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Antimicrobial
therapy
Instructor – Dr. Jesus
George
1
Introduction
 Include: - Antibacterial
- Antiviral
- Antifungal
 Antibiotic: - Chemical substance produced
by a micro organism which has capacity in
dilute solution to inhibit the growth of or kill
other organisms.
2
Cont.
 Chemotherapeutic agent- A drug which is
manufactured entirely by chemical symthesis.
e.g: Sulphonamide, trimethoprim
3
Mechanism of action
 Inibition of cellwall synthesis- Penicillin,
cephalosporin, vancomycin
 Inhibition of cytoplasmic membrane -
antifungal antibiotics
 " protein synthsesis & impairement of
function of ribosomes - Aminolgylocydes,
Macrolides
4
CONT.
 Interference in transcription and translation of
genetic information - Quinolones,
metronidazole
 Antimetabolite action - Sulfonamide,
trimethoprim
 Binding to viral enzymes essential for DNA
synthesis - Acyclovir
5
Classifications
 On the basis of family
 Penicillins
 Cephalosporins
 Sulphonnamides
 Aminoglycosides
 Macrolides
6
Cont.
 On the basis of effect
 Bacteriostatic: Erythromycin
clotrimoxazole
Sulfonamide
 Bactericidal: Penicillins
Cephalosporins
quinolones
Aminoglycosides
7
Selection of Antimicrobials
• Clinical evaluation and diagnosis of
antimicrobiological etiology.
• Study of culture & Sensitivity
• pregnancy and neonatal period
• Severity of disease
• Risk of toxicity of drug .
8
Cont.
 H/O Allergic reaction
 Cost of therapy
 Use of narrow spectrum antibiotic
9
Antibiotic prophylaxis
 Given in followings situation:
 For preventing endocarditis following minor
surgeries.
 In patients with compound musculoskeletal
injuries, penetrating wounds, skull injury,
rhinorrhea, otorrhea
10
Cont.
• Prophylaxis regime for dental & oral procedure
– Amoxycillin: Adult 2.0g, children 50mg/kg orally 1 hr
before procedure.
– In Patient can't use oral –ampicillin - Adult- 2.0g i/m or
i/v & children 50mg/kg i/m or i/v 30min. before
procedure
– Allegric to penicillin- cephalexin adult 2.gm, child
50mg/kg oral, 1hr before procedure or
– Azithromycin adult 500mg, child. 50mg/kg oral 1hr
before procedure
– Allergic to penicillin and unable to take orally
clindamycin adult-600mg, child-50mg/kg 1hr before
procedure.
11
Principles of antibiotic
administration:
 Dosage: Should be adequate
 In renal failure dosage should be decreased
e.g Aminoglycosides, vancomycin
 In severe infection- large initial dose is used.
 Duration: Should be given for Min. 4 to 5 days.
 Severe infection -Duration can be prolonged
12
Cont.
 Route & Frequency of administration:
Antibiotic given by oral route should be acid
stable and absorbed from GIT e.g Penicllin
V, Amoxycillin
 Use of narrow spectrum antibiotic:
To minimize risk of super infection with
resistant organism
13
Beta - lactam Antibiotics
 Include penicillins & Cephalosporins
 Have B-Lactam ring
14
Penicillins:
 Classification
 Natural: Penicllin G and Phenoxymethyl Penicillin
V.
 Semisynthetic:- Short acting:- Ampicillin
-Amoxycillin
- Long acting: -Procaine penicillin, benzathene
penicillin.
15
Cont.
 Administration:
 Oral Route-Safest & Commonly used.
 i/m- Should be given only if surgery is equipped to
deal emergencies
 i/v- Should be given only in hospitalized patients.
 Penicillin are not given orally. Since adequate
level is not achieved.
16
Cont.
 Phenoxymethyl penicillin and ampicillin should be
given 1HR before or 3hrs after meals.
 Amoxicillin can be given after food
17
Cont.
• Measurements
– Expressed in I.U
– 250mg= 4,00,000 I.U
• TOXIC effects
– Allergy: Manifested as skin rash, Dermatitis, Serum
Sickness
– Controlled by withdrawal of penicillin use of
antihistamine
– Anaphylaxis- Life threatening - Characterized by -
Coughing, tonic spasms, Cyanosis, Weak Pulse,
Rapid drop in BP
18
Cont.
 Other Effects:
 Pregnancy-1st choice-Amoxycillin
 Lactation: Phenoxymethyl penicilin is preferred
 Oral Contraceptives: Penicillins may render
OCP in - effective
19
Cephalosporins
• Mode of action
– Bactericidal
– Inhibit cell wall synthesis
• Spectrum of activity
– Staphylococci
– Streptococci
• Indication:
– Alternative drug when penicillin is contraindication
20
Cont.
 Classification
 1st Generation For Gram+ve Microorganisms &
gram –ve except enterococci e.g:- Cephalexin
 Second generation:greater activity against gram
+ve organisms e.g Cefotaxime
 Third Generation: Less activity against gram+ve
than first generation & more activity against
enterobacteria
21
Erythromycin
 Macrolide antibiotic
 Available as azithromycin , Roxithromycin
 Oral only
 Broad Spectrum Antibiotic
 Against Gram +ve resistant to penicillin & Gram
-ve Organisms.
22
Cont.
 Preparation
 Oral, i/m, i/v
 Mode of action
 Bacteriostatic
 Inhibit protein synthesis
 .
23
Cont.
 Pharmacology
 Oral preparation salt available as stearate or
estolate salt
 Stearate salt is acid labile but less absorbed
 Estolate: Well absorbed
 i/M Preparation: erythromycin
 i/V : Erythromycin Lactobionate is used
24
Cont.
• Absorption:
– Absorbed from upper part of small intestine
– Food may delay absorption- So Given the before
food.
• Excretion:
– Excreted by liver and kidney
• Toxic Effect
– Allergic reaction-skin rashes
– Anaphylaxis
– Gastrointestinal effect- Nausea, vomiting,
diarrohea
25
Cont.
• Interaction:
– Antihistamins
– Theophyllin
– Carbamazepine
– Warfarin
– Benzodiazepine
– Ocp
• Use in pregnancy & lactation
– Not teratogenic
– Appears in breast milk
26
Sulfonamides and Trimethoprim
 Bacteriostatic
 Inactivated in presence of pus
 Act by inhibitions of bacterial synthesis of folic
acid from para - amino benzoic acid
 Absorption, distribution, excretion
 Absorbed after oral administration
 Distributed through all body fluids
27
Cont.
 Cross placental barrier & appears in breast milk
 Excreted through kidney
 Presence of sulfonamides in urine is greater than
in blood- leads to formation of crystals of
sulfonamide in urine called crystalurea & leads to
renal damage
28
Cont.
 Toxic effects
 Allergic reaction- Skin rash
 Exfoliative dermatitis
 Steven-johnson syndrome
 Perepheral neuritis
 Photosensitivity
29
Cont.
 Hemopoletic system:
 Macrocytic anemia
 Depression of bone marrow
 A/c hemolytic anemia
 Agranulocytosis
 Aplastic anemia
 Renal Damage
30
Cont.
 Pregnancy & lactation
 Not recommended pregnancy & lactation
 Ocp: becomes ineffective
31
Clotrimoxazole (Sulfamethazole +
Trimethoprim)
 Inhibits bacterial synthesis of DNA & RNA.
 Bacteriostatic
 Spectrum
 Streptococcus- pyogenes
 Most staphylococci
 Hemophil
32
Cont.
 Indication:
 Osteomyelitis secondary to osteoradionecrosis
 Actinomycotic infection
 Preparation:
 Oral: Adult: 80mg trimethoprim + 400mg
sulfumethazole 2 tablets 12th hrly.
 Child 20mg trimethoprim + 100mg sulfamethazole
33
Quinolones
• Mechanism of action
– Inhibit synthesis of bacterial DNA
• Eg: Norfloxacin
ciprofloxacin
ofloxacin
Sparfloxacin
Pefloxacin
34
Cont.
• Spectrum
– Bactericidal
– Against gram+ve gram-ve bacteria
• Absorption, Distibution, Excretion
• GIT Body Fluids Kidney
• Uses
– All except norfloxacin in systemic & serious
infection norfloxacin-UTI & GI infection
35
Cont.
• Adverse Reaction
– GIT:Nausea
Vomiting
Diarrohea
Anorexia
– CNS:Confusion
Nervousness
– Allergy
36
Acyclovir
• Used in- herpes simplex 1 & 2
– Varicella zoster infection
• Action:
– Inhibit viral DNA synthesis
• Dosage:
– Oral, 200mg 5 times/day for 7 days or i/v infusion
• Adverse reaction
– Thrombophlebitis (i.v)
– Blood urea & creatine is increased
– Avoided in pregnancy
37
Cont.
 Preparation:
 Cream 3%
 3% eye ointment
 Tablets 200 mg
38
Aminoglycosides
• Gentamycin
• Vancomycin
• Streptomycin
• Kanamycin
• Neomycin
• Bactericdal
• Inhibit protien synthesis
• Effective against gram-ve bacteria
• Toxic effect on 8th nerve & kidney
39
Gentamycin
• Administration
– i/m
• Spectrum
– Gram+ve & Gram-ve Bacteria
• Indication:
– Severe anaerobic infection
• Dosage:
– Adult: 3-7mg/kg/day in 2-3 divided doses
– Child: 1-3mg/kg/day " " "
40
Cont.
 Toxic effect:
 Ototoxicity
 Nephrotoxicity
 Allergy
 Pregnancy & Lactation - not recommended
41
Vancomycin
• Bactericidal
• Similar to gentamycin
• Indication
– Severe orofacial infection
– patients allergic to penicillin
– Patients with risk of endocarditis
• Dosage -i/v infusion
– Adult: 500mg 6th hrly or 1g 12th hrly
– Child: 44mg/kg/day in divided dose
42
Cont.
 Adverse reaction
 Deafness
 Anaphylaxis
 Hypotension
 Pregnancy & lactation
 Not recommended

43
Antimycotic agents
 Polyenes: Nystatin
 Amphotericin B
 Azoles: Imidazoles
 Triazoles
 Polyenes:
 Commonly used for oral candidiasis
44
Amphotericin B
• Mode of action
– Fungicidal & Fungistatic
• Spectrum
– Fungi causing disease to human
• Absorption:
– Poorly absorbed by GIT
• Administration
– i/v
– Topical
45
Cont.
• Adverse effect
– Nephrotoxicity
– Hypokalemia
– Mild anemia
– A/c hypersensitivity reaction
• Drug interaction:
– Aminoglycosides
– Cyclosporin
– Glucocorticoids
46
Cont.
 Dosage:
 Available as : Ointment
- Suspension
- Cream
- Lozenges - 80mg/day 8th hrly
- i/v infusion 0.25mg/kg/day
47
Nystatin
• For superficial infection of c.albicans
• Similar to amphotericin B
• Adverse effect:
– Systemic toxicity
• Preparations:
– Cream- Angular Chelitis
– Tablets - Oral candidiasis
– Suspension
– Oral Rinse
48
Azoles
 Classified into two
 Imidazoles-Clotrimazole
 Ketoconazole
 Miconazole
 Triazoles-Fluconozole
49
Clotrimazole
• Fungistatic
• Anticandidal & antistaphylococcal
• Use:
– Superficial infection of mouth, skin, vagina
• Adverse effects
– Skin irritation
– Nausea, vomiting
• Preparation
– Cream 1% tds
– Lozenges 10mg
50
Miconozole
 Same as clotrimazole
 Adverse effect
 Thrombophlebits
 Preparation:
 Tablets, cream, oral Gel, i/v, topical, vagina
preparations

51
Ketoconazole
• Mode of action
– Against most of fungi
• Absorption
– Readily absorbed orally
• Adverse effect:
– Nausea
– Vomiting
– Hepatotoxicity
– Painful gynecomastia
– Loss of hair
– Tearatogen
52
Cont.
 Interaction:
 Nonsedative antitistamine-terfenadine
 Preparation:
 Tablets, suspension, cream
 Dose-200-400mg/day
53
Fluconazole
• Water soluble
• Easily absorbed from GIT
• Mode of action:
– Broad spectrum antifungal
– Excreted through kidney
• Adverse effect
– Nausea
– Vomiting
– Allergy
– Headache
– GI discomfort
54
Cont.
• Interaction:
– Antihistamine-Terfenadine
– Phenytoin sodium
– Warfarin
– Cyclosporine
• Preparation:
– Capsule
– I/v
• Dosage:
– 50mg/day for 7-14days. Oropharyngeal candidiasis
– 50mg/day 14-30days, esophageal candidiasis
55
Metronidazole
 In anaerobic infection
 In anug
 Spectrum:
 Gram+ve & gram-ve including bacteriods
 Indications:
 Anug
 C/c destructive periodontal desease
 Juvenile periodontitis
56
Cont.
 Administration, absorption, distribution:
 Absorbed through - GIT
 Distributed in body fluids
 Cross placental barrier
 Appear in breast milk
 Excretion:
 In urine- coloured red or brown
 In saliva
57
Cont.
 Toxic effect & contraindication
 Carcinogenicity
 Teratogenicity
 Bood dyscrasias
 Hypotension
 Dizziness
 Contraindicatsd in pts with phenytoin sodium
58

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7 antimicrobial theapy

  • 2. Introduction  Include: - Antibacterial - Antiviral - Antifungal  Antibiotic: - Chemical substance produced by a micro organism which has capacity in dilute solution to inhibit the growth of or kill other organisms. 2
  • 3. Cont.  Chemotherapeutic agent- A drug which is manufactured entirely by chemical symthesis. e.g: Sulphonamide, trimethoprim 3
  • 4. Mechanism of action  Inibition of cellwall synthesis- Penicillin, cephalosporin, vancomycin  Inhibition of cytoplasmic membrane - antifungal antibiotics  " protein synthsesis & impairement of function of ribosomes - Aminolgylocydes, Macrolides 4
  • 5. CONT.  Interference in transcription and translation of genetic information - Quinolones, metronidazole  Antimetabolite action - Sulfonamide, trimethoprim  Binding to viral enzymes essential for DNA synthesis - Acyclovir 5
  • 6. Classifications  On the basis of family  Penicillins  Cephalosporins  Sulphonnamides  Aminoglycosides  Macrolides 6
  • 7. Cont.  On the basis of effect  Bacteriostatic: Erythromycin clotrimoxazole Sulfonamide  Bactericidal: Penicillins Cephalosporins quinolones Aminoglycosides 7
  • 8. Selection of Antimicrobials • Clinical evaluation and diagnosis of antimicrobiological etiology. • Study of culture & Sensitivity • pregnancy and neonatal period • Severity of disease • Risk of toxicity of drug . 8
  • 9. Cont.  H/O Allergic reaction  Cost of therapy  Use of narrow spectrum antibiotic 9
  • 10. Antibiotic prophylaxis  Given in followings situation:  For preventing endocarditis following minor surgeries.  In patients with compound musculoskeletal injuries, penetrating wounds, skull injury, rhinorrhea, otorrhea 10
  • 11. Cont. • Prophylaxis regime for dental & oral procedure – Amoxycillin: Adult 2.0g, children 50mg/kg orally 1 hr before procedure. – In Patient can't use oral –ampicillin - Adult- 2.0g i/m or i/v & children 50mg/kg i/m or i/v 30min. before procedure – Allegric to penicillin- cephalexin adult 2.gm, child 50mg/kg oral, 1hr before procedure or – Azithromycin adult 500mg, child. 50mg/kg oral 1hr before procedure – Allergic to penicillin and unable to take orally clindamycin adult-600mg, child-50mg/kg 1hr before procedure. 11
  • 12. Principles of antibiotic administration:  Dosage: Should be adequate  In renal failure dosage should be decreased e.g Aminoglycosides, vancomycin  In severe infection- large initial dose is used.  Duration: Should be given for Min. 4 to 5 days.  Severe infection -Duration can be prolonged 12
  • 13. Cont.  Route & Frequency of administration: Antibiotic given by oral route should be acid stable and absorbed from GIT e.g Penicllin V, Amoxycillin  Use of narrow spectrum antibiotic: To minimize risk of super infection with resistant organism 13
  • 14. Beta - lactam Antibiotics  Include penicillins & Cephalosporins  Have B-Lactam ring 14
  • 15. Penicillins:  Classification  Natural: Penicllin G and Phenoxymethyl Penicillin V.  Semisynthetic:- Short acting:- Ampicillin -Amoxycillin - Long acting: -Procaine penicillin, benzathene penicillin. 15
  • 16. Cont.  Administration:  Oral Route-Safest & Commonly used.  i/m- Should be given only if surgery is equipped to deal emergencies  i/v- Should be given only in hospitalized patients.  Penicillin are not given orally. Since adequate level is not achieved. 16
  • 17. Cont.  Phenoxymethyl penicillin and ampicillin should be given 1HR before or 3hrs after meals.  Amoxicillin can be given after food 17
  • 18. Cont. • Measurements – Expressed in I.U – 250mg= 4,00,000 I.U • TOXIC effects – Allergy: Manifested as skin rash, Dermatitis, Serum Sickness – Controlled by withdrawal of penicillin use of antihistamine – Anaphylaxis- Life threatening - Characterized by - Coughing, tonic spasms, Cyanosis, Weak Pulse, Rapid drop in BP 18
  • 19. Cont.  Other Effects:  Pregnancy-1st choice-Amoxycillin  Lactation: Phenoxymethyl penicilin is preferred  Oral Contraceptives: Penicillins may render OCP in - effective 19
  • 20. Cephalosporins • Mode of action – Bactericidal – Inhibit cell wall synthesis • Spectrum of activity – Staphylococci – Streptococci • Indication: – Alternative drug when penicillin is contraindication 20
  • 21. Cont.  Classification  1st Generation For Gram+ve Microorganisms & gram –ve except enterococci e.g:- Cephalexin  Second generation:greater activity against gram +ve organisms e.g Cefotaxime  Third Generation: Less activity against gram+ve than first generation & more activity against enterobacteria 21
  • 22. Erythromycin  Macrolide antibiotic  Available as azithromycin , Roxithromycin  Oral only  Broad Spectrum Antibiotic  Against Gram +ve resistant to penicillin & Gram -ve Organisms. 22
  • 23. Cont.  Preparation  Oral, i/m, i/v  Mode of action  Bacteriostatic  Inhibit protein synthesis  . 23
  • 24. Cont.  Pharmacology  Oral preparation salt available as stearate or estolate salt  Stearate salt is acid labile but less absorbed  Estolate: Well absorbed  i/M Preparation: erythromycin  i/V : Erythromycin Lactobionate is used 24
  • 25. Cont. • Absorption: – Absorbed from upper part of small intestine – Food may delay absorption- So Given the before food. • Excretion: – Excreted by liver and kidney • Toxic Effect – Allergic reaction-skin rashes – Anaphylaxis – Gastrointestinal effect- Nausea, vomiting, diarrohea 25
  • 26. Cont. • Interaction: – Antihistamins – Theophyllin – Carbamazepine – Warfarin – Benzodiazepine – Ocp • Use in pregnancy & lactation – Not teratogenic – Appears in breast milk 26
  • 27. Sulfonamides and Trimethoprim  Bacteriostatic  Inactivated in presence of pus  Act by inhibitions of bacterial synthesis of folic acid from para - amino benzoic acid  Absorption, distribution, excretion  Absorbed after oral administration  Distributed through all body fluids 27
  • 28. Cont.  Cross placental barrier & appears in breast milk  Excreted through kidney  Presence of sulfonamides in urine is greater than in blood- leads to formation of crystals of sulfonamide in urine called crystalurea & leads to renal damage 28
  • 29. Cont.  Toxic effects  Allergic reaction- Skin rash  Exfoliative dermatitis  Steven-johnson syndrome  Perepheral neuritis  Photosensitivity 29
  • 30. Cont.  Hemopoletic system:  Macrocytic anemia  Depression of bone marrow  A/c hemolytic anemia  Agranulocytosis  Aplastic anemia  Renal Damage 30
  • 31. Cont.  Pregnancy & lactation  Not recommended pregnancy & lactation  Ocp: becomes ineffective 31
  • 32. Clotrimoxazole (Sulfamethazole + Trimethoprim)  Inhibits bacterial synthesis of DNA & RNA.  Bacteriostatic  Spectrum  Streptococcus- pyogenes  Most staphylococci  Hemophil 32
  • 33. Cont.  Indication:  Osteomyelitis secondary to osteoradionecrosis  Actinomycotic infection  Preparation:  Oral: Adult: 80mg trimethoprim + 400mg sulfumethazole 2 tablets 12th hrly.  Child 20mg trimethoprim + 100mg sulfamethazole 33
  • 34. Quinolones • Mechanism of action – Inhibit synthesis of bacterial DNA • Eg: Norfloxacin ciprofloxacin ofloxacin Sparfloxacin Pefloxacin 34
  • 35. Cont. • Spectrum – Bactericidal – Against gram+ve gram-ve bacteria • Absorption, Distibution, Excretion • GIT Body Fluids Kidney • Uses – All except norfloxacin in systemic & serious infection norfloxacin-UTI & GI infection 35
  • 36. Cont. • Adverse Reaction – GIT:Nausea Vomiting Diarrohea Anorexia – CNS:Confusion Nervousness – Allergy 36
  • 37. Acyclovir • Used in- herpes simplex 1 & 2 – Varicella zoster infection • Action: – Inhibit viral DNA synthesis • Dosage: – Oral, 200mg 5 times/day for 7 days or i/v infusion • Adverse reaction – Thrombophlebitis (i.v) – Blood urea & creatine is increased – Avoided in pregnancy 37
  • 38. Cont.  Preparation:  Cream 3%  3% eye ointment  Tablets 200 mg 38
  • 39. Aminoglycosides • Gentamycin • Vancomycin • Streptomycin • Kanamycin • Neomycin • Bactericdal • Inhibit protien synthesis • Effective against gram-ve bacteria • Toxic effect on 8th nerve & kidney 39
  • 40. Gentamycin • Administration – i/m • Spectrum – Gram+ve & Gram-ve Bacteria • Indication: – Severe anaerobic infection • Dosage: – Adult: 3-7mg/kg/day in 2-3 divided doses – Child: 1-3mg/kg/day " " " 40
  • 41. Cont.  Toxic effect:  Ototoxicity  Nephrotoxicity  Allergy  Pregnancy & Lactation - not recommended 41
  • 42. Vancomycin • Bactericidal • Similar to gentamycin • Indication – Severe orofacial infection – patients allergic to penicillin – Patients with risk of endocarditis • Dosage -i/v infusion – Adult: 500mg 6th hrly or 1g 12th hrly – Child: 44mg/kg/day in divided dose 42
  • 43. Cont.  Adverse reaction  Deafness  Anaphylaxis  Hypotension  Pregnancy & lactation  Not recommended  43
  • 44. Antimycotic agents  Polyenes: Nystatin  Amphotericin B  Azoles: Imidazoles  Triazoles  Polyenes:  Commonly used for oral candidiasis 44
  • 45. Amphotericin B • Mode of action – Fungicidal & Fungistatic • Spectrum – Fungi causing disease to human • Absorption: – Poorly absorbed by GIT • Administration – i/v – Topical 45
  • 46. Cont. • Adverse effect – Nephrotoxicity – Hypokalemia – Mild anemia – A/c hypersensitivity reaction • Drug interaction: – Aminoglycosides – Cyclosporin – Glucocorticoids 46
  • 47. Cont.  Dosage:  Available as : Ointment - Suspension - Cream - Lozenges - 80mg/day 8th hrly - i/v infusion 0.25mg/kg/day 47
  • 48. Nystatin • For superficial infection of c.albicans • Similar to amphotericin B • Adverse effect: – Systemic toxicity • Preparations: – Cream- Angular Chelitis – Tablets - Oral candidiasis – Suspension – Oral Rinse 48
  • 49. Azoles  Classified into two  Imidazoles-Clotrimazole  Ketoconazole  Miconazole  Triazoles-Fluconozole 49
  • 50. Clotrimazole • Fungistatic • Anticandidal & antistaphylococcal • Use: – Superficial infection of mouth, skin, vagina • Adverse effects – Skin irritation – Nausea, vomiting • Preparation – Cream 1% tds – Lozenges 10mg 50
  • 51. Miconozole  Same as clotrimazole  Adverse effect  Thrombophlebits  Preparation:  Tablets, cream, oral Gel, i/v, topical, vagina preparations  51
  • 52. Ketoconazole • Mode of action – Against most of fungi • Absorption – Readily absorbed orally • Adverse effect: – Nausea – Vomiting – Hepatotoxicity – Painful gynecomastia – Loss of hair – Tearatogen 52
  • 53. Cont.  Interaction:  Nonsedative antitistamine-terfenadine  Preparation:  Tablets, suspension, cream  Dose-200-400mg/day 53
  • 54. Fluconazole • Water soluble • Easily absorbed from GIT • Mode of action: – Broad spectrum antifungal – Excreted through kidney • Adverse effect – Nausea – Vomiting – Allergy – Headache – GI discomfort 54
  • 55. Cont. • Interaction: – Antihistamine-Terfenadine – Phenytoin sodium – Warfarin – Cyclosporine • Preparation: – Capsule – I/v • Dosage: – 50mg/day for 7-14days. Oropharyngeal candidiasis – 50mg/day 14-30days, esophageal candidiasis 55
  • 56. Metronidazole  In anaerobic infection  In anug  Spectrum:  Gram+ve & gram-ve including bacteriods  Indications:  Anug  C/c destructive periodontal desease  Juvenile periodontitis 56
  • 57. Cont.  Administration, absorption, distribution:  Absorbed through - GIT  Distributed in body fluids  Cross placental barrier  Appear in breast milk  Excretion:  In urine- coloured red or brown  In saliva 57
  • 58. Cont.  Toxic effect & contraindication  Carcinogenicity  Teratogenicity  Bood dyscrasias  Hypotension  Dizziness  Contraindicatsd in pts with phenytoin sodium 58