Product image of Naklofen (Diclofenac Sodium) supplied by GNH India

Naklofen

Active Ingredient:
Diclofenac Sodium
Origin:
EU

Naklofen (Diclofenac Sodium)

Diclofenac sodium, the active ingredient in Naklofen, is a nonsteroidal anti-inflammatory drug (NSAID) presented as an injectable solution for intramuscular use. It is employed to relieve mild to moderate pain, reduce inflammation in musculoskeletal conditions, and manage postoperative discomfort in adult patients under medical supervision as prescribed by a qualified healthcare professional.

GNH India supplies Naklofen as a licensed, GDP‑compliant international pharmaceutical supplier serving hospitals and clinics worldwide, with a focus on quality assurance, regulatory compliance, and reliable cold‑chain logistics for injectable products.

Manufacturer / TM Owner

Krka, D.D., Novo Mesto

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Indications & Clinical Uses

Diclofenac sodium is used to treat pain and inflammation associated with musculoskeletal and postoperative conditions.

  • Mild to moderate pain: provides analgesia by reducing inflammatory mediators, improving patient comfort during acute injury or disease.
  • Inflammatory musculoskeletal conditions: decreases swelling and pain in disorders such as osteoarthritis, rheumatoid arthritis, and acute sprains, facilitating mobility.
  • Post‑operative pain: helps control pain after surgical procedures, allowing earlier ambulation and reduced reliance on opioid analgesics.
  • Acute sprains and strains: reduces localized pain and inflammation, supporting early rehabilitation and functional recovery.

How It Works

  • Diclofenac sodium exerts its anti‑inflammatory and analgesic effects by reversibly inhibiting cyclooxygenase enzymes COX‑1 and COX‑2. This inhibition blocks the conversion of arachidonic acid to prostaglandins, which are key mediators of inflammation, pain, and fever. By lowering prostaglandin synthesis at the site of injury, the drug diminishes peripheral sensitization and reduces the inflammatory response. The effect is localized to inflamed tissues, providing targeted relief while preserving normal prostaglandin functions elsewhere.

Side Effects

Like other NSAIDs, injectable diclofenac may be associated with a range of adverse reactions.

Common Side Effects

  • Injection site pain: mild discomfort or erythema at the intramuscular injection site.
  • Gastrointestinal upset: nausea, dyspepsia, or abdominal discomfort may occur.
  • Headache: transient mild to moderate headache reported by some patients.
  • Dizziness: occasional light‑headedness or vertigo, usually self‑limiting.
  • Elevated liver enzymes: mild, reversible increases in hepatic transaminases may be observed.

Serious or Rare Side Effects

  • Severe gastrointestinal bleeding: ulceration or hemorrhage that can be life‑threatening and requires immediate medical attention.
  • Cardiovascular events: increased risk of myocardial infarction or stroke, particularly with prolonged or high‑dose therapy.
  • Renal impairment: acute kidney injury or worsening of chronic kidney disease may develop.
  • Severe skin reactions: Stevens‑Johnson syndrome or toxic epidermal necrolysis, presenting with extensive rash and mucosal involvement.
  • Anaphylaxis: rare systemic allergic reaction characterized by hypotension, bronchospasm, and possible airway compromise.

Precautions & Warnings

When using intramuscular diclofenac, clinicians should observe several precautionary measures to minimize risk.

  • Assess renal function: evaluate baseline kidney status before initiating therapy.
  • Monitor hepatic enzymes: check liver function tests periodically during treatment.
  • Evaluate cardiovascular risk: consider history of heart disease or stroke before use.
  • Avoid in active ulcer disease: contraindicated in patients with active gastrointestinal ulceration.
  • Use lowest effective dose: prescribe the minimal dose needed for symptom control.
  • Store at 2-8°C: keep refrigerated, protect from light, do not freeze or shake.

Avoid Interactions

Diclofenac sodium can interact with several medicines, altering efficacy or safety.

Major Interactions (Avoid)

  • Anticoagulants (e.g., warfarin): increased risk of serious bleeding, requiring close INR monitoring and possible dose adjustment.
  • Other NSAIDs or COX‑2 inhibitors: additive gastrointestinal toxicity that can lead to ulceration or bleeding.
  • High‑dose aspirin: heightened bleeding tendency and potential for renal impairment when combined.

Moderate Interactions (Monitor Closely)

  • ACE inhibitors or ARBs: may reduce renal protective effects and impair kidney function, especially in patients with pre‑existing renal disease.
  • Diuretics: potential for reduced diuretic efficacy and electrolyte imbalance, necessitating periodic assessment of fluid and electrolyte status.
  • Lithium: diclofenac can raise lithium levels, requiring serum monitoring and possible dose modification.
  • Methotrexate: may increase methotrexate toxicity, monitor blood levels and watch for hepatic or bone marrow suppression.

Frequently Asked Questions

Naklofen is an injectable form of diclofenac sodium that is prescribed to manage mild to moderate pain, reduce inflammation in musculoskeletal disorders such as osteoarthritis or rheumatoid arthritis, and control postoperative pain following surgical procedures. It is typically used in hospital or clinical settings where rapid onset of analgesia is required.

Diclofenac sodium works by reversibly inhibiting the cyclooxygenase enzymes COX‑1 and COX‑2, which are essential for converting arachidonic acid into prostaglandins. Prostaglandins mediate inflammation, pain, and fever, so reducing their production lessens these symptoms at the site of injury or inflammation.

The specific dose of Naklofen is determined by the prescribing clinician based on the patient’s condition, weight, and overall health status. Because it is an injectable formulation, the prescriber will decide the appropriate volume and concentration to administer intramuscularly.

Safety data for diclofenac sodium during pregnancy and lactation are limited. Generally, NSAIDs are avoided in the third trimester because of potential fetal complications, and caution is advised during breastfeeding. Healthcare providers should evaluate the risk‑benefit ratio before prescribing to pregnant or nursing mothers.

To request Naklofen, submit an enquiry on the product page at gnhindia.com, specifying the required quantity. GNH India works with hospitals, pharmacies, and procurement teams worldwide, verifies trade or institutional credentials, and then provides pricing, availability, shipping details—including cold‑chain handling if needed—and necessary import documentation.

Naklofen delivers diclofenac sodium via intramuscular injection, offering a faster onset of action compared with oral NSAIDs such as ibuprofen or naproxen. Its injectable route can be advantageous for patients unable to take oral medication, but the safety profile regarding gastrointestinal, cardiovascular, and renal risks remains similar to other NSAIDs.

Naklofen must be stored at 2‑8 °C in a refrigerator, protected from light, and should never be frozen or shaken. The product should be kept in its original packaging until use to maintain stability and potency.

Naklofen is given as an intramuscular injection by a qualified healthcare professional. The injection site is typically a large muscle such as the gluteus maximus or deltoid, using aseptic technique to minimize infection risk and ensure proper absorption.

Serious risks include severe gastrointestinal bleeding, cardiovascular events such as myocardial infarction or stroke, acute renal impairment, life‑threatening skin reactions like Stevens‑Johnson syndrome, and rare anaphylactic reactions. Patients should be monitored closely for signs of these complications, especially during prolonged therapy.

Naklofen is contraindicated in patients with known hypersensitivity to diclofenac or other NSAIDs, active gastrointestinal ulceration or bleeding, severe renal or hepatic impairment, and those with a history of serious cardiovascular events. It should also be avoided in patients receiving anticoagulant therapy unless the benefits outweigh the risks.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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