Syprine

From WikiMD's Food, Medicine & Wellness Encyclopedia

Syprine (INN: Trientine) is a medication used in the management and treatment of Wilson's disease, a rare genetic disorder that causes excessive accumulation of copper in the body. Syprine acts by chelating copper, facilitating its excretion from the body, and thereby reducing its toxic effects. This article provides an overview of Syprine, including its pharmacology, indications, administration, and safety profile.

Pharmacology[edit | edit source]

Syprine, with the active ingredient trientine hydrochloride, functions as a chelating agent. It binds to copper ions, forming a stable complex that can be excreted by the kidneys. Unlike penicillamine, another chelator used in Wilson's disease, Syprine is generally considered to have a more favorable side effect profile, making it a preferred option for some patients.

Indications[edit | edit source]

Syprine is primarily indicated for the treatment of Wilson's disease in patients who are intolerant to penicillamine. It may also be used in cases where penicillamine therapy has been deemed ineffective. Early diagnosis and treatment with Syprine are crucial to prevent irreversible damage caused by copper accumulation, such as liver failure and neurological disorders.

Administration[edit | edit source]

Syprine is administered orally. The dosage and duration of treatment depend on the severity of the disease and the patient's response to therapy. It is important that Syprine is taken on an empty stomach, at least one hour before meals or two hours after, to enhance absorption and efficacy.

Safety Profile[edit | edit source]

While Syprine is generally well-tolerated, it can cause side effects in some patients. Common adverse effects include gastrointestinal disturbances, such as nausea and diarrhea, and, less frequently, neurological symptoms like dizziness and headaches. Long-term use of Syprine requires regular monitoring of liver function and copper levels to ensure safety and effectiveness.

Conclusion[edit | edit source]

Syprine represents a critical option in the management of Wilson's disease, offering benefits for patients who cannot tolerate or do not respond to penicillamine therapy. Its role in facilitating copper excretion helps prevent the progression of this potentially life-threatening condition, underscoring the importance of early diagnosis and treatment.

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