DrugInfoSys

Ergotamine (Tartrate)

Also known as: Cafergot, Migril®,

Drug #282

Ergotamine (Tartrate) is alkaloid derived from ergot, consisting of lysergic acis, ammonia, proline, phenylalanine and pyruvic acid combined in amide linkages. Ergotamine (Tartrate) is used as an analgesic in the treatment of migraine and cluster headaches.

Primary Characteristics

Ergotamine (Tartrate) is also known as Cafergot, Migril®, .

It is of Synthetic origin and belongs to Ergot Alkaloid.

It belongs to Serotonin agonsit pharmacological group on the basis of mechanism of action and also classified in Ergot Derivative pharmacological group. It is also classified under Analgesics and Anti-inflammatory Agents .

Molecular Weight: 1313.43 · pKa: 6.8 · Solubility in Water: 1 in 500 · Solubility in Alcohol: 1 in 500 · Non-proprietary name: Ergotamine (Tartrate).

Molecular structure of Ergotamine (Tartrate)

Pharmacokinetics

Distribution: Ergotamine (Tartrate) has a volume of distribution is 1.85L/kg. plasma protein binding is 93 to 98%.

Elimination: it is metabolised via Hepatic 90%, plasma half-life is 2 & 21 hours, renal excretion is 5% excreted in urine.

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Indications

Ergotamine (Tartrate) is primarily indicated in conditions like Migraine, Prophylactic treatment of vascular headache, Vascular headaches.

Contraindications

Dosage

Ergotamine (Tartrate)'s dosage details are as follows:

DoseSingle DoseFrequencyRouteInstructions
Adult Dosage
1.5 mg1.5 mgInitially as Required
1.5 mg1.5 mgEvery 6hPOMaintenance for a Week
2 mg2 mgEvery 6hRectallyNot more than 4mg in 24 hours. Repeat half an hour or laier. Not more than 6mg should be given in 24 hours
Paediatric Dosage (20kg)
No data.
Neonatal Dosage (3kg)
No data.

Drug Interactions

Unknown3 interactions
8 interactions
Major6 interactions
Moderate5 interactions

Always consult your physician for the change of dose regimen or an alternative drug of choice that may strictly be required.

Side Effects

Ergotamine (Tartrate) in overdosage may give rise to further complications which include Ventricular fibrillation , Retroperitoneal fibrosis , Pleuropulmonary fibrosis , Endocardial fibrosis , Cerebral hemorrhage, Stroke.

Ergotamine (Tartrate) produces potentially life-threatening effects which include Myocardial infarction, Renal failure, Vascular occlusions, Gangrene of extremities, Necrosis of bowel. Careful monitoring is needed with proper medical management.

The signs and symptoms that are produced after acute overdosage of Ergotamine (Tartrate) are Nausea, Vomiting, Tachycardia , Diarrhea, Coma, Extreme Thirst, Confusion , Pallor, Cold extremities, Tingling.

Ergotamine (Tartrate) is known to cause more or less tolerable side effects which are usually transient. These include Abdominal pain, Cyanosis, Muscle pain, Nausea, Numbness , Oedema, Poresthesia, Vomiting , Weakness.

Warnings / Precautions

Avoid prolong administration or excessive dosage of ergotamine because of danger of gangrene, ergotism and patients become dependent upon it. It is Contraindicated in Pregnancy Risk of renal Vasoconstriction Avoid in liver impairment

Interference in Pathology

Ergotamine (Tartrate) may interfere in the diagnosis of False-negative skin test.

Available Brands

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Multi-Ingredient Combinations

Storage Conditions

Ergotamine (Tartrate) should be stored Aerosol. Suppositories. Tab.

Drug Classification

  1. 1.7.1Acute migraine attack

Manufacturers

Manufacturers of Ergotamine (Tartrate) in Pakistan: