“…[14,22] • Sensitzing effect of the heart for catecholamine [33] • α-methyldopa reduces levodopa response [21] • Pyridoxine (B6) increases the peripheral breakdown of levodopa and diminishes its efficacy [22,29,33] • Mequitazine decreases the L-dopa effect [29] • Metoclopramide and antacids increase levodopa resorption [21,29] • Domperidone slightly increases the bioavailability of levodopa [24] • Reduced therapeutic effect by reserpine, classical neuroleptics and opioids [14,22] Dopamine agonists • Ergot-agonists: increased effect of antihypertensive drugs [14,22] • Alpha-DHEC enhances the effect of platelet aggregation inhibitors • Lisuride increases the inclination to bleeding • Inhibition of particular enzymes of the P-450 system by bromocriptine and pergolide • Elevation of the macrolide antibiotic level (up to 4.6 times) by, e. g., cabergoline and bromocriptine • Caution when combining pramipexole with exclusively renally eliminated agents • High dose of Estrogens may increase the ropinirole level • Declining therapeutic effect by reserpine, classical neuroleptics and opioids [14,22] Selegiline • Contraindicated when used concurrently with SSRI (can trigger mania, shivering attacks, excessive sweating) and MAO inhibitors • Use cautiously in combination with TAD or COMT inhibitors (if selegiline > 10mg) • Do not combine with triptans -unpredictable interactions [33] and keep in mind the side effects seen with sibutramine [15] • Caution is required when used simultaneously with QT-interval prolonging agents (antiarrhythmic drugs, amantadine, domperidone) • Interaction with metoprolol (increased level) and several antibiotics • Reduced alcohol tolerance [22] Anticholinergics…”