. J. Clin. Psychiatry
    69:1150ÔÇô1156.
    Biederman, J., R. Fried, C. R. Petty, A. Henin, J. Wozniak, L.
    Corkum, et al. 2012. Examining the association between
    stimulant treatment and cognitive outcomes across the life
    cycle of adults with attention-de´¼ücit/hyperactivity disorder:
    a controlled cross-sectional study. J. Nerv. Ment. Dis.
    200:69ÔÇô75.
    Bloom, B., and R. A. Cohen. 2007. Summary health statistics
    for U.S. children: National Health Interview Survey, 2006.
    Statistics VH 234:1ÔÇô79.
    Bogle, K. E., and B. H. Smith. 2009. Illcit methylphenidate
    use: a review of prevalence, availability, pharmacology,
    and consequences. Curr. Drug Abuse Rev. 2:157ÔÇô
    176.
    Bray, C. L., K. S. Cahill, J. T. Oshier, C. S. Peden, D. W.
    Theriaque, T. R. Flotte, et al. 2004. Methylphenidate does
    not improve cognitive function in healthy sleep-deprived
    young adults. J. Invest. Med. 52:192ÔÇô201.
    Breitenstein, C., S. Wailke, S. Bushuven, S. Kamping, P.
    Zwitserlood, E. B. Ringelstein, et al. 2004. D-amphetamine
    boosts language learning independent of its cardiovascular
    and motor arousing effects. Neuropsychopharmacology
    29:1704ÔÇô1714.
    Breitenstein, C., A. Floel, C. Korsukewitz, S. Waike, S.
    Bushuven, and S. Knecht. 2006. A shift paradigm: from
    noradrenergic to dopaminergic modulation of learning? J.
    Neurol. Sci. 248:42ÔÇô47.
    Brignell, C. M., J. Rosenthal, and H. V. Curran. 2007.
    Pharmacological manipulations of arousal and memory for
    emotional material: effects of a single dose of
    methylphenidate or lorazepam. J. Psychopharmacol.
    21:673ÔÇô683.
    Brown, R. T., R. W. Amler, W. S. Freeman, J. M. Perrin, M.
    T. Stein, H. M. Feldman, et al. 2005. Treatment of
    attention-de´¼ücit/hyperactivity disorder: overview of the
    evidence. Pediatrics 115:e749ÔÇôe757.
    Brumaghim, J. T., and R. Klormart. 1998. MethylphenidateÔÇÖs
    effects on paired-association learning and event-related
    potentials of young adults. Psychophysiology 35:73ÔÇô85.
    Burns, J. T., R. F. House, F. C. Fensch, and J. G. Miller. 1967.
    Effects of magnesium pemoline and dextroamphetamine on
    human learning. Science 155:849ÔÇô851.
    Callaway, E. 1983. Presidential address. 1982: the
    pharmacology of human information processing.
    Psychophysiology 20:359ÔÇô370.
    Camp-Bruno, J. A., and R. L. Herting. 1994. Cognitive effects
    of milacemide and methylphenidate in healthy young adults.
    Psychopharmacology 115:46ÔÇô52.
    Center for Disease Control and Prevention. 2005a. Mental
    health in the United States. Prevalence of diagnosis and
    medication treatment for attention-de´¼ücit/hyperactivity
    disorder ÔÇô United States, 2003. MMWR Morb. Mortal.
    Wkly. Rep. 54:842ÔÇô847.
    Center for Disease Control and Prevention. 2005b. Prevalence
    of diagnosis and medication treatment for attention de´¼ücit/
    hyperactivity disorder ÔÇô United States, 2003. MMWR
    Morbid. Mortal. Wkly. Rep. 54:842ÔÇô847.
    Centers for Disease Control and Prevention. 2010. Increasing
    prevalence of parent-reported attention-de´¼ücit/hyperactivity
    disorder among children ÔÇô United States, 2003 and 2007.
    MMWR Morb. Mortal. Wkly. Rep. 59:1439ÔÇô1443.
    Chen, J. P. 2007. Methamphetamine-associated acute
    myocardial infarction and cardiogenic shock with normal
    coronary arteries: refractory global coronary microvascular
    spasm. J. Invasive Cardiol. 19:E89ÔÇôE92.
    Clatworthy, P. L., S. J. Lewis, L. Brichard, Y. T. Hong, D.
    Izquierdo, L. Clark, et al. 2009. Dopamine release in
    dissociable striatal subregions predicts the different effects of
    oral methylphenidate on reversal learning and spatial
    working memory. J. Neurosci. 29:4690ÔÇô4696.
    Cooper, N. J., H. Keage, D. Hermens, L. M. Williams,
    D. Debrota, and C. R. Clark. 2005. The dose-dependent
    effect of methylphenidate on performance, cognition,
    and psychophysiology. J. Integrative Neurosci. 4:
    123ÔÇô144.
    Cooper, W. O., L. A. Habel, C. M. Sox, K. A. Chan, P. G.
    Arbogast, T. C. Cheetham, et al. 2011. ADHD drugs and
    serious cardiovascular events in children and young adults.
    N. Engl. J. Med. 365:1896ÔÇô1904.
    ?¬ 2012 The Authors. Published by Wiley Periodicals, Inc. 673
    S. E. Lakhan & A. Kirchgessner Stimulants in Individuals With and Without ADHDDepartment of Justice: Drug Enforcement Administration.
    2008. ARCOS2-report 7, United States summary for retail
    drug purchases by grams weight.
    Dodds, C. M., U. Muller, L. Clark, A. van Loon, R. Cools, and
    T. W. Robbins. 2008. Methylphenidate has differential
    effects on blood oxygenation level-dependent signal related
    to cognitive subprocesses of reversal learning. J. Neurosci.
    28:5976ÔÇô5982.
    Dopheide, J. A., and S. R. Pliszka. 2009. Attention-de´¼ücit-
    hyperactivity disorder: an update. Pharmacotherapy 29:
    656ÔÇô679.
    Elia, J., P. J. Ambrosini, and J. L. Rapoport. 1999. Treatment
    of attention-de´¼ücit-hyperactivity disorder. N. Engl. J. Med.
    340:780ÔÇô788.
    Elliott, R., B. J. Sahakian, K. Matthews, A. Bannerjea, J.
    Rimmer, and T. W. Robbins. 1997. Effects of
    methylphenidate on spatial working memory and planning
    in healthy young adults. Psychopharmacology 131:196ÔÇô206.
    European Medicines Agency. 2007. Meeting highlights from
    the committee for medicinal products for human use, 16ÔÇô19
    July 2007, European Medicines Agency, London.
    Farah, M. J., C. Halmm, G. Sankoorikal, M. E. Smith, and A.
    Chatterjee. 2009. When we enhance cognition with Adderall,
    do we sacri´¼üce creativity? A preliminary study
    Psychopharmacology 202:541ÔÇô547.
    Faraone, S. V., and S. J. Glatt. 2010. A comparison of the
    ef´¼ücacy of medications for adult attention-de´¼ücit/
    hyperactivity disorder using meta-analysis of effect sizes. J.
    Clin. Psychiatry 71:754ÔÇô763.
    Faraone, S. V., J. Biederman, J. G. Jetton, and M. T. Tsuang.
    1997. Attention de´¼ücit disorder and conduct disorder:
    longitudinal evidence for a familial subtype. Psychol. Med.
    27:291ÔÇô300.
    Faraone, S. V., J. Sergeant, C. Gillberg, and J. Biederman.
    2007. The worldwide prevalence of ADHD: is it an
    American condition? World Psychiatry 2:104ÔÇô113.
    Fillmore, M. T., T. H. Kelly, and C. A. Martin. 2005. Effects
    of d-amphetamine in human models of information
    processing and inhibitory control. Drug Alcohol Dep.
    77:151ÔÇô159.
    Fitzpatrick, P., R. Klorman, J. T. Brumaghim, and R. W.
    Keefover. 1988. Effects of methylphenidate on stimulus
    evaluation and response processes: evidence from
    performance and event-related potentials. Psychophysiology
    25:292ÔÇô304.
    Fleming, K., L. B. Bigelow, D. R. Weinberger, and T. E.
    Goldberg. 1995. Neuropsychological effects of amphetamine
    may correlate with personality characteristics.
    Psychopharmacol. Bull. 31:357ÔÇô362.
    Gandhi, P. J., G. U. Ezeala, T. T. Luyen, T. C. Tu, and M. T.
    Tran. 2005. Myocardial infarction in an adolescent taking
    Adderall. Am. J. Health Syst. Pharm. 62:1494ÔÇô1497.
    Greydanus, D. E., and V. C. Strasburger. 2006. Adolescent
    medicine. Prim. Care 33:xiiiÔÇôxviii.
    Gualtieri, C. T., and L. G. Johnson. 2008. Medications do not
    necessarily normalize cognition in ADHD patients. J. Atten.
    Disord. 11:459ÔÇô469.
    Habel, L. A., W. O. Cooper, C. M. Sox, K. A. Chan, B. H.
    Fireman, P. G. Arbogast, et al. 2011. ADHD medications
    and risk of serious cardiovascular events in young and
    middle-aged adults. JAMA 306:2673ÔÇô2683.
    Harris, S.. 2009. ÔÇ£I donÔÇÖt see it as a problemÔÇØ: more medical
    students taking prescription stimulants, few see cause for
    concern.
    Herman, L., O. Shtayermman, B. Aksnes, M. Anzalone, A.
    Cormerals, and C. Liodice. 2011. The use of prescription
    stimulants to enhance academic performance among college
    students in health care programs. J. Physician Assist. Educ.
    22:15ÔÇô22.
    Hester, R., L. S. Nandam, R. G. OÔÇÖConnell, J. Wagner, M.
    Strudwick, P. J. Nathan, et al. 2012. Neurochemical
    enhancement of conscious error awareness. J. Neurosci.
    32:2619ÔÇô2627.
    Horrigan, J. P. 2001. Present and future pharacotherapeutic
    options for adult attention de´¼ücit/hyperactivity disorder.
    Exp. Opin. Psychopharmacol. 2:573ÔÇô586.
    Hurst, P. M., R. Radlow, N. C. Chubb, and S. K. Bagley. 1969.
    Effects of D-amphetamine on acquisition, persistence, and
    recall. Am. J. Psychol. 82:307ÔÇô319.
    Jacobs, A. 2005. The Adderall advantage. The New York Times.
    Available at: http://www.nytimes.com/2005/07/31/education/
    edlife/jacobs31.html
    Jensen, P. S., L. E. Arnold, J. M. Swanson, B. Vitiello, H. B.
    Abikoff, L. L. Greenhill, et al. 2007. 3-year follow-up of the
    NIMH MTA study. J. Am. Acad. Child Adolesc. Psychiatry
    46:989ÔÇô1002.
    Jiao, X., S. Velez, J. Ringstad, V. Eyma, D. Miller, and M.
    Bleiberg. 2009. Myocardial infarction associated with
    Adderall XR and alcohol use in a young man. J. Am. Board
    Fam. Med. 22:197ÔÇô201.
    Johnston, L. D., P. M. OÔÇÖMalley, J. G. Bachman, and J. E.
    Schulenberg. 2004. Monitoring the future: national survey
    results on drug use, 1975ÔÇô2003. Pp. 10ÔÇô12 in NIoD, ed.
    Abuse. National Institutes of Health, U.S. Department of
    Health and Human Services, Bethesda, MD.
    Kadison, R. 2005. Getting an edge ÔÇô use of stimulants and
    antidepressants in college. N. Engl. J. Med. 353:1089ÔÇô1091.
    Kennedy, R. S., R. C. Odenheimer, D. R. Baltzley, W. P. Dunlap,
    and C. D. Wood. 1990. Differential effects of scopolamine
    and amphetamine on microcomputer-based performance
    tests. Aviat. Space Environ. Med. 61:615ÔÇô621.
    Kessler, R. C., L. Adler, R. Barkley, J. Biederman, C. K.
    Conners, O. Demler, et al. 2006. The prevalence and
    correlates of adult ADHD in the United Stated: results from
    the national comorbidity survey replication. Am. J.
    Psychiatry 163:716ÔÇô723.
    Klorman, R., L. O. Bauer, H. W. Coons, J. L. Lewis, J.
    Peloquin, R. A. Perlmutter, et al. 1984. Enhancing effects of
    674 ?¬ 2012 The Authors. Published by Wiley Periodicals, Inc.
    Stimulants in Individuals With and Without ADHD S. E. Lakhan & A. Kirchgessnermethylphenidate on normal young adultsÔÇÖ cognitive
    processes. Psychopharmacol. Bull. 20:3ÔÇô9.
    Koelega, H. S. 1993. Stimulant drugs and vigilance
    performance: a review. Psychopharmacology 111:1ÔÇô16.
    Kollins, S. H. 2003. Comparing the abuse potential of
    methylphenidate versus other stimulants: a review of
    available evidence and relevance to the ADHD patient.
    J. Clin. Psychol. 64:14ÔÇô18.
    Kollins, S. H. 2008. ADHD, substance use disorder, and
    psychostimulant treatment current literature and treatment
    guidelines. J. Atten. Disord. 12:115ÔÇô125.
    Kollins, S. H., F. J. McClernon, and B. F. Fuemmeler. 2005.
    Association between smoking and attention-de´¼ücit/
    hyperactivity disorder symptoms in a population-based
    sample of children aged 9 through 16 years. J. Am. Acad.
    Child Adolesc. Psychiatry 62:1142ÔÇô1431.
    Kuczenski, R., and D. S. Segal. 1997. Effects of
    methylphenidate on extracellular dopamine, serotonin, and
    norepinephrine: comparison with amphetamine.
    J. Neurochem. 68:2032ÔÇô2037.
    Kumari, V., P. J. Corr, O. F. Mulligan, P. A. Cotter, S. A.
    Checkley, and I. A. Gray. 1997. Effects of acute
    administration of d-amphetamine and haloperidol on
    procedural learning in man: a preliminary study.
    Psychopharmacology 129:271ÔÇô276.
    Kutcher, J. S. 2011. Treatment of attention-de´¼ücit hyperactivity
    disorder in athletes. Curr. Sports Med. Rep. 10:32ÔÇô36.
    Looby, A., and M. Earleywine. 2011. Expectation to receive
    methylphenidate enhances subjective arousal but not
    cognitive performance. Exp. Clin. Psychopharmacol. 19:433ÔÇô
    444.
    Lord, S., G. Downs, P. Furlaw, A. Chaudhurl, A. Silverstein, A.
    Gammaitoni, et al. 2003. Nonmedical use of prescription
    opiods and stimulants among student pharmacists. J. Am.
    Pharm. Assoc. 49:519ÔÇô528.
    Low, K. G., and A. E. Gendaszek. 2002. Illicit use of
    psychostimulants among college students: a preliminary
    study. Psychol. Health Med. 7:283ÔÇô287.
    Makris, A. P., C. R. Rush, R. C. Frederich, A. C. Taylor, and
    T. H. Kelly. 2007. Behavioral and subjective effects of d-
    ampetamine and moda´¼ünil in healthy adults. Exp. Clin.
    Psychopharmacol. 15:123ÔÇô133.
    Masand, P., P. Pickett, and G. B. Murray. 1991.
    Psychostimulants for secondary depression in medical
    illness. Psychosomatics 32:203ÔÇô208.
    Mattay, V. S., K. F. Berman, J. L. Ostrem, G. Esposito, J. D. Van
    Horn, and L. B. Bigelow. 1996. Dextroamphetamine enhances
    ÔÇ£neural network-speci´¼ücÔÇØ physiological signals: a positron
    emission tomography rCBF study. J. Neurosci. 16:
    4816ÔÇô4822.
    Mattay, V. S., J. H. Callicott, A. Bertolino, I. Heaton, J. A.
    Frank, R. Coppola, et al. 2000. Effects of
    dextroamphetamine on cognitive performance and cortical
    activation. NeuroImage 12:268ÔÇô275.
    Mattay, V. S., T. E. Goldberg, F. Fera, A. R. Hariri, A.
    Tessitore, M. F. Egan, et al. 2003. Catechol O-
    methyltransferase val158-met genotype and individual
    variation in the brain response to amphetamine. Proc. Natl.
    Am. Sci. USA 100:6186ÔÇô6191.
    McCabe, S. E., and C. J. Boyd. 2005. Sources of prescription
    drugs for illicit use. Addict. Behav. 30:1342ÔÇô1350.
    McCabe, S. E., C. J. Teter, and C. J. Boyd. 2004. The use,
    misuse and diversion of prescription stimulants among
    middle and high school students. Subst. Use Misuse
    39:1095ÔÇô1116.
    McCabe, S. E., J. R. Knight, C. J. Teter, and H. Wechsler.
    2005. Nonmedical use of prescription stimulants among US
    college students: prevalence and correlates from a
    nationwide survey. Addiction 100:96ÔÇô106.
    McLaughlin, L. 2011. Adderall: the whole story. Available at:
    http://reesenews.org/2011/10/26/adderall-the-whole-story/
    19843/
    McNiel, A. D., K. B. Muzzin, J. P. DeWald, A. L. McCann, E.
    D. Schneiderman, J. Sco´¼üeld, et al. 2011. The nonmedical
    use of prescription stimulants among dental and dental
    hygiene students. J. Dental Edu. 75:365ÔÇô376.
    Mehta, M. A., A. M. Owen, B. J. Sahakian, N. Mavaddat, J. D.
    Pickard, and T. W. Robbins. 2000. Methylphenidate enhances
    working memory by modulating discrete frontal and parietal
    lobe regions in the human brain. J. Neurosci. 20:RC65.
    Mintzer, M. Z., and R. R. Grif´¼üths. 2007. A triazolam/
    amphetamine dose-effect interaction study: dissociation of
    effects on memory versus arousal. Psychopharmacology
    192:425ÔÇô440.
    Misener, V. L., P. Luca, O. Azeke, J. Crosbie, I. Waldman, R.
    Tannock, et al. 2004. Linkage of the dopamine receptor D1
    gene to attention-de´¼ücit/hyperactivity disorder. Mol.
    Psychiatry 9:500ÔÇô509.
    Mitchell, H.. 2012. Faking ADHD Gets you into Harvard. The
    Daily Beast. Available at: http://www.thedailybeast.com/
    articles/2012/01/25/faking-adhd-gets-you-into-harvard.html
    Molina, B. S. G., S. P. Hinshaw, J. M. Swanson, L. E. Arnold,
    B. Vitiello, P. S. Jensen, et al. 2009. The MTA at 8 years:
    prospective follow-up of children treated for combined type
    ADHD in the multisite study. J. Am. Acad. Child Adolesc.
    Psychiatry. 48:484ÔÇô500.
    Murray, J. B. 1998. Psychophysiological aspects of amphetamine-
    methamphetamine abuse. J. Psychol. 132:227ÔÇô237.
    Musser, C. J., P. A. Ahmann, F. W. Theye, P. Mundt, S. K.
    Broste, and N. Mueller-Rizner. 1998. Stimulant use and the
    potential for abuse in Wisconsin as reported by school
    administrators and longitudinally followed children. J. Dev.
    Behav. Pediatr. 19:187ÔÇô192.
    Oken, B. S., S. S. Kishiyama, and M. C. Salinsky. 1995.
    Pharmacologically induced changes in arousal: effects on
    behavioral and electrophysiologic measures of alertness
    and attention. Electroenceph Clin. Neurophysiol. 95:
    359ÔÇô371.
    ?¬ 2012 The Authors. Published by Wiley Periodicals, Inc. 675
    S. E. Lakhan & A. Kirchgessner Stimulants in Individuals With and Without ADHDPartridge, B. J., S. K. Bell, J. C. Lucke, S. Yeates, and W. D.
    Hall. 2011. Smart drugs ÔÇ£as common as coffeeÔÇØ: media hype
    about neuroenhancement. PLoS One 6:e28416.
    Pelham W. E., Jr, K. McBurnett, G. W. Harper, R. Milich, D.
    A. Murphy, J. Clinton, et al. 1990. Methylphenidate and
    baseball playing in ADHD children: whoÔÇÖs on ´¼ürst?
    J. Consult. Clin. Psychol. 58:130ÔÇô133.
    Piper, B. J., J. B. Fraiman, and J. S. Meyer. 2005. Repeated
    MDMA (ÔÇ£EcstasyÔÇØ) exposure in adolescent male rats alters
    temperature regulation, spontaneous motor activity,
    attention, and serotonin transporter binding. Dev.
    Psychobiol. 47:145ÔÇô157.
    Polanczyk, G., M. S. de Lima, B. L. Horta, J. Biederman, and
    L. A. Rohde. 2007. The worldwide prevalence of ADHD: a
    systematic review and metaregression analysis. Am. J.
    Psychiatry 164:942ÔÇô948.
    Polchert, S. E., and R. M. Morse. 1985. Pemoline abuse. JAMA
    254:946ÔÇô947.
    Putukian, M., J. B. Kreher, D. B. Coppell, J. L. Glazer, D. B.
    McKeag, and R. D. White. 2011. Attention de´¼ücit
    hyperactivity disorder and the athlete: an American Medical
    Society for Sports Medicine position statement. Clin. J.
    Sport Med. 21:392ÔÇô401.
    Rabiner, D. L., A. D. Anastopoulos, E. J. Costello, R. H.
    Hoyle, S. E. McCabe, and H. S. Swartzweder. 2009. The
    misuse and diversion of prescribed ADHD medications by
    college students. J. Atten. Disord. 13:144ÔÇô153.
    Rapoport, J. L., M. S. Buchsbaum, H. Weingartner, T. P.
    Zahn, C. Ludlow, and E. J. Mikkelsen. 1978.
    Dextroamphetamine: cognitive and behavioral effects in
    normal and prepubertal boys. Science 199:560ÔÇô563.
    Rasmussen, P., and C. Gillberg. 2000. Natural outcome of
    ADHD with developmental coordination disorder at age
    22 years: a controlled, longitudinal, community-based
    study. J. Am. Acad. Child Adolesc. Psychiatry 39:1424ÔÇô
    1431.
    Rogers, R. D., A. J. Blackshaw, H. C. Middleton, K. Matthews,
    K. Hawtin, C. Crowley, et al. 1999. Tryptophan depletion
    impairs stimulus-reward learning while methylphenidate
    disrupts attentional control in healthy young adults:
    implications for the monoaminergic basis of impulsive
    behavior. Psychopharmacology 146:482ÔÇô491.
    Rosa-Neto, P., H. C. Lou, P. Cumming, O. Pryds, H.
    Karrebaek, J. Lunding, et al. 2005. Methylphenidate-evoked
    changes in striatal dopamine correlate with inattention and
    impulsivity in adolescents with attention de´¼ücit
    hyperactivity/disorder. Neuroimage 25:868ÔÇô876.
    Rosenthal, E. 2012. Not acute myocardial infarction in a
    teenager due to Adderall XR. Pediatr. Cardiol. 33:679.
    Sahakian, B. J., and A. M. Owen. 1992. Computerized
    assessment in neuropsychiatry using CANTAB: discussion
    paper. J. Royal Soc. Med. 85:399ÔÇô402.
    Schelleman, H., W. B. Bilker, S. E. Kimmel, G. W. Daniel, C.
    Newcomb, J. P. Guevara, et al. 2012. Methylphenidate and
    risk of serious cardiovascular events in adults. Am. J.
    Psychiatry 169:178ÔÇô185.
    Schmedje, J. F., C. M. Oman, R. Letz, and E. L. Baker. 1988.
    Effects of scopolamine and dextroamphetamine on human
    performance. Aviation Space Environ. Med. 59:407ÔÇô410.
    Schroeder, S. R., K. Mann-Koepke, C. T. Gualtieri, D. A.
    Eckerman, and G. R. Breese. 1987. Methylphenidate affects
    strategic choice behavior in normal adult humans.
    Pharmacol. Biochem. Behav. 28:213ÔÇô217.
    Schweitzer, J. B., D. O. Lee, R. B. Hanford, C. F. Zink, T. D.
    Ely, M. A. Tagamets, et al. 2004. Effect of methylphenidate
    on executive functioning in adults with attention de´¼ücit/
    hyperactivity disorder: normalization of behavior but not
    related brain activity. Biol. Psychiatry 56:597ÔÇô606.
    Sciutto, M. J., C. J. Nol´¼ü, and C. Bluhm. 2004. Effects of child
    gender and symptom type on referrals for ADHD by
    elementary school teachers. J. Emotion Behav. Disord.
    12:247ÔÇô253.
    Servan-Schreiber, D., C. S. Carter, R. M. Bruno, and J. D.
    Cohen. 1998. Dopamine and the mechanisms of cognition:
    Part II. D-amphetamine effects in human subjects
    performing a selective attention task. Biol. Psychiatry
    43:723ÔÇô729.
    Silber, B. Y., R. J. Croft, K. Papafotiou, and C. Stough. 2006.
    The acute effects of d-amphetamine and methamphtetamine
    on attention and psychomotor performance.
    Psychopharmacology 187:154ÔÇô169.
    Smith, M. E., and M. J. Farah. 2011. Are prescription
    stimulants ÔÇ£smart pillsÔÇØ? The epidemiology and cognitive
    neuroscience of prescription stimulant use by normal
    healthy individuals. Psychol. Bull. 137:717ÔÇô741.
    Soetens, E., R. Dhooge, and J. Hueting. 1993. Amphetamine
    enhances human-memory consolidation. Neurosci. Lett.
    161:9ÔÇô12.
    Soetens, E., S. Casaer, R. Dhooge, and J. Hueting. 1995. Effect
    of amphetamine on long-term retention of verbal material.
    Psychopharmacology 119:155ÔÇô162.
    Sroufe, L. A. 2012. Ritalin gone wrong. New York Times, 29
    January 2012.
    Strauss, J., J. L. Lewis, R. Klorman, L. J. Peloquin, R. A.
    Perlmatter, and L. F. Salzman. 1984. Effects of
    methylphenidate on young adults performance and event-
    related potentials in a vigilance and a paired-associates
    learning test. Psychophysiology 21:609ÔÇô621.
    Surles, L. K., H. J. May, and J. P. Garry. 2002. Adderall-
    induced psychosis in an adolescent. J. Am. Board Fam.
    Pract. 15:498ÔÇô500.
    Sylvester, A. L., and B. Agarwala. 2012. Acute myocardial
    infarction in a teenager due to Adderall XR. Pediatr.
    Cardiol. 33:155ÔÇô157.
    Teter, C. J., S. E. McCabe, J. A. Cranford, C. J. Boyd, and S.
    K. Guthrie. 2005. Prevalence and motivations for the illicit
    use of prescription stimulants in an undergraduate student
    sample. J. Am. Coll. Health 53:253ÔÇô262.
    676 ?¬ 2012 The Authors. Published by Wiley Periodicals, Inc.
    Stimulants in Individuals With and Without ADHD S. E. Lakhan & A. KirchgessnerThe MTA Cooperative Group. 1999. A 14-month randomized
    clinical trial of treatment strategies for attention-de´¼ücit/
    hyperactivity disorder. Arch. Gen. Psychiatry 56:1073ÔÇô1086.
    Tuttle, J. P., N. E. Scheurich, and J. Ranseen. 2010. Prevalence
    of ADHD diagnosis and nonmedical prescription stimulant
    use in medical students. Acad. Psychiatry 34:220ÔÇô223.
    Unrug, A., A. Coenen, and G. van Luijtelaar. 1997. Effects of
    the tranquilizer diazepam and the stimulant
    methylphenidate on alertness and memory.
    Neuropsychobiology 36:42ÔÇô48.
    Upadhyaya, H. P., K. Rose, W. Wang, K. OÔÇÖRourke, B.
    Sullivan, D. Deas, et al. 2005. Attention-de´¼ücit/hyperactivity
    disorder, medication treatment, and substance use patterns
    among adolescents and young adults. J. Child Adolesc.
    Psychopharmacol. 15:799ÔÇô809.
    Visser, S. N., C. A. Lesesne, and R. Perou. 2012. National
    estimates and factors associated with medication treatment
    for childhood attention-de´¼ücit/hyperactivity disorder.
    Pediatrics 119:S99ÔÇôS107.
    Vitiello, B., G. R. Elliott, J. M. Swanson, L. E. Arnold, L.
    Hechtman, H. Abikoff, et al. 2011. Blood pressure and heart
    rate in the mulimodal treatment of attention de´¼ücit/
    hyperactivity disorder study over 10 years. Am. J.
    Psychiatry. 169:167ÔÇô177.
    Volkow, N. D., Y. S. Ding, J. S. Fowler, G. J. Wang, J. Logan,
    J. S. Gatley, et al. 1995. Is methylphenidate like cocaine?
    Studies on their pharmacokinetics and distribution in the
    human brain. Arch. Gen. Psychiatry 52:456ÔÇô463.
    Volkow, N. D., G. J. Wang, J. Newcorn, F. Telang, M. V.
    Solanto, J. S. Fowler, et al. 2007. Depressed dopamine
    activity in caudate and preliminary evidence of limbic
    involvement in adults with attention-de´¼ücit/hyperactivity
    disorder. Arch. Gen. Psychiatry 64:932ÔÇô940.
    Volkow, N. D., G. J. Wang, D. Tomasi, S. H. Kollins, T. L.
    Wigal, J. H. Newcorn, et al. 2012. Methylphenidate-
    elicited dopamine increases in ventral striatum are
    associated with long-term symptom improvement in
    adults with attention de´¼ücit hyperactivity disorder.
    J. Neurosci. 32:841ÔÇô849.
    Ward, A. S., T. H. Kelly, R. W. Foltin, and M. W. Fischman.
    1997. Effects of d-amphetamine on task performance and
    social behavior of humans in a residential laboratory. Exp.
    Clin. Psychopharmacol. 5:130ÔÇô136.
    Weitzner, M. 1965. Manifest anxiety, amphetamine and
    performance. J. Psychol. 60:71ÔÇô79.
    Weyandt, L. L., and G. DuPaul. 2006. ADHD in college
    students. J. Atten. Disord. 10:9ÔÇô19.
    Wilens, T. E. 2003. Does the medicating ADHD increase or
    decrease the risk for later substance abuse? Rev. Bras.
    Psiquiatr. 25:127ÔÇô128.
    Wilens, T. E., J. Biederman, and T. J. Spencer. 2002. Attention
    de´¼ücit/hyperactivity disorder across the lifespan. Annu. Rev.
    Med. 53:113ÔÇô131.
    Wilens, T. E., S. Faraone, and J. Biederman. 2004.
    Attention-de´¼ücit/hyperactivity disorder in adults. JAMA
    292:619ÔÇô623.
    Wilens, T. E., L. A. Adler, J. Adams, S. Sgambati, J. Rotrosen,
    R. Sawtelle, et al. 2008. Misuse and diversion of stimulants
    prescribed for ADHD: a systematic review of the literature.
    J. Am. Acad. Child Adolesc. Psychiatry 47:21ÔÇô31.
    Willett, R. A. 1962. The effect of a stimulant and a depressant
    drug on the serial rote learning of nonsense syllables.
    Psychopharmacologia 3:23ÔÇô34.
    Wise, R. A. 2002. Brain reward circuitry: insights from
    unsensed incentives. Neuron 36:229ÔÇô240.
    de Wit, H., J. Crean, and J. B. Richards. 2000. Effects of
    d-amphetamine and ethanol on a measure of behavioral
    inhibition in humans. Behav. Neurosci. 114:830ÔÇô837.
    de Wit, H., J. L. Enggasser, and J. B. Richards. 2002. Acute
    administration of d-amphetamine decreases impulsivity
    in healthy volunteers. Neuropsychopharmacology 27:813ÔÇô
    825.
    Zeeuws, I., and E. Soetens. 2007. Verbal memory performance
    improved via an acute administration of D-amphetamine.
    Hum. Psychopharmacol. Clin. Exp. 22:279ÔÇô287.
    Zuvekas, S., and B. Vitiello. 2011. Stimulant medication use in
    children: a 12-year perspective. Am. J. Psychiatry 169:160ÔÇô
    166

    Posted on Leave a comment

    Browse Renewable Energy Products. Seller’s Listings 100% Free!