Vaccines or candidate vaccines used to prevent infection with VIBRIO CHOLERAE. The original cholera vaccine consisted of killed bacteria, but other kinds of vaccines now exist.
An acute diarrheal disease endemic in India and Southeast Asia whose causative agent is VIBRIO CHOLERAE. This condition can lead to severe dehydration in a matter of hours unless quickly treated.
Suspensions of killed or attenuated microorganisms (bacteria, viruses, fungi, protozoa), antigenic proteins, synthetic constructs, or other bio-molecular derivatives, administered for the prevention, amelioration, or treatment of infectious and other diseases.
The interactions between physician and patient.
Vaccines in which the infectious microbial nucleic acid components have been destroyed by chemical or physical treatment (e.g., formalin, beta-propiolactone, gamma radiation) without affecting the antigenicity or immunogenicity of the viral coat or bacterial outer membrane proteins.
An ENTEROTOXIN from VIBRIO CHOLERAE. It consists of two major protomers, the heavy (H) or A subunit and the B protomer which consists of 5 light (L) or B subunits. The catalytic A subunit is proteolytically cleaved into fragments A1 and A2. The A1 fragment is a MONO(ADP-RIBOSE) TRANSFERASE. The B protomer binds cholera toxin to intestinal epithelial cells, and facilitates the uptake of the A1 fragment. The A1 catalyzed transfer of ADP-RIBOSE to the alpha subunits of heterotrimeric G PROTEINS activates the production of CYCLIC AMP. Increased levels of cyclic AMP are thought to modulate release of fluid and electrolytes from intestinal crypt cells.
Use of plants or herbs to treat diseases or to alleviate pain.
Services providing pharmaceutic and therapeutic drug information and consultation.
Printed publications usually having a format with no binding and no cover and having fewer than some set number of pages. They are often devoted to a single subject.
Use of written, printed, or graphic materials upon or accompanying a drug container or wrapper. It includes contents, indications, effects, dosages, routes, methods, frequency and duration of administration, warnings, hazards, contraindications, side effects, precautions, and other relevant information.
The teaching or training of patients concerning their own health needs.
Works about lists of drugs or collections of recipes, formulas, and prescriptions for the compounding of medicinal preparations. Formularies differ from PHARMACOPOEIAS in that they are less complete, lacking full descriptions of the drugs, their formulations, analytic composition, chemical properties, etc. In hospitals, formularies list all drugs commonly stocked in the hospital pharmacy.
That segment of commercial enterprise devoted to the design, development, and manufacture of chemical products for use in the diagnosis and treatment of disease, disability, or other dysfunction, or to improve function.
Computer-based systems for input, storage, display, retrieval, and printing of information contained in a patient's medical record.
Drugs manufactured and sold with the intent to misrepresent its origin, authenticity, chemical composition, and or efficacy. Counterfeit drugs may contain inappropriate quantities of ingredients not listed on the label or package. In order to further deceive the consumer, the packaging, container, or labeling, may be inaccurate, incorrect, or fake.
Activities and programs intended to assure or improve the quality of care in either a defined medical setting or a program. The concept includes the assessment or evaluation of the quality of care; identification of problems or shortcomings in the delivery of care; designing activities to overcome these deficiencies; and follow-up monitoring to ensure effectiveness of corrective steps.
Agreements between two or more parties, especially those that are written and enforceable by law (American Heritage Dictionary of the English Language, 4th ed). It is sometimes used to characterize the nature of the professional-patient relationship.
A system for verifying and maintaining a desired level of quality in a product or process by careful planning, use of proper equipment, continued inspection, and corrective action as required. (Random House Unabridged Dictionary, 2d ed)
A generic concept reflecting concern with the modification and enhancement of life attributes, e.g., physical, political, moral and social environment; the overall condition of a human life.
A sampling methodology using small sample sizes when conducting surveys in small geographical or population-based areas or lots.
Outside services provided to an institution under a formal financial agreement.
Works containing information articles on subjects in every field of knowledge, usually arranged in alphabetical order, or a similar work limited to a special field or subject. (From The ALA Glossary of Library and Information Science, 1983)
NATIONAL LIBRARY OF MEDICINE service for health professionals and consumers. It links extensive information from the National Institutes of Health and other reviewed sources of information on specific diseases and conditions.
A genus of extremely thermophilic heterotrophic archaea, in the family THERMOCOCCACEAE, occurring in heated sea flows. They are anaerobic chemoorganotropic sulfidogens.
Information intended for potential users of medical and healthcare services. There is an emphasis on self-care and preventive approaches as well as information for community-wide dissemination and use.
Platforms that provide the ability and tools to create and publish information accessed via the INTERNET. Generally these platforms have three characteristics with content user generated, high degree of interaction between creator and viewer, and easily integrated with other sites.
A genus of strictly anaerobic ultrathermophilic archaea, in the family THERMOCOCCACEAE, occurring in heated seawaters. They exhibit heterotrophic growth at an optimum temperature of 100 degrees C.
Body of knowledge related to the use of organisms, cells or cell-derived constituents for the purpose of developing products which are technically, scientifically and clinically useful. Alteration of biologic function at the molecular level (i.e., GENETIC ENGINEERING) is a central focus; laboratory methods used include TRANSFECTION and CLONING technologies, sequence and structure analysis algorithms, computer databases, and gene and protein structure function analysis and prediction.
The mulberry plant family of the order Urticales, subclass Hamamelidae, class Magnoliopsida. They have milky latex and small, petalless male or female flowers.
The systematic study of the complete DNA sequences (GENOME) of organisms.
A condition caused by dysfunctions related to the SINOATRIAL NODE including impulse generation (CARDIAC SINUS ARREST) and impulse conduction (SINOATRIAL EXIT BLOCK). It is characterized by persistent BRADYCARDIA, chronic ATRIAL FIBRILLATION, and failure to resume sinus rhythm following CARDIOVERSION. This syndrome can be congenital or acquired, particularly after surgical correction for heart defects.
A device designed to stimulate, by electric impulses, contraction of the heart muscles. It may be temporary (external) or permanent (internal or internal-external).
An organochlorine insecticide that is slightly irritating to the skin. (From Merck Index, 11th ed, p482)
Impaired conduction of cardiac impulse that can occur anywhere along the conduction pathway, such as between the SINOATRIAL NODE and the right atrium (SA block) or between atria and ventricles (AV block). Heart blocks can be classified by the duration, frequency, or completeness of conduction block. Reversibility depends on the degree of structural or functional defects.
Regulation of the rate of contraction of the heart muscles by an artificial pacemaker.
The meaning ascribed to the BASE SEQUENCE with respect to how it is translated into AMINO ACID SEQUENCE. The start, stop, and order of amino acids of a protein is specified by consecutive triplets of nucleotides called codons (CODON).
The utilization of drugs as reported in individual hospital studies, FDA studies, marketing, or consumption, etc. This includes drug stockpiling, and patient drug profiles.
Glycoproteins with a molecular weight of approximately 620,000 to 680,000. Precipitation by electrophoresis is in the alpha region. They include alpha 1-macroglobulins and alpha 2-macroglobulins. These proteins exhibit trypsin-, chymotrypsin-, thrombin-, and plasmin-binding activity and function as hormonal transporters.
Exclusive legal rights or privileges applied to inventions, plants, etc.
A novel composition, device, or process, independently conceived de novo or derived from a pre-existing model.
Property, such as patents, trademarks, and copyright, that results from creative effort. The Patent and Copyright Clause (Art. 1, Sec. 8, cl. 8) of the United States Constitution provides for promoting the progress of science and useful arts by securing for limited times to authors and inventors, the exclusive right to their respective writings and discoveries. (From Black's Law Dictionary, 5th ed, p1014)
Time period from 1701 through 1800 of the common era.
Time period from 1601 through 1700 of the common era.
A mitosporic fungal genus with many reported ascomycetous teleomorphs. Cephalosporin antibiotics are derived from this genus.
A group of antibiotics that contain 6-aminopenicillanic acid with a side chain attached to the 6-amino group. The penicillin nucleus is the chief structural requirement for biological activity. The side-chain structure determines many of the antibacterial and pharmacological characteristics. (Goodman and Gilman's The Pharmacological Basis of Therapeutics, 8th ed, p1065)
A broad-spectrum penicillin antibiotic used orally in the treatment of mild to moderate infections by susceptible gram-positive organisms.
A penicillin derivative commonly used in the form of its sodium or potassium salts in the treatment of a variety of infections. It is effective against most gram-positive bacteria and against gram-negative cocci. It has also been used as an experimental convulsant because of its actions on GAMMA-AMINOBUTYRIC ACID mediated synaptic transmission.
A chronic systemic disease, primarily of the joints, marked by inflammatory changes in the synovial membranes and articular structures, widespread fibrinoid degeneration of the collagen fibers in mesenchymal tissues, and by atrophy and rarefaction of bony structures. Etiology is unknown, but autoimmune mechanisms have been implicated.
Nonsusceptibility of an organism to the action of penicillins.

Protection with antibody to tumor necrosis factor differs with similarly lethal Escherichia coli versus Staphylococcus aureus pneumonia in rats. (1/31)

BACKGROUND: Differing factors may alter the effects of antibody to tumor necrosis factor (TNF) in infection and sepsis. The authors tested whether bacteria type or treatment route alters antibody to TNF in a rat model of bacterial pneumonia. METHODS: Rats (n = 231) received similarly lethal doses of either intratracheal Escherichia coli or Staphylococcus aureus followed by treatment with either intratracheal or intraperitoneal antibody to TNF or control serum. Animals received antibiotics (cefotiam daily dose, 100 mg/kg) starting 4 h after inoculation and were studied for up to 96 h. RESULTS: Compared with S. aureus, E. coli increased serum TNF and interleukin-6 concentrations, lung lavage TNF concentrations, neutrophil counts, and alveolar-to-arterial oxygen gradients and decreased circulating neutrophils and lymphocytes (P > or = 0.05 for all). Compared with controls, with both bacteria, except for lung lavage TNF concentrations (which decreased with intratracheal but not with intraperitoneal antibody to TNF), treatment route did not alter the effects of antibody to TNF on any parameter (P = not significant for all). Antibody to TNF reduced mortality rates (relative risk of death +/- SEM) with both E. coli (-1.6 +/- 0.6; P = 0.006) and S. aureus (-0.5 +/- 0.04; P = 0.185), but these reductions were greater with E. coli than with S. aureus in a trend approaching statistical significance (P = 0.09). Compared with controls, similarly (P = not significant) with both bacteria, antibody to TNF decreased lung lavage and tissue bacteria concentrations (both P < 0.05) and serum TNF concentration (P < 0.09) and increased circulating neutrophils and lymphocytes (both P < or = 0.01). Compared with S. aureus, with E. coli antibody to TNF decreased alveolar-to-arterial oxygen gradients (P = 0.04) and increased serum interleukin-6 concentrations (P = 0.003). CONCLUSION: Antibody to TNF improved host defense and survival rates with both lethal E. coli and S. aureus pneumonia, but protection was greater with E. coli, where TNF concentrations were higher than with S. aureus. The efficacy of antiinflammatory agents in sepsis may be altered by bacteria type.  (+info)

Cl- -dependent upregulation of human organic anion transporters: different effects on transport kinetics between hOAT1 and hOAT3. (2/31)

Chloride ion has a stimulatory effect on the transport of organic anions across renal basolateral membranes. However, the exact mechanisms at molecular levels have been unclear as of yet. Human organic anion transporters hOAT1 and hOAT3 play important roles in renal basolateral membranes. In this study, the effects of Cl(-) on the activities of these transporters were evaluated by using HEK293 cells stably expressing hOAT1 or hOAT3 (HEK-hOAT1 or HEK-hOAT3). The uptake of p-[(14)C]aminohippurate by HEK-hOAT1 and [(3)H]estrone sulfate by HEK-hOAT3 was greater in the presence of Cl(-) than in the presence of SO(4)(2-) or gluconate. Additionally, the uptake of various compounds by HEK-hOAT1 and HEK-hOAT3 was significantly higher in the Cl(-)-containing medium than the gluconate-containing medium, suggesting that the influences of Cl(-) are not dependent on substrate and that Cl(-) directly stimulates the functions of hOAT1 and hOAT3. The substitution of gluconate with Cl(-) did not change the K(m) value for the uptake of p-[(14)C]aminohippurate by HEK-hOAT1 but caused an approximately threefold increase in the maximal uptake rate (V(max)) value. On the other hand, replacement of gluconate with Cl(-) decreased the K(m) value for the uptake of [(3)H]estrone sulfate and cefotiam by HEK-hOAT3 to about one-third, while it did not change the V(max) value. In summary, Cl(-) upregulates the activities of both hOAT1 and hOAT3, but its effects on transport kinetics differ between these transporters. It was suggested that Cl(-) participates in the trans-location process for hOAT1, and the substrate recognition process for hOAT3.  (+info)

Adaptive responses of renal organic anion transporter 3 (OAT3) during cholestasis. (3/31)

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Multidrug-resistant Neisseria gonorrhoeae with reduced cefotaxime susceptibility is increasingly common in men who have sex with men, Amsterdam, the Netherlands. (4/31)

Antimicrobial resistance is an increasing problem in Neisseria gonorrhoeae (NG) treatment. Presently, third-generation parenteral cephalosporins, like ceftriaxone and cefotaxime, are the first option. Resistance to oral, but not to parenteral, third-generation cephalosporins has been reported previously. We analysed the microbial susceptibility (as minimum inhibitory concentration - MIC) of NG cultures obtained from high-risk visitors of the largest Dutch outpatient clinic for sexually transmitted infections (STI) in Amsterdam, the Netherlands. Among 1,596 visitors, we identified 102 patients with at least one NG isolate with reduced susceptibility to cefotaxime (0.125 microg/ml < MIC < or = 0.5 microg/ml). The percentage of NG isolates with reduced susceptibility to cefotaxime rose from 4.8% in 2006 to 12.1% in 2008 (chi2 17.5, p<0.001). With multivariate logistic regression, being a man who has sex with men (MSM) was significantly associated with reduced susceptibility to cefotaxime (p<0.001). Compared to susceptible NG isolates, those with decreased susceptiblity to cefotaxime were more often resistant also to penicillin (16.5% vs. 43.3%), tetracycline (21.5% vs. 68.9%) and ciprofloxacin (44.4% vs. 90.0%, all p<0.001). The increased prevalence of NG strains with reduced susceptibility to cefotaxime among MSM may herald resistance to third-generation parenteral cephalosporins. A considerable proportion of these strains show resistance to multiple antibiotics which could limit future NG treatment options.  (+info)

Molecular-weight-dependent, anionic-substrate-preferential transport of beta-lactam antibiotics via multidrug resistance-associated protein 4. (5/31)

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Interaction of cefpirome and a cephalosporinase from Citrobacter freundii GN7391. (6/31)

The interaction of cefpirome and a cephalosporinase from Citrobacter freundii, including hydrolysis and inhibition, was studied in comparison with those of cefotiam, cefotaxime, and ceftazidime. Cefpirome was hydrolyzed by the enzyme more rapidly at Vmax than were cefotaxime and ceftazidime. However, the low affinity of the enzyme for cefpirome caused a reduction in the hydrolytic rate of cefpirome at a low drug concentration (0.1 microM). The high stability of cefpirome at a low concentration explains the high antimicrobial activity of the agent against cephalosporinase-producing bacteria.  (+info)

Cefotiam disposition in markedly obese athlete patients, Japanese sumo wrestlers. (7/31)

Markedly obese athletes like Japanese sumo wrestlers may frequently suffer various traumas which result in the prophylaxis or treatment of posttraumatic infection with antibiotics. However, appropriate dosage regimens in this group of patients have not been fully known for many antibiotics. Therefore, we studied the kinetic disposition of cefotiam, a parenteral, broad-spectrum cephalosporin with activity against gram-positive and -negative bacteria, after an intravenous dose (2 g) infused over 30 min into 15 sumo wrestler patients with an excess body weight (130 to 220% of ideal body weight) and 10 control patients with a normal weight (90 to 102% of ideal body weight). Mean (+/- standard deviation) clearance and steady-state volume of distribution were significantly greater in the sumo wrestler than in the control group (38.3 +/- 9.4 versus 23.5 +/- 6.0 liters/h, P less than 0.001, and 30.2 +/- 8.0 versus 17.9 +/- 6.1 liters, P less than 0.001). Mean elimination half-life was slightly but significantly longer in the sumo wrestler than in the control group (0.91 +/- 0.14 versus 0.74 +/- 0.20 h, P less than 0.05). However, mean residence time did not differ between the two groups (0.79 +/- 0.10 versus 0.75 +/- 0.14 h). The statistical differences in clearance and volume of distribution between the two groups disappeared when these kinetic parameters were corrected for body surface area, but not for total body weight or ideal body weight. The results suggest that the dosage calculation of cefotiam, a hydrophilic antibiotic, should be made on the basis of body surface area in morbidly obese athlete or sumo wrestler patients. However, whether this recommendation should extend to other nonathlete obese subjects remains to be determined.  (+info)

In vitro evaluation of E1040, a new cephalosporin with potent antipseudomonal activity. (8/31)

E1040 is a new parenteral cephalosporin with a broad antibacterial spectrum and potent antipseudomonal activity. The compound was four- to eightfold more active than ceftazidime and cefsulodin against Pseudomonas aeruginosa (MIC of E1040 for 90% of strains tested [MIC90], 3.13 micrograms/ml). E1040 also showed a potent activity against other glucose-nonfermentative rods, including Acinetobacter species. The activities of E1040 against most species of the family Enterobacteriaceae were roughly comparable to the activities of ceftazidime and cefmenoxime and exceeded that of cefotiam. Against Citrobacter freundii (MIC90, 0.78 micrograms/ml), Enterobacter cloacae (MIC90, 3.13 micrograms/ml), and Enterobacter aerogenes (MIC90, 0.2 micrograms/ml), E1040 was 16- to 256-fold more active than ceftazidime and cefmenoxime. The activities of E1040 against gram-positive cocci and anaerobes were comparable to those of ceftazidime, but the compound was less active than cefmenoxime. E1040 was at least as resistant as ceftazidime and cefmenoxime to hydrolysis by various beta-lactamases and showed high affinities for penicillin-binding protein 3 of both Escherichia coli and P. aeruginosa.  (+info)

Synthesis and biological screening of 5-{[(4,6-disubstituted pyrimidine-2-yl)thio]methyl}-N-phenyl-1,3,4-thiadiazol-2-amines, MA Azam, B.R.P Kumar, S Shalini, B Suresh, TK Reddy, C
TY - JOUR. T1 - Laboratory and clinical studies of loracarbef. AU - Irabu, Yuei. AU - Inadome, Jun. AU - Fukuhara, Hiroshi. AU - Nakamura, Hiroaki. AU - Kaneshima, Hiroshi. AU - Shimoji, Katsuyoshi. AU - Kitsukawa, Keizou. AU - Shigeno, Yoshiteru. AU - Saito, Atsushi. AU - Furugen, Kyouko. AU - Nakasone, Isamu. AU - Taira, Shinko. AU - Kusano, Nobutika. AU - Hokama, Seitetsu. AU - Hokama, Tyoutetsu. PY - 1993. Y1 - 1993. N2 - We performed bacteriological and clinical evaluations of loracarbef (LCBF), a new oral carbacephem, in respiratory tract infections, with the following results. 1) Antimicrobial activity: The minimum inhibitory concentrations (MICs) of LCBF were measured in 302 clinically isolated strains, and compared with those of cefaclor, cefotiam, cefixime, cefteram and amoxicillin, using the MIC-2000 system. LCBF had wide antimicrobial activity against clinically isolated strains except methicillin-resistant Staphylococcus aureus, Enterococcus faecalis, Enterobacter cloacae, Serratia ...
The efficacy of a single dose of cefotiam as prophylaxis for postoperative infection was analyzed in a prospective randomized study of 840 patients undergoing either carniotomy (group I, n= 711) or...
6R,7R)-7-(((3,5-dichloro-4-oxo-1(4H)-pyridinyl) acetyl) amino)-3-(((5-methyl-1,3,4- thiadiazol- 2-yl)thio) methyl)-8 -oxo-5-thia-1-azabicyclo(4.2.0)oct-2-ene-2-carboxylic acid ...
Ethanesulfonic acid, 2-((2-(bis(2-chloroethyl)amino)tetrahydro-2H-1,3,2-oxazaphosphorin-4-yl)thio)-, compd.with cyclohexanamine (1:1) ...
All devices and instrumentations used in this clinical investigation bear the CE mark. They belong to the regular implants used for ACL repair at the study hospital since 2002. Except different graft anchoring, similar treatments apply to patients in both study groups. All participants undergo internationally accepted surgically procedures by a single surgeon (D.C.) with extensive experience in ACL repair using both the BioCryl® screw and RigidFix® cross pins. Also, postoperative care and rehabilitation programs do not differ from those employed outside a clinical trial.. All repairs are carried out under general anaesthesia, with the patient in a supine position. Perioperative antibiotic prophylaxis comprises 2 g of cefotiam. Patients receive 40 mg of enoxaparin daily for prophylaxis of thromboembolic events until full weight bearing.. The knee joint is accessed through two to three standard portals. Meniscal injuries are addressed with partial resection or repair.. Hamstring tendons are ...
Image @sumokyokai Even the best sumo wrestlers cant spend all his time in the dohyō. Sometimes theyve just got to go out and (bend the tree branches down with their super strength so they can) smell the flowers....
This page contains information on the chemical Acetic acid, ((5-((4-methylphenyl)amino)-1,3,4-thiadiazol-2-yl)thio)-, 2-(2-methylphenyl) hydrazide including: 2 synonyms/identifiers.
21-stone nine-time grand champ Harumafuji has apologised for the incident that left fellow wrestler Takanoiwa hospitalised with serious injuries
Buy this product, a biochemical for proteomics research, from Santa Cruz Biotechnology. Molecular Formula: C24H22ClN3O3S2, Molecular Weight: 500.03
An Axon was established in 1996 for the professional manufacturing of Reverse Osmosis unit and its components, starting from the production of Brassware of drinking faucet, diverter valve and the other relative accessory
In this article, youll get to know about the list of top 10 strongest WWE wrestlers. There are many great wrestlers in this industry but we are picking best of the best.
Quite a difference in cultures. Bud Selig, captain of the ship when USA Major League Baseball cruised through a steroid era continues in power and continues to rake in tens of millions of salary dollars. Meanwhile a venerable Japanese sumo wrestler, presiding over the national sport reigns in disgrace when two Russian sumo wrestlers possess marijuana. To the IHT for the summary: (further update with the Guardian; the Russians were the first sumo wrestlers expelled for life) Two popular Russian sumo wrestlers were slapped with lifetime bans from Japans ancient national sport for allegedly using marijuana and the head of...
Cherished for its serenity and deep ties to Japanese culture, sumo wrestling’s floundering reputation was dealt its latest blow yesterday when one of the ritualistic sport’s grand champions retired over a brawl with a junior fighter.
also, I think as long as you eat enough so that you are not getting super lean (and I was a high school wrestler...Ive seen some disquieting leanness...to the point of one tall guy doing 105, getting weaker and being called Skeletor)...but to the extent you dont get that...and muscle adds slow...youre NOT going to turn into Skeletor quickly, then youll be fine. Sure, you could probably get most musclar the fastest if you add a lot of weight like a defensive lineman or a sumo wrestler...but its perfectly reasonable to have ALTERNATE GOALS, which involve staying lean AS you add muscle ...
Chankonabe is wedded to sumo in the same way as whiskey is to the Wild West and cowboys; theyre both fuel for fightin. Terao Tsunefumi, the man behind this eponymous restaurant, is a well-respected sumo wrestler who had a career in the ring spanning ... ...
Jills treatment begins. For a month we catch the tube and thread the carcinogenic city streets to the hospital. She goes to bloods. She gets weighed. She cant lose weight. We must forget her diabetes and plump her up like a sumo wrestler. The chemo ward is full of bone-tired, gaunt and wasted patients being pumped with yards of poison by jolly nurses for hours on end. I bring Jill occasional coffeeless coffees and dying sandwiches. She doesnt want them. Or me. So I visit a place where carers care for carers. It is cringingly well-meaning and full of women who nod a lot and say yes before I finish a sentence and suggest I go Nordic walking or attend a mindfulness course. That should do it. I return to find Jill in a deep stupor. I shake her alive in my now established caring manner ...
Ōuchiyama Heikichi (born Heikichi Ōuchi, 19 June 1926 - 1 November 1985) was a sumo wrestler from Hitachinaka, Ibaraki, Japan. He made his professional debut in 1944, and reached the top makuuchi division in 1949. He reached the second highest rank of ōzeki in 1955, and was a runner-up in two tournaments. He was well known for his extraordinary size - at 2.02 m (6 ft 7 1⁄2 in) tall he was the tallest modern era ōzeki until Akebono in 1992. After his retirement in 1959 he worked as a coach at Tokitsukaze stable and Tatsutagawa stable until his death in 1985. He came from a family of fisherman, and helped out on the fishing boats by diving into the water to catch fish. He was not particularly large in elementary school, but increased rapidly in height after that. During the war he was recruited by the Imperial Japanese Navy, assigned to the anti-submarine patrol unit with his father. He joined Futabayama stable (later Tokitsukaze stable) in 1944 and reached the jūryō division in 1947. He ...
Cefmenoxime is a medicine available in a number of countries worldwide. A list of US medications equivalent to Cefmenoxime is available on the Drugs.com website.
Learn more about 5-amino-2h-tetrazol-2-yl-acetic-acid. We enable science by offering product choice, services, process excellence and our people make it happen.
Product Number , 78097775. CAS Number , 75738-58-8. EC , Molecular Formula , C16H18ClN9O5S3. Molecular Weight , 548.02. Storage Temp , Harmonized Tariff code , 29419000. Signal Word , ...
Furan, 2-[[(4-bromophenyl)thio]methyl]-5-nitro- | C11H8BrNO3S | CID 71397589 - structure, chemical names, physical and chemical properties, classification, patents, literature, biological activities, safety/hazards/toxicity information, supplier lists, and more.
The report comprises precise information, comprehensive analysis in two ways-qualitative and quantitative-industry experts inputs, and information provided by industry analysts and industry participants involved in the entire value chain. The report highlights exhaustive study of major market and their present trends, along with corresponding market segments. The Sulbenicillin Sodium report also provides data regarding various market factors and their impact on the overall market and its segments.. Global Research report analyzes the scope of Sulbenicillin Sodium industry including size, share, analysis, sales, supply, production, definition, specification, classification, demands, application, forecast trends, industry policy, and news. The report focuses on regional as well as global market, its key players, along with market segments including detailed study on various divisions and its applications. The report provides comprehensive information on each and every segment covered of the ...
Research Report on Europe Sulbenicillin Sodium Market Report 2017. The Report includes market price, demand, trends, size, Share, Growth, Forecast, Analysis & Overview.
Take football for instance, many offensive linemen pack on extra weight to play more effectively. Often they would be more healthy at a drastically lower weight. Linemen at the upper levels are up to 100 lbs over their optimal healthy weight, like a sumo wrestler. In (combat) sports where making weight is important, it often has to do with taking weight off. Getting into a sauna to cut water weight is not healthy, nor would competing before re-hydrating. Part of many training camps is working down closer to the proper weight. This comes from diet and lots of exercise. Runners dont try to cut water weight but to lose fat to be light ...
Some of you are most likely aware what a somatotype is. However for those that arent, a somatotype is basically the body shape/structure category that you fit into. To further elaborate, there are 3 somatotypes, an endomorph, mesomorph and ectomorph. An endomorph is generally more likely to store bodyfat, builds muscle fairly easily and usually not very tall. An ectomorph is generally very tall, low level of bodyfat and struggles to build muscle. A mesomorph builds muscle very easily, is very athletic and doesnt hold much bodyfat. Here are 3 examples: Endomorph - sumo wrestler Ectomorph - peter crouch Mesomorph - 100m sprinter Your genetics are what determine your somatotype. Everyone will be born with certain physical characteristics which may make them slightly ectomorphic, endomorphic or mesomorphic. It is however never a simple case of being one or the other. Usually people are somewhere in between 2 or even all 3 but leaning towards one or the other. If you imagine a triangle where the 3 points
The 2,000-year old cocktail: it tastes as bad as it looks... but it works. My back hurts. So does my throat, and I feel like a sumo wrestler is sitting on my head trying to pop my eyes out. Alas, the common cold has got me. Fortunately, I expect to be rid of it in 48-72 hours.
133506-45-3 - JFWAUHPDWGYCOJ-UHFFFAOYSA-N - Glycine, N-(((1-phenyl-1H-tetrazol-5-yl)thio)acetyl)- - Similar structures search, synonyms, formulas, resource links, and other chemical information.
2-(4-((2)-2-(((2)-2-((tert-butoxycarbonyl)amino)-3-phenylpropanoyl)amino)-3-oxo-3-(pentylamino)propyl)-2-(1(2)H-tetrazol-5-yl)phenoxy)acetic acid: structure in first source
Learn more about 5-4-methylpiperidin-1-yl-methyl-1h-tetrazol-1-yl-acetic-acid. We enable science by offering product choice, services, process excellence and our people make it happen.
Becoming a pro wrestler requires many of the same athletic and technical skills as those of a traditional, Olympic-style wrestler, but also has many unique aspects. Professional wrestling, for instance, emphasizes personal style and...
Professional guide for CeFAZolin. Includes: pharmacology, pharmacokinetics, contraindications, interactions, adverse reactions and more.
The Harrappan civilization was already established in India when the Aryans invaded, bringing with them the religion that would later become Hinduism. These people werent just lowly hunter-gatherers, either- they had advanced constructions in which they lived that featured toilets with flowing water sewage systems, the most advanced measurement system in the ancient world, the first dentists (evidence of the first drilled molars were found in Harrappan cities), and one of the oldest writing systems in the world. Despite all of that advancement, they were apparently shitty warriors and got the brakes beat off them by the Aryans, who conquered the Harappans and supplanted their existing culture with Aryan culture and religion. The produce of the Aryan religion were the Vedas, a series of Brahmanical texts written over time, not unlike the books of the Christian Bible. Similarly, these books often contradict each other, though the Vedas are fairly uniform in the stance on meat consumption- its ...
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...hed be struttin his oversized stuff in Sankeien Gardens this week. This basket-ball sized monstrosity was the size of a sumo wrestlers head. I only wish I had taken this photo with one of us little people next to it...
Since TBP is a generalized setting, it s useful in almost any game system. The strong similarity to George R.R. Martin s Wild Cards series may seem to predispose it to superhero games such as Champions, but that s not really the case. GURPS can handle it, obviously, but so can d20 Modern (though the latter would require some adjustments and new Feats to recreate some of the abilities). Because of the tone, it actually bears a stronger resemblance to the World of Darkness games, with their gloomy, dystopian look at reality; or better yet, the little-known sci-fi RPG Underground , by Ray Winninger, in which powers are often balanced with drawbacks. (For example, getting built-in armor at the cost of being built like a sumo wrestler or having skin like a rhinoceros, to say nothing of the insanity table in character generation ...
Reading Time: 4 minutes. Following is the chapter-wise summary of the book Freakonomics by Steven Levitt and Stephen Dubner.. Chapter 1: What do schoolteachers and Sumo wrestlers have in common?. In this chapter, the authors lay great emphasis on incentives and the response of people to the various incentives: economic, social and moral. Incentives are the means of urging people to do more of a good thing and less of a bad thing. The authors believe that Economics is, at the root, the study of incentives. To elaborate upon the different incentive structures involved in different situations, 3 case studies are included in the chapter.. The first case looks at how some teachers in the Chicago Public School System, in a response to the No Child Left Behind Law, manipulated the standardised test results of their students. The law rewarded schools that outperformed other schools in their overall test scores. The cheating teachers were detected by developing a computer algorithm which could detect ...
Just as sushi, Mount Fuji, and sumo wrestlers are synonymous with Japanese culture, so is sake, Japans famous rice wine. Dating back to the third century, sake has played a significant role in Japanese traditions. Around 250 A.D., sakes original recipe greatly differed from what it is today. Rice, millet, and chestnuts were chewed by villagers and then spat out into a communal barrel to ferment. Once the natural fermenting process was completed, the sake, then known as kuchikami no sake, or chewing in the mouth sake, was drank during special religious and social celebrations. Present at weddings and New Years celebrations, sake was also used as an offering to the protectors of the fields in Shinto rituals after each harvest. Sakes first recorded appearance in the United States was in 1885. Newly immigrated Japanese laborers brought their beverage of choice with them when they were first enlisted to work in Hawaiis sugarcane fields. In the last hundred years, sakes popularity has ...
[Study of clinical bacteriological efficacy in a cefmenoxime ototopical solution].: One percent cefmenoxime (CMX) ototopical solution was administered to 302 pa
m-[5-(Methylthio)-1H-tetrazol-1-yl]phenol/ACM94201884 can be provided in Alfa Chemistry. We are dedicated to provide our customers the best products and services.
In 1992, Anoaʻi was contacted by Vince McMahon of the World Wrestling Federation (WWF) and offered a roster spot along with The Samoans (Fatu and Samoan Savage). On an August 17, 1992 episode of Prime Time Wrestling the Samoans (soon to be the Headshrinkers) made their debut. Commentator Gorilla Monsoon made mention of another, larger Samoan that they would soon be seeing in the WWF.[10] Anoai would make his initial debut as Kokina in an untelevised match on September 1, 1992 at a WWF Superstars taping in Hershey, Pennsylvania. Wrestling as Kokina, he defeated Ron Neal.[11] This would be the only time that Anoai wrestled under his former gimmick. Shortly after he was offered a new gimmick: Yokozuna. Managed by Mr. Fuji, Yokozuna debuted on the October 31, 1992 edition of Superstars and portrayed a sumo wrestler competing under the Japanese flag.[2] He wore a sumo thong as part of his ring attire, but wore long tights underneath the thong, something that Vince McMahon and Yokozunas own cousin ...
A spokesman for the sumo association told AFP that a police report had been filed on behalf of the 27-year-old assaulted wrestler - Takanoiwa, also from Mongolia - by the fighters team.. The sumo association has set up a committee to investigate the issue but declined to comment further until we find out the truth about the incident, he said.. Police could not confirm they have received the report, but said: It would be true if the victims side said so.. Generally speaking, police start probing the case when we receive a report, said a spokesman, who declined to give his name.. The alleged assault took place last month when Mongolian wrestlers were relaxing over drinks after a tournament.. According to several media reports, Harumafuji flew into a rage when Takanoiwa tried to take out his phone to take a call during a conversation.. Kyokushuzan, a former Mongolian sumo wrestler who heard details from people who were at the scene, told private broadcaster TBS: When I heard about it, I ...
Tosanoumi Toshio (born February 16, 1972 as Toshio Yamamoto in Aki City, Kōchi Prefecture, Japan), is a former sumo wrestler. He first reached the top division of professional sumo in 1995, winning 13 special prizes and earning 11 kinboshi or gold stars for defeating yokozuna over his long career. The highest rank he reached was sekiwake. He retired in 2010 to become a coach at his stable, Isenoumi stable under the name of Tatekawa. After success in amateur sumo competitions while at Doshisha University, where he was a two-time winner of the All Western Japan Sumo Championships in 1992 and 1993, Yamamoto was recruited by former sekiwake Fujinokawa and joined Isenoumi stable. He was given the shikona of Tosanoumi, meaning sea of Tosa, from his native Kōchi Prefecture. Because of his amateur achievements he had makushita tsukedashi status and entered professional sumo in the third, makushita division in March 1994. He entered jūryō four tournaments later. Another four tournaments later he ...
Many abuse survivors have a high level of resilience as well as a pain threshold that could rival a sumo wrestler or someone walking on hot coals without so much as a grimace. Even if you feel like you can deal with further abuse even after the break-up, consider that this is truly a life or death situation. If you are escaping from a physical abuser, this affirmation hits home. Yet even if youre coming out of an emotionally abusive relationship, it also holds weight. I know many might not think of emotional violence as a life or death situation, but considering the suicides that occur from bullying and domestic violence and the fact that domestic violence survivors are actually at a higher risk of committing suicide, it is truer than we think. Each time we sacrifice our peace of mind for one more hit of the abuse rather than detoxing from the relationship, we also belittle, demean and abuse ourselves. These incidents build up collectively to reenact the same sense of hopelessness we had ...
Saturday evening found me in a rugby club which shall be nameless. A match sponsor had laid on food; entertainment in the shape of a singer was also on the menu. There was hardly anyone there. One worthy, the worst for wear, had to be restrained from throwing the tables and chairs around which everyone thought was great fun. I decided to move on to Kidwelly Hall for the Kidwellys Got Talent competition run by the Netball Club.. Most events in the town struggle for support but this time the hall was packed. The acts were really good and some of the singers sang in tune which was nice. For me the best act was Emily and Jenny who did a dance routine wearing enormous Sumo wrestler outfits. All done in the best possible taste. Only one person asked me for a job.. I was climbing into bed at twenty past one when my phone pinged. Do you fancy a dance? - a text from a female colleague. I think shed done it for a bet. Just a normal Saturday night in Kidwelly.. Assistance Dog ...
Dont specialize! Alexander the Great, long ago, noted that the Olympic athletes of his day turned out to be substandard soldiers- they had specialized to greatly, and only wanted to do the event that they excelled in, rather than being all around soldiers. The same was noted of the gladiators of ancient Rome, who turned out to be inferior soldiers in battle, since they were only skilled at one on one battle, and were mainly trained in pleasing the crowd, not killing quickly and efficiently. Also, as a side note, it is interesting that far from the movie version of gladiators, they were not lean and sporting a six-pack- the gladiators purposely ate lots of wheat, because they knew it would stimulate lots of fat storage. They were the Sumo Wrestlers of their day, since they wanted lots of fat to protect the stabbing swords from reader lives than Football players today. Football is really just kind of Gladiator Light ...
Montelukast Racemate (Acid),Montelukast Acid Racemate ; 1-[[[(1RS)-1-[3-[(1E)-2-(7-Chloro-2-quinolinyl)ethenyl]phenyl]-3-[2-(1-hydroxy-1-methylethyl)phenyl]propyl]thio]methyl]cyclopropaneacetic acid ;
The earliest known masked wrestler in the United States was The Masked Marvel who famously crashed the international tournament, which featured many of the top stars of the Farmer Burns-Frank Gotch era, held at the Manhattan Opera House in 1915. In North America, many professional wrestlers have traditionally worn masks after they had been used in an area, or territory, that their popularity and drawing ability diminished, it would be an easy way for a wrestler to begin working in a new area as a fresh face. (source: Wikipedia) ...
4-oxo-4H-chromene-2-carboxylic acid (2-(2-(4-(2-(6,7-dimethoxy-3,4-dihydro-1H-isoquinolin-2-yl)-ethyl)-phenyl)-2H-tetrazol-5-yl)-4,5-dimethoxyphenyl)amide: structure in first source
Bolivian wrestling (Lucha libre) is one of the most popular sports in the country. Women wrestlers are known as cholitas and have in the last ten years become popular in the sport.
The two famous wrestlers, Balla Gaye 2 and Eumeu Sene, competed in the crunch match dubbed 'Le Choc' at Demba Diop Stadium in the capital of Dakar.
Cefpirome (CAS NO.84957-29-9) is a white to yellowish white crystalline powder, slight specific smell. More easily soluble in water and not very dissolve in eth
Why HOAT? Many people are asking, why must we use HOAT in our PT Cruisers? , Why can t we go with some cheaper mix? , Can we mix in the green
本論文中合成三種類型之光折變高分子材料。第一種材料是將光導電分子混入非線性光學特性之高分子中而製成,透過在極化時之即時(In Situ)量測可了解非線性分子在電場作用下的定向(orientation)機制與熱穩定性。陷阱之位能及對應於不同能量之陷阱密度分布對光折變高分子之特性有決定性之影響, 本研究率先以熱刺激去極化電流(thermally stimulated current TSC) 探討此兩種與有關陷阱之特性,並探討混入之成份及主鏈結構對陷阱之位能及陷阱密度分布之影響。因為光折變高分子的組成成份包括非線性光學分子,電荷生成物種(CGM),電荷傳輸物種(CTM), 三者之吸光範圍彼此不同, 所以本研究除了改變組成成份之分子結構外, 亦嘗試使用不同波長之雷射作為讀寫光源, 也發現其對光折變高分子的特性有很大的影響
Wednesdays convention programming followed Tuesdays standard script: red meat for the base in the early hours, capped off with a slightly sweeter offering in prime time for independent consumption. But there was nothing routine about Bill Clintons speech.
Cefotiam Crowle A, Sbarbaro J, May M (1988). "Effects of isoniazid and of ceforanide against virulent tubercle bacilli in ...
The aminothiazole ring can be seen in the structure of Cefotiam. The majority of third generation cephalosporins have the ...
J01DC07 Cefotiam. J01DC08 Lorakarbef. J01DC09 Cefmetazol. J01DC10 Cefprozil. J01DC11 Ceforanid. J01DC12 Cefminoks. J01DC13 ...
... cefotiam MeSH D02.065.589.099.249.190.190.145 --- ceftizoxime MeSH D02.065.589.099.249.190.190.155 --- ceftriaxone MeSH D02.065 ...
... cefotiam (INN) cefovecin sodium (USAN) cefoxazole (INN) cefoxitin (INN) cefozopran (INN) cefpimizole (INN) cefpiramide (INN) ...
J01DC01 Cefoxitin J01DC02 Cefuroxime J01DC03 Cefamandole J01DC04 Cefaclor J01DC05 Cefotetan J01DC06 Cefonicide J01DC07 Cefotiam ...
... cefotiam 1981 - cefsulodin 1981 - latamoxef 1981 - netilmicin 1982 - ceftriaxone 1982 - micronomicin 1983 - cefmenoxime 1983 - ...
... was launched as Pansporin in February 1981 by Takeda Pharmaceutical of Japan and has been available as a generic since ... Cefotiam is a parenteral second-generation cephalosporin antibiotic. It has broad-spectrum activity against Gram-positive and ... Cefotiam inhibits final cross-linking stage of peptidoglycan production, thus inhibiting bacterial cell wall synthesis. It has ... Kolben M, Mandoki E, Ulm K, Freitag K (2001). "Randomized trial of cefotiam prophylaxis in the prevention of postoperative ...
InChI=1S/C20H22N4O10S/c1-9(25)33-10(2)34-19(28)15-11(7-32-20(21)29)8-35-18-14(17(27)24(15)18)22-16(26)13(23-30-3)12-5-4-6-31-12/h4-6,10,14,18H,7-8H2,1-3H3,(H2,21,29)(H,22,26)/b23-13-/t10?,14-,18-/m1/ ...
The production of benzylpenicillin involves fermentation, recovery and purification of the penicillin.[10] The fermentation process of the production of benzylpencillin is about obtaining the product. The presence of the product in solution inhibits the reaction and reduces the product rate and yield. Thus, in order to obtain the most product and increase the rate of reaction the product, would be continuously extracted out.[11] This is done by having the mold with either glucose, sucrose, lactose, startch, or detrin, nitrate, ammonium salt, corn steep liquor, peptone, meat or yeast extract, and little amounts of inorganic salts.[12] The recovery of the benzylpencillin is the most important part of the production process because it affects the purification steps if done wrong.[10] There are many different types of techniques to recover benzyl penicillin, aqueous two-phase extraction, liquid membrane extraction, microfiltration technique, and solvent subulation[10] Extraction is more commonly ...
... , sold under the brandname Merrem among others, is a broad-spectrum antibiotic used to treat a variety of bacterial infections.[1] Some of these include meningitis, intra-abdominal infection, pneumonia, sepsis, and anthrax.[1] It is given by injection into a vein.[1] Common side effects include nausea, diarrhea, constipation, headache, rash, and pain at the site of injection.[1] Serious side effects include Clostridium difficile infection, seizures, and allergic reactions including anaphylaxis.[1] Those who are allergic to other β-lactam antibiotics are more likely to be allergic to meropenem.[1] Use in pregnancy appears to be safe.[1] It is in the carbapenem family of medications.[1] Meropenem usually results in bacterial death through blocking their ability to make a cell wall.[1] It is more resistant to breakdown β-lactamase producing bacteria.[1] Meropenem was patented in 1983.[2] It was approved for medical use in the United States in 1996.[1] It is on the World Health ...
InChI=1S/C14H15N5O5S2/c1-5-3-25-12-8(11(21)19(12)9(5)13(22)23)17-10(20)7(18-24-2)6-4-26-14(15)16-6/h4,8,12H,3H2,1-2H3,(H2,15,16)(H,17,20)(H,22,23)/b18-7-/t8-,12-/m1/ ...
Bonow RO, Carabello BA, Kanu C, et al. (August 2006). "ACC/AHA 2006 guidelines for the management of patients with valvular heart disease: a report of the American College of Cardiology/American Heart Association Task Force on Practice Guidelines (writing committee to revise the 1998 Guidelines for the Management of Patients With Valvular Heart Disease): developed in collaboration with the Society of Cardiovascular Anesthesiologists: endorsed by the Society for Cardiovascular Angiography and Interventions and the Society of Thoracic Surgeons". Circulation. 114 (5): e84-231. doi:10.1161/CIRCULATIONAHA.106.176857. PMID 16880336 ...
Penicillin V is sometimes used in the treatment of odontogenic infections.. It is less active than benzylpenicillin (penicillin G) against Gram-negative bacteria.[9][10] Phenoxymethylpenicillin has a range of antimicrobial activity against Gram-positive bacteria that is similar to that of benzylpenicillin and a similar mode of action, but it is substantially less active than benzylpenicillin against Gram-negative bacteria.[9][10]. Phenoxymethylpenicillin is more acid-stable than benzylpenicillin, which allows it to be given orally.. Phenoxymethylpenicillin is usually used only for the treatment of mild to moderate infections, and not for severe or deep-seated infections since absorption can be unpredictable. Except for the treatment or prevention of infection with Streptococcus pyogenes (which is uniformly sensitive to penicillin), therapy should be guided by bacteriological studies (including sensitivity tests) and by clinical response.[11] People treated initially with parenteral ...
The in vitro activity of ceftolozane-tazobactam has been examined in five surveillance studies of isolates from Europe and North America.[8] In these studies, ceftolozane-tazobactam was notable for its activity against Pseudomonas aeruginosa, a moderately common cause of hospital-acquired infections that is commonly multi-drug resistant. Ninety percent of P. aeruginosa isolates were inhibited by a ceftolozane-tazobactam at a concentration of 4 μg/mL (MIC90), making it the most potent anti-pseudomonal antibiotic in clinical use. In these same studies, ceftolozane-tazobactam exhibited MIC90 values of ,1 μg/mL for Escherichia coli, Citrobacter koseri, Morganella morganii, Proteus mirabilis, Salmonella species, and Serratia marcescens. Somewhat poorer activity is observed for the Klebsiella and Enterobacter species, with the MIC90 for extended spectrum beta-lactamase (ESBL) expressing Klebsiella pneumonia being ,32 μg/mL. ...
A set of multienzymes (peptide synthase CepA, CepB, and CepC) are responsible for assembling the heptapeptide. (Figure 2). The organization of CepA, CepB, and Cep C closely resembles other peptide synthases such as those for surfactin (SrfA1, SrfA2, and SrfA3) and gramicidin (GrsA and GrsB).[41] Each peptide synthase activates codes for various amino acids to activate each domain. CepA codes for modules 1, 2, and 3. CepB codes for modules 4, 5, and 6, and CepC codes for module 7. The three peptide synthases are located at the start of the region of the bacterial genome linked with antibiotic biosynthesis, and span 27 kb.[41]. After the linear heptapeptide molecule is synthesized, vancomycin has to undergo further modifications, such as oxidative cross-linking and glycosylation, in trans[clarification needed] by distinct enzymes, referred to as tailoring enzymes, to become biologically active (Figure 3). To convert the linear heptapeptide, eight enzymes, open reading frames (ORFs) 7, 8, 9, 10, ...
InChI=1S/C16H21N7O7S3/c1-22-15(19-20-21-22)33-4-7-3-32-14-16(30-2,13(29)23(14)10(7)12(27)28)18-9(24)6-31-5-8(17)11(25)26/h8,14H,3-6,17H2,1-2H3,(H,18,24)(H,25,26)(H,27,28)/t8-,14-,16+/m1/s1 ‹See TfM› ...
... (SEF-di-nir) is a third-generation oral cephalosporin antibiotic sold under the brand names Cefzon and Omnicef. As of 2008, cefdinir, as Omnicef, was the highest-selling cephalosporin antibiotic in the United States, with more than US$585 million in retail sales of its generic versions alone.[1] Cefdinir is structurally similar to cefixime. It was discovered by Fujisawa Pharmaceutical Co., Ltd. (now Astellas) and introduced in 1991 under the brand name Cefzon.[2][3] Warner-Lambert licensed this cephalosporin for marketing in US from Fujisawa.[4] Abbott obtained U.S. marketing rights to Omnicef (cefdinir) in December 1998 through an agreement with Warner-Lambert Company.[5] It was approved by FDA on Dec 4, 1997.[6] It is available in US as Omnicef by Abbott Laboratories and in India as Cednir by Abbott, Kefnir by Glenmark, Cefdair by Xalra Pharma and Cefdiel by Ranbaxy. ...
Ceftolozane exerts bactericidal activities against susceptible gram-negative and gram-positive infections by inhibiting essential penicillin-binding proteins (PBPs), which are required for peptidoglycan cross-linking for bacterial cell wall synthesis, resulting in inhibition of cell wall synthesis and subsequent cell death. Ceftolozane is an inhibitor of PBPs of Pseudomonas aeruginosa (e.g. PBP1b, PBP1c, and PBP3) and E. coli (e.g., PBP3).[6][7] Tazobactam is a potent β-lactamase inhibitor of most common class A and C β-lactamases. Tazobactam has little clinically relevant in vitro activity against bacteria due to its reduced affinity to penicillin-binding proteins; however, it is an irreversible inhibitor of some β-lactamases (certain penicillinases and cephalosporinases) and can covalently bind to some chromosomal and plasmid-mediated bacterial beta-lactamases.[6] The addition of tazobactam strengthens the therapeutic response to ceftolozane, giving it the ability to treat a broader range ...
... is a second-generation cephalosporin antibiotic. It can be used to treat ear infections, skin infections, and other bacterial infections.[citation needed] It comes as a tablet and as a liquid suspension. Although there is a widely quoted cross-allergy risk of 10% between cephalosporins and penicillin, an article[1] has shown no increased risk for cross-allergy for cefprozil and several other second-generation or later cephalosporins. It was patented in 1983 and approved for medical use in 1992.[2] ...
... has the ability to kill a wide variety of bacteria. Imipenem is the active antibiotic agent and works by interfering with their ability to form cell walls, so the bacteria break up and die. Imipenem is rapidly degraded by the renal enzyme dehydropeptidase if administered alone (making it less effective); the metabolites can cause kidney damage.[11] Imipenem is a broad-spectrum betalactam antibiotic used for severe bacterial infections caused by susceptible organisms. Because imipenem is rapidly inactivated by renal dehydropeptidase I, it is given in combination with cilastatin, a DHP-I inhibitor which increases half-life and tissue penetration of imipenem. Imipenem/cilastatin, like other carbapenems, binds to bacterial penicillin-binding proteins and interferes with bacterial cell wall integrity and synthesis. It has activity against many aerobic and anaerobic Gram-positive and Gram-negative organisms, including Staphylococcus aureus, Streptococcus pyogenes, S. agalactiae, S. ...
Cefotaximă# • Ceftriaxonă# • Cefiximă# • Cefoperazon㇠• Cefotiam • Ceftazidimă# • Ceftizoximă • Ceftibuten • Cefditoren ( ...
Cefaclor • Cefamandole • Cefminox • Cefonicid • Ceforanide • Cefotiam • Cefprozil • Cefbuperazone • Cefuroxime • Cefuzonam • ...
InChI=1S/C14H24N2O7/c1-5-4-6(17)14(20)13(21-5)22-12-10(19)7(15-2)9(18)8(16-3)11(12)23-14/h5,7-13,15-16,18-20H,4H2,1-3H3/t5-,7-,8+,9+,10+,11-,12-,13+,14+/m1/s1 ...
سفتریاکسون (آیوپاک آدی: (6R,7R)-7-{[(2Z)-2-(2-amino-1,3-thiazol-4-yl)-,2-(methoxyimino)acetyl]amino}-3-{[(2-methyl-5,6-dioxo-1,2,5,6-tetrahydro-1,2,4-triazin-3-yl)thio]methyl}-8-oxo-5-thia-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylic acid, اینگیلیسجه: Ceftriaxone, (چینجه:頭孢曲松‎)، عربجه: سيفترياكسون‎، روسجا: Цефтриаксон) بیر شیمیایی بیلشیک دواء. بۇ دواءنین مول جرمیسی مول/قرم ۵۵۴٫۵۸ دیر. نیمه عمر یا یاریلانما سۆرعتی ۵٫۸-۸٫۷ ساعات زامان آپاریر و آنتی‌بیوتیک‌ اۆچون ایستیفاده اوْلونور. ...
سیکلوسرین (آیوپاک آدی: (R)-4-Amino-1,2-oxazolidin-3-one, اینگیلیسجه: Cycloserine, عربجه: سيكلوسيرين‎، روسجا: Циклосерин) بیر شیمیایی بیلشیک دواء. بۇ دواءنین مول جرمیسی مول/قرم ۱۰۲٫۰۹۲ دیر. متابولیسمی قاراجییرده باش وئریر. سیکلوسرین آنتی‌بیوتیک‌ اۆچون ایستیفاده اوْلونور. ...
Cefaclor • Cefamandole • Cefminox • Cefonicid • Ceforanide • Cefotiam • Cefprozil • Cefbuperazone • Cefuroxime • Cefuzonam • ...
سیلور سولفادیازین (آیوپاک آدی: Silver [(4-aminophenyl)sulfonyl](pyrimidin-2-yl)azanide, اینگیلیسجه: Silver sulfadiazine, (چینجه:磺胺嘧啶银‎)) بیر شیمیایی بیلشیک دواء. بۇ دواءنین مول جرمیسی مول/قرم ۳۵۷٫۱۴ دیر. سیلور سولفادیازین آنتی‌بیوتیک‌ اۆچون ایستیفاده اوْلونور. ...
... cefotiam, cefixime, cefteram and amoxicillin, using the MIC-2000 system. LCBF had wide antimicrobial activity against ... cefotiam, cefixime, cefteram and amoxicillin, using the MIC-2000 system. LCBF had wide antimicrobial activity against ... cefotiam, cefixime, cefteram and amoxicillin, using the MIC-2000 system. LCBF had wide antimicrobial activity against ... cefotiam, cefixime, cefteram and amoxicillin, using the MIC-2000 system. LCBF had wide antimicrobial activity against ...
Cefotiam was launched as Pansporin in February 1981 by Takeda Pharmaceutical of Japan and has been available as a generic since ... Cefotiam is a parenteral second-generation cephalosporin antibiotic. It has broad-spectrum activity against Gram-positive and ... Cefotiam inhibits final cross-linking stage of peptidoglycan production, thus inhibiting bacterial cell wall synthesis. It has ... Kolben M, Mandoki E, Ulm K, Freitag K (2001). "Randomized trial of cefotiam prophylaxis in the prevention of postoperative ...
Cefradol information about active ingredients, pharmaceutical forms and doses by Ferron, Cefradol indications, usages and related health products lists
Fodiclo information about active ingredients, pharmaceutical forms and doses by Interbat, Fodiclo indications, usages and related health products lists
Buy high quality Cefotiam Hexetil Hydrochloride (mixture of Diastereomers) 95789-30-3 from toronto research chemicals Inc. ... Cefotiam Hexetil Hydrochloride (mixture of Diastereomers). Catalogue number:. C243000. Chemical name: Cefotiam Hexetil ...
... 1-(Cyclohexyloxycarbonyloxy)ethyl ester dihydrochloride,Cefotiam hexetil hydrochloride,SCE-2174,Pansporin T,Taketiam, ... Cefotiam Dihydrochloride,Abbott 48999,CGP-14221/E,Halospor,Pansporin,Pansporine,Spizef,Sporidyn,1-(Cyclohexyloxycarbonyloxy) ... Cefotiam,(6R,7R)-7-[[(2-Amino-4-thiazolyl)acetyl]amino]-3-[[[1-[2-(dimethylamino)ethyl]-1H-tetrazol-5-yl]-thio]methyl]-8-oxo-5- ...
Cefotiam hcl Dosage Forms Injection and infusion Cefotiam hcl Indication For treatment of severe infections caused by ... Cefotiam hcl Patient Information No information avaliable Cefotiam hcl Organisms Affected Enteric bacteria and other eubacteria ... Cefotiam hcl Pharmacology Cefotiam is a third generation beta-lactam cephalosporin antibiotic. It has broad spectrum activity ... Cefotiam works by inhibiting bacterial cell wall biosynthesis. Cefotiam hcl Absorption Rapidly absorbed following intramuscular ...
ChEMBL Compound Description] ID:, InChI_Key:, Tradenames:CERADON , Pansporin, Synonyms:CGP-14221/E , CEFOTIAM HEXETIL ... HYDROCHLORIDE , ABBOTT-48999 , CEFOTIAM HYDROCHLORIDE , SCE 963 , CERADON , Pansporin , Ceradon , CEFOTIAM ... CEFOTIAM. ChEMBL Synonyms CGP-14221/E , CEFOTIAM HEXETIL HYDROCHLORIDE , ABBOTT-48999 , CEFOTIAM HYDROCHLORIDE , SCE 963 , ...
Although certain medicines should not be used together at all, in other cases two different medicines may be used together even if an interaction might occur. In these cases, your doctor may want to change the dose, or other precautions may be necessary. When you are receiving this vaccine, it is especially important that your healthcare professional know if you are taking any of the medicines listed below. The following interactions have been selected on the basis of their potential significance and are not necessarily all-inclusive.. Receiving this vaccine with any of the following medicines is usually not recommended, but may be required in some cases. If both medicines are prescribed together, your doctor may change the dose or how often you use one or both of the medicines.. ...
Detailed drug Information for Vaxchora. Includes common brand names, drug descriptions, warnings, side effects and dosing information.
Clinical evaluation of cefotiam in internal medicine].. Kawamura S, Sakata Y, Chiba Y, Yoshida Y, Aizawa M, Nara H, Yanagiya S ...
cefotiam HCl. antibacterial. glypressin. terlipressin acetate. vasopressor. ilozef. cefazolin Na. antibacterial. kefox. ...
Cefotiam Crowle A, Sbarbaro J, May M (1988). "Effects of isoniazid and of ceforanide against virulent tubercle bacilli in ...
Cefotiam. approved, investigational. yes. inducer. Details. DB00267. Cefmenoxime. approved. yes. inhibitor. Details. ...
An Efficacy of Antimicrobial Drug in the Experimental Model of Intracutaneous Infection in the Guinea-Pig Caused by ,I,Bacteroides fragili,/I, (1984 ...
Acutely Exaggerated Hepatitis B Induced by the Withdrawal of Immunosuppressants in a Seroconverted Renal Transplant Recipient : Report of a Case (2002 ...
Cefotiam hydrochloride. Cefbuperazone sodium. Topiramate. Cefroxadine hydrate. Cefotetan free acid. Cefcapene pivoxil ...
J01DC07 Cefotiam. J01DC08 Lorakarbef. J01DC09 Cefmetazol. J01DC10 Cefprozil. J01DC11 Ceforanid. J01DC12 Cefminoks. J01DC13 ...
Cefotiam: Loop Diuretics may enhance the nephrotoxic effect of Cefotiam. Monitor therapy ...
Cefotiam Dihydrochloride A cephalosporin antibiotic 66309-69-1. sc-394091 100 mg. $240.00 0 ...
Cefotiam. 2. g. P. 4. g. P. J01DC07. 1992 Cefotetan. 2. g. P. 4. g. P. J01DC05. 1992 ...
With intravenous cefotiam (Spizef) 2,0 g three times daily, the inflammation decreased, as seen clinically and with nuclear ... Unter systemischer antibiotischer Therapie mit Cefotiam (Spizef) 2,0 g 3-mal tgl. i.v. war die Entzündung sowohl klinisch als ...
Penicillin, ceftizoxime, and cefotiam are all β-lactam antibiotics. They can inhibit peptide bond formation by competitively ... Among the remaining four antibiotics, the three antibiotics including penicillin, ceftizoxime, and cefotiam are all β-lactam ... In the clinic, penicillin, ceftizoxime, cefotiam, and vancomycin are usually used to treat Gram-positive bacterial infections. ... However, for other antibiotics, including vancomycin, penicillin, ceftizoxime, cefotiam, clindamycin, and tinidazole, when they ...
Cefotiam Hydrochloride; Cefoxitin; Cefoxitin Sodium; Cefpimizole; Cefpimizole Sodium; Cefpiramide; Cefpiramide Sodium; ...
Cefotiam Hydrochloride; Cefoxitin; Cefoxitin Sodium; Cefpimizole; Cefpimizole Sodium; Cefpiramide; Cefpiramide Sodium; ...
J01D C07 - Cefotiam. J01D C08 - Lorakarbef. J01D C09 - Cefmetazol. J01D C10 - Cefprozil ...
J01D C07 - Cefotiam. J01D C08 - Lorakarbef. J01D C09 - Cefmetazol. J01D C10 - Cefprozil ...
Cefotiam hexetil. C21544. D07648. Cefotiam. RC00094. C12861_C21544. D01628. Cefditoren pivoxil. C21546. D07639. Cefditoren. ...
... cefotiam, Takeda Chemical Industries, Ltd.; cefaclor and kanamycin, Sigma Chemical Co., St. Louis, Mo.; cefdinir, Fujisawa ...
  • Cefuroxime, cefotiam and cefaclor are important substances of the second generation of Cephalosporins. (urology-textbook.com)
  • 1) Antimicrobial activity: The minimum inhibitory concentrations (MICs) of LCBF were measured in 302 clinically isolated strains, and compared with those of cefaclor, cefotiam, cefixime, cefteram and amoxicillin, using the MIC-2000 system. (elsevier.com)
  • Cefotiam is a parenteral second-generation cephalosporin antibiotic. (wikipedia.org)
  • Cefotiam is a third generation beta-lactam cephalosporin antibiotic. (pharmacycode.com)
  • The accumulation and the apical-to-basolateral transport of cephradine, cephalexin and cefixime, all p.o. agents, were significantly higher than those of cefotiam, a parenteral agent. (aspetjournals.org)
  • Cefepime (CFPM), cefotiam (CTM), cefozopran (CZOP), and flomoxef (FMOX) were each administered to 8â€"10. (ebscohost.com)
  • and Streptococcus pneumoniae, TOC-39 was twice as active as or more active than cefotiam, ceftazidime, flomoxef, and cefpirome. (asm.org)
  • Against Streptococcus pyogenes, TOC-39 was superior to cefotiam, ceftazidime, and flomoxef and was similar to cefpirome. (asm.org)
  • A 1999 study examined the biodegradability of the antibiotics cefotiam , ciprofloxacin, meropenem , penicillin G , and sulfamethoxazole as well as their toxicity to bacteria. (sourcewatch.org)
  • One study examined the biodegradability of the antibiotics cefotiam , ciprofloxacin , meropenem , penicillin G , and sulfamethoxazole as well as their toxicity to bacteria. (sourcewatch.org)
  • Serrapeptase has also been clinically studied and shown effective for the treatment of chronic bronchitis and venous inflammatory disease, and improving the effects of the antibiotics ofloxacin, cephalexin, and cefotiam. (forresthealth.com)
  • Cefotiam was launched as Pansporin in February 1981 by Takeda Pharmaceutical of Japan and has been available as a generic since February 1993. (wikipedia.org)
  • cefotiam, Takeda Chemical Industries, Ltd. (asm.org)
  • Cefotiam inhibits final cross-linking stage of peptidoglycan production, thus inhibiting bacterial cell wall synthesis. (wikipedia.org)
  • Cefotiam works by inhibiting bacterial cell wall biosynthesis. (pharmacycode.com)