NBDE Part II Pharmacology (From First-Aid) – Flashcards

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Epinehrine
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alpha 1, 2, beta 1,2 - anaphylactic shock, bronchospasm, glaucoma, vasoconstriction (in anesthetics) [Direct acting Adrenergic]
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NE
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alpha 1, alpha 2, beta 1- vasoconstriction, hypotension (NE will inc BP), shock [Direct acting adrenergic]
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Isoproterenol
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Beta 1, Beta 2- Bronchodilator [Direct acting adrenergic]
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Dopamine
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D1=D2 > alpha 1,2, beta 1,2- shock [Direct acting adrenergic}
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Dobutamine
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B1>B2- Congestive Heart Failure [Direct acting adrenergic}
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Phenylephrine
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alpha 1 > alpha 2- nasal decongestion, pupil dilator [Direct acting adrenergic}
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Methoxamine
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alpha 1> alpha 2- Treats BOTH Paroxysmal supraventricular tachycardia & hypotension [Direct acting adrenergic}
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clonidine
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alpha 2 - hypertension [Direct acting adrenergic}
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metaproterenol
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Beta 2 - bronchodilator, bronchospasm [Direct acting adrenergic}
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albuterol
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Beta 2- bronchodilator [Direct acting adrenergic}
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terbutaline
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beta 2- bronchodilator, reduces uterine contractions [Direct acting adrenergic}
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Amphethamine
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Indirect acting general agonist- Narcolepsy, attention deficit disorder
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Ephedrine
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Indirect acting general agonist & directing acting alpha and beta agonist [aka mixed action adrenergic] -hypotension, nasal decongestion, asthma
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1. Alpha 1 2. Alpha 2 3. Beta 1 4. Beta 2
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1. Smooth muscle contraction (vasoconstriction) 2. Bind to receptors pre-synaptically to reduce NE release, they cause a drop in BP (hypotension) 3. Located on kidneys and inc renin thereby inc BP, also located on Heart muscle and inc contraction 4. Lung relaxation - smooth muscle relaxation
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Phenoxybenzamine -irr or rev? -what type of drug? -txs what? -adverse side effects?
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-Irreversible -Nonselective alpha adrenergic blocker -Treats Pheochromocytoma -Adverse side effects: Postural hypotension, reflex tachycardia
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Phentolamine -irr or rev? -what type of drug? -txs what? -adverse side effects?
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-Reversible -Nonselective alpha adrenergic blocker -Treats Pheochromocytoma -Adverse side effects: Postural hypotension, reflex tachycardia
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Pheochromocytoma
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-benign tumor of adrenal gland -you have 2 adrenal glands, one above each kidney -if left untreated, it pumps hormones out continuously that cause high blood pressure
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Doxazosin
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Beta 1 adrenergic blocker Uses: hypertension, urinary retention (makes it easier to pee) Adverse effects: postural hypotension, headache, dizzy Trick: If the drug ends in "sin"--> its a sin to hold it in
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Prazosin
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Alpha 1 adrenergic blocker Uses: hypertension, urinary retention (makes it easier to pee) Adverse effects: postural hypotension, headache, dizzy
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Terazosin
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Alpha 1 adrenergic blocker Uses: hypertension, urinary retention (makes it easier to pee) Adverse effects: postural hypotension, headache, dizzy
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Propanolol 1) Treats 2) Adverse effects 3) type of drug
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1) Hypertension, Angina pectoris, myocardial infarction, glaucoma, migraine 2) Bronchoconstriction, arrhythmias, sexual impairment, fasting hypoglycemia 3) Beta nonselective blocker
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Timolol 1) Treats 2) Adverse effects 3) type of drug
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1) Glaucoma, hypertension 2) More potent than propanolol 3) nonselective beta blocker
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Nadolol 1) Treats 2) Adverse rxns 3) type of drug
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1) Glaucoma, hypertension 2) More potent than propanolol 3) nonselective beta blocker
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Labetalol 1. type of drug 2. treats 3. ad rnxs 4. also blocks?
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1. nonselective beta blocker 2. hypertension 3. orthostatic hypotension, dizziness, bradycardia, fatigue, drowsienss 4. alpha 1
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Acebutolol 1. Type of Drug 2. Txs 3. Adverse Effects
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1. Beta 1 blocker 2. hypertension 3. hypotension, bradycardia, fatigue, drowsiness
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Atenolol 1. Type 2. txs 3. adverse rxns
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1. Beta 1 blocker 2. hypertension 3. hypotension, bradycardia, fatigue, drowsiness
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Metoprolol 1. Type 2. txs 3. ad rxns
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1. Beta 1 blocker 2. hypertension 3. hypotension, bradycardia, fatigue, drowsiness
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Reserpine
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Blocks Mg ++/ATP-dependent transport of NE, SE, DA from cytoplasm into storage vesicles in adrenergic nerves
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Guanethidine
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Inhibits response of adrenergic nerves to stimulation by blocking release of NE
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Cocaine
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Inhibits the reuptake of NE by adrenergic neurons by blocking the Na+/K+ activated ATPase
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Bethanechol 1. Type of drug 2. Action 3. Clinical Application
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1. Cholinergic Agonist (Direct Acting) - hint ends in "chol" 2. Increases intestinal motility and stimulates detrusor muscle of bladdar 3. Atonic bladder
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Carbachol 1. Type of drug 2. Action 3. Clinical Application
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1. Cholinergic Agonist (Direct Acting) - hint ends in "chol" 2. Produces rapid miosis and contraction of ciliary muscles 3. Glaucoma
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Pilocarpine 1. Type of drug 2. Action 3. Clinical Application
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1. Cholinergic Agonist (Direct Acting) - hint ends in "chol" 2. Produces rapid miosis and contraction of ciliary muscles 3. Glaucoma
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Myasthenia gravis
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-skeletal muscle weakness -autoimmune disease which results from antibodies that block nicotinic acetylcholine receptors -prevents nerve impulses from triggering muscle contractions -treated with medications known as acetylcholinesterase inhibitors such as neostigmine and pyridostigmine.
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Edrophonium 1. Actions 2. Clinical Application
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1. Inhibits acetylcholinesterase- increasing Ach in the Neuromuscular junction. 2. Urinary retention, Reversal of neuromuscular junction blockade, Myasthenia gravis, Glaucoma
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Neostigmine 1. Actions 2. Clinical Application
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1. Inhibits acetylcholinesterase- increasing Ach in the Neuromuscular junction. 2. Urinary retention, Reversal of neuromuscular junction blockade, Myasthenia gravis, Glaucoma
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Physostigmine
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1. Inhibits acetylcholinesterase- increasing Ach in the Neuromuscular junction. 2. Urinary retention, Reversal of neuromuscular junction blockade, Myasthenia gravis, Glaucoma
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Echothiophate
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1. Inhibits acetylcholinesterase- increasing Ach in the Neuromuscular junction. 2. Urinary retention, Reversal of neuromuscular junction blockade, Myasthenia gravis, Glaucoma
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Atropine 1. Clinical uses 2. Adverse effects 3. Type of drug
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Antispasmodic (GI and bladdar)- decreases spasms Mydriasis Antisecretory (eyes, airway)- decreases these secretions Antidote for cholinergic agonists 2. Dry mouth, tachycardia, blurred vision, constipation, disorientation 3. Antimuscarinic agent
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Scopalamine 1. Type of drug 2. CLincial uses 3. Adverse
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1. Antimuscarinic agent 2. Antimotion sickness (decreases nerve signals that trigger your stomach to vomit. Scopolamine is used to prevent nausea and vomiting caused by motion sickness or from anesthesia given during surgery), Sedation 3. Same as Atropine
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Ipratropium 1. type of drug 2. Clinical uses
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1. antimuscarinic agent 2. asthma, COPD tip- antimuscarinic drugs are all about stoping secretions
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Succinylcholine 1. type of drug 2. Actions 3. Application
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1. Neuromuscular Blocker 2. Depolarizing neuromuscular junctional (NMJ) blockade 3. Rapid endotracheal intubation
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Tubocurarine
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1. Neuromuscular Blocker 2. Nondepolarizing NMJ blockade 3. Adjunctive in anesthesia for relaxation of skeletal muscles
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Atracurium
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1. Neuromuscular Blocker 2. Nondepolarizing NMJ blockade 3. Adjunctive in anesthesia for relaxation of skeletal muscles
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Doxacurium
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1. Neuromuscular Blocker 2. Nondepolarizing NMJ blockade 3. Adjunctive in anesthesia for relaxation of skeletal muscles
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Pancuronium
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1. Neuromuscular Blocker 2. Nondepolarizing NMJ blockade 3. Adjunctive in anesthesia for relaxation of skeletal muscles
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Hexamethonium
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Nicotinic Ach receptor antagonist
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Benzodiazepines 1. name a bunch 2. action 3. application 4. adverse effects 5. Type of drug
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1. diazepam, lorazepam, chlonazepam, triazolam, midazolam, chlordiazepoxide!!!!!!?!, alprazolam, oxazepam 2. facilitates gamma-aminobutyric acid (GABA) receptor binding by increasing the frequency of Cl- channel opening 3. Anxiety, Sedation, Muscle spasticity, seizures, sleep disorder, alcohol withdrawal 4. Drowsiness and confusion, Dependence, Potentiate alcohol effects and other central nervous system (CNS) depressants 5. Anxiolytic/Hypnotic
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Flumazenil
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Tx of benzodiazepine overdose. competitive GABA receptor.
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Buspirone 1. Type 2. Action 3. Applicationi
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1. Anxiolytic 2. Mediated through SE receptors 3. Anxiety disorder
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Hydroxyzine 1. Type 2. action 3. application
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1. Anxiolytic 2. antihistamine 3. antiemetic (preventing vomiting), anxiety disorder
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Phenobarbital 1. Type 2. Action 3. Application 4. Adverse Effects
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1. Barbiturate 2. potentiates GABA receptor binding by inc the duration of CL channel opening 3. Anesthesia, seizures, anxiety 4. drowsiness, confusion, dependence, potentiate alcohol and other cns depressants, cario and respiratory depressant, drug interactions (induce cytochrome P450)
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Pentobarbital
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1. Barbiturate 2. potentiates GABA receptor binding by inc the duration of CL channel opening 3. Anesthesia, seizures, anxiety 4. drowsiness, confusion, dependence, potentiate alcohol and other cns depressants, cario and respiratory depressant, drug interactions (induce cytochrome P450)
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Thiopental
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1. Barbiturate 2. potentiates GABA receptor binding by inc the duration of CL channel opening 3. Anesthesia, seizures, anxiety 4. drowsiness, confusion, dependence, potentiate alcohol and other cns depressants, cario and respiratory depressant, drug interactions (induce cytochrome P450)
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Secobarbital
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1. Barbiturate 2. potentiates GABA receptor binding by inc the duration of CL channel opening 3. Anesthesia, seizures, anxiety 4. drowsiness, confusion, dependence, potentiate alcohol and other cns depressants, cario and respiratory depressant, drug interactions (induce cytochrome P450)
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Chloral hydrate
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1. Nonbarbituate sedative 2. used for short-term of insomnia (sedative before dental/medical procedures). Its rapidly metabolized into trichloroethanol and trichloroacetic acid Cardio and Respir depressant at high doses
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Antihistamines 1. Type 2. Treats 3. Name two antihistamines?
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1. Nonbarbituate sedatives 2. Treats mild insomnia 3. Diphenhydramine & Doxylamine
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Carbamazepine
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Anticonvulsant Blocks Na channels Adverse effects- Liver toxicity, Blood dyscrasia, Induction of cyt P450
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Phenytoin
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Anticonvulsant blocks na channels adverse effects- gingival hyperplasia, SLE-like syndrome, diplopia (double vision), ataxia (loose muscle control), cyt P450
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Gabapentin
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Anticonvulsant Increases presynaptic GABA release adverse effects: ataxia, sedation
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Valproic Acid
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Anticonvulsant Blocks Na channels and increases GABA conc Adverse effcts: hepatotoxicity, neural tube defects
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Benzodiazepines
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Anticonvulsants Facilitates GABA binding Adverse effects: Sedation, dependence, tolerance
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Selective Serotonin Reuptake Inhibitors 1. Type of Drug 2. Name 3 of these drugs 3. Mechanism 4. Application 5. Adverse effects
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1. Antidepressant 2. Fluoxetine, Sertraline, Paroxetine Parrot serves the flu 3. Specifically inhibits serotonin reuptake 4. Depression 5. Anxiety, nausea, sexual dysfunction "Parrot Serves fruit"
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Tricylclic Antidepressants 1. Name the 6 2. Mechanism 3. Application 4. Adverse Effects
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1. Amitriptyline, Imipramine, Nortriptyline, Desipramine, Trimipramine, Doxepin has "trip" or "pra" in it 2. Inhibits reuptake of NE and SE into presynaptic nerve terminals 3. Depression and panic disorders 4. Antimuscarinic effects, postural hypotension, sedation, convulsions, arrhythmias
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Monoamine Oxidase Inhibitors 1. Name 3 2. Mechanism 3. Applications 4. adverse effects 5. TYpe of drug
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1. Phenelzine, Isocarboxazid, Tranylcypromine 2. Increases monoamine (NE, SE, DA) stores within the neurons and subsequent release of excess neurotransmitters into the synapse 3. Depression, anxiety, phobic states 4. drowsniess, postural hypotension, dry mouth, dysuria (painful urination), constipation 5. Antidepressant
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Lithium 1. Type of drug 2. Mechanism 3. Application 4. Adverse effect
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1. Antidepressant 2. Unknown 3. Bipolar disorder 4. Narrow therapeutic window, tremor, polyuria, hypothyroidism
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Antipsychotics (Neuroleptics) 1. Name 5 2. Mechanism 3. Application 4. Adverse effects
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1. Haloperiodol, Chlorpromazine, Thioridazine, Fluphenazine, Prochlorperazine 2. Block DA D2 receptors 3. Psychosis, acute mania, schizophrenia 4. Extrapyramidal effects, tardive dyskinesia, antimuscarinic effects, postural hypotension
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Antipsychotics (Atypical) 1. name 3 2. Mechanism 3. Application 4. Adverse
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1. Risperidone, Clozapine, Olanzapine 2. Block DA D2 and 5HT2 SE receptors 3. Schizophrenia, mania, depression 4. Lesser extrapyramidal and antimuscarinic effects than neuroleptics
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There are two general types of antipsychotics
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1. Neuroleptics 2. Atypical
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Cardiac Glycosides 1. Name two 2. Mechanism 3. Application 4. Adverse Effects
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1. Digitoxin, Digoxin 2. Inhibits Na+/K+ ATPase (normally pumps Na+ out of cells!) of cardiac cells, inc Na+ intracellularlly. This favors the Na+/Ca+ antiport causing an influx of Ca2++ inside--> increasing contractility! 3. Congestive heart failure 4. Dysrhythmia, nausea, vomiting, blurred vision, digoxin toxicity (narrow therapeutic index)
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Antiarrhythmic Classes of Drugs
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Class I: Na+ channel blockers (either slows phase 0 depolarization or shortens phase 3 repolarization) Quinidine, Lidocaine, Procainamide, Flecainide, Disopyramide Class II: B-Blockers (propanolol, metoprolol, pindolol, esmolol)- Decrease phase 4 deplolarization Class III: K+ channel blockers causing prolonged phase 3 repolarization Sotalol, Amiodarone, Bretylium Class IV: Ca2++ channel blockers (Verapamil, Diltiazem) Shorter action potential
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Diuretics 1.) 2 Types
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1. Loop Diuretics (Furosemide) -Sulfonamide loop diuretic that inhibits the Na+/K+/2Cl- triple co-transporter of the thick ascending loop of Henle -Treats Hypertension & edematous states (accumulation of fluid) -Adverse effects: Hyperuricemia (too much uric acid), ototoxicity (being toxic to the ear), hypokalemia, hypovolemia 2. Thiazide Diuretics (Hydrochlorothiazide) -Inhibits Na+/Cl- reabsorption in the distal convoluted tubules -Treats Hypertension & congestive heart failure - Adverse: Hyperuricemia, hypokalemia
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B-Blockers
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Propanolol, Metoprolol, Atenolol, Labetalol -Lowers cardiac output by decreasing sympathetic outflow from the CNS and inhibits release of renin from kidney -First line drug therapy for hypertension! -Adverse: Bradycardia, hypotension, insomnia, sexual dysfunction
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Alpha-1 Blockers
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Prazosin, Oxazosin, Terazosin - decrease in peripheral vascular resistance - adverse: first dose postural hypotension, headache, dizzy
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ACE inhibitors
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Captopril, Enalapril, Lisinopril, Benazepril -Anti-hypertensives -Blocks angiotensin convertin enzyme resulting in decrease conversioni of angiotensin I to II- potent vasoconstrictor -Adverse: cough, hypotension, hyperkalemia, rashes, fever Side effects of ACE inhibitors: "CAPTOPRIL" -Cough -Angioedema -Potassium excess -Taste changes -Orthostatic hypotension -Pregnancy contraindication -Rash -Indomethacin inhibition -Liver toxicity
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Angiotensin II Antagonist
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Losartan Angiotensin II receptor blocker Adverse: Fetal toxicity
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Ca2++ channel Blocker
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Verapamil, Diltiazem, Nifedipine -Block L-type ca channels in smooth muscle of heart -Adverse: Dizzy, constipation, headache, fatigue, hypotension
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Antianginal Drugs
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1) Nitroglycerin and Isosorbide Dinitrate -Nitric oxide release in smooth muscle cause increase cGMP resulting in relaxation and vasodilation. Affects VEINS greater than arteries -Applications: Angina and pulmonary edema -Adverse effects: dizzy, constipation, headache, fatigue, hypotension 2) B-Blockers -Lowers cardiac output -decreases heart workload (reduces freq and severity of angina attacks)
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Anticoagulants -Go over everything plus their overdose reversal meds
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1) Heparin -Binds and activates antithrombin III resulting in inactivation of thrombin and factor Xa. -Txs: Pulmonary embolism, stroke, deep vein thrombosis. Follow PTT -Adverse: Bleeding, thrombocytopenia (dec in platelets) -Overdose reversal: Protamine sulfate 2) Warfarin -inhibits synthesis of Vit K-dependent clotting factors: II, VII, IX, X as well as regulatory factors protein C and protein S -txs: long term anticoagulation. Follow PT/INR -Adverse: Bleeding and teratogenic -Overdose reversal: Vit K.
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Antihyperlipidemics
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HMG-CoA Reductase Inhibitor -Lovastatin, Pravastatin, Simvastatin, Fluvastatin -Competively inhibits HMG-CoA reductase, the rate-limiting step in de novo (new) cholesterol synthesis -Adverse effects: Rhabdomyolysis (damaged skeletal muscle breaks down rapidly), myopathy (dz of muscle tissue), liver failure
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Penicillin
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-Cell wall synthesis inhibitor -Penicillin V & Penicillin G -Binds penicillin binding proteins; blocks transpeptidase cross linking of bacterial cell walls; activates autolysins in bacterias. Not resistant to beta lactamase. -Spectrum: gram + cocci, gram + rods, gram - cocci, spirochetes -Adverse effects: Hypersensitivity reactions, diarrhea, hemolytic anemia
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Narrow Spectrum Penicillins
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Methicillin, Dicloxacillin, Nafcillin -Mechanism same as penicillin except beta lactamase resistant bc of bulkier R-group -Spectrum: Staph aureus -Adverse: Hypersensitivity reactions, nephritis (inflammation of kidneys)
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Extended Spectrum Penicillins
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Amoxicillin, Ampicillin -Mech same as penicillin but is beta lactamse resistant. It is combined with beta lactamse inhibitors such as clavulanic acid to enhance spectrum. Amoxicillin has more oral bioavailability -Spectrum: gram + (enterococci) and certain gram - rods (H. infuenzae, E. coli, P. Mirabilis, L. Monocytogenes, Salmonella) -Adverse: hypersensitivity rxns, pseudomembranous colitis
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Clavulanic acid
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beta lactamase inhibitor
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Antipseudomonas Penicillins
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Piperacillin, Carbenicillin, Ticarcillin -Same as penicillin but is beta lactamase resistant. Combined with beta lactamase inhibitors such as tazobactam to enhance spectrum -Spectrum: Many gram - bacilli and also pseudomonas aeruginosa -adverse: hypersensitivity rxns
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tazobactam
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beta lactamase inhibitor
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Cephalosporins
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Cell wall synthesis inhibitors -Beta lactam drugs that inhibit cell wall synthesis but more resistant to beta lactamase 1st generation: Cefazolin, cephalexin, cefadroxil Effective against gram + cocci and proteus mirabilis, E.coli, Kleb pneumoniae 2nd generation: Cefaclor, cefoxitin, cefuroxime, cefamandole Has some decreased gram + activity but has inc gram - activity to three additional organisms (Entero aerogenes, H. influenzae, Neisseria species) 3rd generation: Cefotaxime, ceftazidime, ceftriaxone, cefdinir, cefixime Has some dec gram + but compared to 1st and 2nd generation has enhanced gram + and serratia marcescens 4th generation: Cefepime Increased against Pseudomonas and gram + (strep and staph) Adverse effects: Hypersensitivity Cross hypersensitivity with penicillins (5-10%). Disulfiram-like effect with cefamandole. Anti vitamin K effects with cefamandole and cefoperazone causing bleeding.
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Carbapenems
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Imipenem -Beta lactam drug -inhibits cell wall synthesis - they are beta lactamase resistant -Spectrum: broadest beta lactam antibiotic spectrum! effective against pencillinase producing gram + and -, anaerobes, and pseudomonas aeruginosa -Adverse: GI upset
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Antimicrobials- Cell wall synthesis inhibitors
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Penicillins, Cephalosporins, Carbapenems, Monobactams, Vancomycin
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Monobactam
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Aztreonam -Beta lactam drug, resistant to beta lactamase -narrow spectrum primarily against enterobacteria, especially useful against aerobic gram - rods -adverse: skin rash, abnormal liver functions, no cross hypersensitivity with penicillin
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Vancomycin
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inhibits synthesis of cell wall phospholipids by binding D-ala and D-ala portions of cell wall precursors. Bactericidal and resistance occurs with amino acid change of D-ala and D-ala to D-ala and D-lac. spectrum: multi drug resistant gram + (staph and clostridium difficile- pseudomembraneous colitis) Adverse: diffuse flushing (red man syndrome), nephrotoxicity, ototoxicity, phlebitis (inflammation of veins)
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Protein synthesis inhibitors (antimicrobials)
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Clindamycin, Tetracyclines, Macrolies, Aminoclycosides, Chloramphenicol, Fluoroquinolones FATMCC
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Clindamycin
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-Works at 50S ribosomal subunit, Prevents peptide formation -Bacteriostatic -Spectrum: Anaerobic organisms such as bacteroides fragilis and clostridium perfringens -Adverse: pseudomembranous colitis
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Tetracyclines
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Tetracycline, Demeclocycline, Doxycycline, Minocycline -Binds to 30S blocks access of tRNA inhibiting bacterial protein synthesis -avoid taking milk antacids or iron bc divalent cations inhibit its absorption in the gut -spectrum: wide! active against vibrio cholerae, acne, chlamydia, ureaplasma urealyticum, mycoplasma pneumoniae, borrleia burgdorferi, rickettsia, tularemia -adverse: discoloration of teeth, inhibits bone growth in children, photosensitivity, GI irritation, fatal hepatotoxicity in pregnant women
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Macrolides
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Azithromycin, Clarithromycin, Erythromycin (ACE) -Binds to 50S and inhibits translocation steps of protein synthesis -spectrum: upper respiratory infections, pneumonias, mycoplasma, legionella, chlamydia, neisseria, gram + cocci (strep infections in pts allergic to penicillins) (MULPCNS*) -adverse effects: cholestatic hepatitis, GI irritation, ototoxicity
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Aminoglycosides
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Amikacin, Gentamicin, Neomycin, Netilmicin, Streptomycin, Tobramycin - all end in "micin or mycin" -binds to separated 30s interfering with assembly of ribosomal apparatus (requires O2 for uptake) -spectrum: aerobes only. gram - rods and synergistic with beta lactam antibiotics -adverse: teratogen, ototoxicity, nephrotoxicity
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Chloramphenicol
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-Binds 50S inhibits protein synthesis at the peptidyl transferase rxn -spectrum: broad spectrum antibacterial active against H. influenzae, Neisseria meningitidis, and streptococcus pneumoniae. Also active against Rickettsiae -adverse: hemolytic anemias and gray baby syndrome
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Fluoroquinolones
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Ciprofloxacin, Enoxacin, Levofloxacin, Norfloxacin, Ofloxacin, Trovafloxacin -Inhibits DNA gyrase (Topoisomerase II) -Spectrum: Gram negative rods of GI and urinary tracts including Pseudomonas aeruginosa, Neisseria. Has some activity against some gram + -adverse effects: tendonitis and tendon rupture, GI irritation
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Who needs AB Prophylaxis? Also - drug of choice? Allergic?
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1. Hx of prosthetic cardiac valve 2. Hx of previous infective endocarditis 3. Hx of CHD: Unrepaired cyanotic CHD, Completely repaired CHD with prosthetic material during first 6 months, Repaired CHD with residual defects 4. Hx of cardiac transplantation who develop valvulopathy Drug of choice: Amoxicillin 2 grams 30-60 minutes prior to dental procedures If Allergic: -Clind 600 mg 30-60 min -Ceph 2 g 30-60 min -Azithromycin 500 mg 30-60 -Clarithromycin 500 mg 30-60 * IF dosage is not administered before procedure, up to 2 hours after is ok
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Amphotericin B
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-Antifungal -Binds to ergosterol in cell membrane of fungi and forms pores that allows electrolytes and small molecules to leak from the cell causing cell death -Spectrum- wide spectrum of systemic mycoses such as Candida albicans, Histoplasma capsulatum, cryptococcus neoformans, coccidiodes immitis, strains of aspergillus and blastomyces dermatitdis -adverse: nephrotoxicity, arrhythmias, fevers/chills
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Nystatin
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Antifungal similar to amphotericin B spectrum: oral candidiasis adverse: nausea and vomiting
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Azoles
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-Antifungal -Fluconazole, ketoconazole, itraconazole, miconazole, voriconazole -Blocks synthesis of ergosterol -systemic mycoses with same spectrum as ampho B with addition of histoplasmosis -Adverse: Endocrine effects (gynecomastia, impotence, menstrual irregularities, decreased libido) liver dysfunction, fevers/chills
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Flucytosine
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Antifungal Inhibits DNA synthesis by conversion to fluorouracil and inhibiting thymidylate synthetase spectrum: systemic mycoses (cryptococcosis, candidiasis, chromoblastomycosis) adverse: bone marrow depression, hepatic dysfunction, GI irritation
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Name all antifungals
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Amphotericin B, Nystatin, Azoles, Flucytosine, Griseofulvin
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Griseofulvin
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Antifungal Interacts with microtubules to disrupt the mitotic spindle and inhibits mitosis Spectrum: Dermatophytes -(Trichophyton, Microsporum, Epidermophyton) Adverse: well tolerated
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Amantadine
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-Antiviral -Blockade of viral membrane matrix protein, M2, which is required for fusion of the viral membrane with cell membrane - prevents viral penetration and uncoating -Spectrum: Influenza A and Parkinsons disease -Adverse: insomnia, ataxia, and dizzy
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Ribavirin
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Antiviral -Inhibits synthesis of viral mRNA by inhibiting synthesis of guanine nucleosides -Spectrum: broad spec of RNA and DNA viruses including respiratory syncytial virus and hepatitis C -adverse: Hemolytic anemia and teratogenic
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Oseltamivir and Zanamvir
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Antiviral -Influenza neuraminidase inhibitors -Spectrum: Influenza A and B -Adverse: GI irritation
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Acyclovir
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Antiviral -Phosphorylated by herpes virus encoded enzyme, thymidine kinase, and inhibits viral DNA polymerase -Spectrum: herpes viruses HSV-1, HSV-2, VZV (chicken pox), EBV (Ebstein Barr aka herpes 4) -Adverse: Nephrotoxicity, tremors, local irritation depending on route of administration
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Ganciclovir
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Antiviral -Similar mechanism to acyclovir but with a preference for inhibition of CMV DNA polymerase -Spectrum: CMV -Adverse: neutropenia, nephrotoxicity
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Reverse Transcriptase Inhibitors
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HIV Therapy -Nucleosides: Zidovudine (AZT), Didanosine, Zalcitabine, Abacavir -Nonnucleosides: Nevirapine, Delaviridine, Efavirenz -Protease Inhibitors: Ritonavir, saquinavir, nelfinavir, ampreavir Mechanism for Nonnucleosides: -Inhibits HIV reverse transcriptase and thus preventing the incorporation of HIV into host genome. -Adverse effects: bone marrow suppression, megaloblastic anemia, peripheral neuropathy, rash, lactic acidosis Mechanism for Protease Inhibitors: -Blocks protease enzyme thereby inhibiting assembly of virus -Adverse: Thrombocytopenia, GI irriation, hyperglycemia, and lipid abnormalities
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Insulin
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-Diabetes -Mechanism: Binds to insulin receptors. In muscles stimulates uptake of glucose, stimulates glycogen and protein synthesis, stimulates K+ uptake. In adipose tissues, stimulates uptake of glucose and stimulates triglyceride storage. In liver, stimulates storage of glucose to glycogen -Used for diabetes and life-threatening hyperkalemia -toxicities: hypoglycemia
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Sulfonylureas
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Glipizide, Glyburide, Tolbutamide, Chlorpropamide -Stimulation of insulin release from beta cells of pancreas, stimulates binding of insulin to target tissues, decreases serum glucagon levels -Used for type II diabetes (requires presence of beta cells) -Toxicity: hypoglycemia and disulfiram reactions (tolbutamide and chlorpropamide)
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Biguanides
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Metformin -Decrease hepatic gluconeogenesis -used for type II diabetes -toxicity: lactic acidosis
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Glitazones
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Rosiglitazone, Pioglitazone -Increases target cell response to insulin -Used for: Type II diabetes -Toxcitiy: hepatotoxic, weight gain
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Alpha-Glucosidase Inhibitor
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Acarbose, Miglitol -Inhibits alpha-glucosidase in intestinal brush border and therefore decreasing the absorption of starch and disaccharides -Uses: Type II diabetes -Toxicities: Flatulence, diarrhea, abdomina cramping
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Hyperthyroidism
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Propylthiouracil, Methimazole -Inhibition of the coupling and organification steps of thyroid hormone synthesis -Propythiouracil also decreases the peripheral conversion of T4 to T3 -Toxicities: aplastic anemia, agranulocytosis, rash
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Steroid Therapy
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Glucocorticoids- Prednisone, Triamcinolone, Dexamethazone, Beclomethasone, Hydrocortisone Mechanism: Binds to specific intracellular cytoplasmic receptors in tissues. Promotes normal intermediary metabolism to provide increased resistance to stress. Decrease the production of leukotrienes and prostaglandins by inhibiting phospholipase A2 and expression of Cox-2. Uses: inflammation, addisons disease, immune suppression, asthma (aka they are anti-infammatories) toxicities: iatrogenic cushings syndrome Addisons disease- hyposecretion of adrenocortical hormone Cushings syndrome- hypersecretion of adrenocortical hormone
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Opiods -there is 8 of them
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Analgesics -Fentanyl, Morphine, Meperidine, Methadone Sulfentanil, Codeine, Heroin, Dextromethorphan -interact with opioid receptors (mu, delta, kappa) in the CNS and GI tract to modulate synaptic transmission -Uses: pain, reduce cough reflex (dex), diarrhea (loperamide) -Toxicities: respiratory depression, constipation, miosis, additive CND depression and addiction
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NSAIDs
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Analgesics -Aspirin, Ibuprofen, Indomethacin, Naproxen, Etodolac -Aspirin irreversibly inhibits Cox-1 and Cox-2 while the other NSAIDs are reversible inhibitors of 1 & 2. Prostaglandin synthesis is also blocked. -uses: Analgesia, anti-inflammatory, and antipyretic -Toxicity: aplastic anemia, GI ulcers, GI irritation, and Reye's syndrome
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Acetaminophen
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-Inhibition of cyclooxygenase in CNS -Clinical: Antipyretic and analgesic -Toxicities: Hepatotoxicity with overdose. Acetaminophen metabolite depletes glutathione and forms toxic metabolite, NAPQI, in liver. N-acetylcysteine is antidote.
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Cox-2 inhibitors
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Celecoxib, Valdecoxib -Preferential inhibition of cox 2 isoform that is found in inflammatory cells and mediates pain and inflammation. Spares cox-1, which is helpful in maintaining gastric mucosa cells. -uses: rheumatoid and osteoarthritis -toxicities: risk of MI and strokes
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Autacoids
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Prostaglandins -they all end in "prost" (Misoprostol, Carboprost, Dinoprost, Dinoprostone) - Uses: Abortions, induction of labor, prevention of peptic ulcers and maintenance of patent ductus arteriousus -Toxicities: Diarrhea
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Antihistamines
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1) H1 Blockers: Reversible H1 histamine receptor blockers 1st Generation: Diphenhydramine, Dimenhydrinate -Uses: Allergy, motion sickness and nausea, and sedatives 2nd Generation: Fexofenadine, Loratidine -Uses: Allergy, far less sedating that 1st generation -Toxicities: Sedation, antimuscarinic, antialpha adrenergic effects 2) H2 Blockers: Reversible H2 histamine receptor blockers Cimetidine, Ranitidine, Nizatidine, Famotidine -Uses: Peptic ulcers, esophageal reflux, gastritis -Toxicities: potent inhibitor of P450 (cimetidine)
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