Read Mosby's 2014 Nursing Drug Reference Online
Authors: Linda Skidmore-Roth
(toh-pire′ah-mate)
Topamax, Topamax Sprinkle, Topiragen
Func. class.:
Anticonvulsant—miscellaneous
Chem. class.:
Monosaccharide derivative
May prevent seizure spread as opposed to an elevation of seizure threshold, increases GABA activity
Partial seizures in adults and children 2-16 yr old; tonic-clonic seizures; seizures with Lennox-Gastaut syndrome; migraine prophylaxis
Unlabeled uses:
Infantile spasms, bipolar disorder, alcohol dependence, absence seizures, neuropathic pain, cluster headaches, mania
Hypersensitivity, metabolic acidosis, pregnancy (D)
Precautions:
Breastfeeding, children, renal/hepatic disease, acute myopia, secondary closed-angle glaucoma, behavioral disorders, COPD, dialysis, encephalopathy, status asthmaticus, status epilepticus, surgery, paresthesias, maculopathy
• Adult/adolescent/child
≥
10 yr:
PO
25-50 mg/day initially, titrate by 25-50 mg/wk, up to 200-400 mg/day in 2 divided doses
• Child 2-9 yr:
PO
week 1: 25 mg in
PM
, then 25 mg bid if tolerated (week 2), then increase by 25-50 mg/day each week as tolerated over 5 to 7-wk titration period, maintenance given in 2 divided doses; <11 kg, minimum 150 mg/day, max 250 mg/day; 12-22 kg, minimum 200 mg/day, max 300 mg/day; 23-31 kg, minimum 200 mg/day, max 350 mg/day; 32-38 kg, minimum 250 mg/day, max 350 mg/day; >38 kg, minimum 250 mg/day, max 400 mg/day
• Adult:
PO
25 mg/day initially, increase by 25 mg/day/wk up to 100 mg/day in 2 divided doses
• Adult:
PO
CCr <70 ml/min, give 1/2 dose
• Adult/adolescent >16 yr:
PO
50 mg/day, titrate slowly by 50 mg/wk to 100-300 mg tid
• Child 2-16 yr:
PO
0.5-1 mg/kg, max 25 mg, initially daily × 7 days then increase by 0.5-1 mg/kg/day weekly up to 3-6 mg/kg/day in divided doses
• Child:
PO
25 mg/day, may increase by 25 mg q2-3days until spasms controlled, max 24 mg/kg/day
• Adult:
PO
25 mg/day, titrated to max 300 mg/day in divided doses
• Adult:
PO
12.5-25 mg q day or bid × 4 wk then double dose q4wk to max 100-200 mg/day in divided doses
• Adult:
PO
25 mg/day then increase by 25-mg increments to 200 mg/day
Available forms:
Tabs 25, 50, 100, 200 mg; sprinkle caps 15, 25 mg
•
Swallow tabs whole; do not break, crush, or chew tabs; very bitter
•
May take without regard to meals
•
Sprinkle cap can be given whole or opened and sprinkled on soft food; do not chew, drink water after sprinkle
CNS:
Dizziness, fatigue
, cognitive disorders, insomnia,
anxiety
, depression, paresthesia,
memory loss, tremor
, motor retardation,
suicidal ideation
EENT:
Diplopia,
vision abnormality
GI:
Diarrhea,
anorexia, nausea, dyspepsia
, abdominal pain, constipation, dry mouth,
pancreatitis
GU:
Breast pain, dysmenorrhea, menstrual disorder
INTEG:
Rash
MISC:
Weight loss, leukopenia, metabolic acidosis, increased body temperature;
unexplained death (epilepsy)
RESP:
Upper respiratory tract infection, pharyngitis, sinusitis
Well absorbed, peak 2 hr, terminal half-life 19-25 hr, excreted in urine (55%-97% unchanged), crosses placenta, excreted in breast milk, protein binding (9%-17%), steady state 4 days
Increase:
renal stones—carbonic anhydrase inhibitors
Increase:
effect of amitriptyline
Increase:
CNS depression—alcohol, CNS depressants
Increase:
topiramate levels—metformin, hydrochlorothiazide, lamoTRIgine
Decrease:
levels of oral contraceptives, estrogen, digoxin, valproic acid, lithium, risperiDONE
Decrease:
topiramate levels—phenytoin, carBAMazepine, valproic acid, probenecid
•
Seizures:
location, type, duration, aura
•
Bipolar disorder:
mood, behavior
•
Renal studies: urinalysis, BUN, urine creatinine q3mo; symptoms of renal colic
•
Hepatic studies: ALT, AST, bilirubin if patient receiving long-term treatment
•
CBC during long-term therapy (anemia); serum bicarbonate (metabolic acidosis)
•
Migraines: pain location, duration; alleviating factors
Mental status: mood, sensorium, affect, behavioral changes,
suicidal thoughts/behaviors;
if mental status changes, notify prescriber
•
Body weight, evidence of cognitive disorder
•
Storage at room temp away from heat, light
•
Assistance with ambulation during early part of treatment; dizziness occurs
•
Seizure precautions: padded side rails, move objects that may harm patient
•
Therapeutic response: decreased seizure activity
•
To carry emergency ID stating patient’s name, products taken, condition, prescriber’s name and phone number
•
To avoid driving, other activities that require alertness
•
Not to discontinue medication quickly after long-term use
•
To notify prescriber immediately of blurred vision, periorbital pain
•
To maintain adequate fluid intake
•
About administration procedure and expected results
•
To use nonhormonal contraceptive; that effect of oral contraceptives is decreased, pregnancy (D)
•
To drink plenty of fluids to prevent kidney stones
•
May need to increase amount of food consumed, weight loss may occur
Canada only Side effects:
italics
= common;
bold
= life-threatening
Nurse Alert
(toh-poh-tee′kan)
Hycamtin
Func. class.:
Antineoplastic, natural; topoisomerase inhibitor
Chem. class.:
Camptothecin analog
Antitumor product with topoisomerase-I–inhibitory activity; topoisomerase I relieves torsional strain
in DNA by causing single-strand breaks; also causes double-strand DNA damage
Metastatic ovarian cancer after failure of traditional chemotherapy; relapsed small-cell lung cancer; cervical cancer
Unlabeled uses:
Non–small-cell lung cancer (NSCLC), rhabdomyosarcoma
Pregnancy (D), breastfeeding, hypersensitivity, severe bone marrow depression
Black Box Warning:
Neutropenia
Precautions:
Children, renal disease, gelatin hypersensitivity
• Adult:
IV INF
1.5 mg/m
2
over 30 min daily × 5 days starting on day 1 of 21-day course × 4 courses; may be reduced to 0.25 mg/m
2
for subsequent courses if severe neutropenia occurs; relapsed small-cell lung cancer (SCLC) in those with a prior complete or partial response, ≥45 days from end of first-line treatment.
PO
2.3 mg/m
2
/day on days 1-5 of 21-day course
• Adult:
IV
CCr 20-39 ml/min, 0.75 mg/m
2
/day × 5 days starting on day 1 of 21-day course
Available forms:
Lyophilized powder for inj 4 mg; caps 0.25, 1 mg
•
Do not break, crush, chew, or open caps; protect from light
•
Take without regard to food
•
Visually inspect for particulate matter and discoloration prior to use
•
Reconstitute each 4 mg-vial with 4 ml sterile water for injection; use immediately, no preservative
•
Withdraw the appropriate volume of the reconstituted solution; dilute further, dilute in 0.9% NaCl or D5W prior to administration
•
The reconstituted solution is yellow or yellow-green
•
Topotecan injection diluted for infusion is stable at room temperature with normal light for 24 hr
•
Infuse over 30 min
CNS:
Arthralgia,
asthenia, headache
, myalgia,
pain
, weakness
GI:
Abdominal pain, constipation
, diarrhea, obstruction,
nausea
, stomatitis,
vomiting;
increased ALT, AST; anorexia
HEMA:
Neutropenia, leukopenia, thrombocytopenia, anemia, sepsis
INTEG:
Total alopecia
RESP:
Dyspnea, cough,
interstitial lung disease
Rapidly and completely absorbed, excreted in urine and feces as metabolites, half-life 2.8 hr, 7%-35% bound to plasma proteins
•
Avoid use with P-glycoprotein, breast cancer resistance protein inhibitors (amiodarone, clarithromycin, diltiazem, erythromycin, indinavir), quiNIDine, testosterone, verapamil, tamoxifen, itraconazole, mefloquine, RU-486, niCARdipine, vaccines, toxoids
Increase:
myelosuppression when used with CISplatin
Increase:
bleeding risk—NSAIDs, anticoagulants, thrombolytics, platelet inhibitors
•
Avoid use with grapefruit juice
•
Hepatic studies: AST, ALT, alk phos, which may be elevated; creatinine, BUN
Black Box Warning:
CBC, differential, platelet count weekly; withhold product if WBC is <3500/mm
3
or platelet count is <100,000/mm
3
; notify prescriber of results; product should be discontinued
•
Buccal cavity for dryness, sores or ulcerations, white patches, oral pain, bleeding, dysphagia
•
Interstitial lung disease (ILD):
fever, cough, dyspnea, hypoxia, may be fatal
•
Storage of caps in refrigerator; IV INF unopened at room temp; protect both from light
•
Increased fluid intake to 2-3 L/day to prevent dehydration unless contraindicated
•
Rinsing of mouth tid-qid with water, club soda; brushing of teeth bid-tid with soft brush or cotton-tipped applicator for stomatitis; use unwaxed dental floss
•
Therapeutic response: decreased tumor size, spread of malignancy
•
That total alopecia may occur; that hair grows back but is different in color and texture
•
To avoid foods with citric acid or hot or rough texture if stomatitis is present; to drink adequate fluids
•
To report stomatitis and any bleeding, white spots, ulcerations in mouth; to examine mouth daily; to report symptoms
Black Box Warning:
To report signs of anemia: fatigue, headache, faintness, SOB, irritability
•
To use effective contraception during treatment and for ≤6 mo after, pregnancy (D); to avoid breastfeeding
•
To avoid OTC products without approval of prescriber
•
To avoid driving or other activities requiring alertness
•
To avoid vaccines, toxoids