Details
Stereochemistry | ABSOLUTE |
Molecular Formula | C15H24N4O6S2 |
Molecular Weight | 420.504 |
Optical Activity | UNSPECIFIED |
Defined Stereocenters | 6 / 6 |
E/Z Centers | 0 |
Charge | 0 |
SHOW SMILES / InChI
SMILES
[H][C@]12[C@@H](C)C(S[C@@H]3CN[C@H](CNS(N)(=O)=O)C3)=C(N1C(=O)[C@]2([H])[C@@H](C)O)C(O)=O
InChI
InChIKey=AVAACINZEOAHHE-VFZPANTDSA-N
InChI=1S/C15H24N4O6S2/c1-6-11-10(7(2)20)14(21)19(11)12(15(22)23)13(6)26-9-3-8(17-5-9)4-18-27(16,24)25/h6-11,17-18,20H,3-5H2,1-2H3,(H,22,23)(H2,16,24,25)/t6-,7-,8+,9+,10-,11-/m1/s1
Molecular Formula | C15H24N4O6S2 |
Molecular Weight | 420.504 |
Charge | 0 |
Count |
|
Stereochemistry | ABSOLUTE |
Additional Stereochemistry | No |
Defined Stereocenters | 6 / 6 |
E/Z Centers | 0 |
Optical Activity | UNSPECIFIED |
DescriptionSources: www.fda.gov/ohrms/dockets/ac/08/briefing/2008-4364b1-02-johnson.pdfCurator's Comment: Description was created based on several sources including http://www.ncbi.nlm.nih.gov/pmc/articles/PMC2446428/#B1
Sources: www.fda.gov/ohrms/dockets/ac/08/briefing/2008-4364b1-02-johnson.pdf
Curator's Comment: Description was created based on several sources including http://www.ncbi.nlm.nih.gov/pmc/articles/PMC2446428/#B1
Doripenem is a synthetic carbapenem that has broad antibacterial potency against aerobic and anaerobic gram-positive and gram-negative bacteria. Doripenem is structurally related to beta-lactam antibiotics and shares the bactericidal mode of action of other β-lactam antibiotics by targeting penicillin-binding proteins (PBPs) to inhibit the biosynthesis of the bacterial cell wall. Doripenem is resistant to hydrolysis by most β-lactamases and is resistant to inactivation by renal dehydropeptidases. Doripenem has many similarities to the other carbapenems, as well as some important differences, such as greater potency against Pseudomonas aeruginosa. It was found to be similar to comparator agents. The most common adverse effects related to doripenem therapy were headache, nausea, diarrhea, rash, and phlebitis.
CNS Activity
Sources: http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3122383/
Curator's Comment: Doripenem penetrates the intact blood-brain barrier to a small but measurable extent.
Originator
Curator's Comment: Shionogi (Japan) is the drug's originator and markets doripenem under the brand name Finibax. Peninsula Pharmaceuticals acquired development and marketing rights to doripenem in the US in a licensing agreement signed with Shionogi in 2003. Doripenem is part of Johnson &' Johnson's anti-infective R&D portfolio following the acquisition of Peninsula Pharmaceuticals in 2005.
Approval Year
Targets
Primary Target | Pharmacology | Condition | Potency |
---|---|---|---|
Target ID: CHEMBL2354204 |
47.6 µM [IC50] |
Conditions
Condition | Modality | Targets | Highest Phase | Product |
---|---|---|---|---|
Curative | DORIBAX Approved UseIndicated as a single agent for the treatment of complicated intra-abdominal infections caused by Escherichia coli, Klebsiella pneumoniae, Pseudomonas aeruginosa, Bacteroides caccae, Bacteroides fragilis, Bacteroides thetaiotaomicron, Bacteroides uniformis, Bacteroides vulgatus, Streptococcus intermedius, Streptococcus constellatus and Peptostreptococcus micros and as a single agent for the treatment of complicated urinary tract infections, including pyelonephritis caused by Escherichia coli
including cases with concurrent bacteremia, Klebsiella pneumoniae, Proteus mirabilis, Pseudomonas aeruginosa, and Acinetobacter baumannii. To reduce the development of drug-resistant bacteria and maintain the effectiveness of DORIBAX® and other antibacterial drugs, DORIBAX® should be used only to treat infections that are proven or strongly suspected to be caused by susceptible bacteria. Launch Date2007 |
|||
Curative | DORIBAX Approved UseIndicated as a single agent for the treatment of complicated intra-abdominal infections caused by Escherichia coli, Klebsiella pneumoniae, Pseudomonas aeruginosa, Bacteroides caccae, Bacteroides fragilis, Bacteroides thetaiotaomicron, Bacteroides uniformis, Bacteroides vulgatus, Streptococcus intermedius, Streptococcus constellatus and Peptostreptococcus micros and as a single agent for the treatment of complicated urinary tract infections, including pyelonephritis caused by Escherichia coli
including cases with concurrent bacteremia, Klebsiella pneumoniae, Proteus mirabilis, Pseudomonas aeruginosa, and Acinetobacter baumannii. To reduce the development of drug-resistant bacteria and maintain the effectiveness of DORIBAX® and other antibacterial drugs, DORIBAX® should be used only to treat infections that are proven or strongly suspected to be caused by susceptible bacteria. Launch Date2007 |
|||
Curative | DORIBAX Approved UseIndicated as a single agent for the treatment of complicated intra-abdominal infections caused by Escherichia coli, Klebsiella pneumoniae, Pseudomonas aeruginosa, Bacteroides caccae, Bacteroides fragilis, Bacteroides thetaiotaomicron, Bacteroides uniformis, Bacteroides vulgatus, Streptococcus intermedius, Streptococcus constellatus and Peptostreptococcus micros and as a single agent for the treatment of complicated urinary tract infections, including pyelonephritis caused by Escherichia coli
including cases with concurrent bacteremia, Klebsiella pneumoniae, Proteus mirabilis, Pseudomonas aeruginosa, and Acinetobacter baumannii. To reduce the development of drug-resistant bacteria and maintain the effectiveness of DORIBAX® and other antibacterial drugs, DORIBAX® should be used only to treat infections that are proven or strongly suspected to be caused by susceptible bacteria. Launch Date2007 |
Cmax
Value | Dose | Co-administered | Analyte | Population |
---|---|---|---|---|
16.87 μg/mL EXPERIMENT https://pubmed.ncbi.nlm.nih.gov/28920154/ |
500 mg single, intravenous dose: 500 mg route of administration: Intravenous experiment type: SINGLE co-administered: |
DORIPENEM plasma | Homo sapiens population: UNHEALTHY age: ADULT sex: FEMALE / MALE food status: UNKNOWN |
|
12.94 μg/mL EXPERIMENT https://pubmed.ncbi.nlm.nih.gov/28920154/ |
500 mg single, intravenous dose: 500 mg route of administration: Intravenous experiment type: SINGLE co-administered: |
DORIPENEM plasma | Homo sapiens population: UNHEALTHY age: ADULT sex: FEMALE / MALE food status: UNKNOWN |
|
10.2 mg/L EXPERIMENT https://pubmed.ncbi.nlm.nih.gov/29746394/ |
250 mg single, intravenous dose: 250 mg route of administration: Intravenous experiment type: SINGLE co-administered: |
DORIPENEM plasma | Homo sapiens population: HEALTHY age: ADULT sex: FEMALE / MALE food status: UNKNOWN |
|
23 μg/mL |
500 mg single, intravenous dose: 500 mg route of administration: Intravenous experiment type: SINGLE co-administered: |
DORIPENEM plasma | Homo sapiens population: HEALTHY age: ADULT sex: UNKNOWN food status: UNKNOWN |
AUC
Value | Dose | Co-administered | Analyte | Population |
---|---|---|---|---|
52.98 μg × h/mL EXPERIMENT https://pubmed.ncbi.nlm.nih.gov/28920154/ |
500 mg single, intravenous dose: 500 mg route of administration: Intravenous experiment type: SINGLE co-administered: |
DORIPENEM plasma | Homo sapiens population: UNHEALTHY age: ADULT sex: FEMALE / MALE food status: UNKNOWN |
|
70.64 μg × h/mL EXPERIMENT https://pubmed.ncbi.nlm.nih.gov/28920154/ |
500 mg single, intravenous dose: 500 mg route of administration: Intravenous experiment type: SINGLE co-administered: |
DORIPENEM plasma | Homo sapiens population: UNHEALTHY age: ADULT sex: FEMALE / MALE food status: UNKNOWN |
|
13.8 mg × h/L EXPERIMENT https://pubmed.ncbi.nlm.nih.gov/29746394/ |
250 mg single, intravenous dose: 250 mg route of administration: Intravenous experiment type: SINGLE co-administered: |
DORIPENEM plasma | Homo sapiens population: HEALTHY age: ADULT sex: FEMALE / MALE food status: UNKNOWN |
|
36.3 μg × h/mL |
500 mg single, intravenous dose: 500 mg route of administration: Intravenous experiment type: SINGLE co-administered: |
DORIPENEM plasma | Homo sapiens population: HEALTHY age: ADULT sex: UNKNOWN food status: UNKNOWN |
|
47.1 mg*h/L Clinical Trial https://clinicaltrials.gov/ct2/show/NCT01401010 |
500 mg 1 times / 8 hour multiple, intravenous dose: 500 mg route of administration: intravenous experiment type: multiple co-administered: |
DORIPENEM serum | Homo sapiens population: unhealthy age: sex: food status: |
|
66.4 mg*h/L Clinical Trial https://clinicaltrials.gov/ct2/show/NCT01401010 |
1000 mg 1 times / 8 hour multiple, intravenous dose: 1000 mg route of administration: intravenous experiment type: multiple co-administered: |
DORIPENEM serum | Homo sapiens population: unhealthy age: sex: food status: |
T1/2
Value | Dose | Co-administered | Analyte | Population |
---|---|---|---|---|
2.93 h EXPERIMENT https://pubmed.ncbi.nlm.nih.gov/28920154/ |
500 mg single, intravenous dose: 500 mg route of administration: Intravenous experiment type: SINGLE co-administered: |
DORIPENEM plasma | Homo sapiens population: UNHEALTHY age: ADULT sex: FEMALE / MALE food status: UNKNOWN |
|
4.04 h EXPERIMENT https://pubmed.ncbi.nlm.nih.gov/28920154/ |
500 mg single, intravenous dose: 500 mg route of administration: Intravenous experiment type: SINGLE co-administered: |
DORIPENEM plasma | Homo sapiens population: UNHEALTHY age: ADULT sex: FEMALE / MALE food status: UNKNOWN |
|
0.91 h EXPERIMENT https://pubmed.ncbi.nlm.nih.gov/29746394/ |
250 mg single, intravenous dose: 250 mg route of administration: Intravenous experiment type: SINGLE co-administered: |
DORIPENEM plasma | Homo sapiens population: HEALTHY age: ADULT sex: FEMALE / MALE food status: UNKNOWN |
|
1 h |
500 mg single, intravenous dose: 500 mg route of administration: Intravenous experiment type: SINGLE co-administered: |
DORIPENEM plasma | Homo sapiens population: HEALTHY age: ADULT sex: UNKNOWN food status: UNKNOWN |
|
2.2 h Clinical Trial https://clinicaltrials.gov/ct2/show/NCT01401010 |
500 mg 1 times / 8 hour multiple, intravenous dose: 500 mg route of administration: intravenous experiment type: multiple co-administered: |
DORIPENEM serum | Homo sapiens population: unhealthy age: sex: food status: |
|
2.4 h Clinical Trial https://clinicaltrials.gov/ct2/show/NCT01401010 |
1000 mg 1 times / 8 hour multiple, intravenous dose: 1000 mg route of administration: intravenous experiment type: multiple co-administered: |
DORIPENEM serum | Homo sapiens population: unhealthy age: sex: food status: |
Funbound
Value | Dose | Co-administered | Analyte | Population |
---|---|---|---|---|
91.9% |
500 mg single, intravenous dose: 500 mg route of administration: Intravenous experiment type: SINGLE co-administered: |
DORIPENEM plasma | Homo sapiens population: HEALTHY age: ADULT sex: UNKNOWN food status: UNKNOWN |
Doses
Dose | Population | Adverse events |
---|---|---|
2 g 3 times / day multiple, intravenous Highest studied dose Dose: 2 g, 3 times / day Route: intravenous Route: multiple Dose: 2 g, 3 times / day Sources: |
unhealthy, 24 years (rangeL 21–37 years) n = 16 Health Status: unhealthy Condition: cystic fibrosis Age Group: 24 years (rangeL 21–37 years) Sex: M+F Population Size: 16 Sources: |
Disc. AE: Transaminases increased, Allergic reaction... Other AEs: Leukopenia, Diarrhea... AEs leading to discontinuation/dose reduction: Transaminases increased (1 patient) Other AEs:Allergic reaction (1 patient) Leukopenia (1 patient) Sources: Diarrhea (11 patient) Nausea (9 patients) Vomiting (9 patients) Headache (6 patients) Oral candidiasis (3 patients) Rash (2 patients) |
500 mg 3 times / day steady, intravenous Recommended Dose: 500 mg, 3 times / day Route: intravenous Route: steady Dose: 500 mg, 3 times / day Sources: |
unhealthy, 54 years (range: 18-90 years) n = 853 Health Status: unhealthy Condition: intra-abdominal infections Age Group: 54 years (range: 18-90 years) Sex: M+F Population Size: 853 Sources: |
Disc. AE: Nausea, Vulval mycotic infection... AEs leading to discontinuation/dose reduction: Nausea (0.2%) Sources: Vulval mycotic infection (0.1%) Rash (0.1%) |
5 mg/kg single, intravenous Dose: 5 mg/kg Route: intravenous Route: single Dose: 5 mg/kg Sources: |
unknown, <8 weeks n = 26 Health Status: unknown Age Group: <8 weeks Sex: M+F Population Size: 26 Sources: |
Other AEs: Anemia neonatal, Hypoalbuminemia... Other AEs: Anemia neonatal (3 patients) Sources: Hypoalbuminemia (3 patients) Hyperglycemia (2 patients) Peripheral edema (1 patient) Patent ductus arteriosus (2 patients) |
8 mg/kg single, intravenous Dose: 8 mg/kg Route: intravenous Route: single Dose: 8 mg/kg Sources: |
unknown, >8 weeks <44 weeks n = 26 Health Status: unknown Age Group: >8 weeks <44 weeks Sex: M+F Population Size: 26 Sources: |
Other AEs: Anemia neonatal, Peripheral edema... Other AEs: Anemia neonatal (1 patient) Sources: Peripheral edema (1 patient) Dermatitis diaper (2 patients) |
AEs
AE | Significance | Dose | Population |
---|---|---|---|
Leukopenia | 1 patient | 2 g 3 times / day multiple, intravenous Highest studied dose Dose: 2 g, 3 times / day Route: intravenous Route: multiple Dose: 2 g, 3 times / day Sources: |
unhealthy, 24 years (rangeL 21–37 years) n = 16 Health Status: unhealthy Condition: cystic fibrosis Age Group: 24 years (rangeL 21–37 years) Sex: M+F Population Size: 16 Sources: |
Allergic reaction | 1 patient Disc. AE |
2 g 3 times / day multiple, intravenous Highest studied dose Dose: 2 g, 3 times / day Route: intravenous Route: multiple Dose: 2 g, 3 times / day Sources: |
unhealthy, 24 years (rangeL 21–37 years) n = 16 Health Status: unhealthy Condition: cystic fibrosis Age Group: 24 years (rangeL 21–37 years) Sex: M+F Population Size: 16 Sources: |
Transaminases increased | 1 patient Disc. AE |
2 g 3 times / day multiple, intravenous Highest studied dose Dose: 2 g, 3 times / day Route: intravenous Route: multiple Dose: 2 g, 3 times / day Sources: |
unhealthy, 24 years (rangeL 21–37 years) n = 16 Health Status: unhealthy Condition: cystic fibrosis Age Group: 24 years (rangeL 21–37 years) Sex: M+F Population Size: 16 Sources: |
Diarrhea | 11 patient | 2 g 3 times / day multiple, intravenous Highest studied dose Dose: 2 g, 3 times / day Route: intravenous Route: multiple Dose: 2 g, 3 times / day Sources: |
unhealthy, 24 years (rangeL 21–37 years) n = 16 Health Status: unhealthy Condition: cystic fibrosis Age Group: 24 years (rangeL 21–37 years) Sex: M+F Population Size: 16 Sources: |
Rash | 2 patients | 2 g 3 times / day multiple, intravenous Highest studied dose Dose: 2 g, 3 times / day Route: intravenous Route: multiple Dose: 2 g, 3 times / day Sources: |
unhealthy, 24 years (rangeL 21–37 years) n = 16 Health Status: unhealthy Condition: cystic fibrosis Age Group: 24 years (rangeL 21–37 years) Sex: M+F Population Size: 16 Sources: |
Oral candidiasis | 3 patients | 2 g 3 times / day multiple, intravenous Highest studied dose Dose: 2 g, 3 times / day Route: intravenous Route: multiple Dose: 2 g, 3 times / day Sources: |
unhealthy, 24 years (rangeL 21–37 years) n = 16 Health Status: unhealthy Condition: cystic fibrosis Age Group: 24 years (rangeL 21–37 years) Sex: M+F Population Size: 16 Sources: |
Headache | 6 patients | 2 g 3 times / day multiple, intravenous Highest studied dose Dose: 2 g, 3 times / day Route: intravenous Route: multiple Dose: 2 g, 3 times / day Sources: |
unhealthy, 24 years (rangeL 21–37 years) n = 16 Health Status: unhealthy Condition: cystic fibrosis Age Group: 24 years (rangeL 21–37 years) Sex: M+F Population Size: 16 Sources: |
Nausea | 9 patients | 2 g 3 times / day multiple, intravenous Highest studied dose Dose: 2 g, 3 times / day Route: intravenous Route: multiple Dose: 2 g, 3 times / day Sources: |
unhealthy, 24 years (rangeL 21–37 years) n = 16 Health Status: unhealthy Condition: cystic fibrosis Age Group: 24 years (rangeL 21–37 years) Sex: M+F Population Size: 16 Sources: |
Vomiting | 9 patients | 2 g 3 times / day multiple, intravenous Highest studied dose Dose: 2 g, 3 times / day Route: intravenous Route: multiple Dose: 2 g, 3 times / day Sources: |
unhealthy, 24 years (rangeL 21–37 years) n = 16 Health Status: unhealthy Condition: cystic fibrosis Age Group: 24 years (rangeL 21–37 years) Sex: M+F Population Size: 16 Sources: |
Rash | 0.1% Disc. AE |
500 mg 3 times / day steady, intravenous Recommended Dose: 500 mg, 3 times / day Route: intravenous Route: steady Dose: 500 mg, 3 times / day Sources: |
unhealthy, 54 years (range: 18-90 years) n = 853 Health Status: unhealthy Condition: intra-abdominal infections Age Group: 54 years (range: 18-90 years) Sex: M+F Population Size: 853 Sources: |
Vulval mycotic infection | 0.1% Disc. AE |
500 mg 3 times / day steady, intravenous Recommended Dose: 500 mg, 3 times / day Route: intravenous Route: steady Dose: 500 mg, 3 times / day Sources: |
unhealthy, 54 years (range: 18-90 years) n = 853 Health Status: unhealthy Condition: intra-abdominal infections Age Group: 54 years (range: 18-90 years) Sex: M+F Population Size: 853 Sources: |
Nausea | 0.2% Disc. AE |
500 mg 3 times / day steady, intravenous Recommended Dose: 500 mg, 3 times / day Route: intravenous Route: steady Dose: 500 mg, 3 times / day Sources: |
unhealthy, 54 years (range: 18-90 years) n = 853 Health Status: unhealthy Condition: intra-abdominal infections Age Group: 54 years (range: 18-90 years) Sex: M+F Population Size: 853 Sources: |
Peripheral edema | 1 patient | 5 mg/kg single, intravenous Dose: 5 mg/kg Route: intravenous Route: single Dose: 5 mg/kg Sources: |
unknown, <8 weeks n = 26 Health Status: unknown Age Group: <8 weeks Sex: M+F Population Size: 26 Sources: |
Hyperglycemia | 2 patients | 5 mg/kg single, intravenous Dose: 5 mg/kg Route: intravenous Route: single Dose: 5 mg/kg Sources: |
unknown, <8 weeks n = 26 Health Status: unknown Age Group: <8 weeks Sex: M+F Population Size: 26 Sources: |
Patent ductus arteriosus | 2 patients | 5 mg/kg single, intravenous Dose: 5 mg/kg Route: intravenous Route: single Dose: 5 mg/kg Sources: |
unknown, <8 weeks n = 26 Health Status: unknown Age Group: <8 weeks Sex: M+F Population Size: 26 Sources: |
Anemia neonatal | 3 patients | 5 mg/kg single, intravenous Dose: 5 mg/kg Route: intravenous Route: single Dose: 5 mg/kg Sources: |
unknown, <8 weeks n = 26 Health Status: unknown Age Group: <8 weeks Sex: M+F Population Size: 26 Sources: |
Hypoalbuminemia | 3 patients | 5 mg/kg single, intravenous Dose: 5 mg/kg Route: intravenous Route: single Dose: 5 mg/kg Sources: |
unknown, <8 weeks n = 26 Health Status: unknown Age Group: <8 weeks Sex: M+F Population Size: 26 Sources: |
Anemia neonatal | 1 patient | 8 mg/kg single, intravenous Dose: 8 mg/kg Route: intravenous Route: single Dose: 8 mg/kg Sources: |
unknown, >8 weeks <44 weeks n = 26 Health Status: unknown Age Group: >8 weeks <44 weeks Sex: M+F Population Size: 26 Sources: |
Peripheral edema | 1 patient | 8 mg/kg single, intravenous Dose: 8 mg/kg Route: intravenous Route: single Dose: 8 mg/kg Sources: |
unknown, >8 weeks <44 weeks n = 26 Health Status: unknown Age Group: >8 weeks <44 weeks Sex: M+F Population Size: 26 Sources: |
Dermatitis diaper | 2 patients | 8 mg/kg single, intravenous Dose: 8 mg/kg Route: intravenous Route: single Dose: 8 mg/kg Sources: |
unknown, >8 weeks <44 weeks n = 26 Health Status: unknown Age Group: >8 weeks <44 weeks Sex: M+F Population Size: 26 Sources: |
Overview
CYP3A4 | CYP2C9 | CYP2D6 | hERG |
---|---|---|---|
OverviewOther
Other Inhibitor | Other Substrate | Other Inducer |
---|---|---|
Drug as perpetrator
Target | Modality | Activity | Metabolite | Clinical evidence |
---|---|---|---|---|
Page: 15.0 |
no | |||
Page: 15.0 |
no | |||
Page: 15.0 |
no | |||
Page: 15.0 |
no | |||
Page: 15.0 |
no | |||
Page: 15.0 |
no | |||
Page: 15.0 |
no | |||
Page: 15.0 |
no | |||
Page: 15.0 |
no | |||
Page: 15.0 |
no | |||
Page: 15.0 |
unlikely | |||
Page: 15.0 |
unlikely | |||
Page: 15.0 |
unlikely | |||
Page: 15.0 |
unlikely | |||
Page: 15.0 |
unlikely | |||
Page: 15.0 |
unlikely |
Drug as victim
Target | Modality | Activity | Metabolite | Clinical evidence |
---|---|---|---|---|
Page: 13.0 |
no | |||
Sources: https://doi.org/10.1016/j.ijantimicag.2011.11.019 Page: 2.0 |
no |
Tox targets
Target | Modality | Activity | Metabolite | Clinical evidence |
---|---|---|---|---|
Page: 10.0 |
PubMed
Title | Date | PubMed |
---|---|---|
Antibacterial Drug Discovery and Development Summit - Tenth Annual SRI Summit. | 2005 May |
|
Occurrence of PER-1 producing clinical isolates of Pseudomonas aeruginosa in Japan and their susceptibility to doripenem. | 2006 Dec |
|
Pharmacokinetics and tissue penetration of a new carbapenem, doripenem, intravenously administered to laboratory animals. | 2006 Jan-Feb |
|
Comparative review of the carbapenems. | 2007 |
|
Peritoneal penetration of doripenem after intravenous administration in abdominal-surgery patients. | 2007 Dec |
|
Development of an HPLC method for the determination of doripenem in human and mouse serum. | 2007 Jun 15 |
|
Carbapenems in the USA: focus on doripenem. | 2007 Oct |
|
Pharmacodynamic optimization of beta-lactams in the patient care setting. | 2008 |
|
Efficacy and safety of intravenous infusion of doripenem versus imipenem in ventilator-associated pneumonia: a multicenter, randomized study. | 2008 Apr |
|
Pharmacokinetic-pharmacodynamic modeling and simulation for in vivo bactericidal effect in murine infection model. | 2008 Apr |
|
Effects of treatment with antimicrobial agents on the human colonic microflora. | 2008 Dec |
|
New developments in carbapenems. | 2008 Dec |
|
Multidrug-resistant Gram-negative bacterial infections: the emerging threat and potential novel treatment options. | 2008 Feb |
|
Doripenem (Doribax): the newest addition to the carbapenems. | 2008 Jul |
|
The role of carbapenems in the treatment of severe nosocomial respiratory tract infections. | 2008 Mar |
|
Efficacy and tolerability of IV doripenem versus meropenem in adults with complicated intra-abdominal infection: a phase III, prospective, multicenter, randomized, double-blind, noninferiority study. | 2008 May |
|
Quantification of doripenem in human plasma and peritoneal fluid by high-performance liquid chromatography with ultraviolet detection. | 2008 May 1 |
|
Current treatment of pseudomonal infections in the elderly. | 2009 |
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Doripenem: antimicrobial profile and clinical potential. | 2009 Apr |
|
Doripenem activity tested against a global collection of Enterobacteriaceae, including isolates resistant to other extended-spectrum agents. | 2009 Apr |
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In vitro activity of doripenem against Acinetobacter baumannii clinical isolates. | 2009 Feb |
|
Management of severe abdominal infections. | 2009 Jan |
|
Comparative in vitro activities of nemonoxacin, doripenem, tigecycline and 16 other antimicrobials against Nocardia brasiliensis, Nocardia asteroides and unusual Nocardia species. | 2009 Jul |
|
An analysis of current pharmaceutical industry practices for making clinical trial results publicly accessible. | 2009 Jul |
|
Doripenem. | 2009 Jul 15 |
Patents
Sample Use Guides
In Vivo Use Guide
Sources: www.accessdata.fda.gov/drugsatfda_docs/label/2013/022106s014lbl.pdf
Curator's Comment: Administered every 8 hours by intravenous infusion over one hour in patients ≥18 years of age. For complicated intra-abdominal infection 5-14 days, for complicated UTI, including pyelonephritis 10 days.
500 mg administered every 8 hours by intravenous infusion over one hour in patients ≥18 years of age; for complicated intra-abdominal infection 5–14 days, for complicated UTI, including pyelonephritis 10 days.
Route of Administration:
Intravenous
HardyDisk™ Doripenem Antimicrobial Susceptibility Test Disks are used for semi-quantitative in vitro susceptibility testing by the agar diffusion test procedure (Kirby-Bauer) of rapidly growing and certain fastidious bacterial pathogens. The concentration of doripenem 10ug has been shown to be active against most isolates of the following microorganisms both in vitro and in clinical infections: Acinetobacter baumannii, Escherichia coli, Klebsiella pneumoniae, Proteus
mirabilis, Pseudomonas aeruginosa, Streptococcus constellatus, Streptococcus intermedius
Substance Class |
Chemical
Created
by
admin
on
Edited
Fri Dec 15 16:03:18 GMT 2023
by
admin
on
Fri Dec 15 16:03:18 GMT 2023
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Record UNII |
BHV525JOBH
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Record Status |
Validated (UNII)
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Record Version |
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NDF-RT |
N0000011294
Created by
admin on Fri Dec 15 16:03:18 GMT 2023 , Edited by admin on Fri Dec 15 16:03:18 GMT 2023
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NDF-RT |
N0000011294
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admin on Fri Dec 15 16:03:18 GMT 2023 , Edited by admin on Fri Dec 15 16:03:18 GMT 2023
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NDF-RT |
N0000175496
Created by
admin on Fri Dec 15 16:03:18 GMT 2023 , Edited by admin on Fri Dec 15 16:03:18 GMT 2023
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NDF-RT |
N0000011294
Created by
admin on Fri Dec 15 16:03:18 GMT 2023 , Edited by admin on Fri Dec 15 16:03:18 GMT 2023
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NDF-RT |
N0000011294
Created by
admin on Fri Dec 15 16:03:18 GMT 2023 , Edited by admin on Fri Dec 15 16:03:18 GMT 2023
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NCI_THESAURUS |
C260
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EMA ASSESSMENT REPORTS |
DORIBAX (WITHDRAW: URINARY TRACT INFECTIONS)
Created by
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NDF-RT |
N0000011294
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FDA ORPHAN DRUG |
188104
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WHO-ATC |
J01DH04
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NDF-RT |
N0000011294
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NDF-RT |
N0000011294
Created by
admin on Fri Dec 15 16:03:18 GMT 2023 , Edited by admin on Fri Dec 15 16:03:18 GMT 2023
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LIVERTOX |
NBK548111
Created by
admin on Fri Dec 15 16:03:18 GMT 2023 , Edited by admin on Fri Dec 15 16:03:18 GMT 2023
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WHO-VATC |
QJ01DH04
Created by
admin on Fri Dec 15 16:03:18 GMT 2023 , Edited by admin on Fri Dec 15 16:03:18 GMT 2023
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C099245
Created by
admin on Fri Dec 15 16:03:18 GMT 2023 , Edited by admin on Fri Dec 15 16:03:18 GMT 2023
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C65470
Created by
admin on Fri Dec 15 16:03:18 GMT 2023 , Edited by admin on Fri Dec 15 16:03:18 GMT 2023
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DTXSID2046678
Created by
admin on Fri Dec 15 16:03:18 GMT 2023 , Edited by admin on Fri Dec 15 16:03:18 GMT 2023
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BHV525JOBH
Created by
admin on Fri Dec 15 16:03:18 GMT 2023 , Edited by admin on Fri Dec 15 16:03:18 GMT 2023
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4149
Created by
admin on Fri Dec 15 16:03:18 GMT 2023 , Edited by admin on Fri Dec 15 16:03:18 GMT 2023
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DB06211
Created by
admin on Fri Dec 15 16:03:18 GMT 2023 , Edited by admin on Fri Dec 15 16:03:18 GMT 2023
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m4744
Created by
admin on Fri Dec 15 16:03:18 GMT 2023 , Edited by admin on Fri Dec 15 16:03:18 GMT 2023
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PRIMARY | Merck Index | ||
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RR-37
Created by
admin on Fri Dec 15 16:03:18 GMT 2023 , Edited by admin on Fri Dec 15 16:03:18 GMT 2023
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SUB22196
Created by
admin on Fri Dec 15 16:03:18 GMT 2023 , Edited by admin on Fri Dec 15 16:03:18 GMT 2023
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CHEMBL491571
Created by
admin on Fri Dec 15 16:03:18 GMT 2023 , Edited by admin on Fri Dec 15 16:03:18 GMT 2023
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148016-81-3
Created by
admin on Fri Dec 15 16:03:18 GMT 2023 , Edited by admin on Fri Dec 15 16:03:18 GMT 2023
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Doripenem
Created by
admin on Fri Dec 15 16:03:18 GMT 2023 , Edited by admin on Fri Dec 15 16:03:18 GMT 2023
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119771
Created by
admin on Fri Dec 15 16:03:18 GMT 2023 , Edited by admin on Fri Dec 15 16:03:18 GMT 2023
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PRIMARY | RxNorm | ||
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73303
Created by
admin on Fri Dec 15 16:03:18 GMT 2023 , Edited by admin on Fri Dec 15 16:03:18 GMT 2023
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7975
Created by
admin on Fri Dec 15 16:03:18 GMT 2023 , Edited by admin on Fri Dec 15 16:03:18 GMT 2023
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100000089808
Created by
admin on Fri Dec 15 16:03:18 GMT 2023 , Edited by admin on Fri Dec 15 16:03:18 GMT 2023
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DORIPENEM
Created by
admin on Fri Dec 15 16:03:18 GMT 2023 , Edited by admin on Fri Dec 15 16:03:18 GMT 2023
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Related Record | Type | Details | ||
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TARGET ORGANISM->INHIBITOR |
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TARGET ORGANISM->INHIBITOR |
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TARGET ORGANISM->INHIBITOR |
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TARGET ORGANISM->INHIBITOR |
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TARGET ORGANISM->INHIBITOR |
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SOLVATE->ANHYDROUS |
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TARGET ORGANISM->INHIBITOR |
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TARGET ORGANISM->INHIBITOR |
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TARGET ORGANISM->INHIBITOR |
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TARGET ORGANISM->INHIBITOR |
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SALT/SOLVATE -> PARENT |
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TARGET ORGANISM->INHIBITOR |
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TARGET ORGANISM->INHIBITOR |
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Related Record | Type | Details | ||
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METABOLITE INACTIVE -> PARENT |
primarily via dehydropeptidase-I
MAJOR
PLASMA; URINE
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Related Record | Type | Details | ||
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ACTIVE MOIETY |
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