Pharm part 5 Flashcards
Common indications for paroxetine
Depression
Panic d/o
OCD
GAD
MOA of paroxetine
SSRI, clinically unrelated to tricyclic, tetracyclic, or other antidepressants
Presumably, the inhibition of serotonin reuptake from brain synapse stimulated serotonin activity in the brain
Common AEs of paroxetine
Nausea Somnolence HA Sexual dysfunction Dizziness Asthenia Wt gain
Renal or hepatic dose adjustments for paroxetine
CrCl <30 mL/min: adjustment needed
Severe hepatic impairment: adjustment needed
BBW for paroxetine
Increased suicidal thinking and behavior
Clinically sig drug interactions for paroxetine
MAOIs
Chronic use with NSAIDs increases risk of GI bleed
Major counseling points for paroxetine
May cause drowsiness.
Avoid EtOH while taking this med
Therapy may take up to 2 wks to see improvement
Do not abruptly d/c
Pay close attention to any changes in mood, thought, or feelings such as suicidality
Monitoring parameters of paroxetine
Improvement of S/sx of depression/panic/GAD/OCD
Unusual changes in mood
Suicidality
Common indications of clonidine
HTN
Opioid detox
Impulse control/ADHD
MOA of clonidine
Central pre-synaptic alpha 2 receptor antagonist
Reduces the brain’s adrenergic outflow to decrease BP
Common AEs of clonidine
Drowsiness Xerostomia HA Bradycardia Rash (transdermal patch) Dizziness Somnolence
Clinically sig drug interactions of clonidine
TCAs may cause severe hypotension
Avoid CNS depressants
Major counseling points of clonidine
Do not d/c abruptly d/t rebound HTN
Patches are applied on a weekly basis
Patch site must be rotated on a weekly basis
Monitoring parameters of clonidine
Decrease in BP
Improvement of S/sx of ADHD/impulse control
Common indications for promethazine
Nausea
Motion sickness
Cough
MOA of promethazine
Competitively inhibits histamine at the H1 receptor sites, causing spasmolytic and decongestant effects
Common adverse effects of promethazine
Drowsiness Rash Nausea Vomiting Blurred vision Dry mouth Dizziness