Tagitol v (oral and rectal)

Tagitol v (oral and rectal) Medicine

Overdose

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Contraindications

TAGITOL V 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 prior aspiration, tracheo-esophageal fistula, or obtundation;

known hypersensitivity to barium sulfate or any of the excipients of TAGITOL V.

Undesirable effects

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.

Therapeutic indications

TAGITOL V is indicated for use in adult patients for use in computed tomography (CT) colonography as a fecal tagging agent.

Pharmacodynamic properties

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

Date of revision of the text

Aug 2017

Name of the medicinal product

Tagitol V

Fertility, pregnancy and lactation

Risk Summary

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

Qualitative and quantitative composition

Dosage Forms And Strengths

Oral suspension: barium sulfate (40% w/v) supplied as a ready-to-use suspension in a 20 mL, singledose, plastic bottle for oral administration. Each 20 mL bottle contains 8 g of barium sulfate.

TAGITOL V (barium sulfate) is an oral suspension (40% w/v) supplied as a box of three 20 mL HDPE bottles. Each bottle contains 8 grams barium sulfate.

Provided as: 24 boxes, each containing 3 (20 mL) bottles (NDC 32909-814)

Storage And Handling

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

Manufactured by: EZEM Canada Inc, Anjou (Quebec) Canada H1J 2Z4. Revised: Aug 2017

Special warnings and precautions for use

WARNINGS

Included as part of the "PRECAUTIONS" Section

PRECAUTIONS 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, dermal reactions including rashes, urticaria and itching. A history of bronchial asthma, atopy, 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.

Intra-Abdominal Barium Leakage

The use of TAGITOL V is contraindicated in patients at high risk of perforation of the GI tract. Administration of TAGITOL V may result in leakage of barium from the GI tract in the presence of conditions that increase the risk of perforation 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 gastrointestinal tract, especially if it is distal to the stomach. The barium leakage has been associated with peritonitis and granuloma formation.

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 gastrointestinal motility, electrolyte imbalance, dehydration, on a low residue diet, on medications that delay GI motility, constipation, cystic fibrosis, Hirschsprung disease, and the elderly. To reduce the risk of delayed GI transit and obstruction, patients should maintain adequate hydration following a barium sulfate procedure.

Aspiration Pneumonitis

The use of TAGITOL V is contraindicated in patients at high risk of aspiration. 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.

Systemic Embolization

Barium sulfate products may occasionally intravasate into the venous drainage of the large bowel 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 barium sulfate products, monitor patients for potential intravasation when administering barium sulfate.

Patient Counseling Information

After administration, advise patients to:

  • Maintain adequate hydration.
  • Seek medical attention for worsening of constipation or slow gastrointestinal passage.
  • Seek medical attention for any delayed onset of hypersensitivity: rash, urticaria, or respiratory difficulty.
Administration Instructions

TAGITOL V is typically provided to the patient for self-administration. Advise patients to carefully read and follow the Patient Instructions for Use to be provided to the patient.

Provide the patient with any site specific instructions regarding their procedure and when to take meals.

Nonclinical Toxicology Carcinogenesis, Mutagenesis, Impairment Of Fertility

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

Use In Specific Populations Pregnancy Risk Summary

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

Lactation Risk Summary

TAGITOL V 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

Pediatric Use

TAGITOL V is not indicated for pediatric use.

Geriatric Use

Clinical studies of TAGITOL V do 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.

Dosage (Posology) and method of administration

Recommended Dosing
  • The recommended oral dose of TAGITOL V is one 20 mL bottle (8 g barium sulfate) with each meal (breakfast, lunch and dinner) the day before the colonography examination. Total dose = 3 bottles (24 g barium sulfate).
Important Administration Instructions
  • TAGITOL V is typically provided to the patient for self-administration. Advise patients to carefully read and follow the Patient Instructions for Use to be provided to the patient.
  • Shake bottle for 15 seconds prior to administration.
  • For oral use only.
  • Encourage patients to hydrate following the barium sulfate procedure.
  • Discard any unused suspension.

Interaction with other medicinal products and other forms of interaction

SIDE EFFECTS

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.
DRUG INTERACTIONS

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