| Term 
 | Definition 
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 | Definition 
 
        | 3 drops every day in each eye |  | 
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 | Definition 
 
        | every 3 hours or as needed |  | 
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 | Definition 
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        | lec 18 aka Tylenol, relieve pain and fever NOT ANTI-INFLAMMATORY Inhibition of Prostaglandins |  | 
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        | Term 
 | Definition 
 
        | H1 Histamine receptor antagonist -prevent eye irritation caused by allergies. -Can be given to patients as young as 2 years old |  | 
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        | Term 
 | Definition 
 
        | Treatment of gout, works by decreasing uric acid production |  | 
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        | Term 
 | Definition 
 
        | Lec 16 an antipsychotic that blocks postsynaptic dopamine receptors. It is atypical and is therefore effective against both positive and negative symptoms. It is a preferred first line of treatment, lower risk for parkinsonism and tardive dyskinesia. A possible treatment for bipolar disorder |  | 
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        | Term 
 | Definition 
 
        | -lec 14 -a psycho motor non stimulant, used to treat ADHD however it is less addictive than Ritalin (not a controlled substance) -selective Norepinephrine re-uptake inhibitor |  | 
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        | Term 
 | Definition 
 
        | -used to treat rheumatoid arthritis, decreases inflammation   |  | 
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        | Term 
 | Definition 
 
        | -lec 17 -a GABA agonist, used as a muscle relaxant to treat muscle spasm |  | 
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        | Term 
 | Definition 
 
        | -a muscarinic antagonist used to treat Parkinsons, reserved for younger patients who still have a lot of acetylcholine left. Benztropine reaches the CNS better than Atropine |  | 
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        | Term 
 | Definition 
 
        | -alpha adrenergic agonist used to treat glaucoma, works by decreasing aqueous production |  | 
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        | Term 
 | Definition 
 
        | -a topical NSAID given once a day, used to treat pain and inflammation following cataract surgery |  | 
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        | Term 
 | Definition 
 
        | -a direct dopamine agonist used to treat Parkonsin’s -it is also used to treat post partum lactation and acromegaly |  | 
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        | Term 
 | Definition 
 
        | used to treat osteoporosis, a hormonal agent secreted by parafollicular cells, good for patients who cannot take Bisphosphonates or ERT Calcitonin moves calcium from the blood into bone. Source is salmon  |  | 
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        | Term 
 | Definition 
 
        | Lec 15-a second generation anti-epileptic -also used as a treatment for mania or bipolar disorder (anti-convulsant) -works by inhibiting glutamate receptors -may increase risk of suicide |  | 
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        | Term 
 | Definition 
 
        | -a first generation anti-psychotic, blocks post synaptic dopamine receptors, treats positive symptoms (Typical vs. Atypical) -may cause corneal deposits |  | 
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        | Term 
 | Definition 
 
        | -a selective serotonin re-uptake inhibitor used to treat depression and anxiety |  | 
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        | Term 
 | Definition 
 
        | -treats gout by binding to tubules, preventing transport |  | 
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        | Term 
 | Definition 
 
        | -mast cell stabilizer used to prevent symptoms of asthma |  | 
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        | Term 
 | Definition 
 
        | -lec 17-an antispasmodic agent, alleviates skeletal muscle spasms, is similar to TCAs |  | 
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        | Term 
 | Definition 
 
        | -a directly acting skeletal muscle relaxant -also an antidote for malignant hyperthermia -inhibits the release of Ca from storage, thus decreasing muscle contraction |  | 
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        | Term 
 | Definition 
 
        | -a potent, long acting, ketone based, corticosteroid, treats red eye -may increase IOP thus prednisolone is generally preferred |  | 
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        | Term 
 | Definition 
 
        | -increases attention, used to treat narcolepsy and ADHD -indirect agonist of NE and  DA |  | 
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        | Term 
 | Definition 
 
        | -increases GABA, used to treat status epilepticus which is a seizure that lasts 30 min |  | 
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        | Term 
 | Definition 
 
        | -a topical NSAID used as an analgesic  |  | 
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        | Term 
 | Definition 
 
        | -an appetite suppressant, works by stimulating the release of NE and DA |  | 
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        | Term 
 | Definition 
 
        | -an emulsion-form corticosteroid -used to treat ocular pain, inflammation and uveitis |  | 
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        | Term 
 | Definition 
 
        | -a cholinesterase inhibitor used to treat Alzheimers SE of diarrhea, nausea and vomiting |  | 
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        | Term 
 | Definition 
 
        | -a topical carbonic anhydrase inhibitor which reduces aqueous production -found in Cosopt which is a combination glaucoma drug,  |  | 
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        | Term 
 | Definition 
 
        |   -a nonbenzodiazepine drug for treating insomnia, binds GABA type A receptors -has less anxiolytic and anticonvulsant activity than older sleep promoting meds. |  | 
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        | Term 
 | Definition 
 
        | -an antiepileptic the blocks Ca++ channels  |  | 
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        | Term 
 | Definition 
 
        | -a second generation antidepressant -selective serotonin re-uptake inhibitor -Prozac is the longest acting, it can be taken only once/week, safe for younger patients.  -may increase risk of suicide |  | 
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        | Term 
 | Definition 
 
        | -a cholinesterase inhibitor, Alzheimer treatment -cognitive benefits sustained for up to 3 months |  | 
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        | Term 
 | Definition 
 
        | a high potency anti-psychotic used to treat Schizophrenia -Typical (works against positive Sx) |  | 
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        | Term 
 | Definition 
 
        | -used to replace natural corticosteroids in a deficient patient -naturally increases blood sugar, suppresses immune system, and aids in fat, protein and carb metabolism |  | 
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        | Term 
 | Definition 
 
        | -osteoporosis treatment, inhibits osteoclast activity |  | 
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        | Term 
 | Definition 
 
        | prostaglandin synthesis inhibitor, relieves pain and inflammation, prophylaxis of MI and stroke,used to close ductus arteriosus |  | 
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        | Term 
 | Definition 
 
        | -histamine receptor blocker used to treat allergic conjunctivitis |  | 
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        | Term 
 | Definition 
 
        | -mast cell stabilizer and antihistamine -OTC allergy med |  | 
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        | Term 
 | Definition 
 
        | -2nd generation anti-epileptic drug -inhibits glutamate receptors |  | 
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        | Term 
 | Definition 
 
        | -a prostaglandin glaucoma med, decreases IOP by increasing uveosclera outflow.  |  | 
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        | Term 
 | Definition 
 
        | -a mood stabilizer, used to treat bipolar disorder, also a common treatment for manic depression -contraindicated in patients with severe renal disease -has a low therapeutic index. |  | 
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        | Term 
 | Definition 
 
        | -a benzodiazepine, increases the action of GABA, an intermediate acting drug.  -prescribe for patients with alcohol withdrawal |  | 
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        | Term 
 | Definition 
 
        | -an ester based corticosteroid used to treat inflammation,  -may increase IOP |  | 
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        | Term 
 | Definition 
 
        | -an N-methyl-D-aspartate (NMDA) receptor antagonist, since this receptor is activate but glutamate it is in turn a glutamateantagonist  -used to treat Alzheimers (note that most other anti-Alzheimer drugs are cholinesterase inhibitors) -dizziness is a common side effect |  | 
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        | Term 
 | Definition 
 
        | -anti-cancer drug -prevents folic acid synthesis and thus cell replication |  | 
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        | Term 
 | Definition 
 
        | -indirect stimulant of NE and DA, increasing their activity and thus increasing attention and improving learning. -ADHD drug |  | 
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        | Term 
 | Definition 
 
        | -indirect acting sympathomimetic, increases the activity of NE and DA  -used in treatment of ADHD, narcolepsy and obesity |  | 
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        | Term 
 | Definition 
 
        | -a prodrug used to treat pain and inflammation associated with cataract surgery |  | 
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        | Term 
 | Definition 
 
        | -antihistamine and mast cell stabilizer -commonly used to treat ocular allergies -more potent than OTC |  | 
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        | Term 
 | Definition 
 
        | -antiobesity -increases NE and inhibits lipase (so lipids are not broken down) |  | 
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        | Term 
 | Definition 
 
        | -an SSRI -treats depression and anxiety -decreases libido |  | 
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        | Term 
 | Definition 
 
        | -MAOI-mono amine oxidase inhibitor-thus inhibits the breakdown of catecholamies like NE. -antidepressant |  | 
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        | Term 
 | Definition 
 
        | -an appetite suppressant for short term management of obesity  -increases release of NE and DA and inhibits their re-uptake |  | 
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        | Term 
 | Definition 
 
        | -epilepsy med, especially status epilepticus -blocks Na+ channels thus inhibiting transmission of impulse,  |  | 
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        | Term 
 | Definition 
 
        | -a preferred treatment for ocular inflammation, a ketone based corticosteroid -treats uveitis and episcleritis |  | 
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        | Term 
 | Definition 
 
        | -gout med -increases excretion of urate by preventing reabsorption in the kidney |  | 
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        | Term 
 | Definition 
 
        | -a SERM (selective estrogen receptor modulator) -an estrogen antagonist, decreases bone absorption, thus increasing bone mass and density -treatment of osteoporosis, also decreases risk of breast cancer |  | 
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        | Term 
 | Definition 
 
        | -binds with high affinity to melatonin receptors, treatment for insomnia |  | 
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        | Term 
 | Definition 
 
        | -a cholinesterase inhibitor used in the treatment Of Alzheimers -taken with food to prevent nausea |  | 
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        | Term 
 | Definition 
 
        | -MAOI type B  -Parkinsons treatment and neuroprotective properties -used in earlier stages of Parkinsons while patient’s own DA is still present |  | 
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        | Term 
 | Definition 
 
        | -antidepressant -SSRI -blocks 5-HT which is a serotonin receptor   |  | 
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        | Term 
 | Definition 
 
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 -a potassium sparing diuretic, treats edema |  | 
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        | Term 
 | Definition 
 
        |   -low potency first generation anti-psychotic -tx for schizophrenia as well as a sedative, can cause retinal problems and corneal deposits |  | 
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        | Term 
 | Definition 
 
        | -a beta blocker, glaucoma and migraine med |  | 
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        | Term 
 | Definition 
 
        | -alpha 2 agonist -antispasmodic agent |  | 
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        | Term 
 | Definition 
 
        | -COMT inhibitor (Catechol-O-methyl-Transferase inhibitor) -treatment of parkinsons -given in combination with levodopa, prevents conversion of levodopa, so as to lengthen its half life-allows it to be active longer. -ineffective on its own |  | 
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        | Term 
 | Definition 
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        | Term 
 | Definition 
 
        | -an anticonvulsant -contraindicated in patients with hepatic impairment -treatment of acute mania -prophylaxis for recurrent manic and depressive episodes |  | 
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        | Term 
 | Definition 
 
        | -for erectile dysfunction -increases blood flow by inhibiting phosphodiesterase |  | 
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        | Term 
 | Definition 
 
        | -prevention of osteoporosis -decrease osteoclast formation and activity -increases osteoclast destruction -inhibit cholesterol biosynthetic pathway which is important for osteoclast function |  | 
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        | Term 
 | Definition 
 
        | -a non-benzodiazepine type hypnotic agent used to treat insomnia -has greater specificity at one GABA type A receptor. |  | 
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        | Term 
 
        | Name the 4 drugs on our drug list used to treat Alzheimers and differentiate their mechanisms of action |  | Definition 
 
        | Donepezil Galantamine Rivastigmine Mementine The first 3 are Cholinesterase inhibitors, Mementine is an NMDA receptor antagonist |  | 
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        | Term 
 
        | Name the four drugs on our list used to treat Parkinsons disease and differentiate their mechanisms of action |  | Definition 
 
        | Bromocriptine-dopamine agonist Benztropine-cholinergic antagonist Selegiline MAOI (type B) Tolcapone -extends the life of L-Dopa   |  | 
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        | Term 
 
        | Name 3 drugs used to treat insomnia, how are they different from one another? |  | Definition 
 
        | Eszopiclone Ramelteon Zolpidem Ramelteon binds to melatonin receptors, the other 2 are nonbenzodiazepine hypnotic agents that bind to GABA type A receptors |  | 
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        | Term 
 
        | Name 5 drugs used to treat epilepsy and their respective mechanisms |  | Definition 
 
        | Carbamazepine-blocks glutamate receptors Diazepam-increases GABA Ethosuximide-blocks Ca++ channels Lamotrigine-blocks glutamate receptors Phenytoin-blocks Na+ channels   |  | 
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        | Term 
 
        | Name the 3 drugs listed to treat obesity (appetite suppressants) What is their main mechanism? |  | Definition 
 
        | Diethylpropion Orlistat Phentermine   They stimulate NE Orlistat also inhibits lipase |  | 
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        | Term 
 
        | Which 3 drugs are used to treat gout? |  | Definition 
 
        | Allopurinol Colchicine Probenecid |  | 
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        | Term 
 
        | Name 4 drugs we learned that are used to treat osteoporosis and their respective mechanisms |  | Definition 
 
        | Calcitonin-moves calcium from blood to bone Ibandronate-inhibits osteoclasts Raloxifene-estrogen antagonist Zoledronic Acid-disrupts osteoclast synthesis and activity |  | 
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        | Term 
 
        | Describe 4 drugs for glaucoma treatment and how their mechanisms differ |  | Definition 
 
        | Brimonidine is an alpha adrenergic agonist and it decreases aqueous production as well as increases outflow Dorzolamide is a Carbonic Anhydrase Inhibitor and it decreases aqueous production Latanoprost increases uveoscleral outflow Timolol is a non selective beta blocker and it decreases production |  | 
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        | Term 
 
        | Name 4 drugs used to treat ADHD |  | Definition 
 
        | Atomoxetine Dextroamphetamine Methylphenidate Mixed Amphetamine   |  | 
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        | Term 
 
        | Name 2 drugs used to treat Schizophrenia |  | Definition 
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