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CLAVULANIC ACID

Classification   |    Detailed evidence-based information

Therapeutic Toxic Class

    A) Clavulanic acid is a beta-lactamase inhibitor found in combination products with amoxicillin or ticarcillin to enhance antibacterial activity of the penicillin against resistant strains.

Specific Substances

    A) CLAVULANIC ACID
    1) BRL 14151
    2) Clavulanic acid
    3) MM 14151
    4) CAS 58001-44-8 (clavulanic acid)
    5) CAS 58001-44-8
    POTASSIUM CLAVULANATE
    1) Clavulanate potassium
    2) CAS 61177-45-5
    3) BRL 14151K
    SODIUM CLAVULANATE
    1) Sodium clavulanate
    2) CAS 57943-81-4

Available Forms Sources

    A) FORMS
    1) Clavulanic acid is only available in combination with either amoxicillin (amoxicillin/clavulanate potassium) or ticarcillin (ticarcillin disodium with clavulanate potassium) (Prod Info AUGMENTIN(R) oral tablets, oral powder for suspension, oral chewable tablets, 2013; Prod Info TIMENTIN(R) intravenous injection, 2012; Prod Info AUGMENTIN(R) powder for oral suspension , chewable tablets, 2009; Prod Info Amoxicillin/Clavulanate Potassium oral tablets, 2008; Prod Info AUGMENTIN ES-600(R) powder for oral suspension, 2006; Prod Info AUGMENTIN XR(R) extended release tablets, 2006).
    2) TICARCILLIN DISODIUM WITH CLAVULANATE POTASSIUM
    a) Intravenous powder for solution: Clavulanate potassium - ticarcillin disodium: 1 g-30 g, 100 mg-3 g (Prod Info TIMENTIN(R) intravenous injection, 2012)
    b) Intravenous solution: Clavulanate potassium - ticarcillin disodium): 100 mg/100 mL- 3 g/100 mL (Prod Info TIMENTIN(R) intravenous injection, 2012)
    3) AMOXICILLIN WITH CLAVULANATE POTASSIUM
    a) Oral tablet: Amoxicillin - clavulanate potassium: 250 mg-125 mg, 500 mg-125 mg, 875 mg-125 mg
    b) Oral tablet: chewable: Amoxicillin - clavulanate potassium: 125 mg-31.25 mg, 200 mg-28.5 mg, 250 mg-62.5 mg, 400 mg-57 mg
    c) Oral tablet, extended release: Amoxicillin - clavulanate potassium: 1000 mg-62.5 mg
    d) Oral powder for suspension: Amoxicillin - clavulanate potassium: 125 mg/5 mL-31.25 mg/5 mL, 200 mg/5 mL-28.5 mg/5 mL, 250 mg/5 mL-62.5 mg/5 mL, 400 mg/5 mL-57 mg/5 mL, 600 mg/5 mL-42.9 mg/5 mL
    e) References: (Prod Info AUGMENTIN(R) oral tablets, oral powder for suspension, oral chewable tablets, 2013; Prod Info TIMENTIN(R) intravenous injection, 2012; Prod Info AUGMENTIN(R) powder for oral suspension , chewable tablets, 2009; Prod Info Amoxicillin/Clavulanate Potassium oral tablets, 2008; Prod Info AUGMENTIN ES-600(R) powder for oral suspension, 2006; Prod Info AUGMENTIN XR(R) extended release tablets, 2006).
    B) USES
    1) Combination products containing amoxicillin/clavulanate potassium and ticarcillin disodium with clavulanate potassium are used in the treatment of various bacterial infections (Haemophilus influenzae, Moraxella (Branhamella) catarrhalis, various strains of Staphylococcus aureus, E. coli and Klebsiella spp.) (Prod Info AUGMENTIN(R) oral tablets, oral powder for suspension, oral chewable tablets, 2013; Prod Info TIMENTIN(R) intravenous injection, 2012; Prod Info AUGMENTIN(R) powder for oral suspension , chewable tablets, 2009; Prod Info Amoxicillin/Clavulanate Potassium oral tablets, 2008; Prod Info AUGMENTIN ES-600(R) powder for oral suspension, 2006; Prod Info AUGMENTIN XR(R) extended release tablets, 2006).

Life Support

    A) This overview assumes that basic life support measures have been instituted.

Clinical Effects

    0.2.1) SUMMARY OF EXPOSURE
    A) USES: Combination products containing amoxicillin with clavulanate potassium and ticarcillin disodium with clavulanate potassium are used in the treatment of various bacterial infections (Haemophilus influenzae, Moraxella (Branhamella) catarrhalis, various strains of Staphylococcus aureus, E. coli and Klebsiella spp.). Most available literature discusses the use of clavulanic acid as a combination product; therefore, the effects reported may not be directly related to clavulanic acid, but related to the penicillin used. Refer to "PENICILLINS" management for more information.
    B) PHARMACOLOGY: Clavulanic acid is a beta-lactamase inhibitor produced by Streptomyces clavuligerus which has been shown to inhibit staphylococcal beta-lactamases and numerous beta-lactamases produced by gram-negative organisms. Clavulanic acid also inhibits beta-lactamases produced by Bacteroides species including B fragilis. When combined with beta-lactam antibiotics, the activity of the antibiotic is extended against beta-lactamase-producing organisms which would otherwise be resistant.
    C) EPIDEMIOLOGY: Overdose is rare.
    D) WITH THERAPEUTIC USE
    1) Nausea, vomiting, and/or diarrhea are the most common (up to 30%) adverse effects seen with therapeutic oral use of clavulanic acid; these effects are dose-related. Other effects include electrolyte disturbances, dizziness, behavioral changes, urticaria-arthralgia, hypersensitivity reaction, rash, candidal vaginitis, non-thrombocytopenic purpura, thrombocytosis, neutropenia, and eosinophilia. Tachycardia and/or hypotension may accompany systemic allergic reactions, which are rare. Liver injury, primarily cholestasis, has been reported. Persistent hepatic injury resulted in liver transplantation in a toddler after amoxicillin/clavulanic acid therapy.
    E) WITH POISONING/EXPOSURE
    1) Most patients are asymptomatic or experience mild gastrointestinal symptoms of abdominal pain, nausea, vomiting and diarrhea following overdose with combination agents. Rash, hyperactivity, or drowsiness have occurred in a small number of patients.
    0.2.20) REPRODUCTIVE
    A) Clavulanic acid would be expected to appear in human breast milk. Clavulanic acid also crosses the placenta in levels similar to maternal serum levels. No effects on fertility have been demonstrated. No teratogenic effects have been demonstrated.

Laboratory Monitoring

    A) Monitor vital signs and mental status.
    B) Monitor serum electrolytes after large overdose as hyperkalemia may develop. Other routine laboratory studies are generally not necessary after overdose unless otherwise clinically indicated.
    C) Monitor fluid status in patients with severe vomiting and/or diarrhea.
    D) Obtain a baseline ECG and institute continuous cardiac monitoring in patients with significant hypersensitivity/anaphylactoid reaction.
    E) Plasma concentrations clavulanic acid and the associated antibiotics are not clinically useful in overdose situations.

Treatment Overview

    0.4.2) ORAL/PARENTERAL EXPOSURE
    A) MANAGEMENT OF MILD TO MODERATE TOXICITY
    1) Treatment is symptomatic and supportive. Treat significant vomiting and diarrhea with IV fluids; administer antiemetics, as needed. HYPERSENSITIVITY REACTION: Administer antihistamines, with or without inhaled beta agonists, corticosteroids or epinephrine.
    B) MANAGEMENT OF SEVERE TOXICITY
    1) ANAPHYLAXIS: Acute anaphylaxis is more likely to occur after parenteral exposure, but may develop with all routes. Administer oxygen, aggressive airway management, antihistamines, epinephrine, corticosteroids, ECG monitoring, and IV fluids. SEIZURES: Treat seizures with IV benzodiazepines; barbiturates or propofol may be needed if seizures persist or recur.
    C) DECONTAMINATION
    1) PREHOSPITAL: GI decontamination is generally not necessary as toxicity is limited.
    2) HOSPITAL: GI decontamination is generally not necessary as toxicity is limited .
    D) AIRWAY MANAGEMENT
    1) Airway management is unlikely following overdose; however, aggressive airway management is indicated in patients that develop a significant hypersensitivity/anaphylactoid reaction.
    E) ANTIDOTE
    1) None
    F) ENHANCED ELIMINATION PROCEDURE
    1) HEMODIALYSIS: Ampicillin-class antibiotics, amoxicillin and ticarcillin are removed from the circulation by hemodialysis, but as severe toxicity is highly unlikely, hemodialysis is almost never indicated.
    G) PATIENT DISPOSITION
    1) HOME CRITERIA: Asymptomatic children and those with mild GI effects after inadvertent ingestions of pediatric preparations can generally be managed at home. A number of children ingesting more than 250 mg/kg of amoxicillin have developed crystalluria, hematuria and transient renal insufficiency; any patient who develops urinary symptoms should be referred to a healthcare facility.
    2) OBSERVATION CRITERIA: Patients with deliberate overdose or with more than mild symptoms should be evaluated in a health care facility. All patients with a history of penicillin allergy or evidence of a hypersensitivity reaction should be referred immediately to a healthcare facility. Patients should be observed until symptoms resolve and clinical parameters (eg, vital signs, mental status) are within normal limits.
    3) ADMISSION CRITERIA: Patients with ongoing symptoms should be admitted.
    4) CONSULT CRITERIA: Consult a poison center or medical toxicologist for assistance in patients with persistent renal or cardiovascular symptoms.
    H) PITFALLS
    1) Toxicity is limited; do not overtreat. If significant toxicity develops, an alternative etiology should be sought.
    I) PHARMACOKINETICS
    1) SELECT AGENTS: AMOXICILLIN: Approximately, 25% bound to plasma proteins. Half-life after oral administration is 1.3 hours. Amoxicillin is approximately 50% to 70% excreted unchanged in the urine during the first 6 hours after a single 250 mg or 500 mg tablet. TICARCILLIN: Approximately, 45% bound to serum proteins. There is an inverse relationship between the serum half-life and creatinine clearance; half-life approximately 1.1 hours in healthy patients.
    J) PREDISPOSING CONDITIONS
    1) Underlying renal impairment; hepatic insufficiency.
    K) DIFFERENTIAL DIAGNOSIS
    1) Ingestion of a GI irritant, gastroenteritis.

Range Of Toxicity

    A) TOXICITY: Amoxicillin/Clavulanate - Most patients are asymptomatic following overdosage or experience only mild gastrointestinal symptoms. Clavulanic acid combinations are available in numerous formulations; total drug exposure is variable.
    B) THERAPEUTIC DOSES: Varies by indication and formulation: ADULTS: Amoxicillin/clavulanate potassium: 500 or 875 mg orally every 12 hours or 250 or 500 mg orally every 8 hours, depending on the severity and type of infection. Ticarcillin disodium/clavulanate potassium: Systemic and urinary tract infections: The recommended dose is 3.1 g every 4 to 6 hours, administered via an IV infusion over a 30-minute period. Gynecologic infections: Based on the ticarcillin component, the recommended dose is 200 to 300 mg/kg/day in divided doses every 4 to 6 hours, depending on the severity of infection, and administered via an IV infusion over a 30-minute period. CHILDREN: Amoxicillin/clavulanate potassium: Based on the amoxicillin component, the amoxicillin/clavulanate combination product is dosed as follows: ORAL: Neonates and infants less than 3 months of age: Using the 125 mg/5 mL oral suspension of amoxicillin/clavulanate potassium, the recommended dose is 30 mg/kg/day every 12 hours. 3 months or older and less than 40 kg: 25 to 45 mg/kg/day in divided doses every 12 hours, or 20 to 40 mg/kg/day in divided doses every 8 hours, depending on the severity of infection and product strength. 40 kg or more: 500 or 875 mg every 12 hours or 250 or 500 mg every 8 hours, depending on the severity and type of infection. Ticarcillin disodium/clavulanate potassium: Based on the ticarcillin component, the ticarcillin/clavulanate combination product is dosed as follows: INTRAVENOUS: Less than 60 kg: 200 to 300 mg/kg/day in divided doses every 4 to 6 hours, depending on the severity of infection, and administered via an IV infusion over a 30-minute period. 60 kg or more: 3.1 g every 4 to 6 hours, depending on the severity of infection, and administered via an IV infusion over a 30-minute period.

Summary Of Exposure

    A) USES: Combination products containing amoxicillin with clavulanate potassium and ticarcillin disodium with clavulanate potassium are used in the treatment of various bacterial infections (Haemophilus influenzae, Moraxella (Branhamella) catarrhalis, various strains of Staphylococcus aureus, E. coli and Klebsiella spp.). Most available literature discusses the use of clavulanic acid as a combination product; therefore, the effects reported may not be directly related to clavulanic acid, but related to the penicillin used. Refer to "PENICILLINS" management for more information.
    B) PHARMACOLOGY: Clavulanic acid is a beta-lactamase inhibitor produced by Streptomyces clavuligerus which has been shown to inhibit staphylococcal beta-lactamases and numerous beta-lactamases produced by gram-negative organisms. Clavulanic acid also inhibits beta-lactamases produced by Bacteroides species including B fragilis. When combined with beta-lactam antibiotics, the activity of the antibiotic is extended against beta-lactamase-producing organisms which would otherwise be resistant.
    C) EPIDEMIOLOGY: Overdose is rare.
    D) WITH THERAPEUTIC USE
    1) Nausea, vomiting, and/or diarrhea are the most common (up to 30%) adverse effects seen with therapeutic oral use of clavulanic acid; these effects are dose-related. Other effects include electrolyte disturbances, dizziness, behavioral changes, urticaria-arthralgia, hypersensitivity reaction, rash, candidal vaginitis, non-thrombocytopenic purpura, thrombocytosis, neutropenia, and eosinophilia. Tachycardia and/or hypotension may accompany systemic allergic reactions, which are rare. Liver injury, primarily cholestasis, has been reported. Persistent hepatic injury resulted in liver transplantation in a toddler after amoxicillin/clavulanic acid therapy.
    E) WITH POISONING/EXPOSURE
    1) Most patients are asymptomatic or experience mild gastrointestinal symptoms of abdominal pain, nausea, vomiting and diarrhea following overdose with combination agents. Rash, hyperactivity, or drowsiness have occurred in a small number of patients.

Neurologic

    3.7.2) CLINICAL EFFECTS
    A) DIZZINESS
    1) WITH THERAPEUTIC USE
    a) Dizziness is a rare effect reported following therapeutic use of amoxicillin/clavulanic acid (Prod Info Augmentin(R), amoxicillin/clavulanate potassium, 1998).
    B) AGGRESSIVE BEHAVIOR
    1) WITH THERAPEUTIC USE
    a) Reversible irritability and aggressive behavior occurred in patients taking amoxicillin/clavulanic acid. Symptoms disappeared upon drug withdrawal, and recurred upon rechallenge (Prod Info Augmentin(R), amoxicillin/clavulanate potassium, 1998). Amoxicillin alone did not cause these symptoms (Macknin, 1987).
    C) ANXIETY
    1) WITH THERAPEUTIC USE
    a) Anxiety has been reported with amoxicillin/clavulanate potassium (Prod Info AUGMENTIN(R) oral tablets, oral powder for suspension, oral chewable tablets, 2013; Prod Info AUGMENTIN ES-600(R) powder for oral suspension, 2006; Prod Info AUGMENTIN XR(R) extended release tablets, 2006).
    D) PSYCHOMOTOR AGITATION
    1) WITH THERAPEUTIC USE
    a) Agitation has been reported with amoxicillin/clavulanate potassium (Prod Info AUGMENTIN(R) oral tablets, oral powder for suspension, oral chewable tablets, 2013; Prod Info AUGMENTIN ES-600(R) powder for oral suspension, 2006; Prod Info AUGMENTIN XR(R) extended release tablets, 2006).
    E) CLOUDED CONSCIOUSNESS
    1) WITH THERAPEUTIC USE
    a) Confusion has been reported with amoxicillin/clavulanate potassium (Prod Info AUGMENTIN(R) oral tablets, oral powder for suspension, oral chewable tablets, 2013; Prod Info AUGMENTIN ES-600(R) powder for oral suspension, 2006; Prod Info AUGMENTIN XR(R) extended release tablets, 2006).
    F) SEIZURE
    1) WITH THERAPEUTIC USE
    a) Seizures have been reported with amoxicillin/clavulanate potassium (Prod Info AUGMENTIN(R) oral tablets, oral powder for suspension, oral chewable tablets, 2013; Prod Info AUGMENTIN ES-600(R) powder for oral suspension, 2006; Prod Info AUGMENTIN XR(R) extended release tablets, 2006).
    b) Seizures were reported during postmarketing use of ticarcillin and clavulanate therapy. The risk for seizures increases when the dose of ticarcillin and clavulanate exceeds the recommended dose, particularly in patients with impaired renal function (Prod Info TIMENTIN(R) intravenous injection, 2012).
    G) DIZZINESS
    1) WITH THERAPEUTIC USE
    a) Dizziness has been reported with amoxicillin/clavulanate potassium (Prod Info AUGMENTIN(R) oral tablets, oral powder for suspension, oral chewable tablets, 2013; Prod Info AUGMENTIN ES-600(R) powder for oral suspension, 2006; Prod Info AUGMENTIN XR(R) extended release tablets, 2006).
    H) HEADACHE
    1) WITH THERAPEUTIC USE
    a) Headache was reported during postmarketing use of ticarcillin and clavulanate therapy (Prod Info TIMENTIN(R) intravenous injection, 2012).

Gastrointestinal

    3.8.2) CLINICAL EFFECTS
    A) DRUG-INDUCED GASTROINTESTINAL DISTURBANCE
    1) WITH THERAPEUTIC USE
    a) Nausea, vomiting, and/or diarrhea are the most frequent adverse effects seen with therapeutic oral use of clavulanic acid; these effects are dose-related (Prod Info Augmentin(R), amoxicillin/clavulanate potassium, 1998).
    b) INCIDENCE: The estimated incidence of diarrhea is 10% to 30% in usual oral therapeutic administration of clavulanic acid combined with amoxicillin. (Stein & Gurwith, 1984). In clinical trials, diarrhea was reported in 2.9% to 14.5% of patients treated with amoxicillin/clavulanate potassium therapy. Side effects increased with higher doses (Prod Info AUGMENTIN XR(R) extended release tablets, 2006).
    2) WITH POISONING/EXPOSURE
    a) Although most patients remain asymptomatic following overdose, gastrointestinal symptoms of abdominal pain, vomiting and diarrhea are the most frequently reported effects (Prod Info Augmentin(R), amoxicillin/clavulanate potassium, 1998).
    b) In clinical trials, diarrhea and loose stools were reported in 9% of patients treated with amoxicillin/clavulanate potassium therapy. Side effects increased with higher doses (Prod Info AUGMENTIN(R) oral tablets, oral powder for suspension, oral chewable tablets, 2013).
    B) ABDOMINAL PAIN
    1) WITH THERAPEUTIC USE
    a) Abdominal pain has also been reported as a consequence of therapeutic use of clavulanic acid combined with amoxicillin (Iravani et al, 1988; Stein & Gurwith, 1984).
    C) ANTIBIOTIC ENTEROCOLITIS
    1) WITH THERAPEUTIC USE
    a) PSEUDOMEMBRANOUS COLITIS has also occurred with use of this combination (Abramowicz, 1984; Prod Info Augmentin(R), amoxicillin/clavulanate potassium, 1998).
    b) Enterocolitis has been reported with amoxicillin/clavulanate potassium (Prod Info AUGMENTIN(R) oral tablets, oral powder for suspension, oral chewable tablets, 2013; Prod Info AUGMENTIN ES-600(R) powder for oral suspension, 2006; Prod Info AUGMENTIN XR(R) extended release tablets, 2006).
    D) PSEUDOMEMBRANOUS ENTEROCOLITIS
    1) WITH THERAPEUTIC USE
    a) Hemorrhagic or pseudomembranous colitis has been reported with amoxicillin/clavulanate potassium (Prod Info AUGMENTIN(R) oral tablets, oral powder for suspension, oral chewable tablets, 2013; Prod Info AUGMENTIN ES-600(R) powder for oral suspension, 2006; Prod Info AUGMENTIN XR(R) extended release tablets, 2006).

Hepatic

    3.9.2) CLINICAL EFFECTS
    A) CHOLESTATIC HEPATITIS
    1) SUMMARY: A causal relationship between cholestatic jaundice and the administration of amoxicillin/clavulanic acid may exist. Several cases of cholestatic hepatitis have been reported in the literature (Reddy et al, 1989; Schneider et al, 1989; Verhamme et al, 1989).
    2) CASE REPORTS
    a) In a toddler, progressive cholestasis resulted in orthotopic liver transplantation after receiving amoxicillin/clavulanic acid therapy (Chawla et al, 2000).
    b) Three cases reported to the Australian Adverse Drug Reactions Committee suggested an association between amoxicillin/clavulanic acid therapy and jaundice (ADRAC, 1988).
    c) Eighteen cases of hepatic dysfunction were related to amoxicillin/clavulanic acid therapy. Cholestatic and hepatocellular syndromes were seen, but were benign and reversible in all cases (Reddy et al, 1989).
    d) A 37-year-old man with no past medical history was given a 10-day course of amoxicillin-clavulanate for treatment of pneumonia and developed jaundice, rash, pruritus, and increasing fatigue approximately one month later. A liver biopsy revealed centrilobular cholestasis. Despite symptomatic care, the patient developed an acute onset of renal failure and a skin rash consistent with toxic epidermal necrolysis approximately 60 days after initial therapy. High dose corticosteroid therapy was ineffective and the patient died (Limauro et al, 1999).
    e) PEDIATRIC: A 2.9-year-old male was treated for otitis media with a 10-day course of amoxicillin-clavulanic acid and developed an initial rash followed by jaundice and pruritus over the next several days. One month after symptoms began, a liver biopsy revealed centrolobular cholestasis consistent with a drug reaction. Due to ongoing symptoms of pruritus, failure to grow and extensive xanthomatosis, the child underwent successful liver transplantation; the native liver had signs of biliary cirrhosis with ductular proliferation and ductopenia (Chawla et al, 2000).
    B) LIVER ENZYMES ABNORMAL
    1) CASE REPORT: An adult developed elevated liver enzymes following the therapeutic use of amoxicillin-clavulanic acid. Similar liver injury occurred after receiving erythromycin 2 years later. In both incidences, liver function returned to normal within several weeks (Horsmans & Geubel, 1994).
    C) TOXIC LIVER DISEASE
    1) WITH THERAPEUTIC USE
    a) Liver injury (ie, hepatitis and cholestatic jaundice, increases in serum transaminases, serum bilirubin and/or alkaline phosphatase) has been reported with amoxicillin/clavulanate potassium therapy and during postmarketing surveillance. It has been reported more frequently in the elderly, in men, or in patients on prolonged therapy. Liver injury following amoxicillin/clavulanic acid has resulted in death (less than 1 death reported per estimated 4 million prescriptions worldwide); however, these cases have generally been associated with serious underlying diseases or concomitant medications. Onset of symptoms of liver injury may occur during or several weeks after stopping therapy. Although the liver injury may be severe, the condition is generally reversible (Prod Info AUGMENTIN(R) oral tablets, oral powder for suspension, oral chewable tablets, 2013; Prod Info AUGMENTIN ES-600(R) powder for oral suspension, 2006; Prod Info AUGMENTIN XR(R) extended release tablets, 2006).

Genitourinary

    3.10.2) CLINICAL EFFECTS
    A) VAGINITIS
    1) Candidal vaginitis has been reported following therapeutic use of clavulanic acid/amoxicillin (Stein & Gurwith, 1984).
    B) INTERSTITIAL NEPHRITIS
    1) WITH THERAPEUTIC USE
    a) Interstitial nephritis has been reported with amoxicillin/clavulanate potassium (Prod Info AUGMENTIN(R) oral tablets, oral powder for suspension, oral chewable tablets, 2013; Prod Info AUGMENTIN ES-600(R) powder for oral suspension, 2006; Prod Info AUGMENTIN XR(R) extended release tablets, 2006).
    C) BLOOD IN URINE
    1) WITH THERAPEUTIC USE
    a) Hematuria has been reported with amoxicillin/clavulanate potassium (Prod Info AUGMENTIN(R) oral tablets, oral powder for suspension, oral chewable tablets, 2013; Prod Info AUGMENTIN ES-600(R) powder for oral suspension, 2006; Prod Info AUGMENTIN XR(R) extended release tablets, 2006).
    D) CRYSTALLURIA
    1) WITH THERAPEUTIC USE
    a) Crystalluria has been reported with amoxicillin/clavulanate potassium (Prod Info AUGMENTIN(R) oral tablets, oral powder for suspension, oral chewable tablets, 2013; Prod Info AUGMENTIN ES-600(R) powder for oral suspension, 2006; Prod Info AUGMENTIN XR(R) extended release tablets, 2006).
    E) SERUM BLOOD UREA NITROGEN RAISED
    1) WITH THERAPEUTIC USE
    a) Isolated reports of increases in blood-urea nitrogen have occurred (Brogden et al, 1981a; Mashimo, 1981).
    F) SERUM CREATININE RAISED
    1) WITH THERAPEUTIC USE
    a) Isolated reports of increases in serum creatinine levels have occurred (Brogden et al, 1981a; Mashimo, 1981).

Hematologic

    3.13.2) CLINICAL EFFECTS
    A) PLATELET AGGREGATION
    1) WITH THERAPEUTIC USE
    a) No direct hematologic effects of clavulanic acid have been demonstrated. However, high doses of ticarcillin (with which clavulanic acid is frequently combined) have been reported to cause impaired coagulation by impairing platelet function (Jackson et al, 1985).
    b) Prolonged prothrombin time and bleeding time have also been observed with ticarcillin/clavulanic acid therapy (Prod Info Timentin(R), ticarcillin disodium/clavulanate potassium, 1998).
    B) THROMBOCYTOSIS
    1) WITH THERAPEUTIC USE
    a) Thrombocytosis was reported after 48 hours of ticarcillin/clavulanic acid therapy. Platelet count remained high during antibiotic treatment, but resolved upon discontinuation of the drug (Prod Info TIMENTIN(R) intravenous injection, 2012; Moody & Pawlicki, 1987; Prod Info Timentin(R), ticarcillin disodium/clavulanate potassium, 1998).
    b) Thrombocytopenia has been reported with amoxicillin/clavulanate potassium. Effects were reversible after withdrawal of treatment and are believed to be hypersensitivity related (Prod Info AUGMENTIN(R) oral tablets, oral powder for suspension, oral chewable tablets, 2013; Prod Info AUGMENTIN ES-600(R) powder for oral suspension, 2006; Prod Info AUGMENTIN XR(R) extended release tablets, 2006).
    C) THROMBOCYTOPENIC PURPURA
    1) WITH THERAPEUTIC USE
    a) Thrombocytopenic purpura has been reported with amoxicillin/clavulanate potassium. Effects were reversible after withdrawal of treatment and are believed to be hypersensitivity related (Prod Info AUGMENTIN(R) oral tablets, oral powder for suspension, oral chewable tablets, 2013; Prod Info AUGMENTIN ES-600(R) powder for oral suspension, 2006; Prod Info AUGMENTIN XR(R) extended release tablets, 2006).
    D) LEUKOPENIA
    1) WITH THERAPEUTIC USE
    a) Severe neutropenia developed after 45 days of amoxicillin/clavulanic acid therapy. Six days after cessation of the drug, normal myelopoiesis resumed (Desgrandchamps & Schnyder, 1987).
    b) Leukopenia has been reported with amoxicillin/clavulanate potassium. Effects were reversible after withdrawal of treatment and are believed to be hypersensitivity related (Prod Info AUGMENTIN(R) oral tablets, oral powder for suspension, oral chewable tablets, 2013; Prod Info AUGMENTIN ES-600(R) powder for oral suspension, 2006; Prod Info AUGMENTIN XR(R) extended release tablets, 2006).
    c) Leukopenia was reported during postmarketing use of ticarcillin and clavulanate therapy (Prod Info TIMENTIN(R) intravenous injection, 2012).
    E) EOSINOPHIL COUNT RAISED
    1) WITH THERAPEUTIC USE
    a) Eosinophilia has been reported with amoxicillin/clavulanate potassium. Effects were reversible after withdrawal of treatment and are believed to be hypersensitivity related (Prod Info AUGMENTIN(R) oral tablets, oral powder for suspension, oral chewable tablets, 2013; Prod Info AUGMENTIN ES-600(R) powder for oral suspension, 2006; Prod Info AUGMENTIN XR(R) extended release tablets, 2006).
    b) Eosinophil counts increased 5% to 8% in 14% of patients treated in the series. These changes were transient and returned to normal within 2 weeks after completion of treatment (Iravani & Richard, 1982).
    F) ANEMIA
    1) WITH THERAPEUTIC USE
    a) Anemia has been reported with amoxicillin/clavulanate potassium. Effects were reversible after withdrawal of treatment and are believed to be hypersensitivity related (Prod Info AUGMENTIN(R) oral tablets, oral powder for suspension, oral chewable tablets, 2013; Prod Info AUGMENTIN ES-600(R) powder for oral suspension, 2006; Prod Info AUGMENTIN XR(R) extended release tablets, 2006).
    G) HEMOLYTIC ANEMIA
    1) WITH THERAPEUTIC USE
    a) Hemolytic anemia has been reported with amoxicillin/clavulanate potassium. Effects were reversible after withdrawal of treatment and are believed to be hypersensitivity related (Prod Info AUGMENTIN(R) oral tablets, oral powder for suspension, oral chewable tablets, 2013; Prod Info AUGMENTIN ES-600(R) powder for oral suspension, 2006; Prod Info AUGMENTIN XR(R) extended release tablets, 2006).
    H) AGRANULOCYTOSIS
    1) WITH THERAPEUTIC USE
    a) Agranulocytosis has been reported with amoxicillin/clavulanate potassium. Effects were reversible after withdrawal of treatment and are believed to be hypersensitivity related (Prod Info AUGMENTIN(R) oral tablets, oral powder for suspension, oral chewable tablets, 2013; Prod Info AUGMENTIN ES-600(R) powder for oral suspension, 2006; Prod Info AUGMENTIN XR(R) extended release tablets, 2006).
    I) NEUTROPENIA
    1) WITH THERAPEUTIC USE
    a) Neutropenia was reported during postmarketing use of ticarcillin and clavulanate therapy (Prod Info TIMENTIN(R) intravenous injection, 2012).

Dermatologic

    3.14.2) CLINICAL EFFECTS
    A) ERUPTION
    1) WITH THERAPEUTIC USE
    a) Skin rashes, including urticaria, have been attributed to clavulanic acid administered concurrently with amoxicillin (Stein & Gurwith, 1984; Schiano, 1989; Prod Info Augmentin(R), amoxicillin/clavulanate potassium, 1998).
    B) ITCHING OF SKIN
    1) WITH THERAPEUTIC USE
    a) Pruritus has been reported with amoxicillin/clavulanate potassium (Prod Info AUGMENTIN(R) oral tablets, oral powder for suspension, oral chewable tablets, 2013; Prod Info AUGMENTIN ES-600(R) powder for oral suspension, 2006; Prod Info AUGMENTIN XR(R) extended release tablets, 2006). Generalized pruritus has also been reported (Stein & Gurwith, 1984).
    C) ACUTE GENERALIZED EXANTHEMATOUS PUSTULOSIS
    1) WITH THERAPEUTIC USE
    a) Acute generalized exanthematous pustulosis has been reported with amoxicillin/clavulanate potassium (Prod Info AUGMENTIN(R) oral tablets, oral powder for suspension, oral chewable tablets, 2013; Prod Info AUGMENTIN ES-600(R) powder for oral suspension, 2006; Prod Info AUGMENTIN XR(R) extended release tablets, 2006).
    D) PURPURA
    1) WITH THERAPEUTIC USE
    a) CASE REPORT: Henoch-Schonlein purpura syndrome occurred in a patient after a short course of amoxicillin/clavulanate, which recurred upon rechallenge. Symptoms resolved with steroid therapy (Wakefield & Hunter, 1988).
    E) DRUG-INDUCED TOXIC PUSTULODERMA
    1) CASE REPORT: A 40-year-old woman developed pustular lesions on her face, neck and upper third of the trunk following 6 days of therapy with amoxicillin-clavulanic acid for pharyngitis and fever. Histological exam was positive for toxic pustuloderma. The patient was treated with antihistamines with improvement noted within one week (Corbalan-Velez et al, 2000).
    F) STEVENS-JOHNSON SYNDROME
    1) Stevens-Johnson syndrome has been reported with amoxicillin/clavulanate potassium (Prod Info AUGMENTIN(R) oral tablets, oral powder for suspension, oral chewable tablets, 2013; Prod Info AUGMENTIN ES-600(R) powder for oral suspension, 2006; Prod Info AUGMENTIN XR(R) extended release tablets, 2006).
    2) CASE REPORT: A 37-year-old man with no past medical history was given a 10-day course of amoxicillin-clavulanate for treatment of pneumonia and developed jaundice, rash, pruritus and increasing fatigue approximately one month later. A liver biopsy revealed centrilobular cholestasis. Despite symptomatic care, the patient developed an acute onset of renal failure and a skin rash consistent with toxic epidermal necrolysis approximately 60 days after initial therapy. High dose corticosteroid therapy was ineffective and the patient died (Limauro et al, 1999).
    G) ERYTHEMA MULTIFORME
    1) WITH THERAPEUTIC USE
    a) Erythema multiforme has been reported with amoxicillin/clavulanate potassium (Prod Info AUGMENTIN(R) oral tablets, oral powder for suspension, oral chewable tablets, 2013; Prod Info AUGMENTIN ES-600(R) powder for oral suspension, 2006; Prod Info AUGMENTIN XR(R) extended release tablets, 2006).

Musculoskeletal

    3.15.2) CLINICAL EFFECTS
    A) JOINT PAIN
    1) WITH THERAPEUTIC USE
    a) CASE REPORT: A serum-sickness-like reaction (urticaria-arthralgia syndrome) occurred in a patient following a 10-day course of amoxicillin/clavulanic acid (dose not stated). The patient refused penicillin skin testing. Gradual, but spontaneous and complete resolution of symptoms occurred within 2 weeks (Schiano, 1989).

Immunologic

    3.19.2) CLINICAL EFFECTS
    A) ANAPHYLACTOID REACTION
    1) WITH THERAPEUTIC USE
    a) Hypersensitivity reactions which may include skin rashes, pruritus, urticaria, angioedema, serum sickness-like reactions, erythema multiforme (rare) and exfoliative dermatitis (rare) have been reported with therapeutic use of amoxicillin/clavulanic acid (Prod Info Augmentin(R), amoxicillin/clavulanate potassium, 1998).
    b) Similar reports of skin rash, pruritus, and urticaria have been reported with the combination of ticarcillin and clavulanic acid. Other effects which were also considered to be a hypersensitivity response included: arthralgia, myalgia, drug fever, chills, and chest discomfort (Prod Info Timentin(R), ticarcillin disodium/clavulanate potassium, 1998).

Reproductive

    3.20.1) SUMMARY
    A) Clavulanic acid would be expected to appear in human breast milk. Clavulanic acid also crosses the placenta in levels similar to maternal serum levels. No effects on fertility have been demonstrated. No teratogenic effects have been demonstrated.
    3.20.2) TERATOGENICITY
    A) LACK OF EFFECT
    1) No reports have attributed human teratogenic effects to clavulanic acid.
    3.20.3) EFFECTS IN PREGNANCY
    A) PLACENTAL BARRIER
    1) Clavulanic acid crosses the placenta (in rats and mice) in concentrations similar to those in maternal serum. No direct effect on pregnancy outcomes has been reported, however (Jackson et al, 1985).
    B) PREGNANCY CATEGORY
    POTASSIUM CLAVULANATEB
    Reference: Briggs et al, 1998
    3.20.4) EFFECTS DURING BREAST-FEEDING
    A) BREAST MILK
    1) Clavulanic acid passes into breast milk of lactating animals (Jackson et al, 1985). Although human data are very limited, a risk of sensitization of the infant would seem to exist.

Genotoxicity

    A) The Ames test for mutagenicity did not demonstrate increases in the rate of mutations. No chromosomal damage was seen in cultured human lymphocytes (Jackson et al, 1985).

Monitoring Parameters Levels

    4.1.1) SUMMARY
    A) Monitor vital signs and mental status.
    B) Monitor serum electrolytes after large overdose as hyperkalemia may develop. Other routine laboratory studies are generally not necessary after overdose unless otherwise clinically indicated.
    C) Monitor fluid status in patients with severe vomiting and/or diarrhea.
    D) Obtain a baseline ECG and institute continuous cardiac monitoring in patients with significant hypersensitivity/anaphylactoid reaction.
    E) Plasma concentrations clavulanic acid and the associated antibiotics are not clinically useful in overdose situations.

Life Support

    A) Support respiratory and cardiovascular function.

Patient Disposition

    6.3.1) DISPOSITION/ORAL EXPOSURE
    6.3.1.1) ADMISSION CRITERIA/ORAL
    A) Patients with ongoing symptoms should be admitted.
    6.3.1.2) HOME CRITERIA/ORAL
    A) Asymptomatic children and those with mild GI effects after inadvertent ingestions of pediatric preparations can generally be managed at home. A number of children ingesting more than 250 mg/kg of amoxicillin have developed crystalluria, hematuria and transient renal insufficiency; any patient who develops urinary symptoms should be referred to a healthcare facility.
    6.3.1.3) CONSULT CRITERIA/ORAL
    A) Consult a poison center or medical toxicologist for assistance in patients with persistent renal or cardiovascular symptoms.
    6.3.1.5) OBSERVATION CRITERIA/ORAL
    A) Patients with deliberate overdose or with more than mild symptoms should be evaluated in a health care facility. All patients with a history of penicillin allergy or evidence of a hypersensitivity reaction should be referred immediately to a healthcare facility. Patients should be observed until symptoms resolve and clinical parameters (eg, vital signs, mental status) are within normal limits.

Monitoring

    A) Monitor vital signs and mental status.
    B) Monitor serum electrolytes after large overdose as hyperkalemia may develop. Other routine laboratory studies are generally not necessary after overdose unless otherwise clinically indicated.
    C) Monitor fluid status in patients with severe vomiting and/or diarrhea.
    D) Obtain a baseline ECG and institute continuous cardiac monitoring in patients with significant hypersensitivity/anaphylactoid reaction.
    E) Plasma concentrations clavulanic acid and the associated antibiotics are not clinically useful in overdose situations.

Oral Exposure

    6.5.1) PREVENTION OF ABSORPTION/PREHOSPITAL
    A) GI decontamination is generally not necessary as toxicity is limited.
    6.5.2) PREVENTION OF ABSORPTION
    A) GI decontamination is generally not necessary as toxicity is limited.
    6.5.3) TREATMENT
    A) SUPPORT
    1) MANAGEMENT OF MILD TO MODERATE TOXICITY
    a) Treatment is symptomatic and supportive. Treat significant vomiting and diarrhea with IV fluids; administer antiemetics, as needed. HYPERSENSITIVITY REACTION: Administer antihistamines, with or without inhaled beta agonists, corticosteroids or epinephrine.
    2) MANAGEMENT OF SEVERE TOXICITY
    a) ANAPHYLAXIS: Acute anaphylaxis is more likely to occur after parenteral exposure, but may develop with all routes. Administer oxygen, aggressive airway management, antihistamines, epinephrine, corticosteroids, ECG monitoring, and IV fluids. SEIZURES: Treat seizures with IV benzodiazepines; barbiturates or propofol may be needed if seizures persist or recur.
    B) MONITORING OF PATIENT
    1) Monitor vital signs and mental status.
    2) Monitor electrolytes after very large overdose as hyperkalemia may develop.
    3) Obtain a baseline ECG and institute continuous cardiac monitoring in patients with significant hypersensitivity/anaphylactoid reaction.
    4) Plasma concentrations of clavulanic acid of the associated antibiotics are not clinically useful in overdose situations.
    C) FLUID/ELECTROLYTE BALANCE REGULATION
    1) If losses are substantial, fluid and electrolyte replacement should be provided as indicated by the patient's clinical status and the results of serum electrolyte determinations.
    D) HYPOTENSIVE EPISODE
    1) SUMMARY
    a) Infuse 10 to 20 milliliters/kilogram of isotonic fluid and keep the patient supine. If hypotension persists, administer dopamine or norepinephrine. Consider central venous pressure monitoring to guide further fluid therapy.
    2) DOPAMINE
    a) DOSE: Begin at 5 micrograms per kilogram per minute progressing in 5 micrograms per kilogram per minute increments as needed (Prod Info dopamine hcl, 5% dextrose IV injection, 2004). If hypotension persists, dopamine may need to be discontinued and a more potent vasoconstrictor (eg, norepinephrine) should be considered (Prod Info dopamine hcl, 5% dextrose IV injection, 2004).
    b) CAUTION: If ventricular dysrhythmias occur, decrease rate of administration (Prod Info dopamine hcl, 5% dextrose IV injection, 2004). Extravasation may cause local tissue necrosis, administration through a central venous catheter is preferred (Prod Info dopamine hcl, 5% dextrose IV injection, 2004).
    3) NOREPINEPHRINE
    a) PREPARATION: 4 milligrams (1 amp) added to 1000 milliliters of diluent provides a concentration of 4 micrograms/milliliter of norepinephrine base. Norepinephrine bitartrate should be mixed in dextrose solutions (dextrose 5% in water, dextrose 5% in saline) since dextrose-containing solutions protect against excessive oxidation and subsequent potency loss. Administration in saline alone is not recommended (Prod Info norepinephrine bitartrate injection, 2005).
    b) DOSE
    1) ADULT: Dose range: 0.1 to 0.5 microgram/kilogram/minute (eg, 70 kg adult 7 to 35 mcg/min); titrate to maintain adequate blood pressure (Peberdy et al, 2010).
    2) CHILD: Dose range: 0.1 to 2 micrograms/kilogram/minute; titrate to maintain adequate blood pressure (Kleinman et al, 2010).
    3) CAUTION: Extravasation may cause local tissue ischemia, administration by central venous catheter is advised (Peberdy et al, 2010).
    E) ACUTE ALLERGIC REACTION
    1) SUMMARY
    a) Mild to moderate allergic reactions may be treated with antihistamines with or without inhaled beta adrenergic agonists, corticosteroids or epinephrine. Treatment of severe anaphylaxis also includes oxygen supplementation, aggressive airway management, epinephrine, ECG monitoring, and IV fluids.
    2) BRONCHOSPASM
    a) ALBUTEROL
    1) ADULT: 2.5 to 5 milligrams in 2 to 4.5 milliliters of normal saline delivered per nebulizer every 20 minutes up to 3 doses. If incomplete response administer 2.5 to 10 mg every 1 to 4 hours as needed, or 10 to 15 mg/hr by continuous nebulization as needed (National Heart,Lung,and Blood Institute, 2007). CHILD: 0.15 milligram/kilogram (minimum 2.5 milligrams) per nebulizer every 20 minutes up to 3 doses. If incomplete response administer 0.15 to 0.3 mg/kg (up to 10 mg) every 1 to 4 hours as needed, or 0.5 mg/kg/hr by continuous nebulization (National Heart,Lung,and Blood Institute, 2007).
    3) CORTICOSTEROIDS
    a) Consider systemic corticosteroids in patients with significant bronchospasm.
    b) PREDNISONE: ADULT: 40 to 80 milligrams/day. CHILD: 1 to 2 milligrams/kilogram/day (maximum 60 mg) in 1 to 2 divided doses divided twice daily (National Heart,Lung,and Blood Institute, 2007).
    4) MILD CASES
    a) DIPHENHYDRAMINE
    1) SUMMARY: Oral diphenhydramine, as well as other H1 antihistamines can be used as indicated (Lieberman et al, 2010).
    2) ADULT: 50 milligrams orally, or 10 to 50 mg intravenously at a rate not to exceed 25 mg/min or may be given by deep intramuscular injection. A total of 100 mg may be administered if needed. Maximum daily dosage is 400 mg (Prod Info diphenhydramine HCl intravenous injection solution, intramuscular injection solution, 2013).
    3) CHILD: 5 mg/kg/24 hours or 150 mg/m(2)/24 hours. Divided into 4 doses, administered intravenously at a rate not exceeding 25 mg/min or by deep intramuscular injection. Maximum daily dosage is 300 mg (Prod Info diphenhydramine HCl intravenous injection solution, intramuscular injection solution, 2013).
    5) MODERATE CASES
    a) EPINEPHRINE: INJECTABLE SOLUTION: It should be administered early in patients by IM injection. Using a 1:1000 (1 mg/mL) solution of epinephrine. Initial Dose: 0.01 mg/kg intramuscularly with a maximum dose of 0.5 mg in adults and 0.3 mg in children. The dose may be repeated every 5 to 15 minutes, if no clinical improvement. Most patients respond to 1 or 2 doses (Nowak & Macias, 2014).
    6) SEVERE CASES
    a) EPINEPHRINE
    1) INTRAVENOUS BOLUS: ADULT: 1 mg intravenously as a 1:10,000 (0.1 mg/mL) solution; CHILD: 0.01 mL/kg intravenously to a maximum single dose of 1 mg given as a 1:10,000 (0.1 mg/mL) solution. It can be repeated every 3 to 5 minutes as needed. The dose can also be given by the intraosseous route if IV access cannot be established (Lieberman et al, 2015). ALTERNATIVE ROUTE: ENDOTRACHEAL ADMINISTRATION: If IV/IO access is unavailable. DOSE: ADULT: Administer 2 to 2.5 mg of 1:1000 (1 mg/mL) solution diluted in 5 to 10 mL of sterile water via endotracheal tube. CHILD: DOSE: 0.1 mg/kg to a maximum of 2.5 mg administered as a 1:1000 (1 mg/mL) solution diluted in 5 to 10 mL of sterile water via endotracheal tube (Lieberman et al, 2015).
    2) INTRAVENOUS INFUSION: Intravenous administration may be considered in patients poorly responsive to IM or SubQ epinephrine. An epinephrine infusion may be prepared by adding 1 mg (1 mL of 1:1000 (1 mg/mL) solution) to 250 mL D5W, yielding a concentration of 4 mcg/mL, and infuse this solution IV at a rate of 1 mcg/min to 10 mcg/min (maximum rate). CHILD: A dosage of 0.01 mg/kg (0.1 mL/kg of a 1:10,000 (0.1 mg/mL) solution up to 10 mcg/min (maximum dose 0.3 mg) is recommended for children (Lieberman et al, 2010). Careful titration of a continuous infusion of IV epinephrine, based on the severity of the reaction, along with a crystalloid infusion can be considered in the treatment of anaphylactic shock. It appears to be a reasonable alternative to IV boluses, if the patient is not in cardiac arrest (Vanden Hoek,TL,et al).
    7) AIRWAY MANAGEMENT
    a) OXYGEN: 5 to 10 liters/minute via high flow mask.
    b) INTUBATION: Perform early if any stridor or signs of airway obstruction.
    c) CRICOTHYROTOMY: Use if unable to intubate with complete airway obstruction (Vanden Hoek,TL,et al).
    d) BRONCHODILATORS are recommended for mild to severe bronchospasm.
    e) ALBUTEROL: ADULT: 2.5 to 5 milligrams in 2 to 4.5 milliliters of normal saline delivered per nebulizer every 20 minutes up to 3 doses. If incomplete response administer 2.5 to 10 mg every 1 to 4 hours as needed, or 10 to 15 mg/hr by continuous nebulization as needed (National Heart,Lung,and Blood Institute, 2007).
    f) ALBUTEROL: CHILD: 0.15 milligram/kilogram (minimum 2.5 milligrams) per nebulizer every 20 minutes up to 3 doses. If incomplete response administer 0.15 to 0.3 milligram/kilogram (maximum 10 milligrams) every 1 to 4 hours as needed OR administer 0.5 mg/kg/hr by continuous nebulization (National Heart,Lung,and Blood Institute, 2007).
    8) MONITORING
    a) CARDIAC MONITOR: All complicated cases.
    b) IV ACCESS: Routine in all complicated cases.
    9) HYPOTENSION
    a) If hypotensive give 500 to 2000 milliliters crystalloid initially (20 milliliters/kilogram in children) and titrate to desired effect (stabilization of vital signs, mentation, urine output); adults may require up to 6 to 10 L/24 hours. Central venous or pulmonary artery pressure monitoring is recommended in patients with persistent hypotension.
    1) VASOPRESSORS: Should be used in refractory cases unresponsive to repeated doses of epinephrine and after vigorous intravenous crystalloid rehydration (Lieberman et al, 2010).
    2) DOPAMINE: Initial Dose: 2 to 20 micrograms/kilogram/minute intravenously; titrate to maintain systolic blood pressure greater than 90 mm Hg (Lieberman et al, 2010).
    10) H1 and H2 ANTIHISTAMINES
    a) SUMMARY: Antihistamines are second-line therapy and are used as supportive therapy and should not be used in place of epinephrine (Lieberman et al, 2010).
    1) DIPHENHYDRAMINE: ADULT: 25 to 50 milligrams via a slow intravenous infusion or IM. PEDIATRIC: 1 milligram/kilogram via slow intravenous infusion or IM up to 50 mg in children (Lieberman et al, 2010).
    b) RANITIDINE: ADULT: 1 mg/kg parenterally; CHILD: 12.5 to 50 mg parenterally. If the intravenous route is used, ranitidine should be infused over 10 to 15 minutes or diluted in 5% dextrose to a volume of 20 mL and injected over 5 minutes (Lieberman et al, 2010).
    c) Oral diphenhydramine, as well as other H1 antihistamines, can also be used as indicated (Lieberman et al, 2010).
    11) DYSRHYTHMIAS
    a) Dysrhythmias and cardiac dysfunction may occur primarily or iatrogenically as a result of pharmacologic treatment (epinephrine) (Vanden Hoek,TL,et al). Monitor and correct serum electrolytes, oxygenation and tissue perfusion. Treat with antiarrhythmic agents as indicated.
    12) OTHER THERAPIES
    a) There have been a few reports of patients with anaphylaxis, with or without cardiac arrest, that have responded to vasopressin therapy that did not respond to standard therapy. Although there are no randomized controlled trials, other alternative vasoactive therapies (ie, vasopressin, norepinephrine, methoxamine, and metaraminol) may be considered in patients in cardiac arrest secondary to anaphylaxis that do not respond to epinephrine (Vanden Hoek,TL,et al).
    F) SEIZURE
    1) SUMMARY
    a) Attempt initial control with a benzodiazepine (eg, diazepam, lorazepam). If seizures persist or recur, administer phenobarbital or propofol.
    b) Monitor for respiratory depression, hypotension, and dysrhythmias. Endotracheal intubation should be performed in patients with persistent seizures.
    c) Evaluate for hypoxia, electrolyte disturbances, and hypoglycemia (or, if immediate bedside glucose testing is not available, treat with intravenous dextrose).
    2) DIAZEPAM
    a) ADULT DOSE: Initially 5 to 10 mg IV, OR 0.15 mg/kg IV up to 10 mg per dose up to a rate of 5 mg/minute; may be repeated every 5 to 20 minutes as needed (Brophy et al, 2012; Prod Info diazepam IM, IV injection, 2008; Manno, 2003).
    b) PEDIATRIC DOSE: 0.1 to 0.5 mg/kg IV over 2 to 5 minutes; up to a maximum of 10 mg/dose. May repeat dose every 5 to 10 minutes as needed (Loddenkemper & Goodkin, 2011; Hegenbarth & American Academy of Pediatrics Committee on Drugs, 2008).
    c) Monitor for hypotension, respiratory depression, and the need for endotracheal intubation. Consider a second agent if seizures persist or recur after repeated doses of diazepam .
    3) NO INTRAVENOUS ACCESS
    a) DIAZEPAM may be given rectally or intramuscularly (Manno, 2003). RECTAL DOSE: CHILD: Greater than 12 years: 0.2 mg/kg; 6 to 11 years: 0.3 mg/kg; 2 to 5 years: 0.5 mg/kg (Brophy et al, 2012).
    b) MIDAZOLAM has been used intramuscularly and intranasally, particularly in children when intravenous access has not been established. ADULT DOSE: 0.2 mg/kg IM, up to a maximum dose of 10 mg (Brophy et al, 2012). PEDIATRIC DOSE: INTRAMUSCULAR: 0.2 mg/kg IM, up to a maximum dose of 7 mg (Chamberlain et al, 1997) OR 10 mg IM (weight greater than 40 kg); 5 mg IM (weight 13 to 40 kg); INTRANASAL: 0.2 to 0.5 mg/kg up to a maximum of 10 mg/dose (Loddenkemper & Goodkin, 2011; Brophy et al, 2012). BUCCAL midazolam, 10 mg, has been used in adolescents and older children (5-years-old or more) to control seizures when intravenous access was not established (Scott et al, 1999).
    4) LORAZEPAM
    a) MAXIMUM RATE: The rate of intravenous administration of lorazepam should not exceed 2 mg/min (Brophy et al, 2012; Prod Info lorazepam IM, IV injection, 2008).
    b) ADULT DOSE: 2 to 4 mg IV initially; repeat every 5 to 10 minutes as needed, if seizures persist (Manno, 2003; Brophy et al, 2012).
    c) PEDIATRIC DOSE: 0.05 to 0.1 mg/kg IV over 2 to 5 minutes, up to a maximum of 4 mg/dose; may repeat in 5 to 15 minutes as needed, if seizures continue (Brophy et al, 2012; Loddenkemper & Goodkin, 2011; Hegenbarth & American Academy of Pediatrics Committee on Drugs, 2008; Sreenath et al, 2010; Chin et al, 2008).
    5) PHENOBARBITAL
    a) ADULT LOADING DOSE: 20 mg/kg IV at an infusion rate of 50 to 100 mg/minute IV. An additional 5 to 10 mg/kg dose may be given 10 minutes after loading infusion if seizures persist or recur (Brophy et al, 2012).
    b) Patients receiving high doses will require endotracheal intubation and may require vasopressor support (Brophy et al, 2012).
    c) PEDIATRIC LOADING DOSE: 20 mg/kg may be given as single or divided application (2 mg/kg/minute in children weighing less than 40 kg up to 100 mg/min in children weighing greater than 40 kg). A plasma concentration of about 20 mg/L will be achieved by this dose (Loddenkemper & Goodkin, 2011).
    d) REPEAT PEDIATRIC DOSE: Repeat doses of 5 to 20 mg/kg may be given every 15 to 20 minutes if seizures persist, with cardiorespiratory monitoring (Loddenkemper & Goodkin, 2011).
    e) MONITOR: For hypotension, respiratory depression, and the need for endotracheal intubation (Loddenkemper & Goodkin, 2011; Manno, 2003).
    f) SERUM CONCENTRATION MONITORING: Monitor serum concentrations over the next 12 to 24 hours. Therapeutic serum concentrations of phenobarbital range from 10 to 40 mcg/mL, although the optimal plasma concentration for some individuals may vary outside this range (Hvidberg & Dam, 1976; Choonara & Rane, 1990; AMA Department of Drugs, 1992).
    6) OTHER AGENTS
    a) If seizures persist after phenobarbital, propofol or pentobarbital infusion, or neuromuscular paralysis with general anesthesia (isoflurane) and continuous EEG monitoring should be considered (Manno, 2003). Other anticonvulsants can be considered (eg, valproate sodium, levetiracetam, lacosamide, topiramate) if seizures persist or recur; however, there is very little data regarding their use in toxin induced seizures, controlled trials are not available to define the optimal dosage ranges for these agents in status epilepticus (Brophy et al, 2012):
    1) VALPROATE SODIUM: ADULT DOSE: An initial dose of 20 to 40 mg/kg IV, at a rate of 3 to 6 mg/kg/minute; may give an additional dose of 20 mg/kg 10 minutes after loading infusion. PEDIATRIC DOSE: 1.5 to 3 mg/kg/minute (Brophy et al, 2012).
    2) LEVETIRACETAM: ADULT DOSE: 1000 to 3000 mg IV, at a rate of 2 to 5 mg/kg/min IV. PEDIATRIC DOSE: 20 to 60 mg/kg IV (Brophy et al, 2012; Loddenkemper & Goodkin, 2011).
    3) LACOSAMIDE: ADULT DOSE: 200 to 400 mg IV; 200 mg IV over 15 minutes (Brophy et al, 2012). PEDIATRIC DOSE: In one study, median starting doses of 1.3 mg/kg/day and maintenance doses of 4.7 mg/kg/day were used in children 8 years and older (Loddenkemper & Goodkin, 2011).
    4) TOPIRAMATE: ADULT DOSE: 200 to 400 mg nasogastric/orally OR 300 to 1600 mg/day orally divided in 2 to 4 times daily (Brophy et al, 2012).

Enhanced Elimination

    A) HEMODIALYSIS
    1) Hemodialysis is expected to remove clavulanic acid from serum. Amoxicillin and ticarcillin, which may be combined with clavulanic acid, are removed from the serum by hemodialysis (Prod Info Augmentin(R), amoxicillin/clavulanate potassium, 1998; Prod Info Timentin(R), ticarcillin disodium/clavulanate potassium, 1998).

Summary

    A) TOXICITY: Amoxicillin/Clavulanate - Most patients are asymptomatic following overdosage or experience only mild gastrointestinal symptoms. Clavulanic acid combinations are available in numerous formulations; total drug exposure is variable.
    B) THERAPEUTIC DOSES: Varies by indication and formulation: ADULTS: Amoxicillin/clavulanate potassium: 500 or 875 mg orally every 12 hours or 250 or 500 mg orally every 8 hours, depending on the severity and type of infection. Ticarcillin disodium/clavulanate potassium: Systemic and urinary tract infections: The recommended dose is 3.1 g every 4 to 6 hours, administered via an IV infusion over a 30-minute period. Gynecologic infections: Based on the ticarcillin component, the recommended dose is 200 to 300 mg/kg/day in divided doses every 4 to 6 hours, depending on the severity of infection, and administered via an IV infusion over a 30-minute period. CHILDREN: Amoxicillin/clavulanate potassium: Based on the amoxicillin component, the amoxicillin/clavulanate combination product is dosed as follows: ORAL: Neonates and infants less than 3 months of age: Using the 125 mg/5 mL oral suspension of amoxicillin/clavulanate potassium, the recommended dose is 30 mg/kg/day every 12 hours. 3 months or older and less than 40 kg: 25 to 45 mg/kg/day in divided doses every 12 hours, or 20 to 40 mg/kg/day in divided doses every 8 hours, depending on the severity of infection and product strength. 40 kg or more: 500 or 875 mg every 12 hours or 250 or 500 mg every 8 hours, depending on the severity and type of infection. Ticarcillin disodium/clavulanate potassium: Based on the ticarcillin component, the ticarcillin/clavulanate combination product is dosed as follows: INTRAVENOUS: Less than 60 kg: 200 to 300 mg/kg/day in divided doses every 4 to 6 hours, depending on the severity of infection, and administered via an IV infusion over a 30-minute period. 60 kg or more: 3.1 g every 4 to 6 hours, depending on the severity of infection, and administered via an IV infusion over a 30-minute period.

Therapeutic Dose

    7.2.1) ADULT
    A) SPECIFIC SUBSTANCE
    1) AMOXICILLIN AND CLAVULANATE (COMBINATION PRODUCT)
    a) 500 or 875 mg orally every 12 hours or 250 or 500 mg orally every 8 hours, depending on the severity and type of infection (Prod Info AUGMENTIN(R) oral tablets, oral powder for suspension, oral chewable tablets, 2013).
    2) TICARCILLIN AND CLAVULANATE (COMBINATION PRODUCT)
    a) Systemic and urinary tract infections: The recommended dose is 3.1 g every 4 to 6 hours, administered via an IV infusion over a 30-minute period (Prod Info TIMENTIN(R) intravenous injection, 2012).
    b) Gynecologic infections: Based on the ticarcillin component, the recommended dose is 200 to 300 mg/kg/day in divided doses every 4 to 6 hours, depending on the severity of infection, and administered via an IV infusion over a 30-minute period (Prod Info TIMENTIN(R) intravenous injection, 2012).
    7.2.2) PEDIATRIC
    A) SPECIFIC SUBSTANCE
    1) AMOXICILLIN AND CLAVULANATE (COMBINATION PRODUCT)
    a) Based on the amoxicillin component, the amoxicillin/clavulanate combination product is dosed as follows:
    b) ORAL
    1) Neonates and infants less than 3 months of age: Using the 125 mg/5 mL oral suspension of amoxicillin/clavulanate potassium, the recommended dose is 30 mg/kg/day every 12 hours (Prod Info AUGMENTIN(R) oral tablets, oral powder for suspension, oral chewable tablets, 2013).
    2) 3 months or older and less than 40 kg: 25 to 45 mg/kg/day in divided doses every 12 hours, or 20 to 40 mg/kg/day in divided doses every 8 hours, depending on the severity of infection and product strength (Prod Info AUGMENTIN(R) oral tablets, oral powder for suspension, oral chewable tablets, 2013).
    3) 40 kg or more: 500 or 875 mg every 12 hours or 250 or 500 mg every 8 hours, depending on the severity and type of infection (Prod Info AUGMENTIN(R) oral tablets, oral powder for suspension, oral chewable tablets, 2013).
    2) TICARCILLIN AND CLAVULANATE (COMBINATION PRODUCT)
    a) Based on the ticarcillin component, the ticarcillin/clavulanate combination product is dosed as follows:
    b) INTRAVENOUS
    1) Less than 60 kg: 200 to 300 mg/kg/day in divided doses every 4 to 6 hours, depending on the severity of infection, and administered via an IV infusion over a 30-minute period (Prod Info TIMENTIN(R) intravenous injection, 2012).
    2) 60 kg or more: 3.1 g every 4 to 6 hours, depending on the severity of infection, and administered via an IV infusion over a 30-minute period (Prod Info TIMENTIN(R) intravenous injection, 2012).

Maximum Tolerated Exposure

    A) Clavulanic acid is often combined with penicillin products which can result in neuromuscular hyperirritability or seizures (Prod Info Timentin(R), ticarcillin disodium/clavulanate potassium, 1998).
    B) Amoxicillin/Clavulanate: Most patients are asymptomatic following overdosage or experience only mild gastrointestinal symptoms (Prod Info Augmentin(R), amoxicillin/clavulanate potassium, 1998).

Serum Plasma Blood Concentrations

    7.5.2) TOXIC CONCENTRATIONS
    A) TOXIC CONCENTRATION LEVELS
    1) GENERAL
    a) THERAPEUTIC LEVELS - Peak serum levels of 2 to 3 micrograms/milliliter clavulanic acid have occurred after single doses of 125 milligrams (Brogden et al, 1981).

Toxicity Information

    7.7.1) TOXICITY VALUES
    A) ANIMAL DATA
    1) LD50- (INTRAPERITONEAL)MOUSE:
    a) 1531 mg/kg ((RTECS, 2000))
    2) LD50- (ORAL)MOUSE:
    a) 4526 mg/kg ((RTECS, 2000))
    3) LD50- (SUBCUTANEOUS)MOUSE:
    a) 2185 mg/kg ((RTECS, 2000))
    4) LD50- (INTRAPERITONEAL)RAT:
    a) 1399 mg/kg ((RTECS, 2000))
    5) LD50- (ORAL)RAT:
    a) 7936 mg/kg ((RTECS, 2000))
    6) LD50- (SUBCUTANEOUS)RAT:
    a) 1393 mg/kg ((RTECS, 2000))

Pharmacologic Mechanism

    A) Clavulanate is produced by the fermentation of Streptomyces clavuligerus (Prod Info Augmentin(R), amoxicillin/clavulanate potassium, 1998).
    B) Clavulanic acid itself has poor antimicrobial activity. However, it binds to and inactivates bacterial beta-lactamases. As a result, compounds such as amoxicillin, which would normally be hydrolyzed, are spared (Todd & Benfield, 1990).
    1) It has the ability to act against plasmid mediated beta-lactameases which are frequently responsible for transferred drug resistance to penicillins and cephalosporins (Prod Info Augmentin(R), amoxicillin/clavulanate potassium, 1998), which makes the antibiotic effective against normally resistant organisms (Todd & Benfield, 1990).

Physical Characteristics

    A) Clavulanic acid is supplied with amoxicillin as a powder for reconstitution for oral use, and as tablets. Clavulanic acid is supplied with ticarcillin as a powder for reconstitution for parenteral use.
    B) Each gram of clavulanate potassium contains 5.1 mEq of potassium.

Molecular Weight

    A) Clauvulanic acid: 199.16
    B) Potassium clavulanate: 237.25

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