Cefoperazone
Sulbactam
A beta-lactamase inhibitor with very weak antibacterial action. The compound prevents antibiotic destruction of beta-lactam antibiotics by inhibiting beta-lactamases, thus extending their spectrum activity. Combinations of sulbactam with beta-lactam antibiotics have been used successfully for the therapy of infections caused by organisms resistant to the antibiotic alone.
Moxalactam
Broad- spectrum beta-lactam antibiotic similar in structure to the CEPHALOSPORINS except for the substitution of an oxaazabicyclo moiety for the thiaazabicyclo moiety of certain CEPHALOSPORINS. It has been proposed especially for the meningitides because it passes the blood-brain barrier and for anaerobic infections.
Cephalosporins
Cephamycins
Cefotetan
Aztreonam
Microbial Sensitivity Tests
Ceftazidime
Enterobacter
Enoxacin
Bacteria
One of the three domains of life (the others being Eukarya and ARCHAEA), also called Eubacteria. They are unicellular prokaryotic microorganisms which generally possess rigid cell walls, multiply by cell division, and exhibit three principal forms: round or coccal, rodlike or bacillary, and spiral or spirochetal. Bacteria can be classified by their response to OXYGEN: aerobic, anaerobic, or facultatively anaerobic; by the mode by which they obtain their energy: chemotrophy (via chemical reaction) or PHOTOTROPHY (via light reaction); for chemotrophs by their source of chemical energy: CHEMOLITHOTROPHY (from inorganic compounds) or chemoorganotrophy (from organic compounds); and by their source for CARBON; NITROGEN; etc.; HETEROTROPHY (from organic sources) or AUTOTROPHY (from CARBON DIOXIDE). They can also be classified by whether or not they stain (based on the structure of their CELL WALLS) with CRYSTAL VIOLET dye: gram-negative or gram-positive.
beta-Lactams
Four-membered cyclic AMIDES, best known for the PENICILLINS based on a bicyclo-thiazolidine, as well as the CEPHALOSPORINS based on a bicyclo-thiazine, and including monocyclic MONOBACTAMS. The BETA-LACTAMASES hydrolyze the beta lactam ring, accounting for BETA-LACTAM RESISTANCE of infective bacteria.
Piperacillin
Bacteroides fragilis
beta-Lactamases
Cefamandole
Enterobacteriaceae
A family of gram-negative, facultatively anaerobic, rod-shaped bacteria that do not form endospores. Its organisms are distributed worldwide with some being saprophytes and others being plant and animal parasites. Many species are of considerable economic importance due to their pathogenic effects on agriculture and livestock.
Cefmetazole
Imipenem
Semisynthetic thienamycin that has a wide spectrum of antibacterial activity against gram-negative and gram-positive aerobic and anaerobic bacteria, including many multiresistant strains. It is stable to beta-lactamases. Clinical studies have demonstrated high efficacy in the treatment of infections of various body systems. Its effectiveness is enhanced when it is administered in combination with CILASTATIN, a renal dipeptidase inhibitor.
Cefsulodin
Penicillanic Acid
Drug Resistance, Microbial
Ceftizoxime
A semisynthetic cephalosporin antibiotic which can be administered intravenously or by suppository. The drug is highly resistant to a broad spectrum of beta-lactamases and is active against a wide range of both aerobic and anaerobic gram-positive and gram-negative organisms. It has few side effects and is reported to be safe and effective in aged patients and in patients with hematologic disorders.
In-vitro susceptibility of 1982 respiratory tract pathogens and 1921 urinary tract pathogens against 19 antimicrobial agents: a Canadian multicentre study. Canadian Antimicrobial Study Group. (1/172)
A total of 3903 pathogens from 48 Canadian medical centres were tested against 19 antimicrobial agents. Five agents showed activity against > or = 90% of all 1982 respiratory tract pathogens tested (ciprofloxacin, 90%; cefoperazone, 91%; ticarcillin/clavulanate, 92%; ceftazidime and imipenem, 93% each). Nine agents had > or = 90% activity against Enterobacteriaceae from respiratory tract infection (cefotaxime and ticarcillin/clavulanate, 90% each; aztreonam, ceftizoxime and ceftriaxone, 91% each; ceftazidime, 93%; ciprofloxacin, 97%; imipenem and netilmicin, 98% each). Similarly, five agents had activity against > or = 90% of all 1921 urinary tract pathogens tested (ciprofloxacin and ticarcillin/clavulanate, 90% each; cefoperazone and netilmicin, 91% each; imipenem, 99%). Nine agents had > or = 95% activity against Enterobacteriaceae from urinary tract infection (ciprofloxacin, 95%; cefotetan, 97%; aztreonam, cefotaxime, ceftazidime, ceftizoxime, ceftriaxone and netilmicin, 98% each; imipenem, 99%). Seventeen agents had activity against > or = 95% of Staphylococcus aureus strains. Susceptibility of Pseudomonas aeruginosa isolates ranged from 2% to 91%. (+info)Markedly different rates and resistance profiles exhibited by seven commonly used and newer beta-lactams on the selection of resistant variants of Enterobacter cloacae. (2/172)
Seven beta-lactam antibiotics (cefepime, cefoperazone, ceftazidime, ceftriaxone, cefamandole, imipenem and meropenem) were tested for their potential to select resistance in standard and clinical strains of Enterobacter cloacae (n = 9). The strains were subcultured daily with the test antibiotics at doubling concentrations starting at 0.125 x MIC. Development of resistance throughout the passages was detected by a disc diffusion test. Ceftazidime, ceftriaxone and cefamandole selected resistance at a faster rate than cefoperazone, cefepime and meropenem. Imipenem did not select resistance in the nine strains tested and was the only antibiotic that eradicated all the strains during selection. The resistance patterns of strains selected by meropenem, cefepime and the other cephalosporins were markedly different, although cross-resistance to the early generation cephalosporins was common. The resistance phenotypes of most strains remained stable upon serial passages in antibiotic-free medium. The findings of this study highlight the importance of the choice of antibiotic for therapy not only on the basis of its antibacterial activity, but also on its potential to select resistance to itself and other antibiotics. (+info)Investigation of the synergic effects of aminoglycoside-fluoroquinolone and third-generation cephalosporin combinations against clinical isolates of Pseudomonas spp. (3/172)
Antimicrobial synergy resulting from antibiotic combination therapy is often important in the treatment of serious bacterial infections. Previous studies have demonstrated synergy between an aminoglycoside and beta-lactam antibiotics in the treatment of Pseudomonas aeruginosa infections. The present paper investigates the synergic effects of aminoglycosides (amikacin and netilmicin) and fluoroquinolones (ciprofloxacin, ofloxacin and pefloxacin) in combination with third-generation cephalosporins (cefoperazone, ceftriaxone and ceftazidime) against 18 clinical isolates of Pseudomonas spp. The effects of these drugs were examined by three methods (disc diffusion, 'chequerboard' titration and the time-killing method), to evaluate the activities of the antibiotics alone and in combination against selected isolates. Fractional inhibitory concentration indices were calculated for all isolates with all combinations. Use of the disc diffusion method revealed that amikacin and netilmicin in combination with the three cephalosporins exhibited synergy against 7-12 isolates, whereas the combinations of quinolones and ceftazidime displayed synergic effects only in the case of 3-5 isolates. On 'chequerboard' titration, amikacin and ceftriaxone exerted synergy against seven of the isolates. The other combinations showed synergy against fewer isolates, but every combination demonstrated synergic effect against some of the isolates. The tested combinations had different effects against various Pseudomonas spp. With the time-killing method, the 1/2 x MIC of amikacin or ciprofloxacin in combination with the 1/2 x MIC of third-generation cephalosporins proved to be most effective. No antagonism was found with these combinations. Discrepancies in the detection of synergy were observed for the different methods. (+info)Cefoperazone prevents the inactivation of alpha(1)-antitrypsin by activated neutrophils. (4/172)
At sites of neutrophilic inflammation, tissue injury by neutrophil elastase is favored by phagocyte-induced hypochlorous acid-dependent inactivation of the natural elastase inhibitor alpha(1)-antitrypsin. In the present study, cefoperazone prevented alpha(1)-antitrypsin inactivation by neutrophils and reduced the recovery of hypochlorous acid from these cells. Moreover, the antibiotic reduced the free elastase activity in a neutrophil suspension supplemented with alpha(1)-antitrypsin without affecting the cells' ability to release elastase. These data suggest that the drug inactivates hypochlorous acid before its reaction with alpha(1)-antitrypsin, thereby permitting the antiprotease-mediated blockade of released elastase. In conclusion, cefoperazone appears to have the potential for limiting elastase-antielastase imbalances, attenuating the related tissue injury at sites of inflammation. (+info)Prevalence of Campylobacter, Arcobacter, Helicobacter, and Sutterella spp. in human fecal samples as estimated by a reevaluation of isolation methods for Campylobacters. (5/172)
The aims of this study were to investigate the prevalence of campylobacteria including Campylobacter jejuni subsp. jejuni (C. jejuni) and Campylobacter coli in human clinical samples and in samples from healthy individuals and to reevaluate the efficacies of conventional selective methods for isolation of Campylobacter spp. Two charcoal-based selective media, modified charcoal cefoperazone deoxycholate agar (mCCDA) and cefoperazone-amphotericin-teicoplanin (CAT) agar, were compared with Skirrow's blood-based medium and with a filter method (filter) applied to a yeast-enriched blood agar. A total of 1,376 specimens were tested on all four media, and the percentages of thermophilic Campylobacter-positive specimens isolated on Skirrow's medium, filters, CAT agar, and mCCDA were 82, 83, 85, and 95%, respectively. When additional samples were processed with the three selective media, mCCDA recovered significantly more thermophilic Campylobacter spp. than Skirrow's medium (P = 0.0034). No significant difference between Skirrow's medium and CAT agar was observed in this study. Another six taxa were identified, namely, Campylobacter concisus, Campylobacter curvus-like bacteria, Arcobacter butzleri, Arcobacter cryaerophilus, Helicobacter cinaedi, and Sutterella wadsworthensis. Most of these strains were isolated after 5 to 6 days of incubation by use of the filter technique. This paper provides evidence for the existence of S. wadsworthensis in human feces from clinical cases of gastrointestinal disorders and in feces from a healthy individual. Furthermore, C. concisus was isolated from a large number of diarrheal cases, particularly those at the extremes of age, but was additionally isolated from the feces of healthy people. Further investigations to establish the role of C. concisus and S. wadsworthensis in enteric disease is needed. We conclude that a range of campylobacteria may cause infections in Denmark. (+info)Multilocular pyogenic hepatic abscess complicating ascaris lumbricoides infestation. (6/172)
A 74-year-old man was admitted to our hospital with frequent right flank pain. The multiple multilocular hepatic abscesses were revealed by computed tomography. Radiographs following a barium meal showed a linear filling defect in the ileum consistent with ascariasis. One day after treatment with pyrantel pamoate, an Ascaris was passed in the stool. The pyogenic hepatic abscesses gradually healed with both antibiotics and continuous drainage. After 2 months, he was discharged. In this case, the pyogenic hepatic abscesses were thus considered to have been caused by an inflammation which spread through the portal vein. (+info)Susceptibility of clinical isolates of Bacteroides fragilis group strains to cefoxitin, cefoperazone and ticarcillin/clavulanate. (7/172)
A total of 40 strains of the B. fragilis group was isolated from clinical specimens in two hospital centers in Fortaleza from 1993 to 1997. The most frequently isolated species was Bacteroides fragilis (19 strains) and most isolates came from intra-abdominal and wound infections. The susceptibility profile was traced for cefoxitin, cefoperazone and ticarcillin-clavulanate by using the agar dilution reference method. All isolates were susceptible to ticarcillin-clavulanate (128/2 microg/ml). Resistance rates of 15 and 70% were detected to cefoxitin (64 microg/ml) and cefoperazone (64 microg/ml), respectively. Such regional results permit a better orientation in choosing this group of antibiotics for prophylaxis and therapy especially in relation to cefoxitin, which is frequently used in the hospital centers studied. (+info)In-vitro susceptibility of Burkholderia pseudomallei to cefoperazone-sulbactam combination. (8/172)
Melioidosis is endemic in Malaysia. Emerging resistance with new and current antimicrobial agents has underscored the need to look further for new antimicrobial agents for the treatment of melioidosis. Hence, we evaluated the in-vitro susceptibility of fifty locally isolated strains of Burkholderia pseudomallei, the causative agent of melioidosis to cefoperazone-sulbactam combination using the method of NCCLS. All the fifty strains tested were susceptible in-vitro to cefoperazone-sulbactam. The MIC90 of the organism for cefoperazone-sulbactam was 4 mg/L. The results of our findings suggested that cefoperazone-sulbactam may be useful in the treatment of melioidosis. (+info) Enterobacteriaceae Infections: Bacterial infections caused by members of the family Enterobacteriaceae, which includes several genera such as Escherichia (E. coli, E. aerogenes), Klebsiella (K. pneumoniae, K. oxytoca), Proteus (P. mirabilis, P. vulgaris), and Providencia. These bacteria are commonly found in the gastrointestinal tract and urinary tract, and can cause a variety of infections, including urinary tract infections, pneumonia, bloodstream infections, and surgical site infections.
Previous article'Etiology' Next article 'Esophageal Cancer'
Cefoperazone
... /sulbactam (Sulperazon) is a co-formulation with sulbactam. Cefoperazone has a broad spectrum of activity and has ... Cefoperazone is a third-generation cephalosporin antibiotic, marketed by Pfizer under the name Cefobid. It is one of few ... Cefoperazone exerts its bactericidal effect by inhibiting the bacterial cell wall synthesis, and sulbactam acts as a beta- ... "Cefoperazone (Cefobid) - The Antimicrobial Index Knowledgebase - TOKU-E". antibiotics.toku-e.com. Stork CM (2006). "Antibiotics ...
Campylobacter fetus
Modified charcoal cefoperazone deoxycholate (CCD) agar is a growth medium designed to isolate Campylobacters from feces. On CCD ... Identification of C. fetus species in infected animals or people is routinely performed by culture on blood or cefoperazone ... "Charcoal cefoperazone deoxycholate (CCD) agar - Modified". Culture Media for Food Microbiology. Progress in Industrial ...
Melioidosis
There are no differences between using cefoperazone/sulbactam or ceftazidime to treat melioidosis as both shows similar death ... However, data are lacking to recommend cefoperazone/sulbactam usage. For those with kidney impairment, the dosage of ... Apisarnthanarak A, Little JR (March 2002). "The role of cefoperazone-sulbactam for treatment of severe melioidosis". Clinical ... Meropenem, imipenem and the cefoperazone-sulbactam combination (Sulperazone) are also effective. Intravenous amoxicillin- ...
Sulbactam
The combination cefoperazone/sulbactam (Sulperazon) is available in many countries. Recently, its use in treating Acinetobacter ...
Cephalosporin
These include latamoxef (moxalactam), cefmenoxime, cefoperazone, cefamandole, cefmetazole, and cefotetan. This is thought to be ...
Ceftriaxone
However, unlike ceftazidime and cefoperazone, ceftriaxone does not have useful activity against Pseudomonas aeruginosa. It is ...
Typhoid fever
... cefoperazone, and other newer cephalosporins". Reviews of Infectious Diseases. 9 (4): 719-36. doi:10.1093/clinids/9.4.719. ...
Shashank Shah
"Cefoperazone-Sulbactam for Treatment of Intra-Abdominal Infections: Results from a Randomized, Parallel Group Study in India". ...
Proteus vulgaris
Ciprofloxacin Ceftazidime Netilmicin Sulbactam or cefoperazone Meropenem Piperacillin/tazobactam Ampicillin/sulbactam Proteus ...
List of drugs: Cb-Ce
... cefoperazone (INN) ceforanide (INN) cefoselis (INN) Cefotan cefotaxime (INN) cefotetan (INN) cefotiam (INN) cefovecin sodium ( ...
Pseudomonas aeruginosa
... cefoperazone, cefpirome, ceftobiprole, but not cefuroxime, cefotaxime, or ceftriaxone) antipseudomonal penicillins: ...
Antibiotic
... s such as metronidazole, tinidazole, cephamandole, latamoxef, cefoperazone, cefmenoxime, and furazolidone, cause a ...
ATCvet code QJ51
QJ51DB04 Cefazolin QJ51DB08 Cefapirin QJ51DB10 Cefacetrile QJ51DB90 Cefalonium QJ51DC02 Cefuroxime QJ51DD12 Cefoperazone ...
List of MeSH codes (D02)
... cefoperazone MeSH D02.065.589.099.249.160 - cefazolin MeSH D02.065.589.099.249.177 - cefonicid MeSH D02.065.589.099.249.185 - ...
Disulfiram-like drug
... cefoperazone, cefotetan, ceftriaxone, and latamoxef (moxalactam); thought to be due to common N-methylthiotetrazole metabolite ...
Mycoplasma alligatoris
65 mg cefoperazone 1 −1 and 20% (v/v) fetal bovine serum in 5% CO2 atmosphere or in ambient air. Isolates were then grown at ...
Disulfiram
... including cefoperazone, cefamandole and cefotetan, that have a N-methylthio-tetrazole moiety Griseofulvin, an oral antifungal ...
Proteus penneri
... amikacin piperacillin cefoperazone All tested strains have been found resistant to: penicillin ampicillin tetracycline ...
Pasteurella canis
... and cefoperazone), ciprofloxacin (quinolones), trimethoprim/sulfamethoxazole (sulfonamides), chloramphenicol, most ...
Prototheca zopfii
... cefoperazone, cephalexin, enrofloxacin, lincomycin, oxytetracycline, miconazole, colistin, a combination of amoxicillin with ...
Β-Lactamase inhibitor
... or cefoperazone (Sulperazon) Tazobactam, usually combined with piperacillin (Zosyn and Tazocin) β-lactamase inhibitors with a ...
ATC code J01
... combinations J01DD62 Cefoperazone and beta-lactamase inhibitor J01DD63 Ceftriaxone and beta-lactamase inhibitor J01DD64 ... Latamoxef J01DD07 Ceftizoxime J01DD08 Cefixime J01DD09 Cefodizime J01DD10 Cefetamet J01DD11 Cefpiramide J01DD12 Cefoperazone ...
Timeline of antibiotics
... cefoperazone/sulbactam 1986 - co-ticarclav (ticarcillin/clavulanic acid) 1987 - ampicillin/sulbactam 1987 - cefixime 1987 - ... cefoperazone 1981 - cefotiam 1981 - cefsulodin 1981 - latamoxef 1981 - netilmicin 1982 - ceftriaxone 1982 - micronomicin 1983 ...
Cefoperazone - www.micromasterlab.com
99% Cefoperazone, Cefoperazone Sodium Sterile in Stock
CEFOPERAZONE SULBACTAMS FOR INJECTION Manufacturer in Gujarat,Supplier,Exporter
Get More Detail For CEFOPERAZONE SULBACTAMS FOR INJECTION based in Vadodara, Gujarat, India. ... Manufacturer wide range of Pharmaceutical Products like CEFOPERAZONE SULBACTAMS FOR INJECTION with reasonable price offered by ... Cefoperazone + Sulbactam is a combination of two medicines: Cefoperazone and Sulbactam. Cefoperazone is an antibiotic. It works ... USES: Cefoperazone + Sulbactam is used in the treatment of bacterial infections. ...
Cefoperazone | Davis's Drug Guide for Rehabilitation Professionals | F.A. Davis AT Collection | McGraw Hill Medical
Cefoperazone. In: Ciccone CD. Ciccone C.D.(Ed.),Ed. Charles D. Ciccone.eds. Daviss Drug Guide for Rehabilitation Professionals ... "Cefoperazone." Daviss Drug Guide for Rehabilitation Professionals Ciccone CD. Ciccone C.D.(Ed.),Ed. Charles D. Ciccone. McGraw ... Cefoperazone. Ciccone CD. Ciccone C.D.(Ed.),Ed. Charles D. Ciccone. (2016). Daviss Drug Guide for Rehabilitation Professionals ...
Table - RmtC and RmtF 16S rRNA Methyltransferase in NDM-1-Producing Pseudomonas aeruginosa - Volume 21, Number 11-November 2015...
Melioidosis - Wikipedia
However, data are lacking to recommend cefoperazone/sulbactam usage.[47][48] For those with kidney impairment, the dosage of ... Meropenem, imipenem and the cefoperazone-sulbactam combination (Sulperazone) are also effective.[1] Intravenous amoxicillin- ... There are no differences between using cefoperazone/sulbactam or ceftazidime to treat melioidosis as both shows similar death ... "The role of cefoperazone-sulbactam for treatment of severe melioidosis". Clinical Infectious Diseases. 34 (5): 721-723. doi ...
Randomized noninferiority trial of cefoperazone-sulbactam versus cefepime in the treatment of hospital-acquired and healthcare...
Cefoperazone-sulbactam at 2 g every 12 h was noninferior to cefepime at 2 g every 2 h for patients with HCAP. ... Cefoperazone-sulbactam at 2 g every 12 h was noninferior to cefepime at 2 g every 2 h for patients with HCAP.", ... Cefoperazone-sulbactam at 2 g every 12 h was noninferior to cefepime at 2 g every 2 h for patients with HCAP. ... Cefoperazone-sulbactam at 2 g every 12 h was noninferior to cefepime at 2 g every 2 h for patients with HCAP. ...
gmcsf, Leukine (sargramostim) dosing, indications, interactions, adverse effects, and more
MESH TREE NUMBER CHANGES - 2008 MeSH
Chloramphenicol Injection: MedlinePlus Drug Information
Frontiers | Selective Essential Oils from Spice or Culinary Herbs Have High Activity against Stationary Phase and Biofilm...
Cephalosporin-resistant Escherichia coli among Summer Camp Attendees with Salmonellosis - Volume 9, Number 10-October 2003 -...
Vitamin K - Health Professional Fact Sheet
Ampicillin/sulbactam Disease Interactions - Drugs.com
Global gene expression analysis of Escherichia coli K-12 DH5α after exposure to 2.4 GHz wireless fidelity radiation - Elham...
National Ambulatory Medical Care Survey, 1994
DeCS
Cefoperazone Sodium Salt Salt, Cefoperazone Sodium Sodium Salt, Cefoperazone Sodium, Cefoperazone T1551 - Narrower Concept UI. ... Cefoperazone Sodium Salt. Céfobis. Salt, Cefoperazone Sodium. Sodium Salt, Cefoperazone. Sodium, Cefoperazone. T 1551. T-1551. ... Cefoperazone - Preferred Concept UI. M0003720. Scope note. Semisynthetic broad-spectrum cephalosporin with a tetrazolyl moiety ...
INJECTIONS
Cephalosporins, Parenteral - LiverTox - NCBI Bookshelf
Pielonefrite/diagnóstico
Value Set Concept Details
Words that contain ZO (637 words) - WordMom
Is Tobramycin Safe in Breastfeeding
2023 Drugs Underdosing ICD-10-CM Codes
CEFOBID3
- CEFOBID ® (sterile cefoperazone), formerly known as sterile cefoperazone sodium, contains cefoperazone as cefoperazone sodium. (nih.gov)
- CEFOBID (sterile cefoperazone) contains 34 mg sodium (1.5 mEq) per gram (g). (nih.gov)
- CEFOBID (sterile cefoperazone) in crystalline form is supplied in vials containing 1 g or 2 g cefoperazone as cefoperazone sodium for intravenous or intramuscular administration. (nih.gov)
Third-generation ce2
- Cefoperazone, a third-generation cephalosporin, interferes with cell wall synthesis by binding to the penicillin-binding proteins (PBPs), thus preventing cross-linking of nascent peptidoglycan. (nih.gov)
- Cefoperazone is a semisynthetic, broad-spectrum, third-generation cephalosporin with antibacterial activity. (synzeal.com)
Cefotaxime1
- Cefotaxime does not cause a significant incidence of coagulopathies, as observed with some cephalosporins (e.g., cefamandole and cefoperazone), nor is it associated with the development of pseudocholelithiasis as seen with ceftriaxone. (nih.gov)
Cephalosporin1
- Cebanex Forte 3Gm Inj is a combination of two antibiotics, namely: Cefoperazone (cephalosporin antibiotic) and sulbactam (beta-lactamase inhibitor). (apollopharmacy.in)
Cefepime2
- These results indicated the noninferiority of cefoperazone-sulbactam to cefepime, which was confirmed by per-protocol analysis. (tmu.edu.tw)
- Cefoperazone-sulbactam at 2 g every 12 h was noninferior to cefepime at 2 g every 2 h for patients with HCAP. (tmu.edu.tw)
Cefoxitin1
- One hundred one women undergoing elective abdominal hysterectomy were given perioperative cefoperazone or cefoxitin in a prospective randomized blinded study. (elsevierpure.com)
Antibiotic1
- Cefoperazone is an antibiotic. (oceanpharmaproducts.com)
Broad-spectrum1
- Cefoperazone, a third-generation cephamycin with broad-spectrum antibacterial activity and the ability to permeate bacterial cell membranes, is active against commonly encountered multidrug-resistant pathogens for hospital-acquired pneumonia (HAP) and health care-associated pneumonia (HCAP). (tmu.edu.tw)
Works by preventing th1
- Cefoperazone works by preventing the formation of bacterial cell covering, which is necessary for their survival. (apollopharmacy.in)
Infection1
- Fecal samples were collected from individual mice after cefoperazone treatment and immediately before the infection to analyze the gut microbiota constitution and quantify the fecal AA levels. (news-medical.net)
Treatment2
- Cefoperazone + Sulbactam is used in the treatment of bacterial infections. (oceanpharmaproducts.com)
- To clarify the clinical effects of cefoperazone-sulbactam in the treatment of HAP and HCAP, we conducted an openlabel, randomized, noninferiority trial that recruited patients aged ≥18 years suffering HAP/HCAP. (tmu.edu.tw)
Patients3
- En tout, 38 patients ont contracté 43 infections nosocomiales liées aux dispositifs médicaux (1,13 épisode par patient). (who.int)
- 28. Pharmacokinetics of cefoperazone in patients with normal and impaired hepatic and renal function. (nih.gov)
- 29. Pharmacokinetics of multiple-dose cefoperazone in hemodialysis patients. (nih.gov)
Effects1
- Limited information indicates cefoperazone produces low levels in milk that are not expected to cause adverse effects in breastfed infants. (nih.gov)
Activity1
- On the other hand, sulbactam works by decreasing bacterial resistance and enhancing the activity of cefoperazone against the bacteria. (apollopharmacy.in)
Combination1
- Cefoperazone + Sulbactam is a combination of two medicines: Cefoperazone and Sulbactam. (oceanpharmaproducts.com)
Sulbactam9
- Matsuda S, Kashiwagura T, Hirayama H. Passage into the human milk and clinical evaluation of sulbactam/cefoperazone. (nih.gov)
- Neurosurgical patients (over 18 years old) with an indwelling ventricular drainage pipe after neurological surgery who were treated with cefoperazone/sulbactam for prevention of intracranial infection were eligible. (medscape.com)
- Cefoperazone/sulbactam (Sulperazon, Pfizer, New York, USA) in 1.5-g ampoules with cefoperazone 1.0 g/sulbactam 0.5g was given to all included patients. (medscape.com)
- All the patients were given cefoperazone/sulbactam 3.0 g in 50-mL saline by intravenous injection for 3 hours every 6 hours after craniotomy. (medscape.com)
- Cefoperazone and sulbactam concentrations were measured with liquid chromatography mass spectrometry (LC-MS/MS). (medscape.com)
- The ratio (Y) of the cefoperazone-sulbactam peak area (AS) and to the IS peak area (AI) was calculated, and the cefoperazone-sulbactam plasma concentration (X) was weighted (1/x2) for regression calculation. (medscape.com)
- The correlation coefficient R of the serum cefoperazone concentration and the serum sulbactam was 0.9958 and 0.9913, respectively. (medscape.com)
- The respective correlation coefficient R of CSF cefoperazone concentration and CSF sulbactam concentration was 0.9921 and 0.9532. (medscape.com)
- The peak area of the main component in the sample solution was brought into the working standard curve to calculate cefoperazone/sulbactam content in each sample solution. (medscape.com)
Gram2
Milk1
- Limited information indicates cefoperazone produces low levels in milk that are not expected to cause adverse effects in breastfed infants. (nih.gov)