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54 Cards in this Set

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MAOIs
-MAO breaks down excess catecholamines
-MAOIs bind irreversibly to MAO
-efficient antidepressant and anti-anxiety agents
-rarely used today b/c of serious SE
MAOI types
1. Nardil
2. Parnate
3. Marplan
4. EmSam: no dietary restriction on lower doses because it avoids "first pass"
MAOIs SE
1. hypertensive crisis: caused by eating tyramine-containing foods, with increase NE in the body such as:
-alcohol, foreign cheeses, excess caffeine or chocolate
-smoked or fermented meats
-avacados, raisins, figs
2. Serotonin syndrome: AMS, hyperpyrexia, muscle rigidity
3. Sympathomimetic syndrome: HTN, tachy, anxiety
-WAIT 2 WKS WHEN SWITCHING FROM AN MAOI TO ANOTHER ANTIDEPRESSANT
Tricyclic antidepressants (TCAs)
-bind to reuptake pumps and block reuptake of serotonin and NE
-antidepressants and antianxiety agents
-SECOND LINE because of SE's
TCAs types
1. Elavil
2. Anafranik
3. Norpramin
4. Pamelor
5. Tofranil
TCA SE
1. Serotonine: GAS
-GI upset
-Arousal
-Sexual: dec libido, erectile dysfunction
2. NE:
-inc BP, tachy, tremor
-anxiety, incomnia, HA
-dec appetite, nausea
3. Anticholinergic: dry mouth, constipation, drowsiness, confusion, urinary retention, blurred vision
TCA SE cont
4. Alpha 1: orthostatic hypptension, syncope, dizziness
5. Cadiac: prolongs QT interval

-use caution in pts with conduction disorders!
SSRIs
-inhibit presynaptic reuptake of serotonin only
-antidepressant and antianxiety agents
-good for premenstrual syndrome and PMDD
-first line antidepressant because of MILD SE profile!
-not all alike!
-relatively safe in OD
-may inc levels of other antidepressants!
SSRI types
1. prozac
2. paxil
3. zoloft
4. luvox
5. celexa
6. lexapro
SSRI SE
1. N/D
2. vomiting
3 anorexia
4 anxiety
5 insomnia
6. sedation
7. dec libido, erectile dysfunction
-may dec plt function!
-may inc INR in combo with coumadin
-w/drawal syndromes: Dizziness, GI distress, fatigue, anxiety palpitations
Serotonin-2 Antagonistd
-increased serotonin leads to:
5HT-1 - Decreased depression and anxiety
5HT-2 - Anxiety, decreased libido, dysorgasmia
5HT-3 – Nausea, vomiting
5HT-4 – Abdominal cramping, diarrhea
serotonin-2 antagonists- basics
-Block Serotonin at the postsynaptic Serotonin-2 receptor, where many unwanted side effects occur, such as anxiety and sexual dysfunction
-results in dec depression and anxiety, with fewer sexual SE
-most commonly used to treat insomnia
-Desyrel
serotonin-2 antagonists SE
1. sedation
2. wt gain
3. orthostatic hypotension
4. dizzines
5. sedation
-priapism in 1/10,000 male pts!
SNRIs
-inhibits presynaptic reuptake of serotonin and NE
-may be more effective than SSRIs alone
-good for depression, anxiety, pain disorders
1. Effexor XR
2. Pristiq
3. Cymbalta
SNRIa SE
1. anxiety, jitteriness, insomnia, sedation
2. N/D. vomiting, anorexia
3. dec libido
4. inc BP, tachy, tremor
5. HA
Dopamine-NE reuptake inhibitors (NDRIs)
-inhibit presynaptic reuptake of NE and DA
-lower sexual SE and wt gain potential than other antidepressants!
-good for depression, seasonal affective disorder, smoking cessation and ADHA
-no indication fo anxiety disorders
1. Welbutrin, Welbutrin SR, Welbutrin XL
NDRIs SE
1. inc BP, tachy, tremor
2. anxiety, insomina, HA
3. decreased appetitie, nausea
3. increased libido
-increased seizure risk!
-paranois, psychosis!
Alpha-2 Antagonists
-inhibit presynaptic alpha-2 activity
-increase levels of synpatic serotonin and NE
-Remeron
alpha-2 antagonists SE
1. aniexty, agittion, insomnia, sedation
2. N/D
3/ dec libido
4. inc BP, tachy, tremor
5. HA
6. sedation
7. wt gain
Lithium
-acts on ion channels to "desensitize" the CNS
-good for mania and bipolar
-effective in decreasing recurrences of mania
-NOT metabolized by liver
-excreted through kidneys
Lithium SE
1. sedation
2. N/V/D
3. acne
4. alopecia
5. tremor, seizures
6. wt gain
7. hypothyroidism
8. polyuria, polydipsia
9, benign EKG changes, arrhythmia
10, leukocytosis
lithium- cautin
-narrow TI
-Toxicity; N/V, abd pain, lethargy, ataxia
-CAT D
-labs: BUN/Creat, lytes, TFTs, CBC, U/A, EKG, HcG
-f/u every 6 months
Antoconvulsants
-act on ion channels to "desensitize the CNS
Depakote: for acute mania only
Equetro: Bipolar Disorder
Lamictal: long-term treatment of Bipolar Disorder.
Depakote SE
1. GI upset
2. sedation
3. tramor
4. wt gain
5. alopecia
6. thrombocytopenia, inc LFTs
7. hepatotoxicity
Lab: CBC, plts, LFTs
Equetro SE
1. sedation
2. GI distress
3. dec appetite
4. hepatitis
5. leukopenia, thrombocytopenia
6. inc LFTs
7. agranulocytosis, aplastic anemia
Labs: CBC, plts, LFTs, HCG
Lamictal SE
1. sedaiton
2. GI
3. exfoliative dermatitis
4. SJS
-Depakote + Lamictal increases levels of both medications and the risk of Stevens-Johnsons Syndrome,
Antopsychotics
-lower DA in CNS
-used in acute and maintenance tx of mania
-all can cause varying degrees of sedation, dry mouth, constipation, lightheadedness
When treating anxiety disorders...
Starting dose is lower than for Depression
Therapeutic dose is often higher than for Depression
Side Effects are more common than in Depression
Rule of Thumb: “Start low, go slow, end high.”
Benzodiazepines
-GABA attaches to the GABA receptors of the Cl channel, allowing Cl ions to pass
-the greater the number of Cl ions, the greater the inhibition of the CNS
-benzos attach to the benzo receptor of the Cl channel
-in the presence of GABA, more Cl ions are to pass through
-without GABA benzos are useless!
Benzos- basics
-enhance GABA activity
-Sedative-hypnotics:
1. in lower doses, the reduce anxiety
2. in higher dose, the induce sleep
-NOT first line tx, due to TOLERANCE, DEPENDENCE, WITHDRAWAL AND SEDATION
Long acting benzos
1. Klonopin 6-10 hr duration
2. Valium 6-10 hrs
intermediate acting benzos
1. Xanax 4-5 hrs
2. ativan "
short acting benzos
1. Halcoin 1-2 hrs
Benzo SE
1. sedation
2. confusion
3. impaired memory
4. ataxia
5. behavioral disinhibition
6. resp depression
-caution: hass additvie effect with alcohol
-may lead to death in pts with impaired respt function!
Primary tx for insomnia is
-non-benzodiazepine hypnotics
Non-Benzodiazepine Hypnotics
- bind to a receptor site NEAR benzo receptors to increase GABA activity
-benefits over benzos:
1. rapid onset, short duration
2. less rebound, witdrawal, dependence and loss of efficacy
3. less confusion, memory impairment and ataxia
non benzo hypnotics types
1. Ambien (shortest half life)
2. Sonata
3. Lunesta
4. Restoril (longest half life)
Melatonin agonists
-Rozerem
-increases activity at the MT-1 and MT-2 receptors
-no evidence of dependence or tolerance!
-may take up to 2 wks to work
-SE: depression, possible dec test and increase prolactin
second line tx for insomnia
1. short-acting benzos
2. sedating antidepressants: TCAs, Trazadone, Remeron
3. 1st gen antihistamines
4. natural supps: melatonin
Hypersomnolence txs
1. sleep if primary cause is sleep deprivation
2. caffeine: adenosine receptor antagonist. DA and NE agonist
-Adenosine is a by-product of ATP metabolism. As it builds up in your system, it increases your sleep drive.
Psychotimulants
-Ritalin, Adderal
-MOA: block Da and NE reuptake. May relase DA and NE as weel
-SE: inc BP, tachy, anxiety, insomnia, HA, dec appetite, wt loss
Histamine Agonist
-Provigil
-increases histamine release in the "sleep/wake" center of the brain
-increased alertness with dec sympathetic SE
-dec potential for tol and dependence
-dec potential for abuse
antipsychotics affect 4 major areas of the brain:
1) Mesolimbic Pathway – Positive Symptoms
2) Mesocortical Pathway – Negative and Cognitive Symptoms
3) Nigrostriatal Pathway – Body Movement
4) Tuberoinfundibular Pathway - Prolactin Release
Haldol SE
1. dystonia
2. ESPEs
3. TD
4. prolactinemia
Clozapine SE
-2nd gen
1. agranulocystosis
2. seizures
3. leukopenia
Risperdal SE
-2nd gen
1. hyperprolactinemia
Zyprexa SE
-2nd gen
1. hyperglycemia
2. hyperlipidemia
Seroquel Se
-2nd gen
-sedation
Geodon SE
-2nd gen
-QTC prolongation
Abilify Se
-3rd gen
-Akathesia
Acetylcholinesterase inhibitors
-block the enzyme that breast down Ach
-slowing in the degenerative course of Alzheimers
Ach inhibitor types
1. Aricept: N/V/D
2. Exelon: GI upset
3. Razadyne
4. Cognex: heptatotoxicity- 2nd line
NMDA antagonists
-Namenda
-tx moderate ot severe alzheimers
-inhibits excess NMDA and NMDA-induced neurodegeneration
-should inhibit disease progression
ADHD tx
1. psychostimulatns: first line!
2. non-stimulants: increase levels of NE in the brain
-SE: anxiety, insomnia, sedation, dry mouth, constipation, urinary retention