| Term 
 | Definition 
 
        | Muscarinic agonist over nicotinic agonist stimulates GI motility
 contracts bladder
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        | Term 
 | Definition 
 
        | muscarinic agonist induces vomiting
 treates glaucoma
 contracts ciliary muscle contraction
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        | Term 
 | Definition 
 
        | Muscarinic antagonist, alkaloid preanesthetic, decreases respiratory secretion
 treats vagal hyperactivity, decreases gastric motility, causes hypohidrosis, decreases lacrimation, xerostomia (dry mouth), myadrysis, urinary retention
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        | Term 
 | Definition 
 
        | M1 antagonist, treats ulcers |  | 
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        | Term 
 | Definition 
 
        | cholinergic agonistcauses vasodilation, treats ergot poisoning |  | 
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        | Term 
 | Definition 
 
        | cholinergic agonist, treat colic and impaction |  | 
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        | Term 
 | Definition 
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        | Term 
 | Definition 
 
        | muscarinic agonist decrease heart rate and blood pressure
 may cause dyspnea-bronchoconstriction
 |  | 
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        | Term 
 | Definition 
 
        | Reversible, cholinesterase inhibitor causes miosis and decreases intraocular pressure, treats non-obstructive atony
 |  | 
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        | Term 
 | Definition 
 
        | Reversible, cholinesterase inhibitor |  | 
        |  | 
        
        | Term 
 | Definition 
 
        | Reversible, cholinesterase inhibitor |  | 
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        | Term 
 | Definition 
 
        | irreversible cholinesterase inhibitor |  | 
        |  | 
        
        | Term 
 | Definition 
 
        | reactivates cholinesterase |  | 
        |  | 
        
        | Term 
 
        | DFP-diisopropyl phosphofluridate |  | Definition 
 | 
        |  | 
        
        | Term 
 
        | tetraethyl-phosphate (TEPP) |  | Definition 
 | 
        |  | 
        
        | Term 
 | Definition 
 | 
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        | Term 
 | Definition 
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        | Term 
 | Definition 
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        | Term 
 | Definition 
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        | Term 
 | Definition 
 | 
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        | Term 
 | Definition 
 
        | muscarinic antagonist, alkaloid |  | 
        |  | 
        
        | Term 
 | Definition 
 
        | muscarinic antagonist, alkaloid |  | 
        |  | 
        
        | Term 
 | Definition 
 
        | muscarinic antagonist, used s a preanesthetic, does not cause tachycardia, reduces gastric and respiratory secretions, lasts longer than atropine |  | 
        |  | 
        
        | Term 
 | Definition 
 
        | similar to atropine, shorter duration, fewer GI, CV side effects |  | 
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        | Term 
 | Definition 
 
        | D1 adrenergic receptor, improves tissue perfusion partial agonist/antagonist
 catecholamine
 |  | 
        |  | 
        
        | Term 
 | Definition 
 
        | B1 adrenergic agonist, dilates peripheral blood vessels, improves cardiac contractility, catecholamine |  | 
        |  | 
        
        | Term 
 | Definition 
 
        | D1, D2 agonist, improves renal bloodflow, increase cardiac contractility, catecholamine |  | 
        |  | 
        
        | Term 
 | Definition 
 
        | adrenergic agonist, CNS stimulant, respiratory stimulant, reverse barbituate, noncatecholamine |  | 
        |  | 
        
        | Term 
 | Definition 
 
        | non-cholaminergic agent, adrenergic agonist, nasal spray, decrease bleeding from surgical procedures |  | 
        |  | 
        
        | Term 
 | Definition 
 
        | non catecholamine, adrenergic agonist, causes weight reduction, treats urinary incontinence in dogs, |  | 
        |  | 
        
        | Term 
 | Definition 
 
        | non catecholamine, alpha and beta adrenergic agonist, |  | 
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        | Term 
 | Definition 
 
        | B2 agonist, used to treat COPD |  | 
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        | Term 
 | Definition 
 | 
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        | Term 
 | Definition 
 
        | synthetic adrenergic antagonist, treats visceral ischemia due to circulatory shock |  | 
        |  | 
        
        | Term 
 | Definition 
 
        | synthetic adrenergic antagonist, treats visceral ischemia due to circulatory shock |  | 
        |  | 
        
        | Term 
 | Definition 
 
        | alpha 1 adrenergic antagonist |  | 
        |  | 
        
        | Term 
 | Definition 
 
        | alpha 2 adrenergic antagonist, reverse anesthesia in large wild animals |  | 
        |  | 
        
        | Term 
 | Definition 
 
        | beta adrenergic antagonist, treats atrial fibrillation or flutter |  | 
        |  | 
        
        | Term 
 | Definition 
 
        | beta adrenergic antagonist, treats atrial fibrillation or flutter |  | 
        |  | 
        
        | Term 
 | Definition 
 
        | beta adrenergic antagonist, treats atrial fibrillation or flutter |  | 
        |  | 
        
        | Term 
 | Definition 
 
        | prevent NE release, treats hypertension |  | 
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        | Term 
 | Definition 
 | 
        |  | 
        
        | Term 
 
        | Alpha methyl paratyrosine |  | Definition 
 
        | blocks tyrosine hydroxylase, inhibits NE synthesis |  | 
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        | Term 
 | Definition 
 
        | used for parkinson's, improve mood, mental health, increase catecholamine and serotonin in the brain |  | 
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        | Term 
 
        | Salicylate or carboxylic acid |  | Definition 
 
        | NSAIDs, suppresses inflammation, prevent making arachidonic acid |  | 
        |  | 
        
        | Term 
 | Definition 
 
        | NSAIDs suppresses inflammation, prevent making arachidonic acid |  | 
        |  | 
        
        | Term 
 | Definition 
 
        | NSAIDs, suppresses inflammation, prevent making arachidonic acid |  | 
        |  | 
        
        | Term 
 | Definition 
 
        | NSAIDs, suppresses inflammation, prevent making arachidonic acid |  | 
        |  | 
        
        | Term 
 | Definition 
 
        | NSAIDs, suppresses inflammation, prevent making arachidonic acid may cause chronic renal failure, inhibits COX1 and 2, |  | 
        |  | 
        
        | Term 
 | Definition 
 
        | NSAIDs, suppresses inflammation, prevent making arachidonic acid |  | 
        |  | 
        
        | Term 
 | Definition 
 
        | NSAID, inhibits COX, stabilizes lysosomes, inhibits formation of kinins, antithrombotics, |  | 
        |  | 
        
        | Term 
 | Definition 
 
        | NSAID, small therapeutic index, treats arthritis, spondylitis, and laminitis |  | 
        |  | 
        
        | Term 
 
        | Flunixin Meglumine (banamine) |  | Definition 
 
        | NSAID, nicotinic acid derivative, analgesic, treats visceral pain, acute cow mastitis |  | 
        |  | 
        
        | Term 
 | Definition 
 
        | NSAID, treats soft tissue infflamation, large margin of safety |  | 
        |  | 
        
        | Term 
 | Definition 
 
        | NSAID, targets COX-2 only so limited gastric injury, postoperative analgesic, good for osteoarthritis, can affect cartilage formation |  | 
        |  | 
        
        | Term 
 | Definition 
 
        | NSAID, reversibly binds COX, causes gastric lesions |  | 
        |  | 
        
        | Term 
 | Definition 
 
        | NSAID, slow onset of action, treats laminitis |  | 
        |  | 
        
        | Term 
 | Definition 
 
        | NSAID, inhibits COX, LO and bradykinin |  | 
        |  | 
        
        | Term 
 | Definition 
 
        | NSAID, osteoarthritis in dogs, |  | 
        |  | 
        
        | Term 
 | Definition 
 
        | NSAID, treats osteoarthritis |  | 
        |  | 
        
        | Term 
 
        | polysulfated glycoaminoglycan |  | Definition 
 
        | chondroprotetctive, proteolytic enzymes are inhibited, lysosomes are stabilized |  | 
        |  | 
        
        | Term 
 | Definition 
 
        | dual pathway NSAID, blocks COX and lipoxygenase, decreases gastric irritation and ulceration, metabolized to its active form tepoxalin pyrazole acid, treats osteoarthritis |  | 
        |  | 
        
        | Term 
 | Definition 
 
        | NSAID, specific COX2 inhibitor |  | 
        |  | 
        
        | Term 
 | Definition 
 
        | lubricant in synovial fluid, inhibits phagocytosis and lymphocyte migration |  | 
        |  | 
        
        | Term 
 
        | dimethyl sulfoxide (DMSO) |  | Definition 
 
        | scavenges free radicals, useful for CNS inflammation, inhibits platelet aggregation, treats acute swelling, acute ofr chronic otitis, skin wounds, acral lick dermatitis |  | 
        |  | 
        
        | Term 
 | Definition 
 
        | steroidal anti-inflammatory, found in creams and ointments |  | 
        |  | 
        
        | Term 
 | Definition 
 
        | steroidal anti-inflammatory, converts to cortisol by the liver |  | 
        |  | 
        
        | Term 
 | Definition 
 
        | steroidal anti-inflammatory, converted by the liver into prednisolone, little to no mineralcorticoid effect |  | 
        |  | 
        
        | Term 
 | Definition 
 
        | steroidal anti-inflammatory, used if liver is non-functional, little to no mineralcorticoid effect |  | 
        |  | 
        
        | Term 
 | Definition 
 
        | steroidal anti-inflammatory, little to no mineralcorticoid effect |  | 
        |  | 
        
        | Term 
 
        | isoflupredone or 9-flouroprednisolone |  | Definition 
 
        | high power steroidal anti-inflammatory, used in large animals |  | 
        |  | 
        
        | Term 
 | Definition 
 
        | intermediate power steroidal anti-inflammatory,not ideal for alternate day therapy |  | 
        |  | 
        
        | Term 
 | Definition 
 
        | long acting steroidal anti-inflammatory, no mineralcorticoid effect, used more commonly in large animals due to cost and availability issues |  | 
        |  | 
        
        | Term 
 | Definition 
 
        | long acting steroidal anti-inflammatory, no mineralcorticoid effect, used more commonly in large animals due to |  | 
        |  | 
        
        | Term 
 | Definition 
 
        | long acting steroidal anti-inflammatory, no mineralcorticoid effect, used more commonly in large animals due to |  | 
        |  | 
        
        | Term 
 | Definition 
 | 
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