Deg Neuro Pharmacological Therapy Flashcards
Riluzole
ALS
Glutamate blocker; prolong survival 3-6 months
Baclofen
ALS, MS
Treat muscle spasms, spasticity
SE: dizziness, weakness, confusion, nausea
Diazepam
ALS, Huntingtons
Treats anxiety, muscle spasms, seizures; chorea tx
SE: dizziness, weakness, confusion, nausea
Dantrolene sodium
ALS
Treat muscle spasms; treat/prevent malignant hyperthermia
SE: dizziness, weakness, confusion, nausea
Glycopyrrolate
ALS
Treats severe drooling
SE: constipation
IVIG
Guillain-Barre
Stops the antibodies, decreases circulating antibodies; given during first couple weeks of dz
Tx HTN, tachy
Treat hypotension with fluids
Tetrabenazine (xenazine)
Huntington
Tx chorea
Levodopa
Huntington
treat patients with rigidity; may give Parkinson’s disease drugs
Amantadine HCl
MS, P
Reduces rigidity, tremor, bradykinesia, postural changes
SE: mood changes, confusion, depression, hallucinations, LE edema, nausea, epigastric distress, urinary retention, HA, visual impairment
Mitoxantrone (Novantrone)
MS
Reduce clinical relapses (risk of cardiac toxicity)
Gabapentin (Neurontin)
MS
anticonvulsant, nerve pain medication
Oxybutynin
MS
Tx bladder urgency; bladder relaxant
Baclofen (lioresal)
MS
Muscle relaxant, decrease spasticity
Methylprednisolone
MS
Shortens duration of relapse (no LT benefit); anti-inflammatory effect on T-cells and cytokines
Glatiramer
MS
Reduces frequency of relapses, but not progression of disability
Dimethyl fumarate
MS
Decreases number of episodes of worsening MS
Interferon 1A (Avonex, Rebif)
MS
Slows disease worsening, decrease flare ups; immunomodulator medications
SE: flu-like symptoms
Interferon 1B (Betaseron, Extavia)
MS
Reduce flare ups; immunomodulator
SE: flu-like symptoms
IVIG (MG)
Myasthenia gravis
Tx exacerbations;
Consists of immune globulins and acts to destroy and neutralize autoantibodies in the blood stream and block the production of new autoantibodies
AE: HA, migraine, flu-like symptoms
Pyridostigmine bromide (mesitonin)
Myasthenia gravis
Anti-cholinesterase; inhibits breakdown of ach; usually given QID
SE: take with food/milk, diarrhea, abdominal cramps, excessive saliva
Prednisone
Myasthenia gravis
Second line; most common long term; susceptible to oral infections
Azathioprine
Myasthenia gravis
3rd line; inhibits T-lymphocytes and b-cell proliferation and reduce ach receptor antibody levels; therapeutic effects may take 3-12 months
AE: leukopenia, hepatotoxicity
Carbidopa-levodopa
Parkinson’s disease
Increases presence of dopamine in brain
*carbidopa added to avoid metabolism of levodopa before it reaches brain
SE: NV, appetite loss, decreased BP, dystopia, dyskinesia, confusion
Amantadine HCl
Parkinson’s disease
Reduces rigidity, tremor, bradykinesia, postural changes
SE: mood changes, confusion, depression, hallucinations, LE edema, nausea, epigastric distress, urinary retention, HA, visual impairment