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MEDICINE MONOGRAPH CODE: [7.3] ID: TIP-MED-000105

Aceclofenac

Active Ingredient / Scientific Identity: Aceclofenac • Class: Non-Steroidal Anti-Inflammatory Drug (NSAID); Phenylacetic Acid Derivative (Preferential COX-2 Inhibitor, Prodrug of 4'-Hydroxyaceclofenac & Diclofenac)

⚖️ Compare Profile
Generic / Entity NameAceclofenac ([7.3])
Verified Indian Brands / RefVoveran (Novartis), Dynapar (Troikka), Reactin (Cipla)
Pharmacological ClassNon-Steroidal Anti-Inflammatory Drug (NSAID); Phenylacetic Acid Derivative (Preferential C
Available Dosage FormsOral Film-Coated Tablets: 100 mg; Sustained/Controlled-Release (SR/CR) Tablets: 200 mg
Regulatory ClassificationSchedule H Prescription Drug (To be sold by retail on the prescription of a Registere
Key Warning & Review DateRenal: Contraindicated in severe CKD (eGFR <30 mL/min); avoid in moderate CKD (eGFR 30–59 mL/min). Hepatic: Reduce initial do
Reviewed: 2026-11-10
Safety Matrix:⚖️ Legal Status: Schedule H Prescription Drug (To be sold by retail o✔️ Standard Clinical Dispensing Precautions

1. Clinical & Scientific Overview

Aceclofenac (TIP-MED-000105, Reference Code [7.3]) is classified under Pain, Inflammation, Rheumatology & Gout Medicines (Ch 07) as a Non-Steroidal Anti-Inflammatory Drug (NSAID); Phenylacetic Acid Derivative (Preferential COX-2 Inhibitor, Prodrug of 4'-Hydroxyaceclofenac & Diclofenac). Within the Indian regulatory and compendial framework, it is governed under Schedule H Prescription Drug (To be sold by retail on the prescription of a Registered Medical Practitioner only — Drugs Rules 1945).

Verified Indian Market Examples / Compendial Status:
Voveran (Novartis), Dynapar (Troikka), Reactin (Cipla)
Representative Indian Market Examples (Edition 2.7 Ch 07 [7.3], p. 80): Zerodol (Ipca), Hifenac (Intas), Aceclo (Aristo), Movon; In FDC with Paracetamol: Zerodol-P, Hifenac-P; With Paracetamol + Serratiopeptidase: Zerodol-SP; With Thiocolchicoside: Zerodol-MR; Sustained-Release: Zerodol-CR 200 mg — Strengths & Dosage Forms: Oral Film-Coated Tablets: 100 mg; Sustained/Controlled-Release (SR/CR) Tablets: 200 mg
Dosage Forms & Available Strengths:
Oral Film-Coated Tablets: 100 mg; Sustained/Controlled-Release (SR/CR) Tablets: 200 mg
Routes: Oral / Parenteral / Topical as specified by formulation

3. Mechanism of Action & Pharmacodynamics

Non-Steroidal Anti-Inflammatory Drug (NSAID); Phenylacetic Acid Derivative (Preferential COX-2 Inhibitor, Prodrug of 4'-Hydroxyaceclofenac & Diclofenac) acting on target receptor/enzyme pathways in Pain, Inflammation, Rheumatology & Gout Medicines (Ch 07): clinical efficacy is mediated via Non-Steroidal Anti-Inflammatory Drug (NSAID); Phenylacetic Acid Derivative (Preferential COX-2 Inhibitor, Prodrug of 4'-Hydroxyaceclofenac & Diclofenac) for Osteoarthritis, rheumatoid arthritis, ankylosing spondylitis, acute lumbago (low back pain), dental pain, and postoperative musculoskeletal inflammation..

4. Therapeutic Indications & Evidence-Supported Uses

  • Osteoarthritis, rheumatoid arthritis, ankylosing spondylitis, acute lumbago (low back pain), dental pain, and postoperative musculoskeletal inflammation

🇮🇳 Jurisdiction & Indication Note: Indications and schedules reflect Indian compendial and regulatory records (CDSCO / Indian Pharmacopoeia & NFI / NLEM 2022). Where international reference labels (US FDA DailyMed / NCBI StatPearls) are cited for pharmacokinetic or mechanistic parameters, international approvals do not automatically imply CDSCO approval in India.

5. Educational Dosage Context, Formulations & Administration

Educational Dosing & Regimen Summary: General Adult Reference: 100 mg twice daily (morning and evening after meals), or 200 mg SR/CR once daily (Maximum 200 mg/day). Follow physician prescription.

Administration & Meal Timing: Take WITH or immediately AFTER food with a full glass of water. | Twice daily after breakfast and dinner (for 100 mg IR) or once daily after dinner (for 200 mg SR/CR).

6. Pharmacokinetics, Metabolism & Renal/Hepatic Adjustment

Absorption & Disposition:
Absorption, distribution, metabolism, and excretion follow class pharmacokinetic profile; verify patient renal/hepatic function.
Metabolism & Biotransformation:
Renal: Contraindicated in severe CKD (eGFR <30 mL/min); avoid in moderate CKD (eGFR 30–59 mL/min). Hepatic: Reduce initial dose to 100 mg once daily in mild-to-moderate hepatic impairment; contraindicated in severe liver disease.
Elimination & Renal Adjustment:
Renal: Contraindicated in severe CKD (eGFR <30 mL/min); avoid in moderate CKD (eGFR 30–59 mL/min). Hepatic: Reduce initial dose to 100 mg once daily in mild-to-moderate hepatic impairment; contraindicated in severe liver disease.
Hepatic Impairment Considerations:
Renal: Contraindicated in severe CKD (eGFR <30 mL/min); avoid in moderate CKD (eGFR 30–59 mL/min). Hepatic: Reduce initial dose to 100 mg once daily in mild-to-moderate hepatic impairment; contraindicated in severe liver disease.

7. Contraindications, Precautions & High-Risk Warnings

Contraindications & Red-Flag Precautions:
  • Same cardiovascular, renal, and gastrointestinal contraindications as Diclofenac! (Because aceclofenac is partially metabolised to diclofenac in vivo, it is contraindicated in established IHD, heart failure, stroke, PAD, active peptic ulcer, eGFR <30–45 mL/min, pregnancy 3rd trimester, and Dengue).

Key Clinical Precautions: Renal: Contraindicated in severe CKD (eGFR <30 mL/min); avoid in moderate CKD (eGFR 30–59 mL/min). Hepatic: Reduce initial dose to 100 mg once daily in mild-to-moderate hepatic impairment; contraindicated in severe liver disease.

8. Adverse Effects Profile

Common & Mechanism-Related Adverse Effects:
  • Dyspepsia, abdominal pain, nausea, diarrhoea, dizziness, mild elevation of hepatic transaminases (slightly better upper GI tolerability than conventional diclofenac/piroxicam, but ulcer risk remains significant).
  • GI ulceration and haemorrhage, acute kidney injury, cardiovascular thrombotic events, Stevens-Johnson syndrome, hepatotoxicity.
Serious / Dose-Limiting Adverse Effects:
  • Monitor for severe hypersensitivity, organ toxicity, or dose-limiting adverse events.

9. Major Drug–Drug, Drug–Food & Drug–Herb Interactions

  • Blunts antihypertensive efficacy of ACE inhibitors, ARBs, beta-blockers, and diuretics ('Triple Whammy' AKI risk)
  • Increases bleeding risk with aspirin, clopidogrel, DOACs, warfarin, and steroids
  • Increases lithium, digoxin, and methotrexate toxicity
  • Combined with fluoroquinolones (ciprofloxacin), increases CNS seizure risk

10. Clinical Monitoring, Patient Counselling & Storage

Clinical & Laboratory Monitoring: Monitor clinical response, baseline renal/hepatic parameters, and relevant serum biomarkers.

Pharmacist Patient Counselling Points:

  • Patient Counselling Checklist: Zerodol-P and Zerodol-SP are among the top-selling prescription tablets in Indian orthopaedic OPDs. Remind patients that '-P' and '-SP' already contain 325 mg of Paracetamol, to take them strictly after meals, and to stop using them as soon as acute joint pain resolves rather than refilling them monthly like a blood pressure pill.
  • Meal & Clock Timing Instruction: Take WITH or immediately AFTER food with a full glass of water. (Twice daily after breakfast and dinner (for 100 mg IR) or once daily after dinner (for 200 mg SR/CR).)
  • Missed Dose Protocol: Take after food if remembered; skip if close to next dose. Never double.
  • Geriatric Dispensing Pearl: Ensure gastroprotection (Pantoprazole 40 mg OD) if prescribed short-term to an elderly patient, and strictly screen out use in CGHS beneficiaries with CKD, heart failure, or coronary stents.

Storage, Stability & Dispensing Safeguards: Store below 25°C–30°C in original moisture- and light-resistant packaging out of reach of children. Available forms: Oral Film-Coated Tablets: 100 mg; Sustained/Controlled-Release (SR/CR) Tablets: 200 mg

11. Visual Pharmacology & Mechanism Diagram (svg-v339-01-adme-12-step-journey)

THE 12-STEP ORAL DRUG JOURNEY THROUGH THE HUMAN BODY (LADME) Note: IV bolus enters Step 6 directly (F = 100%); Sublingual & Transdermal routes bypass Step 4–5 Portal First-Pass Metabolism 1. Oral Administration • Tablet / Capsule swallowed • Gastric emptying to duodenum pH 1.5–3.5 (Stomach) 2. Disintegration & Dissolution • Tablet breaks into granules • API dissolves in GI fluid Noyes-Whitney Dissolution Rate 3. GI Epithelial Absorption • Crosses intestinal villi • Passive / Active / P-gp efflux Small Intestine (Large Surface Area) 4. Portal Circulation • Mesenteric veins → Portal vein • Delivers blood to liver sinusoids Pre-systemic Venous Conduit 5. First-Pass Metabolism • Gut & hepatic CYP450 extraction • High: GTN, Propranolol, Morphine Determines Bioavailability (F = f_a × (1-E_H)) 6. Systemic Circulation • Hepatic vein → IVC → Heart • Unbound vs Albumin-bound drug Only FREE drug is active 7–8. Tissue Distribution (Vd) • Capillary permeation to organs • Blood-Brain & Placental barriers Vd = Dose / C_0 (L or L/kg) 9. Target Site of Action • Receptors (GPCR, Ion channel) • Enzymes & Carrier Transporters Pharmacodynamic Effect (E_max, EC50) 10. Hepatic Biotransformation • Phase I (CYP450 Oxidation/Hydrolysis) • Phase II (Glucuronidation/Sulfation) Converts lipophilic drug → hydrophilic metabolite 11. Renal & Biliary Elimination • Nephron: Filtration + Secretion − Reabsorption • Biliary excretion & Enterohepatic recycling Total Clearance CL_tot = CL_renal + CL_hepatic 12. Excretion from the Body • Urine (Primary polar metabolite route) • Bile/Faeces, Expired Air, Sweat, Milk Elimination Half-Life t1/2 = (0.693 × Vd) / CL
svg-v339-01-adme-12-step-journey — 8.1 Complete 12-Step Journey of an Orally Administered Drug (ADME): Figure 8.1: The 12-step physiological journey of a typical orally administered solid dosage form through Liberation, Absorption, Distribution, Metabolism, and Excretion (LADME). Note: Parenteral (IV), sublingual, and inhalational routes bypass gastrointestinal absorption and/or hepatic first-pass metabolism.

12. Authoritative References, Regulatory Sources & Editorial Disclaimer

Primary Compendial & Guideline Reference: Indian Pharmacist Desk Reference — Professional Edition 2.7 (2026–27) • Ch 07 [7.3] (p. 80)

Official Verification Portals: Indian Pharmacopoeia Commission (IPC) & National Formulary of India (NFI) • Central Drugs Standard Control Organization (CDSCO) • Ministry of Health & Family Welfare — NLEM 2022 • NCBI Bookshelf / StatPearls Pharmacology Reference • DailyMed (US FDA Official Prescribing Reference)

Last Medically & Pharmaceutically Reviewed: 2026-11-10 • Verification Status: HANDBOOK_SOURCE_CONTENT

Educational & Clinical Disclaimer: This reference profile is published solely for pharmacy education, academic study, and professional clinical reference. It does not substitute for patient-specific clinical judgement, qualified specialist oncology/medical supervision, or official CDSCO/IP prescribing information. Never self-medicate with prescription, Schedule H/H1/X, NDPS, or oncology medicines.