Skip to Main Content

++

INTRODUCTION

++

tegaserod (te-gas-er-od)

Zelnorm

Classification

Therapeutic: anti-irritable bowel syndrome agents

Pharmacologic: 5-HT4 agonists

++
Indications
++

Short-term treatment of irritable bowel syndrome (IBS) in women whose primary symptom is constipation in patients younger than 55 yr. Chronic idiopathic constipation in patients younger than 55 yr for whom no other treatment has provided satisfactory relief and/or who had satisfactory improvement previously with tegaserod. Only available under an emergency investigational new drug (IND) process. To qualify, patients must have a condition characterized as immediately life threatening or requiring hospitalization. Physicians would need to make the request for emergency use through the FDA.

++
Action
++

Acts as a partial agonist of 5-hydroxytryptamine (5-HT, serotonin) at the 5-HT4 receptor site. Agonist activity causes the release of other neurotransmitters and results in increased peristalsis, increased intestinal secretion, and decreased visceral sensitivity. Therapeutic Effects: Decreased constipation.

++
Adverse Reactions/Side Effects
++

CNS: headache. GI: diarrhea.

++

PHYSICAL THERAPY IMPLICATIONS

++
Examination and Evaluation
++

  • Monitor GI symptoms (constipation, abdominal pain, bloating, cramps) to help document whether drug therapy is successful in reducing these symptoms.

++
Patient/Client-Related Instruction
++

  • Advise patient to avoid alcohol and foods that may increase GI irritation and constipation.

  • Instruct patient to report other bothersome side effects such as severe or prolonged headache or diarrhea.

++
Pharmacokinetics
++

Absorption: 10% absorbed following oral administration.

++

Distribution: Extensively distributed to tissues.

++

Protein Binding: 98% bound to plasma proteins.

++

Metabolism and Excretion: 66% excreted unchanged in feces; remainder is metabolized in the GI tract and by the liver. Metabolites are renally excreted.

++

Half-life: 11 hr.

++

Table Graphic Jump Location
Favorite Table | Download (.pdf) | Print

TIME/ACTION PROFILE

ROUTE ONSET PEAK DURATION
PO unknown 1 hr* 1–2wk

*Blood levels.

Return of symptoms following discontinuation.

++
Contraindications/Precautions
++

Contraindicated in: Hypersensitivity; Moderate-to-severe hepatic impairment; Severe renal impairment; History of bowel obstruction, gallbladder disease, sphincter of Oddi dysfunction, or intra-abdominal adhesions; Concurrent or frequent diarrhea; Exclusion criteria for emergency access include history, current diagnosis, or symptoms of CV disease, Presence of CV risk factors, Uncompensated depression or anxiety, Suicidal ideation or behavior.

++

Use Cautiously in: Mild hepatic impairment; Geri: Safety not established; OB: Pregnancy, lactation, or children <18 yr (safety not established).

++
Interactions
++

Drug-Drug: None known.

++
Route/Dosage
++

PO (Adults): 6 mg bid before meals.

++
Availability
++

Tablets: 2 mg, 6 mg.

Pop-up div Successfully Displayed

This div only appears when the trigger link is hovered over. Otherwise it is hidden from view.