Mosby's 2014 Nursing Drug Reference (423 page)

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vitamin A (Rx,
PO-OTC
, Rx-IM)

Aquasol A, Vitamin A

Func. class.:
Vitamin, fat soluble

Chem. class.:
Retinol

ACTION:

Needed for normal bone, tooth development; visual dark adaptation; skin disease; mucosa tissue repair; assists with production of adrenal steroids, cholesterol, RNA

USES:

Vit A deficiency

CONTRAINDICATIONS:

Pregnancy (X) (IM), hypersensitivity to vit A, malabsorption syndrome, hypervitaminosis A, IV administration

Precautions:
Pregnancy (C) (PO), breastfeeding, impaired renal function, children, hepatic disease, infants, alcoholism, hepatitis

DOSAGE AND ROUTES
Calculator

• Adult and child >8 yr:
PO
100,000-500,000 international units/day × 3 days then 50,000/day × 2 wk; dose based on severity of deficiency; maintenance 10,000-20,000 international units for 2 mo

• Child 1-8 yr:
IM
5000-15,000 international units/day × 10 days

• Infant <1 yr:
IM
5000-15,000 international units × 10 days

Maintenance

• Child 4-8 yr:
IM
15,000 international units/day × 2 mo

• Child <4 yr:
IM
10,000 international units/day × 2 mo

Available forms:
Caps 10,000, 25,000, 50,000 international units; drops 5000 international units; inj 50,000 international units/ml; tabs 10,000, 25,000, 50,000 international units

Administer:
PO route

• 
With food (PO) for better absorption

• 
Do not administer IV because of risk of anaphylactic shock; IM only

• 
Oral preparations not indicated for vit A deficiency in those with malabsorption syndrome

IM route

• 
Give deep in large muscle mass; do not use deltoid muscle for administration of >1 ml

SIDE EFFECTS

CNS:
Headache,
increased intracranial pressure, intracranial hypertension,
lethargy, malaise

EENT:
Gingivitis, papilledema, exophthalmos, inflammation of tongue and lips

GI:
Nausea, vomiting, anorexia, abdominal pain,
jaundice

INTEG:
Drying of skin, pruritus, increased pigmentation, night sweats, alopecia

META:
Hypomenorrhea, hypercalcemia

MS:
Arthralgia, retarded growth, hard areas on bone

PHARMACOKINETICS

Stored in liver, kidneys, fat; excreted (metabolites) in urine, feces

INTERACTIONS

Increase:
levels of vit A—corticosteroids, oral contraceptives

Decrease:
absorption of vit A—mineral oil, cholestyramine, colestipol

Drug/Lab Test

False increase:
bilirubin, serum cholesterol

NURSING CONSIDERATIONS
Assess:

• 
Nutritional status: yellow and dark green vegetables, yellow/orange fruits, vit-A–fortified foods, liver, egg yolks

• 
Vit A deficiency:
decreased growth; night blindness; dry, brittle nails; hair loss; urinary stones; increased infection; hyperkeratosis of skin; drying of cornea

Perform/provide:

• 
Storage in tight, light-resistant container

Evaluate:

• 
Therapeutic response: increased growth rate, weight; absence of dry skin and mucous membranes, night blindness

Teach patient/family:

• 
That, if dose is missed, it should be omitted

• 
That ophthalmic exams may be required periodically throughout therapy

• 
Not to use mineral oil while taking this product

• 
To notify prescriber of nausea, vomiting, lip cracking, loss of hair, headache

• 
Not to take more than prescribed amount

TREATMENT OF OVERDOSE:

Discontinue product

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

vitamin E (
OTC
)

Aquasol E

Func. class.:
Vit E

Chem. class.:
Fat soluble

ACTION:

Needed for digestion and metabolism of polyunsaturated fats; decreases platelet aggregation, blood clot formation; promotes normal growth and development of muscle tissue, prostaglandin synthesis

USES:

Vit E deficiency, impaired fat absorption, hemolytic anemia in premature neonates, prevention of retrolental fibroplasia, sickle cell anemia, supplement for malabsorption syndrome

CONTRAINDICATIONS:

IV use in infants

Precautions:
Pregnancy (A), anemia, breastfeeding, hypoprothrombinemia

DOSAGE AND ROUTES
Calculator
Deficiency

• Adult:
PO
60-75 international units/day

• Child:
PO
1 international units/kg (malabsorption)

Prevention of deficiency

• Adult:
PO
30 international units/day;
TOP
apply to affected areas

• Infant:
PO
5 international units/day

Available forms:
Caps 100, 200, 400, 500, 600, 1000 international units; tabs 100, 200, 400 international units; drops 50 mg/ml; chew tabs 400 units; ointment; cream; lotion; oil

Administer:
PO route

• 
Administer with or after meals

• 
Chew chewable tabs well

• 
Sol may be dropped in mouth or mixed with food

Topical route

• 
To moisturize dry skin

SIDE EFFECTS

CNS:
Headache, fatigue

CV:
Increased risk for thrombophlebitis

EENT:
Blurred vision

GI:
Nausea, cramps, diarrhea

GU:
Gonadal dysfunction

INTEG:
Sterile abscess, contact dermatitis

META:
Altered metabolism of hormones (thyroid, pituitary, adrenal), altered immunity

MS:
Weakness

PHARMACOKINETICS

PO:
Metabolized in liver, excreted in bile

INTERACTIONS

Increase:
action of oral anticoagulants

Decrease:
absorption—cholestyramine, colestipol, mineral oil, sucralfate

NURSING CONSIDERATIONS
Assess:

• 
Nutritional status: wheat germ; dark green, leafy vegetables; nuts; eggs; liver; vegetable oils; dairy products; cereals

Perform/provide:

• 
Storage in tight, light-resistant container

Evaluate:

• 
Therapeutic response: absence of hemolytic anemia, adequate vit E levels, improvement in skin lesions, decreased edema

Teach patient/family:

• 
About the necessary foods for diet

• 
To omit dose if missed

• 
To avoid vitamin supplements unless directed by prescriber

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

voriconazole (Rx)

(vohr-i-kahn′a-zol)

Vfend

Func. class.:
Antifungal, systemic

Chem. class.:
Triazole derivative

ACTION:

Inhibits fungal CYP 450-mediation demethylation; needed for biosynthesis; causes leakage from cell membrane

USES:

Invasive aspergillosis, serious fungal infections (
Candida
sp.,
Scedosporium apiospermum, Fusarium
sp.,
Monosporium, Apiospermum
)

Unlabeled uses:
Acremonium sp., Blastomyces dermatitidis, Coccidioides immitis, Cryptococcus neoformans
, febrile neutropenia, fungal keratitis,
Histoplasma capsulatum
, oropharyngeal candidiasis,
Rhodotorula sp., Scedosporium sp.
, cutaneous aspergillosis, candidemia (premature neonates), fungal infections in children ≥12 yr

CONTRAINDICATIONS:

Pregnancy (D), breastfeeding, children, hypersensitivity, severe bone marrow depression, severe hepatic disease

Precautions:
Renal disease (IV); patients of Asian/African descent; cardiomyopathy, cholestasis, chemotherapy, lactase deficiency, visual disturbances, renal failure, pancreatitis, QT prolongation, hypokalemia; ventricular dysrhythmias, torsades de pointes

DOSAGE AND ROUTES
Calculator
Esophageal candidiasis

• Adult/geriatric/child ≥12 yr and ≥40 kg:
PO
200 mg q12hr; <40 kg, 100 mg q12hr

• Adult/geriatric/child ≥12 yr:
IV INF
Loading dose 6 mg/kg q12hr × 2 dose then 4 mg/kg q12hr; may switch to oral dosing

Candidemia of the skin, kidney, bladder wall, abdomen (nonneutropenic patients)

• Adult/child ≥12 yr:
IV
loading dose 6 mg/kg q12hr × 24 hr then 3-4 mg/kg q12hr × ≥14 days and ≥7 days after resolution of symptoms;
PO
after loading dose >
40 kg
200 mg q12hr × ≥14 days and ≥7 days after resolution of symptoms; <
40 kg
100 mg q12hr × ≥14 days and ≥7 days after resolution of symptoms

Invasive aspergillosis

• Adults/adolescents:
IV
6 mg/kg q12hr (loading dose) then 4 mg/kg q12hr, may reduce to 3 mg/kg q12hr if intolerable

• Child ≥12 yr:
IV
6 mg/kg q12hr, then 4 mg/kg q12hr

CNS blastomycosis/blastomycosis meningitis (unlabeled)

• Adult:
PO
200-400 mg bid × at least 12 mo and until resolution of CSF abnormalities

Renal dose

• Adult:
PO
CCr <50 ml/min, use orally only

Hepatic dose

• Adult:
PO
6 mg/kg q12hr × 2 doses then 2 mg/kg q12hr or 100 mg q12hr if >40 kg; 50 mg q12hr if <40 kg

Available forms:
Tabs 50, 200 mg; powder for inj, lyophilized 200 mg voriconazole, powder for oral susp 45 g (40 mg/ml after reconstitution)

Administer:
PO route

• 
Oral susp: tap bottle; add 46 ml of water to bottle; shake well; remove cap; push bottle adaptor into neck of bottle; replace cap; write expiration date (14 days); shake well before each use; administer using only oral dispenser supplied, 1 hr before or after meals; tabs and susp may be interchanged

Intermittent IV INF route

• 
Product only after C&S confirms organism, product needed to treat condition; make sure product used in life-threatening infections

• 
Reconstitute powder with 19 ml water for inj to 10 mg/ml, shake until dissolved; infuse over 1-2 hr at conc of ≤5 mg/ml; do not admix with other products, 4.2% sodium bicarbonate inf

• 
Store at room temp (powder, tabs)

Y-site compatibilities:
Acyclovir, alfentanil, allopurinol, amifostine, amikacin, aminocaproic acid, aminophylline, amiodarone, amphotericin B liposome, ampicillin, ampicillin/sulbactam, anidulafungin, azithromycin, aztreonam, bivalirudin, bleomycin, bumetanide, bu
prenorphine, butorphanol, calcium acetate/chloride/gluconate, CARBOplatin, carmustine, caspofungin, ceFAZolin, cefotaxime, cefoTEtan, cefOXitin, cefTAZidime, ceftizoxime, cefTRIAXone, chloramphenicol, chlorproMAZINE, cimetidine, ciprofloxacin, cisatracurium, CISplatin, clindamycin, cyclophosphamide, cytarabine, dacarbazine, DACTINomycin, DAPTOmycin, DAUNOrubicin, dexamethasone, dexmedetomidine, dexrazoxane, digoxin, diltiazem, diphenhydrAMINE, DOBUTamine, DOCEtaxel, dolasetron, DOPamine, doripenem, doxacurium, doxycycline, droperidol, enalaprilat, ePHEDrine, EPINEPHrine, epirubicin, ertapenem, erythromycin, esmolol, etoposide, etoposide phosphate, famotidine, fenoldopam, fentaNYL, fluconazole, fludarabine, fluorouracil, foscarnet, fosphenytoin, furosemide, ganciclovir, gemcitabine, gentamicin, glycopyrrolate, granisetron, haloperidol, heparin, hydrALAZINE, hydrocortisone, ifosfamide, imipenem/cilastatin, inamrinone, insulin, irinotecan, isoproterenol, ketorolac, labetalol, leucovorin, levofloxacin, lidocaine, linezolid, LORazepam, magnesium sulfate, mannitol, mechlorethamine, melphalan, meperidine, meropenem, mesna, metaraminol, methohexital, methotrexate, methyldopate, methylPREDNISolone, metoclopramide, metoprolol, metroNIDAZOLE, midazolam, milrinone, mitoMYcin, morphine, nafcillin, nalbuphine, naloxone, niCARdipine, nitroglycerin, norepinephrine, octreotide, ondansetron, oxaliplatin, oxytocin, PACLitaxel, pamidronate, pancuronium, pentamidine, pentazocine, PENTobarbital, PHENobarbital, phentolamine, phenylephrine, piperacillin/tazobactam, potassium chloride/phosphates, procainamide, promethazine, propranolol, quinupristin/dalfopristin, remifentanil, rocuronium, sodium acetate/bicarbonate/phosphates, streptozocin, succinylcholine, SUFentanil, tacrolimus, teniposide, theophylline, thiotepa, ticarcillin/clavulanate, tirofiban, tobramycin, topotecan, trimethobenzamide, trimethoprim/sulfamethoxazole, vancomycin, vasopressin, vecuronium, verapamil, vinBLAStine, vinCRIStine, vinorelbine, zidovudine

SIDE EFFECTS

CNS:
Headache
, paresthesias, peripheral neuropathy, hallucinations, psychosis, EPS, depression, Guillain-Barré syndrome, insomnia, suicidal ideation, dizziness

CV:
Tachycardia,
hypo/hypertension, vasodilation,
atrial arrhythmias, atrial fibrillation, AV block, bradycardia, CHF, MI, QT prolongation, torsades de pointes

EENT:
Blurred vision, eye hemorrhage

GI:
Nausea, vomiting, anorexia
, diarrhea, cramps,
hemorrhagic gastroenteritis, acute hepatic failure, hepatitis, intestinal perforation, pancreatitis

GU:
Hypokalemia
, azotemia,
renal tubular necrosis, permanent renal impairment, anuria, oliguria

HEMA:
Anemia,
eosinophilia,
hypomagnesemia,
thrombocytopenia, leukopenia, pancytopenia

INTEG:
Burning, irritation
, pain, necrosis at inj site with extravasation, dermatitis, rash, photosensitivity

MISC:
Respiratory disorder

SYST:
Stevens-Johnson syndrome, toxic epidermal necrolysis, sepsis;
melanoma (photosensitivity reactions)

PHARMACOKINETICS

By CYP3A4, CYP2C9 enzymes; max serum conc 1-2 hr after dosing; eliminated via hepatic metabolism; protein binding 58%; elimination half-life 6 hr (dose dependent)

INTERACTIONS

Increase:
effects of benzodiazepines, calcium channel blockers, cycloSPORINE, ergots, HMG-CoA reductase inhibitors, pimozide, quiNIDine, prednisoLONE, sirolimus, sulfonylureas, tacrolimus, vinca alkaloids, warfarin, rifabutin, proton pump inhibitors, NNRTIs, protease inhibitors, phenytoin

Increase:
nephrotoxicity—other nephrotoxic antibiotics (aminoglycosides, CISplatin, vancomycin, cycloSPORINE, polymyxin B)

Increase:
hypokalemia—corticosteroids, digoxin, skeletal muscle relaxants, thiazides

 
Increase:
QT prolongation—class IA/III antidysrhythmics, some phenothiazines, β agonists, local anesthetics, tricyclics, haloperidol, chloroquine, droperidol, pentamidine; CYP3A4 inhibitors (amiodarone, clarithromycin, erythromycin, telithromycin, troleandomycin), arsenic trioxide, levomethadyl; CYP3A4 substrates (methadone, pimozide, QUEtiapine, quiNIDine, risperiDONE, ziprasidone)

Drug/Herb

• 
Do not use with St. John’s wort

Drug/Food

• 
Avoid use with high-fat meals, take 1 hr before or after meal

Drug/Lab Test

Increase:
AST/ALT, alk phos, creatinine, bilirubin

Decrease:
Hgb/Hct, platelets, WBC

NURSING CONSIDERATIONS
Assess:

• 
VS q15-30min during first inf; note changes in pulse, B/P

• 
I&O ratio; watch for decreasing urinary output, change in specific gravity; discontinue product to prevent permanent damage to renal tubules

• 
Blood studies: CBC, K, Na, Ca, Mg q2wk; BUN, creatinine weekly

• 
Weight weekly; if weight increases >2 lb/wk, edema is present; renal damage should be considered

 
Renal toxicity:
increasing BUN, serum creatinine; if BUN is >40 mg/dl or if serum creatinine >3 mg/dl, product may be discontinued or dosage reduced

 
Hepatotoxicity:
increasing AST, ALT, alk phos, bilirubin, baseline and periodically

• 
Allergic reaction:
dermatitis, rash; product should be discontinued, antihistamines (mild reaction) or epinephrine (severe reaction) administered

• 
Hypokalemia:
anorexia, drowsiness, weakness, decreased reflexes, dizziness, increased urinary output, increased thirst, paresthesias

• 
Ototoxicity:
tinnitus (ringing, roaring in ears), vertigo, loss of hearing (rare); visual disturbance

• 
QT prolongation:
ECG, ejection fraction; assess for chest pain, palpitations, dyspnea

Evaluate:

• 
Therapeutic response: decreased fever, malaise, rash, negative C&S for infecting organism

Teach patient/family:

• 
That long-term therapy may be needed to clear infection (2 wk-3 mo, depending on type of infection)

• 
To notify prescriber of bleeding, bruising, soft-tissue swelling, dark urine, persistent nausea or diarrhea, headache, rash, yellow skin/eyes

• 
Take 1 hr before or after meal (PO)

• 
Do not drive at night because of vision changes

• 
Avoid strong, direct sunlight

• 
Women of childbearing age should use effective contraceptive, pregnancy (D)

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

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