Mosby's 2014 Nursing Drug Reference (169 page)

BOOK: Mosby's 2014 Nursing Drug Reference
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HIGH ALERT
factor IX complex
(human) (Rx)

AlphaNine SD, Bebulin, BeneFIX, Mononine, Profilnine SD

Func. class.:
Hemostatic

Chem. class.:
Factors II, VII, IX, X

ACTION:

Causes an increase in blood levels of clotting factors II, VII, IX, X; factor IX (human) has IX activity

USES:

Hemophilia B (Christmas disease), factor IX deficiency, anticoagulant reversal, control of bleeding in patients with factor VIII inhibitors, reversal of overdose of anticoagulants in emergencies

CONTRAINDICATIONS:

Hypersensitivity to mouse or hamster protein, DIC, mild factor IX deficiency

Precautions:
Pregnancy (C), neonates/infants, hepatic disease, elective surgery

DOSAGE AND ROUTES
Calculator
Factor IX complex (human) bleeding in hemophilia B

• Adult and child:
IV
establish 25% of normal factor IX or 60-75 units/kg then 10-20 units/kg/day 1-2×/wk

Prophylaxis for bleeding in hemophilia B (long term)

• Adult and child:
IV
25-40 units/kg 2×/wk

Bleeding in hemophilia A/inhibitors of factor VIII (Proplex T, Konyne 80)

• Adult and child:
IV
75 units/kg, repeat after 12 hr

Oral anticoagulant reversal (Factor IX complexer only) (unlabeled)

• Adult and child:
IV
20-50 units/kg

Factor VII deficiency (use Proplex T only)

• Adult and child:
IV
0.5 units/kg × weight (kg) × desired factor IX increase (% of normal); repeat q4-6hr if needed

Factor IX (human) minor to moderate hemorrhage

Use only Alpha-Nine, Alpha-Nine SD

• Adult and child:
IV
dose to increase factor IX level to 20%-30% in one dose

Serious hemorrhage

• Adult and child:
IV
dose to increase factor IX to 30%-50% as daily inf

Minor hemorrhage (mononine only)

• Adult and child:
IV
dose to increase factor IX to 15%-25% (20-30 units/kg), repeat after 24 hr if needed

Major hemorrhage

• Adult and child:
IV
dose to increase factor IX to 25%-50% (75 units/kg) q18-30hr × ≤10 days

Available forms:
Inj (number of units noted on label)

Administer:

• 
Hepatitis B vaccine before administration

• 
IV after warming to room temp ≤3 ml/min, with plastic syringe only; do not admix

• 
After dilution with provided diluent, 50 units/ml or 25 units/ml; do not exceed 10 ml/min; decrease rate if fever, headache, flushing, tingling occur

• 
After cross-matching if patient has blood type A, B, AB to determine incompatibility with factor

BeneFIX

• 
Allow vials of concentrate/diluent to warm to room temp

• 
After removing flip-top cap from vial, wipe top of vial with alcohol swab; allow to dry

• 
Peel back cover from vial adapter package; do not remove

• 
Place vial adapter over vial; press firmly until it snaps; attach plunger rod to diluent syringe and break plastic tip cap from diluent syringe

• 
Lift package away from adapter and connect diluent syringe; depress plunger; swirl contents

SIDE EFFECTS

CNS:
Headache, dizziness, malaise, paresthesia,
lethargy, chills, fever, flushing

CV:
Hypotension
, tachycardia,
MI
,
venous thrombosis, pulmonary embolism

GI:
Nausea, vomiting, abdominal cramps, jaundice,
viral hepatitis

HEMA:
Thrombosis, hemolysis, AIDS, DIC

INTEG:
Rash, flushing,
urticaria
, inj site reactions

RESP:
Bronchospasm

PHARMACOKINETICS

IV:
Half-life factor IX: 22 hr; rapidly cleared from plasma

INTERACTIONS

• 
Incompatible with protein products

 
Increase:
thrombosis risk—aminocaproic acid; do not administer

Decrease:
effect of warfarin

NURSING CONSIDERATIONS
Assess:

• 
Blood studies: coagulation factor assays by % normal: 5% prevents spontaneous hemorrhage, 30%-50% for surgery, 80%-100% for severe hemorrhage; APTT, clotting inhibitor titers, D-dimer, factor IX, VII concentration, fibrin degradation products, fibrinogen, platelets, PT, thrombin time

• 
Increased B/P, pulse

• 
For bleeding q15-30min; immobilize and apply ice to affected joints

• 
I&O; if urine becomes orange or red, notify prescriber

• 
Allergic or pyrogenic reaction:
fever, chills, rash, itching, slow inf rate if not severe

 
DIC:
bleeding, ecchymosis, hypersensitivity, changes in coagulation tests

• 
For tingling sensation; if present, reduce rate

Perform/provide:

• 
Storage of reconstituted sol for 3 hr at room temp or for ≤2 yr with refrigeration (powder); check expiration date

Evaluate:

• 
Therapeutic response: prevention of hemorrhage

Teach patient/family:

• 
To report any signs of bleeding: gums, under skin, urine, stools, emesis; calf pain, joint pain, yellowing of eyes/skin

• 
About the risk for viral hepatitis, AIDS; to be tested q2-3mo for HIV, although low risk

• 
That immunization for hepatitis B may be given first

• 
To carry emergency ID identifying disease; to avoid salicylates, NSAIDs; to inform other health professionals of condition

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

famciclovir (Rx)

(fam-cy′clo-veer)

Famvir

Func. class.:
Antiviral

Chem. class.:
Guanosine nucleoside

ACTION:

Inhibits DNA polymerase and viral DNA synthesis by conversion of this guanosine nucleoside to penciclovir

USES:

Treatment of acute herpes zoster (shingles), genital herpes; recurrent mucocutaneous herpes simplex virus (HSV) in patients with HIV; initial episodes of herpes genitalis; herpes labialis in the immunocompromised

Unlabeled uses:
Bell’s palsy, herpes labialis prophylaxis, postherpetic neuralgia prophylaxis

CONTRAINDICATIONS:

Hypersensitivity to this product, penciclovir, acyclovir, ganciclovir, valacyclovir, valganciclovir

Precautions:
Pregnancy (B), breastfeeding, renal disease

DOSAGE AND ROUTES
Calculator
Herpes zoster

• Adult:
PO
500 mg q8hr for 7 days

Renal dose

• Adult:
PO
CCr ≥60 ml/min, 500 mg q8hr; CCr 40-59 ml/min, 500 mg q12hr; CCr 20-39 ml/min, 500 mg q24hr; CCr <20 ml/min, 250 mg q24hr

Recurrent herpes simplex virus

• Adult:
PO
125 mg q12hr × 5 days

Renal dose

• Adult:
PO
40-59 ml/min 500 mg bid; CCr 20-39 ml/min 500 q day; CCr <20 ml/min 250 mg q day

Suppression of recurrent herpes simplex virus

• Adult:
PO
250 mg q12hr up to 1 yr

Renal dose

• Adult:
PO
CCr 20-39 ml/min, 125 mg q12hr × 5 days; CCr <20 ml/min, 125 mg q24hr × 5 days

Genital herpes/herpes labialis (recurrent)

• Adult:
PO
125 mg bid × 5 days or 1000 mg bid for 1 day; begin treatment at 1st sign of recurrence; immunocompetent herpes labialis 1500 mg as a single dose

Suppression of recurrent genital herpes

• Adult:
PO
250 mg bid for up to 1 yr

Herpes genitalis initial episodes

• Adult:
PO
250 mg tid × 7-10 days

Bell’s palsy (unlabeled)

• Adult:
PO
750 mg tid × 7 days with predniSONE

Varicella-zoster virus (shingles); chickenpox (unlabeled)

• Adult:
PO
500 mg q8hr × 7 days, preferably within 48 hr of onset

Herpes zoster in HIV (unlabeled)

• Adult/adolescent:
PO
500 mg tid × 7-10 days

Available forms:
Tabs 125, 250, 500 mg

Administer:

• 
Without regard to meals

• 
As soon as diagnosed; for herpes zoster within 72 hr

SIDE EFFECTS

CNS:
Headache, fatigue, dizziness
, paresthesia, somnolence, fever

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

GU:
Decreased sperm count

INTEG:
Pruritus

MS:
Back pain, arthralgia

RESP:
Pharyngitis, sinusitis

PHARMACOKINETICS

Bioavailability 77%, 20% protein binding, 73% excreted via kidneys, terminal plasma half-life 2-3 hr

INTERACTIONS

Decrease:
renal excretion—theophylline, probenecid, digoxin

Decrease:
metabolism—cimetidine

NURSING CONSIDERATIONS
Assess:

• 
Herpes zoster:
number, distribution of lesions; burning, itching, pain, which are early symptoms of herpes infection; assess daily during therapy

• 
Renal studies: urine CCr; BUN before and during treatment if decreased renal function; dose may have to be lowered

• 
Bowel pattern before, during treatment; diarrhea may occur

• 
Posttherapeutic neuralgia during and after treatment

Evaluate:

• 
Therapeutic response: decreased size, spread of lesions

Teach patient/family:

• 
How to recognize beginning infection

• 
How to prevent spread of infection; that this medication does not prevent spread to others; that condoms should be used

• 
About the reason for medication, expected results

• 
That women with genital herpes should have yearly Pap smears; that cervical cancer is more likely

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