Mosby's 2014 Nursing Drug Reference (181 page)

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Do not confuse:
Prolixin
/Proloid

ACTION:

Depresses cerebral cortex, hypothalamus, limbic system, which control activity and aggression; blocks neurotransmission produced by DOPamine at synapse; exhibits strong α-adrenergic and anticholinergic blocking action; mechanism for antipsychotic effects is unclear

USES:

Psychotic disorders, schizophrenia

CONTRAINDICATIONS:

Hypersensitivity, circulatory collapse, hepatic damage, cerebral arteriosclerosis, coronary disease, severe hypo/hypertension,
blood dyscrasias, coma, brain damage, closed-angle glaucoma, bone marrow depression, alcohol and barbiturate withdrawal

Precautions:
Pregnancy (C), breastfeeding, children <12 yr, geriatric patients, seizure disorders, hypertension, cardiac/hepatic disease

 

Black Box Warning:

Increased mortality in elderly patients with dementia-related psychosis

DOSAGE AND ROUTES
Calculator
Decanoate

• Adult and child >16 yr:
IM/SUBCUT
12.5-25 mg q1-3wk, may increase slowly

• Child 12-16 yr:
IM/SUBCUT
6.25-18.75 mg, then repeat q1-3wk, then increase slowly; max 25 mg

• Child 5-12 yr:
IM/SUBCUT
3.125-12.5 mg, then repeat q1-3wk, increase slowly

HCl

• Adult:
PO
2.5-10 mg in divided doses q6-8hr, max 40 mg/day;
IM
initially 1.25 mg then 2.5-10 mg in divided doses q6-8hr

• Child:
PO
0.25-3.5 mg/day in divided doses q4-6hr, max 10 mg/day

Available forms:
Decanoate:
inj 25 mg/ml;
HCl:
tabs 1, 2.5, 5, 10 mg; inj 2.5 mg/ml; elixir 2.5 mg/5 ml; oral solution 5 mg/ml

Administer:
PO route

• 
Give with food, milk, or a full glass of water to minimize gastric irritation

• 
Oral concentrate:
Give using a calibrated measuring device. Dilute just before use with 120–240 ml of water, saline, milk, 7-Up, carbonated orange beverage, or apricot, orange, pineapple, prune, tomato, or V-8 juice. Do not mix with beverages containing caffeine (coffee, cola), tannics (tea), or pectinates (apple juice) or with other liquid medications. Avoid spilling the solution on the skin and clothing

• 
Oral elixir:
Give using a calibrated measuring device. Avoid spilling the solution on the skin and clothing

Injectable routes

• 
Visually inspect for particulate matter and discoloration before use, slight yellow to amber color does not alter potency, markedly discolored solutions should be discarded

IM route (fluPHENAZine HCl only)

• 
No dilution necessary; if irritation occurs, subsequent IM doses may be diluted with NS for injection or 2% procaine

• 
Inject slowly and deeply into the upper outer quadrant of the gluteal muscle using a dry syringe and needle, aspirate before injection

• 
Keep patient in a recumbent position for at least 30 min following injection to minimize hypotensive effects

• 
Rotate the site of injection to avoid irritation or sterile abscess formation with repeat use

IM depot injection (fluPHENAZine decanoate or fluPHENAZine enanthate)

• 
FluPHENAZine decanoate or enanthate injections are administered IM or subcut, do not give IV

• 
FluPHENAZine depot injections must be drawn up using a dry syringe and needle of at least 21-G, do not dilute

• 
Inject slowly and deeply into the upper outer quadrant of the gluteal muscle, aspirate before injection

• 
Keep patient in a recumbent position for at least 30 min following the initial injection to minimize hypotensive effects. Once patient is dose-stabilized on depot formulation, this precaution may be modified. Rotate the site of injection to avoid irritation or sterile abscess formation with repeat administration

Subcut injection route (fluPHENAZine decanoate or fluPHENAZine enanthate)

• 
FluPHENAZine decanoate or enanthate injections are administered via IM or SC injection only, do not administer IV

• 
FluPHENAZine depot injection solutions must be drawn up using a dry syringe and a needle of at least 21-G, do not dilute

• 
Inject subcut, taking care not to inject intradermally

• 
Keep patient in a recumbent position for at least 30 min following the initial injection to minimize hypotensive effects. Once patient is dose-stabilized on depot formulation, this precaution may be modified for ambulatory patients; rotate the injection sites

SIDE EFFECTS

CNS:
EPS: pseudoparkinsonism, akathisia, dystonia, tardive dyskinesia, drowsiness, headache
,
seizures, neuroleptic malignant syndrome

CV:
Orthostatic hypotension
, hypertension,
cardiac arrest,
ECG changes,
tachycardia

EENT:
Blurred vision, glaucoma, dry eyes

GI:
Dry mouth, nausea, vomiting, anorexia, constipation
, diarrhea, jaundice, weight gain,
paralytic ileus, hepatitis,
cholecystic jaundice

GU:
Urinary retention, urinary frequency, enuresis, impotence, amenorrhea, gynecomastia

HEMA:
Anemia,
leukopenia, leukocytosis, agranulocytosis, aplastic anemia, thrombocytopenia

INTEG:
Rash
, photosensitivity, dermatitis

RESP:
Laryngospasm,
dyspnea,
respiratory depression

PHARMACOKINETICS

Metabolized by liver, excreted in urine (metabolites), crosses placenta, enters breast milk, protein binding >90%, not dialyzable

PO/IM (HCl):
Onset 1 hr, peak 2-4 hr, duration 6-8 hr, half-life 3.5-4 days

IM/SUBCUT (decanoate):
Onset 1-3 days; peak 1-2 days, duration over 4 wk, single-dose half-life 6.8-9.6 days, multiple dose 14.3 days

INTERACTIONS

Increase:
serotonin syndrome, neuroleptic malignant syndrome—SSRIs, SNRIs, serotonin-receptor agonists

Increase:
QT prolongation, torsades de pointes (at higher doses)—amiodarone, arsenic trioxide, astemizole, dasatinib, disopyramide, dofetilide, droperidol, erythromycin, flecainide, gatifloxacin, ibutilide, levomethadyl, ondansetron, paliperidone, palonosetron, some antidepressants, vorinostat, ziprasidone, haloperidol

Increase:
sedation—other CNS depressants, alcohol, barbiturate anesthetics, haloperidol, metyrosine, risperiDONE

Increase:
toxicity—EPINEPHrine

Increase:
anticholinergic effects—anticholinergics

Decrease:
effects of levodopa, lithium

Decrease:
fluPHENAZine effects—smoking, barbiturates

Drug/Lab Test

Increase:
LFTs, cardiac enzymes, cholesterol, blood glucose, prolactin, bilirubin, cholinesterase

Decrease:
hormones (blood and urine)

False positive:
pregnancy tests, PKU urinary steroids, 17-OHCS

NURSING CONSIDERATIONS
Assess:

 

Black Box Warning:

Increased mortality in elderly patients with dementia-related psychosis

• 
Serotonin syndrome, neuroleptic malignant syndrome:
severe EPS, increased CPK, altered mental state, sinus tachycardia, change in B/P, sweating, often occurs in young men, heat stress, physical exhaustion, dehydration, organic brain disease

 
QT prolongation, torsades de pointes:
ECG for changes

• 
Bilirubin, CBC, LFTs monthly

• 
Urinalysis recommended before and during prolonged therapy

• 
Affect, orientation, LOC, reflexes, gait, coordination, sleep pattern disturbances

• 
B/P standing and lying; pulse and respirations q4hr during initial treatment; establish baseline before starting treatment; report drops of 30 mm Hg

• 
Dizziness, faintness, palpitations, tachycardia on rising

• 
EPS
including akathisia (inability to sit still, no pattern to movements), tardive dyskinesia (bizarre movements of jaw,
mouth, tongue, extremities), pseudoparkinsonism (rigidity, tremors, pill rolling, shuffling gait)

• 
Constipation, urinary retention daily; if these occur, increase bulk, water in diet

Perform/provide:

• 
Supervised ambulation until stabilized on medication; do not involve patient in strenuous exercise; fainting possible; patient should not stand still for long periods

Evaluate:

• 
Therapeutic response: decrease in emotional excitement, hallucinations, delusions, paranoia, reorganization of patterns of thought, speech

Teach patient/family:

• 
That orthostatic hypotension occurs often; to rise from sitting or lying position gradually; to avoid hazardous activities until stabilized on medication

• 
To avoid hot tubs, hot showers, tub baths because hypotension may occur; that in hot weather, heat stroke may occur; to take extra precautions to stay cool

 
To avoid abrupt withdrawal of this product or EPS may result; that product should be withdrawn slowly

• 
To avoid OTC preparations (cough, hay fever, cold) unless approved by prescriber; that serious product interactions may occur; to avoid use with alcohol, CNS depressants; that increased drowsiness may occur

• 
To use a sunscreen to prevent burns

• 
About the importance of compliance with product regimen

• 
About EPS and the need for meticulous oral hygiene because oral candidiasis may occur

• 
To report sore throat, malaise, fever, bleeding, mouth sores; if these occur, CBC should be drawn, product discontinued

• 
That urine may turn pink to reddish brown

TREATMENT OF OVERDOSE:

Lavage; if orally ingested, provide an airway;
do not induce vomiting

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

BOOK: Mosby's 2014 Nursing Drug Reference
9.93Mb size Format: txt, pdf, ePub
ads

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