section name header

Pronunciation

pin-ah-VEER-ee-um

Classifications

Therapeutic Classification: anti irritable bowel syndrome agents

Pharmacologic Classification: calcium channel blockers

Indications

Canada-Approved Medicine

This monograph describes a medication approved for use in Canada by the Therapeutic Products Directorate, a division of Health Canada’s Health Products and Food Branch. The medication is not approved by the United States Food and Drug Administration; however, a similar formulation carrying a different generic or brand name might be available in the US.

REMS

Action

Therapeutic Effects:

Pharmacokinetics

Absorption: Poorly absorbed (1–10%).

Distribution: Distributes selectively to digestive tract.

Protein Binding: 97%.

Metabolism/Excretion: Minimal enterohepatic cycling, eliminated almost entirely in feces. Some metabolism.

Half-life: 1.5 hr.

Time/Action Profile

(blood levels)

ROUTEONSETPEAKDURATION
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Contraind./Precautions

Contraindicated in:

Use Cautiously in:

Adv. Reactions/Side Effects

All less than 1%

CNS: drowsiness, headache, vertigo.

GI: constipation, diarrhea, distention, dry mouth, epigastric pain/fullness, esophageal irritation, nausea.

Derm: rash.

Interactions

Drug-Drug:

Route/Dosage

Availability

Assessment

Implementation

Patient/Family Teaching

Evaluation/Desired Outcomes

Canadian Brand Names

Dicetel

Pot. Nursing Diagnoses