Apomorphine
Non-selective dopamine agonist (high D2/D3 affinity) acting centrally to modulate neural drive and arousal. Unlike PDE5 inhibitors, it targets the central nervous system to initiate response rather than maintaining vascular engorgement.
Indications & Usage
FDA Label Indications
NEUROLOGY- ▸ Target: Parkinson's Disease (Advanced).
- ▸ Condition: Acute intermittent treatment of hypomobility ("off" episodes).
Off-Label / Functional Use
CLINICAL PRACTICE- ▸ Target: Men & Women (Central Activation).
- ▸ Condition: Psychogenic ED, Delayed Ejaculation, Hypoactive Desire (HSDD).
Dosing Protocols
Select administration route to view specific protocols.
SUBLINGUAL TROCHE
GOLD STANDARDPlace under tongue. Allow full dissolution (approx 10 mins). Do not swallow saliva immediately.
Start with 2.0 mg test dose to assess nausea tolerance. Titrate up to 3.0-4.0 mg if needed at next trial. Doses >4mg significantly increase nausea risk.
Nausea is the primary dose-limiting side effect. The "Yawn" reflex typically precedes therapeutic onset by 5-10 minutes.
Cycling & Safety Limits
The "Pre/60/120" Rule
Pre-Medicate (Tigan)
Initiate Trimethobenzamide 300mg TID, 3 days prior to first dose to prevent severe emesis.
60 Minute Window
Therapeutic window is short. Activity should be planned 45-60 mins post-dose (SL).
120 Min Washout
Wait at least 2 hours between doses to allow receptor reset and prevent accumulation.
DO NOT COMBINE with 5HT3 Antagonists (Zofran). Risk of severe hypotension.