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Piroxicam

NSAID (non-selective COX inhibitor, oxicam class) · Analgesic

Also known as Piroxicam betadex, Piroxicam cyclodextrin

START
20 mg OD with food; check baseline renal function, BP, and GI history; use PPI gastroprotection if GI risk factors
TYPICAL MAX
20 mg/day (40 mg x 2 days only for acute conditions)
STOP IF
GI bleeding, severe rash, jaundice, eGFR <30, signs of heart failure, CV event
WATCH
BP, renal function, LFTs, GI symptoms, signs of bleeding
CDSCO approvedSchedule HJan AushadhiATC M01AC01
Dose laddermg/d
10start20titrate40ceiling
Renal dose adjustmenteGFR mL/min/1.73m²
FULLStandard 20 mg OD; monitor BP and ren…60CAUTIONUse lowest effective dose; monitor c…30AVOIDAvoid - high risk of nephrotoxicity90

KDIGO 2024 + manufacturer label

Pharmacokineticsplasma · t hours
1.5hONSET4hPEAK2d1dDURATION
ONSET
1.5h · Onset of analgesia
PEAK
4h · Peak plasma concentration
2d · Very long half-life (45-50 hours)
DURATION
1d · Once-daily dosing covers 24h
EXCRETION
Urine (metabolites)
route + CYP
INTERACTIONS
12 major
incl. contraindicated
PREGNANCY
Avoid in third trimester; use only if clearly needed in first and second trimesters
FDA category + note
Top interactionssee all 12
  • AlcoholContraindicatedTextbook-citedKDT 7e · p950
  • MethylprednisoloneContraindicatedTextbook-citedKDT 7e · p950
  • CiprofloxacinSevereTextbook-citedKDT 7e · p949
  • DexamethasoneSevereTextbook-citedKDT 7e · p950
Available in India

313 branded formulations and 4 fixed-dose combinations. Look up specific brands in the Drugs workspace.

Jan Aushadhi — generic available at GoI pharmacies

Mechanism

Non-selective inhibition of cyclo-oxygenase-1 (COX-1) and cyclo-oxygenase-2 (COX-2), reducing prostaglandin synthesis throughout the body. The enolic acid structure provides long half-life enabling once-daily dosing.

Indications

Rheumatoid arthritisOsteoarthritisAnkylosing spondylitisAcute musculoskeletal disordersAcute gout

Dosing

Adult
20 mg once daily (usual dose); may use 10-20 mg daily. Acute conditions: 40 mg once daily x 2 days then 20 mg daily
Pediatric
Not recommended under 12 years; 12-17 years: limited data
Renal adjustment
Avoid if eGFR <30; use lowest effective dose if eGFR 30-60
Hepatic adjustment
Avoid in severe hepatic impairment; reduce dose in mild-moderate
Geriatric
Start at 10 mg/day; increased risk of GI bleeding and renal impairment
Max dose
20 mg/day (40 mg/day for first 2 days of acute conditions only)

Pharmacokinetics

Onset
1-2 hours
Peak effect
3-5 hours (Tmax); steady-state by day 7-12
Duration
24-48 hours
Half-life
45-50 hours (long half-life enables once-daily dosing)
Bioavailability
100%
Protein binding
99%
Metabolism
Hepatic CYP2C9 (major) and CYP3A4 (minor); hydroxylation and glucuronidation
Excretion
Urine (major, as metabolites); fecal (minor)

Contraindications

  • Active peptic ulcer disease or GI bleeding
  • History of GI perforation/ulcer/bleeding with NSAIDs
  • Severe heart failure
  • Severe renal impairment (eGFR <30)
  • Severe hepatic impairment
  • Third trimester pregnancy
  • Hypersensitivity to piroxicam or other NSAIDs
  • Aspirin-induced asthma

Side effects

Common
DyspepsiaNauseaAbdominal painDiarrheaConstipationFlatulenceHeadacheDizzinessRashEdema
Serious
  • GI bleeding, ulceration, perforation
  • Cardiovascular thrombotic events (MI, stroke)
  • Nephrotoxicity
  • Hepatotoxicity
  • Severe skin reactions (Stevens-Johnson, TEN)
  • Agranulocytosis
  • Anaphylaxis

Pregnancy & lactation

Pregnancy

Avoid in third trimester; use only if clearly needed in first and second trimesters

Lactation

Excreted in breast milk; use with caution during breastfeeding

Drug interactions

Alcohol
Contraindicated
Textbook-cited

Increased risk of gastric bleeding

Concurrent use is contraindicated

Source: KDT 7e · p950

Methylprednisolone
Contraindicated
Textbook-cited

Significantly increased GI bleeding risk.

Concurrent use is contraindicated; if unavoidable, add PPI

Source: KDT 7e · p950

Ciprofloxacin
Severe
Textbook-cited

Enhanced CNS toxicity including seizures.

Avoid concurrent use

Source: KDT 7e · p949

Dexamethasone
Severe
Textbook-cited

Significantly increased GI bleeding risk.

Concurrent use is contraindicated; if unavoidable, add PPI

Source: KDT 7e · p950

Glibenclamide
Severe
Textbook-cited

Hypoglycemia

Avoid concurrent use; substitute with paracetamol if analgesic needed

Source: KDT 7e · p949

Gliclazide
Severe
Textbook-cited

Hypoglycemia

Avoid concurrent use; substitute with paracetamol if analgesic needed

Source: KDT 7e · p949

Glimepiride
Severe
Textbook-cited

Hypoglycemia

Avoid concurrent use; substitute with paracetamol if analgesic needed

Source: KDT 7e · p949

Glipizide
Severe
Textbook-cited

Hypoglycemia

Avoid concurrent use; substitute with paracetamol if analgesic needed

Source: KDT 7e · p949

Heparin
Severe
Textbook-cited

Increased bleeding risk.

Avoid concurrent use

Source: KDT 7e · p949

Hydrocortisone
Severe
Textbook-cited

Significantly increased GI bleeding risk

Concurrent use is contraindicated; if unavoidable, add PPI

Source: KDT 7e · p950

Levofloxacin
Severe
Textbook-cited

Enhanced CNS toxicity, seizure risk.

Avoid concurrent use

Source: KDT 7e · p949

Moxifloxacin
Severe
Textbook-cited

Enhanced CNS toxicity, seizure risk

Avoid concurrent use

Source: KDT 7e · p949

Related guidelines

Ask House about Piroxicam

Continue into a citation-backed clinical answer with the drug context already attached.

Sources: KD Tripathi 7e, Goodman & Gilman 14e, Katzung, BNF·Verified: 2026-05-19 · House clinical team·Cockpit curated: 2026-05-19