Use LEFT and RIGHT arrow keys to navigate between flashcards;
Use UP and DOWN arrow keys to flip the card;
H to show hint;
A reads text to speech;
45 Cards in this Set
- Front
- Back
Bromocriptine - Indication |
Dopamine agonist in PKD. (Also used to treat hyperprolactinemia)
|
|
Pramipexole - Indication
|
Dopamine agonist in PKD. (Also used to treat restless legs sysndrome) |
|
Ropinirole - Indication
|
Dopamine agonist in PKD. (Also used to treat restless legs sysndrome)
|
|
Amantadine - Indication
|
Increases dopamine in PKD. (Also used as an antiviral against influenza A and rubella)
|
|
Selegiline - Indication
|
Adjunctive agent to L-dopa in treatment of Parkinson's disease
|
|
Entacapone - Indication
|
Adjunctive (only) agent to L-dopa in treatment of Parkinson disease.
|
|
Tolcapone - Indication
|
Adjunctive (only) agent to L-dopa in treatment of Parkinson disease.
|
|
Benztropine - Indication
|
Improves tremor and rigidity (little effect on bradykinsia)
|
|
Rasagiline - Indication
|
Adjunctive agent to L-dopa in treatment of Parkinson's disease; possible neuroprotective action.
|
|
L-dopa (leveodpa)/carbidopa - Indication
|
Increases level of dopamine in the brain in Parkinson's disease
|
|
Memantine - Indication
|
Moderate to severe Alzheimer's Disease
|
|
Donepezil, galantamine, rivastigmine - Indication
|
Alzheimer's Disease |
|
Tetrabenazine - Indication
|
Chorea; Huntington's Disease
|
|
Reserpine - Indication
|
Chorea; Huntington's Disease (also used for blood pressure control, older medication)
|
|
Sumatriptan - Indication
|
Acute migraine, cluster headache attacks
|
|
Bromocriptine - Mechanism
|
Ergot - stimulates dopamine receptors directly
|
|
Pramipexole- Mechanism
|
Non-ergot - stimulates dopamine receptors directly; D2 family - higher affinity for D3 receptor sub-type
|
|
Ropinirole- Mechanism
|
Non-ergot - stimulates dopamine receptors directly; D2 family - higher affinity for D3 receptor sub-type
|
|
Amantadine- Mechanism
|
May stimulate dopamine release
|
|
Selegiline- Mechanism
|
Selective MAO type B inhibitor, irreversible, does not interact with tyramine; prevents dopamine breakdown leading to increased dopamine availability |
|
Entacapone- Mechanism
|
COMT inhibitor. Prevents dopamine breakdown (blocks peripheral conversion of L-dopa to O-methyl dopa) leading to increased dopamine availability
|
|
Tolcapone- Mechanism
|
COMT inhibitor. Prevents dopamine breakdown (blocks peripheral conversion of L-dopa to O-methyl dopa) leading to increased dopamine availability
|
|
Benztropine- Mechanism
|
Antimuscarinic; curbs excess cholinergic activity. (Balances dopaminergic-cholinergic systems by reducing cholinergic dominance.)
|
|
Rasagiline- Mechanism
|
Selective MAO type B inhibitor, irreversible, does not interact with tyramine; prevents dopamine breakdown leading to increased dopamine availability
|
|
L-dopa (leveodpa)/carbidopa- Mechanism
|
Unlike dopamine, L-dopa can cross blood-brain barrier and is converted by dopa decarboxylase in the CNS to dopamine. Carbidopa, a peripheral decarboxylase inhibitor, is givin with L-dopa to increase the bioavilability of L-dopa in the brain and to limit peripheral side effects.
|
|
Memantine- Mechanism
|
NMDA receptor antagonist; helps prevent excitotoxicity (mediated by Ca2+).
|
|
Donepezil, galantamine, rivastigmine- Mechanism
|
Acetylcholinesterase (AChE) inhibitors; increases neurotransmitter acetylcholine by blocking the enzyme that metabolizes it
|
|
Tetrabenazine- Mechanism
|
Inhibits vesicular monoamine transporter (VMAT); limits dopamine vesicle packaging and release.
|
|
Reserpine- Mechanism
|
Inhibits vesicular monoamine transporter (VMAT); limits dopamine vesicle packaging and release.
|
|
Sumatriptan- Mechanism
|
5-HT 1B/1D agonist. Inhibits trigeminal nerve activation; prevents vasoative peptide release; induces vasoconstriction. Half-life less than 2 hours.
|
|
Bromocriptine- Side Effect
|
Confusion and hallucinations. (Newer non-ergots more specific and preferred.)
|
|
Pramipexole- Side Effect
|
Confusion and hallucinations, somnolence, compulsive behaviors, orthostasis
|
|
Ropinirole- Side Effect
|
Confusion and hallucinations, somnolence, compulsive behaviors, orthostasis
|
|
Amantadine- Side Effect
|
Ataxia, conufsion and hallucinations, especially if used in combination with other PKD drugs
|
|
Selegiline- Side Effect
|
May enhance adverse effects of L-dopa. Conufsion, hallucinations, especially when added to other PKD meds. Metabolizes to amphetamine and has largely been replaced by rasageline (Azilect).
|
|
Entacapone- Side Effect
|
May enhance adverse effects of L-dopa.
|
|
Tolcapone- Side Effect
|
Acute liver failure (entacapone preferred). May enhance adverse effects of L-dopa.
|
|
Benztropine- Side Effect
|
Dry mouth, blurred vision, constipation and urinary retention, sedation, mental confusion.
|
|
Rasagiline- Side Effect
|
May enhance adverse effects of L-dopa. Conufsion, hallucinations, especially when added to other PKD meds.
|
|
L-dopa (leveodpa)/carbidopa- Side Effect
|
Arrhythmias occur from increased peripheral formation of catecholamines. Long-term use can lead to dyskinesia following administration ("on-off" phenomenon), akinesia between doses. Somnolence, orthostasis, confusion may occur.
|
|
Memantine- Side Effect
|
Dizziness, confusion, hallucination.
|
|
Donepezil, galantamine, rivastigmine- Side Effect
|
Nausea, dizziness, insominia, diarrhea.
|
|
Tetrabenazine- Side Effect
|
Depression, suicidal ideation, sedation, anxiety (preferred due to increased effectiveness)
|
|
Reserpine- Side Effect
|
Sedation, dizziness, depression
|
|
Sumatriptan- Side Effect
|
Coronary vasospasm (contraindicated in patients with CAD or Prinzmetal angina), mild tingling.
|