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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

Contraind./Precautions

Contraindicated in:

Use Cautiously in:

Adv. Reactions/Side Effects

CNS: dizziness, headache.

GI: dyspepsia, flatulence, gastritis, abdominal distension, abdominal pain, appetite, cholestasis, constipation, diarrhea, nausea.

GU: erectile dysfunction, renal failure.

Derm: alopecia, pruritus, urticaria, photosensitivity reaction, alopecia, rash.

MS: RHABDOMYOLYSIS, muscle cramps, muscular weakness, myalgia.

Misc: hypersensitivity reactions including anaphylaxis.

Interactions

Drug-Drug:

Availability

Route/Dosage

Action

Therapeutic Effects:

Classifications

Therapeutic Classification: lipid-lowering agents

Pharmacologic Classification: fibric acid derivatives

Pharmacokinetics

Absorption: Well absorbed (100%) following oral admininistration.

Distribution: Unknown.

Metabolism/Excretion: 50% metabolized, 50% excreted unchanged in urine, remainder as metabolites. 3% excreted in feces.

Half-life: 1–2 hr.

Canadian Brand Names

Bezalip SR

Time/Action Profile

(blood levels)

ROUTEONSETPEAKDURATION
POunknown3–4 hr24 hr

Patient/Family Teaching

Pronunciation

bezz-uh-FIBE-rate