Monograph Details
|
|
Musculoskeletal Disorders
> Arthritis/rheumatic disorders
|
|
DAYPRO |
| Manufacturer |
|
Pfizer Labs |
| Legal Classification |
|
Rx
|
| Pharmacological Class |
|
NSAID (propionic acid deriv.). |
| Generic Name |
|
Oxaprozin 600 mg; scored caplets. |
| Indications |
|
Rheumatoid arthritis (RA). Osteoarthritis (OA). Juvenile rheumatoid arthritis (JRA). |
| Children |
|
<6 years: not recommended. JRA: 6–16 years (22–31 kg): 600 mg once daily; (32–54 kg): 900 mg once daily; (≥55 kg): 1.2 g once daily. |
| Adults |
|
RA (≥16 years) or OA: 1.2 g once daily; max 1.8 g or 26 mg/kg daily, whichever is less, in divided doses. Low body weight, milder disease, or on dialysis: initially 600 mg once daily; max 1.2g daily. |
| Contraindications |
|
Aspirin allergy. 3rd trimester pregnancy. Coronary artery bypass graft surgery. |
| Precautions |
|
Advanced renal disease: not recommended. Renal or hepatic dysfunction. Discontinue if renal or hepatic disease develops. History of GI bleed/ulcer. Bleeding disorders. Monitor CBC, hepatic, and renal function in chronic use; and for GI bleed/ulcer. Heart failure. Hypertension. Asthma. Alcoholism. Dehydrated. Elderly. Debilitated. Labor & delivery. Pregnancy (Cat.C). Nursing mothers: not recommended. |
| Interactions |
|
Potentiates methotrexate, lithium, protein bound drugs. Increased risk of GI bleed with aspirin, corticosteroids, smoking, anticoagulants. May antagonize, or increase risk of renal failure with ACEIs, diuretics. Monitor oral anticoagulants, antihypertensives. |
| Adverse Reactions |
|
GI upset, CNS effects, tinnitus, blurred vision, dysuria, edema, photosensitivity, GI ulcer/bleed, blood dyscrasias, renal or hepatic dysfunction, rash (discontinue if occurs). See literature re: risk of cardiovascular events. |
| How Supplied |
|
Caplets—100, 500 |
| Additional Resources |
|
• Related Prescribing Note |
|
|
|
|