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ergoloid mesylates (Hydergine)

 

Classes: Ergot Derivatives

Dosing and uses of Hydergine (ergoloid mesylates)

 

Adult dosage forms and strengths

tablet

  • 1mg

 

Age-Related Mental Decline & Alzheimer's Dementia

1 mg PO q8hr

May administer up to 4.5-12 mg/day therapeutic trial should be 6 months in duration

 

Pediatric dosage forms and strengths

Safety & efficacy not established

 

Geriatric dosage forms and strengths

 

Age-Related Mental Decline & Alzheimer's Dementia

1 mg PO q8hr

May administer up to 4.5-12 mg/day therapeutic trial should be 6 months in duration

 

Hydergine (ergoloid mesylates) adverse (side) effects

Frequency not defined

Flushing

Headache

Rash

Nausea

Vomiting

Nasal congestion

Blurred vision

Bradycardia or bradyarrhythmia

Orthostatic hypotension

 

Warnings

Contraindications

Hypersensitivity, psychosis; consider other CNS disease before starting

CYP3A4 inhibitors (azole anifungals, protease inhibitors, macrolide antibiotics)

 

Pregnancy and lactation

Pregnancy category: N/A

Lactation: unknown

 

Pregnancy categories

A: Generally acceptable. Controlled studies in pregnant women show no evidence of fetal risk.

B: May be acceptable. Either animal studies show no risk but human studies not available or animal studies showed minor risks and human studies done and showed no risk.

C: Use with caution if benefits outweigh risks. Animal studies show risk and human studies not available or neither animal nor human studies done.

D: Use in LIFE-THREATENING emergencies when no safer drug available. Positive evidence of human fetal risk.

X: Do not use in pregnancy. Risks involved outweigh potential benefits. Safer alternatives exist.

NA: Information not available.

 

Pharmacology of Hydergine (ergoloid mesylates)

Mechanism of action

Contains derivatives of three naturally occurring ergot alkaloids which have some peripheral alpha blocking activity and also depress CNS vasomotor nerve activity resulting in slight decrease in BP and HR; mechanism of action in dementia is largely unknown

 

Pharmacokinetics

Half-Life elimination: 3.5 hr

Onset: 3-4 wk

Peak Plasma Time: ~1 hr

Concentration: 576 pg/mL

Bioavailability: 9%

Metabolism: Liver