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

Modifenac

Active Ingredient:
Diclofenac Sodium
Origin:
EU

Modifenac (Diclofenac Sodium)

Diclofenac Sodium, the active ingredient in Modifenac, is a nonsteroidal anti-inflammatory drug (NSAID) presented as an oral formulation for systemic use. It is employed to relieve pain and reduce inflammation in conditions such as osteoarthritis and rheumatoid arthritis, particularly in adult patients requiring symptomatic management.

GNH India supplies Modifenac as a licensed, GDP‑compliant international pharmaceutical supplier serving hospitals, pharmacies and clinics worldwide. The company adheres to stringent quality standards and provides reliable logistics for global distribution. All shipments are accompanied by full regulatory documentation.

Manufacturer / TM Owner

Teva B.V

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Indications & Clinical Uses

  • Modifenac, a diclofenac‑based NSAID, acts on inflammatory pathways to alleviate symptoms in several musculoskeletal conditions.
  • Pain: Provides symptomatic relief of mild to moderate pain.
  • Inflammation: Reduces swelling and inflammatory response in affected tissues.
  • Osteoarthritis: Improves joint function and decreases pain associated with osteoarthritis.
  • Rheumatoid arthritis: Helps control pain and inflammation in rheumatoid arthritis flares.

How It Works

  • Diclofenac sodium exerts its anti‑inflammatory and analgesic effects by reversibly inhibiting cyclooxygenase‑1 (COX‑1) and cyclooxygenase‑2 (COX‑2) enzymes. This inhibition decreases the conversion of arachidonic acid to prostaglandins, which are mediators of pain, fever and inflammation. By lowering prostaglandin synthesis, the drug diminishes peripheral sensitisation of nociceptors and reduces inflammatory exudate formation, leading to relief of pain and swelling.

Side Effects

Adverse reactions to Modifenac may vary in frequency and severity.

Common Side Effects

  • Gastrointestinal discomfort such as dyspepsia or nausea.
  • Headache.
  • Dizziness.
  • Elevated liver enzymes.

Serious or Rare Side Effects

  • Peptic ulcer disease or gastrointestinal bleeding.
  • Severe skin reactions, for example Stevens‑Johnson syndrome.
  • Hepatotoxicity or significant liver injury.
  • Renal impairment or acute kidney injury.

Precautions & Warnings

  • When prescribing Modifenac, clinicians should consider several precautionary measures to minimise risk.
  • Assess gastrointestinal risk: evaluate history of ulcers, bleeding or NSAID use.
  • Monitor liver function: perform baseline and periodic liver enzyme tests.
  • Check renal function: assess creatinine clearance before and during therapy.
  • Avoid in patients with known hypersensitivity to diclofenac or other NSAIDs.
  • Store at ambient temperature below 25°C: keep in original packaging, protect from moisture.

Avoid Interactions

Modifenac can interact with other medicines, altering its efficacy or safety profile.

Major Interactions (Avoid)

  • Anticoagulants (e.g., warfarin): increased risk of serious bleeding.
  • Selective serotonin reuptake inhibitors (SSRIs) or other serotonergic agents: heightened bleeding risk.

Moderate Interactions (Monitor Closely)

  • ACE inhibitors or diuretics: may reduce renal function, monitor kidney parameters.
  • Lithium: diclofenac can increase lithium levels, monitor serum concentration.
  • Methotrexate: reduced clearance may raise toxicity, monitor hepatic and renal function.

Frequently Asked Questions

Modifenac contains diclofenac sodium, an NSAID that is commonly prescribed to manage mild to moderate pain, reduce inflammation, and improve joint function in conditions such as osteoarthritis and rheumatoid arthritis. It may also be used for other acute musculoskeletal pains where an anti‑inflammatory effect is desired.

Diclofenac sodium works by reversibly inhibiting the cyclooxygenase enzymes COX‑1 and COX‑2, which are essential for converting arachidonic acid into prostaglandins. By lowering prostaglandin production, the drug decreases inflammation, pain signalling, and fever, providing symptomatic relief in affected tissues.

The appropriate dose of Modifenac is determined by the prescribing clinician based on the patient’s specific condition, severity of symptoms, age, renal and hepatic function, and any concomitant medications. Dosage regimens are individualized and should follow the prescriber’s instructions and local regulatory guidelines.

Safety of diclofenac during pregnancy and lactation has not been fully established. It is generally advised to avoid NSAIDs, including diclofenac, in the third trimester because of potential fetal cardiovascular effects. Breastfeeding mothers should consult their healthcare provider, as diclofenac can be excreted in breast milk.

To request Modifenac, submit an enquiry on the product page at gnhindia.com indicating the required quantity. GNH India supplies hospitals, pharmacies and procurement teams worldwide, and will ask for trade or institutional credentials. The sales team then provides pricing, availability, shipping details and any necessary import documentation.

Modifenac (diclofenac) is a potent NSAID with a relatively short half‑life, offering strong analgesic and anti‑inflammatory effects. Compared with ibuprofen, it often provides longer pain relief but may carry a higher risk of gastrointestinal and cardiovascular adverse events. Choice of NSAID should be based on individual risk factors and therapeutic goals.

Modifenac should be stored at ambient temperature below 25 °C, in its original packaging, and protected from moisture and direct sunlight. Keep the product out of reach of children and avoid storing it in bathrooms or other humid environments to maintain stability.

Modifenac is intended for oral administration. The tablet or capsule should be swallowed whole with a full glass of water, preferably with food or milk to minimise gastrointestinal irritation. Patients should follow the dosing schedule prescribed by their healthcare professional.

The most serious risks include gastrointestinal bleeding or ulceration, severe skin reactions such as Stevens‑Johnson syndrome, hepatotoxicity, and renal impairment. Cardiovascular events such as myocardial infarction or stroke may also occur, particularly with long‑term use or in patients with existing cardiovascular disease.

Modifenac should be avoided in individuals with known hypersensitivity to diclofenac or any NSAID, those with active peptic ulcer disease, severe heart failure, uncontrolled hypertension, or significant liver or kidney disease. It is also contraindicated in patients who have experienced serious cardiovascular events related to NSAID therapy.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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