Mosby's 2014 Nursing Drug Reference (193 page)

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

ganciclovir ophthalmic

 

gatifloxacin

(ga-ti-floks′a-sin)

Zymar, Zymaxid

Func. class.:
Ophthalmic anti-infective

Chem. class.:
Fluoroquinolone

Do not confuse:
gatifloxacin/levofloxacin/moxifloxacin

ACTION:

Inhibits DNA gyrase, thereby decreasing bacterial replication

USES:

Bacterial conjunctivitis

CONTRAINDICATIONS:

Hypersensitivity to this product or fluoroquinolones, infants <1 yr

Precautions:
Pregnancy (C), breastfeeding

DOSAGE AND ROUTES
Calculator
Bacterial conjunctivitis

• Adult/adolescent/child ≥1 yr:
OPHTH SOL
Instill 1 drop in affected eye(s) every 2 hr while awake × 2 days, then 1 drop up to qid × 5 more days or
Zymaxid 1 drop every 2 hr while awake first day, then bid to qid while awake days 2 to 7

Available forms:
Ophthalmic solution 0.3%, 0.5%

Administer:
Ophthalmic route

• 
Commercially available ophthalmic solutions are not for injection subconjunctivally or into the anterior chamber of the eye

• 
Apply topically to the eye, taking care to avoid contamination

• 
Do not touch the tip of the dropper to the eye, fingertips, or other surface

• 
Apply pressure to lacrimal sac for 1 min after instillation

• 
Avoid wearing contact lenses during treatment

SIDE EFFECTS

EENT:
Hypersensitivity, irritation, redness, tearing, keratitis, blepharitis, taste changes

PHARMACOKINETICS

Unknown

NURSING CONSIDERATIONS
Assess:

• 
Allergic reaction
: hypersensitivity, discontinue product

Evaluate:

• 
Decreased ophthalmic infection

Teach patient/family:
Ophthalmic route

• 
To apply topically to the eye, taking care to avoid contamination; for ophthalmic use only

• 
Not to touch the tip of the dropper to the eye, fingertips, or other surface

• 
To apply pressure to lacrimal sac for 1 min after instillation

• 
To avoid wearing contact lenses during treatment

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

gefitinib (Rx)

(ge-fi′tye-nib)

Iressa

Func. class.:
Antineoplastic—miscellaneous

Chem. class.:
Epidermal growth factor receptor inhibitor

ACTION:

Not fully understood; inhibits intracellular phosphorylation of cell surface receptors associated with epidermal growth factor receptors

USES:

Advanced/metastatic non–small cell lung cancer (NSCLC) in those who have not responded to platinum or DOCEtaxel products

CONTRAINDICATIONS:

Pregnancy (D), breastfeeding, children, hypersensitivity

Precautions:
Geriatric patients, ocular/pulmonary/renal/hepatic disorders

DOSAGE AND ROUTES
Calculator

• Adult:
PO
250 mg/day

Available forms:
Tabs 250 mg

SIDE EFFECTS

EENT:
Amblyopia, conjunctivitis, eye pain, corneal erosion/ulcer

GI:
Nausea, diarrhea, vomiting
, anorexia,
pancreatitis,
mouth ulceration,
hepatotoxicity

INTEG:
Rash
, pruritus,
acne, dry skin
,
toxic epidermal necrolysis, angioedema

MISC:
Peripheral edema,
hemorrhage

RESP:
Interstitial lung disease,
cough, dyspnea, pneumonia

PHARMACOKINETICS

Slowly absorbed; excreted in feces (86%), urine (<4%); elimination halflife 48 hr; metabolism by CYP3A4

INTERACTIONS

Increase:
gefitinib concentrations—ketoconazole, itraconazole, erythromycin, clarithromycin

Increase:
bone marrow suppression—cloZAPine

Increase:
plasma concentration of warfarin, metoprolol

Decrease:
gefitinib levels—phenytoin, rifampin, cimetidine, ranitidine, sodium bicarbonate

Drug/Herb

Decrease:
gefitinib levels—St. John’s wort

NURSING CONSIDERATIONS
Assess:

 
Pulmonary changes: lung sounds, cough, dyspnea; interstitial lung disease may occur, may be fatal; discontinue therapy if confirmed

• 
Ocular changes: eye irritation, corneal erosion/ulcer, aberrant eyelash growth

 
Pancreatitis: abdominal pain, levels of amylase, lipase

 
Toxic epidermal necrolysis, angioedema

• 
GI symptoms: frequency of stools, if diarrhea is poorly tolerated, therapy may be discontinued for up to 14 days; LFTs baseline and periodically

Administer:

• 
Without regard to food; avoid grapefruit juice

• 
May be dispersed in half-glass of water (noncarbonated), rinse glass and drink liquid, may be given through NG tube

Evaluate:

• 
Therapeutic response: decreased NSCLC

Teach patient/family:

 
To report adverse reactions immediately: shortness of breath, severe abdominal pain, ocular changes, skin eruptions

• 
Reason for treatment, expected results

• 
Use contraception during treatment; avoid breastfeeding

• 
Avoid persons with infections

BOOK: Mosby's 2014 Nursing Drug Reference
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ads

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