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Lisdexamfetamine: Difference between revisions

From Pharmacopedia
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{{MedTemplate
{{MedTemplate
| generic           = Lisdexamfetamine
| generic           = Lisdexamfetamine (dimesylate)
| brand             = Vyvanse
| brand             = Vyvanse, Elvanse (EU)
| structure         =  
| structure         =
| classes           = Amphetamine, Psychostimulant
| classes           = [[:Category:Psychostimulants|Psychostimulant]], [[:Category:Amphetamines|Amphetamine]], [[:Category:ADHD medicines|ADHD medicine]], [[:Category:Schedule II controlled substances|Schedule II controlled substance]]
| mechanism          = Prodrug of dextroamphetamine
| uses             = <vote slug="adhd-lisdex-use">Attention-deficit/hyperactivity disorder (FDA, ages 6+ and adult)</vote>, <vote slug="binge-eating-disorder-use">Binge-eating disorder in adults (FDA)</vote>
| uses               =  
| starting_dose     = ADHD: 30 mg PO once daily in the morning; titrate by 10-20 mg weekly to clinical effect. Binge-eating disorder: 30 mg/day, titrate to 50-70 mg/day
| starting_dose     =  
| preparations     = Capsules 10, 20, 30, 40, 50, 60, 70 mg; chewable tablets 10, 20, 30, 40, 50, 60 mg
| preparations       =  
| fda_max           = 70 mg/day
| fda_max          =  
| pill_id           =
| routes             =  
| routes           = Oral
| onset             =  
| onset             = 1-2 hours (slower than immediate-release amphetamine because activation requires enzymatic cleavage in red blood cells)
| duration           =  
| duration         = 10-12 hours (smoother profile than immediate-release amphetamine salts)
| halflife           =
| halflife          = Parent lisdexamfetamine <1 hour; dextroamphetamine 10-12 hours after release<ref name="vyvanse-label">FDA Prescribing Information, Vyvanse (lisdexamfetamine dimesylate), Takeda/Shire, current revision. https://www.accessdata.fda.gov/drugsatfda_docs/label/2017/021977s045lbl.pdf</ref>
| bioavailability    =
| bioavailability   = ~96% after red blood cell hydrolytic cleavage releases dextroamphetamine<ref name="vyvanse-label" />
| pregnancy         =  
| pregnancy        = Limited human data; the amphetamine class is associated with intrauterine growth restriction and neonatal withdrawal symptoms.{{citation needed}}
| legal              =  
| legal             = [[USLegal:Schedule II|Schedule II controlled substance]] in US<ref name="vyvanse-label" />
| intro              =
| mechanism         = <vote slug="lisdexamfetamine-mech-claim">Lisdexamfetamine is an inactive lysine-conjugated parent compound that requires enzymatic cleavage by red blood cell hydrolases to release active dextroamphetamine. The red-blood-cell-dependent conversion provides a slower, smoother release profile than immediate-release amphetamine salts, and is the basis of the abuse-deterrent design: IV administration bypasses the necessary RBC cleavage and produces no peak effect, and intranasal misuse offers little kinetic advantage over oral administration.</vote> Once converted, dextroamphetamine acts by displacing dopamine and norepinephrine from presynaptic vesicles via VMAT-2 and reversing DAT and NET transport, the shared mechanism of all amphetamine-class agents<ref name="vyvanse-label" />.
| pharmacokinetics   =  
| pharmacodynamics  =  
| indications        =  
| dosing             =  
| effects            =
| interactions      = <pharmaInteractions/>
| pregnancy_details  =
| monitoring         =  
| counseling        =  
| anecdotes          =
| seealso            =
| references        =  
}}
}}
== References ==
<references />


[[Category:Psychostimulants]]
[[Category:Psychostimulants]]
[[Category:Amphetamines]]
[[Category:ADHD medicines]]
[[Category:Schedule II controlled substances]]