Mosby's 2014 Nursing Drug Reference (411 page)

BOOK: Mosby's 2014 Nursing Drug Reference
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trospium (Rx)

(trose′pee-um)

Sanctura, Sanctura XR

Func. class.:
Anticholinergic, urinary antispasmodic

Chem. class.:
Muscarinic receptor antagonist

ACTION:

Relaxes smooth muscles in bladder by inhibiting acetylcholine effect on muscarinic receptors

USES:

Overactive bladder (urinary frequency, urgency)

CONTRAINDICATIONS:

Hypersensitivity, uncontrolled closed-angle glaucoma, urinary retention, gastric retention, myasthenia gravis

Precautions:
Pregnancy (C), breastfeeding, children, geriatric patients, renal/hepatic disease, controlled closed-angle glaucoma, ulcerative colitis, intestinal atony, bladder outflow obstruction

DOSAGE AND ROUTES
Calculator

• Adult
<
75 yr:
PO
20 mg bid 1 hr before meals or on empty stomach;
ER
60 mg in
AM

• Geriatric

75 yr:
PO
titrate down to 20 mg/day based on response and tolerance

Renal dose

• Adult:
PO
CCr <30 ml/min, 20 mg/day at bedtime, ext rel product not recommended

Available forms:
Tabs 20 mg; caps ext rel 60 mg

Administer:

• 
1 hr before meals or on empty stomach (reg rel); in
AM
(ext rel) ≥1 hr before meal

SIDE EFFECTS

CNS:
Fatigue, dizziness, headache

CV:
Tachycardia

EENT:
Dry eyes, vision abnormalities

GI:
Flatulence, abdominal pain,
constipation, dry mouth
, dyspepsia

GU:
Urinary retention, UTI

INTEG:
Dry skin,
angioedema

MISC:
Heat stroke, fever

PHARMACOKINETICS

Rapidly absorbed (10%); peak 5-6 hr; protein bound (50%-85%); extensively metabolized; excreted in urine, feces; excreted in urine by active tubular secretion; half-life 20 hr

INTERACTIONS

Increase:
drowsiness—CNS depressants, alcohol

Increase or decrease:
trospium effect—products excreted by active renal secretion (aMILoride, digoxin, morphine), metformin, quiNIDine, procainamide, ranitidine, tenofovir, triamterene, vancomycin

Drug/Food

Decrease:
absorption—high-fat meal

NURSING CONSIDERATIONS
Assess:

• 
Urinary patterns:
distention, nocturia, frequency, urgency, incontinence, voiding patterns

Evaluate:

• 
Therapeutic response: correction of urinary status: absence of dysuria, frequency, nocturia, incontinence

Teach patient/family:

• 
To avoid hazardous activities because dizziness may occur

• 
That alcohol may increase drowsiness

• 
About anticholinergic effects that may occur

• 
That overheating may occur with strenuous exercise

• 
To avoid all other products unless approved by prescriber

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

undecylenic acid topical

 

unoprostone
ophthalmic

 

ustekinumab (Rx)

(us′te-kin′ue-mab)

Stelara

Func. class.:
Antipsoriatic agent

ACTION:

Interleukin (IL)-12, IL-23 Antagonist

USES:

Plaque psoriasis

CONTRAINDICATIONS:

Hypersensitivity, sepsis, active infections

Precautions:
Pregnancy (B), breast-feeding, children ≤18 yr, geriatric patients, surgery, TB, diabetes mellitus, immunosuppression

DOSAGE AND ROUTES
Calculator

• Adult

100 kg:
SUBCUT
90 mg, repeat in 4 wk, then 90 mg q12wk starting wk 16

• Adult

100 kg:
SUBCUT
45 mg, repeat in 4 wk, then 45 mg q12wk starting wk 16

Available forms:
Solutions for inj 45 mg/0.5 mc

Administer:

• 
Visually inspect for particulate matter or discoloration; solution should be slightly yellow and may contain a few small translucent or white particles; do not use if discolored, cloudy or if foreign
particulate matter is present; do not shake

• 
Use at 27 G, 0.5 inch needle

• 
May be administered subcut into upper arm, abdomen, or thigh; rotate inj sites

SIDE EFFECTS

CNS:
Headache, leukoencephalopathy

HEMA:
Bleeding

INTEG:
Inj site reaction
, pruritus, skin irritation, erythema

SYST:
Serious infections, malignancies

PHARMACOKINETICS

Maximum serum concentration: 13.5 days after a single 45 mg subcut dose, 7 days after a single 90 mg subcut dose; half-life 14.9-45.6 days

INTERACTIONS

• 
Do not give concurrently with vaccines; immunizations should be brought up to date before treatment

• 
Avoid use with immunosuppressives

NURSING CONSIDERATIONS
Assess:

• 
For inj site pain, swelling

Evaluate:

• 
Therapeutic response: decreased plaque psoriasis

Teach patient/family:

• 
That product must be continued for prescribed time to be effective

• 
Not to receive live vaccinations during treatment

• 
To notify prescriber of possible infection (upper respiratory or other)

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

valACYclovir (Rx)

(val-a-sye′kloh-vir)

Valtrex

Func. class.:
Antiviral

Chem. class.:
Synthetic purine nucleoside analog

Do not confuse:
valACYclovir
/valGANciclovir
Valtrex
/Valcyte

ACTION:

Interferes with DNA synthesis by conversion to acyclovir, thereby causing decreased viral replication, time of lesional healing

USES:

Treatment or suppression of herpes zoster (shingles), genital herpes, herpes labialis (cold sores), varicella, varicella-zoster

Unlabeled uses:
CMV with advanced HIV, posttransplant patients, Bell’s palsy, herpes simplex virus prophylaxis, acute retinal necrosis (ARN), encephalitis

CONTRAINDICATIONS:

Hypersensitivity to this product or acyclovir, valGANciclovir

Precautions:
Pregnancy (B), breastfeeding, geriatric patients, hepatic/renal disease, electrolyte imbalance, dehydration, penciclovir, famciclovir, ganciclovir, hypersensitivity, varicella

DOSAGE AND ROUTES
Calculator
Herpes zoster (shingles)

• Adult:
PO
1 g tid × 1 wk

Genital herpes (suppressive, initial)

• Adult:
PO
1 g bid × 10 days initially

Genital herpes (recurrent episodes)

• Adult:
PO
500 mg bid × 3 days

Genital herpes (suppressive therapy)

• Adult:
PO
1 g/day with normal immune function; 500 mg/day for those with ≤9 recurrences/yr; 500 mg bid for HIV-infected patients with CD4 count ≥100

Reduction of transmission

• Adult:
PO
500 mg/day for source partner

Herpes labialis

• Adult:
PO
2 g bid × 1 day at 1st sign of lesions

Varicella (chickenpox) in immunocompetent patients

• Adolescent and child ≥2 yr:
PO
20 mg/kg/dose tid × 5 days, max 3 g/day; start at 1st sign, preferably within 24 hr of rash

Renal dose

• Adult:
PO
CCr 30-49 ml/min, 1 g q12hr (for regimens 1 g q8hr); 1 g q12hr × 1 day (herpes labialis); CCr 10-29 ml/min, 1 g q24hr (genital herpes/herpes zoster); 500 mg q24hr (recurrent genital herpes); CCr <10 ml/min, 500 mg q24hr (genital herpes/herpes zoster), 500 mg q24hr (recurrent genital herpes)

Available forms:
Tabs 500 mg, 1 g

Administer:

• 
As soon as possible (herpes labialis, genital herpes); within 24 hr of rash (varicella)

• 
Within 72 hr of outbreak (herpes zoster)

• 
Without regard to food

• 
Caps may be made into susp by pharmacy

SIDE EFFECTS

CNS:
Tremors, lethargy,
dizziness, headache
, weakness, depression

ENDO:
Dysmenorrhea

GI:
Nausea
, vomiting, diarrhea, abdominal pain, constipation,
increased AST

HEMA:
Thrombocytopenic purpura, hemolytic uremic syndrome

INTEG:
Rash

PHARMACOKINETICS

Onset unknown; terminal half-life 2½-3½ hr; converted to acyclovir that crosses placenta, enters breast milk; excreted in urine primarily as acyclovir; protein binding 13.5%-17.9%

INTERACTIONS

Increase:
blood levels of valACYclovir—cimetidine, probenecid; only significant with renal disease

Drug/Lab Test

Increase:
LFTs, creatinine

Decrease:
WBC, platelets

NURSING CONSIDERATIONS
Assess:

• 
Infection;
characteristics of lesions; therapy should be started at 1st sign or symptom of herpes; most effective within 72 hr of outbreak

 
Thrombocytopenic purpura, hemolytic uremic syndrome; may be fatal

• 
C&S before product therapy; product may be taken as soon as culture is taken; repeat C&S after treatment; determine presence of other sexually transmitted diseases

• 
Bowel pattern before, during treatment

• 
Skin eruptions: rash

• 
Allergies before treatment, reaction of each medication

Perform/provide:

• 
Storage at room temp; protect from light, moisture

Evaluate:

• 
Therapeutic response: absence of itching, painful lesions; crusting and healed lesions

Teach patient/family:

• 
To take as prescribed; if dose is missed, to take as soon as remembered up to 2 hr before next dose; not to double dose

• 
That product may be taken orally before infection occurs; that product should be taken when itching or pain occurs, usually before eruptions

• 
That partners need to be told that patient has herpes because they can become infected; that condoms must be worn to prevent reinfections

• 
That product does not cure infection, just controls symptoms; that product does not prevent infection of others

BOOK: Mosby's 2014 Nursing Drug Reference
9.29Mb size Format: txt, pdf, ePub
ads

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