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Enantyum 25 mg (Dexketoprofen Trometamol)

Enantyum 25 mg

Enantyum 25 mg contains the active ingredient dexketoprofen trometamol, a potent non-steroidal anti-inflammatory drug (NSAID) belonging to the arylpropionic acid class. Developed as the water-soluble tromethamine salt of dexketoprofen (the active S-enantiomer of ketoprofen), it provides rapid analgesia for mild to moderate acute pain. This review synthesizes evidence-based information on its pharmacology, clinical applications, safety profile, and risk mitigation strategies.

1. Pharmacology and Mechanism of Action

  • COX Inhibition: Dexketoprofen reversibly inhibits cyclooxygenase (COX)-1 and COX-2 enzymes, reducing prostaglandin synthesis. This suppresses inflammation, pain, and fever.
  • Rapid Absorption:
    • Oral solution/granules: Peak plasma concentration in 15–30 minutes when fasted 213.
    • Tablets: Peak in 30–50 minutes.
  • Half-life: ~1–2 hours, with excretion primarily renal (70–80%).

2. Approved Indications and Usage

Short-term symptomatic treatment (max 3–4 days) of:

  • Musculoskeletal pain: Acute muscle/joint injuries.
  • Dysmenorrhea: Primary menstrual pain.
  • Dental pain: Post-procedural toothache.
  • Other: Headache, post-traumatic pain.

Note: Not approved for chronic pain, fever, or pediatric use (<18 years)

3. Dosage and Administration

Patient GroupStandard DoseMax Daily DoseSpecial Adjustments
Adults (≥18 yrs)25 mg every 8 hrs75 mg (3 doses)None
Elderly25 mg every 12 hrs50 mg (2 doses)Increase to 75 mg if tolerated 
Hepatic/Renal Impairment (mild)25 mg every 12 hrs50 mgAvoid in moderate-severe disease 

Key Administration Guidelines:

  • Acute pain: Take 15–30 minutes before meals for faster absorption.
  • GI risk mitigation: Take with food if tolerability is a concern.
  • Granules/oral solution: Dissolve 1 sachet in water (contains 2.4 g sucrose; caution in diabetes)

4. Contraindications and Boxed Warnings

Absolute Contraindications:

  • Hypersensitivity: To dexketoprofen, aspirin, or other NSAIDs (risk of anaphylaxis).
  • Cardiovascular: Severe heart failure, post-CABG surgery.
  • Gastrointestinal: Active peptic ulcer, history of GI bleeding/perforation.
  • Renal/Hepatic: Severe impairment (CrCl <60 ml/min; Child-Pugh score ≥10).
  • Third-trimester pregnancy: Risk of fetal ductus arteriosus closure.

High-Risk Populations:

  • Asthma with nasal polyps: 10–20% risk of bronchospasm.
  • Inflammatory bowel disease: May exacerbate ulcerative colitis/Crohn’s.

5. Adverse Effects

Frequency-Based Classification:

FrequencyAdverse Effects
Common (≥1/100)Nausea, vomiting, abdominal pain, diarrhea, dyspepsia
Uncommon (≥1/1,000)Dizziness, headache, gastritis, rash, hypertension
Rare (≥1/10,000)GI ulcer/bleeding, anaphylaxis, acute renal failure, Stevens-Johnson syndrome

Serious Risks:

  • GI complications: Ulceration/bleeding (up to 1% in long-term users; higher in elderly).
  • Cardiovascular: Myocardial infarction/stroke risk ↑ with high doses or pre-existing CVD.
  • Renal toxicity: Acute kidney injury in dehydrated patients or those on diuretics.

6. Drug Interactions

High-Risk Combinations:

  • Anticoagulants (warfarin, heparin): ↑ Bleeding risk (avoid).
  • SSRIs (e.g., fluoxetine): ↑ GI ulcer risk.
  • ACE inhibitors (e.g., lisinopril): Reduced antihypertensive effect.
  • Methotrexate: ↑ Toxicity at doses >15 mg/week.

Other Notable Interactions:

  • Lithium: ↑ Plasma levels (risk of toxicity).
  • Diuretics: ↑ Nephrotoxicity.

7. Special Populations

  • Pregnancy:
    • First/second trimester: Use only if essential (possible embryotoxicity).
    • Third trimesterContraindicated (risk of premature ductal closure).
  • Lactation: Avoid (excretion in milk unknown).
  • Fertility: May impair ovulation (discontinue pre-conception).
  • Elderly: Start at 50 mg/day; ↑ monitoring for GI/renal/CV effects. 

8. Overdose and Management

  • Symptoms: Nausea, vomiting, lethargy, GI bleeding, acute renal failure.
  • Treatment:
    • Activated charcoal if recent ingestion.
    • Supportive care (IV fluids, antiemetics).
    • Hemodialysis ineffective (high protein binding).

9. Formulations and Storage

FormulationKey FeaturesStorage
Oral granules25 mg/sachet; contains sucrose (diabetes caution)≤30°C; protect from light
Film-coated tablets25 mg; no sucrose/sodium≤30°C; in original blister
Oral solution25 mg/sachet; contains methyl parahydroxybenzoateRoom temperature

10. Clinical Considerations and Conclusion

Enantyum 25 mg is a valuable option for acute pain due to its rapid onset and proven efficacy. However, its use mandates strict adherence to:

  1. Short duration (≤3–4 days) to minimize risks.
  2. Dose individualization in elderly/renal/hepatic impairment.
  3. Vigilance for GI/CV events, especially in high-risk patients.
  4. Avoidance in children, pregnancy, and severe comorbidities.

Conclusion: While dexketoprofen offers superior analgesia for acute conditions, its safety profile necessitates careful patient selection and adherence to prescribing guidelines. Always weigh benefits against risks, particularly cardiovascular and gastrointestinal hazards inherent to NSAIDs.

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