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Methysergide
Pronunciation
U.S. Brand Names
Generic Available
Synonyms
Pharmacological Index
Use
Pregnancy Risk Factor
Contraindications
Warnings/Precautions
Adverse Reactions
Overdosage/Toxicology
Drug Interactions
Mechanism of Action
Pharmacodynamics/Kinetics
Usual Dosage
Dietary Considerations
Mental Health: Effects on Mental Status
Mental Health: Effects on Psychiatric Treatment
Dental Health: Local Anesthetic/Vasoconstrictor Precautions
Dental Health: Effects on Dental Treatment
Patient Information
Nursing Implications
Dosage Forms

Pronunciation
(meth i SER jide)

U.S. Brand Names
Sansert®

Generic Available

No


Synonyms
Methysergide Maleate

Pharmacological Index

Ergot Derivative


Use

Prophylaxis of vascular headache


Pregnancy Risk Factor

X


Contraindications

Peripheral vascular disease, severe arteriosclerosis, pulmonary disease, severe hypertension, phlebitis, serious infections, pregnancy


Warnings/Precautions

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

Tablet, as maleate: 2 mg


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