Dihydroergocryptine
Dihydroergocryptine used in the symptomatic treatment of mental deterioration associated with cerebrovascular insufficiency and in peripheral vascular disease
Primary Characteristics
It is of Synthetic origin and belongs to Ergot Alkaloid.
It is classified in Ergot Alkaloid pharmacological group. It is also classified under Psychotherapeutic Drugs .
Molecular Weight: 673.8 · Solubility in Water: null · Solubility in Alcohol: null · Non-proprietary name: Dihydroergocryptine.

Pharmacokinetics
Elimination: plasma half-life is 12-16 hr.
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Indications
Dihydroergocryptine is primarily indicated in conditions like Cerebro-vascular insufficiency, Chronic venous insufficiency, Ischaemic heart disease, Migraine, Parkinsonism.
Dihydroergocryptine is also indicated for secondary conditions like Behavioural disorders, Lactation inhibition, Peripheral vascular disease, Psychiatric disease, Raynaud's disease.
Contraindications
Dihydroergocryptine is contraindicated in conditions like Psychosis, Hypersensitivity to the drug.
Dosage
Dihydroergocryptine's dosage details are as follows:
| Dose | Single Dose | Frequency | Route | Instructions |
|---|---|---|---|---|
| Adult Dosage | ||||
| 90 mg | 90 mg | — | Maintainance doses for parkinsoinism. | |
| 20 mg | 20 mg | Every 24h | PO | For migraine |
| Paediatric Dosage (20kg) | ||||
| No data. | ||||
| Neonatal Dosage (3kg) | ||||
| No data. | ||||
Drug Interactions
None recorded.
Side Effects
Dihydroergocryptine is known to cause more or less tolerable side effects which are usually transient. These include Nausea.
Warnings / Precautions
Available Brands
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Multi-Ingredient Combinations
Storage Conditions
Drug Classification
- 1.12.8 — Other cardiovascular preparations