Medically reviewed on December 15, 2017.
Applies to the following strengths: 2 mg
Usual Adult Dose for:
Additional dosage information:
Usual Adult Dose for Migraine
Initial dose: 2 mg sublingually at first sign of a migraine attack; may repeat dose at half-hour intervals not to exceed maximum doses
Maximum dose: 6 mg/24 hours; 10 mg/7-day period
-This drug should not be used for chronic daily administration.
Use: To abort or prevent vascular headaches, such as a migraine, migraine variants, or "histaminic cephalalgia".
Renal Dose Adjustments
Liver Dose Adjustments
US BOXED WARNING: CONCOMITANT ADMINISTRATION WITH POTENT CYP450 3A4 INHIBITORS:
-Serious and/or life-threatening peripheral ischemia has been associated with the coadministration of this drug with potent CYP450 3A4 inhibitors including protease inhibitors and macrolide antibiotics. Because CYP450 3A4 inhibition elevates the serum levels of this drug, the risk for vasospasm leading to cerebral ischemia and/or ischemia of the extremities is increased.
Safety and efficacy have not been established in patients younger than 18 years.
Consult WARNINGS section for additional precautions.
Data not available: Contraindicated in renal impairment
-Place under tongue at first sign of an attack; do not exceed maximum doses
-Protect from light; store between 68F and 77F (20C to 25C)
-This drug should only be used when a clear diagnosis of migraine headache has been established.
-Safe administration of ergot alkaloids require patients at risk of coronary artery disease (CAD) have a satisfactory cardiovascular (CV) evaluation prior to starting therapy; due to the possibility of CV testing not detecting underlying CAD, it is strongly recommended that first dose administration occur in a medically equipped facility and an ECG be obtained after dosing.
-Consider ECG monitoring following the first dose in patients with risk factors for coronary artery disease (CAD) who have satisfactorily completed a cardiovascular evaluation; patients with cardiovascular risk factors and those who acquire risk factors predictive of CAD should undergo periodic cardiovascular evaluation
-Patients should report to their healthcare provider any numbness or tingling in toes or fingers, muscle pain in the arms and legs, weakness in legs, chest pain, changes in heart rate, swelling, or itching.
-Patients should be advised to talk with their doctor or pharmacist before taking any new medications or supplements.
-Patients should be aware of the risk of serious cardiovascular side effects and the importance of seeking medical advice promptly if they occur.
-Patients should be instructed not to take more than the prescribed amount of medication without talking to their healthcare provider.
-This drug cause dizziness; have patient avoid driving or operating machinery until adverse effects are determined.
-Advise patient to speak to physician or health care professional if pregnant, intend to become pregnant, or are breastfeeding.
Always consult your healthcare provider to ensure the information displayed on this page applies to your personal circumstances.
More about ergotamine
- Ergotamine Side Effects
- During Pregnancy or Breastfeeding
- Drug Images
- Drug Interactions
- Support Group
- En Español
- 4 Reviews
- Drug class: antimigraine agents
Other brands: Ergomar