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

Dicloflex

Active Ingredient:
Diclofenac Sodium
Origin:
EU

Dicloflex (Diclofenac Sodium)

Dicloflex is a topical medication that contains the non‑steroidal anti‑inflammatory drug (NSAID) diclofenac sodium. It is formulated for cutaneous application and is marketed in the European Union. The product delivers diclofenac sodium through the skin to provide localized analgesic and anti‑inflammatory effects without systemic administration. It is intended for short‑term use on intact skin over painful joints or muscles, and it is supplied without a prescription in many EU countries.

Manufacturer / TM Owner

Inspharma D.O.O.

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Indications & Clinical Uses

Dicloflex is applied to the skin to manage localized pain and inflammation associated with musculoskeletal conditions.

  • Relief of mild to moderate pain from osteoarthritis of the knee or other joints.
  • Reduction of inflammation and discomfort from sprains, strains, and bruises.
  • Management of tendonitis or bursitis symptoms in the affected area.
  • Adjunctive therapy for postoperative or post‑traumatic pain where oral NSAIDs are unsuitable.
  • Temporary relief of back or shoulder muscle aches.

Side Effects

Topical diclofenac may cause skin‑related and systemic side effects, most of which are mild and reversible.

Common

  • Local skin irritation, redness, or itching at the application site.
  • Burning or stinging sensation shortly after application.
  • Dryness or peeling of the treated skin.
  • Mild headache.

Serious

  • Allergic skin reactions such as rash, hives, or swelling.
  • Severe skin ulceration or necrosis.
  • Signs of systemic NSAID toxicity (e.g., gastrointestinal bleeding, dizziness).
  • Liver enzyme elevation or hepatic dysfunction.

Precautions & Warnings

When using Dicloflex, certain precautions help minimize risks and ensure safe use.

  • Apply only to intact, unbroken skin and avoid mucous membranes.
  • Do not cover the treated area with occlusive dressings unless directed by a healthcare professional.
  • Limit use to the recommended duration, typically not exceeding 7‑10 days without medical advice.
  • Avoid use on large body surface areas to reduce systemic absorption.
  • Discontinue if signs of allergic reaction or severe skin irritation develop.
  • Consult a physician before use in patients with known cardiovascular, renal, or hepatic disease.
  • Keep out of reach of children; accidental ingestion may cause systemic NSAID effects.

Avoid Interactions

Dicloflex can interact with other medicines, especially those that affect bleeding, kidney function, or systemic NSAID exposure.

Avoid

  • Concurrent use of oral or injectable NSAIDs, aspirin, or anticoagulants (e.g., warfarin, clopidogrel) that increase bleeding risk.
  • Systemic corticosteroids or other anti‑inflammatory agents that may heighten gastrointestinal toxicity.
  • Other topical products containing diclofenac or similar NSAIDs, which could raise total diclofenac exposure.

Use with caution

  • Diuretics or ACE inhibitors in patients with renal impairment, as NSAIDs can affect kidney function.
  • Lithium therapy, because NSAIDs may increase lithium serum levels.
  • Methotrexate, as NSAIDs can reduce its clearance.
  • Antihypertensive medications, where NSAIDs might blunt their effect.

Frequently Asked Questions

Dicloflex is intended for short‑term relief of localized pain and inflammation associated with osteoarthritis, sprains, strains, tendonitis, bursitis, and minor muscle aches.

Clean and dry the affected area, then apply a thin layer of the gel and gently rub it in. Wash hands after use and avoid covering the area with airtight dressings unless advised.

Generally, use should not exceed 7‑10 days without medical supervision; prolonged use may increase systemic absorption and risk of side effects.

The most frequently reported effects are local skin irritation, redness, itching, burning sensation, and mild headache.

Discontinue if you develop severe skin reactions such as rash, swelling, blistering, or signs of systemic toxicity like stomach pain or unusual bleeding.

It is advisable to avoid simultaneous use of other NSAIDs, including oral diclofenac, aspirin, or ibuprofen, to reduce the risk of excessive NSAID exposure.

The safety of topical diclofenac during pregnancy or lactation has not been fully established; consult a healthcare professional before use.

Yes, using Dicloflex with anticoagulants such as warfarin or clopidogrel may increase bleeding risk and should be avoided or closely monitored.

Seek medical attention promptly, as systemic exposure to diclofenac can cause gastrointestinal or renal effects.

No, the product should only be applied to intact skin; applying it to cuts, abrasions, or irritated skin can increase irritation and systemic absorption.

Diclofenac sodium inhibits cyclooxygenase enzymes (COX‑1 and COX‑2), decreasing prostaglandin synthesis, which reduces inflammation and pain signals at the site of application.

Topical diclofenac is generally not recommended for children under 12 years of age unless directed by a physician.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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