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Organism no. tested ; E. cloacae 1, 246 ; Ceftazidime-susceptible 924 ; Ceftazidime-resistant 276 ; Cefepime-susceptible 218 ; Cefepime-resistant 39 ; E. aerogenes 336 ; Ceftazidime-susceptible 236 ; Ceftazidime-resistant 83 ; Cefepime-susceptible 77 ; Cefepime-resistant 2 ; C. freundii 186 ; Ceftazidime-susceptible 148 ; Ceftazidime-resistant 32 ; Cefepime-susceptible 25 ; Cefepime-resistant 5 ; S. marcescens 645 ; Ceftazidime-susceptible 618 ; Ceftazidime-resistant 13 ; Cefepime-susceptible 12 ; Cefepime-resistant 1.
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Benztropine .26 BETA-2 ADRENERGIC DRUGS .65 BETA-ADRENERGIC ANTAGONIST DRUGS .34 betaine .67 betamethasone .40 BETASERON.49 beta-val.40 betaxolol .34, 62 bethanechol.67 bevacizumab .21 bexarotene .24 BEXXAR.21 BEXXAR 131 IODINE .21 bicalutamide .21 BICNU.21 bidhist .64 bisoprol hydrochlorothizide.37 bisoprolol.34 bleomycin.21 BLOOD DETOXICANTS.55 BOOSTRIX .50 borofair.42 bortezomib .25 bosentan.35 BOTOX .64 botulinum toxin type a .64 bpm .64 brimonidine.62 brinzolamide .62 bromocriptine .31 brompheniramine.64 bubbli-pred .44 budeprion sr.31 budesonide.48, 67 bumetanide .36 BUPHENYL.46 buprenorphine .29 buprenorphine naloxone.29 buproban .33 bupropion sr .33 bupropion, er, sr .31 buspirone .28 butalbital compound codeine.29 butorphanol .25, 29 b-vex .65 BYETTA .44 CANASA . 48 captopril. 33, 37 captopril hydrochlorothiazide. 37 CARAFATE SUSPENSION. 48 carbamazepine . 28 CARBAMAZEPINES . 28 carbenicillin . 18 carbidopa . 31 carbidopa levodopa entacapone . 31 carbidopa levodopa, cr . 31 carbinoxamine. 65 carboplatin . 21 carboptic . 62 CARDIAC GLYCOSIDES . 35 CARDIOVASCULAR MEDICATIONS. 33 carisoprodal aspirin codeine . 52 carisoprodol . 52 carisoprodol compound. 52 carmustine. 21 carteolol . 62 cartia xt . 35 carvedilol . 34 CASODEX. 21 CEENU . 21 cefaclor, er . 15 cefadroxil . 15 cefazolin . 15 cefdinir . 15 cefepime . 15 cefotaxime . 15 cefoxitin. 15 cefpodoxime . 15 cefprozil. 15 CEFTIN SUSPENSION. 15 ceftriaxone. 15 cefuroxime. 15 CELEBREX . 53 celecoxib. 53 CELLCEPT. 21 CELONTIN. 33 CENTRALLY ACTING ANTIHYPERTENSIVES . 35 cephalexin . 15 CEPHALOSPORINS . 15 CEREZYME . 46 cerovel. 41 cesia . 59 cetuximab . 22 CHEMET . 46 chloral hydrate . 32 CHLORAL HYDRATE . 32 chlorambucil . 23 chloramphenicol. 15 CHLORAMPHENICOLS . 15 chlorhexidine. 43 CHLORHEXIDINE . 43 chlorhexidine gluconate . 43 chloroquine . 19 CHLOROQUINE. 19 chlorothiazide. 38 chlorpheniramine . 65 chlorpromazine . 26. Introduction IV to oral switch is the prompt conversion of IV antibiotic therapy to oral. Patients may be considered candidates for switching from IV to oral therapy once the patient has shown clinical improvement and is medically stable. Rationale The majority of patients with a severe infection who are adequately absorbing oral medication and initially require IV therapy can be safely switched to oral therapy within 48 hours. There are a number of advantages to support the prompt switch from IV to oral therapy these are as follows1, 2, 3: Reduction in the likelihood of hospital acquired bacteraemia and infected phlebitic IV lines. Saves both medical and nursing time. Reduces discomfort for patients and enables improved mobility and the possibility of earlier hospital discharge. Potential to significantly reduce treatment costs. Patient is more likely to receive antibiotics at the correct time. Potential reduction in the risk of adverse effects; errors in preparation are significantly higher with parenteral drugs, compared to oral formulation. Considerations for the early switch to oral therapy COMS1, 2, 3, 4 review at 24-48 hours. 24 III. THE DECISION BELOW ERRONEOUSLY DENIES PATENT-HOLDERS ANY RECOURSE FOR GOVERNMENT TAKINGS OF THEIR PROPERTY. Once it is established that Zoltek's patent rights are property under the Fifth Amendment, and that the conduct of the government or its authorized agents infringed upon, and hence took, that property, all that remains is to determine what remedies are available. The Fifth Amendment, of course, provides a "self-executing" constitutional remedy by imposing a duty on the government to pay just compensation for its taking of property. An adequate statutory or legal remedy, of course, will provide the required "just compensation" and avoid the perfection of a Fifth Amendment claim. Absent adequate statutory compensation, however, the Fifth Amendment itself provides a constitutional claim for compensation. In this case, the initial issue thus is whether 1498 provides compensation for the taking here and, if it does not, the issue of the constitutional remedy arises. The essential point, however, is that some remedy must exist, either by statute or under the Constitution, because to deny any remedy whatsoever, as did the court below, would violate the Fifth Amendment. A. Statutory Compensation for the Infringement in this Case Is Available under 28 U.S.C. 1498. The court below held that Zoltek lacked a claim for compensation under 1498 because some or all of the steps of the accused processes were performed outsides the United States. While the court was deeply conflicted as to the source of such geographic limitation whether through incorporation of 271 a ; directly into 1498 a ; or through the exclusion set out in 1498 c ; the net result was the same. But, under a proper construction of 1498 in light of constitutional concerns, neither of the court's rationales supports excluding a claim for compensation for the 271 g ; -based infringement at issue here. Samples were mixed with 0.25 volume of buffer B 250 mM Tris-HCl, pH 6.8, 10% [wt vol] SDS, 25% vol vol ; glycerol, 0.2% wt vol ; bromphenol blue, and 5% vol vol ; -mercaptoethanol ; , boiled for 5 min at 95C, and then subjected to 7.5% or 10% SDS-PAGE. After electrophoresis, the proteins were transferred to Hybond-C nitrocellulose filters GE Healthcare ; . Incubations with primary antibodies were performed at 4C using the following antibodies: 5 g ml IgG-7D4 SREBP-2 5 g ml IgG-R139 SCAP 0.4 g ml anti-Myc IgG-9E10 Myc-Insig-1 1: 1000 dilution of polyclonal Phospho-Akt Ser473 ; antibody P-Akt ; , and 1: 1000 dilution of Akt antibody total Akt and cefixime. Plasmid-mediated, extended-spectrum -lactamases ESBLs ; , so named because of their increased spectrum of activity, confer resistance to third- and fourthgeneration cephalosporins eg, ceftriaxone, cefotaxime, ceftazidime, cefepime and cefpirome ; and monobactams eg, aztreonam ; . ESBLs are inhibited by -lactamase inhibitors such as clavulanic acid and tazobactam. They are usually derived from earlier, narrow-spectrum -lactamases and differ from the parent enzyme by a few point mutations, which confer an extended spectrum of activity. The parent enzymes include the TEM, SHV and OXA families of -lactamases. To date, over 150 different ESBLs have been described. Isolations of ESBL-producing Enterobacteriaceae have been monitored in New Zealand since the mid-1990s. This paper reports: the trends in ESBL-producing isolates between 1996 and 2002 the performance of the ESBL-producing isolates identified in 2002 in phenotypic screening and confirmatory tests.

Legend: CAZ ceftazidime ; , AZT aztreonam ; , CTX cefotaxime ; , CRO ceftriaxone ; , AMC co-amoxiclav ; , TZP piperacillin tazobactam ; , AMK amikacin ; , NET netilmicin ; , FEP cefepime ; , FOX cefoxitin ; , SXT cotrimoxazole ; , IPM imipenem ; , CIP ciprofloxacin ; , CXM cefuroxime ; , AMP ampicillin ; Figure 1. Susceptibility Patterns of ESL Positive Cases and Controls and suprax.
Table 3. Influence of Physiologically High Vagal Tone and Administration of Acetylcholine on Refractory Period at 22 Atrial Sites Autonomic blockade RP msec ; High vagal tone RP ARP ARP msec ; msec ; % ; 123 128 127 Acetylcholine ARP ARP msec ; msec. Brand drugs pages lowest price phendimetrazine free and buy cheap time, phendimetrazine you pharmacy similar discount the net and cefpodoxime. RESULTS: The final cohort included 199 subjects and Streptococcus pneumoniae was the most frequent pathogen. In 40% of cases antibiotics were not in accordance with IDSA recommendations. At baseline there were few differences between the two groups as a function of guideline adherence. In unadjusted analysis, the duration of MV was longer in persons given IDSA-treatment regimens 11 days vs. 10 days ; . In a multivariate Cox proportional hazard model, two variables were independently associated with greater durations of MV: development of acute renal failure Hazard Ratio [HR] 1.47, 95% CI: 1.02-2.12 ; and prescription of an IDSA non-compliant regimen HR 1.40, 95% CI: 1.02-1.93 ; . Adjusted analysis indicated that patients not receiving a regimen consistent with IDSA guidelines spent an added 3 days on MV. Excluding the immunosuppressed subjects from the analysis n 17 ; did not alter our findings. CONCLUSION: Failure to follow formal antibiotic recommendations for the treatment of SCAP increases the need for continuing MV. CLINICAL IMPLICATIONS: Given the costs associated with MV, enhanced guideline compliance represents a means for both improving outcomes and enhancing resource utilization in the ICU. DISCLOSURE: Andrew Shorr, None. ANTIBIOTIC SUSCEPTIBILITY OF PSEUDOMONAS AERUGINOSA AND STAPHYLOCOCCUS AUREUS ISOLATES FROM US HOSPITAL INTENSIVE CARE UNITS ICUS ; : RESULTS OF THE ANTIMICROBIAL RESISTANCE MANAGEMENT ARM ; PROGRAM, 1997-2005 John G. Gums PharmD * University of Florida, Gainesville, FL PURPOSE: Risk factors for hospital-acquired pneumonia HAP ; include an ICU stay. The ARM Program, an ongoing project of the University of Florida, has collected antibiogram sensitivity report data from 364 US institutions. These data comprise a national aggregate database containing 29.5 million drug isolate comparisons. This study examined ICU isolate antimicrobial susceptibility rates of P aeruginosa and S aureus, two of the most common causes of HAP. METHODS: P aeruginosa and S aureus ICU isolate drug comparisons for 1997-2005 were reviewed for antibiotics used to treat HAP: carbapenems imipenem ; , aminoglycosides amikacin, gentamicin, tobramycin ; , fluoroquinolones ciprofloxacin, levofloxacin ; , cephalosporins ceftazidime, cefepime ; , extended-spectrum penicillin antibiotics piperacillin ; , or the combination of piperacillin and tazobactam a beta-lactamase inhibitor ; . Data were available for Northeast, Southeast, and Southwest, summed for a national total. RESULTS: For P aeruginosa n 17, 883 ; , national susceptibility to imipenem was 78.2% range, 58.1% in Southwest to 85.7% in Southeast to amikacin, 89.5% 87.7% in Southeast to 92.9% in Southwest gentamicin, 72.7% 53.8% in Southwest to 76% in Southeast tobramycin, 86.1% 71% in Southeast to 88.2% in Northeast ciprofloxacin, 67.2% 66.5% in Northeast to 67.6% in Southeast levofloxacin, 56.9% 46% in Southwest to 60.9% in Northeast ceftazidime, 78.7% 56.9% in Southwest to 81.9% in Northeast cefepime, 71.2% 57.9% in Southwest to 76.7% in Northeast piperacillin, 81.6% 62% in Southwest to 84.6% in Southeast and piperacillin tazobactam, 86.3% 80.8% in Southwest to 85.9% in Northeast. For S aureus n 8128 ; , national susceptibility rates ranged from 98% for amikacin and 96.2% to gentamicin to 37.5% for levofloxacin; these rates were 52.4% for imipenem and 53.6% for ciprofloxacin. CONCLUSION: P aeruginosa ICU isolates are most resistant to fluoroquinolones and most susceptible to amikacin, piperacillin tazobactam, and tobramycin. S aureus ICU isolates are most resistant to levofloxacin and most susceptible to amikacin and gentamicin. CLINICAL IMPLICATIONS: Optimal therapy for HAP should include assessment of risk factors, including local antimicrobial resistance patterns. These data suggest HAP should not be treated with fluoroquinolones if P aeruginosa or S aureus are suspected of being the infectious organisms. DISCLOSURE: John Gums, Grant monies from industry related sources ; AstraZeneca, Roche Pharmaceuticals. EFFECTS OF EARLY ENTERAL FEEDING ON THE OUTCOME OF CRITICALLY ILL MECHANICALLY VENTILATED MEDICAL PATIENTS ON VASOPRESSORS Pratik Doshi MD * Bruno DiGiovine MD, MPH Henry Ford Hospital, Detroit, MI PURPOSE: To determine the impact of early enteral feeding on the outcome of critically ill mechanically ventilated medical patients who are on vasopressors. METHODS: Retrospective analysis of prospectively collected multiinstitutional intensive care unit database of 1, 174 patients requiring mechanical ventilation and vasopressor medications. RESULTS: All patients were on vasopressors for at least 1 day, they were then divided according to whether or not they received enteral feeding within 48 hours of onset of mechanical ventilation. The 707 patients 60% ; who did were labeled as the "early feeding group" and the remaining 467 patients 40% ; were labeled as the "late feeding group". The overall ICU and hospital mortality was lower in the early feeding group 22.5% versus 28.3%, p 0.03 and 34% versus 44%, p 0.0006, respectively ; . The lower mortality rates in the early feeding group were more evident in the sickest group as defined by quartiles of severity illness scores. Three separate models were done using each of the different scores APACHE-II, SAPS-II and MPM-0 ; . In all models, early enteral feeding was associated with an approximately 20% decrease in ICU mortality and 25% decrease in hospital mortality, even in light of vasopressor use. We also analyzed the data after controlling for confounding by matching for propensity score. In this analysis, early feeding was. 070.0, 070.1, 070.20 070.44 , 070.49 , 070.51, 070.52, 070.53, Appendix A Appendix A Appendix A Appendix A Appendix A Appendix A Appendix B Appendix B Appendix B Appendix B Appendix B Appendix B Appendix B Table 5.10 Table 5.11 Table 5.12 Table 5.14 The addition of Table 5.10 will provide the ICD-9-CM procedure codes used to determine the initial population for all SCIP measures. The addition of Table 5.11 will provide the ICD-9-CM procedure codes used to determine the population for SCIP-Inf-4. The addition of Table 5.12 will provide the list of ICD-9-CM procedure codes used to determine the population for SCIP-Inf-7. 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You should also be aware that you must always consult your doctors professional before ordering online offline or taking using prescription cefepime as side effects can occur. Pseudomonas aeruginosa peritonitis * oral quinolone as one of the antibiotics * Alternative drugs include ceftazidime, cefepime tobramycin or piperacillin * piperacillin : 4 g every 12 hours IV in adults. cannot be added to with aminoglycosides and keftab.
The stents we currently use most often, except for two, are mostly bare metal they are not coated with any drug.

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71 ; ORION CORPORATION [FI FI]; Orionintie 1, FIN-02200 Espoo FI ; . for all designated States except pour tous les tats dsigns sauf US ; 72, 75 ; HAPPONEN, Pertti [FI FI]; Lakkapolku 2 H, FIN-70280 Kuopio FI ; . SERKKOLA, Elina [FI FI]; Kuusmiehentie 34 C 5, FIN-00670 Helsinki FI ; . NISSINEN, Erk ki [FI FI]; Ellipsipolku 4 A 23, FIN-02210 Espoo FI ; . 74 ; ORION CORPORATION; Orion Pharma, Industrial Property Rights, P.O. Box 65, FIN02101 Espoo FI ; . 81 ; ZW. 84 ; AP GH A61K 31 00 11 ; 061638 21 ; PCT CA03 00077 22 ; 27 Jan jan 2003 27.01.2003 ; 25 ; en 30 ; 350, 954 ; en 25 Jan jan 2002 25.01.2002 ; US 13 ; A2 and cinnarizine. 2006: Abbott enters into a partnership with Earvin "Magic" Johnson and the Magic Johnson Foundation to address the alarming rise of HIV infections in the African-American community. The "I Stand With Magic" campaign istandwithmagic ; , launched on World AIDS Day, December 1, 2006, is a multi-year, multi-million dollar effort to provide educational tools and resources for African Americans and other minority communities to slow the spread of HIV. 2006: Abbott Fund and Baylor open a new pediatric AIDS clinic in Lilongwe, Malawi in November. Today, this clinic serves more than 1, 000 children living with HIV AIDS. Baylor has opened clinics, modeled after the first clinic in Romania, in Malawi, Botswana, Leshotho, Swaziland and Uganda. An additional clinic is under construction in Burkina Faso. 2006: Abbott announces the Aluvia tablet would cost 0 per patient per year in Africa and the LDCs. In August, Abbott expands the differential pricing program to create a new tier for low and lower middle-income countries, as defined by the World Bank and the United Nations. 2007: Abbott Fund opens an office in Dar es Salaam, Tanzania its first outside of Illinois. The Fund also brings on new partners to help advance its Abbott Global AIDS Care programs, including Catholic Medical Mission Board, Elizabeth Glaser Pediatric AIDS Foundation and Family Health International. 2007: In April, Abbott announces a further reduction in the price to , 000 per patient per year in low and lower middle-income countries. After these reductions in the price in low- and lower middle-income countries, Kaletra and Aluvia are now the most affordable protease inhibitors, compared to other boosted or unboosted protease inhibitors that are recommended in the World Health Organization WHO ; , U.S. Department of Health and Human Services DHHS ; , the British HIV Association BHIVA ; , and the International AIDS Society IAS ; -USA guidelines.
In May, Canon announced two new printers, the 17-inch output iPF5100 and the 24-inch output iPF6100. Both printers feature reformulated black, matte black, gray and photo gray inks to reduce bronzing and increase scratch resistance. Because the print heads on the new models are also all-new, the reformulated inks are not backward compatible with the iPF5000. With these models, Canon introduces a color calibration system, with the goal of bringing the print performance to a known state for consistent color accuracy, print to print and printer to printer. This should mean that a custom profile created for one printer-paper combination will be suitable for another printer using the same system and other similar Canon printers. Canon claims color variance between different printers will average no more than 2 delta-E based on Canon's tests with Canon Premium Matte Paper ; . A 1 delta-E difference is considered a tonal difference, and is barely visible. A difference of 3 delta-E is considered acceptable for most purposes. The new printers' calibration system is not to be confused with ICC profiling capability. For that you'll need printer profiling tools like the GretagMacbeth X-rite Eye-One Photo, Eye-One Pro and ProfileMaker 5 Photostudio. Canon does say that the printers will ship with a much improved set of generic profiles. These printers also introduce Canon Kyuanos color technology, which should make it simpler to factor in the viewing conditions where the print will be displayed. It might be possible to use an Eye-One Display 2 or Eye-One Pro spectrophotometer to read the exact light, then have Canon's optional PosterArtist 2007 software use this data to apply an appropriate rendering correction during printing. The downside is that the system is compatible only with the Microsoft Windows Vista operating system--no Windows XP or Apple OS X support. If you have a newer Mac with an Intel processor, it should be possible to set up a bootable partition on a hard drive using VISTA as the OS. The iPF6100 sports a larger LCD panel that graphically displays the ink level in each of the 12 cartridges. The display is accessed through the Info button on the printer or through the print drivers on your computer. At press time it seemed likely that the iPF6100 will include a printer stand as standard equipment. Canon says that it has improved printer documentation in response to customer feedback, with search capability and online Web links throughout the user manual, printer driver and software, and the LCD panel on the iPF6100 will also display illustrated instructions. Both printers feature rollfeed units, but the iPF6100 has no cassette feed option. Expected for release this month, the iPF6100 will have an MSRP of about , 495. The iPF5100, scheduled to ship in August, will have an MSRP of about , 995. Also shipping this month, Poster Artist 2007 will sell for 9 and domperidone.

Ceftriaxone category interpretation based on NCCLS 2001 guidelines M100-S11 ; . In January, 2002, the NCCLS modified the interpretive standard for pneumococci when testing ceftriaxone, cefotaxime and cefepime Document M100-S12 ; . The MIC breakpoints for these drugs for pneumococci isolated from patients with meningitis are now interpreted differently from pneumococci isolated from nonmeningitis cases. The new interpretation for all three antibiotics is provided in Table 12. Table 12.Jan, 2002 NCCLS ceftriaxone, cefotaxime & cefepime interpretive standards for S. pneumoniae Susceptible Intermediate Resistant MIC breakpoint MIC breakpoint MIC breakpoint 0.5 g ml 1.0 g ml 2.0 g ml Meningitis Nonmeningitis 1.0 g ml 2.0 g ml 4.0 g ml.
Plan to have two weeks' extra medication squirreled away in case you can't access your doctor, or the idc pharmacy has staffing or delivery problems and cisapride and cefepime. Mental health professionals should consider consulting a similar publication from the tapa center for jail diversion: working with people with mental illness involved in the criminal justice system: what mental health service providers need to know, which is available at: gainsctr pdfs tapa massaro!

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Yaksh, T. L., and Malkmus, S. A. 1999 ; . Animal models of intrathecal and epidural drug delivery. In Spinal Drug Delivery T. L. Yaksh, ed., pp. 317-344. Elsevier Science B.V., Amsterdam.

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Thus, there is a high rate of clinical failure when cephalosporins are given for enterobacter bacteremia, even when the initial culture results indicated susceptibility other options for treating enterobacter infections include cefepime, quinolones, carbapenems, or amtnoglycosides. 5.1.1 Penicillins 5.1.1.3 Broad-spectrum penicillinsa amoxycillin ampicillin co-amoxiclav 5.1.1.4 Anti-pseudomonal penicillins piperacillin tazobactam ticarcillin clavulanate 5.1.2 Cephalosporins, cephamycins & other -lactams Cephalosporins and cephamycins cefaclor cefadroxil cefepime cefixime cefodizime cefotaxime cefotetan cefoxitin cefoperazone cefpirome cefpodoxime cefprozil ceftazidime ceftibuten ceftriaxone cefuroxime cephalexin cefamandole cephazolin Cephradine. 2. Health care providers should be aware of the option of using continuous or extended combined hormonal contraception and consider offering it to women for contraception, medical reasons, and personal preferences. III-A and cefixime. If your doctor says you have had a hypersensitivity reaction to this medicine, never take this medicine again.
Deb new medicare drug benefits plan june 12, 2005 9: good morning professionals, the medicare modernization act of 2005 prescription drug benefit, part d, is due to take effect january 1, 200 education is important for providers and beneficiaries since the new benefit will impact many seniors.

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Uses: this medication is used for external genital and external anal.

Can she be suffering from drug interactions. Has obtained permission to use one of the most well-known methods of causality evaluation within the adverse drug reaction module. This scale, known as the Naranjo algorithm7, is regarded by many as the most valid and consistently reproducible scale. The algorithm is a series of ten questions with each individual question assigned a weighted value dependent upon the response of "Yes, " "No, " and "Don't Know." The sum of these values has a corresponding probability assignment. After completing the series of questions and selecting the desired responses, a calculation tool within the program computes the sum and carries forward one of the four probability values, Highly Probable, Probable, Possible, or Doubtful. This algorithm is accessed through the product page, and is applicable to each individual suspected medication associated with a report. Hospitalized patient 1st dose antibiotic should be given in 4 hrs of presentation ; Recommended EMPIRIC regimens: 1. General medical ward: Preferred - 3rd gen. cephalosporin cefotaxime ceftriaxone ; + macrolide Alternate - anti-pneumococcal fluoroquinolone alone 2. ICU without suspicion for pseudomonas combination therapy suggested ; : Preferred - beta-lactam cefotaxime ceftriaxone, ampicillin sulbactam, piperacillin tazobactam ; + macrolide Alternate - beta-lactam + fluoroquinolone Beta-lactam allergy - anti-pneumococcal fluoroquinolone + - clindamycin 3. Suspected aspiration - anti-pneumococal fluoroquinolone + - a betalactam beta-lactamase inhibitor ampicillin sulbactam, piperacillin tazobactam ; or clindamycin or metronidazole 4. Suspicion for pseudomonas - antipseudomonal agent piperacillin, piperacillin tazobactam, a carbepenem, cefepime or aztreonam ; + ciprofloxacin; or antipseudomonal agent + an aminoglycoside + either macrolide or fluoroquinolone 5. Influenza with bacterial superinfection - beta-lactam see above ; or anti-pneumococcal fluoroquinolone Note: Antibiotic therapy should be adjusted to narrow-spectrum, pathogen-specific therapy whenever possible based on sputum blood or other culture results.
Responsibility for treatment In addition to their other responsibilities, a * licensed veterinarian is responsible to the * Corporation for the consequences of the administration, prescription, or provision of any * drug, medicine, or * foreign substance to or for a * race horse and any other veterinary treatment provided to the * horse by the veterinarian. Reporting deaths of horses The * licensed owner of a * horse registered with a * licensed operator to * race in Alberta, or a * licensed veterinarian, must report to an * official veterinarian the death of a horse, whether the death is from natural causes or by euthanasia, immediately after the death occurs. Division 3 Veterinary Care at Race Meetings.