| Term 
 
        | Chlor-promazine (Thorazine) -category -mode of action -effect -side effects |  | Definition 
 
        | -Phenothiazine --Dopamine (D2) antagonist -Antipsychotic -TCA side effects (dirty drug) |  | 
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        | Term 
 
        | Pro-Methazine (Phenergan) -category -mode of action -effect |  | Definition 
 
        | -phenothiazine -anti-histamine, blocks M, blocks H1 in brain -treats pruitis (itching); motion sickness; and acts as a sedative (TCA like) |  | 
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        | Term 
 
        | Pro-Chlor-Perazine (Compazine) -category -mode of action -effect |  | Definition 
 
        | -Phenothiazine -TCA-like, D2 blocker -for drug induced nausea and migraine (but better to use sertrons aka 5-HT3 blockers) |  | 
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        | Term 
 
        | Flu-Phenazine (Permitil) and Tri-Fluo-Perazine (Stelazine) -category -mode of action -effect |  | Definition 
 
        | -Phenothiazines -TCA like (D2 blocker) -long-term antipsychotic for non-compliant patients   |  | 
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        | Term 
 
        | 4 categories of neuroleptic (antipsychotic) drugs |  | Definition 
 
        | -Phenothiazines (TCA like) -Butyrophenones -Thioxanthenes -Benzamides   |  | 
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        | Term 
 
        | Haloperidol -category -mode of action -effect -side effects |  | Definition 
 
        | -Butryophenones -More selective D2 blocker without TCA side effects -antipsychotic -D2 blocker related: extrapyramidal symptoms (Parkinson-like, motor side effects), the worst being tardive dyskinesia which is irreversible   |  | 
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        | Term 
 
        | Pseudo Parkinsonism drugs -mode of action -four examples |  | Definition 
 
        | -decrease in dopamine leads to increase in Ach, so these drugs counter that with atropine, anti-cholinergenic effects -Benztropine (esp for dystonia), Trihexyphenidyl (also anti M), Diphenhydramine (Benadryl, also antihistamine), Amantadine |  | 
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        | Term 
 
        | Clozapine (Di-Benzo-diazepine) -Category -Mode of action -Effects -Side effects -Metabolism |  | Definition 
 
        | -Atypical neuroleptic (all P450 metabolized) -D4 and 5-HT2 antagonists (high affinity) and low affinity D2 antagonist. -Antipsychotic (effective against negative symptoms like withdrawal...as opposed to positive symptoms like hearing voices) -TCA-like: sedation (H2 blocker), orthostasis/reflex tackycardia (β1 blocker), QT prolongation (K+ channel blocker) hypersalivation (rare for a TCA), hyperthermia (anticholinergic effect in periphery) and seizures (due to hyperthermia), but less EPS (extra pyramidal, Parkinson-like symptoms like dystonia etc.); Agranulocytosis: supressed red blood cell production needing blood monitoring; weight gain (10 by 10 = 10 lbs by 10 weeks) -P450 1A2 like Xanthines  |  | 
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        | Term 
 
        | Olanzapine -category -effects -side effects -metabolism |  | Definition 
 
        | -Atypical neuroleptic -D4 and 5-HT2 antagonists (high affinity) and low affinity D2 antagonist. -Antipsychotic (effective against negative symptoms like withdrawal...as opposed to positive symptoms like hearing voices)...NO Agranulocytosis! -TCA-like: sedation (H2 blocker), orthostasis/reflex tackycardia (β1 blocker), QT prolongation (K+ channel blocker) hypersalivation (rare for a TCA), hyperthermia (anticholinergic effect in periphery) and seizures (due to hyperthermia), but less EPS (extra pyramidal, Parkinson-like symptoms like dystonia etc.); ; weight gain (10 by 10 = 10 lbs by 10 weeks) -P450 1A2 like Xanthines |  | 
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        | Term 
 
        | Ziprasidone (Geodon) -Mode of action -Effect -Side effect |  | Definition 
 
        | -5-HT2 antagonist and NASRI (SNRI) reuptake inhibitor (little effect on D2 receptor) -Anti-depressant -QT prolongation (K+ channel blocker) |  | 
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        | Term 
 
        | Quetiapine -Category -Effect -Side effects |  | Definition 
 
        | -Atypical neuroleptic -anti-psychotic -Sedating, cataract development, hypothyroidism |  | 
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        | Term 
 
        | Aripiprazole (Abilify) -Mode of action -Effect -Side effect? -Metabolism |  | Definition 
 
        | -5HT2 antagonist; 5HT1A partial agonist (Buspirone-like); D2 partial agonist -antipsychotic -less weight gain -P450 2D6 & 3A4 |  | 
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        | Term 
 
        | Parkinson's therapy -3 part way of increasing dopamine |  | Definition 
 
        | -Carbidopa (Decarboxylase Inhibitor that stays in blood, allowing Levodopa to pass blood brain barrier before being converted to dopamine which cannot pass barrier) -Levadopa -Entacapone (COMT ie methyl transferase inhibitor, which stops Levadopa from being metabolized in the brain) -Stalevo (combines all three)   |  | 
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        | Term 
 
        | Selegeline (Antiparkin) -Mode of action -Effect |  | Definition 
 
        | -MAO-B (metabolizes dopamine) inhibitor -treats Parkinson disease by increasing dopamine levels |  | 
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        | Term 
 
        | Bromcriptine and Pergolide -Category -Mode of action -Effect -Side effects |  | Definition 
 
        | -Ergotamine derivatives -Dopamine receptor agonists -psychosis, nausea and vomitting (D2 agonist in CRTZ), orthostatic hypotension (usually α1 blocker, but also D2 agonist in periphery causes vasodilation), fibrosis (pulmonary and retroperitoneal), vasospasm and GI ulceration   |  | 
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        | Term 
 
        | Pramipexole and Ropinrole -Category -Mode of action -effect -Side effects |  | Definition 
 
        | -Non-ergotamine derivatives -Dopamine receptor agonists -Anti-Parkinson with NO fibrosis or vasospasms -Same as erotamine derivatives (psychosis, N&V, orthostatic hypotension, GI ulceration) with NO fibrosis or vasospasms |  | 
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