Mosby's 2014 Nursing Drug Reference (359 page)

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

rizatriptan (Rx)

(rye-zah-trip′tan)

Maxalt, Maxalt-MLT

Func. class.:
Migraine agent

Chem. class.:
5-HT
1D
receptor agonist, abortive agent-triptan

ACTION:

Binds selectively to the vascular 5-HT
1B/1D
receptor subtype; exerts antimigraine effect; causes vasoconstriction of the cranial arteries

USES:

Acute treatment of migraine

CONTRAINDICATIONS:

Angina pectoris, history of MI, documented silent ischemia, Prinzmetal’s angina, ischemic heart disease, concurrent ergotamine-containing preparations, uncontrolled hypertension, hypersensitivity, basilar or hemiplegic migraine

Precautions:
Pregnancy (C), breastfeeding, children, geriatric patients, postmenopausal women, men >40 yr, risk factors for CAD, hypercholesterolemia, obesity, diabetes, impaired renal/hepatic function

DOSAGE AND ROUTES
Calculator

• Adult:
PO
5-10 mg single dose, redosing separated by ≥2 hr, max 30 mg/24 hr; use 5 mg for patient receiving propranolol, max 15 mg/24 hr

Available forms:
Tabs (Maxalt) 5, 10 mg; orally disintegrating tabs (Maxalt-MLT) 5, 10 mg

Administer:

• 
Orally disintegrating tab:
do not open blister until use; peel blister open with dry hands; place tab on patient’s tongue, where it will dissolve, and have patient swallow with saliva (contains phenylalanine)

SIDE EFFECTS

CNS:
Dizziness, drowsiness, headache, fatigue
, warm/cold sensations, flushing

CV:
MI, ventricular fibrillation, ventricular tachycardia, coronary artery vasospasm,
palpitations, hypertension, peripheral vascular ischemia, ECG changes

ENDO:
Hot flashes, mild increase in growth hormone

GI:
Nausea
, dry mouth, diarrhea, abdominal pain, ischemic colitis

RESP:
Chest tightness, pressure, dyspnea

PHARMACOKINETICS

Onset of pain relief 10 min-2 hr; peak 1-1½ hr; duration 14-16 hr; 14% plasma protein binding; metabolized in liver (metabolite); excreted in urine (82%), feces (12%); half-life 2-3 hr

INTERACTIONS

 
Weakness, hyperreflexia, incoordination: SSRIs

Increase:
levels of sibutramine

Increase:
rizatriptan action—cimetidine, oral contraceptives, MAOIs, nonselective MAOI (type A and B), isocarboxazide, pargyline, phenelzine, propranolol, tranylcypromine

Increase:
vasospastic effects—ergot, ergot derivatives, other 5-HT receptor agonists

Drug/Herb

 
Serotonin syndrome: St. John’s wort

NURSING CONSIDERATIONS
Assess:

• 
Migraine symptoms:
visual disturbances, aura, intensity, nausea, vomiting, photophobia

• 
Stress level, activity, recreation, coping mechanisms

• 
Neurologic status: LOC, blurring vision, nausea, vomiting, tingling in extremities preceding headache

• 
Ingestion of tyramine foods
(pickled products, beer, wine, aged cheese), food additives, preservatives, colorings, artificial sweeteners, chocolate, caffeine, which may precipitate these types of headaches

• 
Renal status: urine output

Perform/provide:

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

Evaluate:

• 
Therapeutic response: decrease in frequency, severity of headache

Teach patient/family:

• 
About use of orally disintegrating tab:
instruct patient not to open blister until use, to peel blister open with dry hands, to place tab on tongue, where it will dissolve, and to swallow with saliva (contains phenylalanine)

• 
To report any side effects to prescriber

• 
To use alternative contraception while taking product if oral contraceptives are being used

• 
That product does not prevent or reduce number of migraines; if 1st dose does not relieve pain, do not use more, notify prescriber

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

roflumilast

Daliresp

Func. class.:
Respiratory anti-inflammatory agent

Chem. class.:
Phosphodiesterase-4 (PDE4) inhibitor

ACTION:

Roflumilast (and the active metabolite roflumilast N-oxide) selectively inhibit phosphodiesterase-4 (PDE4); not a bronchodilator; inhibition of the PDE4 enzyme blocks the hydrolyses and inactivation of cyclic adenosine monophosphate (cAMP), resulting in intracellular cAMP accumulation; decreases inflammatory activity, PDE4 inhibition may affect migration and actions of pro-inflammatory cells (neutrophils, other leukocytes, T-lymphocytes, monocytes, macrophages, fibroblasts)

USES:

For the prevention of COPD exacerbations in patients with severe COPD associated with chronic bronchitis and a history of exacerbations

CONTRAINDICATIONS:

Moderate to severe hepatic disease
(Child-Pugh B or C)

Precautions:
Pregnancy (category C), breastfeeding, neonates, infants, children, adolescents, acute bronchospasm, anxiety, insomnia, depression, suicidal ideation or behavior

DOSAGE AND ROUTES
Calculator

• Adult:
PO
500 mcg/day

Available forms:
Tabs 500 mcg

Administer:
PO route

• 
Give without regard to meals

SIDE EFFECTS

CNS:
Insomnia, anxiety, depression, headache, dizziness, tremor,
suicidal ideation

EENT:
Rhinitis, sinusitis

GI:
Weight loss, diarrhea
,
nausea
, anorexia, abdominal pain, dyspepsia, gastritis, vomiting

GU:
Urinary tract infection

MS:
Back pain, muscle cramps/spasm

SYST:
Infections, influenza

PHARMACOKINETICS

80% absolute bioavailability; protein binding 99% (roflumilast); 97% (N-oxide metabolite); low penetration across the blood–brain barrier; extensively metabolized (liver); metabolism by CYP3A4 and CYP1A2 produces (active metabolite N-oxide); half-life parent drug 17 hr, metabolite 30; steady state 4 days (parent drug), 6 days (metabolite); 70% excreted in urine; parent drug peak 1 hr (range, 0.5-2 hr), metabolite peak 8 hr (range, 4-13 hr); contraindicated in moderate to severe hepatic impairment; use with caution in patients with mild hepatic

INTERACTIONS

Increase:
roflumilast effect—CYP3A4/CYP1A2 inhibitors (enoxacin, cimetidine, delavirdine, indinavir, isoniazid, itraconazole, dalfopristin, quinupristin, tipranavir)

Increase:
roflumilast effect—oral contraceptives (gestodene and ethinyl estradiol)

Decrease:
roflumilast effect—CYP3A4 inducers (rifampin, barbiturates, carBAMazepine, phenytoin, erythromycin, ketoconazole, fluvoxaMINE, alcohol, etravirine, ritonavir, bexarotene, rifabutin, OXcarbazepine, nevirapine, modafinil, metyrapone, PHENobarbital, bosentan, dexamethasone)

Altered effect of:
fosamprenavir

Drug/Herb

Decrease:
roflumilast effect—St. John’s wort

NURSING CONSIDERATIONS
Assess:

• 
Lung sounds and respiratory function baseline and periodically thereafter

 
Behavioral changes including mood, depression, suicidal thoughts/behaviors

• 
Liver function tests baseline and periodically thereafter; if increases in liver function studies occur, product should be discontinued

• 
Weight; weight loss is common

Perform/provide:

• 
Storage at room temperature

Evaluate:

• 
Decreasing exacerbations in COPD

Teach patient/family:

• 
To take product as directed, not to skip or double doses, to take missed doses as soon as remembered unless almost time for next dose

• 
Not to use OTC or other products without prescriber approval; not to discontinue other respiratory products unless approved by prescriber

• 
Not to be used for acute bronchospasm but may be continued during acute asthma attacks

 
Suicidal thoughts/behaviors:
To notify prescriber of worsening depression or suicidal thoughts/behaviors

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