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Pronunciation |
|
(meth
i SER
jide) |
|
|
U.S. Brand
Names |
|
Sansert® |
|
|
Generic
Available |
|
No |
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|
Synonyms |
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Methysergide Maleate |
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|
Pharmacological Index |
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Ergot Derivative |
|
|
Use |
|
Prophylaxis of vascular headache |
|
|
Pregnancy Risk
Factor |
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X |
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Contraindications |
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Peripheral vascular disease, severe arteriosclerosis, pulmonary disease,
severe hypertension, phlebitis, serious infections,
pregnancy |
|
|
Warnings/Precautions |
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Patients receiving long-term therapy may develop retroperitoneal fibrosis,
pleuropulmonary fibrosis and fibrotic thickening of the cardiac valves. Fibrosis
occurs rarely when therapy is interrupted for 3-4 weeks every 6 months. Use
caution in patients with impairment of renal of hepatic function; some products
may contain tartrazine. |
|
|
Adverse
Reactions |
|
>10%:
Cardiovascular: Postural hypotension, peripheral ischemia
Central nervous system: Insomnia
Gastrointestinal: Nausea, vomiting, abdominal pain, diarrhea
1% to 10%:
Cardiovascular: Peripheral edema, tachycardia, bradycardia
Dermatologic: Rash
Gastrointestinal: Heartburn |
|
|
Overdosage/Toxicology |
|
Symptoms of overdose include hyperactivity, limb spasms, impaired mental
function, and impaired circulation. Treatment is
supportive. |
|
|
Drug
Interactions |
|
Beta-blockers may cause peripheral ischemia |
|
|
Mechanism of
Action |
|
Ergotamine congener, however actions appear to differ; methysergide has
minimal ergotamine-like oxytocic or vasoconstrictive properties, and has
significantly greater serotonin-like properties |
|
|
Pharmacodynamics/Kinetics |
|
Serum half-life, plasma elimination: ~10 hours |
|
|
Usual Dosage |
|
Adults: Oral: 4-8 mg/day with meals; if no improvement is noted after 3
weeks, drug is unlikely to be beneficial; must not be given continuously for
longer than 6 months, and a drug-free interval of 3-4 weeks must follow each
6-month course |
|
|
Dietary
Considerations |
|
May be administered with food or milk |
|
|
Mental Health: Effects
on Mental Status |
|
Insomnia is common; may rarely cause drowsiness, euphoria, depression, or
confusion |
|
|
Mental Health:
Effects on Psychiatric
Treatment |
|
None reported |
|
|
Dental Health: Local
Anesthetic/Vasoconstrictor
Precautions |
|
No information available to require special precautions |
|
|
Dental Health:
Effects on Dental Treatment |
|
No effects or complications reported |
|
|
Patient
Information |
|
This drug is meant to prevent migraine headaches, not treat acute attacks.
Take as directed; do not take more than recommended and do not discontinue
without consulting prescriber (must be discontinued slowly). You may experience
weight gain (monitor dietary intake and exercise) or dizziness or vertigo (use
caution when driving or engaging in tasks that require alertness until response
to drug is known). Small frequent meals may reduce nausea or vomiting. Diarrhea
will lessen with use. Report cold, numb, tingling, or painful extremities or leg
cramps, chest pain, difficulty breathing or shortness of breath, or pain on
urination. Pregnancy/breast-feeding precautions: Inform prescriber if
you are pregnant. Do not get pregnant during or for 1 month following therapy.
Consult prescriber for instruction on appropriate barrier contraceptive
measures. This drug may cause severe fetal defects. Do not
breast-feed. |
|
|
Nursing
Implications |
|
Advise patient to make position changes slowly |
|
|
Dosage Forms |
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Tablet, as maleate: 2 mg |
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