Drilldown: Medicines
Use the filters below to narrow your results.
generic:
None (1) ·
Agomelatine (1) ·
Amantadine (1) ·
Amoxapine (1) ·
Apomorphine (1) ·
Benztropine (1) ·
Biperiden (1) ·
Bromocriptine (1) ·
Cabergoline (1) ·
Carbidopa/levodopa (1) ·
Clomipramine (1) ·
Desipramine (1) ·
Duloxetine (1) ·
Entacapone (1) ·
Imipramine (1) ·
Isocarboxazid (1) ·
Levodopa (1) ·
Levomilnacipran (1) ·
Maprotiline (1) ·
Milnacipran (1) ·
Moclobemide (1) ·
Nefazodone (1) ·
Opicapone (1) ·
Phenelzine (1) ·
Protriptyline (1) ·
Rasagiline (1) ·
Reboxetine (1) ·
Rotigotine (1) ·
Safinamide (1) ·
Selegiline (1) ·
Sertraline (1) ·
Tianeptine (1) ·
Tolcapone (1) ·
Tranylcypromine (1) ·
Trihexyphenidyl (1) ·
Trimipramine (1)
brand:
None (2) ·
Akineton (1) ·
Anafranil (1) ·
Apokyn (1) ·
Artane (1) ·
Aurorix (1) ·
Azilect (1) ·
Cogentin (1) ·
Comtan (1) ·
Cymbalta, Drizalma Sprinkle, Irenka, Yentreve (1) ·
Dostinex (1) ·
Edronax (1) ·
Eldepryl (1) ·
Fetzima (1) ·
Ludiomil (1) ·
Marplan (1) ·
Nardil (1) ·
Neupro (1) ·
Norpramin (1) ·
Ongentys (1) ·
Parlodel (1) ·
Parnate (1) ·
Rexulti (1) ·
Savella (1) ·
Serzone (1) ·
Sinemet (1) ·
Stablon (1) ·
Surmontil (1) ·
Symmetrel (1) ·
Tasmar (1) ·
Tofranil (1) ·
Valdoxan (1) ·
Vivactil (1) ·
Xadago (1) ·
Zoloft (1)
classes: (Click arrow to add another value)
mechanism:
Central and peripheral COMT inhibitor (1) ·
D1/D2/D3 receptor agonist (1) ·
D2 agonist; D1 partial agonist (1) ·
D2 receptor agonist (1) ·
Dopamine precursor (1) ·
Dopamine precursor + DOPA decarboxylase inhibitor (1) ·
Irreversible non-selective MAO inhibitor (3) ·
Irreversible selective MAO-B inhibitor (2) ·
MAO-B inhibitor; sodium channel blocker; glutamate release inhibitor (1) ·
Melatonin receptor agonist; 5-HT2C antagonist (1) ·
Mu-opioid agonist; modulates glutamate AMPA receptors (1) ·
Muscarinic receptor antagonist (1) ·
Muscarinic receptor antagonist; dopamine reuptake inhibitor (1) ·
NMDA antagonist; dopamine releasing agent (1) ·
Non-selective dopamine receptor agonist (1) ·
Once-daily COMT inhibitor (1) ·
Partial agonist at D2 and 5HT1A. Antagonist at 5HT2A, α1A, α1B, α2C. More potent 5HT2A antagonism, 5HT1A partial agonism, and α1 antagonism (relative to D2 partial agonism) than aripiprazole, proposed to reduce akathisia and enhance affective/cognitive effects. (1) ·
Peripheral COMT inhibitor (1) ·
Potent serotonin reuptake inhibitor; also NRI (1) ·
Reversible inhibitor of MAO-A (1) ·
Selective M1 muscarinic antagonist (1) ·
Selective norepinephrine reuptake inhibitor (3) ·
Serotonin and norepinephrine reuptake inhibitor (3) ·
Serotonin reuptake inhibitor and 5-HT2A antagonist (1) ·
Serotonin–norepinephrine reuptake inhibition (balanced) (1) ·
Serotonin–norepinephrine reuptake inhibitor (2) ·
TrkB/BDNF'"`UNIQ--ref-00000084-QINU`"' '"`UNIQ--vote-00000085-QINU`"' (1) ·
Weak SRI; primarily H1/D2/alpha antagonist (1)
uses:
None (34) ·
Depression, anxiety, neuropathic pain, fibromyalgia, chronic musculoskeletal pain (1) ·
Schizophrenia (FDA-approved 2015). Adjunctive treatment of major depressive disorder (2015). '''Agitation associated with dementia due to Alzheimer disease''' (FDA-approved May 2023, first agent specifically approved for this problem). Investigational for PTSD (combined with sertraline). (1)
starting dose:
preparations:
fda max:
onset:
duration:
halflife:
bioavailability:
pregnancy:
legal:
Showing below up to 36 results in range #1 to #36.