Mosby's 2014 Nursing Drug Reference (55 page)

BOOK: Mosby's 2014 Nursing Drug Reference
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azelastine nasal agent

See
Appendix B

 

azilsartan

Edarbi

Func. class.:
Antihypertensive

Chem. class.:
Angiotensin II receptor antagonist

ACTION:

Antagonizes angiotensin II at the AT
1
receptor in tissues like vascular smooth muscle and the adrenal gland. Two angiotensin II receptors, AT
1
and AT
2
, have been identified; azilsartan exhibits more than 10,000-fold greater affinity for the AT
1
receptor than the AT
2
receptor.

USES:

Hypertension, alone or in combination with other antihypertensives

CONTRAINDICATIONS:

 

Black Box Warning:

Pregnancy (D) 2nd/3rd trimesters

Precautions:
Pregnancy (C) 1st trimester, breastfeeding, children, geriatric patients, angioedema, African descent, renal disease, renal artery stenosis, heart failure, hypovolemia

DOSAGE AND ROUTES:
Calculator

• Adult: PO
80 mg/day, may give an initial dose of 40 mg/day in patients receiving high-dose diuretic therapy

Available forms:
Tabs 40, 80 mg

Administer:

• 
May administer without regard to food

SIDE EFFECTS

CNS:
Dizziness, fatigue, asthenia

CV:
Hypotension, orthostatic hypotension

GI:
Nausea, diarrhea

HEMA:
Anemia

INTEG:
Angioedema

MS:
Muscle cramps

RESP:
Cough

SYST:
Secondary malignancy

PHARMACOKINETICS:

Protein binding >99% to serum albumin; metabolized by CYP2C9; elimination half-life 11 hr, steady state within 5 days and no accumulation in plasma occurs with once-daily dosing; elimination 55% in feces, 42% in urine; hydrolyzed to the active metabolite, azilsartan, in GI tract during absorption, rapidly absorbed, peak 1.5-3 hr; absolute bioavailability (60%) not affected by food

INTERACTIONS:

Increase:
hypotensive effect—other antihypertensives, other angiotensin receptor antagonists, MAOIs

Increase:
hypoglycemia—antidiabetics

Increase:
renal failure risk—cyclosporine, diuretics, NSAIDs in those with poor renal function; monitor closely

Increase:
lithium toxicity—lithium

Increase:
phosphate nephropathy—sodium phosphate monobasic monohydrate; sodium phosphate dibasic anhydrous

Drug/Herb:

Increase:
antihypertensive effect—Hawthorn

Decrease:
antihypertensive effect—ephedra

NURSING CONSIDERATIONS
Assess:

 
Angioedema:
Assess for facial swelling, difficulty breathing

 

Black Box Warning:

For pregnancy (D) 2nd/3rd trimester, can cause fetal death

• 
Response and adverse reactions especially in renal disease

• 
B/P, pulse when beginning therapy and periodically thereafter; note rhythm, rate, quality; obtain electrolytes before beginning therapy

Perform/provide:

• 
Use original package to protect from light and moisture beat

Evaluate:

• 
Therapeutic response: decreased B/P

Teach patient/family:

• 
To comply with dosage schedule even if feeling better

 
To notify prescriber of facial swelling; if pregnancy is planned or suspected (category D 2nd/3rd trimester)

• 
That diarrhea, dehydration, excessive perspiration, vomiting, may lead to fall in B/P; to consult prescriber if these occur

• 
To rise slowing from lying or sitting to minimize orthostatic hypotension; that product may cause dizziness

• 
To avoid OTC medications unless approved by prescriber; to inform all health care providers of product use

• 
To use proper technique for obtaining B/P

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

azithromycin (Rx)

(ay-zi-thro-my′sin)

Zithromax, Zmax, Zithromax Tri Pak, Zithromax Z Pak

Func. class.:
Antiinfective

Chem. class.:
Macrolide (azalide)

Do not confuse:
azithromycin
/erythromycin
Zithromax
/Zinacef

ACTION:

Binds to 50S ribosomal subunits of susceptible bacteria and suppresses protein synthesis; much greater spectrum of activity than erythromycin; more effective against gram-negative organisms

USES:

Mild to moderate infections of the upper respiratory tract, lower respiratory tract; uncomplicated skin and skin structure infections caused by
Moraxella catarrhalis, Streptococcus pneumoniae, Streptococcus pyogenes, Staphylococcus aureus, Streptococcus agalactiae, Mycoplasma pneumoniae, Haemophilus influenzae, Clostridium, Legionella pneumophila;
NGU or cervicitis due to
Chlamydia trachomatis;
in children: acute otitis media
(H. influenzae, M. catarrhalis, S. pneumoniae)
PO;
acute pharyngitis/tonsillitis (group A streptococcal)
PO;
acute skin/soft tissue infections
PO;
community-acquired pneumonia
(Chlamydia pneumoniae, H. influenzae, M. pneumoniae, S. pneumoniae)
PO;
pharyngitis/tonsillitis
(S. pyogenes);
prophylaxis of disseminated
Mycobacterium avium
complex (MAC)

Unlabeled uses:
Babesiosis, cholera, cystic fibrosis, dental abscess/infection, endocarditis prophylaxis, granuloma inguinale,
Helicobacter pylori, Klebsiella granulomatis
, Legionnaire’s disease, Lyme disease, lymphogranuloma venereum, MAC,
Mycoplasma hominis
, periodontitis, pertussis, prostatitis,
Rickettsia tsutsugamushi, Salmonella typhi
,
shigellosis, syphilis, toxoplasmosis, typhoid fever

CONTRAINDICATIONS:

Hypersensitivity to azithromycin, erythromycin, any macrolide

Precautions:
Pregnancy (B), breastfeeding; geriatric patients; renal/hepatic/cardiac disease; <6 mo for otitis media; <2 yr for pharyngitis, tonsillitis

DOSAGE AND ROUTES
Calculator
Most infections

• Adult: PO
500 mg on day 1 then 250 mg/day on days 2-5 for a total dose of 1.5 g or 500 mg a day × 3 days

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