ibuprofen
(eye byoo' proe fen)
Advil, Advil Liqui-Gels, Advil Migraine, Apo-Ibuprofen (CAN), Children's Advil, Children's Motrin, Genpril, Infants' Motrin, Junior Strength Advil, Junior Strength Motrin, Menadol, Midol, Midol Maximum Strength Cramp Formula, Motrin, Motrin IB, Motrin Migraine Pain, Novo-Profen (CAN), Nuprin, PediaCare Fever, Pediatric Advil Drops
Pregnancy Category B
Pregnancy Category D (third trimester)
Drug classes
NSAID
Analgesic (nonopioid)
Propionic acid derivative
Therapeutic actions
Anti-inflammatory, analgesic, and antipyretic activities largely related to inhibition of prostaglandin synthesis; exact mechanisms of action are not known. Inhibits both cyclooxygenase (COX) 1 and 2. Ibuprofen is slightly more selective for COX-1.
Indications
· Relief of signs and symptoms of rheumatoid arthritis and osteoarthritis
· Relief of mild to moderate pain
· Treatment of primary dysmenorrhea
· Fever reduction
· Unlabeled uses: Prophylactic for migraine; abortive treatment for migraine
Contraindications and cautions
· Contraindicated with allergy to ibuprofen, salicylates, or other NSAIDs (more common in patients with rhinitis, asthma, chronic urticaria, nasal polyps).
· Use cautiously with CV dysfunction, hypertension; peptic ulceration, GI bleeding; pregnancy; lactation; impaired hepatic or renal function.
Available forms
Tablets—100, 200, 400, 600, 800 mg; chewable tablets—50, 100 mg; capsules—200 mg; suspension—100 mg/2.5 mL, 100 mg/5 mL; oral drops—40 mg/mL
Dosages
ADULTS
Do not exceed 3,200 mg/day.
· Mild to moderate pain: 400 mg q 4–6 hr PO.
· Osteoarthritis or rheumatoid arthritis: 1,200–3,200 mg/day PO (300 mg qid or 400, 600, 800 mg tid or qid; individualize dosage. Therapeutic response may occur in a few days, but often takes 2 wk).
· Primary dysmenorrhea: 400 mg q 4 hr PO.
· OTC use: 200–400 mg q 4–6 hr PO while symptoms persist; do not exceed 1,200 mg/day. Do not take for more than 10 days for pain or 3 days for fever, unless so directed by health care provider.
PEDIATRIC PATIENTS
· Juvenile arthritis: 30–40 mg/kg/day PO in three to four divided doses; 20 mg/kg/day for milder disease.
· Fever (6 mo–12 yr): 5–10 mg/kg PO q 6–8 hr; do not exceed 40 mg/kg/day.
Pharmacokinetics
Route | Onset | Peak | Duration |
Oral | 30 min | 1–2 hr | 4–6 hr |
Metabolism: Hepatic; T1/2: 1.8–2.5 hr
Distribution: Crosses placenta; may enter breast milk
Excretion: Urine
Adverse effects
· CNS: Headache, dizziness, somnolence, insomnia, fatigue, tiredness, dizziness, tinnitus, ophthalmologic effects
· CV: Hypertension, palpitations, arrhythmia
· Dermatologic: Rash, pruritus, sweating, dry mucous membranes, stomatitis
· GI: Nausea, dyspepsia, GI pain, diarrhea, vomiting, constipation, flatulence, GI bleeding
· GU: Dysuria, renal impairment, menorrhagia
· Hematologic: Bleeding, platelet inhibition with higher doses, neutropenia, eosinophilia, leukopenia, pancytopenia, thrombocytopenia, agranulocytosis,granulocytopenia, aplastic anemia, decreased Hgb or Hct, bone marrow depression
· Respiratory: Dyspnea, hemoptysis, pharyngitis, bronchospasm, rhinitis
· Other: Peripheral edema, anaphylactoid reactions to anaphylactic shock
Interactions
Drug-drug
· Increased toxic effects of lithium with ibuprofen
· Decreased diuretic effect with loop diuretics—bumetanide, furosemide, ethacrynic acid
· Potential decrease in antihypertensive effect of beta-adrenergic blocking agents and ACE inhibitors
· Increased risk of gastric ulceration with bisphosphates
· Increased risk of bleeding with anticoagulants
Nursing considerations
Assessment
· History: Allergy to ibuprofen, salicylates or other NSAIDs; CV dysfunction, hypertension; peptic ulceration, GI bleeding; impaired hepatic or renal function; pregnancy; lactation
· Physical: Skin color, lesions; T; orientation, reflexes, ophthalmologic evaluation, audiometric evaluation, peripheral sensation; P, BP, edema; R, adventitious sounds; liver evaluation, bowel sounds; CBC, clotting times, urinalysis, LFTs, renal function tests, serum electrolytes, stool guaiac
Interventions
· Administer drug with food or after meals if GI upset occurs.
· Arrange for periodic ophthalmologic examination during long-term therapy.
· Discontinue drug if eye changes, symptoms of liver dysfunction, or renal impairment occur.
· WARNING: Institute emergency procedures if overdose occurs: Gastric lavage, induction of emesis, supportive therapy.
· Use drug only as suggested; avoid overdose. Take the drug with food or after meals if GI upset occurs. Do not exceed the prescribed dosage.
· Avoid over-the-counter drugs. Many of these drugs contain similar medications, and serious overdosage can occur.
· You may experience these side effects: Nausea, GI upset, dyspepsia (take drug with food); diarrhea or constipation; drowsiness, dizziness, vertigo, insomnia (use caution when driving or operating dangerous machinery).
· Report sore throat, fever, rash, itching, weight gain, swelling in ankles or fingers, changes in vision, black or tarry stools.
Adverse effects in Italic are most common; those in Bold are life-threatening.
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