HOW SUPPLIED SECTION.


HOW SUPPLIED. Penicillin Sodium for injection, USP, for IM or IV use, is supplied in dry powder form in vials containing 5,000,000 units (5 million units) of crystalline penicillin as the sodium salt, with 1.68 mEq of sodium per million units of penicillin G, in tray packs of 10 (NDC 0781-6153-95) and in tray packs of 50 (NDC 0781-6153-97).. STORAGE. Store dry powder at 20 to 25C (68 to 77F) (see USP Controlled Room Temperature).Sterile constituted solution may be kept in refrigerator (2 to 8C) for days without significant loss of potency.Manufactured by Sandoz GmbH for Sandoz Inc., Princeton, NJ 0854046270951May 2020.

TERATOGENIC EFFECTS SECTION.


Teratogenic Effects. Reproduction studies performed in the mouse, rat, and rabbit have revealed no evidence of impaired fertility or harm to the fetus due to penicillin G. Human experience with the penicillins during pregnancy has not shown any positive evidence of adverse effects on the fetus. There are, however, no adequate and well controlled studies in pregnant women showing conclusively that harmful effects of these drugs on the fetus can be excluded. Because animal reproduction studies are not always predictive of human response, this drug should be used during pregnancy only if clearly needed.

ADVERSE REACTIONS SECTION.


ADVERSE REACTIONS. Body as Whole. The Jarisch-Herxheimer reaction is systemic reaction, that may occur after the initiation of penicillin therapy in patients with syphilis or other spirochetal infections (i.e., Lyme disease and Relapsing fever). The reaction begins one to two hours after initiation of therapy and disappears within 12 to 24 hours. It is characterized by fever, chills, myalgias, headache, exacerbation of cutaneous lesions, tachycardia, hyperventiliation, vasodilation with flushing and mild hypotension. The pathogenesis of the Herxheimer reaction may be due to the release from the spirochaete of host stable pyrogen.. Hypersensitivity Reactions. The reported incidence of allergic reactions to all penicillins ranges from 0.7 to 10 percent in different studies (see WARNINGS). Sensitization is usually the result of previous treatment with penicillin, but some individuals have had immediate reactions when first treated. In such cases, it is postulated that prior exposure to penicillin may have occurred via trace amounts present in milk or vaccines.Two types of allergic reactions to penicillin are noted clinically Immediate and delayed.Immediate reactions usually occur within 20 minutes of administration and range in severity from urticaria and pruritus to angloneurotic edema, laryngospasm, bronchospasm, hypotension, vascular collapse and death (see WARNINGS). Such immediate anaphylactic reactions are very rare and usually occur after parenteral therapy, but few cases of anaphylaxis have been reported following oral therapy. Another type of immediate reaction, an accelerated reaction, may occur between 20 minutes and 45 hours after administration and may include urticaria, pruritus, fever and, occasionally, laryngeal edema.Delayed reactions to penicillin therapy usually occur within to weeks after initiation of therapy. Manifestations include serum sickness-like symptoms, i.e., fever, malaise, urticaria, myalgia, arthralgia, abdominal pain and various skin rashes, ranging from maculopapular eruptions to exfoliative dermatitis.Contact dermatitis has been observed in individuals who prepare penicillin solutions.. Gastrointestinal System. Pseudomembranous colitis has been reported with the onset occurring during or after penicillin treatment. Nausea, vomiting, stomatitis, black or hairy tongue, and other symptoms of gastrointestinal irritation may occur, especially during oral therapy.. Hematologic System. Reactions include neutropenia, which resolves after penicillin therapy is discontinued; Coombs-positive hemolytic anemia, an uncommon reaction, occurs in patients treated with intravenous penicillin in doses greater than 10 million units/day and who have previously received large doses of the drug; and with large doses of penicillin, bleeding diathesis, can occur secondary to platelet dysfunction.. Metabolic. Penicillin Sodium for injection, USP (1 million units contains 1.68 mEq of sodium ion) may cause serious and even fatal electrolyte disturbances when given intravenously in large doses.. Cardiovascular System. High dosage of penicillin sodium may result in congestive heart failure due to high sodium intake.. Nervous System. Neurotoxic reactions including hyperreflexia, myoclonic twitches, seizures and coma have been reported following the administration of massive intravenous doses, and are more likely in patients with impaired renal function.. Urogenital System. Renal tubular damage and interstitial nephritis have been associated with large intravenous doses of penicillin G. Manifestations of this reaction may include fever, rash, eosinophilia, proteinuria, eosinophiluria, hematuria and rise in serum urea nitrogen. Discontinuation of penicillin results in resolution in the majority of patients.. Local Reactions. Phlebitis and thrombophlebitis may occur with intravenous administration.

CARCINOGENESIS & MUTAGENESIS & IMPAIRMENT OF FERTILITY SECTION.


Carcinogenesis, Mutagenesis, Impairment of Fertility. No long-term animal studies have been conducted with this drug.

CLINICAL PHARMACOLOGY SECTION.


CLINICAL PHARMACOLOGY. After an intravenous infusion of penicillin G, peak serum concentrations are attained immediately after completion of the infusion. In study of ten patients administered single million unit dose of penicillin intravenously over to minutes, the mean serum concentrations were 400 mcg/mL, 273 mcg/mL and mcg/mL at to minutes, 10 minutes and hours after completion of the injection, respectively. In separate study, five healthy adults were administered one million units of penicillin intravenously, either as bolus over minutes or as an infusion over 60 minutes. The mean serum concentration eight minutes after completion of the bolus was 45 mcg/mL and eight minutes after completion of the infusion was 14.4 mcg/mL.The mean -phase serum half-life of penicillin administered by the intravenous route in ten patients with normal renal function was 42 minutes, with range of 31 to 50 minutes.The clearance of penicillin in normal individuals is predominantly via the kidney. The renal clearance, which is extremely rapid, is the result of glomerular filtration and active tubular transport, with the latter route predominating. Urinary recovery is reported to be 58 to 85% of the administered dose. Renal clearance of penicillin is delayed in premature infants, neonates and in the elderly due to decreased renal function. The serum half-life of penicillin correlates inversely with age and clearance of creatinine and ranges from 3.2 hours in infants to days of age to 1.4 hours in infants 14 days of age or older.Nonrenal clearance includes hepatic metabolism and, to lesser extent, biliary excretion. The latter routes become more important with renal impairment.Probenecid blocks the renal tubular secretion of penicillin. Therefore, the concurrent administration of probenecid prolongs the elimination of penicillin and, consequently, increases the serum concentrations.Penicillin is distributed to more areas of the body including lung, liver, kidney, muscle, bone and placenta. In the presence of inflammation, levels of penicillin in abscesses, middle ear, pleural, peritoneal and synovial fluids are sufficient to inhibit most susceptible bacteria. Penetration into the eye, brain, cerebrospinal fluid (CSF) or prostate is poor in the absence of inflammation. With inflamed meninges, the penetration of penicillin into the CSF improves, such that the CSF/serum ratio is to 6%. Inflammation also enhances its penetration into the pericardial fluid. Penicillin is actively secreted into the bile resulting in levels at least 10 times those achieved simultaneously in serum. Penicillin penetrates poorly into human polymorphonuclear leukocytes.In the presence of impaired renal function, the -phase serum half-life of penicillin is prolonged. -phase serum half-lives of one to two hours were observed in azotemic patients with serum creatinine concentrations <3 mg/100 mL and ranged as high as 20 hours in anuric patients. linear relationship, including the lowest range of renal function, is found between the serum elimination rate constant and renal function as measured by creatinine clearance.In patients with altered renal function, the presence of hepatic insufficiency further alters the elimination of penicillin G. In one study, the serum half-lives in two anuric patients (excreting <400 mL urine/day) were 7.2 and 10.1 hours. totally anuric patient with terminal hepatic cirrhosis had penicillin half-life of 30.5 hours, while another patient with anuria and liver disease had serum half-life of 16.4 hours.The dosage of penicillin should be reduced in patients with severe renal impairment, with additional modifications when hepatic disease accompanies the renal impairment.Hemodialysis has been shown to reduce penicillin serum levels.. Microbiology. Penicillin is bactericidal against penicillin-susceptible microorganisms during the stage of active multiplication. It acts by inhibiting biosynthesis of cell-wall mucopeptide. It is not active against the penicillinase-producing bacteria, which include many strains of staphylococci. Penicillin is highly active in vitro against staphylococci (except penicillinase-producing strains), streptococci (groups A, B, C, G, H, and M), pneumococci and Neisseria meningitidis. Other organisms susceptible in vitro to penicillin are Neisseria gonorrhoeae, Corynebacterium diphtheriae, Bacillus anthracis, clostridia, Actinomyces species, Spirillum minus, Streptobacillus monillformis, Listeria monocytogenes, and leptospira; Treponema pallidum is extremely susceptible.Some species of gram-negative bacilli were previously considered susceptible to very high intravenous doses of penicillin (up to 80 million units/day) including some strains of Escherichia coli, Proteus mirabilis, salmonella, shigella, Enterobacter aerogenes (formerly Aerobacter aerogenes) and Alcaligenes faecalis. Penicillin is no longer considered drug of choice for infections caused by these organisms.. Susceptibility Testing. For specific information regarding susceptibility test interpretive criteria and associated test methods and quality control standards recognized by FDA for this drug, please see: https://www.fda.gov/STIC.

CONTRAINDICATIONS SECTION.


CONTRAINDICATIONS. history of hypersensitivity (anaphylactic) reaction to any penicillin is contraindication.

DESCRIPTION SECTION.


DESCRIPTION. Penicillin sodium for Injection, USP is sterile penicillin sodium powder for reconstitution. It is an antibacterial agent intended for intravenous or intramuscularly use.Chemically, penicillin sodium is designated 4-Thia-1-azabicyclo(3.2.0)-heptane-2-carboxylic acid,3,3-dimethyl-7-oxo-6-[(phenylacetyl)amino]-, [2S -(2, 5, 6)]-, monosodium salt and has the following structural formula:Penicillin sodium, water soluble benzylpenicillin, is white to almost white crystalline powder which is almost odorless and/or after reconstitution colorless solution. The pH of freshly constituted solutions usually ranges from 5.0 to 7.5.Penicillin sodium for Injection, USP is supplied in vials equivalent to 5,000,000 units (5 million units) of penicillin as the sodium salt, with 1.68 mEq of sodium per million units of penicillin G.. chemical-structure.

DOSAGE & ADMINISTRATION SECTION.


DOSAGE AND ADMINISTRATION. Penicillin Sodium for injection, USP may be given intravenously or intramuscularly. The usual dose recommendations are as follows:. Adult Patients Clinical IndicationDosageSerious infections due to susceptible strains ofstreptococci (including S. pneumoniae) andstaphylococci-septicemia, empyema, pneumonia,pericarditis, endocarditis and meningitis5 to 24 million units/day depending on the infection and its severity administered in equally divided doses every to hoursAnthraxMinimum of million units/day in divided doses every hours. Higher doses may be required depending on susceptibility of organism.Actinomycosis Cervicofacial disease Thoracic and abdominal disease1 to million units/day()10 to 20 million units/day()Clostridial infections Botulism (adjunctive therapy to antitoxin) Gas gangrene (debridement and/or surgery as indicated) Tetanus (adjunctive therapy to human tetanus immune globulin)20 million units/day()Diphtheria (adjunctive therapy to antitoxin and for the prevention of the carrier state)2 to million units/day in divided doses for 10 to12 days()Erysipelothrixendocarditis12 to 20 million units/day for to weeks()Fusospirochetosis(severe infections of the oropharnyx [Vincents], lower respiratory tract and genital area)5 to 10 million units/day()Listeria infections Meningitis Endocarditis15 to 20 million units/day for weeks()15 to 20 million units/day for weeks()Pasteurella infections including bacteremia and meningitis4 to million units/day for weeks()Haverhill fever, Rat-bite fever12 to 20 million units/day for to weeks()Disseminated gonococcal infections, such as meningitis endocarditis, arthritis, etc., caused by penicillin- susceptible organisms10 million units/day();duration depends on the type of infectionSyphilis (neurosyphilis)12 to 24 million units/day, as to MU every hours for 10 to 14 days; many experts recommend additional therapy with Benzathine PCN 2.4 MU IM weekly for doses after completion ofIV therapyMeningococcal meningitis and/or septicemia24 million units/day as million units every hoursSerious infections, such as pneumonia and endocarditis, due to susceptible strains ofstreptococci (including S. pneumoniae) andmeningococcus150,000 units/kg/day divided in equal doses every4 to hours; duration depends on infecting organism and type of infectionMeningitis caused by susceptible strains of pneumococcus and meningococcus250,000 units/kg/day divided in equal doses every4 hours for to 14 days depending on the infectingorganism (maximum dose of 12 to 20 million units/day)Disseminated Gonococcal infections (penicillin-susceptible strains)weight less than 45 kg: Arthritis100,000 units/kg/day in equally divided doses for to 10 days Meningitis250,000 units/kg/day in equal doses every hours for 10 to 14 days Endocarditis250,000 units/kg/day in equal doses every hoursfor weeksArthritis, meningitis, endocarditisweight 45 kg or greater:10 million units/day in equally divided doses with the duration of therapy depending on the type of infectionSyphilis (congenital and neurosyphilis) after thenewborn period200,000 to 300,000 units/kg/day (administered as50,000 units/kg every to hours) for 10 to 14 daysDiphtheria (adjunctive therapy to antitoxin and for prevention of the carrier state)150,000 to 250,000 units/kg/day in equal dosesevery hours for to 10 daysRat-bite fever; Haverhill fever (with endocarditis caused by S. moniliformis)150,000 to 250,000 units/kg/day in equal dosesevery hours for weeksBecause of its short half-life, Penicillin is administered in divided doses, usually every to hours with the exception of meningococcal meningitis/septicemia, i.e., every hours.. Pediatric Patients. This product should not be administered to patients requiring less than one million units per dose. (see PRECAUTIONS: Pediatric Use).. Renal Impairment. Penicillin is relatively nontoxic, and dosage adjustments are generally required only in cases of severe renal impairment.The recommended dosage regimens are as follows:Creatinine clearance less than 10 mL/min/1.73 m2; administer full loading dose (see recommended dosages in the tables above) followed by one-half of the loading dose every to 10 hours.Uremic patients with creatinine clearance greater than 10 mL/min/1.73m2; administer full loading dose (see recommended dosages in the tables above) followed by one-half of the loading dose every to hours.Additional dosage modifications should be made in patients with hepatic disease and renal impairment.For most acute infections, treatment should be continued for at least 48 to 72 hours after the patient becomes asymptomatic. Antibiotic therapy for Group -hemolytic streptococcal infections should be maintained for at least 10 days to reduce the risk of rheumatic fever.Parenteral drug products should be inspected visually for particulate matter and discoloration prior to administration whenever solution and container permit.. Preparation of Solution. Solutions of penicillin should be prepared as follows: Loosen powder. Hold vial horizontally and rotate it while slowly directing the stream of diluent against the wall of the vial. Shake vial vigorously after all the diluent has been added. Depending on the route of administration, use Sterile Water for Injection, USP, 0.9% Sodium Chloride Injection, USP, or Dextrose Injections, USP.Note: Penicillins are rapidly inactivated in the presence of carbohydrate solutions at alkaline pH.PREPARATION OF SOLUTION 5 million unitsDiluent AddedFinal Concentration8 mL 500,000 units/mL3 mL 1,000,000 units/mL.

DRUG & OR LABORATORY TEST INTERACTIONS SECTION.


Drug/Laboratory Test Interactions. After treatment with penicillin G, false-positive reaction for glucose in the urine may occur with Benedicts solution, Fehlings solution or Clinitest(R) tablet, but not with the enzyme-based tests, such as Clinistix(R) and Tes-Tape(R).Penicillin has been associated with pseudoproteinuria by certain test methods.

DRUG INTERACTIONS SECTION.


Drug Interactions. Bacteriostatic antibacterials (i.e., chloramphenicol, erythromycins, sulfonamides or tetracyclines) may antagonize the bactericidal effect of penicillin, and concurrent use of these drugs should be avoided. This has been documented in vitro, however, the clinical significance of this interaction is not well-documented.Penicillin blood levels may be prolonged by concurrent administration of probenecid which blocks the renal tubular secretion of penicillins.Other drugs may compete with Penicillin for renal tubular secretion and thus prolong the serum half-life of penicillin. These drugs include: aspirin, phenylbutazone, sulfonamides, indomethacin, thiazide diuretics, furosemide and ethacrynic acid.

GENERAL PRECAUTIONS SECTION.


General. Penicillin should be used with caution in individuals with histories of significant allergies and/or asthma (see WARNINGS). Whenever allergic reactions occur, penicillin should be withdrawn unless, in the opinion of the physician, the condition being treated is life-threatening and amenable only to penicillin therapy.Penicillin Sodium for injection, USP by the intravenous route in high doses (above 10 million units) should be administered slowly because of the potential adverse effects of electrolyte imbalance from the sodium content of the penicillin. Penicillin Sodium for injection, USP contains 1.68 mEq of sodium per million units of penicillin G.The use of antibiotics may promote overgrowth of nonsusceptible organisms, including fungi. Indwelling intravenous catheters encourage superinfections. Should superinfection occur, appropriate measures should be taken.When indicated, incision and drainage or other surgical procedures should be performed in conjunction with antibiotic therapy.Prescribing penicillin sodium in the absence of proven or strongly suspected bacterial infection or prophylactic indication is unlikely to provide benefit to the patient and increases the risk of the development of drug-resistant bacteria.

INDICATIONS & USAGE SECTION.


INDICATIONS AND USAGE. Therapy. Penicillin Sodium for Injection, USP is indicated in the treatment of serious infections caused by susceptible strains of the designated microorganisms in the conditions listed below. Appropriate culture and susceptibility tests should be done before treatment in order to isolate and identify organisms causing infection and to determine their susceptibility to penicillin G. Therapy with Penicillin Sodium for Injection, USP may be initiated before results of such tests are known when there is reason to believe the infection may involve any of the organisms listed below, however, once these results become available, appropriate therapy should be continued.Clinical IndicationInfecting OrganismSepticemia, empyema,pneumonia, pericarditis,endocarditis, meningitisStreptococcus pyogenes(group -hemolyticstreptococcus), other-hemolytic streptococciincluding groups C, H, G, Land M, Streptococcus pneumoniae andStaphylococcus species (non-penicillinase producing strains)AnthraxBacillus anthracisActinomycosis (cervico-facial disease andthoracic and abdominaldisease)Actinomyces IsraelilBotulism (adjunctivetherapy to antitoxin),gas gangrene, andtetanus (adjunctivetherapy to humantetanus immune globulin)Clostridium speciesDiphtheria (adjunctivetherapy to antitoxin andprevention of the carrierstate)CorynebacteriumdiphtheriaeErysipelothrix endocarditisErysipelothrixrhusiopthiaeFusospirochetosis(severe infections of theoropharynx [Vincents],lower respiratory tractand genital area)Fusobacterium speciesand spirochetesListeria infectionsincluding meningitis andendocarditisListeria monocytogenesPasteurella infectionsincluding bacteremia andmeningitisPasteurella multocidaHaverhill feverStreptobacillusmoniliformisRat-bite feverSpirillum minus orStreptobacillusmoniliformisDisseminated gonococcalinfectionsNeisseria gonorrhoeae(penicillin-susceptible)Syphilis (congenital andneurosyphilis)Treponema pallidumMeningococcalmeningitis and/orsepticemiaNeisseria meningitidisGram-negative bacillaryinfections (bacteremias)Escherichia coli,Enterobacter aerogenes,Alcaligenes faecalis,salmonella, shigella andProteus mirabilis, Penicillin Gis not the drug of choice in thetreatment of gram-negativebacillary infections.To reduce the development of drug-resistant bacteria and maintain the effectiveness of penicillin sodium and other antibacterial drugs, penicillin sodium should be used only to treat or prevent infections that are proven or strongly suspected to be caused by susceptible bacteria. When culture and susceptibility information are available, they should be considered in selecting or modifying antibacterial therapy. In the absence of such data, local epidemiology and susceptibility patterns may contribute to the empiric selection of therapy.

INFORMATION FOR PATIENTS SECTION.


Information for Patients. Patients should be counseled that antibacterial drugs including penicillin sodium should only be used to treat bacterial infections. They do not treat viral infections (e.g., the common cold). When penicillin sodium is prescribed to treat bacterial infection, patients should be told that although it is common to feel better early in the course of therapy, the medication should be taken exactly as directed. Skipping doses or not completing the full course of therapy may: (1) decrease the effectiveness of the immediate treatment, and (2) increase the likelihood that bacteria will develop resistance and will not be treatable by penicillin sodium or other antibacterial drugs in the future.Diarrhea is 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.

LABORATORY TESTS SECTION.


Laboratory Tests. Periodic assessment of organ system function, including frequent evaluation of electrolyte balance, hepatic, renal and hematopoietic systems, and cardiac and vascular status should be performed during prolonged therapy with high doses of intravenous penicillin (see ADVERSE REACTIONS). If any impairment of function is suspected or known to exist, reduction in the total dosage should be considered (see DOSAGE AND ADMINISTRATION).In suspected staphylococcal infections, proper laboratory studies, including susceptibility tests should be performed.All infections due to Group beta-hemolytic streptococci should be treated for at least 10 days.Patients being treated for gonococcal infection should have serologic test for syphilis before receiving penicillin. All cases of penicillin treated syphilis should receive adequate follow-up including clinical and serological examinations. The recommended follow-up varies with the stage of syphilis being treated. See CDC recommendations.

NURSING MOTHERS SECTION.


Nursing Mothers. Penicillins are excreted in human milk. Caution should be exercised when penicillins are administered to nursing woman.

OVERDOSAGE SECTION.


OVERDOSAGE. Dose related toxicity may arise with the use of massive doses of intravenous penicillins (40 to 100 million units per day), particularly in patients with severe renal impairment (see PRECAUTIONS). The manifestations may include agitation, confusion, asterixis, hallucinations, stupor, coma, multifocal myocionus, seizures and encephalopathy. Hypernatremia is also possible (see ADVERSE REACTIONS: Metabolic).In case of over-dosage, discontinue penicillin, treat symptomatically and institute supportive measures as required. If necessary, hemodialysis may be used to reduce blood levels of penicillin G, although the degree of effectiveness of this procedure is questionable.

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL.


5,000,000 Unit Vial Label. NDC 0781-6153-95Penicillin Sodiumfor Injection, USP5,000,000 Units(5 million units)Rx OnlyFor IM or IV use10 VialsSANDOZ. 5-million-case-label.

PEDIATRIC USE SECTION.


Pediatric Use. lncompletely developed renal function in newborns may delay elimination of penicillin; therefore, appropriate reductions in the dosage and frequency of administration should be made in these patients. All newborns treated with penicillins should be monitored closely for clinical and laboratory evidence of toxic or adverse effects (see PRECAUTIONS).Pediatric doses are generally determined on weight basis and should be calculated for each patient individually. Recommended guidelines for pediatric dosages are presented in DOSAGE AND ADMINISTRATION.The potential for toxic effects in children from chemicals that may leach from the single dose premixed intravenous preparation in plastic containers has not been evaluated.

PRECAUTIONS SECTION.


PRECAUTIONS. General. Penicillin should be used with caution in individuals with histories of significant allergies and/or asthma (see WARNINGS). Whenever allergic reactions occur, penicillin should be withdrawn unless, in the opinion of the physician, the condition being treated is life-threatening and amenable only to penicillin therapy.Penicillin Sodium for injection, USP by the intravenous route in high doses (above 10 million units) should be administered slowly because of the potential adverse effects of electrolyte imbalance from the sodium content of the penicillin. Penicillin Sodium for injection, USP contains 1.68 mEq of sodium per million units of penicillin G.The use of antibiotics may promote overgrowth of nonsusceptible organisms, including fungi. Indwelling intravenous catheters encourage superinfections. Should superinfection occur, appropriate measures should be taken.When indicated, incision and drainage or other surgical procedures should be performed in conjunction with antibiotic therapy.Prescribing penicillin sodium in the absence of proven or strongly suspected bacterial infection or prophylactic indication is unlikely to provide benefit to the patient and increases the risk of the development of drug-resistant bacteria.. Laboratory Tests. Periodic assessment of organ system function, including frequent evaluation of electrolyte balance, hepatic, renal and hematopoietic systems, and cardiac and vascular status should be performed during prolonged therapy with high doses of intravenous penicillin (see ADVERSE REACTIONS). If any impairment of function is suspected or known to exist, reduction in the total dosage should be considered (see DOSAGE AND ADMINISTRATION).In suspected staphylococcal infections, proper laboratory studies, including susceptibility tests should be performed.All infections due to Group beta-hemolytic streptococci should be treated for at least 10 days.Patients being treated for gonococcal infection should have serologic test for syphilis before receiving penicillin. All cases of penicillin treated syphilis should receive adequate follow-up including clinical and serological examinations. The recommended follow-up varies with the stage of syphilis being treated. See CDC recommendations.. Drug Interactions. Bacteriostatic antibacterials (i.e., chloramphenicol, erythromycins, sulfonamides or tetracyclines) may antagonize the bactericidal effect of penicillin, and concurrent use of these drugs should be avoided. This has been documented in vitro, however, the clinical significance of this interaction is not well-documented.Penicillin blood levels may be prolonged by concurrent administration of probenecid which blocks the renal tubular secretion of penicillins.Other drugs may compete with Penicillin for renal tubular secretion and thus prolong the serum half-life of penicillin. These drugs include: aspirin, phenylbutazone, sulfonamides, indomethacin, thiazide diuretics, furosemide and ethacrynic acid.. Drug/Laboratory Test Interactions. After treatment with penicillin G, false-positive reaction for glucose in the urine may occur with Benedicts solution, Fehlings solution or Clinitest(R) tablet, but not with the enzyme-based tests, such as Clinistix(R) and Tes-Tape(R).Penicillin has been associated with pseudoproteinuria by certain test methods.. Carcinogenesis, Mutagenesis, Impairment of Fertility. No long-term animal studies have been conducted with this drug.. Pregnancy. Teratogenic Effects. Reproduction studies performed in the mouse, rat, and rabbit have revealed no evidence of impaired fertility or harm to the fetus due to penicillin G. Human experience with the penicillins during pregnancy has not shown any positive evidence of adverse effects on the fetus. There are, however, no adequate and well controlled studies in pregnant women showing conclusively that harmful effects of these drugs on the fetus can be excluded. Because animal reproduction studies are not always predictive of human response, this drug should be used during pregnancy only if clearly needed.. Nursing Mothers. Penicillins are excreted in human milk. Caution should be exercised when penicillins are administered to nursing woman.. Pediatric Use. lncompletely developed renal function in newborns may delay elimination of penicillin; therefore, appropriate reductions in the dosage and frequency of administration should be made in these patients. All newborns treated with penicillins should be monitored closely for clinical and laboratory evidence of toxic or adverse effects (see PRECAUTIONS).Pediatric doses are generally determined on weight basis and should be calculated for each patient individually. Recommended guidelines for pediatric dosages are presented in DOSAGE AND ADMINISTRATION.The potential for toxic effects in children from chemicals that may leach from the single dose premixed intravenous preparation in plastic containers has not been evaluated.. Information for Patients. Patients should be counseled that antibacterial drugs including penicillin sodium should only be used to treat bacterial infections. They do not treat viral infections (e.g., the common cold). When penicillin sodium is prescribed to treat bacterial infection, patients should be told that although it is common to feel better early in the course of therapy, the medication should be taken exactly as directed. Skipping doses or not completing the full course of therapy may: (1) decrease the effectiveness of the immediate treatment, and (2) increase the likelihood that bacteria will develop resistance and will not be treatable by penicillin sodium or other antibacterial drugs in the future.Diarrhea is 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.

PREGNULLNCY SECTION.


Pregnancy. Teratogenic Effects. Reproduction studies performed in the mouse, rat, and rabbit have revealed no evidence of impaired fertility or harm to the fetus due to penicillin G. Human experience with the penicillins during pregnancy has not shown any positive evidence of adverse effects on the fetus. There are, however, no adequate and well controlled studies in pregnant women showing conclusively that harmful effects of these drugs on the fetus can be excluded. Because animal reproduction studies are not always predictive of human response, this drug should be used during pregnancy only if clearly needed.

SPL UNCLASSIFIED SECTION.


Rx OnlyTo reduce the development of drug-resistant bacteria and maintain the effectiveness of penicillin sodium and other antibacterial drugs, penicillin sodium should be used only to treat or prevent infections that are proven or strongly suspected to be caused by bacteria.

STORAGE AND HANDLING SECTION.


STORAGE. Store dry powder at 20 to 25C (68 to 77F) (see USP Controlled Room Temperature).Sterile constituted solution may be kept in refrigerator (2 to 8C) for days without significant loss of potency.Manufactured by Sandoz GmbH for Sandoz Inc., Princeton, NJ 0854046270951May 2020.

WARNINGS SECTION.


WARNINGS. SERIOUS AND OCCASIONULLLLY FATAL HYPERSENSITIVITY (anaphylactic) REACTIONS HAVE BEEN REPORTED IN PATIENTS ON PENICILLIN THERAPY. THESE REACTIONS ARE MORE LIKELY TO OCCUR IN INDIVIDUALS WITH HISTORY OF PENICILLIN HYPERSENSITIVITY AND/OR HISTORY OF SENSITIVITY TO MULTIPLE ALLERGENS. THERE HAVE BEEN REPORTS OF INDIVIDUALS WITH HISTORY OF PENICILLIN HYPERSENSITIVITY WHO HAVE EXPERIENCED SEVERE REACTIONS WHEN TREATED WITH CEPHALOSPORINS. BEFORE INITIATING THERAPY WITH PENICILLIN G, CAREFUL INQUIRY SHOULD BE MADE CONCERNING PREVIOUS HYPERSENSITIVITY REACTIONS TO PENICILLINS, CEPHALOSPORINS, OR OTHER ALLERGENS. IF AN ALLERGIC REACTION OCCURS, PENICILLIN SHOULD BE DISCONTINUED AND APPROPRIATE THERAPY INSTITUTED. SERIOUS ANULLPHYLACTIC REACTIONS REQUIRE IMMEDIATE EMERGENCY TREATMENT WITH EPINEPHRINE. OXYGEN, INTRAVENOUS STEROIDS, AND AIRWAY MANULLGEMENT, INCLUDING INTUBATION, SHOULD ALSO BE ADMINISTERED AS INDICATED.Clostridium difficile associated diarrhea (CDAD) has been reported with use of nearly all antibacterial agents, including penicillin sodium, 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 and 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.