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

Motusol

Active Ingredient:
Diclofenac Sodium
Origin:
EU

Motusol (Diclofenac Sodium)

Diclofenac sodium, the active ingredient in Motusol, is a nonsteroidal anti‑inflammatory drug presented as a topical formulation for external use. It is employed to relieve pain and reduce inflammation associated with musculoskeletal conditions, arthritis and soft‑tissue injuries. The medication is applied directly to the affected skin area, allowing localized drug delivery while minimizing systemic exposure.

GNH India supplies Motusol as a licensed, GDP‑compliant international pharmaceutical supplier serving hospitals, pharmacies, clinics and research institutions worldwide. The company ensures reliable logistics and strict quality assurance throughout the supply chain.

Manufacturer / TM Owner

Teva Uk Limited

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Indications & Clinical Uses

  • Diclofenac sodium is used topically to manage inflammatory and painful conditions of the musculoskeletal system.
  • Musculoskeletal pain: provides localized analgesia and reduces inflammation at the site of pain.
  • Arthritis: alleviates joint swelling and stiffness, improving mobility.
  • Soft‑tissue inflammation: diminishes swelling and erythema in tendons, bursae or bruised areas.

How It Works

  • Diclofenac sodium exerts its anti‑inflammatory effect by reversibly inhibiting cyclooxygenase‑1 (COX‑1) and cyclooxygenase‑2 (COX‑2) enzymes in peripheral tissues. This inhibition blocks the conversion of arachidonic acid to prostaglandins, which are mediators of pain, fever and inflammation. Topical delivery concentrates the drug in the dermal and subdermal layers, achieving therapeutic concentrations at the target site while limiting systemic exposure.

Side Effects

Topical diclofenac may cause local and systemic adverse reactions, which are categorized by frequency and severity.

Common Side Effects

  • Skin irritation: redness, itching or burning at the application site.
  • Dryness: mild peeling or flaking of the skin.
  • Pruritus: localized itching.
  • Mild headache: occasional transient headache.

Serious or Rare Side Effects

  • Severe allergic reaction: angioedema, urticaria or anaphylaxis requiring immediate medical attention.
  • Contact dermatitis: intense rash or blistering beyond mild irritation.
  • Systemic toxicity: gastrointestinal ulceration or bleeding, though rare with topical use.

Precautions & Warnings

  • When using Motusol, observe the following precautions to ensure safe and effective therapy.
  • Avoid application on broken or infected skin: limit use to intact epidermis.
  • Do not cover treated area with occlusive dressings unless directed by a healthcare professional.
  • Limit exposure to sunlight: avoid prolonged UV radiation on treated skin.
  • Monitor for signs of systemic NSAID effects: gastrointestinal discomfort, cardiovascular symptoms.
  • Pregnancy and lactation: consult a physician before use, as safety data are limited.
  • Store below 25°C: keep in original container, protect from moisture and light.

Avoid Interactions

Diclofenac sodium can interact with other medicines, altering its safety or effectiveness.

Major Interactions (Avoid)

  • Anticoagulants (e.g., warfarin): increased risk of bleeding.
  • Lithium: diclofenac may raise lithium serum levels, risking toxicity.
  • Methotrexate: reduced clearance leading to enhanced toxicity.

Moderate Interactions (Monitor Closely)

  • ACE inhibitors or ARBs: may diminish renal function, especially in volume‑depleted patients.
  • Diuretics: potential for reduced kidney perfusion.
  • Selective serotonin reuptake inhibitors (SSRIs): modestly increased bleeding risk.

Frequently Asked Questions

Motusol is a topical formulation of diclofenac sodium indicated for the relief of musculoskeletal pain, reduction of inflammation in arthritis, and treatment of soft‑tissue inflammatory conditions such as tendonitis or bursitis.

Diclofenac sodium inhibits the cyclooxygenase enzymes COX‑1 and COX‑2, which reduces the synthesis of prostaglandins—key mediators of pain, fever and inflammation. By limiting prostaglandin production at the site of application, it provides localized analgesic and anti‑inflammatory effects.

The appropriate dose of Motusol is determined by the prescribing healthcare professional based on the severity of symptoms, the area to be treated and individual patient factors. Patients should follow the specific instructions provided by their prescriber.

Safety data for topical diclofenac in pregnancy and lactation are limited. Women who are pregnant, planning to become pregnant, or breastfeeding should discuss potential risks and benefits with their physician before using Motusol.

To request Motusol, submit an enquiry on the product page at gnhindia.com specifying the required quantity. GNH India supplies hospitals, pharmacies and procurement teams worldwide, verifies trade or institutional credentials, and then provides pricing, availability, shipping details and any necessary import documentation.

Motusol delivers diclofenac directly to the skin, achieving high local concentrations while minimizing systemic exposure compared with oral NSAIDs. This can reduce the risk of gastrointestinal and cardiovascular side effects, but topical therapy may be less suitable for widespread systemic inflammation.

Motusol should be stored below 25 °C in its original packaging. Keep the container tightly closed, protect it from moisture and direct light, and avoid freezing to maintain product stability.

Apply a thin layer of Motusol to clean, dry, intact skin over the affected area, typically 2–4 times daily as directed by a healthcare professional. Gently rub the gel in until it disappears; do not cover with occlusive dressings unless advised.

Serious risks include severe allergic reactions such as angioedema or anaphylaxis, extensive contact dermatitis, and, rarely, systemic NSAID toxicity leading to gastrointestinal ulceration or bleeding. Immediate medical attention is required if any of these occur.

Motusol should be avoided in individuals with known hypersensitivity to diclofenac or other NSAIDs, those with active skin infections or open wounds at the application site, and patients with a history of severe cardiovascular, renal or gastrointestinal disease unless specifically approved by a physician.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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