Mosby's 2014 Nursing Drug Reference (282 page)

BOOK: Mosby's 2014 Nursing Drug Reference
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Canada only   Side effects:
italics
= common;
bold
= life-threatening   
Nurse Alert

naltrexone (Rx)

(nal-trex′one)

ReVia, Vivitrol

Func. class.:
Opioid antagonist

Chem. class.:
Thebaine derivative

Do not confuse:
naloxone
/naltrexone

ACTION:

Competes with opioids at opioid-receptor sites

USES:

Blockage of opioid analgesics; used for treatment of opiate addiction, alcoholism

Unlabeled uses:
Nicotine withdrawal, opiate-agonist withdrawal, pruritus

CONTRAINDICATIONS:

Hypersensitivity, opioid dependence

 

Black Box Warning:

Hepatic failure, hepatitis

Precautions:
Pregnancy (C), breastfeeding, children, renal disease, depression, suicidal ideation

 

Black Box Warning:

Hepatic disease

DOSAGE AND ROUTES
Calculator
Adjunct in opiate-agonist dependence

• Adult:
PO
25 mg; if no withdrawal symptoms in 1 hr, then 25 mg additionally; if no withdrawal symptoms, then 50-150 mg/day or in divided doses

Adjunct in alcoholism treatment

• Adult:
PO
50 mg/day with food × 12 wk;
IM
(Vivitrol) 380 mg q4wk

Pruritus (unlabeled)

• Adult:
PO
50 mg/day × 7 days to 4 wk

Nicotine withdrawal (unlabeled)

• Adult:
PO
50 mg/day

Ultrarapid opiate detoxification (unlabeled)

• Adult:
PO
50 mg prior to sedation with midazolam

Available forms:
Tabs 50 mg; powder for inj 380 mg

Administer:
PO route

• 
Give with food, antacid to prevent nausea, vomiting

IM route

• 
Do not give until opioid-free for 7-10 days to prevent opioid withdrawal

• 
IM deep in gluteal, alternate inj sites; use supplied needle to prevent inj site reaction; aspirate before inj

• 
Only if resuscitative equipment is nearby

• 
Not to use IV or SUBCUT

SIDE EFFECTS

CNS:
Stimulation, drowsiness
, dizziness, confusion,
seizures,
headache, flushing, hallucinations, nervousness, irritability,
suicidal ideation,
syncope, anxiety

CV:
Rapid pulse,
pulmonary edema,
hypertension,
DVT

EENT:
Tinnitus, hearing loss, blurred vision

GI:
Nausea, vomiting, diarrhea, heartburn
, anorexia,
hepatitis,
constipation, abdominal pain

GU:
Delayed ejaculation, decreased potency

INTEG:
Rash
, urticaria, bruising, oily skin, acne, pruritus, inj site reactions

MISC:
Increased thirst, chills, fever

MS:
Joint and muscle pain

RESP:
Wheezing, hyperpnea, nasal congestion, rhinorrhea, sneezing, sore throat, pneumonia

PHARMACOKINETICS

Metabolized by liver, excreted by kidneys; crosses placenta, excreted in breast milk; half-life 4 hr; extensive first-pass metabolism; protein binding 21%-28%

PO:
Onset 15-30 min, peak 1-2 hr, duration is dose dependent

IM:
Peak 2 hr

INTERACTIONS

Increase:
lethargy—phenothiazines

Increase:
hepatotoxicity—disulfiram

Increase:
bleeding risk—anticoagulants

Decrease:
effect of analgesics, antidiarrheals, cough preparations

NURSING CONSIDERATIONS
Assess:

 

Black Box Warning:

Hepatic status: LFTs, jaundice, hepatitis, hepatic failure

• 
ABGs including P
O
2
, P
CO
2
, LFTs, VS q3-5min

• 
Signs of withdrawal in drug-dependent individuals, use naltrexone challenge to test opioid dependence; must be free of opioids for 7-10 days before using this product, or withdrawal symptoms can occur

• 
Cardiac status: tachycardia, hypertension

• 
Respiratory dysfunction: respiratory depression,
character, rate, rhythm; if respirations <10/min, respiratory stimulant should be administered

• 
Mental status: depression,
suicidal ideation

Perform/provide:

• 
Storage in tight container

Evaluate:

• 
Therapeutic response: blocking opiate ingestion; successful nicotine, alcohol withdrawal

Teach patient/family:

• 
That patient must be drug-free to start treatment

 
That using opioid while taking this product could prove fatal because high dose is needed to overcome this antagonist; not to self-dose with OTC products unless approved by prescriber

• 
To carry emergency ID stating product used

• 
That, if surgery is needed, all involved should be aware of this product

• 
To use caution while driving or performing other hazardous tasks until effect is known

 
That suicidal thoughts/behaviors may occur; to report these immediately

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

naphazoline nasal agent

 

naphazoline
(ophthalmic)

(na-faz′oh-leen)

Advanced Eye Relief, Redness Maximum Relief, Ak-Con, All Clear, Clear Eyes, Naphcon Forte
, Vasoclear

Func. class.:
Ophthalmic vasoconstrictor

Chem. class.:
Sympathomimetic

ACTION:

Acts on the blood vessels in the eye to produce vasoconstriction

USES:

Ocular congestion, irritation, itching of the eye

CONTRAINDICATIONS:

Hypersensitivity, acute angle-closure glaucoma, 0.1% solution in children/infants

Precautions:
Hyperthyroidism, diabetes mellitus, hypertension, cardiac conditions

DOSAGE AND ROUTES
Calculator

• Adult:
OPHTH
Instill 1-2 drops in affected eye in the conjunctival sac every 3-4 hr, up to qid

Available forms:
Ophthalmic solution 0.012%, 0.1%, 0.02%

Administer:

• 
Store at room temperature, keep tightly closed

SIDE EFFECTS

CNS:
Headache

EENT:
Blurred vision, irritation, photophobia, dilation, stinging, elevated IOP, keratitis

PHARMACOKINETICS

Onset 10 min, duration up to 6 hr

INTERACTIONS

Increase:
Systemic effects—β-blockers

• 
Do not use within 14 days of MAOIs

NURSING CONSIDERATIONS
Assess:

• 
Ocular itching, congestion, irritation: should show improvement quickly, avoid using more than 3 days, long-term use or exceeding dosage can lead to rebound congestion; report eye pain, blurred vision

Evaluate:

• 
Decreasing ocular itching, congestion, irritation

Teach patient/family:

• 
Method for instilling drops

• 
To notify prescriber of eye pain, blurred vision

• 
That ocular itching, congestion, irritation should show improvement quickly

• 
To avoid using longer than 3 days; that long-term use or exceeding dosage can lead to rebound congestion

• 
To wait for at least 15 min before wearing contact lenses

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