CeleBREXGenetic ImplicationsPregnancy CategoryCategory CTher. class.antirheumaticsnonsteroidal anti inflammatory agentsPharm. class.
cox 2 inhibitors
Relief of signs and symptoms of osteoarthritis, rheumatoid arthritis, ankylosing spondylitis and juvenile rheumatoid arthritis.
Management of acute pain including primary dysmenorrhea.
Inhibits the enzyme COX-2. This enzyme is required for the synthesis of prostaglandins.
Has analgesic, anti-inflammatory, and antipyretic properties.Therapeutic Effect(s):
Decreased pain and inflammation caused by arthritis or spondylitis.
Absorption: Bioavailability unknown.
Distribution: 97% bound to plasma proteins; extensive tissue distribution.
Metabolism and Excretion: Mostly metabolized by the hepatic CYP2C9 isoenzyme; the CYP2C9 enzyme system exhibits genetic polymorphism; poor metabolizers may have significantly ↑ celecoxib concentrations and an ↑ risk of adverse effects; <3% excreted unchanged in urine and feces.
Half-life: 11 hr.
TIME/ACTION PROFILE (pain reduction)
|PO||2448 hr||unknown||1224 hr|
Cross-sensitivity may exist with other NSAIDs, including aspirin;
History of allergic-type reactions to sulfonamides;
History of asthma, urticaria, or allergic-type reactions to aspirin or other NSAIDs, including the aspirin triad (asthma, nasal polyps, and severe hypersensitivity reactions to aspirin);
Advanced renal disease;
Severe hepatic dysfunction;
Peri-operative pain from coronary artery bypass graft (CABG) surgery;
OB: Should not be used in late pregnancy (may cause premature closure of the ductus arteriosus).Use Cautiously in:
Cardiovascular disease or risk factors for cardiovascular disease (may ↑ risk of serious cardiovascular thrombotic events, myocardial infarction, and stroke, especially with prolonged use);
Pre-existing renal disease, heart failure, liver dysfunction, concurrent diuretic or ACE inhibitor therapy (↑ risk of renal impairment);
Hypertension or fluid retention;
Renal insufficiency (may precipitate acute renal failure);
Serious dehydration (correct deficits before administering);
Patients who are known or suspected to be poor CYP2C9 metabolizers (↓ initial dose by 50%);
Pedi: Safety not established in children <2 yrs or for longer than 6 mo;
Geri: Concurrent therapy with corticosteroids or anticoagulants, long duration of NSAID therapy, history of smoking, alcoholism, geriatric patients, or poor general health status (↑ risk of GI bleeding);
Lactation: Lactation.Exercise Extreme Caution in:
History of ulcer disease or GI bleeding.
Adverse Reactions/Side Effects
CNS: dizziness, headache, insomnia.
CV: MYOCARDIAL INFARCTION, STROKE, THROMBOSIS, edema.
GI: GI BLEEDING, abdominal pain, diarrhea, dyspepsia, flatulence, nausea.
Derm: EXFOLIATIVE DERMATITIS, STEVENS-JOHNSON SYNDROME, TOXIC EPIDERMAL NECROLYSIS, rash.
*CAPITALS indicates life-threatening.
*italic indicates most frequent.
CYP2C9 inhibitors may ↑ levels.
May ↓ effectiveness of ACE inhibitors , thiazide diuretics , and furosemide .
Fluconazole ↑ levels (use lowest recommended dosage).
May ↑ risk of bleeding with warfarin and aspirin .
May ↑ serum lithium levels.
Does not inhibit the cardioprotective effect of low-dose aspirin .
PO (Adults): Osteoarthritis200 mg once daily or 100 mg twice daily. Rheumatoid arthritis100200 mg twice daily. Ankylosing spondylitis200 mg once daily or 100 mg twice daily; dose may be ↑ after 6 wk to 400 mg daily. Acute pain, including dysmenorrhea400 mg initially, then a 200-mg dose if needed on the first day; then 200 mg twice daily as needed..Hepatic Impairment
PO (Adults): Moderate hepatic impairment (Child-Pugh Class B)↓ dose by 50%..
PO (Children ≥2 yrs, ≥10 kg≤25 kg): Juvenile rheumatoid arthritis50 mg twice daily..
PO (Children ≥2 yrs, ≥25 kg): Juvenile rheumatoid arthritis100 mg twice daily..
Capsules: 50 mg, 100 mg, 200 mg, 400 mg
» Cost: 50 mg $249.93/180, 100 mg $474.93/180, 200 mg $796.98/180, 400 mg $601.98/90.
Assess range of motion, degree of swelling, and pain in affected joints before and periodically throughout therapy.
Assess patient for allergy to sulfonamides, aspirin, or NSAIDs. Patients with these allergies should not receive celecoxib.
Assess patient for skin rash frequently during therapy. Discontinue at first sign of rash; may be life-threatening. Stevens-Johnson syndrome may develop. Treat symptomatically; may recur once treatment is stopped.Lab Test Considerations
May cause ↑ AST and ALT levels.
» May cause hypophosphatemia and ↑ BUN.
Potential Nursing Diagnoses
Impaired physical mobility (Indications)
Acute pain (Indications)
Do not confuse with Celexa (citalopram) or Cerebyx (fosphenytoin).
: May be administered without regard to meals. Capsules may be opened and sprinkled on applesauce and ingested immediately with water. Mixture may be stored in the refrigerator for up to 6 hr.
Instruct patient to take celecoxib exactly as directed. Do not take more than prescribed dose. Increasing doses does not appear to increase effectiveness. Use lowest effective dose for shortest period of time.
Advise patient to notify health care professional promptly if sign or symptom of GI toxicity (abdominal pain, black stools), skin rash, unexplained weight gain, edema, or chest pain occurs. Patients should discontinue celecoxib and notify health care professional if signs and symptoms of hepatotoxicity (nausea, fatigue, lethargy, pruritus, jaundice, upper right quadrant tenderness, flu-like symptoms) occur.
Advise patient to notify health care professional if pregnancy is planned or suspected.
Reduction in joint pain in patients with osteoarthritis.
Reduction in joint tenderness, pain, and joint swelling in patients with rheumatoid arthritis and juvenile rheumatoid arthritis.
Decreased pain with dysmenorrhea.