Label: VARIBAR THIN LIQUID- barium sulfate powder, for suspension

  • Category: HUMAN PRESCRIPTION DRUG LABEL

Drug Label Information

Updated April 30, 2019

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  • HIGHLIGHTS OF PRESCRIBING INFORMATION
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    VARIBAR THIN LIQUID safely and effectively.
    See full prescribing information for VARIBAR THIN LIQUID.

    VARIBAR THIN LIQUID (barium sulfate) for oral suspension

    Initial U.S. Approval: 2016

    INDICATIONS AND USAGE

    VARIBAR THIN LIQUID is a radiopaque contrast agent indicated for use in modified barium swallow examinations to evaluate the oral and pharyngeal function and morphology in adult and pediatric patients (1)

    DOSAGE AND ADMINISTRATION

    For oral use only– once reconstituted, administer by infant bottle, syringe, spoon, or cup. The recommended dose is:

      ● Adults: 5 mL
      ● Pediatric patients 6 months and older: 1 mL to 3 mL
      ● Pediatric patients younger than 6 months of age: 0.5 mL to 1 mL

    • During a single modified barium swallow examination, multiple doses may be administered
    • Maximum cumulative dose: 80 mL (2.1)
    • Must reconstitute supplied powder with water prior to use. See Full Prescribing Information for reconstitution instructions (2.2)

    DOSAGE FORMS AND STRENGTHS

    For oral suspension: 120 g barium sulfate (81% w/w) supplied in a multiple-dose bottle for reconstitution (3)

    CONTRAINDICATIONS

    • Known or suspected perforation of the gastrointestinal (GI) tract (4)
    • Known obstruction of the GI tract (4)
    • Conditions associated with high risk of GI perforation or aspiration (4)
    • Known hypersensitivity to barium sulfate or any of the excipients of VARIBAR THIN LIQUID (4)

    WARNINGS AND PRECAUTIONS

    • Hypersensitivity reactions: Emergency equipment and trained personnel should be immediately available (5.1)
    • Intra-abdominal leakage: May occur in conditions such as GI fistula, ulcer, inflammatory bowel disease, appendicitis or diverticulitis, severe stenosis or obstructing lesions of the GI tract (5.2)
    • Delayed GI transit and obstruction: Patients should maintain adequate hydration in days following barium sulfate procedure to avoid obstruction or impaction (5.3)
    • Aspiration pneumonitis: Aspiration may occur during the modified barium swallow examination, monitor the patient for aspiration (5.4)

    ADVERSE REACTIONS

    Common adverse reactions include nausea, vomiting, diarrhea and abdominal cramping (6)


    To report SUSPECTED ADVERSE REACTIONS, contact Bracco Diagnostics Inc at 1-800-257-5181 or FDA at 1-800-FDA-1088 or www.fda.gov/medwatch

    See 17 for PATIENT COUNSELING INFORMATION.

    Revised: 4/2019

  • Table of Contents
  • 1 INDICATIONS AND USAGE

    VARIBAR THIN LIQUID is indicated for modified barium swallow examinations to evaluate the oral and pharyngeal function and morphology in adult and pediatric patients.

  • 2 DOSAGE AND ADMINISTRATION

    2.1 Recommended Dosing and Administration Instructions

    • The recommended dose of reconstituted VARIBAR THIN LIQUID administered orally by infant bottle, syringe, spoon, or cup is:
      • Adults: 5 mL
      • Pediatric patients 6 months and older: 1 mL to 3 mL
      • Pediatric patients younger than 6 months of age: 0.5 mL to 1 mL
    • During a single modified barium swallow examination, multiple doses of VARIBAR THIN LIQUID may be administered, to assess the patient during multiple swallows and different radiographic views.
    • The maximum cumulative dose is 80 mL.
    • For oral use only
    • Advise patients to hydrate following the barium sulfate procedure.

    2.2 Instructions for Reconstitution

    The VARIBAR THIN LIQUID powder must be reconstituted prior to administration by a healthcare provider according to the following instructions:

    • Add water to the fill line on the bottle label
    • Replace the lid securely
    • Invert the bottle and tap with fingers to mix the powder into the water
    • Shake vigorously for 30 seconds. Let stand for 5 minutes
    • Refill with water to the fill line on the bottle label and reshake thoroughly.
    • Once reconstituted, write the discard after date on the immediate container label. After reconstitution, store in refrigerator at 2°C to 8°C (36ºF to 46ºF) for up to 72 hours.
    • Reconstitution yields approximately 300 mL of VARIBAR THIN LIQUID oral suspension containing 0.4 grams of barium sulfate per mL (40% w/v) and should be homogeneous and white to lightly colored.
  • 3 DOSAGE FORMS AND STRENGTHS

    For oral suspension: 120 grams of barium sulfate supplied as a white to lightly colored powder (81% w/w) in a multiple-dose plastic bottle for reconstitution.

  • 4 CONTRAINDICATIONS

    VARIBAR THIN LIQUID is contraindicated in patients with:

    • known or suspected perforation of the gastrointestinal (GI) tract
    • known obstruction of the GI tract
    • high risk of GI perforation such as those with a recent GI perforation, acute GI hemorrhage or ischemia, toxic megacolon, severe ileus, post GI surgery or biopsy, acute GI injury or burn, or recent radiotherapy to the pelvis
    • high risk of aspiration such as those with known or suspected tracheo-esophageal fistula or obtundation
    • known severe hypersensitivity to barium sulfate or any of the excipients of VARIBAR THIN LIQUID
  • 5 WARNINGS AND PRECAUTIONS

    5.1 Hypersensitivity Reactions

    Barium sulfate preparations contain a number of excipients, including natural and artificial flavors and may induce serious hypersensitivity reactions. The manifestations include hypotension, bronchospasm and other respiratory impairments, and dermal reactions including rashes, urticaria and itching. A history of bronchial asthma, atopy, food allergies, or a previous reaction to a contrast agent may increase the risk for hypersensitivity reactions. Emergency equipment and trained personnel should be immediately available for treatment of a hypersensitivity reaction.

    5.2 Intra-abdominal Barium Leakage

    The use of VARIBAR THIN LIQUID is contraindicated in patients at high risk of perforation of the GI tract [see Contraindications (4)]. Administration of VARIBAR THIN LIQUID may result in leakage of barium from the GI tract in the presence of conditions such as carcinomas, GI fistula, inflammatory bowel disease, gastric or duodenal ulcer, appendicitis, or diverticulitis, and in patients with a severe stenosis at any level of the GI tract, especially if it is distal to the stomach. The barium leakage has been associated with peritonitis and granuloma formation.

    5.3 Delayed Gastrointestinal Transit and Obstruction

    Orally administered barium sulfate may accumulate proximal to a constricting lesion of the colon, causing obstruction or impaction with development of baroliths (inspissated barium associated with feces) and may lead to abdominal pain, appendicitis, bowel obstruction, or rarely perforation. Patients with the following conditions are at higher risk for developing obstruction or baroliths: severe stenosis at any level of the GI tract, impaired GI motility, electrolyte imbalance, dehydration, on a low residue diet, taking medications that delay GI motility, constipation, pediatric patients with cystic fibrosis or Hirschsprung disease, and the elderly [see Use in Specific Populations (8.4, 8.5)]. To reduce the risk of delayed GI transit and obstruction, patients should maintain adequate hydration after the barium sulfate procedure.

    5.4 Aspiration Pneumonitis

    The use of VARIBAR THIN LIQUID is contraindicated in patients with trachea-esophageal fistula [see Contraindications (4)]. Oral administration of barium is associated with aspiration pneumonitis, especially in patients with a history of food aspiration or with compromised swallowing mechanism. Vomiting following oral administration of barium sulfate may lead to aspiration pneumonitis.

    In patients at risk for aspiration, begin the procedure with a small ingested volume of VARIBAR THIN LIQUID. Monitor the patient closely for aspiration, discontinue administration of VARIBAR THIN LIQUID if aspiration is suspected, and monitor for development of aspiration pneumonitis.

    5.5 Systemic Embolization

    Barium sulfate products may occasionally intravasate into the venous drainage of the GI tract and enter the circulation as a "barium embolus" leading to potentially fatal complications which include systemic and pulmonary embolism, disseminated intravascular coagulation, septicemia and prolonged severe hypotension. Although this complication is exceedingly uncommon after oral administration of a barium sulfate suspension, monitor patients for potential intravasation when administering barium sulfate.

  • 6 ADVERSE REACTIONS

    The following adverse reactions have been identified from spontaneous reporting or clinical studies of barium sulfate administered orally. Because the reactions are reported voluntarily from a population of uncertain size, it is not always possible to reliably estimate their frequency or to establish a causal relationship to drug exposure:

    • Nausea, vomiting, diarrhea and abdominal cramping
    • Serious adverse reactions and fatalities include aspiration pneumonitis, barium sulfate impaction, intestinal perforation with consequent peritonitis and granuloma formation, vasovagal and syncopal episodes
  • 8 USE IN SPECIFIC POPULATIONS

    8.1 Pregnancy

    Risk Summary

    VARIBAR THIN LIQUID is not absorbed systemically following oral administration, and maternal use is not expected to result in fetal exposure to the drug.

    8.2 Lactation

    Risk Summary

    VARIBAR THIN LIQUID is not absorbed systemically by the mother following oral administration, and breastfeeding is not expected to result in exposure of the infant to the drug.

    8.4 Pediatric Use

    The efficacy of VARIBAR THIN LIQUID in pediatric patients is based on successful opacification of the pharynx during modified barium swallow examinations [see Clinical Pharmacology (12.1)]. Safety and dosing recommendations in pediatric patients are based on clinical experience.

    VARIBAR THIN LIQUID is contraindicated in pediatric patients with trachea-esophageal fistula. [see Contraindications (4)]. Pediatric patients with a history of asthma or food allergies may be at increased risk for development of hypersensitivity reactions [see Warnings and Precautions (5.1)]. Monitor patients with cystic fibrosis or Hirschsprung disease for bowel obstruction after use [see Warnings and Precautions (5.3)].

    8.5 Geriatric Use

    Clinical studies of VARIBAR THIN LIQUID did not include sufficient numbers of subjects aged 65 and over to determine whether they respond differently from younger subjects. Other reported clinical experience has not identified differences in responses between the elderly and younger patients. In general, dose selection for an elderly patient should be cautious, usually starting at the low end of the dosing range, reflecting the greater frequency of decreased hepatic, renal, or cardiac function, and of concomitant disease or other drug therapy.

  • 11 DESCRIPTION

    VARIBAR THIN LIQUID (barium sulfate) is a radiographic contrast agent that is supplied as a white to lightly colored powder for suspension (81% w/w) with an apple aroma for oral administration. The active ingredient barium sulfate is designated chemically as BaSO4 with a molecular weight of 233.4 g/mol, a density of 4.5 g/cm3, and the following chemical structure:

    Barium Sulfate Chemical Structure

    VARIBAR THIN LIQUID has a viscosity of <15 cPs when reconstituted and contains the following excipients: carboxymethylcellulose sodium, citric acid, maltodextrin, natural and artificial apple flavor, polysorbate 80, saccharin sodium, simethicone, sodium citrate, sorbitol and xylitol.

  • 12 CLINICAL PHARMACOLOGY

    12.1 Mechanism of Action

    Due to its high atomic number, barium (the active ingredient in VARIBAR THIN LIQUID) is opaque to x-rays and therefore acts as a positive contrast agent for radiographic studies.

    12.2 Pharmacodynamics

    Barium sulfate is biologically inert and has no known pharmacological effects.

    12.3 Pharmacokinetics

    Under physiological conditions, barium sulfate passes through the gastrointestinal tract in an unchanged form and is absorbed only in small, pharmacologically insignificant amounts.

  • 13 NONCLINICAL TOXICOLOGY

    13.1 Carcinogenesis, Mutagenesis, Impairment of Fertility

    No animal studies have been performed to evaluate the carcinogenic potential of barium sulfate or potential effects on fertility.

  • 16 HOW SUPPLIED/STORAGE AND HANDLING

    16.1 How Supplied

    VARIBAR THIN LIQUID is supplied as a white to lightly colored powder in a multiple-dose polyethylene bottle containing 120 grams of barium sulfate (81% w/w).

    Provided as: 24 x 148 g bottles (NDC 32909-105-10)

    16.2 Storage and Handling

    Store at USP controlled room temperature 20°C to 25°C (68° F to 77° F).

  • 17 PATIENT COUNSELING INFORMATION

    After administration, advise patients to:

    • Maintain adequate hydration [see Dosage and Administration (2.2) and Warnings and Precautions (5.3)].
    • Seek medical attention for worsening of constipation or slow gastrointestinal passage [see Warnings and Precautions (5.3)].
    • Seek medical attention for any delayed onset of hypersensitivity: rash, urticaria, or respiratory difficulty [see Warnings and Precautions (5.1)].


    Rx Only

    Manufactured by
    EZEM Canada Inc
    Anjou (Quebec) Canada H1J 2Z4

    For
    Bracco Diagnostics Inc.
    Monroe Township, NJ 08831

    VARIBAR is a registered trademark of E-Z-EM, Inc.

  • PRINCIPAL DISPLAY PANEL

    Varibar® Thin Liquid - Barium Sulfate for Suspension
    NDC: 32909-105-10

    Varibar Thin Liquid - Internal
    Varibar Thin Liquid - External
  • INGREDIENTS AND APPEARANCE
    VARIBAR THIN LIQUID 
    barium sulfate powder, for suspension
    Product Information
    Product TypeHUMAN PRESCRIPTION DRUGItem Code (Source)NDC:32909-105
    Route of AdministrationORAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    Barium Sulfate (UNII: 25BB7EKE2E) (Barium Sulfate - UNII:25BB7EKE2E) Barium Sulfate.81 g  in 1 g
    Inactive Ingredients
    Ingredient NameStrength
    anhydrous citric acid (UNII: XF417D3PSL)  
    carboxymethylcellulose sodium (UNII: K679OBS311)  
    dimethicone 1000 (UNII: MCU2324216)  
    maltodextrin (UNII: 7CVR7L4A2D)  
    polysorbate 80 (UNII: 6OZP39ZG8H)  
    silicon dioxide (UNII: ETJ7Z6XBU4)  
    sorbitol (UNII: 506T60A25R)  
    trisodium citrate dihydrate (UNII: B22547B95K)  
    xylitol (UNII: VCQ006KQ1E)  
    saccharin sodium (UNII: SB8ZUX40TY)  
    Product Characteristics
    ColorWHITEScore    
    ShapeSize
    FlavorAPPLEImprint Code
    Contains    
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:32909-105-1024 in 1 CASE04/30/2019
    1148 g in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    NDANDA20803604/30/2019
    Labeler - E-Z-EM Canada Inc (204211163)
    Registrant - E-Z-EM, INC. (002041226)
    Establishment
    NameAddressID/FEIBusiness Operations
    E-Z-EM Canada Inc204211163PACK(32909-105) , LABEL(32909-105) , MANUFACTURE(32909-105) , ANALYSIS(32909-105)