Tobramycin

APP Pharmaceuticals, LLC

Tobramycin for Injection, USP

FULL PRESCRIBING INFORMATION: CONTENTS*

• TOBRAMYCIN DESCRIPTION
• CLINICAL PHARMACOLOGY
  • Microbiology
  • Susceptibility Tests
• TOBRAMYCIN INDICATIONS AND USAGE
• TOBRAMYCIN CONTRAINDICATIONS
• WARNINGS
• PRECAUTIONS
  • Information for Patients
  • Pregnancy Category D
  • Pediatric Use
  • Geriatric Use
• TOBRAMYCIN ADVERSE REACTIONS
  • Neurotoxicity
  • Nephrotoxicity
• OVERDOSAGE
  • Signs and Symptoms
  • Treatment
• TOBRAMYCIN DOSAGE AND ADMINISTRATION
  • Administration for Patients with Normal Renal Function
  • Adults with Life-Threatening Infections
  • Pediatric patients (greater than 1 week of age)
  • Premature or full-term neonates 1 week of age or less
  • Dosage in Patients with Cystic Fibrosis
  • Administration for Patients with Impaired Renal Function
  • Reduced dosage at 8-hour intervals
  • Normal dosage at prolonged intervals
  • Dosage in Obese Patients
  • Intravenous Administration
• PREPARATION AND STORAGE
  • Directions for Proper Use of Pharmacy Bulk Package-Not for direct infusion
• HOW SUPPLIED
• REFERENCES

FULL PRESCRIBING INFORMATION

Rx only

This vial is intended for use by the hospital pharmacist in the extemporaneous preparation of IV solutions.

TOBRAMYCIN DESCRIPTION

Tobramycin sulfate, a water-soluble antibiotic of the aminoglycoside group, is derived from the actinomycete Streptomyces tenebrarius.  Tobramycin for Injection, USP is supplied as a sterile dry powder and is intended for reconstitution with 30 mL of Sterile Water for Injection, USP.  Each vial contains 1,200 mg of tobramycin activity.  After dilution, the solution will contain 40 mg of tobramycin per mL.  The product contains no preservative or sodium bisulfite.

Tobramycin sulfate is O- 3-amino-3-deoxy- α -D-glucopyranosyl-(1→4)- O- [2,6-diamino-2,3,6-trideoxy- α -D- ribo -hexopyranosyl-(1→6)]-2-deoxy-L-streptamine, sulfate (2:5)(salt) and has the molecular formula (C₁₈H₃₇N₅O₉)₂•5H₂SO₄.  The molecular weight is 1425.45.

The structural formula for tobramycin is as follows:

The pharmacy bulk package of tobramycin is a sterile preparation for parenteral use that contains multiple single doses.  It is intended for use in a pharmacy admixture program.  Package use is restricted to the preparation of admixtures for intravenous infusion or to the filling of empty sterile syringes for intravenous injections for patients with individualized dosing requirements.

CLINICAL PHARMACOLOGY

Tobramycin is rapidly absorbed following intramuscular administration.  Peak serum concentrations of tobramycin occur between 30 and 90 minutes after intramuscular administration.  Following an intramuscular dose of 1 mg/kg of body weight, maximum serum concentrations reach about 4 mcg/mL, and measurable levels persist for as long as 8 hours.  Therapeutic serum levels are generally considered to range from 4 to 6 mcg/mL.  When tobramycin is administered by intravenous infusion over a 1-hour period, the serum concentrations are similar to those obtained by intramuscular administration.  Tobramycin is poorly absorbed from the gastrointestinal tract.

In patients with normal renal function, except neonates, tobramycin administered every 8 hours does not accumulate in the serum.  However, in those patients with reduced renal function and in neonates, the serum concentration of the antibiotic is usually higher and can be measured for longer periods of time than in normal adults.  Dosage for such patients must, therefore, be adjusted accordingly (see DOSAGE AND ADMINISTRATION ).

Following parenteral administration, little, if any, metabolic transformation occurs, and tobramycin is eliminated almost exclusively by glomerular filtration.  Renal clearance is similar to that of endogenous creatinine.  Ultrafiltration studies demonstrate that practically no serum protein binding occurs.  In patients with normal renal function, up to 84% of the dose is recoverable from the urine in 8 hours and up to 93% in 24 hours.

Peak urine concentrations ranging from 75 to 100 mcg/mL have been observed following the intramuscular injection of a single dose of 1 mg/kg.  After several days of treatment, the amount of tobramycin excreted in the urine approaches the daily dose administered.  When renal function is impaired, excretion of tobramycin is slowed, and accumulation of the drug may cause toxic blood levels.

The serum half-life in normal individuals is 2 hours.  An inverse relationship exists between serum half-life and creatinine clearance, and the dosage schedule should be adjusted according to the degree of renal impairment (see DOSAGE AND ADMINISTRATION ).  In patients undergoing dialysis, 25% to 70% of the administered dose may be removed, depending on the duration and type of dialysis.

Tobramycin can be detected in tissues and body fluids after parenteral administration.  Concentrations in bile and stools ordinarily have been low, which suggests minimum biliary excretion.  Tobramycin has appeared in low concentration in the cerebrospinal fluid following parenteral administration, and concentrations are dependent on dose, rate of penetration, and degree of meningeal inflammation.  It has also been found in sputum, peritoneal fluid, synovial fluid, and abscess fluids, and it crosses the placental membranes.  Concentrations in the renal cortex are several times higher than the usual serum levels.

Probenecid does not affect the renal tubular transport of tobramycin.

Microbiology

Tobramycin acts by inhibiting synthesis of protein in bacterial cells.  In vitro tests demonstrate that tobramycin is bactericidal.

Tobramycin has been shown to be active against most strains of the following organisms both in vitro and in clinical infections as described in INDICATIONS AND USAGE  section:

     Aerobic Gram-positive microorganisms

     Staphylococcus aureus

     Aerobic Gram-negative microorganisms

     Citrobacter species

     Enterobacter species

     Escherichia coli

     Klebsiella species

     Morganella morganii

     Pseudomonas aeruginosa

     Proteus mirabilis

     Proteus vulgaris

     Providencia species

     Serratia species

Aminoglycosides have a low order of activity against most gram-positive organisms, including Streptococcus pyogenes , Streptococcus pneumoniae , and enterococci.

Although most strains of enterococci demonstrate in vitro resistance, some strains in this group are susceptible. In vitro studies have shown that an aminoglycoside combined with an antibiotic that interferes with cell-wall synthesis affects some enterococcal strains synergistically.  The combination of penicillin G and tobramycin results in a synergistic bactericidal effect in vitro against certain strains of Enterococcus faecalis .  However, this combination is not synergistic against other closely related organisms, e.g., Enterococcus faecium .  Speciation of enterococci alone cannot be used to predict susceptibility.  Susceptibility testing and tests for antibiotic synergism are emphasized.

Cross-resistance between aminoglycosides may occur.

Susceptibility Tests

Diffusion Techniques  

Quantitative methods that require measurement of zone diameters give the most precise estimates of susceptibility of bacteria to antimicrobial agents.  One such procedure is the National Committee for Clinical Laboratory Standards (NCCLS)-approved procedure.¹  This method has been recommended for use with disks to test susceptibility to tobramycin.  Interpretation involves correlation of the diameters obtained in the disk test with minimum inhibitory concentrations (MIC) for tobramycin.

Reports from the laboratory giving results of the standard single-disk susceptibility test with a 10 mcg tobramycin disk should be interpreted according to the following criteria:

A report of “Susceptible” indicates that the pathogen is likely to be inhibited by generally achievable blood levels.  A report of “Intermediate” suggests that the organism would be susceptible if high dosage is used or if the infection is confined to tissues and fluids in which high antimicrobial levels are obtained.  A report of “Resistant” indicates that achievable concentrations are unlikely to be inhibitory and other therapy should be selected.

Standardized procedures require the use of laboratory control organisms.  The 10 mcg tobramycin disk should give the following zone diameters:

Dilution Techniques

Broth and agar dilution methods, such as those recommended by the NCCLS², may be used to determine MICs of tobramycin.  MIC test results should be interpreted according to the following criteria:

As with standard diffusion methods, dilution procedures require the use of laboratory control organisms.  Tobramycin laboratory reagent should give the following MIC values:

TOBRAMYCIN INDICATIONS AND USAGE

Tobramycin for Injection, USP is indicated for the treatment of serious bacterial infections caused by susceptible strains of the designated microorganisms in the diseases listed below:

Septicemia in the pediatric patient and adult caused by P. aeruginosa , E. coli , and Klebsiella spp.

Lower respiratory tract infections caused by P. aeruginos a, Klebsiella spp, Enterobacter spp, Serratia spp, E. coli , and S. aureus (penicillinase- and non-penicillinase-producing strains).

Serious central-nervous-system infections (meningitis) caused by susceptible organisms.

Intra-abdominal infections, including peritonitis, caused by E. coli , Klebsiella spp, and Enterobacter spp.

Skin, bone, and skin structure infections caused by P. aeruginosa , Proteus spp, E. coli , Klebsiella spp, Enterobacter spp, and S. aureus.

Complicated and recurrent urinary tract infections caused by P. aeruginosa , Proteus spp, (indole-positive and indole-negative), E. coli , Klebsiella spp, Enterobacter spp, Serratia spp, S. aureus , Providencia spp, and Citrobacter spp.

Aminoglycosides, including tobramycin sulfate injection, USP are not indicated in uncomplicated initial episodes of urinary tract infections unless the causative organisms are not susceptible to antibiotics having less potential toxicity.  Tobramycin for Injection, USP may be considered in serious staphylococcal infections when penicillin or other potentially less toxic drugs are contraindicated and when bacterial susceptibility testing and clinical judgment indicate its use.

Bacterial cultures should be obtained prior to and during treatment to isolate and identify etiologic organisms and to test their susceptibility to tobramycin.  If susceptibility tests show that the causative organisms are resistant to tobramycin, other appropriate therapy should be instituted.  In patients in whom a serious life-threatening gram-negative infection is suspected, including those in whom concurrent therapy with a penicillin or cephalosporin and an aminoglycoside may be indicated, treatment with tobramycin may be initiated before the results of susceptibility studies are obtained.  The decision to continue therapy with tobramycin should be based on the results of susceptibility studies, the severity of the infection, and the important additional concepts discussed in the WARNINGS  box above.

TOBRAMYCIN CONTRAINDICATIONS

A hypersensitivity to any aminoglycoside is a contraindication to the use of tobramycin.  A history of hypersensitivity or serious toxic reactions to aminoglycosides may also contraindicate the use of any other aminoglycoside because of the known cross-sensitivity of patients to drugs in this class.

WARNINGS

See WARNINGS box above.

Serious allergic reactions including anaphylaxis and dermatologic reactions including exfoliative dermatitis, toxic epidermal necrolysis, erythema multiforme, and Stevens-Johnson Syndrome have been reported rarely in patients on tobramycin therapy.  Although rare, fatalities have been reported (see CONTRAINDICATIONS ).

If an allergic reaction occurs, the drug should be discontinued and appropriate therapy instituted.

Clostridium difficile associated diarrhea (CDAD) has been reported with use of nearly all antibacterial agents, including Tobramycin for Injection, USP, and may range in severity from mild diarrhea to fatal colitis.  Treatment with antibacterial agents alters the normal flora of the colon leading to overgrowth of C. difficile.

C. difficile produces toxins A and B which contribute to the development of CDAD.  Hypertoxin producing strains of C. difficile cause increased morbidity and mortality, as these infections can be refractory to antimicrobial therapy and may require colectomy.  CDAD must be considered in all patients who present with diarrhea following antibiotic use.  Careful medical history is necessary since CDAD has been reported to occur over two months after the administration of antibacterial agents.

If CDAD is suspected or confirmed, ongoing antibiotic use not directed against C. difficile may need to be discontinued.  Appropriate fluid and electrolyte management, protein supplementation, antibiotic treatment of C. difficile, and surgical evaluation should be instituted as clinically indicated.

PRECAUTIONS

Serum and urine specimens for examination should be collected during therapy, as recommended in the WARNINGS box.  Serum calcium, magnesium, and sodium should be monitored.

Peak and trough serum levels should be measured periodically during therapy.  Prolonged concentrations above 12 mcg/mL should be avoided.  Rising trough levels (above 2 mcg/mL) may indicate tissue accumulation.  Such accumulation, advanced age, and cumulative dosage may contribute to ototoxicity and nephrotoxicity.  It is particularly important to monitor serum levels closely in patients with known renal impairment.

A useful guideline would be to perform serum level assays after 2 or 3 doses, so that the dosage could be adjusted if necessary, and at 3- to 4-day intervals during therapy.  In the event of changing renal function, more frequent serum levels should be obtained and the dosage or dosage interval adjusted according to the guidelines provided in DOSAGE AND ADMINISTRATION .

In order to measure the peak level, a serum sample should be drawn about 30 minutes following intravenous infusion or 1 hour after an intramuscular injection.  Trough levels are measured by obtaining serum samples at 8 hours or just prior to the next dose of tobramycin.  These suggested time intervals are intended only as guidelines and may vary according to institutional practices.  It is important, however, that there be consistency within the individual patient program unless computerized pharmacokinetic dosing programs are available in the institution.  These serum-level assays may be especially useful for monitoring the treatment of severely ill patients with changing renal function or of those infected with less susceptible organisms or those receiving maximum dosage.

Neuromuscular blockade and respiratory paralysis have been reported in cats receiving very high doses of tobramycin (40 mg/kg).  The possibility of prolonged or secondary apnea should be considered if tobramycin is administered to anesthetized patients who are also receiving neuromuscular blocking agents, such as succinylcholine, tubocurarine, or decamethonium, or to patients receiving massive transfusions of citrated blood.  If neuromuscular blockade occurs, it may be reversed by the administration of calcium salts.

Cross-allergenicity among aminoglycosides has been demonstrated.

In patients with extensive burns or cystic fibrosis, altered pharmacokinetics may result in reduced serum concentrations of aminoglycosides.  In such patients treated with tobramycin, measurement of serum concentration is especially important as a basis for determination of appropriate dosage.

Elderly patients may have reduced renal function that may not be evident in the results of routine screening tests, such as BUN or serum creatinine.  A creatinine clearance determination may be more useful.  Monitoring of renal function during treatment with aminoglycosides is particularly important in such patients.

An increased incidence of nephrotoxicity has been reported following concomitant administration of aminoglycoside antibiotics and cephalosporins.

Aminoglycosides should be used with caution in patients with muscular disorders, such as myasthenia gravis or parkinsonism, since these drugs may aggravate muscle weakness because of their potential curare-like effect on neuromuscular function.

Aminoglycosides may be absorbed in significant quantities from body surfaces after local irrigation or application and may cause neurotoxicity and nephrotoxicity.

Aminoglycosides have not been approved for intraocular and/or subconjunctival use.  Physicians are advised that macular necrosis has been reported following administration of aminoglycosides, including tobramycin, by these routes.

See WARNINGS  box regarding concurrent use of potent diuretics and concurrent and sequential use of other neurotoxic or nephrotoxic drugs.

The inactivation of tobramycin and other aminoglycosides by ß-lactam-type antibiotics (penicillins or cephalosporins) has been demonstrated in vitro and in patients with severe renal impairment.  Such inactivation has not been found in patients with normal renal function who have been given the drugs by separate routes of administration.

Therapy with tobramycin may result in overgrowth of nonsusceptible organisms.  If overgrowth of nonsusceptible organisms occurs, appropriate therapy should be initiated.

Information for Patients

Diarrhea is a common problem caused by antibiotics which usually ends when the antibiotic is discontinued.  Sometimes after starting treatment with antibiotics, patients can develop watery and bloody stools (with or without stomach cramps and fever) even as late as two or more months after having taken the last dose of the antibiotic.  If this occurs, patients should contact their physician as soon as possible.

Pregnancy Category D

Aminoglycosides can cause fetal harm when administered to a pregnant woman.  Aminoglycoside antibiotics cross the placenta, and there have been several reports of total irreversible bilateral congenital deafness in children whose mothers received streptomycin during pregnancy.  Serious side effects to mother, fetus, or newborn have not been reported in the treatment of pregnant women with other aminoglycosides.  If tobramycin is used during pregnancy or if the patient becomes pregnant while taking tobramycin, she should be apprised of the potential hazard to the fetus.

Pediatric Use

See INDICATIONS AND USAGE  and DOSAGE AND ADMINISTRATION .

Geriatric Use

Elderly patients may be at a higher risk of developing nephrotoxicity and ototoxicity while receiving tobramycin (see WARNINGS , PRECAUTIONS , and OVERDOSAGE ).  Other factors that may contribute to nephrotoxicity and ototoxicity are rising trough levels, excessive peak concentrations, dehydration, concomitant use of other neurotoxic or nephrotoxic drugs, and cumulative dose.  Peak and trough serum levels should be measured periodically during therapy to assure adequate levels and to avoid potentially toxic levels (see WARNINGS and PRECAUTIONS ).

Tobramycin 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.  Dose reduction is required for patients with impaired renal function (see DOSAGE AND ADMINISTRATION ).  Elderly patients may have reduced renal function that may not be evident in the results of routine screening tests, such as BUN or serum creatinine.  A creatinine clearance determination may be more useful.  Monitoring of renal function during treatment with aminoglycosides is particularly important in the elderly (see PRECAUTIONS ).

This product does not contain sodium.

TOBRAMYCIN ADVERSE REACTIONS

Neurotoxicity

Adverse effects on both the vestibular and auditory branches of the eighth nerve have been noted, especially in patients receiving high doses or prolonged therapy, in those given previous courses of therapy with an ototoxin, and in cases of dehydration.  Symptoms include dizziness, vertigo, tinnitus, roaring in the ears, and hearing loss.  Hearing loss is usually irreversible and is manifested initially by diminution of high-tone acuity.  Tobramycin and gentamicin sulfates closely parallel each other in regard to ototoxic potential.

Nephrotoxicity

Renal function changes, as shown by rising BUN, NPN, and serum creatinine and by oliguria, cylindruria, and increased proteinuria, have been reported, especially in patients with a history of renal impairment who are treated for longer periods or with higher doses than those recommended.  Adverse renal effects can occur in patients with initially normal renal function.

Clinical studies and studies in experimental animals have been conducted to compare the nephrotoxic potential of tobramycin and gentamicin.  In some of the clinical studies and in the animal studies, tobramycin caused nephrotoxicity significantly less frequently than gentamicin.  In some other clinical studies, no significant difference in the incidence of nephrotoxicity between tobramycin and gentamicin was found.

Other reported adverse reactions possibly related to tobramycin include anemia, granulocytopenia, and thrombocytopenia; and fever, rash, exfoliative dermatitis, itching, urticaria, nausea, vomiting, diarrhea, headache, lethargy, pain at the injection site, mental confusion, and disorientation.  Laboratory abnormalities possibly related to tobramycin include increased serum transaminases (AST, ALT); increased serum LDH and bilirubin; decreased serum calcium, magnesium, sodium, and potassium; and leukopenia, leukocytosis, and eosinophilia.

OVERDOSAGE

Signs and Symptoms

The severity of the signs and symptoms following a tobramycin overdose are dependent on the dose administered, the patient’s renal function, state of hydration, and age and whether or not other medications with similar toxicities are being administered concurrently.  Toxicity may occur in patients treated more than 10 days, in adults given more than 5 mg/kg/day, in pediatric patients given more than 7.5 mg/kg/day, or in patients with reduced renal function where dose has not been appropriately adjusted.

Nephrotoxicity following the parenteral administration of an aminoglycoside is most closely related to the area under the curve of the serum concentration versus time graph.  Nephrotoxicity is more likely if trough blood concentrations fail to fall below 2 mcg/mL and is also proportional to the average blood concentration.  Patients who are elderly, have abnormal renal function, are receiving other nephrotoxic drugs, or are volume depleted are at greater risk for developing acute tubular necrosis.  Auditory and vestibular toxicities have been associated with aminoglycoside overdose.  These toxicities occur in patients treated longer than 10 days, in patients with abnormal renal function, in dehydrated patients, or in patients receiving medications with additive auditory toxicities.  These patients may not have signs or symptoms or may experience dizziness, tinnitus, vertigo, and a loss of high-tone acuity as ototoxicity progresses.  Ototoxicity signs and symptoms may not begin to occur until long after the drug has been discontinued.

Neuromuscular blockade or respiratory paralysis may occur following administration of aminoglycosides.  Neuromuscular blockade, respiratory failure, and prolonged respiratory paralysis may occur more commonly in patients with myasthenia gravis or Parkinson’s disease.  Prolonged respiratory paralysis may also occur in patients receiving decamethonium, tubocurarine, or succinylcholine.  If neuromuscular blockade occurs, it may be reversed by the administration of calcium salts but mechanical assistance may be necessary.

If tobramycin were ingested, toxicity would be less likely because aminoglycosides are poorly absorbed from an intact gastrointestinal tract.

Treatment

In all cases of suspected overdosage, call your Regional Poison Control Center to obtain the most up-to-date information about the treatment of overdose.  This recommendation is made because, in general, information regarding the treatment of overdosage may change more rapidly than the package insert.  In managing overdosage, consider the possibility of multiple drug overdoses, interaction among drugs, and unusual drug kinetics in your patient.

The initial intervention in a tobramycin overdose is to establish an airway and ensure oxygenation and ventilation.  Resuscitative measures should be initiated promptly if respiratory paralysis occurs.

Patients who have received an overdose of tobramycin and who have normal renal function should be adequately hydrated to maintain a urine output of 3 to 5 mL/kg/hr.  Fluid balance, creatinine clearance, and tobramycin plasma levels should be carefully monitored until the serum tobramycin level falls below 2 mcg/mL.

Patients in whom the elimination half-life is greater than 2 hours or whose renal function is abnormal may require more aggressive therapy.  In such patients, hemodialysis may be beneficial.

TOBRAMYCIN DOSAGE AND ADMINISTRATION

The patient’s pretreatment body weight should be obtained for calculation of correct dosage.  It is desirable to measure both peak and trough serum concentrations (see WARNINGS  box and PRECAUTIONS ).

Administration for Patients with Normal Renal Function

3 mg/kg/day in 3 equal doses every 8 hours (see Table 1).

Adults with Life-Threatening Infections

Up to 5 mg/kg/day may be administered in 3 or 4 equal doses (see Table 1).  The dosage should be reduced to 3 mg/kg/day as soon as clinically indicated. To prevent increased toxicity due to excessive blood levels, dosage should not exceed 5 mg/kg/day unless serum levels are monitored (see WARNINGS box and PRECAUTIONS ).

*Applicable to all product forms except the tobramycin injection, USP, (Pediatric).

Pediatric patients (greater than 1 week of age)

6 to 7.5 mg/kg/day in 3 or 4 equally divided doses (2 to 2.5 mg/kg every 8 hours or 1.5 to 1.89 mg/kg every 6 hours).

Premature or full-term neonates 1 week of age or less

Up to 4 mg/kg/day may be administered in 2 equal doses every 12 hours.

It is desirable to limit treatment to a short term.  The usual duration of treatment is 7 to 10 days.  A longer course of therapy may be necessary in difficult and complicated infections.  In such cases, monitoring of renal, auditory, and vestibular functions is advised, because neurotoxicity is more likely to occur when treatment is extended longer than 10 days.

Dosage in Patients with Cystic Fibrosis

In patients with cystic fibrosis, altered pharmacokinetics may result in reduced serum concentrations of aminoglycosides.  Measurement of tobramycin serum concentration during treatment is especially important as a basis for determining appropriate dose.  In patients with severe cystic fibrosis, an initial dosing regimen of 10 mg/kg/day in 4 equally divided doses is recommended.  This dosing regimen is suggested only as a guide.  The serum levels of tobramycin should be measured directly during treatment due to wide interpatient variability.

Administration for Patients with Impaired Renal Function

Whenever possible, serum tobramycin concentrations should be monitored during therapy.

Following a loading dose of 1 mg/kg, subsequent dosage in these patients must be adjusted, either with reduced doses administered at 8-hour intervals or with normal doses given at prolonged intervals.  Both of these methods are suggested as guides to be used when serum levels of tobramycin cannot be measured directly.  They are based on either the creatinine clearance level or the serum creatinine level of the patient because these values correlate with the half-life of tobramycin.  The dosage schedule derived from either method should be used in conjunction with careful clinical and laboratory observations of the patient and should be modified as necessary.  Neither method should be used when dialysis is being performed.

Reduced dosage at 8-hour intervals

When the creatinine clearance rate is 70 mL or less per minute or when the serum creatinine value is known, the amount of the reduced dose can be determined by multiplying the normal dose from Table 1 by the percent of normal dose from the accompanying nomogram.

An alternate rough guide for determining reduced dosage at 8-hour intervals (for patients whose steady-state serum creatinine values are known) is to divide the normally recommended dose by the patient’s serum creatinine.

Normal dosage at prolonged intervals

If the creatinine clearance rate is not available and the patient’s condition is stable, a dosage frequency in hours for the dosage given in Table 1 can be determined by multiplying the patient’s serum creatinine by 6.

Dosage in Obese Patients

The appropriate dose may be calculated by using the patient’s estimated lean body weight plus 40% of the excess as the basic weight on which to figure mg/kg.

Intravenous Administration

For intravenous administration, the usual volume of diluent (0.9% Sodium Chloride Injection or 5% Dextrose Injection) is 50 to 100 mL for adult doses.  For pediatric patients, the volume of diluent should be proportionately less than that for adults.  The diluted solution usually should be infused over a period of 20 to 60 minutes.  Infusion periods of less than 20 minutes are not recommended because peak serum levels may exceed 12 mcg/mL (see WARNINGS box).

Tobramycin should not be physically premixed with other drugs but should be administered separately according to the recommended dose and route.

PREPARATION AND STORAGE

Directions for Proper Use of Pharmacy Bulk Package-Not for direct infusion

The pharmacy bulk package is for use in the Hospital Pharmacy Admixture Service and only in a suitable work area, such as a laminar flow hood.  Using aseptic technique, the closure may be penetrated only 1 time after reconstitution using a suitable sterile transfer device or dispensing set, which allows measured dispensing of the contents.  Use of a syringe and needle is not recommended as it may cause leakage.  After entry, entire contents of bulk vial should be dispensed within 24 hours.

Tobramycin for Injection, USP is supplied as a dry powder.  The contents of the vial should be diluted with 30 mL of Sterile Water for Injection, USP, to provide a solution containing 40 mg of tobramycin per mL.  Prior to reconstitution, the vial should be stored at 20° to 25°C (68° to 77°F) [see USP Controlled Room Temperature].  After reconstitution, the solution should be kept in a refrigerator and used within 96 hours.  If kept at room temperature, the solution must be used within 24 hours.

Prior to administration, parenteral drug products should be inspected visually for particulate matter and discoloration whenever solution and container permit.

HOW SUPPLIED

Vial stoppers do not contain natural rubber latex.

REFERENCES

• National Committee for Clinical Laboratory Standards, Performance Standards for Antimicrobial Disk Susceptibility Tests–Sixth Edition.  Approved Standard NCCLS Document M2-A6, Vol. 17, No. 1, NCCLS, Wayne, PA, 1997.
• National Committee for Clinical Laboratory Standards, Methods for Dilution Antimicrobial Susceptibility Tests for Bacteria that Grow Aerobically–Fourth Edition.  Approved Standard NCCLS Document M7-A4, Vol. 17, No. 2, NCCLS, Wayne, PA, 1997.

45932C

Revised: December 2008

PACKAGE LABEL - PRINCIPAL DISPLAY - Tobramycin 1.2 g Vial Label

NDC 63323-303-51

300351

Tobramycin for Injection, USP

PHARMACY BULK PACKAGE - NOT FOR DIRECT INFUSION

equivalent to

1.2 g

Tobramycin

Rx only

PACKAGE LABEL - PRINCIPAL DISPLAY - Tobramycin 1.2 g Tray Label

NDC 63323-303-51

300351

Tobramycin for Injection, USP

PHARMACY BULK PACKAGE - NOT FOR DIRECT INFUSION

equivalent to

1.2 g

Tobramycin

Rx only