Mosby's 2014 Nursing Drug Reference (361 page)

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

rosiglitazone (Rx)

(ros-ih-glit′ah-zone)

Avandia

Func. class.:
Antidiabetic, oral

Chem. class.:
Thiazolidinedione

ACTION:

Improves insulin resistance by hepatic glucose metabolism, insulin receptor kinase activity, insulin receptor phosphorylation

USES:

Type 2 diabetes mellitus, alone or in combination with sulfonylureas, metformin, insulin

Unlabeled uses:
Increased ovulation frequency in those with polycystic ovary syndrome; reduced in-stent restenosis in those with diabetes

CONTRAINDICATIONS:

Breastfeeding, children, hypersensitivity to thia
zolidinediones, diabetic ketoacidosis, jaundice

 

Black Box Warning:

NYHA III, IV acute heart failure, heart failure

Precautions:
Pregnancy (C), geriatric patients, thyroid disease, renal/hepatic disease, heart failure, class I, II NYHA

 

Black Box Warning:

MI

DOSAGE AND ROUTES
Calculator

• Adult:
PO
4 mg/day or in 2 divided doses, may increase to 8 mg/day or in 2 divided doses after 12 wk; may be added to metformin, sulfonylurea for adult dose

Available forms:
Tabs 2, 4, 8 mg

Administer:
PO route

• 
Once or in 2 divided doses, without regard to food

• 
Tabs crushed and mixed with food or fluids for patients with difficulty swallowing

• 
Only through the REMS Program 1-800-Avandia

SIDE EFFECTS

CNS:
Fatigue,
headache

CV:
MI, CHF, death (geriatric patients)

ENDO:
Hypo/hyperglycemia

GI:
Weight gain,
hepatotoxicity,
increase total, LDL, HDL cholesterol; decrease free fatty acids, diarrhea

MISC:
Accidental injury, URI, sinusitis, anemia, back pain, diarrhea, edema, bone fractures (female)

SYST:
Anaphylaxis, Stevens-Johnson syndrome, lactic acidosis

PHARMACOKINETICS

Maximal reductions in FBS after 6-12 wk; protein binding 99.8%; excreted in urine, feces; elimination half-life 3-4 hr; may be excreted in breast milk

INTERACTIONS

Increase:
hypoglycemia—gemfibrozil, fluvoxaMINE, ketoconazole, trimethoprim; monitor glucose

• 
Avoid concurrent use with insulin, nitrates

• 
May increase or decrease level: CYP2C5 inducer/inhibitors

Drug/Herb

Increase:
antidiabetic effect—garlic, horse chestnut

Drug/Lab Test

Increase:
ALT, HDL, LDL, total cholesterol, blood glucose

Decrease:
Hgb/Hct

NURSING CONSIDERATIONS
Assess:

 

Black Box Warning:

CHF/MI:
dyspnea, crackles, edema, weight gain ≥5 lb, jugular venous distention; may need to change dose or discontinue product, do not use in acute coronary syndrome, NYHA Class 3/IV heart failure

 
Lactic acidosis:
dyspnea, abdominal pain, muscle pain; notify prescriber

• 
Hypoglycemic reactions (sweating, weakness, dizziness, anxiety, tremors, hunger), hyperglycemic reactions soon after meals

 
Systemic reactions: anaphylaxis, Stevens-Johnson syndrome, lactic acidosis

 
Hepatotoxicity:
LFTs periodically AST, ALT (if ALT >2.5 × ULN, do not use product)

• 
Fasting blood sugar, A1c, plasma lipids/lipoproteins, B/P, body weight during treatment

• 
To use product provider/patient must be enrolled in the Avandia-Rosiglitazone Medicines Access Program

Perform/provide:

• 
Conversion from other oral hypoglycemic agents if needed; change may be made without gradual dosage change; monitor blood glucose during conversion

• 
Storage in tight container in cool environment

Evaluate:

• 
Therapeutic response: decrease in polyuria, polydipsia, polyphagia; clear sensorium; absence of dizziness; stable gait; blood glucose, A1c improvement

Teach patient/family:

• 
To monitor blood glucose; that periodic liver function tests mandatory; to report edema, weight gain

• 
About the symptoms of hypo/hyperglycemia, what to do about each

• 
That product must be continued on daily basis; about the consequences of discontinuing the product abruptly

• 
To avoid OTC medications, herbal preparations, nitrates, or insulin unless approved by prescriber

• 
That diabetes is lifelong; that product is not a cure, only controls symptoms

• 
That all food included in diet plan must be eaten to prevent hypoglycemia

• 
To carry emergency ID and glucagon emergency kit

 
To report symptoms of hepatic dysfunction (nausea, vomiting, abdominal pain, fatigue, anorexia, dark urine, jaundice)

• 
That 2 wk is needed to see reduction in blood glucose level and 2-3 mo needed to see full effect of product

• 
To notify prescriber if oral contraceptives are used

• 
Not to use if breastfeeding, may be secreted in breast milk

• 
That a medication guide should be dispensed with each prescription/refill

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

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