Doripenem: Difference between revisions
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==Adult Dosing== | ==Adult Dosing== | ||
===Intra-abdominal [[infection]], complicated=== | |||
*500mg IV q8h x5-14 days | |||
===[[UTI]], complicated=== | |||
*500mg IV q8h x10 days | |||
===[[Anthrax]], systemic=== | |||
*500mg IV q8h for at least 2 wk as part of multi-drug regimen | |||
==Pediatric Dosing== | ==Pediatric Dosing== | ||
===[[Anthrax]], systemic=== | |||
*Neonates >32 weeks gestation | |||
**20-30 mg/kg/day IV divided q8-12h for two weeks as part of multi-drug regimen | |||
*1+ month old | |||
**120 mg/kg/day IV divided q8h for at least two weeks as part of multi-drug regimen | |||
***Max: 1 g/dose | |||
==Special Populations== | ==Special Populations== | ||
*[[Drug Ratings in Pregnancy|Pregnancy Rating]]: | *[[Drug Ratings in Pregnancy|Pregnancy Rating]]: B | ||
*Lactation: | *Lactation: May use while breastfeeding | ||
*Renal Dosing | *Renal Dosing | ||
**Adult | **Adult | ||
***CrCl 30-50: 250mg IV q8h | |||
***CrCl 10-30: 250mg IV q12h | |||
***CrCl <10: Not defined | |||
***HD: Not defined | |||
**Pediatric | **Pediatric | ||
***May be required, but specifics not defined | |||
*Hepatic Dosing | *Hepatic Dosing | ||
**Adult | **Adult | ||
***No adjustment | |||
**Pediatric | **Pediatric | ||
***May be required, but specifics not defined | |||
==Contraindications== | ==Contraindications== | ||
*Allergy to class/drug | *Allergy to class/drug | ||
*Anaphylactic reaction to [[beta-lactams]] | |||
*Inhalational use | |||
*Ventilator-associated [[pneumonia]] | |||
*Caution: | |||
**Hypersensitivity to [[beta-lactams]] | |||
**Hypersensitivity to multiple allergens | |||
**Renal impairment | |||
**CNS disorder | |||
**[[Seizure]] history or risk | |||
**Recent abx-associated colitis | |||
==Adverse Reactions== | ==Adverse Reactions== | ||
===Serious=== | ===Serious=== | ||
*Hypersensitivity Reaction | |||
*[[Anaphylaxis]] | |||
*[[Stevens-Johnson Syndrome]], Toxic epidermal necrolysis | |||
*[[Seizures]] | |||
*C. diff associated [[diarrhea]] | |||
*[[Pneumonia]], interstitial | |||
===Common=== | ===Common=== | ||
*[[Headache]] | |||
*[[Nausea]], [[Diarrhea]] | |||
*[[Anemia]] | |||
*[[Phlebitis]], [[rash]], [[pruritus]] | |||
*ALT, AST Elevation | |||
*[[Candidiasis]], vuvlovaginal | |||
==Pharmacology== | ==Pharmacology== | ||
*Half-life: | *Half-life: 1h | ||
*Metabolism: | *Metabolism: Kidney minimally | ||
*Excretion: | *Excretion: Urine 85% (70% unchanged), feces <1% | ||
*Mechanism of Action: | *Mechanism of Action: Inhibits cell wall synthesis | ||
==[[Antibiotic Sensitivities]]<ref>Sanford Guide to Antimicrobial Therapy 2014</ref>== | ==[[Antibiotic Sensitivities]]<ref>Sanford Guide to Antimicrobial Therapy 2014</ref>== | ||
Revision as of 17:14, 20 September 2017
General
- Type: Carbapenem (broad-spectrum beta-lactamase)
- Dosage Forms: IV
- Common Trade Names: Doribax
Adult Dosing
Intra-abdominal infection, complicated
- 500mg IV q8h x5-14 days
UTI, complicated
- 500mg IV q8h x10 days
Anthrax, systemic
- 500mg IV q8h for at least 2 wk as part of multi-drug regimen
Pediatric Dosing
Anthrax, systemic
- Neonates >32 weeks gestation
- 20-30 mg/kg/day IV divided q8-12h for two weeks as part of multi-drug regimen
- 1+ month old
- 120 mg/kg/day IV divided q8h for at least two weeks as part of multi-drug regimen
- Max: 1 g/dose
- 120 mg/kg/day IV divided q8h for at least two weeks as part of multi-drug regimen
Special Populations
- Pregnancy Rating: B
- Lactation: May use while breastfeeding
- Renal Dosing
- Adult
- CrCl 30-50: 250mg IV q8h
- CrCl 10-30: 250mg IV q12h
- CrCl <10: Not defined
- HD: Not defined
- Pediatric
- May be required, but specifics not defined
- Adult
- Hepatic Dosing
- Adult
- No adjustment
- Pediatric
- May be required, but specifics not defined
- Adult
Contraindications
- Allergy to class/drug
- Anaphylactic reaction to beta-lactams
- Inhalational use
- Ventilator-associated pneumonia
- Caution:
- Hypersensitivity to beta-lactams
- Hypersensitivity to multiple allergens
- Renal impairment
- CNS disorder
- Seizure history or risk
- Recent abx-associated colitis
Adverse Reactions
Serious
- Hypersensitivity Reaction
- Anaphylaxis
- Stevens-Johnson Syndrome, Toxic epidermal necrolysis
- Seizures
- C. diff associated diarrhea
- Pneumonia, interstitial
Common
- Headache
- Nausea, Diarrhea
- Anemia
- Phlebitis, rash, pruritus
- ALT, AST Elevation
- Candidiasis, vuvlovaginal
Pharmacology
- Half-life: 1h
- Metabolism: Kidney minimally
- Excretion: Urine 85% (70% unchanged), feces <1%
- Mechanism of Action: Inhibits cell wall synthesis
Antibiotic Sensitivities[1]
Key
- S susceptible/sensitive (usually)
- I intermediate (variably susceptible/resistant)
- R resistant (or not effective clinically)
- S+ synergistic with cell wall antibiotics
- U sensitive for UTI only (non systemic infection)
- X1 no data
- X2 active in vitro, but not used clinically
- X3 active in vitro, but not clinically effective for Group A strep pharyngitis or infections due to E. faecalis
- X4 active in vitro, but not clinically effective for strep pneumonia
See Also
References
- ↑ Sanford Guide to Antimicrobial Therapy 2014
