Use LEFT and RIGHT arrow keys to navigate between flashcards;
Use UP and DOWN arrow keys to flip the card;
H to show hint;
A reads text to speech;
84 Cards in this Set
- Front
- Back
Classification of atropine?
|
Cholinergic (ANS) blocking agent
|
|
Atropine's MOA?
|
Acts by competitive inhibition (antagonism) of AcH at the postganglionic axon in the parasympathetic nervous system. Blocks action & binding of AcH at muscarinic receptors of effector cells.
|
|
What is atropine used for?
|
Tx of diarrhea and vomiting by decreasing GI motility, preanesthetic to dry secretions and prevent bradycardia, pupil dilation to aid for ophthalmic exam, relieve ciliary spasm of eye
|
|
Other name for polyflex?
|
Ampicillin
|
|
Class of polyflex?
|
Beta lactam antibiotic, Aminopenicillin
|
|
MOA of polyflex?
|
Inhibits cell wall synthesis, bactericidal
|
|
Class of Naxcel?
|
3rd generation cephalosporin
|
|
What species can be treated with Naxcel?
|
Cattle and swine
|
|
MOA of Naxcel?
|
Inhibits cell wall synthesis,
bactericidal, works against gram- and gram+ bacteria, time-dependent antibiotic |
|
What is tetanus antitoxin derived from?
|
Prepared from the blood of horses hyperimmunized with Clostridium tetani toxoid
|
|
Prednisone's drug class?
|
Glucocorticoid
|
|
Prednisone's MOA?
|
GC receptor agonist,
Prednisone is metabolized to bioactive prednisolone, which then crosses cell membranes and binds specific cytoplasmic receptors. Results in inhibition of steroid hormone action/affects on target tissues. |
|
What is Mestinon?
|
Pyridostigmine bromide
|
|
Mestinon's drug class?
|
Anticholinesterase (cholinesterase inhibitor)
Muscle relaxant antagonists |
|
Mestinon's MOA?
|
Inhibits the hydrolysis of acetylcholine by cholinesterases. AcH accumulates and its action is prolonged.
|
|
What are the indications of Mestinon?
|
Tx of myasthenia gravis, prophylaxis of organophosphate poisoning
|
|
Hydromorphone's drug class?
|
Opioid analgesic (anesthetic adjunct)
|
|
Hydromorphone's MOA?
|
Binds to G protein-coupled opioid receptors located in the brain & spinal cord regions involved in transmission and modulation of pain. Interaction w/G protein-coupled receptors affectes ion channel gating, calcium disposition, and protein phosphorylation.
|
|
Acepromazine's drug class?
|
Phenothiazine derivative (psychotropic drug/antipsychotic agen)
Tranquilizer |
|
Acepromazine's MOA?
|
Acts w/in CNS to inhibit dopamine & serotonin receptors w/in basal ganglia, limbic system, RAS, hypothalamus, and brainstem
|
|
Acepromazine's indications?
|
Sedation
Antiadrenergic Anticholinergic Antihistaminic Antidopaminergic Antiemetic |
|
Acepromazine's contraindications?
|
Lowers seizure threshold.
May paralyze penis in horses. |
|
Propofol's drug class?
|
Anesthetic (injectable)
|
|
Propofol's MOA?
|
CNS depression by enhancing GABA activity in the brain and decreasing cerebral metabolic rate through GABA-A receptors. Modulates the inhibitory function.
|
|
Glycopyrrolate's drug class?
|
Antimuscarinic (cholinergic antagonist)
Anticholinergic agent |
|
Glycopyrrolate's MOA?
|
Binds competitively to muscarinic AcH receptors. Binding inhibits AcH action on structures innervated by postganglionic cholinergic nerves and on smooth muscles that respond to AcH but lack cholinergic innervation.
|
|
Glycopyrrolate's indications?
|
Preoperative antimuscarinic to reduce salivary, tracheobronchial, and pharyngeal secretions, to reduce the volume & free acidity of gastric secretions and to block cardiac vagal inhibitory reflexes during induction of anesthesia and intubation
|
|
Cefazolin's drug class?
|
Cephalosporin (1st generation), broad-spectrum antibiotic
|
|
Cefazolin's MOA?
|
Binds to active site of PBP;
inhibits bacterial growth by interfering with the transpeptidation reaction of bacterial cell wall synthesis |
|
Compare generations of Cephalosporins
|
1- gram+ cocci
2- gram+ cocci & gram- 3- more gram- & can cross blood-brain barrier 4- more resistant to hydrolysis by beta-lactamases |
|
Name for hetastarch?
|
Hydroxyethyl starch (HES)
|
|
Hetastarch's drug class?
|
Synthetic colloid (volume expander)
|
|
Clavamox's scientific name?
|
Amoxillin/clavulanic acid
|
|
Other brand name for Clavamox?
|
Augmentin
|
|
Clavamox's drug class?
|
Beta lactam aminopenicillin (time-dependent bacteriacidal)
|
|
Clavamox's MOA?
|
Inhibits bacterial cell wall synthesis through binding to transpepsidase.
Clavulanic acids binds competitively and irreversibly to beta lactamases. |
|
Other name for diazepam?
|
Valium
|
|
Diazepam's drug class?
|
Benzodiazepine
Spamolytic drug Skeletal relaxant w/ sedative properties Sedative-hypnotic drug |
|
Diazepam's MOA?
|
Facilitate GABA action at GABA-A receptors; enhances membrane hyperpolarization
|
|
Diazepam's indications?
|
Sedative, hypnotic, anesthesia adjunct
|
|
Isoflurane's drug class?
|
Inhalational anesthetic
Skeletal muscle relaxant (neuromuscular blocking drug) |
|
Isoflurane's MOA?
|
Facilitates GABA-mediated inhibition of GABA-A receptor sites
|
|
Fentanyl's drug class?
|
Opiod agonist/analgesic
Phenylpiperidine |
|
Fentanyl's MOA?
|
Binds specific G protein-coupled receptors located in the brain and spinal cord regions involved in the transmission and modulation of pain
|
|
Fentanyl's indications?
|
Moderate to severe intra-operative pain
Analgesioa, sedation 75-125X as potent as morphine |
|
Pyrantel pamoate's drug class?
|
Antiparasitic, tetrahydropyrimidine, endoparasiticide
|
|
Pyrantel pamoate's MOA?
|
Interferes w/ parasitic nerve transmission as cholinergic stimulants, leading to neuromuscular spastic paralysis. Acts as a depolarizing, neuromuscular-blocking agent.
|
|
Pyrantel pamoate's indications?
|
Roundworms (nematodes) - adult and larvae
|
|
Other name for Droncit?
|
Praziquantel
|
|
Droncit's drug class?
|
Cestocide
|
|
Droncit's drug class?
|
Cestocide
|
|
Droncit's MOA?
|
Induces calcium influx across the parasite tegument causing immediate muscular spasm
|
|
Droncit's indications?
|
Effective against all tapeworms (cestode)
|
|
Methazolamide's drug class?
|
Carbonic anhydrase inhibitor
|
|
Methazolamide's MOA?
|
Decreases aqueous humor production by reducing synthesis of bicarbonate in the ciliary body
|
|
Methazolamide's indications?
|
Used in reduction of aqueous humor formation to decrease intraocular pressure
|
|
Dorzolamide HCL's drug class?
|
Carbonic anhydrase inhibitor
|
|
Dorzolamide HCL's MOA?
|
Inhibition of enzyme prevents of H2CO3 and hydration of CO2
|
|
Indication of dorzolamide HCL?
|
Reduces IOP
|
|
Enrofloxacin's drug class?
|
Fluoroquinolone
Antimicrobial Bacteriacidal |
|
Enrofloxacin's MOA?
|
Inhibits bacterial DNA gyrase, which is an enzyme important to bacterial DNA replication
|
|
Enrofloxacin's indications?
|
Broad gram-negative spectrum
|
|
Which drugs make up Panalog?
|
Nystatin, neomycin sulfate, thiostreptin, triamcinolone acetonide
|
|
Panalog's drug class?
|
Topical antibacterial
|
|
Panalog's MOA?
|
Nystatin: fungistatic
Neomycin: aminoglycoside bacteriacidal antibiotic, active against gram neg & some gram pos. Triamcinolone acetonide: GC Thiostreptin: antimicrobial, highly active against gram pos. |
|
Panalog's indications?
|
Anti-inflammatory
Antipuritic Antifungal Antibacterial |
|
Selamectin's brand name?
|
Revolution
|
|
Selamectin's drug class?
|
Semi-synthetic avermectin
|
|
Selamectin's MOA?
|
Binds to glutamate gated Cl channels in parasite's nervous system, causing them to remain open. This leads to hyperpolarization of cell, which blocks neurotransmission.
|
|
Selamectin's indications?
|
Endoparasites, GI roundworms, heartworm prophylaxis, ectoparasites
|
|
What are the active ingredients in Frontline?
|
Fipronil and (s)-methoprene
|
|
Fipronil's drug class?
|
Phenylpyrazole
|
|
Fipronil's MOA?
|
Blocks the action of neurotransmitter GABA-regulated Cl channels by binding to GABA receptor. Results in excitation of nervous system.
|
|
Fipronil's indications?
|
Control of fleas and ticks in dogs and cats
|
|
(s)-methoprene's drug class?
|
Insect growth regulator and juvenile hormone analog
|
|
What is (s)-methoprene's MOA?
|
Mimics the activity of naturally-occurring juvenile hormones; prevents metamorphosis to the adult stage by arresting larval development
|
|
(s)-methoprene's indications?
|
Used to combat fleas in dogs and cats
|
|
What are the active ingredients in Heartguard?
|
Ivermectin and pyrantel pamoate
|
|
Ivermectin's drug class?
|
Avermectin
|
|
Ivermectin's MOA?
|
Binds to glutamate gated Cl channels in parasite's nervous system, causing them to stay open. This leads to hyperpolarization of cell, which blocks neurotransmission.
|
|
Ivermectin's indications?
|
Endoparasites, GI roundworms, heartworm prophylaxis, ectoparasites
|
|
What is PZ insulin?
|
Protamine Zinc Insulin (long-acting hormone)
|
|
PZI's MOA?
|
Insulin binds to insulin receptor, which stimulates tyrosine kinase activity. Autophosphorylation follows. Activated IRS lead to activation of signaling molecules.
|
|
What is Acarexx otic suspension composed of?
|
Ethyl alcohol and 0.01% Ivermectin
|