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VANCOMYCIN
Mohammed – Alrjoub
 General info
 Clinical info
1- indications
2- dosage and administration
3- CI
4- DI
5- precautions
 Pharmaceutical info: dosage forms and storage
conditions
GENERAL INFORMATION
 MOA: Cell wall synthesis inhibitor
 Antibacterial spectrum: G+ organisms ( most
important MRSA and drug resistant enterococci)
CLINICAL INFO:
INDICATION
 For serious G+ infections or those who have an
allergy to penicillin
 MRSA and MRSE
 Orally for life threatening Clostridium Difficile
associated colitis
 With aminoglycosides for enterococcal endocarditis
CLINICAL INFO:
DOSAGE AND ADMINISTRATION
 By slow iv infusion over 60-90 min depending on
dose
a. 500mg q.6.h over 1h or 1g bid over 100min
b. at a rate no more than 10mg/min
 Preferred to be intermittent iv inf.
 Dose depends on CLcr , age, and B.wt.
CLINICAL INFO:
DOSAGE AND ADMINISTRATION
 Preparation:
1- Add 10 ml of sterile WFI to a 500 mg vial of
Vancomycin powder >> 50 mg/ml
2- Reconstituted solutions containing 500 mg vancomycin
must be diluted with at least
100 ml diluent. (NaCl soln. or Dextrose soln.)
CLINICAL INFO:
C/I
 History of deafness
 Renal impairment (adjust dose)
CLINICAL INFO:
S/E
 Red man syndrome: flushing and shock if infused
rapidly
 Ototoxicity
 Nephrotoxicity
 Fever ,chills and phlebitis
CLINICAL INFO:
DI
 Aminoglycosides, furosemide
 Anesthetics: hypersensitivity
PRECAUTIONS
 Renal impairment
 Rapid infusion
 Monitor renal function and hearing
 Pregnancy: BM
 Breast feeding: oral absorption is poor but problems
with bowels normal flora and allergic effects have
been reported
PHARMACEUTICAL INFO:
DOSAGE FORM AND STORAGE CONDITIONS
 Vancocin
 Vancoled
500 mg vial
 Store in airtight container and protect from light
TEICOPLANIN
GENERAL INFORMATION
 Glycopeptide antibiotic
 MOA: Cell wall synthesis inhibitor
 Antibacterial spectrum: G+ organisms ( most
important MRSA and drug resistant enterococci)
CLINICAL INFO:
INDICATION
 For serious G+ infections or those who have an allergy
to penicillin
 MRSA and MRSE
 Orally for life threatening Clostridium Difficile associated
colitis
 For endocarditis
 Treating infection of the abdominal cavity (peritonitis)
associated with peritoneal dialysis.
CLINICAL INFO:
DOSAGE AND ADMINISTRATION
 ROA: Intraperitoneally, IM, IV (inf and bolus), po
 Given once daily after the loading dose
 Dose depends on age, CLcr, and wt
CLINICAL INFO:
DOSAGE AND ADMINISTRATION
 Preperation:
1- add water from the ampoule into the vial (3ml)
2- rotate gently between hands to dissolve the
powder be careful not to form foam…. If foam
develops leave the soln to stand for 15min
3- dilute with NaCl soln, Lactate Ringers, or
Dextrose soln or NaCl with dextrose soln.
4- add lidocaine 0.5 or 1% if IM
** the final soln. is stable for about 24hrs at 2-8◦ c
(beware of contamination)
CLINICAL INFO:
C/I
 Hypersensitivity
 Renal impairment (adjust dose)
CLINICAL INFO:
S/E
 Common: pain, fever, rash, itching, redness of skin,
NVD
 Hearing loss and balance disorders
 Liver and kidney function changes
 Rare: change in blood cell count
CLINICAL INFO:
DI
 Aminoglycosides
 furosemide
 Amphotericin B
 Cyclosporine
PRECAUTIONS
 Renal impairment
 Allergy to vancomycin (cross-allergy)
 Monitor renal function, liver function,hearingand
blood
 Superinfection
 Pregnancy, breast feeding: unknown
 Contains 24.8mg Na
PHARMACEUTICAL INFO:
DOSAGE FORM AND STORAGE CONDITIONS
 Targocid (Sanofi Aventis)
200,400 mg vial
 Store under 25◦ c

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Vancomycin

  • 2.  General info  Clinical info 1- indications 2- dosage and administration 3- CI 4- DI 5- precautions  Pharmaceutical info: dosage forms and storage conditions
  • 3. GENERAL INFORMATION  MOA: Cell wall synthesis inhibitor  Antibacterial spectrum: G+ organisms ( most important MRSA and drug resistant enterococci)
  • 4. CLINICAL INFO: INDICATION  For serious G+ infections or those who have an allergy to penicillin  MRSA and MRSE  Orally for life threatening Clostridium Difficile associated colitis  With aminoglycosides for enterococcal endocarditis
  • 5. CLINICAL INFO: DOSAGE AND ADMINISTRATION  By slow iv infusion over 60-90 min depending on dose a. 500mg q.6.h over 1h or 1g bid over 100min b. at a rate no more than 10mg/min  Preferred to be intermittent iv inf.  Dose depends on CLcr , age, and B.wt.
  • 6. CLINICAL INFO: DOSAGE AND ADMINISTRATION  Preparation: 1- Add 10 ml of sterile WFI to a 500 mg vial of Vancomycin powder >> 50 mg/ml 2- Reconstituted solutions containing 500 mg vancomycin must be diluted with at least 100 ml diluent. (NaCl soln. or Dextrose soln.)
  • 7. CLINICAL INFO: C/I  History of deafness  Renal impairment (adjust dose)
  • 8. CLINICAL INFO: S/E  Red man syndrome: flushing and shock if infused rapidly  Ototoxicity  Nephrotoxicity  Fever ,chills and phlebitis
  • 9. CLINICAL INFO: DI  Aminoglycosides, furosemide  Anesthetics: hypersensitivity
  • 10. PRECAUTIONS  Renal impairment  Rapid infusion  Monitor renal function and hearing  Pregnancy: BM  Breast feeding: oral absorption is poor but problems with bowels normal flora and allergic effects have been reported
  • 11. PHARMACEUTICAL INFO: DOSAGE FORM AND STORAGE CONDITIONS  Vancocin  Vancoled 500 mg vial  Store in airtight container and protect from light
  • 13. GENERAL INFORMATION  Glycopeptide antibiotic  MOA: Cell wall synthesis inhibitor  Antibacterial spectrum: G+ organisms ( most important MRSA and drug resistant enterococci)
  • 14. CLINICAL INFO: INDICATION  For serious G+ infections or those who have an allergy to penicillin  MRSA and MRSE  Orally for life threatening Clostridium Difficile associated colitis  For endocarditis  Treating infection of the abdominal cavity (peritonitis) associated with peritoneal dialysis.
  • 15. CLINICAL INFO: DOSAGE AND ADMINISTRATION  ROA: Intraperitoneally, IM, IV (inf and bolus), po  Given once daily after the loading dose  Dose depends on age, CLcr, and wt
  • 16. CLINICAL INFO: DOSAGE AND ADMINISTRATION  Preperation: 1- add water from the ampoule into the vial (3ml) 2- rotate gently between hands to dissolve the powder be careful not to form foam…. If foam develops leave the soln to stand for 15min 3- dilute with NaCl soln, Lactate Ringers, or Dextrose soln or NaCl with dextrose soln. 4- add lidocaine 0.5 or 1% if IM ** the final soln. is stable for about 24hrs at 2-8◦ c (beware of contamination)
  • 17. CLINICAL INFO: C/I  Hypersensitivity  Renal impairment (adjust dose)
  • 18. CLINICAL INFO: S/E  Common: pain, fever, rash, itching, redness of skin, NVD  Hearing loss and balance disorders  Liver and kidney function changes  Rare: change in blood cell count
  • 19. CLINICAL INFO: DI  Aminoglycosides  furosemide  Amphotericin B  Cyclosporine
  • 20. PRECAUTIONS  Renal impairment  Allergy to vancomycin (cross-allergy)  Monitor renal function, liver function,hearingand blood  Superinfection  Pregnancy, breast feeding: unknown  Contains 24.8mg Na
  • 21. PHARMACEUTICAL INFO: DOSAGE FORM AND STORAGE CONDITIONS  Targocid (Sanofi Aventis) 200,400 mg vial  Store under 25◦ c