Drilldown: Medicines
Use the filters below to narrow your results.
generic:
brand:
None (69) ·
Delysid (historical, Sandoz, withdrawn 1965) (1) ·
Provigil (US, 100 mg and 200 mg tablets); Alertec (Canada); Modiodal (France, original market). See also: Armodafinil (Nuvigil), the R-enantiomer, a related eugeroic approved 2007 with a longer effective half-life. (1) ·
Vyvanse, Elvanse (EU) (1)
classes: (Click arrow to add another value)
mechanism:
1-acetyl-LSD; prodrug of LSD (1) ·
5-HT2A agonist (26) ·
5-HT2A agonist; D2 partial agonist (1) ·
5-HT2A agonist; long duration (1) ·
5-HT2A agonist; MAO inhibitor (1) ·
5-HT2A agonist; milder than other 2C-x (1) ·
5-HT2A agonist; minor psilocybin mushroom alkaloid (1) ·
5-HT2A agonist; primarily auditory effects (1) ·
5-HT2A agonist; sigma-1 agonist (1) ·
5-HT2A partial agonist (1) ·
Contains bufotenin and DMT (1) ·
Contains LSA (2) ·
Contains mescaline (2) ·
Contains psilocybin and psilocin (1) ·
DMT + MAOI (harmine/harmaline); 5-HT2A agonist (1) ·
Extremely potent 5-HT2A agonist; vasoconstrictor (1) ·
Extremely potent 5-HT2A agonist; very long duration (1) ·
LSD analogue; 5-HT2A agonist (4) ·
Lysergic acid 2,4-dimethylazetidide; 5-HT2A agonist (1) ·
Lysergic acid hydroxyethylamide; 5-HT2A agonist (1) ·
Monoamine releasing agent; 5-HT2A agonist (1) ·
Potent 5-HT2A agonist (5) ·
Potent 5-HT2A agonist; no oral activity (1) ·
Potent 5-HT2A agonist; sigma-1 agonist (1) ·
Potent 5-HT2A agonist; very long duration (1) ·
Prodrug of 4-HO-DET; 5-HT2A agonist (1) ·
Prodrug of 4-HO-DiPT; 5-HT2A agonist (1) ·
Prodrug of 4-HO-MET; 5-HT2A agonist (1) ·
Prodrug of 4-HO-MiPT; 5-HT2A agonist (1) ·
Prodrug of LSD; 5-HT2A agonist (4) ·
Prodrug of psilocin; 5-HT2A agonist (1) ·
Serotonin/dopamine/norepinephrine releasing agent; 5-HT2A agonist (1) ·
Very potent 5-HT2A agonist; long duration (1) ·
'"`UNIQ--vote-00000013-QINU`"' 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'"`UNIQ--ref-00000014-QINU`"'. (1) ·
'"`UNIQ--vote-00000049-QINU`"' (1)
starting dose:
None (70) ·
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 (1) ·
Narcolepsy/OSA: 200 mg PO once daily in the morning. Shift work disorder: 200 mg PO approximately 1 hour before the start of the work shift. Lower starting dose (100 mg) can be considered in elderly patients or those with hepatic impairment. (1)
preparations:
fda max:
routes:
onset:
None (69) ·
1-2 hours (slower than immediate-release amphetamine because activation requires enzymatic cleavage in red blood cells) (1) ·
30–60 minutes (1) ·
Peak plasma concentrations 2-4 hours after oral dose. Wakefulness-promoting effect onset correlates with peak plasma; subjective alertness typically reported within 1-2 hours of dosing. (1)
duration:
None (69) ·
10-12 hours (smoother profile than immediate-release amphetamine salts) (1) ·
8–12 hours (1) ·
Effective wakefulness promotion through approximately 12-15 hours reflecting the half-life of the predominant R-enantiomer. For shift-work use, 200 mg taken 1 hour before shift provides coverage through most 8-12 hour shifts. (1)
halflife:
bioavailability:
pregnancy:
Showing below up to 72 results in range #1 to #72.