Mosby's 2014 Nursing Drug Reference (102 page)

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clomiPRAMINE (Rx)

(kloe-mip′ra-meen)

Anafranil

Func. class.:
Antidepressant, tricyclic

Chem. class.:
Tertiary amine

Do not confuse:
clomiPRAMINE
/clomiPHENE/chlorproMAZINE/desipramine/Norpramin

ACTION:

Potentiates serotonin and norepinephrine; moderate anticholinergic effect

USES:

Obsessive-compulsive disorder

Unlabeled uses:
Panic disorder, autism, depression, premature ejaculation, dysphoria, phobias, anxiety, agoraphobia

CONTRAINDICATIONS:

Hypersensitivity, immediate post-MI

Precautions:
Pregnancy (C), breastfeeding, geriatric patients, seizures, cardiac disease, glaucoma, prostatic hypertrophy, urinary retention

 

Black Box Warning:

Children, suicidal ideation

DOSAGE AND ROUTES
Calculator
Obsessive-compulsive disorder

• Adult:
PO
25 mg at bedtime, increase gradually over 4 wk to 75-250 mg/day in divided doses

• Child 10-18 yr:
PO
25 mg/day gradually increase over 2 wk; max 3 mg/kg/day or 200 mg/day, whichever is smaller

Autism (unlabeled)

• Adult:
PO
25 mg/day, may increase to 75-100 mg/day, max 250 mg/day

• Child:
PO
25 mg/day, may increase if needed

Premature ejaculation (unlabeled)

• Adult:
PO
25-50 mg/day

Depression (unlabeled)

• Adult:
PO
25 mg at bedtime and increase gradually over 4 wk to 75-250 mg/day in divided doses

• Child 10-18 yr:
PO
25-50 mg/day gradually increased; max 3 mg/kg/day or 200 mg/day, whichever is smaller

Available forms:
Caps 25, 50, 75 mg

Administer:

• 
Do not break, crush, or chew caps

• 
Increased fluids, bulk in diet for constipation, especially for geriatric patients

• 
Without regard to food, during initial dosing and titration give with meals

• 
After titration, may be given as a single dose at bedtime to reduce daytime sedation

SIDE EFFECTS

CNS:
Dizziness, tremors, mania
,
seizures,
aggressiveness, EPS, drowsiness, headache,
neuroleptic malignant syndrome,
insomnia, agitation

CV:
Hypotension, tachycardia,
cardiac arrest

EENT:
Blurred vision

ENDO:
Galactorrhea, hyperprolactinemia

GI:
Constipation, dry mouth, nausea, dyspepsia
, weight gain,
hepatic toxicity

GU:
Delayed ejaculation, anorgasmia
, urinary retention, decreased libido

HEMA:
Agranulocytosis, neutropenia, pancytopenia

INTEG:
Diaphoresis, photosensitivity

META:
Hyponatremia

SYST:
Suicide in children, adolescents

PHARMACOKINETICS

Onset ≥2 wk (depression), 4-10 wk (OCD); peak 2-6 hr; extensively bound to tissue and plasma proteins; demethylated in liver; active metabolites excreted in urine (50%-60%), feces (24%-32%); half-life 20-30 hr; steady state 1-2 wk

INTERACTIONS

Increase:
hypertensive crisis, seizures, hypertensive episode—MAOIs

Increase:
Serotonin syndrome-SSRIs, SNRIs serotonin syndrome, linezolid, methylene blue IV

Increase:
clomiPRAMINE levels—cimetidine, FLUoxetine, fluvoxaMINE, sertraline; do not use together

Increase:
hypertensive effect—cloNIDine, EPINEPHrine, norepinephrine

Increase:
clomiPRAMINE level—CYP1A2, CYP2D6

Increase:
CNS depression—alcohol, CNS depressants, general anesthetics

Increase:
QT prolongation—other tricyclics, phenothiazines, quinolones

Decrease:
effect of cloNIDine, levodopa, skeletal muscle relaxants, haloperidol, opiates

Decrease:
clomiPRAMINE levels—barbiturates, carBAMazepine, phenytoin

Drug/Herb

Increase:
serotonin syndrome—St. John’s wort; do not use concurrently

Increase:
CNS depression—hops, kava, valerian

Drug/Lab Test

Increase:
prolactin, TBG, AST, ALT, blood glucose

Decrease:
serum thyroid hormone (T
3
, T
4
)

NURSING CONSIDERATIONS
Assess:

• 
B/P lying, standing; pulse q4hr; if systolic B/P drops 20 mm Hg, withhold product, notify prescriber; take VS q4hr in patients with CV disease

• 
Serotonin syndrome:
hyperpyrexia, rigidity, irregular pulse, diaphoresis

• 
ECG
for flattening of T wave, QTc prolongation, bundle branch block, AV block, dysrhythmias in cardiac patients, may lead to cardiac collapse

• 
Blood studies: CBC, leukocytes, differential, cardiac enzymes if patient is receiving long-term therapy and signs of blood dyscrasias

• 
Hepatic studies: AST, ALT, bilirubin

 

Black Box Warning:

Mental status: mood, sensorium, affect, suicidal tendencies; increase in psychiatric symptoms: depression, panic, frequency of obsessive-compulsive behaviors; watch closely for evidence of suicidal thoughts in children, adolescents; seizure disorders

• 
Urinary retention, constipation; constipation more likely in children

• 
Withdrawal symptoms:
headache, nausea, vomiting, muscle pain, weakness; not usual unless product discontinued abruptly

• 
Alcohol consumption; if alcohol consumed, withhold dose until
AM

Perform/provide:

• 
Storage in tight container at room temp; do not freeze

• 
Assistance with ambulation during beginning therapy, since drowsiness, dizziness occurs

• 
Gum, hard candy, or frequent sips of water for dry mouth

Evaluate:

• 
Therapeutic response: decreased anxiety, depression

Teach patient/family:

• 
That the effects may take 4-6 wk to appear

• 
About risk for seizures

• 
To use caution when driving, performing other activities that require alertness because drowsiness, dizziness, blurred vision may occur

• 
To avoid alcohol, other CNS depressants

• 
Not to discontinue medication quickly
after long-term use because this may cause nausea, headache, malaise

 

Black Box Warning:

That suicidal thoughts/behaviors may occur in children, young adults, report immediately

• 
To wear sunscreen, protective clothing to prevent photosensitivity

• 
To notify prescriber if pregnancy is planned, suspected

• 
That men may experience a high incidence of sexual dysfunction

• 
Serotonin syndrome:
report immediately sweating, diarrhea, twitching

• 
Abrupt discontinuation:
do not stop abruptly

TREATMENT OF OVERDOSE:

ECG monitoring; induce emesis; lavage, activated charcoal; anticonvulsant; diazepam IV

Canada only   Side effects:
italics
= common;
bold
= life-threatening   
Nurse Alert

clonazePAM (Rx)

(kloe-na′zi-pam)

Klonopin

Func. class.:
Anticonvulsant

Chem. class.:
Benzodiazepine derivative

 

Controlled Substance Schedule IV

Do not confuse:
clonazePAM
/LORazepam/clorazepate/cloNIDine
KlonoPIN
/cloNIDine

ACTION:

Inhibits spike, wave formation during absence seizures (petit mal); decreases amplitude, frequency, duration, spread of discharge during minor motor seizures

USES:

Absence, atypical absence, akinetic, myoclonic seizures; Lennox-Gastaut syndrome, panic disorder

Unlabeled uses:
Anxiety, insomnia, nystagmus, restless leg syndrome

CONTRAINDICATIONS:

Pregnancy (D), hypersensitivity to benzodiazepines, acute closed-angle glaucoma, psychosis, severe hepatic disease

Precautions:
Breastfeeding, geriatric patients, open-angle glaucoma, chronic respiratory disease, renal/hepatic disease

DOSAGE AND ROUTES
Calculator
Lennox-Gastaut syndrome/atypicals absence seizures/akinetic and myclonic seizures

• Adult:
PO
up to 1.5 mg/day in 3 divided doses; may be increased 0.5-1 mg q3days until desired response, max 20 mg/day

• Geriatric:
PO
0.25 daily-bid initially, increase by 0.25/day q7-14days as needed

• Child <10 yr or <30 kg:
PO
0.01-0.03 mg/kg/day in divided doses q8hr, max 0.05 mg/kg/day; may be increased 0.25-0.5 mg q3days until desired response, max 0.1-0.2 mg/kg/day

Panic disorder

• Adult:
PO
0.25 mg bid increase to 1 m daily after 3 days, max 4 mg/day

Restless leg syndrome (RLS) (unlabeled)

• Adult:
PO
0.5 mg tid or 0.5 mg in the evening and 30 min before bedtime

Insomnia/anxiety (unlabeled)

• Adult:
PO
0.125-0.25 mg at bedtime, titrate up q3-4days as needed

Available forms:
Tabs 0.5, 1, 2 mg; orally disintegrating tabs 0.125, 0.25, 0.5, 1, 2 mg

Administer:
PO route

• 
With food, milk for GI symptoms

• 
Orally disintegrating tablets:
open pouch by peeling back foil on blister pack (do not push tab through foil), place on tongue, allow to dissolve; may be swallowed with/without water

• 
Store at room temperature

SIDE EFFECTS

CNS:
Drowsiness
, dizziness, confusion, behavioral changes, tremors, insomnia, headache,
suicidal tendencies,
slurred speech, anterograde amnesia

CV:
Palpitations, bradycardia, tachycardia

EENT:
Increased salivation, nystagmus, diplopia
, abnormal eye movements

GI:
Nausea, constipation
, polyphagia, anorexia, xerostomia, diarrhea, gastritis, sore gums

GU:
Dysuria, enuresis, nocturia, retention, libido changes

HEMA:
Thrombocytopenia, leukocytosis, eosinophilia

INTEG:
Rash, alopecia, hirsutism

RESP:
Respiratory depression,
dyspnea, congestion

PHARMACOKINETICS

PO:
Peak 1-2 hr, metabolized by liver, excreted in urine, half-life 18-50 hr, duration 6-12 hr, protein binding 85%

INTERACTIONS

Increase:
clonazePAM effects—CYP3A4 inhibitors (azoles, cimetidine, clarithromycin, diltiazem, erythromycin, FLUoxetine), oral contraceptives

Increase:
CNS depression—alcohol, barbiturates, opiates, antidepressants, other anticonvulsants, general anesthetics, hypnotics, sedatives

Decrease:
clonazePAM effect—CYP3A4 inducers (carBAMazepine, PHENobarbital, phenytoin)

Drug/Herb

Increase:
CNS depression—kava, chamomile, valerian

Increase:
clonazePAM effect—ginkgo, melatonin

Decrease:
clonazePAM effect—ginseng, St. John’s wort

Drug/Lab Test

Increase:
AST, alk phos, bilirubin

Decrease:
Platelets, WBC

NURSING CONSIDERATIONS
Assess:

• 
Seizures:
duration, type, intensity, with/without aura

• 
Blood studies: RBC, Hct, Hgb, reticulocyte counts every wk for 4 wk then monthly

• 
Hepatic studies: ALT, AST, bilirubin, creatinine

• 
Abrupt discontinuation:
Do not discontinue abruptly, seizures may increase

• 
Signs of physical withdrawal if medication suddenly discontinued

 
Mental status:
mood, sensorium, affect, oversedation, behavioral changes,
suicidal thoughts/behaviors;
if mental status changes, notify prescriber

• 
Eye problems: need for ophthalmic exam before, during, after treatment (slit lamp, funduscopy, tonometry)

• 
Allergic reaction: red, raised rash; product should be discontinued

 
Blood dyscrasias:
fever, sore throat, bruising, rash, jaundice

• 
Toxicity:
bone marrow depression, nausea, vomiting, ataxia, diplopia, CV collapse; drug levels during initial treatment (therapeutic 20-80 ng/ml)

Perform/provide:

• 
Assistance with ambulation during early part of treatment; dizziness occurs, especially among geriatric patients

Evaluate:

• 
Therapeutic response: decreased seizure activity

Teach patient/family:

• 
To carry emergency ID bracelet stating name, products taken, condition; prescriber’s name, phone number

• 
To avoid driving, other activities that require alertness

• 
To avoid alcohol, other CNS depressants; increased sedation may occur

• 
Not to discontinue medication quickly after long-term use; to taper off over several wk

• 
To notify prescriber of yellowing of skin/eyes, clay-colored stools, bleeding, fever, extreme fatigue, sore throat, suicidal thoughts/behaviors

• 
To notify prescriber immediately if suicidal thoughts, behaviors occur

TREATMENT OF OVERDOSE:

Lavage, activated charcoal, flumazenil, monitor electrolytes, VS, administer vasopressors

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