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oxacillin (Bactocill)

 

Classes: Penicillins, Penicillinase-Resistant

Dosing and uses of Bactocill (oxacillin)

 

Adult dosage forms and strengths

infusion solution

  • 1g/50mL
  • 2g/50mL

powder for injection

  • 1g
  • 2g
  • 10g

 

Staphylococcal Infections

Mild to moderate infections: 250-500 mg IV/IM q4-6hr

Severe infections: 1 g IV/IM q4-6hr

Acute/chronic osteomyelitis/staphylococci infections: 1.5-2 g IV q4-6hr

 

Renal Infection

CrCl < 10 mL/min: May consider adjusting to the lower range of the usually recommended dose depending on severity of infection

 

Pediatric dosage forms and strengths

infusion solution

  • 1g/50mL
  • 2g/50mL

powder for injection

  • 1g
  • 2g
  • 10g

 

Susceptible Staph Infections in Infants & Children

Mild to moderate infections: 100-200 mg/kg/day IV/IM divided q6hr

Severe infections: 150-200 mg/kg/day IV/IM divided q6hr

Maximum 4g/day for mild to moderate infections

Maximum 12g/day for severe infections

 

Susceptible Staph Infections in Neonates

(<7 days old, <2 kg) OR (>7 days old, <1.2 kg): 50 mg/kg/day divided q12hr IV/Im

(<7 days old, >2 kg) OR (>7 days old, 1.2-2 kg): 75 mg/kg/day divided q8hr IV/Im

>7 days old, >2 kg: 100 mg/kg/day divided q6hr IV/Im

 

Bactocill (oxacillin) adverse (side) effects

1-10%

Diarrhea

Nausea

Fever

Rash

 

<1%

Eosinophilia

Leukopenia

Neutropenia

Thrombocytopenia

Hepatotoxicity

Elevated ASt

Acute interstitial nephritis

Serum sickness-like reaction

 

Warnings

Contraindications

Allergy to penicillins, cephalosporins, imipenem

Solutions containing dextrose may be contraindicated in patients with known allergy to corn or corn products

 

Cautions

Evaluate renal, hepatic, hematologic systems periodically during prolonged treatment

Monitor neonates for renal impairment

Monitor organ systems/serum concentrations of drug in neonates

Prolonged treatment may result in bacterial or fungal superinfection

Clostridium difficile associated diarrhea (CDAD) must be considered in all patients who present with diarrhea following antibiotic; CDAD has been reported to occur over two months after the administration of antibacterial agents; careful medical history is necessary; if CDAD suspected or confirmed, ongoing antibiotic use not directed against C. difficile may need to be discontinued; appropriate fluid and electrolyte management, protein supplementation, antibiotic treatment of C. difficile, and surgical evaluation should be instituted as indicated

 

Pregnancy and lactation

Pregnancy category: B

Lactation: excreted in breast milk; use caution

 

Pregnancy categories

A: Generally acceptable. Controlled studies in pregnant women show no evidence of fetal risk.

B: May be acceptable. Either animal studies show no risk but human studies not available or animal studies showed minor risks and human studies done and showed no risk.

C: Use with caution if benefits outweigh risks. Animal studies show risk and human studies not available or neither animal nor human studies done.

D: Use in LIFE-THREATENING emergencies when no safer drug available. Positive evidence of human fetal risk.

X: Do not use in pregnancy. Risks involved outweigh potential benefits. Safer alternatives exist.

NA: Information not available.

 

Pharmacology of Bactocill (oxacillin)

Mechanism of action

Bactericidal antibiotic that inhibits cell wall synthesis by binding to one or more of the penicillin binding proteins. Used in the treatment of infections caused by penicillinase-producing staphylococci. May be used to initiate therapy when a staphylococcal infection is suspected.

 

Pharmacokinetics

Half-Life: 23-60 min (adults; prolonged in renal insufficiency); 0.9-1.8 hr (children)

Peak Plasma Time: 30-60 min

Protein binding: 94%

Distribution: Bile, synovial, pleural, peritoneal, pericardial fluids

Metabolism: Hepatic to active metabolites

Excretion: Urine and feces

 

Administration

IV Incompatibilities

Additive: amikacin(?), cytarabine

Syringe: caffeine

Y-site: Na bicarb, verapamiL

Aminoglycosides & tetracyclines, but compatibility depends on several factors (eg, concentrations of the drugs, specific diluents used, resulting pH, temperature)

 

IV Compatibilities

Solution: compatible w/ most common solvents

Additive: Chloramphenicol Na succinate, dopamine, KCl, verapamiL

Y-site (partial list): Acyclovir, diltiazem, fluconazole, heparin, hydromorphone, MgSO4, meperidine, morphine, KCl, vit B/C, zidovudine

 

IV/IM Preparation

IM Injection

  • For IM injection, reconstitute by adding 5.7 or 11.4 mL of SWI to a vial containing 1 or 2 g of oxacillin, respectively, to provide solutions containing 167 mg of oxacillin per mL (250 mg/1.5 mL)
  • Shake vials well

IV Injection

  • For direct injection, prepare a solution containing approximately 100 mg/mL by adding 10 or 20 mL SWI, ½NS or NS to vials containing 1 or 2 g of oxacillin, respectively

Intermittent or Continuous IV Infusion

  • For intermittent IV infusion, reconstitute vials containing 1 or 2 g as for direct IV injection & further dilute with a compatible IV solution to a concentration of 0.5-40 mg/mL
  • Alternatively, reconstitute ADD-Vantage vials containing 1 or 2 g according to the mfr's directions

 

IV/IM Administration

Administer by IM injection or slow IV injection or infusion

IM: deep into a large muscle (eg, gluteus maximus) & care should be taken to avoid sciatic nerve injury

IV Injection: slowly over about 10 min

Intermittent or Continuous IV Infusion: injections should not be used in series connections with other plastic containers: could result in air embolism from residual air being drawn from primary container before administration of fluid from secondary container is complete

 

Storage

Oxacillin powder: store at controlled room temp

Oxacillin in dextrose injection: store <-20°C