Invanz

Business Editors/Health & Pharmaceutical Writers

WHITEHOUSE STATION, N.J.--(BUSINESS WIRE)--Nov. 29, 2001

Merck & Co., Inc. announced today that the Food and Drug Administration has approved Invanz(TM)(ertapenem sodium), a new once-a-day injectable antibiotic for the treatment of moderate to severe infections in adults caused by many common gram-positive and gram-negative aerobic and anaerobic bacteria.

Invanz is a structurally unique 1-(beta) methyl-carbapenem related to the class of antibiotics known as beta-lactams, which includes penicillins and cephalosporins.

Invanz (pronounced in-vance) is given as a 1-gram dose, once a day, by intravenous infusion or intramuscular injection for the treatment of the following infections caused by susceptible strains of the designated bacteria:

These infections are caused by a range of bacteria and are often community-acquired. Complicated intra-abdominal, complicated skin and skin structure, and acute pelvic infections are typically "mixed" infections, in that they are polymicrobial and involve both aerobic and anaerobic bacteria.

"Invanz offers physicians a new once-a-day treatment option, with excellent aerobic and extensive anaerobic coverage of many bacteria, making it suitable for first-line treatment of complicated intra-abdominal and skin/skin structure infections," said Robin Isaacs, M.D., senior director, Clinical Research, Merck Research Laboratories. "In clinical trials, Invanz was compared to the antibiotics Rocephin(R)(6) and Zosyn(R)(7) and demonstrated excellent clinical efficacy and overall safety and tolerability."

Excellent clinical efficacy demonstrated across all indications

studied

The efficacy, safety and tolerability of Invanz was evaluated in over 1,900 patients enrolled in 13 multi-center clinical trials that compared Invanz to either ceftriaxone or piperacillin/tazobactam. The studies evaluated the overall clinical and microbiological response to Invanz in five infectious disease categories. The primary analysis for all the studies was assessment of response to treatment at pre-specified, post-therapy follow-up visits. Therapy with Invanz ranged from 3 to 14 days. In some of the clinical studies, treatment with Invanz was followed by therapy with an appropriate oral antibiotic.

Study results from the pivotal Phase IIb/III trials showed success rates with Invanz were equivalent to those of the comparator antibiotics. Specifically:

-- Complicated intra-abdominal infections: 83.6 percent (163 of

195) of patients on Invanz were clinically and

microbiologically cured at four to six weeks post-therapy

compared with 80.4 percent (152 of 189) for

piperacillin/tazobactam;

-- Complicated skin and skin structure infections: 83.9 percent

(141 of 168) of patients on Invanz were clinically cured 10 to

21 days post-therapy compared with 85.3 percent (145 of 170)

for piperacillin/tazobactam;

-- Community-acquired pneumonia: In the first study, 92.3 percent

(168 of 182) of patients on Invanz were clinically cured 7 to

14 days post-therapy compared with 91.0 percent (183 of 201)

for ceftriaxone; and in the second study, 91.0 percent (91 of

100) of patients on Invanz were clinically cured 7 to 14 days

post-therapy compared with 91.8 percent (45 of 49) for

ceftriaxone;

-- Complicated urinary tract infections: 89.5 percent (229 of

256) of patients on Invanz were microbiologically cured five

to nine days post-therapy compared with 91.1 percent (204 of

224) for ceftriaxone in the combined studies; and

-- Acute pelvic infections: 93.9 percent (153 of 163) of patients

on Invanz were clinically cured two to four weeks post-therapy

compared with 91.5 percent (140 of 153) for

piperacillin/tazobactam.

Excellent overall safety and tolerability profile demonstrated in clinical studies

The overall safety and tolerability profile of Invanz in the clinical studies was comparable to ceftriaxone and piperacillin/tazobactam. Across studies in five infectious disease categories, the most common clinical side effects thought to be drug-related that occurred in one percent or more of patients receiving Invanz in the trials, including those who were switched to therapy with an oral antimicrobial, were diarrhea (5.5 percent), infused vein complications (3.7 percent), nausea (3.1 percent), headache (2.2 percent), vaginitis in females (2.1 percent), vein inflammation (phlebitis/ thrombophlebitis) (1.3 percent) and vomiting (1.1 percent).

In one of the 13 clinical studies, death occurred in 4.7 percent (15 of 316) of patients receiving Invanz and 2.6 percent (8 of 307) of patients receiving comparator drug for treatment of complicated intra-abdominal infections. These deaths occurred in patients with significant co-morbidity and/or severe baseline infections. Investigators considered these events to be unrelated to study drugs.

In the clinical studies, the rate of seizures reported during therapy plus the 14-day follow-up period in patients treated with Invanz was 0.5 percent, irrespective of drug relationship. These experiences have occurred most commonly in patients with central nervous system disorders and/or compromised renal function.

Pseudomembranous colitis (inflammation of the large intestine) has been reported with nearly all antibacterial agents, including Invanz, and may range in severity from mild to life threatening. It is important to consider this diagnosis in patients who present with diarrhea subsequent to the administration of antibacterial agents.

Invanz: a structure and spectrum unlike other carbapenems

Invanz is a structurally unique, 1-(beta) methyl-carbapenem related to the class of antibiotics known as beta-lactams. Invanz has a spectrum of bacterial activity that is distinct from other carbapenems in that Invanz does not cover Pseudomonas and Acinetobacter species - pathogens typically associated with hospital-acquired infections. Like other beta-lactams, Invanz works by blocking the formation of bacterial cell wall, thereby causing cell death.

Coverage suitable for first-line use in complicated intra-abdominal and skin and skin structure infections

The treatment of complicated intra-abdominal and skin and skin structure infections often requires multiple daily doses of a single antibiotic or combination therapy with multiple antibiotics to ensure appropriate coverage of suspected bacteria. Invanz, a once-a-day antibiotic, offers a simplified dosing regimen versus multiple daily dosing and combination therapy. In addition, Invanz can be administered initially (empirically) while awaiting tests to determine the bacteria causing the infection.

Important information about Invanz

Invanz should not be used in patients with known hypersensitivity to any component of the product, or to other drugs in the same class, or patients who have demonstrated anaphylactic reactions to beta-lactams. Invanz administered intramuscularly should not be used in patients with a known hypersensitivity to local anesthetics of the amide type. Serious and occasionally fatal hypersensitivity (anaphylactic) reactions have been reported in patients receiving therapy with beta-lactams.

As with other antibiotics, prolonged use of Invanz may result in overgrowth of nonsusceptible organisms. Repeated evaluation of the patient's condition is essential. If a new infection occurs during therapy, appropriate measures should be taken. Appropriate specimens for examination of bacteria should be obtained in order to isolate and identify the causative organisms and to determine their susceptibility to Invanz.

Invanz for intravenous or intramuscular administration

Invanz will be supplied in single-dose vials for administration either intravenously or intramusclularly following reconstitution or dilution. The dose of Invanz in adults is 1 gram given once a day. Invanz is expected to be available early in the first quarter of 2002.

About Merck

Merck & Co., Inc. has a long-standing history of anti-infective research, including antimicrobial, antiviral, antifungal and antiparasitic agents. Merck's anti-infectives development began over 60 years ago with research into sulfonamides and penicillin in the 1930s. The approval of Invanz marks the 15th marketed antimicrobial for Merck. Many of these agents have made important contributions in the treatment of community-acquired, mixed, and hospital-acquired infections.

Merck & Co., Inc. is a leading research-driven pharmaceutical products and services company. Merck discovers, develops, manufactures and markets a broad range of innovative products to improve human and animal health, directly or through its joint ventures. Merck-Medco Managed Care manages pharmacy benefits for employers, insurers and other plan sponsors, encouraging the appropriate use of medicines and providing disease management programs. Through these complementary capabilities, Merck works to improve quality of life and contain overall health-care costs.

Full prescribing information for Invanz(TM) is attached.

Editor's Note: The clinical studies to evaluate the efficacy

and safety of Invanz did not include treatment against anthrax

infections. Invanz is not indicated for the treatment of

anthrax.

--------

(1) Complicated intra-abdominal infections due to Escherichia

coli, Clostridium clostridiiforme, Eubacterium lentum,

Peptostreptococcus species, Bacteroides fragilis, Bacteroides

distasonis, Bacteroides ovatus, Bacteroides thetaiotaomicron,

or Bacteroides uniformis.

(2) Complicated skin and skin structure infections due to

Staphylococcus aureus (methicillin susceptible strains only),

Streptococcus pyogenes, Escherichia coli, or

Peptostreptococcus species.

(3) Community acquired pneumonia due to Streptococcus pneumoniae

(penicillin susceptible strains only) including cases with

concurrent bacteremia, Haemophilus influenzae (beta-lactamase

negative strains only), or Moraxella catarrhalis.

(4) Complicated urinary tract infections due to Escherichia coli,

including cases with concurrent bacteremia, or Klebsiella

pneumoniae.

(5) Acute pelvic infections due to Streptococcus agalactiae,

Escherichia coli, Bacteroides fragilis, Porphyromonas

asaccharolytica, Peptostreptococcus species, or Prevotella

bivia.

(6) Rocephin(R)is the registered trademark for ceftriaxone sodium

marketed by Hoffman-LaRoche Inc.

(7) Zosyn(R) is the registered trademark for piperacillin

sodium/tazobactam sodium marketed by Wyeth-Ayerst

Laboratories.

Invanz(TM) is the Merck trademark for ertapenem sodium.

VERSION: 9500000 - November 2001 INVANZ(TM) (ERTAPENEM FOR INJECTION)

For Intravenous or Intramuscular Use

DESCRIPTION

INVANZ(a) (Ertapenem for Injection) is a sterile, synthetic, parenteral, 1-(beta) methyl-carbapenem that is structurally related to beta-lactam antibiotics.

Chemically, INVANZ is described as (4R-(3(3S*,5S*),4(alpha), 5(beta),6(beta)(R*)))-3-((5-(((3-carboxyphenyl)amino)carbonyl)-3- pyrrolidinyl)thio)-6-(1-hydroxyethyl)-4-methyl-7-oxo-1-azabicyclo (3.2.0)hept-2-ene-2-carboxylic acid monosodium salt. Its molecular weight is 497.50. The empirical formula is C22H24N3O7SNa, and its structural formula is:

(GRAPHIC OMITTED)

Ertapenem sodium is a white to off-white hygroscopic, weakly crystalline powder. It is soluble in water and 0.9% sodium chloride solution, practically insoluble in ethanol, and insoluble in isopropyl acetate and tetrahydrofuran.

INVANZ is supplied as sterile lyophilized powder for intravenous infusion after reconstitution with appropriate diluent (see DOSAGE AND ADMINISTRATION, PREPARATION OF SOLUTION) and transfer to 50 mL 0.9% Sodium Chloride Injection or for intramuscular injection following reconstitution with 1% lidocaine hydrochloride. Each vial contains 1.046 grams ertapenem sodium, equivalent to 1 gram ertapenem. The sodium content is approximately 137 mg (approximately 6.0 mEq).

Each vial of INVANZ contains the following inactive ingredients: 175 mg sodium bicarbonate and sodium hydroxide to adjust pH to 7.5.

CLINICAL PHARMACOLOGY

Pharmacokinetics

Average plasma concentrations (mcg/mL) of ertapenem following a single 30-minute infusion of a 1 g intravenous (IV) dose and administration of a single 1 g intramuscular (IM) dose in healthy young adults are presented in Table 1.

The area under the plasma concentration-time curve (AUC) of ertapenem increased less-than dose-proportional based on total ertapenem concentrations over the 0.5 to 2 g dose range, whereas the AUC increased greater-than dose proportional based on unbound ertapenem concentrations. Ertapenem exhibits non-linear pharmacokinetics due to concentration-dependent plasma protein binding at the proposed therapeutic dose. (See CLINICAL PHARMACOLOGY, Distribution.)

(a) Trademark of MERCK & CO., Inc.

COPYRIGHT(c)MERCK & CO., Inc., 2001

All rights reserved

There is no accumulation of ertapenem following multiple IV or IM 1 g daily doses in healthy adults. Absorption

Ertapenem, reconstituted with 1% lidocaine HCl injection, USP (in saline without epinephrine), is almost completely absorbed following intramuscular (IM) administration at the recommended dose of 1 g. The mean bioavailability is approximately 90%. Following 1 g daily IM administration, mean peak plasma concentrations (Cmax) are achieved in approximately 2.3 hours (Tmax).

Distribution

Ertapenem is highly bound to human plasma proteins, primarily albumin. In healthy young adults, the protein binding of ertapenem decreases as plasma concentrations increase, from approximately 95% bound at an approximate plasma concentration of less than 100 micrograms (mcg)/mL to approximately 85% bound at an approximate plasma concentration of 300 mcg/mL.

The apparent volume of distribution at steady state (Vss) of ertapenem is approximately 8.2 liters.

The concentrations of ertapenem achieved in suction-induced skin blister fluid at each sampling point on the third day of 1 g once daily IV doses are presented in Table 2. The ratio of AUC0-24 in skin blister fluid/AUC0-24 in plasma is 0.61.

The concentration of ertapenem in breast milk from 5 lactating women with pelvic infections (5 to 14 days postpartum) was measured at random time points daily for 5 consecutive days following the last 1 g dose of intravenous therapy (3-10 days of therapy). The concentration of ertapenem in breast milk within 24 hours of the last dose of therapy in all 5 women ranged from less than 0.13 (lower limit of quantitation) to 0.38 mcg/mL; peak concentrations were not assessed. By day 5 after discontinuation of therapy, the level of ertapenem was undetectable in the breast milk of 4 women and below the lower limit of quantitation (less than 0.13 mcg/mL) in 1 woman.

Metabolism

In healthy young adults, after infusion of 1 g IV radiolabeled ertapenem, the plasma radioactivity consists predominantly (94%) of ertapenem. The major metabolite of ertapenem is the inactive ring-opened derivative formed by hydrolysis of the beta-lactam ring.

In vitro studies in human liver microsomes indicate that ertapenem does not inhibit metabolism mediated by any of the following cytochrome p450 (CYP) isoforms: 1A2, 2C9, 2C19, 2D6, 2E1 and 3A4. (See DRUG INTERACTIONS.)

In vitro studies indicate that ertapenem does not inhibit P-glycoprotein-mediated transport of digoxin or vinblastine and that ertapenem is not a substrate for P-glycoprotein-mediated transport. (See PRECAUTIONS, Drug Interactions.)

Elimination

Ertapenem is eliminated primarily by the kidneys. The mean plasma half-life in healthy young adults is approximately 4 hours and the plasma clearance is approximately 1.8 L/hour.

Following the administration of 1 g IV radiolabeled ertapenem to healthy young adults, approximately 80% is recovered in urine and 10% in feces. Of the 80% recovered in urine, approximately 38% is excreted as unchanged drug and approximately 37% as the ring-opened metabolite.

In healthy young adults given a 1 g IV dose, the mean percentage of the administered dose excreted in urine was 17.4% during 0-2 hours postdose, 5.4% during 4-6 hours postdose, and 2.4% during 12-24 hours postdose.

Special Populations

Renal Insufficiency

Total and unbound fractions of ertapenem pharmacokinetics were investigated in 26 adult subjects (31 to 80 years of age) with varying degrees of renal impairment. Following a single 1 g IV dose of ertapenem, the unbound AUC increased 1.5-fold and 2.3-fold in subjects with mild renal insufficiency (CLCR 60-90 mL/min/1.73 m2) and moderate renal insufficiency (CLCR 31-59 mL/min/1.73 m2), respectively, compared with healthy young subjects (25 to 45 years of age). No dosage adjustment is necessary in patients with CLCR greater than or equal to31 mL/min/1.73 m2. The unbound AUC increased 4.4-fold and 7.6-fold in subjects with advanced renal insufficiency (CLCR 5-30 mL/min/1.73 m2) and end-stage renal insufficiency (CLCR less than 10 mL/min/1.73 m2), respectively, compared with healthy young subjects. The effects of renal insufficiency on AUC of total drug were of smaller magnitude. The recommended dose of ertapenem in patients with CLCR less than or equal to 30 mL/min/1.73 m2 is 0.5 grams every 24 hours. Following a single 1 g IV dose given immediately prior to a 4 hour hemodialysis session in 5 patients with end-stage renal insufficiency, approximately 30% of the dose was recovered in the dialysate. A supplementary dose of 150 mg is recommended if ertapenem is administered within 6 hours prior to hemodialysis. (See DOSAGE AND ADMINISTRATION.)

Hepatic Insufficiency

The pharmacokinetics of ertapenem in patients with hepatic insufficiency have not been established. However, ertapenem does not appear to undergo hepatic metabolism based on in vitro studies and approximately 10% of an administered dose is recovered in the feces. (See PRECAUTIONS and DOSAGE AND ADMINISTRATION.)

Gender

The effect of gender on the pharmacokinetics of ertapenem was evaluated in healthy male (n=8) and healthy female (n=8) subjects. The differences observed could be attributed to body size when body weight was taken into consideration. No dose adjustment is recommended based on gender.

Geriatric Patients

The impact of age on the pharmacokinetics of ertapenem was evaluated in healthy male (n=7) and healthy female (n=7) subjects greater than or equal to65 years of age. The total and unbound AUC increased 37% and 67%, respectively, in elderly adults relative to young adults. These changes were attributed to age-related changes in creatinine clearance. No dosage adjustment is necessary for elderly patients with normal (for their age) renal function.

Pediatric Patients

The pharmacokinetics of ertapenem in pediatric patients have not been established.

Microbiology

Ertapenem has in vitro activity against gram-positive and gram-negative aerobic and anaerobic bacteria. The bactericidal activity of ertapenem results from the inhibition of cell wall synthesis and is mediated through ertapenem binding to penicillin binding proteins (PBPs). In Escherichia coli, it has strong affinity toward PBPs 1a, 1b, 2, 3, 4 and 5 with preference for PBPs 2 and 3. Ertapenem is stable against hydrolysis by a variety of beta-lactamases, including penicillinases, and cephalosporinases and extended spectrum beta-lactamases. Ertapenem is hydrolyzed by metallo-beta-lactamases.

Ertapenem has been shown to be active against most strains of the following microorganisms in vitro and in clinical infections. (See INDICATIONS AND USAGE): Aerobic gram-positive microorganisms:

Staphylococcus aureus (methicillin susceptible strains only)

Streptococcus agalactiae

Streptococcus pneumoniae (penicillin susceptible strains only)

Streptococcus pyogenes

Note: Methicillin-resistant staphylococci and Enterococcus spp.

are resistant to ertapenem. Aerobic gram-negative microorganisms:

Escherichia coli

Haemophilus influenzae (Beta-lactamase negative strains only)

Klebsiella pneumoniae

Moraxella catarrhalis Anaerobic microorganisms:

Bacteroides fragilis

Bacteroides distasonis

Bacteroides ovatus

Bacteroides thetaiotaomicron

Bacteroides uniformis

Clostridium clostridioforme

Eubacterium lentum

Peptostreptococcus species

Porphyromonas asaccharolytica

Prevotella bivia

The following in vitro data are available, but their clinical significance is unknown.

At least 90% of the following microorganisms exhibit an in vitro minimum inhibitory concentration (MIC) less than or equal to the susceptible breakpoint for ertapenem; however, the safety and effectiveness of ertapenem in treating clinical infections due to these microorganisms have not been established in adequate and well-controlled clinical studies:

Aerobic gram-positive microorganisms:

Streptococcus pneumoniae (penicillin-intermediate strains only) Aerobic gram-negative microorganisms:

Citrobacter freundii

Citrobacter koseri

Enterobacter aerogenes

Enterobacter cloacae

Haemophilus influenzae (Beta-lactamase positive strains)

Haemophilus parainfluenzae

Klebsiella oxytoca (excluding ESBL producing strains)

Morganella morganii

Proteus mirabilis

Proteus vulgaris

Serratia marcescens Anaerobic microorganisms:

Clostridium perfringens

Fusobacterium spp. Susceptibility Tests:

When available, the results of in vitro susceptibility tests should be provided to the physician as periodic reports which describe the susceptibility profile of nosocomial and community-acquired pathogens. These reports should aid the physician in selecting the most effective antimicrobial.

Dilution Techniques:

Quantitative methods are used to determine antimicrobial minimum inhibitory concentrations (MICs). These MICs provide estimates of the susceptibility of bacteria to antimicrobial compounds. The MICs should be determined using a standardized procedure. Standardized procedures are based on a broth dilution method1,4 or equivalent with standardized inoculum concentrations and standardized concentrations of ertapenem powder. The MIC values should be interpreted according to the following criteria:

Note: Staphylococcus spp. can be considered susceptible to ertapenem if the penicillin MIC is less than or equal to 0.12 (mu)g/mL. If the penicillin MIC is greater than 0.12 (mu)g/mL, then test oxacillin. Staphylococcus aureus can be considered susceptible to ertapenem if the oxacillin MIC is less than or equal to 2.0 (mu)g/mL and resistant to ertapenem if the oxacillin MIC is greater than or equal to 4.0 (mu)g/mL. Coagulase negative staphylococci can be considered susceptible to ertapenem if the oxacillin MIC is less than or equal to 0.25 (mu)g/mL and resistant to ertapenem if the oxacillin MIC greater than or equal to0.5 (mu)g/mL.

(a)This interpretive standard is applicable only to broth microdilution susceptibility tests with Haemophilus spp. using Haemophilus Test Medium (HTM)1 inoculated with a direct colony suspension and incubated in ambient air at 35(degree)C for 20-24 hrs.

(b)The current absence of data in resistant strains precludes defining any results other than "Susceptible". Strains yielding MIC results suggestive of a "nonsusceptible" category should be submitted to a reference laboratory for further testing.

(c)This interpretive standard is applicable only to broth microdilution susceptibility tests using cation-adjusted Mueller-Hinton broth with 2-5% lysed horse blood inoculated with direct colony suspension and incubated in ambient air at 35(degree)C for 20-24 hrs.

(d)Streptococcus pneumoniae that are susceptible to penicillin (penicillin MIC less than or equal to 0.06 (mu)g/mL) can be considered susceptible to ertapenem. Testing of ertapenem against penicillin- intermediate or penicillin-resistant isolates is not recommended since reliable interpretive criteria for ertapenem are not available.

(e)Streptococcus spp. that are susceptible to penicillin (MIC less than or equal to 0.12 (mu)g/mL) can be considered susceptible to ertapenem. Testing of ertapenem against penicillin-intermediate or penicillin-resistant isolates is not recommended since reliable interpretive criteria for ertapenem are not available.

A report of "Susceptible" indicates that the pathogen is likely to be inhibited if the antimicrobial compound in blood reaches the concentrations usually achievable. A report of "Intermediate" indicates that the result should be considered equivocal, and, if the microorganism is not fully susceptible to alternative, clinically feasible drugs, the test should be repeated. This category implies possible clinical applicability in body sites where the drug is physiologically concentrated or in situations where high dosage of drug can be used. This category also provides a buffer zone which prevents small uncontrolled technical factors from causing major discrepancies in interpretation. A report of "Resistant" indicates that the pathogen is not likely to be inhibited if the antimicrobial compound in the blood reaches the concentrations usually achievable; other therapy should be selected.

Standardized susceptibility test procedures require the use of laboratory control microorganisms to control the technical aspects of the laboratory procedures. Quality control microorganisms are specific strains of organisms with intrinsic biological properties. QC strains are very stable strains which will give a standard and repeatable susceptibility pattern. The specific strains used for microbiological quality control are not clinically significant. Standard ertapenem powder should provide the following MIC values.

(f)This quality control range is applicable to only H. influenzae ATCC 49766 tested by the broth microdilution procedure using HTM(1) inoculated with a direct colony suspension and incubated in ambient air at 35(degree)C for 20-24 hrs.

(g)This quality control range is applicable to only S. pneumoniae ATCC 49619 tested by a broth microdilution procedure using cation-adjusted Mueller-Hinton broth with 2-5% lysed horse blood inoculated with a direct colony suspension and incubated in ambient air at 35(degree)C for 20-24 hrs.

Diffusion Techniques:

Quantitative methods that require measurement of zone diameters also provide reproducible estimates of the susceptibility of bacteria to antimicrobial compounds. One such standardized procedure(2,4) requires the use of standardized inoculum concentrations. This procedure uses paper disks impregnated with 10-(mu)g ertapenem to test the susceptibility of microorganisms to ertapenem.

Reports from the laboratory providing results of the standard single-disk susceptibility test with a 10-(mu)g ertapenem disk should be interpreted according to the following criteria:

Note: Staphylococcus spp. can be considered susceptible to ertapenem if the penicillin (10 U disk) zone is greater than or equal to 29 mm. If the penicillin zone is less than or greater to 28 mm, then test oxacillin by disk diffusion (1 (mu)g disk). Staphylococcus aureus can be considered susceptible to ertapenem if the oxacillin (1 (mu)g disk) zone is greater than or equal to 13 mm and resistant to ertapenem if the oxacillin zone is less than or equal to 10 mm. Coagulase negative staphylococci can be considered susceptible to ertapenem if the oxacillin zone is greater than or equal to 18 mm and resistant to ertapenem if the oxacillin (1 (mu)g disk) zone is less than or equal to 17 mm.

(h)This zone diameter standard is applicable only to tests performed by disk diffusion with Haemophilus spp. using HTM(2) inoculated with a direct colony suspension and incubated in 5% CO2 at 35(degree)C for 16-18 hrs.

(i)These zone diameter standards apply only to tests performed using Mueller-Hinton agar supplemented with 5% sheep blood inoculated with a direct colony suspension and incubated in 5% CO2 at 35(degree)C for 20-24 hrs.

(j)Streptococcus pneumoniae that is susceptible to penicillin (1-(mu)g oxacillin disk zone diameter greater than or equal to 20 mm), can be considered susceptible to ertapenem. Isolates with 1-(mu)g oxacillin zone diameter less than or equal to 19 mm should be tested against ertapenem using an MIC method.

(k)These zone diameter standards apply only to tests performed using Mueller-Hinton agar supplemented with 5% sheep blood inoculated with a direct colony suspension and in ambient air at 35(degree)C for 20-24 hrs.

(l)Beta-hemolytic Streptococcus spp. that are susceptible to penicillin (10-units penicillin disk zone diameter greater than or equal to 24 mm), can be considered susceptible to ertapenem. Isolates with 10-units penicillin disk zone diameter less than 24 mm should be tested against ertapenem using an MIC method. Penicillin disk diffusion interpretive criteria are not available for viridans group streptococci and they should not be tested against ertapenem.

Interpretation should be as stated above for results using dilution techniques. Interpretation involves correlation of the diameter obtained in the disk test with the MIC for ertapenem.

As with standardized dilution techniques, diffusion methods require the use of laboratory control microorganisms that are used to control the technical aspects of the laboratory procedures. Quality control microorganisms are specific strains of organisms with intrinsic biological properties. QC strains are very stable strains that will give a standard and repeatable susceptibility pattern. The specific strains used for microbiological quality control are not clinically significant. For the diffusion technique, the 10-(mu)g ertapenem disk should provide the following zone diameters in these laboratory quality control strains:

(m)This quality control range is applicable to Haemophilus influenzae ATCC 49766 tested by disk diffusion using HTM2 agar inoculated with a direct colony suspension and incubated in 5% CO2 at 35(degree)C for 16-18 hrs.

(n)This quality control range is applicable to Streptococcus pneumoniae ATCC 49619 tested by disk diffusion using Mueller-Hinton agar supplemented with 5% sheep blood inoculated with a direct colony suspension and incubated in 5% CO2 at 35(degree)C for 20-24 hrs.

Anaerobic Techniques:

For anaerobic bacteria, the susceptibility to ertapenem as MICs can be determined by standardized test methods(3). The MIC values obtained should be interpreted according to the following criteria:

Interpretation is identical to that stated above for results using dilution techniques.

As with other susceptibility techniques, the use of laboratory control microorganisms is required to control the technical aspects of the laboratory standardized procedures. Standardized ertapenem powder should provide the following MIC values:

(O)These quality control ranges are applicable only to agar dilution using Brucella agar supplemented with hemin, vitamin K1 and 5% defibrinated or laked sheep blood inoculated with a direct colony suspension or a 6- to 24-hour fresh culture in enriched thioglycollate medium and incubated in an anaerobic jar or chamber at 35-37(degree)C for 42-48 hrs.

INDICATIONS AND USAGE

INVANZ is indicated for the treatment of adult patients with the following moderate to severe infections caused by susceptible strains of the designated microorganisms. (See DOSAGE AND ADMINISTRATION):

Complicated Intra-abdominal Infections due to Escherichia coli, Clostridium clostridioforme, Eubacterium lentum, Peptostreptococcus species, Bacteroides fragilis, Bacteroides distasonis, Bacteroides ovatus, Bacteroides thetaiotaomicron, or Bacteroides uniformis.

Complicated Skin and Skin Structure Infections due to Staphylococcus aureus (methicillin susceptible strains only), Streptococcus pyogenes, Escherichia coli, or Peptostreptococcus species.

Community Acquired Pneumonia due to Streptococcus pneumoniae (penicillin susceptible strains only) including cases with concurrent bacteremia, Haemophilus influenzae (beta-lactamase negative strains only), or Moraxella catarrhalis.

Complicated Urinary Tract Infections including pyelonephritis due to Escherichia coli, including cases with concurrent bacteremia, or Klebsiella pneumoniae.

Acute Pelvic Infections including postpartum endomyometritis, septic abortion and post surgical gynecologic infections due to Streptococcus agalactiae, Escherichia coli, Bacteroides fragilis, Porphyromonas asaccharolytica, Peptostreptococcus species, or Prevotella bivia.

Appropriate specimens for bacteriological examination should be obtained in order to isolate and identify the causative organisms and to determine their susceptibility to ertapenem. Therapy with INVANZ (ertapenem) may be initiated empirically before results of these tests are known; once results become available, antimicrobial therapy should be adjusted accordingly.

CONTRAINDICATIONS

INVANZ is contraindicated in patients with known hypersensitivity to any component of this product or to other drugs in the same class or in patients who have demonstrated anaphylactic reactions to beta-lactams.

Due to the use of lidocaine HCl as a diluent, INVANZ administered intramuscularly is contraindicated in patients with a known hypersensitivity to local anesthetics of the amide type. (Refer to the prescribing information for lidocaine HCl.)

WARNINGS

SERIOUS AND OCCASIONALLY FATAL HYPERSENSITIVITY (ANAPHYLACTIC) REACTIONS HAVE BEEN REPORTED IN PATIENTS RECEIVING THERAPY WITH BETA-LACTAMS. THESE REACTIONS ARE MORE LIKELY TO OCCUR IN INDIVIDUALS WITH A HISTORY OF SENSITIVITY TO MULTIPLE ALLERGENS. THERE HAVE BEEN REPORTS OF INDIVIDUALS WITH A HISTORY OF PENICILLIN HYPERSENSITIVITY WHO HAVE EXPERIENCED SEVERE HYPERSENSITIVITY REACTIONS WHEN TREATED WITH ANOTHER BETA-LACTAM. BEFORE INITIATING THERAPY WITH INVANZ, CAREFUL INQUIRY SHOULD BE MADE CONCERNING PREVIOUS HYPERSENSITIVITY REACTIONS TO PENICILLINS, CEPHALOSPORINS, OTHER BETA-LACTAMS AND OTHER ALLERGENS. IF AN ALLERGIC REACTION TO INVANZ OCCURS, DISCONTINUE THE DRUG IMMEDIATELY. SERIOUS ANAPHYLACTIC REACTIONS REQUIRE IMMEDIATE EMERGENCY TREATMENT WITH EPINEPHRINE, OXYGEN, INTRAVENOUS STEROIDS, AND AIRWAY MANAGEMENT, INCLUDING INTUBATION. OTHER THERAPY MAY ALSO BE ADMINISTERED AS INDICATED.

Seizures and other CNS adverse experiences have been reported during treatment with INVANZ. (See PRECAUTIONS and ADVERSE REACTIONS.)

Pseudomembranous colitis has been reported with nearly all antibacterial agents, including ertapenem, and may range in severity from mild to life-threatening. Therefore, it is important to consider this diagnosis in patients who present with diarrhea subsequent to the administration of antibacterial agents.

Treatment with antibacterial agents alters the normal flora of the colon and may permit overgrowth of clostridia. Studies indicate that a toxin produced by Clostridium difficile is a primary cause of "antibiotic-associated colitis".

After the diagnosis of pseudomembranous colitis has been established, therapeutic measures should be initiated. Mild cases of pseudomembranous colitis usually respond to drug discontinuation alone. In moderate to severe cases, consideration should be given to management with fluids and electrolytes, protein supplementation and treatment with an antibacterial drug clinically effective against Clostridium difficile colitis.

Lidocaine HCl is the diluent for intramuscular administration of INVANZ. Refer to the prescribing information for lidocaine HCl.

PRECAUTIONS

General

During clinical investigations in adult patients treated with INVANZ (1 g once a day), seizures, irrespective of drug relationship, occurred in 0.5% of patients during study therapy plus 14-day follow-up period. (See ADVERSE REACTIONS.) These experiences have occurred most commonly in patients with CNS disorders (e.g., brain lesions or history of seizures) and/or compromised renal function. Close adherence to the recommended dosage regimen is urged, especially in patients with known factors that predispose to convulsive activity. Anticonvulsant therapy should be continued in patients with known seizure disorders. If focal tremors, myoclonus, or seizures occur, patients should be evaluated neurologically, placed on anticonvulsant therapy if not already instituted, and the dosage of INVANZ re-examined to determine whether it should be decreased or the antibiotic discontinued. Dosage adjustment of INVANZ is recommended in patients with reduced renal function. (See DOSAGE AND ADMINISTRATION.)

As with other antibiotics, prolonged use of INVANZ may result in overgrowth of non-susceptible organisms. Repeated evaluation of the patient's condition is essential. If superinfection occurs during therapy, appropriate measures should be taken.

Caution should be taken when administering INVANZ intramuscularly to avoid inadvertent injection into a blood vessel. (See DOSAGE AND ADMINISTRATION.)

Lidocaine HCl is the diluent for intramuscular administration of INVANZ. Refer to the prescribing information for lidocaine HCl for additional precautions. Laboratory Tests

While INVANZ possesses toxicity similar to the beta-lactam group of antibiotics, periodic assessment of organ system function, including renal, hepatic, and hematopoietic, is advisable during prolonged therapy.

Drug Interactions

When ertapenem is co-administered with probenecid (500 mg p.o. every 6 hours), probenecid competes for active tubular secretion and reduces the renal clearance of ertapenem. Based on total ertapenem concentrations, probenecid increased the AUC by 25% and reduced the plasma and renal clearances by 20% and 35%, respectively. The half-life increased from 4.0 to 4.8 hours. Because of the small effect on half-life, the coadministration with probenecid to extend the half-life of ertapenem is not recommended.

In vitro studies indicate that ertapenem does not inhibit P-glycoprotein-mediated transport of digoxin or vinblastine and that ertapenem is not a substrate for P-glycoprotein-mediated transport. In vitro studies in human liver microsomes indicate that ertapenem does not inhibit metabolism mediated by any of the following six cytochrome p450 (CYP) isoforms: 1A2, 2C9, 2C19, 2D6, 2E1 and 3A4. Drug interactions caused by inhibition of P-glycoprotein-mediated drug clearance or CYP-mediated drug clearance with the listed isoforms are unlikely. (See CLINICAL PHARMACOLOGY, Distribution and Metabolism.)

Other than with probenecid, no specific clinical drug interaction studies have been conducted. Carcinogenesis, Mutagenesis, Impairment of Fertility

No long-term studies in animals have been performed to evaluate the carcinogenic potential of ertapenem.

Ertapenem was neither mutagenic nor genotoxic in the following in vitro assays: alkaline elution/rat hepatocyte assay, chromosomal aberration assay in Chinese hamster ovary cells, and TK6 human lymphoblastoid cell mutagenesis assay; and in the in vivo mouse micronucleus assay.

In mice and rats, IV doses of up to 700 mg/kg/day (for mice, approximately 3 times the recommended human dose of 1 g based on body surface area and for rats, approximately 1.2 times the human exposure at the recommended dose of 1 g based on plasma AUCs) resulted in no effects on mating performance, fecundity, fertility, or embryonic survival.

Pregnancy: Teratogenic Effects

Pregnancy Category B: In mice and rats given IV doses of up to 700 mg/kg/day (for mice, approximately 3 times the recommended human dose of 1 g based on body surface area and for rats, approximately 1.2 times the human exposure at the recommended dose of 1 g based on plasma AUCs), there was no evidence of developmental toxicity as assessed by external, visceral, and skeletal examination of the fetuses. However, in mice given 700 mg/kg/day, slight decreases in average fetal weights and an associated decrease in the average number of ossified sacrocaudal vertebrae were observed. Ertapenem crosses the placental barrier in rats.

There are, however, no adequate and well-controlled studies in pregnant women. Because animal reproduction studies are not always predictive of human response, this drug should be used during pregnancy only if clearly needed. Nursing Mothers

Ertapenem is excreted in human breast milk. (See CLINICAL PHARMACOLOGY, Distribution.) Caution should be exercised when INVANZ is administered to a nursing woman. INVANZ should be administered to nursing mothers only when the expected benefit outweighs the risk. Labor and delivery

INVANZ has not been studied for use during labor and delivery. Pediatric Use

Safety and effectiveness in pediatric patients have not been established. Therefore, use in patients under 18 years of age is not recommended.

Geriatric Use

Of the 1,835 patients in Phase IIb/III studies treated with INVANZ, approximately 26 percent were 65 and over, while approximately 12 percent were 75 and over. No overall differences in safety or effectiveness were observed between these patients and younger patients. Other reported clinical experience has not identified differences in responses between the elderly and younger patients, but greater sensitivity of some older individuals cannot be ruled out.

This drug is known to be substantially excreted by the kidney, and the risk of toxic reactions to this drug may be greater in patients with impaired renal function. Because elderly patients are more likely to have decreased renal function, care should be taken in dose selection, and it may be useful to monitor renal function. (See DOSAGE AND ADMINISTRATION.)

Hepatic Insufficiency

The pharmacokinetics of ertapenem in patients with hepatic insufficiency have not been established. Of the total number of patients in clinical studies, 37 patients receiving ertapenem 1 g daily and 36 patients receiving comparator drugs were considered to have Child-Pugh Class A, B, or C liver impairment. The incidence of adverse experiences in patients with hepatic impairment was similar between the ertapenem group and the comparator groups.

ANIMAL PHARMACOLOGY

In repeat-dose studies in rats, treatment-related neutropenia occurred at every dose-level tested, including the lowest dose (2 mg/kg, 12 mg/m(2)).

Studies in rabbits and Rhesus monkeys were inconclusive with regard to the effect on neutrophil counts.

ADVERSE REACTIONS

Clinical studies enrolled 1954 patients treated with ertapenem; in some of the clinical studies, parenteral therapy was followed by a switch to an appropriate oral antimicrobial. (See CLINICAL STUDIES.) Most adverse experiences reported in these clinical studies were described as mild to moderate in severity. Ertapenem was discontinued due to adverse experiences in 4.7% of patients. Table 3 shows the incidence of adverse experiences reported in greater than or equal to 1.0% of patients in these studies. The most common drug-related adverse experiences in patients treated with INVANZ, including those who were switched to therapy with an oral antimicrobial, were diarrhea (5.5%), infused vein complication (3.7%), nausea (3.1%), headache (2.2%), vaginitis in females (2.1%), phlebitis/thrombophlebitis (1.3%), and vomiting (1.1%).

In patients treated for complicated intra-abdominal infections, death occurred in 4.7% (15/316) of patients receiving ertapenem and 2.6% (8/307) of patients receiving comparator drug. These deaths occurred in patients with significant co-morbidity and/or severe baseline infections. Deaths were considered unrelated to study drugs by investigators.

In clinical studies, seizure was reported during study therapy plus 14-day follow-up period in 0.5% of patients treated with ertapenem, 0.3% of patients treated with piperacillin/tazobactam and 0% of patients treated with ceftriaxone. (See PRECAUTIONS.)

Additional adverse experiences that were reported with INVANZ with an incidence greater than 0.1% within each body system are listed below:

Body as a whole: abdominal distention, pain, chills, septicemia, septic shock, dehydration, gout, malaise, necrosis, candidiasis, weight loss, facial edema, injection site induration, injection site pain, flank pain, and syncope;

Cardiovascular System: heart failure, hematoma, cardiac arrest, bradycardia, arrhythmia, atrial fibrillation, heart murmur, ventricular tachycardia,

asystole, and subdural hemorrhage;

Digestive System: gastrointestinal hemorrhage, anorexia, flatulence, C. difficile associated diarrhea, stomatitis, dysphagia, hemorrhoids, ileus, cholelithiasis, duodenitis, esophagitis, gastritis, jaundice, mouth ulcer, pancreatitis, and pyloric stenosis;

Nervous System & Psychiatric: nervousness, seizure (see WARNINGS and PRECAUTIONS), tremor, depression, hypesthesia, spasm, paresthesia, aggressive behavior, and vertigo;

Respiratory System: pleural effusion, hypoxemia, bronchoconstriction, pharyngeal discomfort, epistaxis, pleuritic pain, asthma, hemoptysis, hiccups, and voice disturbance;

Skin & Skin Appendage: sweating, dermatitis, desquamation, flushing, and urticaria;

Special Senses: taste perversion;

Urogenital System: renal insufficiency, oliguria/anuria, vaginal pruritus, hematuria, urinary retention, bladder dysfunction, vaginal candidiasis, and vulvovaginitis. Adverse Laboratory Changes

Laboratory adverse experiences that were reported during therapy in equal to or greater than 1.0% of patients treated with INVANZ in clinical studies are presented in Table 4. Drug-related laboratory adverse experiences that were reported during therapy in equal to or greater than 1.0% of patients treated with INVANZ, including those who were switched to therapy with an oral antimicrobial, in clinical studies were ALT increased (6.0%), AST increased (5.2%), serum alkaline phosphatase increased (3.4%), platelet count increased (2.8%), and eosinophils increased (1.1%). Ertapenem was discontinued due to laboratory adverse experiences in 0.3% of patients.

Additional laboratory adverse experiences that were reported during therapy in greater than 0.1% but less than 1.0% of patients treated with INVANZ in clinical studies include: increases in BUN, direct and indirect serum bilirubin, serum sodium, monocytes, PTT, urine epithelial cells; decreases in serum bicarbonate.

OVERDOSAGE

No specific information is available on the treatment of overdosage with INVANZ. Intentional overdosing of INVANZ is unlikely. Intravenous administration of INVANZ at a dose of 2 g over 30 min or 3 g over 1-2h in healthy volunteers resulted in an increased incidence of nausea. In clinical studies, inadvertent administration of three 1 g doses of INVANZ in a 24 hour period resulted in diarrhea and transient dizziness in one patient.

In the event of an overdose, INVANZ should be discontinued and general supportive treatment given until renal elimination takes place.

INVANZ can be removed by hemodialysis; the plasma clearance of the total fraction of ertapenem was increased 30% in subjects with end-stage renal insufficiency when hemodialysis (4 hour session) was performed immediately following administration. However, no information is available on the use of hemodialysis to treat overdosage.

DOSAGE AND ADMINISTRATION

The dose of INVANZ in adults is 1 gram (g) given once a day.

INVANZ may be administered by intravenous infusion for up to 14 days or intramuscular injection for up to 7 days. When administered intravenously, INVANZ should be infused over a period of 30 minutes.

Intramuscular administration of INVANZ may be used as an alternative to intravenous administration in the treatment of those infections for which intramuscular therapy is appropriate.

DO NOT MIX OR CO-INFUSE INVANZ WITH OTHER MEDICATIONS. DO NOT USE DILUENTS CONTAINING DEXTROSE ((alpha)-D-GLUCOSE).

Patients with Renal Insufficiency: INVANZ may be used for the treatment of infections in patients with renal insufficiency. In patients whose creatinine clearance is greater than 30 mL/min/1.73 m2, no dosage adjustment is necessary. Patients with advanced renal insufficiency (creatinine clearance less than or equal to30 mL/min/1.73 m2) and end-stage renal insufficiency (creatinine clearance less than or equal to10 mL/min/1.73 m2) should receive 500 mg daily.

Patients on Hemodialysis: When patients on hemodialysis are given the recommended daily dose of 500 mg of INVANZ within 6 hours prior to hemodialysis, a supplementary dose of 150 mg is recommended following the hemodialysis session. If INVANZ is given at least 6 hours prior to hemodialysis, no supplementary dose is needed. There are no data in patients undergoing peritoneal dialysis or hemofiltration.

When only the serum creatinine is available, the following formula(b) may be used to estimate creatinine clearance. The serum creatinine should represent a steady state of renal function.

(b) Cockcroft and Gault equation: Cockcroft DW, Gault MH.

Prediction of creatinine clearance from serum creatinine.

Nephron. 1976

Patients with Hepatic Insufficiency: No dose adjustment recommendations can be made in patients with impaired hepatic function. (See CLINICAL PHARMACOLOGY, Special Populations, Hepatic Insufficiency and PRECAUTIONS.)

No dosage adjustment is recommended based on age or gender. (See CLINICAL PHARMACOLOGY, Special Populations.)

PREPARATION OF SOLUTION

Preparation for intravenous administration:

DO NOT MIX OR CO-INFUSE INVANZ WITH OTHER MEDICATIONS. DO NOT USE DILUENTS CONTAINING DEXTROSE ((alpha)-D-GLUCOSE). INVANZ MUST BE RECONSTITUTED AND THEN DILUTED PRIOR TO ADMINISTRATION.

1. Reconstitute the contents of a 1 g vial of INVANZ with 10 mL

of one of the following: Water for Injection, 0.9% Sodium

Chloride Injection or Bacteriostatic Water for Injection.

2. Shake well to dissolve and immediately transfer contents of

the reconstituted vial to 50 mL of 0.9% Sodium Chloride

Injection.

3. Complete the infusion within 6 hours of reconstitution.

Preparation for intramuscular administration:

INVANZ MUST BE RECONSTITUTED PRIOR TO ADMINISTRATION.

1. Reconstitute the contents of a 1 g vial of INVANZ with 3.2 mL

of 1.0% lidocaine HCl injection(c) (without epinephrine).

Shake vial thoroughly to form solution.

2. Immediately withdraw the contents of the vial and administer

by deep intramuscular injection into a large muscle mass (such

as the gluteal muscles or lateral part of the thigh).

3. The reconstituted IM solution should be used within 1 hour

after preparation. NOTE: THE RECONSTITUTED SOLUTION SHOULD NOT

BE ADMINISTERED INTRAVENOUSLY.

Parenteral drug products should be inspected visually for particulate matter and discoloration prior to use, whenever solution and container permit. Solutions of INVANZ range from colorless to pale yellow. Variations of color within this range do not affect the potency of the product.

STORAGE AND STABILITY

Before reconstitution

Do not store lyophilized powder above 25(Degree)C (77(Degree)F).

Reconstituted and infusion solutions

The reconstituted solution, immediately diluted in 0.9% Sodium Chloride Injection (see DOSAGE AND ADMINISTRATION, PREPARATION OF SOLUTION), may be stored at room temperature (25 degrees C) and used within 6 hours or stored for 24 hours under refrigeration (5 degrees C) and used within 4 hours after removal from refrigeration. Solutions of INVANZ should not be frozen.

HOW SUPPLIED

INVANZ is supplied as a sterile lyophilized powder in single dose vials containing ertapenem for intravenous infusion or for intramuscular injection as follows:

No. 3843--1 g ertapenem equivalent

NDC 0006-3843-71 in trays of 10 vials

No. 3843--1 g ertapenem equivalent

NDC 0006-3843-45 in trays of 25 vials.

CLINICAL STUDIES

Complicated Intra-Abdominal Infections

Ertapenem was evaluated in adults for the treatment of complicated intra-abdominal infections in a clinical trial. This study compared ertapenem (1 g intravenously once a day) with piperacillin/tazobactam (3.375 g intravenously every 6 hours) for 5 to 14 days and enrolled 665 patients with localized complicated appendicitis, and any other complicated intra-abdominal infection including colonic, small intestinal, and biliary infections and generalized peritonitis. The combined clinical and microbiologic success rates in the microbiologically evaluable population at 4 to 6 weeks posttherapy (test of cure) were 83.6% (163/195) for ertapenem and 80.4% (152/189) for piperacillin/tazobactam.

(c) Refer to the prescribing information for lidocaine HCl.

Complicated Skin and Skin Structure Infections

Ertapenem was evaluated in adults for the treatment of complicated skin and skin structure infections in a clinical trial. This study compared ertapenem (1 g intravenously once a day) with piperacillin/tazobactam (3.375 g intravenously every 6 hours) for 7 to 14 days and enrolled 540 patients including patients with deep soft tissue abscess, posttraumatic wound infection and cellulitis with purulent drainage. The clinical success rates at 10 to 21 days posttherapy (test of cure) were 83.9% (141/168) for ertapenem and 85.3% (145/170) for piperacillin/tazobactam.

Community Acquired Pneumonia

Ertapenem was evaluated in adults for the treatment of community acquired pneumonia in two clinical trials. Both studies compared ertapenem (1 g parenterally once a day) with ceftriaxone (1 g parenterally once a day) and enrolled a total of 866 patients. Both regimens allowed the option to switch to oral amoxicillin/clavulanate for a total of 10 to 14 days of treatment (parenteral and oral). In the first study the primary efficacy parameter was the clinical success rate in the clinically evaluable population and success rates were 92.3% (168/182) for ertapenem and 91.0% (183/201) for ceftriaxone at 7 to 14 days posttherapy (test of cure). In the second study the primary efficacy parameter was the clinical success rate in the microbiologically evaluable population and success rates were 91% (91/100) for ertapenem and 91.8% (45/49) for ceftriaxone at 7 to 14 days posttherapy (test of cure).

Complicated Urinary Tract Infections Including Pyelonephritis

Ertapenem was evaluated in adults for the treatment of complicated urinary tract infections including pyelonephritis in two clinical trials. Both studies compared ertapenem (1 g parenterally once a day) with ceftriaxone (1 g parenterally once a day) and enrolled a total of 850 patients. Both regimens allowed the option to switch to oral ciprofloxacin (500 mg twice daily) for a total of 10 to 14 days of treatment (parenteral and oral). The microbiological success rates (combined studies) at 5 to 9 days posttherapy (test of cure) were 89.5% (229/256) for ertapenem and 91.1% (204/224) for ceftriaxone.

Acute Pelvic Infections Including Endomyometritis, Septic Abortion

And Post-Surgical Gynecological Infections

Ertapenem was evaluated in adults for the treatment of acute pelvic infections in a clinical trial. This study compared ertapenem (1 g intravenously once a day) with piperacillin/tazobactam (3.375 g intravenously every 6 hours) for 3 to 10 days and enrolled 412 patients including 350 patients with obstetric/postpartum infections and 45 patients with septic abortion. The clinical success rates in the clinically evaluable population at 2 to 4 weeks posttherapy (test of cure) were 93.9% (153/163) for ertapenem and 91.5% (140/153) for piperacillin/tazobactam.

REFERENCES

1. National Committee for Clinical Laboratory Standards. Methods

for Dilution Antimicrobial Susceptibility Tests for Bacteria

that Grow Aerobically. Fifth Edition; Approved Standard, NCCLS

Document M7-A5, Vol. 17, No. 2 NCCLS, Wayne, PA, December

2000.

2. National Committee for Clinical Laboratory Standards.

Performance Standards for Antimicrobial Disk Susceptibility

Tests. Seventh Edition; Approved Standard, NCCLS Document

M2-A7, Vol. 17, No. 1 NCCLS, Wayne, PA, January 2000.

3. National Committee for Clinical Laboratory Standards. Methods

for Antimicrobial Susceptibility Testing of Anaerobic Bacteria

- Fourth Edition; Approved Standard, NCCLS Document M11-A4,

Vol. 17, No. 22. NCCLS, Wayne, PA, December 1997.

4. National Committee for Clinical Laboratory Standards.

Performance Standards for Antimicrobial Susceptibility Testing

- Eleventh Informational Supplement. Approved Standard, NCCLS

Document M100-S11, Vol. 21, No. 1. NCCLS, Wayne, PA, January

2001.

Issued November 2001 Printed in USA

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