DORIPENEM MONOHYDRATE

US Previously Marketed

Details

Stereochemistry	ABSOLUTE
Molecular Formula	C15H24N4O6S2.H2O
Molecular Weight	438.52
Optical Activity	UNSPECIFIED
Defined Stereocenters	6 / 6
E/Z Centers	0
Charge	0

SHOW SMILES / InChI

Structure Search

SMILES

O.[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=NTUBEBXBDGKBTJ-WGLOMNHJSA-N

InChI=1S/C15H24N4O6S2.H2O/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);1H2/t6-,7-,8+,9+,10-,11-;/m1./s1

HIDE SMILES / InChI

Description
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

Originator

Approval Year

Targets

Primary Target	Pharmacology	Condition	Potency
Bacterial penicillin-binding protein 233 Target ID: CHEMBL2354204 Sources: http://www.accessdata.fda.gov/drugsatfda_docs/label/2007/022106lbl.pdf	Inhibitor 8297		47.6 µM [IC50]

Conditions

Condition	Modality	Highest Phase	Product
Complicated urinary tract infections 11 Sources: http://www.accessdata.fda.gov/drugsatfda_docs/label/2007/022106lbl.pdf	Curative	Approved 8429	DORIBAX Approved Use Indicated 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 Date 2007
Nosocomial pneumonia (NP), including ventilator associated pneumonia (VAP). 2 Sources: http://www.sciencedirect.com/science/article/pii/S0924857913000277	Curative	Withdrawn	DORIBAX Approved Use Indicated 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 Date 2007
Complicated intra-abdominal infections 20 Sources: http://www.accessdata.fda.gov/drugsatfda_docs/label/2007/022106lbl.pdf	Curative	Approved 8429	DORIBAX Approved Use Indicated 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 Date 2007

C_max

Value	Dose	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 DRUG LABEL https://www.accessdata.fda.gov/drugsatfda_docs/label/2009/022106s002s005lbl.pdf	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	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 DRUG LABEL https://www.accessdata.fda.gov/drugsatfda_docs/label/2009/022106s002s005lbl.pdf	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:

T_1/2

Value	Dose	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 DRUG LABEL https://www.accessdata.fda.gov/drugsatfda_docs/label/2009/022106s002s005lbl.pdf	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:

F_unbound

Value	Dose	Co-administered	Analyte	Population
91.9% DRUG LABEL https://www.accessdata.fda.gov/drugsatfda_docs/label/2009/022106s002s005lbl.pdf	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: https://pubmed.ncbi.nlm.nih.gov/27298719	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: https://pubmed.ncbi.nlm.nih.gov/27298719	Disc. AE: Transaminases increased, Allergic reaction... Other AEs: Leukopenia, Diarrhea... AEs leading to discontinuation/dose reduction: Transaminases increased (1 patient) Allergic reaction (1 patient) Other AEs: Leukopenia (1 patient) Diarrhea (11 patient) Nausea (9 patients) Vomiting (9 patients) Headache (6 patients) Oral candidiasis (3 patients) Rash (2 patients) Sources: https://pubmed.ncbi.nlm.nih.gov/27298719
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: https://www.accessdata.fda.gov/drugsatfda_docs/label/2007/022106lbl.pdf	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: https://www.accessdata.fda.gov/drugsatfda_docs/label/2007/022106lbl.pdf	Disc. AE: Nausea, Vulval mycotic infection... AEs leading to discontinuation/dose reduction: Nausea (0.2%) Vulval mycotic infection (0.1%) Rash (0.1%) Sources: https://www.accessdata.fda.gov/drugsatfda_docs/label/2007/022106lbl.pdf
5 mg/kg single, intravenous Dose: 5 mg/kg Route: intravenous Route: single Dose: 5 mg/kg Sources: https://pubmed.ncbi.nlm.nih.gov/26014957	unknown, <8 weeks n = 26 Health Status: unknown Age Group: <8 weeks Sex: M+F Population Size: 26 Sources: https://pubmed.ncbi.nlm.nih.gov/26014957	Other AEs: Anemia neonatal, Hypoalbuminemia... Other AEs: Anemia neonatal (3 patients) Hypoalbuminemia (3 patients) Hyperglycemia (2 patients) Peripheral edema (1 patient) Patent ductus arteriosus (2 patients) Sources: https://pubmed.ncbi.nlm.nih.gov/26014957
8 mg/kg single, intravenous Dose: 8 mg/kg Route: intravenous Route: single Dose: 8 mg/kg Sources: https://pubmed.ncbi.nlm.nih.gov/26014957	unknown, >8 weeks <44 weeks n = 26 Health Status: unknown Age Group: >8 weeks <44 weeks Sex: M+F Population Size: 26 Sources: https://pubmed.ncbi.nlm.nih.gov/26014957	Other AEs: Anemia neonatal, Peripheral edema... Other AEs: Anemia neonatal (1 patient) Peripheral edema (1 patient) Dermatitis diaper (2 patients) Sources: https://pubmed.ncbi.nlm.nih.gov/26014957

AEs

Overview

CYP3A4	CYP2C9	CYP2D6	hERG
	inhibitor 1767 inducer 389	inhibitor 1852	inhibitor 1612

OverviewOther

Other Inhibitor	Other Substrate	Other Inducer
CYP1A2 1524 CYP2A6 707 CYP2B6 810 CYP2C8 911 CYP2C19 1478 CYP2E1 882 CYP3A4/5 278 CYP4A11 21	CYP450 65 P-gp 1537	CYP1A2 701 CYP2B6 547 CYP2C19 293 CYP3A4/5 124 UGT1A1 69

Drug as perpetrator

Target	Modality	Activity
CYP1A2 1692	inhibitor 3277 Sources: https://www.accessdata.fda.gov/drugsatfda_docs/label/2007/022106lbl.pdf#page=15 Page: 15.0	no
CYP2A6 739	inhibitor 3277 Sources: https://www.accessdata.fda.gov/drugsatfda_docs/label/2007/022106lbl.pdf#page=15 Page: 15.0	no
CYP2B6 1001	inhibitor 3277 Sources: https://www.accessdata.fda.gov/drugsatfda_docs/label/2007/022106lbl.pdf#page=15 Page: 15.0	no
CYP2C19 1553	inhibitor 3277 Sources: https://www.accessdata.fda.gov/drugsatfda_docs/label/2007/022106lbl.pdf#page=15 Page: 15.0	no
CYP2C8 965	inhibitor 3277 Sources: https://www.accessdata.fda.gov/drugsatfda_docs/label/2007/022106lbl.pdf#page=15 Page: 15.0	no
CYP2C9 1819	inhibitor 3277 Sources: https://www.accessdata.fda.gov/drugsatfda_docs/label/2007/022106lbl.pdf#page=15 Page: 15.0	no
CYP2D6 1891	inhibitor 3277 Sources: https://www.accessdata.fda.gov/drugsatfda_docs/label/2007/022106lbl.pdf#page=15 Page: 15.0	no
CYP2E1 970	inhibitor 3277 Sources: https://www.accessdata.fda.gov/drugsatfda_docs/label/2007/022106lbl.pdf#page=15 Page: 15.0	no
CYP3A4/5 335	inhibitor 3277 Sources: https://www.accessdata.fda.gov/drugsatfda_docs/label/2007/022106lbl.pdf#page=15 Page: 15.0	no
CYP4A11 25	inhibitor 3277 Sources: https://www.accessdata.fda.gov/drugsatfda_docs/label/2007/022106lbl.pdf#page=15 Page: 15.0	no
CYP1A2 1692	inducer 1573 Sources: https://www.accessdata.fda.gov/drugsatfda_docs/label/2007/022106lbl.pdf#page=15 Page: 15.0	unlikely
CYP2B6 1001	inducer 1573 Sources: https://www.accessdata.fda.gov/drugsatfda_docs/label/2007/022106lbl.pdf#page=15 Page: 15.0	unlikely
CYP2C19 1553	inducer 1573 Sources: https://www.accessdata.fda.gov/drugsatfda_docs/label/2007/022106lbl.pdf#page=15 Page: 15.0	unlikely
CYP2C9 1819	inducer 1573 Sources: https://www.accessdata.fda.gov/drugsatfda_docs/label/2007/022106lbl.pdf#page=15 Page: 15.0	unlikely
CYP3A4/5 335	inducer 1573 Sources: https://www.accessdata.fda.gov/drugsatfda_docs/label/2007/022106lbl.pdf#page=15 Page: 15.0	unlikely
UGT1A1 254	inducer 1573 Sources: https://www.accessdata.fda.gov/drugsatfda_docs/label/2007/022106lbl.pdf#page=15 Page: 15.0	unlikely

Drug as victim

Target	Modality	Activity	Metabolite	Clinical evidence
CYP450 65	substrate 3367 Sources: https://www.accessdata.fda.gov/drugsatfda_docs/label/2007/022106lbl.pdf#page13 Page: 13.0	no
P-gp 1537	substrate 3367 Sources: https://doi.org/10.1016/j.ijantimicag.2011.11.019 Page: 2.0	no

Tox targets

Target	Modality	Activity	Metabolite	Clinical evidence
hERG 1647	inhibitor 1626 Sources: https://www.accessdata.fda.gov/drugsatfda_docs/nda/2007/022106s000_MedR_P8.pdf#page=10 Page: 10.0

Sourcing

Vendor/Aggregator	ID	URL
AA Blocks	AA006UL2	https://www.aablocks.com/goods/Goods/detail?id=AA006UL2
AHH Chemical co.,ltd	MT-50713	http://www.ahhchemical.com/product/MT-50713.html
Aaron Chemicals	AR006VCU	http://www.aaronchem.com/148016-81-3
Achemo Scientific Limited	AC-66571	http://www.achemo.com/search/?Keyword= 148016-81-3
Achemtek	0104-012333	http://www.achemtek.com/364622-82-2
Active Biopharma	ABP000725	http://www.activebiopharma.com/364622-82-2
Adooq BioScience	A12818	https://www.adooq.com/doripenem.html
Angene	AGN-PC-0Q17TG	http://www.angenechemical.com/productshow/AGN-PC-0Q17TG.html
ApexBio Technology	A2036	http://www.apexbt.com/doripenem-hydrate.html
ApexBio Technology	B1076	http://www.apexbt.com/doripenem.html
Aurora Fine Chemicals LLC	A30.257.818	http://online.aurorafinechemicals.com/info?ID=A30.257.818
AvaChem Scientific	2211	http://www.avachem.com/productSearch.asp?2211
BLD Pharm	BD31996	http://www.bldpharm.com/products/148016-81-3.html
BioCrick	BCC4094	http://www.biocrick.com/Doripenem-BCC4094.html
CSNpharm	CSN16169	https://www.csnpharm.com/products/doripenem.html
Chem Scene	CS-2075	http://www.chemscene.com/148016-81-3.html
ChemMol	49401510	http://www.chemmol.com/chemmol/49401510.html
ChemMol	99046355	http://www.chemmol.com/chemmol/99046355.html
Chemspace	CSSB00000055739	https://chem-space.com/CSSB00000055739
Clearsynth	CS-O-01336	http://www.clearsynth.com/en/CSO01336.html
Glentham Life Sciences	GA9212	http://www.glentham.com/products/product/GA9212/
Hefei Hirisun Pharmatech Co., Ltd	HR131453	http://hirisunpharm.com/148016-81-3.html
Lab Network	LN01314809	https://labnetwork.com/frontend-app/p/#!/moleculedetails/LN01314809
Matrix Scientific	146744	https://www.matrixscientific.com/146744.html
MedChem Express	HY-B0187	https://www.medchemexpress.com/doripenem.html
MuseChem	I001815	https://www.musechem.com/product/I001815.html
OChem	7587	http://www.ocheminc.com/index.php?act=psearch&pid=016D813
Parchem	28774	http://www.parchem.com/chemical-supplier-distributor/Doripenem-018774.aspx
Renno Tech	RL01870	http://www.rennotech.com/product_show.asp?id=2119
Selleck Chemicals	S5531	http://www.selleckchem.com/products/doripenem.html
Smolecule	S560427	https://www.smolecule.com/products/s560427
TCI (Tokyo Chemical Industry)	D5249	http://www.tcichemicals.com/eshop/en/us/commodity/D5249/index.html
THE BioTek	bt-288875	https://www.thebiotek.com/product/others/bt-288875
abcr GmbH	AB452160	http://www.abcr.com/shop/en/AB452160
eNovation Chemicals	D320169	http://www.enovationchem.com/productDetails.asp?productID=D320169
iChemical	EBD29332	http://www.ichemical.com/products/148016-81-3.html?utm_source=PubChem&utm_medium=website&utm_campaign=product%20catalogs

PubMed

Title	Date	PubMed
Antimicrobial-induced release of endotoxin from Pseudomonas aeruginosa: comparison of in vitro and animal models.	2003 Feb	12562702
Comparative in vitro antimicrobial activity of a new carbapenem, doripenem: tentative disc diffusion criteria and quality control.	2005 Jun	15872043
Comparative review of the carbapenems.	2007	17488146
Empiric treatment options in the management of complicated intra-abdominal infections.	2007 Aug	17847176
Peritoneal penetration of doripenem after intravenous administration in abdominal-surgery patients.	2007 Dec	17884833
Biochemical characterisation of the CTX-M-14 beta-lactamase.	2007 Feb	17207608
Carbapenems in the USA: focus on doripenem.	2007 Oct	17914914
An overview of harms associated with beta-lactam antimicrobials: where do the carbapenems fit in?	2008	18495060
"The truth, if it exists, is in the details".	2008 Apr	18379272
Pharmacokinetic-pharmacodynamic modeling and simulation for in vivo bactericidal effect in murine infection model.	2008 Apr	17705288
Effects of treatment with antimicrobial agents on the human colonic microflora.	2008 Dec	19337440
Gateways to clinical trials. December 2008.	2008 Dec	19271026
[In-vitro activity of panipenem against clinical isolates in 2006].	2008 Feb	18536215
Doripenem (Doribax)--a new parenteral carbapenem.	2008 Jan 28	18219262
New drugs08, part 2.	2008 Jul	18580663
Efficacy and safety of doripenem versus piperacillin/tazobactam in nosocomial pneumonia: a randomized, open-label, multicenter study.	2008 Jul	18549664
Compatibility of doripenem with other drugs during simulated Y-site administration.	2008 Jul 1	18574017
Doripenem: antimicrobial profile and clinical potential.	2009 Apr	19302929

Patents

Sample Use Guides

In Vivo Use Guide

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

In Vitro Use Guide

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

Name

Type

Language

DORIPENEM MONOHYDRATE

Common Name

English

DRIPENEM HYDRATE

Common Name

English

FINIBAX

Common Name

English

DORIPENEM HYDRATE [MI]

Common Name

English

DORIPENEM HYDRATE

Common Name

English

Doripenem monohydrate [WHO-DD]

Common Name

English

DORIPENEM HYDRATE [JAN]

Common Name

English

(4R,5.BETA.)-3-(((3S)-5.BETA.-((SULFAMOYLAMINO)METHYL)PYRROLIDINE-3.BETA.-YL)THIO)-4.ALPHA.-METHYL-6.BETA.-((1R)-1-HYDROXYETHYL)-7-OXO-1-AZABICYCLO(3.2.0)HEPTA-2-ENE-2-CARBOXYLIC ACID HYDRATE

Common Name

English

Classification Tree Code System Code

EMA ASSESSMENT REPORTS

DORIBAX (WITHDRAWN: PNEUMONIA, VENTILATOR-ASSOCIATED)