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Piroxicam

Class
Nonsteroidal anti-inflammatory drugs
Subclass
Oxicams
Substance name
Piroxicam
Brand names
Feldene®
Common formulations
Capsule
Dosage and administration
Adults patients
Symptomatic relief
Osteoarthritis
20 mg PO daily
Rheumatoid arthritis
20 mg PO daily
Treatment
Treatment of osteoarthritis
20 mg PO daily
Indications for use
Labeled indications
Adults
Symptomatic relief of osteoarthritis
Symptomatic relief of rheumatoid arthritis
Treatment of osteoarthritis
Treatment of rheumatoid arthritis
Safety risks
Contraindications
A recent history of CABG surgery
Aspirin-sensitive asthma or the aspirin triad
Chronic use of piroxicam and a history of or active Gastrointestinal disease
Salicylate hypersensitivity or NSAID hypersensitivity
Warnings and precautions
Abnormal LFTs
Use caution with hepatic disease.
Fluid retention
Use caution with renal disease, or renal impairment.
Hematologic disorder
Use caution with a history of immunosuppression or other risk factors for developing hematological disease (e.g., coagulopathy or hemophilia or thrombocytopenia).
Thromboembolism
Use caution with known heart disease.
Specific populations
Renal impairment
eGFR 20-50 mL/min/1.73 m²
Avoid use as much as possible. Monitor serum creatinine. Monitor for reduction in intrarenal autocoid synthesis.
eGFR 10-20 mL/min/1.73 m²
Avoid use as much as possible. Monitor serum creatinine. Monitor for reduction in intrarenal autocoid synthesis.
eGFR < 10 mL/min/1.73 m²
Avoid use as much as possible. Monitor serum creatinine. Monitor for reduction in intrarenal autocoid synthesis.
Renal replacement therapy
Continuous renal replacement
Avoid use as much as possible. Dose as in eGFR 10-20 mL/min/1.73 m². Monitor serum creatinine. Monitor for reduction in intrarenal autocoid synthesis.
Intermittent hemodialysis
Avoid use as much as possible. Dose as in eGFR < 10 mL/min/1.73 m². Monitor serum creatinine. Monitor for reduction in intrarenal autocoid synthesis.
Peritoneal dialysis
Avoid use as much as possible. Dose as in eGFR < 10 mL/min/1.73 m². Monitor serum creatinine. Monitor for reduction in intrarenal autocoid synthesis.
Hepatic impairment
Any severity
Reduce dose.
Substantial chronic alcohol consumption
Use with caution.
Pregnancy and breastfeeding
Pregnancy
< 20 weeks of gestation • Australia Category: C
Use only if benefits outweigh potential risks.
20-30 weeks of gestation • Australia Category: C
Use only if benefits outweigh potential risks. Monitor for oligohydramnios. If oligohydramnios occurs, discontinue NSAID and treat it properly.
> 30 weeks of gestation • Australia Category: C
Avoid use.
Breastfeeding
Consider alternative agents that may be safer.
Low excretion in breastmilk (5-25%).
Undetectable levels in breastfed infants.
No overt adverse effects reported in breastfed infants.
Adverse reactions
Very common > 10%
↑ LFTs
Common 1-10%
AKI, abdominal pain, constipation, diarrhea, dizziness, flatulence, generalized pruritus, headache, heartburn, loss of appetite, nausea, skin rash, tinnitus, vomiting
Rare < 0.1%
Agranulocytosis, aplastic anemia, hemolytic anemia
Unknown frequency
Acute liver failure, acute intermittent porphyria, acute pancreatitis, alopecia, anaphylaxis, asthma, bronchospasm, cerebrovascular accident, colitis, congestive heart failure, DRESS syndrome, ↓ WBC count, ↓ blood neutrophil count, ↓ fertility, ↓ platelet count, ↓ serum sodium, edema, erythema multiforme, erythroderma, esophagitis, fixed drug eruption, fluid retention, gastrointestinal bleeding, gastrointestinal perforation, gastrointestinal ulceration, glomerulonephritis, gouty arthritis, hepatic necrosis, hepatitis, hypertension, inflammatory bowel disease, ↑ serum potassium, jaundice, myocardial infarction, osteoarthritis, pancytopenia, pemphigus vulgaris, photosensitivity of skin, ↑bleeding time, renal failure, bleeding, blurred vision, systemic lupus erythematosus, Stevens-Johnson syndrome, toxic epidermal necrolysis, tubulointerstitial nephritis
Interactions
Drug(s)
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