Mosby's 2014 Nursing Drug Reference (396 page)

BOOK: Mosby's 2014 Nursing Drug Reference
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Canada only   Side effects:
italics
= common;
bold
= life-threatening   
Nurse Alert

tinidazole (Rx)

(tye-ni′da-zole)

Tindamax

Func. class.:
Antiprotozoal

Chem. class.:
Nitroimidazole derivative

ACTION:

Interferes with DNA/RNA synthesis in protozoa

USES:

Amebiasis, giardiasis, trichomoniasis

Unlabeled uses:
Bacteroides
sp.,
Clostridium
sp.,
Eubacterium
sp.,
Fusobacterium
sp.,
Peptococcus
sp.,
Peptostreptococcus
sp., gingivitis, urethritis,
Veillonella
sp.

CONTRAINDICATIONS:

Pregnancy, breastfeeding; hypersensitivity to this product or nitroimidazole derivative

Precautions:
Children, geriatric patients, hepatic disease, CNS depression, blood dyscrasias, candidiasis, seizures, viral infection, alcoholism, pregnancy (C)

 

Black Box Warning:

Secondary malignancy

DOSAGE AND ROUTES
Calculator
Intestinal amebiasis/amebic involvement of the liver

• Adult:
PO
2 g daily × 3 days

• Child ≥3 yr/adolescent:
PO
50 mg/kg/day × 3 days, max 2 g/day

Giardiasis

• Adult:
PO
2 g as a single dose

• Child ≥3 yr:
PO
50 mg/kg as a single dose, max 2 g

Trichomoniasis

• Adult:
PO
2 g as a single dose

Bacterial vaginosis

• Adult (nonpregnant woman):
PO
2 g/day × 2 days with food or 1 g/day × 5 days with food

Available forms:
Tabs 250, 500 mg

Administer:

• 
Tabs can be crushed and mixed with artificial cherry syrup for children

• 
With food to increase plasma concentrations, minimize epigastric distress and other GI effects

SIDE EFFECTS

CNS:
Dizziness, headache
,
seizures,
peripheral neuropathy
, malaise, fatigue

GI:
Nausea, vomiting
, anorexia, increased AST/ALT, constipation, abdominal pain, indigestion, altered taste

HEMA:
Leukopenia,
neutropenia

INTEG:
Pruritus, urticaria,
rash
, oral candidiasis

SYST:
Angioedema,
cramping

PHARMACOKINETICS

Peak 1½ hr; metabolized extensively in liver; excreted unchanged (20%-25%) in urine, (12%) feces; half-life 12-14 hr; crosses blood-brain barrier

INTERACTIONS

• 
Do not use within 2 wk of disulfiram

Increase:
tinidazole action—CYP3A4 inhibitors (cimetidine, ketoconazole): increased action of tinidazole

Increase:
action of anticoagulants, cycloSPORINE, tacrolimus, fluorouracil, hydantoins, lithium

Decrease:
tinidazole action—CYP3A4 inducers (PHENobarbital, rifampin, phenytoin); cholestyramine, oxytetracycline: decreased action of tinidazole

Drug/Herb

Increase or decrease:
tinidazole level—St. John’s wort

Drug/Lab Test

Increase:
triglycerides, LDH, AST/ALT, glucose

Decrease:
WBCs

NURSING CONSIDERATIONS
Assess:

• 
Giardiasis:
obtain 3 stool samples several days apart beginning q3-4wk after treatment

• 
Amebic liver abscess:
Monitor CBC, ESR, amebic gel diffusion test, ultrasound; also total and differential leukocyte count

 

Black Box Warning:

Secondary malignancy: avoid unnecessary use

• 
Signs of infection, anemia

• 
Bowel pattern before, during treatment

Evaluate:

• 
Therapeutic response: decrease in infection as evidenced by negative culture

Teach patient/family:

• 
To take with food to increase plasma concentrations, minimize epigastric distress and other GI effects; not to use alcoholic beverages during or for 3 days after treatment

• 
Trichomoniasis:
both partners should be treated at the same time

• 
To avoid alcohol, may cause disulfiram reaction

• 
To avoid doing hazardous activities until reaction is known

• 
That product causes taste

• 
Not to use OTC, Rx, or herbal products unless approved by prescriber

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

HIGH ALERT
tinzaparin (Rx)

(tin-zay-par′in)

Innohep

Func. class.:
Anticoagulant

Chem. class.:
Unfractionated porcine heparin

ACTION:

Increases the inhibitory effect of antithrombin factor Xa, thrombin

USES:

Treatment of DVT, PE after abdominal, knee, or hip surgery or after knee or hip replacement

Unlabeled uses:
Antiphospholipid antibody syndrome, arterial thromboembolism prophylaxis, cerebral thromboembolism, DVT prophylaxis, PE prophylaxis, thrombosis prophylaxis

CONTRAINDICATIONS:

Hypersensitivity to this product, heparin, pork or benzyl alcohol, sulfites; hemophilia, leukemia with bleeding, peptic ulcer disease, thrombocytopenic purpura, heparin-induced thrombocytopenia

Precautions:
Pregnancy (B), breastfeeding, children, geriatric patients, alcoholism, severe renal/hepatic disease, blood dyscrasias; severe, uncontrolled hypertension; subacute bacterial endocarditis, acute nephritis; geriatric patients >70 yr (renal disease with DVT/PE)

 

Black Box Warning:

Spinal/epidural anesthesia, lumbar puncture

DOSAGE AND ROUTES
Calculator
Treatment of DVT

• Adult:
SUBCUT
175 anti-Xa international units/kg/day ≥6 days and until adequate anticoagulation with warfarin (therapeutic INR ≥2 for 2 consecutive days)

Prophylaxis of DVT in orthopedic procedures (unlabeled)

• Adult:
75 anti-Xa units/kg/day started 12-24 hr after surgery

Prophylaxis of dvt/thromboembolism/pe (unlabeled)

• Adult:
3500 anti-Xa units (50 anti-Xa units/kg) daily beginning 1-2 hr prior to surgery and continued for 5-10 days

Available forms:
Inj 20,000 international units/1 ml

Administer:

• 
Only after screening patient for bleeding disorders

• 
For 6 days, until warfarin has been given to result in adequate coagulation

• 
SUBCUT only; do not give IM

• 
To recumbent patient; give SUBCUT; rotate inj sites (left/right anterolateral, left/right posterolateral abdominal wall)

• 
Insert whole length of needle into skin fold held with thumb and forefinger

 
Only this product when ordered; not interchangeable with heparin (unfractionated) or LMWHs

• 
At same time each day to maintain steady blood levels

• 
Do not massage area or aspirate when giving SUBCUT inj

• 
Do not mix with other products or inf fluids

• 
Alternate inj sites

• 
For excessive bruising at inj site, may use ice before SUBCUT inj

SIDE EFFECTS

CNS:
Fever, confusion, dizziness, insomnia

CV:
Angina, dysrhythmias, peripheral edema, tachycardia, hypo/hypertension

GI:
Nausea, constipation, flatulence, dyspepsia,
hepatitis

GU:
UTI, hematuria, urinary retention, dysuria

HEMA:
Hemorrhage,
anemia, thrombocytopenia,
bleeding

INTEG:
Ecchymosis, inj site reaction

MISC:
Headache, chest/back pain, hypersensitivity

SYST:
Stevens-Johnson syndrome

PHARMACOKINETICS

Onset 2-3 hr, max antithrombin activity (3-5 hr), elimination half-life 4.5 hr

INTERACTIONS

Increase:
action of tinzaparin—oral anticoagulants, salicylates, thrombolytics, NSAIDs, platelet inhibitors, ticlopidine, clopidogrel

NURSING CONSIDERATIONS
Assess:

 

Black Box Warning:

Spinal/epidermal anesthesia, lumbar puncture: monitor neurological impairment; if impairment occurs, urgent treatment needed

• 
Blood studies (Hct, platelets, occult blood in stools), anti-Xa; thrombocytopenia may occur

• 
Bleeding:
gums, petechiae, ecchymosis, black tarry stools, hematuria, decreased Hct, Hgb

• 
Hypersensitivity (fever, urticaria, chills); report to prescriber

• 
Inj site reactions; do not use IM inj

Perform/provide:

• 
Storage at 77° F (25° C); do not freeze

Evaluate:

• 
Therapeutic response: resolution of DVT

Teach patient/family:

• 
To report any signs of bleeding: gums, under skin, urine, stools

TREATMENT OF OVERDOSE:

Protamine 1 mg/100 anti-Xa international units of tinzaparin

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