Product image of Olfen Patch (Diclofenac Sodium) supplied by GNH India

Olfen Patch

Active Ingredient:
Diclofenac Sodium
Origin:
EU

Olfen Patch (Diclofenac Sodium)

Diclofenac Sodium, the active ingredient in Olfen Patch, is a nonsteroidal anti‑inflammatory drug (NSAID) presented as a topical patch for cutaneous use. It reduces pain and inflammation in musculoskeletal conditions and is applied to the skin of adults.

GNH India supplies Olfen Patch as a licensed, GDP‑compliant international pharmaceutical supplier serving hospitals, pharmacies and clinics worldwide.

Manufacturer / TM Owner

Teva B.V

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Indications & Clinical Uses

Diclofenac Sodium is an NSAID that works locally to relieve pain and inflammation in musculoskeletal and joint conditions.

  • Localized musculoskeletal pain: provides targeted analgesia and reduces inflammation at the application site.
  • Osteoarthritis of the knee: alleviates joint pain and improves function when applied over the affected knee.
  • Post‑operative incision pain: diminishes discomfort and swelling after minor surgical procedures.

How It Works

  • Diclofenac Sodium inhibits cyclooxygenase‑1 and cyclooxygenase‑2 enzymes in the skin, decreasing the synthesis of prostaglandins that mediate inflammation, pain, and fever. By limiting prostaglandin production at the site of application, the patch delivers localized anti‑inflammatory and analgesic effects while minimizing systemic exposure.

Side Effects

Adverse reactions may occur with topical diclofenac use. Most are mild and limited to the skin, but rare systemic events have been reported.

Common Side Effects

  • Skin irritation: redness or discomfort at the application site.
  • Pruritus: itching of the treated area.
  • Burning sensation: transient warmth or stinging on the skin.

Serious or Rare Side Effects

  • Allergic dermatitis: severe rash, swelling, or blistering.
  • Stevens‑Johnson syndrome or toxic epidermal necrolysis: life‑threatening skin reactions.
  • Systemic NSAID toxicity: gastrointestinal ulceration, renal impairment, or cardiovascular events in susceptible individuals.

Precautions & Warnings

Before using Olfen Patch, consider the following safety measures.

  • Assess skin integrity: ensure the area is clean, intact, and free of lesions before application.
  • Avoid use on broken or infected skin: damaged skin may increase systemic absorption and irritation.
  • Limit duration: follow prescriber instructions and do not exceed the recommended wear time.
  • Monitor for systemic NSAID effects: watch for gastrointestinal, renal, or cardiovascular symptoms.
  • Avoid concurrent topical NSAIDs: using more than one NSAID patch can increase local irritation.
  • Store at room temperature: keep in the original packaging, protect from moisture and direct sunlight.

Avoid Interactions

Diclofenac Sodium can interact with other medicines, affecting safety or efficacy.

Major Interactions (Avoid)

  • Anticoagulants (e.g., warfarin): increased risk of bleeding.
  • Other NSAIDs or COX‑2 inhibitors: additive gastrointestinal and renal toxicity.
  • Lithium: diclofenac may raise lithium serum levels, risking toxicity.

Moderate Interactions (Monitor Closely)

  • ACE inhibitors or diuretics: may reduce renal function, especially in dehydrated patients.
  • Methotrexate: diclofenac can raise methotrexate concentrations, requiring dose adjustment.

Frequently Asked Questions

Olfen Patch is a transdermal system that delivers diclofenac sodium to the skin. It is used to relieve localized pain and inflammation associated with musculoskeletal conditions such as minor injuries, osteoarthritis of superficial joints, and postoperative incision discomfort.

Diclofenac sodium blocks the cyclooxygenase‑1 and cyclooxygenase‑2 enzymes in the skin, reducing the production of prostaglandins that cause pain, swelling, and fever. By acting directly at the site of application, the patch provides targeted anti‑inflammatory and analgesic effects.

The specific dose and wear time of Olfen Patch are determined by the prescribing healthcare professional based on the patient’s condition, age, and treatment response. Patients should follow the prescriber’s instructions and not exceed the recommended duration of use.

Safety data for topical diclofenac during pregnancy and lactation are limited. Healthcare providers usually weigh the potential benefits against possible risks before prescribing. Women who are pregnant, planning pregnancy, or breastfeeding should discuss alternative options with their clinician.

To request Olfen Patch, 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, and any necessary import documentation.

Olfen Patch delivers diclofenac directly to the skin, offering localized pain relief with lower systemic exposure compared with oral tablets. This can reduce the risk of gastrointestinal and cardiovascular side effects common to oral NSAIDs, but skin irritation may be more frequent with the patch.

Olfen Patch should be stored at room temperature, below 25 °C, in its original packaging. Keep the patches away from moisture, excessive heat, and direct sunlight to maintain their adhesive properties and drug stability.

The patch is applied to clean, dry, and intact skin on the affected area. Remove the protective liner, press the patch firmly for several seconds, and ensure full contact. Follow the prescriber’s guidance on how long the patch should remain in place and when to replace it.

Serious risks include severe allergic skin reactions such as Stevens‑Johnson syndrome or toxic epidermal necrolysis, systemic NSAID toxicity (e.g., gastrointestinal bleeding, renal impairment, cardiovascular events), and rare cases of photosensitivity. Immediate medical attention is required if these symptoms develop.

Olfen Patch should be avoided in individuals with known hypersensitivity to diclofenac or any component of the patch, those with broken or infected skin at the application site, and patients with a history of severe NSAID‑related adverse events such as gastrointestinal ulcers or cardiovascular disease unless specifically advised by a physician.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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