Mosby's 2014 Nursing Drug Reference (227 page)

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ixabepilone (Rx)

(ix-ab-ep′i-lone)

Ixempra

Func. class.:
Antineoplastic—miscellaneous

Chem. class.:
Epothilone

ACTION:

Microtubule stabilizing agent; microtubules are needed for cell division

USES:

Breast cancer

CONTRAINDICATIONS:

Pregnancy (D), breastfeeding, hypersensitivity to products with polyoxyethylated castor oil, neutropenia of <1500/mm
3
, thrombocytopenia

 

Black Box Warning:

Hepatic disease

Precautions:
Children, geriatric patients, alcoholism, bone marrow suppression, cardiac dysrhythmias, cardiac/renal disease, diabetes mellitus, peripheral neuropathy, ventricular dysfunction

DOSAGE AND ROUTES
Calculator
Breast cancer, metastatic or locally advanced given with capecitabine and resistant to anthracycline, taxane

• Adult: IV INF
40 mg/m
2
over 3 hr q3wk plus capecitabine
PO
2000 mg/m
2
/day in 2 divided doses on days 1-14 q21days; in those with BSA >2.2 m
2
, dose should be calculated for a BSA of 2.2 m
2

Breast cancer, metastatic or locally advanced resistant/refractory to anthracycline, taxane, capecitabine

• Adult: IV INF
40 mg/m
2
over 3 hr q3wk; in those with BSA >2.2 m
2
, dose should be calculated for a BSA of 2.2 m
2

Dosage reduction in those taking a strong CYP3A4 inhibitor

• Adult: IV INF
20 mg/m
2
over 3 hr q3wk

Available forms:
Powder for inj 15, 45 mg

Administer:

• 
Premedicate with histamine antagonists 1 hr before use, prevents hypersensitivity

• 
Antiemetic 30-60 min before product and prn

IV route

• 
Let kit stand at room temp for 30 min; to reconstitute, withdraw supplied diluent (8 ml for 15-mg vials, 23.5 ml for 45-mg vials); slowly inject sol into vial; gently swirl and invert to mix, final conc 2 mg/ml; further dilute in LR in DEHP-free bags, final conc should be between 0.2 and 0.6 mg/ml; after added, mix by manual rotation

• 
Diluted sol stable for 6 hr at room temp; inf must be completed within 6 hr

• 
Use in-line filter, 0.2-1.2 micron

• 
Give over 3 hr

SIDE EFFECTS

CNS:
Peripheral neuropathy
, impaired cognition, chills, fatigue, fever, flushing, headache, insomnia,
asthenia

CV:
Bradycardia,
hypotension
,
abnormal ECG,
angina,
atrial flutter, cardiomyopathy,
chest pain, edema,
MI,
vasculitis

GI:
Nausea, vomiting, diarrhea
, abdominal pain, anorexia, colitis, constipation, gastritis, jaundice, GERD, hepatic failure, trismus

GU:
Renal failure

HEMA:
Neutropenia, thrombocytopenia, anemia,
infections, coagulopathy

INTEG:
Alopecia
, rash, hot flashes

META:
Hypokalemia, metabolic acidosis

MS:
Arthralgia, myalgia

RESP:
Bronchospasm,
cough, dyspnea

SYST:
Hypersensitivity reactions
,
anaphylaxis,
dehydration,
radiation recall reaction

PHARMACOKINETICS

Metabolized in liver by P45CYP3A4; excreted in feces (65%) and urine (21%); terminal half-life 52 hr

INTERACTIONS

Increase:
ixabepilone level—CYP3A4 inhibitors (amiodarone, amprenavir, aprepitant, atazanavir, chloramphenicol, clarithromycin, conivaptan, cycloSPORINE, danazol, darunavir, dalforpistin, delavirdine, diltiazem, erythromycin, estradiol, fluconazole, fluvoxaMINE, fosamprenavir, imatinib, indinavir, isoniazid, itraconazole, ketoconazole, lopinavir, miconazole, nefazodone, nelfinavir, propoxyphene, ritonavir, RU-486, saquinavir, tamoxifen, telithromycin, troleandomycin, verapamil, voriconazole, zafirlukast)

Decrease:
ixabepilone levels—CYP3A4 inducers (aminoglutethimide, barbiturates, bexarotene, bosentan, carBAMazepine, dexamethasone, efavirenz, griseofulvin, modafinil, nafcillin, nevirapine, OXcarbazepine, phenytoin, rifamycin, topiramate)

Drug/Herb

• 
Avoid use with St. John’s wort

Drug/Food

• 
Avoid use with grapefruit products

NURSING CONSIDERATIONS
Assess:

• 
CBC, differential, platelet count prior to treatment and weekly; withhold product if WBC is <1500/mm
3
or platelet count is <100,000/mm
3
, notify prescriber

• 
Monitor temp q4hr (may indicate beginning infection)

 

Black Box Warning:

Liver function tests before, during therapy (bilirubin, AST, ALT, LDH) prn or monthly; check for jaundiced skin and sclera, dark urine, clay-colored stools, itchy skin, abdominal pain, fever, diarrhea

• 
VS during 1st hr of infusion; check IV site for signs of infiltration

 
Hypersensitivity reactions, anaphylaxis
including hypotension, dyspnea, angioedema, generalized urticaria; discontinue inf immediately; keep emergency equipment available

• 
Effects of alopecia on body image; discuss feelings about body changes

Evaluate:

• 
Therapeutic response: decreased tumor size, spread of malignancy

Teach patient/family:

• 
To report signs of infection: fever, sore throat, flulike symptoms

• 
To report signs of anemia: fatigue, headache, faintness, SOB

• 
To report any complaints or side effects to nurse or prescriber

• 
That hair may be lost during treatment; that a wig or hairpiece may make patient feel better; that new hair may be different in color, texture

• 
That pain in muscles and joints 2-5 days after inf is common

• 
To use nonhormonal type of contraception

• 
To avoid receiving vaccinations while receiving product

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

ketoconazole (Rx)

(kee-toe-koe′na-zole)

Func. class.:
Antifungal

Chem. class.:
Imidazole derivative

ACTION:

Alters cell membrane permeability and inhibits several fungal enzymes, thereby leading to cell death

USES:

Systemic candidiasis, chronic mucocandidiasis, oral thrush, candiduria, coccidioidomycosis, histoplasmosis, chromomycosis, paracoccidioidomycosis, blastomycosis; tinea cruris, tinea corporis, tinea versicolor,
Pityrosporum ovale

Unlabeled uses:
Cushing’s syndrome, advanced prostatic cancer, candidiasis/fungal prophylaxis, fungal keratitis, leishmaniasis

CONTRAINDICATIONS:

Breastfeeding, hypersensitivity, fungal meningitis

 

Black Box Warning:

Coadministration with other products (ergot derivatives, cisapride, or triazolam) may cause fatal cardiac arrhythmias due to inhibition of CYP3A4 enzyme system

Precautions:
Pregnancy (C), children <2 yr, renal disease, achlorhydria (product-induced)

 

Black Box Warning:

Hepatic disease

DOSAGE AND ROUTES
Calculator

• Adult:
PO
200-400 mg/day for 1-2 wk (candidiasis), 6 wk (other infections)

• Child ≥2 yr:
PO:
3.3-6.6 mg/kg/day as a single daily dose

Prostate cancer (unlabeled)

• Adult:
PO
400 mg tid

Available forms:
Tabs 200 mg; oral susp 100 mg/5 ml

Administer:

• 
In the presence of acid products only; do not use alkaline products, proton pump inhibitors, H
2
-antagonists, antacids within 2 hr of product; may give coffee, tea, acidic fruit juices, cola

• 
With food to decrease GI symptoms

• 
With HCl if achlorhydria is present; dissolve tab/4 ml of aqueous sol 0.2 N hydrochloric acid; use straw to avoid contact; rinse with water afterward and swallow

SIDE EFFECTS

CNS:
Headache, dizziness, somnolence

GI:
Nausea, vomiting, anorexia, diarrhea, abdominal pain,
hepatotoxicity

GU:
Gynecomastia, impotence

HEMA:
Thrombocytopenia, leukopenia, hemolytic anemia

INTEG:
Pruritus, fever, chills, photophobia, rash, dermatitis, purpura, urticaria

SYST:
Anaphylaxis, angioedema

PHARMACOKINETICS

PO:
Peak 1-2 hr; half-life 2 hr, terminal 8 hr; metabolized in liver; excreted in bile, feces; requires acid pH for absorption; distributed poorly to CSF; highly protein bound

INTERACTIONS

Increase:
effect of CNS depression—chlordiazePOXIDE, clonazePAM, clorazepate, diazepam, estazolam, flurazepam, prazepam, quazepam, avoid concurrent use

Decrease:
effect of—theophylline

Decrease:
metabolism of PACLitaxel

Increase:
hepatotoxicity—other hepatotoxic products, alcohol

Increase:
anticoagulant effect—warfarin, anticoagulants

Increase:
effect of toxicity: alfentanil, ALPRAZolam, amprenavir, ARIPiprazole, atorvastatin, calcium channel blockers, carBAMazepine, clarithromycin, corticosteroids, cyclophosphamide, cycloSPORINE, donepezil, eletriptan, erythromycin, fentaNYL, ifosfamide, indinavir, lovastatin, midazolam, nelfinavir, nisoldipine, quiNIDine, ritonavir, saquinavir, sildenafil, simvastatin, SUFentanil, tamoxifen, triazolam, vinBLAStine, vinca alkaloids, vinCRIStine, zolpidem

Decrease:
action of ketoconazole—antacids, H
2
-receptor antagonists, anticholinergics, phenytoin, isoniazid, rifampin, ddI, gastric acid pump inhibitors

Drug/Lab Test

Increase:
alkaline phosphatase, LFTs, lipids

Decrease:
Hgb, WBC, platelets

NURSING CONSIDERATIONS
Assess:

• 
Infection symptoms before and after treatment

• 
C&S before starting treatment

• 
Allergic reaction: rash, photosensitivity, urticaria, dermatitis

 

Black Box Warning:

Hepatotoxicity: nausea, vomiting, jaundice, clay-colored stools, fatigue; hepatic studies (ALT, AST, bilirubin) if patient receiving long-term therapy, use cautiously in those with hepatic disease

• 
Using with CYP3A4 inhibitors can lead to increased product level, toxicity

Perform/provide:

• 
Storage in tight container at room temp

Evaluate:

• 
Therapeutic response: decreased fever, malaise, rash, negative C&S for infectious organism, absence of scaling

Teach patient/family:

• 
That long-term therapy may be needed to clear infection (1 wk-6 mo, depending on infection)

• 
To avoid hazardous activities if dizziness occurs

• 
To take 2 hr before administration of other products that increase gastric pH (antacids, H
2
-blockers, omeprazole, sucralfate, anticholinergics)

• 
About the importance of compliance with product regimen, that testing will be done periodically to indicate if infection has been eradicated

• 
To decrease nausea, divide dose with meals

• 
Not to use any products (OTC, herbal) unless approved by prescriber

 

Black Box Warning:

To notify prescriber of GI symptoms, signs of hepatic dysfunction (fatigue, nausea, anorexia, vomiting, dark urine, pale stools)

• 
To use sunglasses to prevent photophobia (rare)

• 
To notify prescriber if pregnancy is planned or suspected; do not breastfeed

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