Mosby's 2014 Nursing Drug Reference (189 page)

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

HIGH ALERT
fospropofol (Rx)

(fos-proe′poe-fol)

Lusedra

Func. class.:
General anesthetic

ACTION:

Produces dose-dependent CNS depression by activation of GABA receptor

USES:

Induction or maintenance of anesthesia as part of balanced anesthetic technique; sedation in mechanically ventilated patients

CONTRAINDICATIONS:

Hypersensitivity to product

Precautions:
Pregnancy (B), breastfeeding, children, geriatric patients, respiratory depression, severe respiratory disorders, cardiac dysrhythmias, labor/delivery, renal disease, hyperlipidemia

DOSAGE AND ROUTES
Calculator
Induction/Maintenance

• Adult <65 (healthy), >90 kg:
577.5
IV BOL,
may give supplemental doses up to max of 140 mg, give no more frequently than q4min; 61-89 kg 6.5 mg/kg (max 577.5 mg)
IV BOL
may give supplemental doses up to 1.6 mg/kg/dose (max 140 mg/dose; give no more frequently than q4min); <60 kg 385 mg
IV BOL,
may give supplemental doses up to max 105 mg/dose, give no more frequently than q4min

• Adult: <65 yr (severe systemic disease), ≥90 kg
437.5 mg
IV BOL,
give supplemental doses up to max 105 mg/dose, give no more frequently than q4min; 61-89 kg 4.875 mg/kg (max 437.5 mg) give supplemental doses of 75% of standard dose/up to 1.2 mg/kg/dose (max 105 mg/dose) give no more frequently than q4min; <60 kg 297.5
IV BOL,
give supplemental doses up to max 70 mg/dose, give no more frequently than q4min

• Geriatric ≥90 kg:
IV BOL
437.5 then supplemental doses up to max 105 mg; give no more frequently than q4min; 61-89 kg,
IV BOL
give 75% standard dosing regimen (4.875 mg/kg), give no more frequently than q4min (max 105 mg/dose)

Available forms:
Inj 1050 mg/30 ml

Administer:
IV Bolus route

• 
Visually inspect for particulate matter and discoloration

• 
Each vial is single patient/single use

• 
Draw from vial, discard unused portion

• 
Do not mix with other drugs prior to use

• 
Give by IV BOL in free-flowing peripheral IV line of D
5
W, 5% dextrose/0.2% NaCl, 5% dextrose/0.45% NaCl D
5
LR, LR, 0.45% NaCl, NS, 5% dextrose/0.45% NaCl/20 mEq KCI; do not mix with other fluids, flush line with NS before and after administration

• 
No filtration needed

• 
Give only with resuscitative equipment available

• 
Only qualified persons trained in anesthesia should administer

SIDE EFFECTS

CNS:
Involuntary movement, headache, jerking, fever, dizziness, shivering, tremor, confusion, somnolence, paresthesia, agitation, abnormal dreams, euphoria, fatigue,
increased intracranial pressure, impaired cerebral flow, seizures

CV:
Bradycardia, hypotension
, hypertension, PVC, PAC, tachycardia, abnormal ECG, ST segment depression,
asystole, bradydysrhythmias

EENT:
Blurred vision, tinnitus, eye pain, strange taste, diplopia

GI:
Nausea, vomiting, abdominal cramping
, dry mouth, swallowing, hypersalivation,
pancreatitis

GU:
Urine retention, green urine, cloudy urine, oliguria

INTEG:
Flushing, phlebitis, hives, burning/stinging at inj site
, rash, pain of extremities

MS:
Myalgia

RESP:
Apnea,
cough, hiccups
, dyspnea, hypoventilation, sneezing, wheezing, tachypnea, hypoxia, respiratory acidosis

PHARMACOKINETICS

Onset 15-30 sec, rapid distribution, half-life 1-8 min, terminal half-life .81-.88 hr; 70% excreted in urine; metabolized in liver by conjugation to inactive metabolites, 95%-99% protein binding

INTERACTIONS

 
Do not use within 10 days of MAOIs

Increase:
CNS depression—alcohol, opioids, sedative/hypnotics, antipsychotics, skeletal muscle relaxants, inhalational anesthetics

Drug/Herb

Increase:
fospropofol effect—St. John’s wort

Drug/Lab Test

Increase:
LFTs, bilirubin

NURSING CONSIDERATIONS
Assess:

• 
Inj site: phlebitis, burning, stinging

• 
ECG
for changes: PVC, PAC, ST segment changes; monitor VS

• 
CNS changes: movement, jerking, tremors, dizziness, LOC, pupil reaction

• 
Allergic reactions: hives

• 
Respiratory depression,
character, rate, rhythm; notify prescriber if respirations are <10/min; hypoxemia detectable by pulse oximetry

Perform/provide:

• 
Storage of unopened vials at room temp

Evaluate:

• 
Therapeutic response: induction of anesthesia

Teach patient/family:

• 
That this medication will cause dizziness, drowsiness, sedation

TREATMENT OF OVERDOSE:

Discontinue product; administer vasopressor agents or anticholinergics, artificial ventilation

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

frovatriptan (Rx)

(froh-vah-trip′tan)

Frova

Func. class.:
Antimigraine agent

Chem. class.:
5-HT
1
-Receptor agonist

ACTION:

Binds selectively to the vascular 5-HT
1B
, 5-HT
1D
receptor subtypes; exerts antimigraine effect; binds to benzodiazepine receptor sites, causes vasoconstriction in cranium

USES:

Acute treatment of migraine with/without aura

CONTRAINDICATIONS:

Hypersensitivity, angina pectoris, history of MI, documented silent ischemia, Prinzmetal’s angina, ischemic heart disease; concurrent ergotamine-containing preparations; uncontrolled hypertension; basilar or hemiplegic migraine; ischemic bowel disease; peripheral vascular disease, severe hepatic disease, prophylactic migraine treatment

Precautions:
Pregnancy (C), breastfeeding, children, geriatric patients, post
menopausal women, men >40 yr, risk factors for CAD, hypercholesterolemia, obesity, diabetes, impaired hepatic function, seizure disorder

DOSAGE AND ROUTES
Calculator

• Adult:
PO
2.5 mg; a 2nd dose may be taken after ≥2 hr; max 3 tabs (7.5 mg/day)

Available form:
Tabs 2.5 mg

Administer:

• 
Swallow tabs whole; do not break, crush, or chew

• 
With fluids

• 
2 days/wk or less; rebound headache may occur

SIDE EFFECTS

CNS:
Hot/cold sensation
, paresthesia,
dizziness
, headache, fatigue, insomnia, anxiety, somnolence,
seizures

CV:
Flushing
, chest pain, palpitation

GI:
Dry mouth, dyspepsia, abdominal pain, diarrhea, vomiting, nausea

MS:
Skeletal pain

PHARMACOKINETICS

Onset of pain relief 2-3 hr, terminal half-life 25-29 hr, protein binding 15%, metabolized liver by CYP1A2

INTERACTIONS

Increase:
frovatriptan levels—CYP1A2 inhibitors (cimetidine, ciprofloxacin, erythromycin), estrogen, propranolol, oral contraceptives

Increase:
toxicity—SSRIs, other serotonin agonists (dextromethorphan, traMADol, antidepressants)

NURSING CONSIDERATIONS
Assess:

• 
Migraine symptoms:
aura, unable to view light; ingestion of tyramine-containing foods (pickled products, beer, wine, aged cheese), food additives, preservatives, colorings, artificial sweeteners, chocolate, caffeine, which may precipitate these types of headaches

• 
B/P; signs, symptoms of coronary vasospasms

• 
For stress level, activity, recreation, coping mechanisms

Perform/provide:

• 
Quiet, calm environment with decreased stimulation from noise, bright light, excessive talking

Evaluate:

• 
Therapeutic response: decrease in frequency, severity of migraine

Teach patient/family:

• 
To report any side effects to prescriber

• 
To use contraception while taking product; to inform prescriber if pregnant or planning to become pregnant

• 
To consult prescriber if breastfeeding

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