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单词 relafen
释义

Relafen


Thesaurus
Noun1.Relafen - a nonsteroidal anti-inflammatory drug (trade name Relafen)nabumetonenonsteroidal anti-inflammatory, nonsteroidal anti-inflammatory drug, NSAID - an anti-inflammatory drug that does not contain steroids; "NSAIDs inhibit the activity of both Cox-1 and Cox-2 enzymes"ketone - any of a class of organic compounds having a carbonyl group linked to a carbon atom in each of two hydrocarbon radicalsbrand, brand name, marque, trade name - a name given to a product or service

Relafen


nabumetone

(na-byoo-me-tone) nabumetone,

Relafen

(trade name)

Classification

Therapeutic: antirheumatics
Pregnancy Category: C

Indications

Symptomatic management of rheumatoid arthritis and osteoarthritis.

Action

Inhibits prostaglandin synthesis.

Therapeutic effects

Suppression of pain and inflammation.

Pharmacokinetics

Absorption: Nabumetone (a prodrug) is 80% absorbed after oral administration; 35% is rapidly converted to 6-methoxy-2-naphthylacetic acid (6-MNA), which is the active drug.Distribution: Unknown.Protein Binding: >99%.Metabolism and Excretion: 6-MNA is metabolized by the liver to inactive compounds.Half-life: 24 hr (increased in severe renal impairment).

Time/action profile (analgesia/anti-inflammatory effects)

ROUTEONSETPEAKDURATION
PO1–2 daysfew days–2 wk12–24 hr

Contraindications/Precautions

Contraindicated in: Hypersensitivity;Use with other NSAIDs, including aspirin; cross-sensitivity may occur;Active GI bleeding or ulcer disease;Peri-operative pain from coronary artery bypass graft (CABG) surgery; Lactation: Lactation.Use Cautiously in: Severe renal, or hepatic disease;History of ulcer disease; Obstetric: Avoid using during 2nd half of pregnancy due to potential of NSAIDs to cause premature closure of ductus arteriosus; Pediatric: Safety not established.

Adverse Reactions/Side Effects

Central nervous system

  • agitation
  • anxiety
  • confusion
  • depression
  • dizziness
  • drowsiness
  • fatigue
  • headache
  • insomnia
  • malaise
  • weakness

Ear, Eye, Nose, Throat

  • abnormal vision
  • tinnitus

Respiratory

  • dyspnea
  • hypersensitivity pneumonitis

Cardiovascular

  • edema
  • fluid retention
  • vasculitis

Gastrointestinal

  • gi bleeding (life-threatening)
  • abdominal pain (most frequent)
  • diarrhea (most frequent)
  • ↑ liver function tests
  • anorexia
  • constipation
  • dry mouth
  • dyspepsia
  • flatulence
  • gastritis
  • gastroenteritis
  • ↑ appetite
  • nausea
  • stomatitis
  • vomiting

Genitourinary

  • albuminuria
  • azotemia
  • interstitial nephritis

Dermatologic

  • exfoliative dermatitis (life-threatening)
  • stevens-johnson syndrome (life-threatening)
  • toxic epidermal necrolysis (life-threatening)
  • increased sweating
  • photosensitivity
  • pruritus
  • rash

Hematologic

  • prolonged bleeding time

Metabolic

  • weight gain

Neurologic

  • paresthesia
  • tremor

Miscellaneous

  • allergic reactions including anaphylaxis (life-threatening)
  • angioneurotic edema (life-threatening)

Interactions

Drug-Drug interaction

↑ adverse GI effects with aspirin, other NSAIDs, potassium supplements, corticosteroids, or alcohol.Chronic use with acetaminophen may ↑ risk of adverse renal reactions.May ↓ effectiveness of diuretics or antihypertensives.May ↑ hypoglycemic effects of insulins or oral hypoglycemic agents.↑ risk of toxicity from methotrexate.↑ risk of bleeding with cefotetan, cefoperazone, valproic acid, anticoagulants, ticlopidine, clopidogrel, eptifibatide, tirofiban, or thrombolytic agents.↑ risk of adverse hematologic reactions with antineoplastics or radiation therapy.Concurrent use with cyclosporine may ↑ risk of renal toxicity.

Route/Dosage

Oral (Adults) 1000 mg/day as a single dose or divided dose twice daily; may be ↑ up to 2000 mg/day; use lowest effective dose during chronic therapy.

Availability (generic available)

Tablets: 500 mg, 750 mg

Nursing implications

Nursing assessment

  • Patients who have asthma, aspirin-induced allergy, and nasal polyps are at increased risk for developing hypersensitivity reactions. Monitor for rhinitis, asthma, and urticaria.
  • Assess pain and range of motion before and periodically throughout therapy.
  • Lab Test Considerations: Evaluate BUN, serum creatinine, CBC, and liver function periodically in patients receiving prolonged therapy.
    • Serum potassium, BUN, serum creatinine, alkaline phosphatase, LDH, AST, and ALT tests may show ↑ levels. Blood glucose, hemoglobin, and hematocrit concentrations, leukocyte and platelet counts, and CCr may be ↓.
    • May cause prolonged bleeding time.

Potential Nursing Diagnoses

Acute pain (Indications)
Impaired physical mobility (Indications)

Implementation

  • Administration in higher than recommended doses does not provide increased effectiveness but may cause increased side effects. Use lowest effective dose for the shortest duration possible to minimize cardiac risks.
  • Oral: Administer with meals or antacids to decrease GI irritation and increase absorption.

Patient/Family Teaching

  • Advise patient to take this medication with a full glass of water and to remain in an upright position for 15–30 min after administration.
  • Instruct patient to take medication as directed. Take missed doses as soon as remembered but not if almost time for the next dose. Do not double dose.
  • May cause drowsiness, dizziness, or visual disturbances. Advise patient to avoid driving or other activities requiring alertness until response to the medication is known.
  • Advise patient to use sunscreen and protective clothing to prevent photosensitivity reactions.
  • Caution patient to avoid the concurrent use of alcohol, aspirin, acetaminophen, or other OTC medications without consulting health care professional.
  • Advise patient to inform health care professional of medication regimen before treatment or surgery.
  • Advise patient to consult health care professional if rash, itching, visual disturbances, tinnitus, weight gain, edema, black stools, persistent headache, or influenza-like syndrome (chills, fever, muscle aches, pain) occurs.

Evaluation/Desired Outcomes

  • Decreased pain and improved joint mobility. Partial arthritic relief is usually seen within 1 wk, but maximum effectiveness may require 2 wk or more of continuous therapy. Patients who do not respond to one NSAID may respond to another.

Relafen

(rĕl′ə-fĕn′) A trademark for the drug nabumetone.

Relafen


Related to Relafen: Norflex
  • noun

Synonyms for Relafen

noun a nonsteroidal anti-inflammatory drug (trade name Relafen)

Synonyms

  • nabumetone

Related Words

  • nonsteroidal anti-inflammatory
  • nonsteroidal anti-inflammatory drug
  • NSAID
  • ketone
  • brand
  • brand name
  • marque
  • trade name
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更新时间:2024/11/12 12:53:31