Pharm4 Flashcards

1
Q

Precautions of Aminoglycosides

A
  • Use with caution in animals w/ renal disease or poor renal blood perfusion
  • Gentamicin, amikacin, kanamycin, and tobramycin should not be mixed w/ penicillin
  • Inactivated by organic debris
  • Not to be used in adult food animals
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2
Q

Quinolones

A
  • Newest antibiotic group
  • Reserve use for treatment of more serious infections
  • Examples: enrofloxacin, marbofloxacin, orbifloxacin, ciprofloxacin
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3
Q

Mechanism of action of Quinolones

A

Disruption of bacterial DNA molecule

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4
Q

Absorption of Quinolones

A
  • Well absorbed after oral or parenteral administration
  • GI absorption poor in mature ruminants- absorption in abomasum
  • Absorbed more slowly in the presence of food
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5
Q

Distribution, Metabolism, Elimination of Quinolones

A
  • Distribution– penetrates most tissues, except CNS
  • metabolized in by liver
  • Elimination– metabolites excreted through urine and bile
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6
Q

Spectrum of activity of Quinolones

A
  • Proven efficacy against most G- and some G+ bacteria

- not effective vs. anaerobic bacteria

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7
Q

Precautions of Quinolones

A
  • May cause damage to articular cartilage of growing dogs and horses (<3yrs).
  • Not recommended for pregnant animals- harmful to fetus
  • Vomiting, nausea, diarrhea observed in some animals
  • May cause crystal formation in urine
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8
Q

Tetracyclines

A
  • One of the oldest group of antibiotics
  • Use mostly in large animals
  • Examples: tetracycline, oxytetracycline, doxycycline
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9
Q

Mechanism of action of Tetracyclines

A
  • Bind to bacterial ribosomes and disrupt protein synthesis

* Bacteriostatic

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10
Q

Absorption of Tetracyclines

A

-Absorbed well after oral or parenteral administration
-These products interfere with absorption of tetracyclines from the GI tract:
 dairy products
 antidiarrheal agents
 antacids

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11
Q

Distribution and Elimination of Tetracyclines

A

• Distribution– Distributed to most tissues, except CNS
• Elimination:
-Excreted through bile but most reabsorbed from intestine
-Most elimination occurs via renal excretion

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12
Q

Spectrum of activity of Tetracyclines

A

Effective vs. G+ and G- bacteria (rickettsia, spirochetes, Chlamydia, Mycoplasma, salmon poisoning)

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13
Q

Precautions of Tetracyclines

A
  • Cause yellow discoloration of teeth and bones in young, growing animals
  • Cause retardation of bone growth in the fetus
  • Can cause vomiting, diarrhea, and anorexia
  • Do not use in animals w/ renal disease
  • Do not use in combination w/ penicillins or cephalosporins
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14
Q

Sulfonamides and Potentiated Sulfonamides

A
  • One of the oldest group of antibiotics used in animals
  • Examples: sulfadimethoxine, sulfamethazine, sulfachlorpyridazine, sulfadiazine-timethoprim, sulfadimethoxine-ormetoprim
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15
Q

Potentiated Sulfonamides

A

Have a sulfonamide mixed with another antibiotic. Increase the spectrum of activity.

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16
Q

Mechanism of action of Sulfonamides and Potentiated Sulfonamides

A

Interfere with the formation of folic acid by bacteria

17
Q

Absorption and Distribution of Sulfonamides and Potentiated Sulfonamides

A

Absorbed well after oral administration

Distributed well to body tissues, except CNS

18
Q

Metabolism and Elimination of Sulfonamides and Potentiated Sulfonamides

A

Metabolized by the liver

Elimination– Metabolites are excreted in urine; unchanged molecules are also excreted in urine

19
Q

Spectrum of activity of Sulfonamides and Potentiated Sulfonamides

A

Effective vs. G+ and G- bacteria, some protozoa

20
Q

Precautions of Sulfonamides and Potentiated Sulfonamides

A
  • Allergic reactions have been reported: fever, facial swelling, rashes, shock
  • Bone marrow suppression can occur w/ prolonged use
  • Can cause KCS in some dogs
  • May cause crystal formation in urine
21
Q

Metronidazole

A
  • Effective vs. anaerobic bacteria (Clostridium) and some protozoa (Giardia)
  • Anti-iflammatory effect in GI tract
  • Toxicity possible with high dose and prolonged useà CNS abnormalities
22
Q

Lincosamides

A

• Often used to treat G+ anaerobic bacterial infections in animals
o Examples: lincomycin, clindamycin

23
Q

Mechanism of action of Lincosamides

A

Bind to bacterial ribosome and interfere w/ protein synthesis

24
Q

Absorption and Distribution of Lincosamides

A

Absorbed well after parenteral and oral administration

Good distribution to body tissues, except CNS

25
Q

Metabolism and Elimination of Lincosamides

A

Metabolized by the liver

Excreted through urine and bile

26
Q

Spectrum of activity of Lincosamides

A

Effective vs. G+ bacteria, anaerobic bacteria, protozoa (Toxoplasma)

27
Q

Precautions of Lincosamides

A
  • Can cause vomiting and diarrhea
  • Do not use w/ antidiarrheal products
  • Do not use in guinea pigs, hamsters, or rabbits
28
Q

Chloramphenicol

A
  • Powerful broad spectrum antibiotic used only occasionally in animals
  • Should not be used in food animals
29
Q

Mechanism of action of Chloramphenicol

A

Binds the bacterial ribosome and interferes w/ protein synthesis

30
Q

Absorption and Distribution of Chloramphenicol

A

Absorbed well after oral administration

Distribution– Penetrates all tissues, including the CNS!!

31
Q

Metabolism and Elimination of Chloramphenicol

A

Metabolized by liver

Excreted in urine and bile

32
Q

Spectrum of activity of Chloramphenicol

A

Effective vs. G+ and G- bacteria (rickettsia, Chlamydia, Mycoplasma)

33
Q

Precautions of Chloramphenicol

A
  • Can cause bone marrow suppression in mammals
  • Do not use in animals w/ liver disease
  • Cats have a decreased ability to metabolize chloramphenicol
  • Do not use in combination w/ penicillins or cephalosporins