Product image of Naproxen Sodium Aurobindo (Naproxen Sodium) supplied by GNH India

Naproxen Sodium Aurobindo

Active Ingredient:
Naproxen Sodium
Origin:
EU

Naproxen Sodium Aurobindo (Naproxen Sodium)

Naproxen sodium, the active ingredient in Naproxen Sodium Aurobindo, is a nonsteroidal anti‑inflammatory drug (NSAID) presented as an oral dosage form for systemic use. It is employed to relieve pain, reduce inflammation, and lower fever in adults and adolescents when indicated.

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

Manufacturer / TM Owner

Aurobindo Pharma B.V.

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Indications & Clinical Uses

Naproxen sodium is an NSAID that acts on inflammatory pathways to manage several painful and inflammatory conditions.

  • Musculoskeletal pain: alleviates discomfort associated with osteoarthritis, rheumatoid arthritis and other joint disorders.
  • Acute pain: provides relief for dental, postoperative or injury‑related pain.
  • Dysmenorrhea: reduces menstrual cramps and associated inflammation.
  • Fever: lowers elevated body temperature in febrile states.

How It Works

  • Naproxen sodium reversibly inhibits cyclooxygenase‑1 (COX‑1) and cyclooxygenase‑2 (COX‑2) enzymes, decreasing the conversion of arachidonic acid to prostaglandins. The reduction in prostaglandin synthesis leads to diminished inflammation, pain signaling, and fever generation at the site of tissue injury or infection.

Side Effects

Naproxen sodium may cause a range of adverse reactions, from mild to severe.

Common Side Effects

  • Gastrointestinal upset: dyspepsia, nausea, abdominal pain.
  • Headache or dizziness.
  • Mild skin rash or pruritus.
  • Elevated blood pressure.
  • Fluid retention or peripheral edema.

Serious or Rare Side Effects

  • Gastrointestinal ulceration or bleeding.
  • Severe renal impairment or acute kidney injury.
  • Cardiovascular events such as myocardial infarction or stroke.
  • Life‑threatening skin reactions (e.g., Stevens‑Johnson syndrome).
  • Anaphylaxis or severe hypersensitivity reactions.

Precautions & Warnings

Before initiating therapy, consider patient‑specific risk factors and monitor appropriately.

  • Assess gastrointestinal risk: evaluate history of ulcers or bleeding before use.
  • Monitor renal function: especially in patients with dehydration, heart failure or pre‑existing kidney disease.
  • Avoid in known hypersensitivity to naproxen or other NSAIDs.
  • Use caution in cardiovascular disease: weigh benefits against potential thrombotic risk.
  • Review concomitant anticoagulant or antiplatelet therapy to prevent excess bleeding.
  • Store at room temperature: keep in the original container, protect from moisture and heat.

Avoid Interactions

Naproxen sodium can interact with several drug classes, altering efficacy or safety.

Major Interactions (Avoid)

  • Anticoagulants (e.g., warfarin): increased risk of serious bleeding.
  • Other NSAIDs or COX‑2 inhibitors: heightened gastrointestinal toxicity.
  • Selective serotonin reuptake inhibitors (SSRIs): elevated hemorrhage risk.

Moderate Interactions (Monitor Closely)

  • ACE inhibitors or diuretics: may reduce renal function, especially in volume‑depleted patients.
  • Lithium: naproxen can raise lithium serum concentrations.
  • Methotrexate: concurrent use may increase methotrexate toxicity.

Frequently Asked Questions

Naproxen Sodium Aurobindo is an oral NSAID indicated for the relief of mild to moderate pain, reduction of inflammation in musculoskeletal disorders such as osteoarthritis and rheumatoid arthritis, treatment of dysmenorrhea, and the management of fever. It works by targeting inflammatory pathways to provide symptomatic control in these conditions.

Naproxen sodium exerts its effect by reversibly inhibiting the cyclooxygenase‑1 and cyclooxygenase‑2 enzymes, which are essential for the synthesis of prostaglandins. By lowering prostaglandin levels, the drug diminishes inflammation, pain signaling, and fever responses at the site of tissue injury or infection.

The specific dose of naproxen sodium is determined by the prescribing clinician based on the individual’s condition, age, renal function and other factors. Typical adult regimens range from 250 mg to 500 mg taken twice daily, but the exact amount and frequency must be set by a qualified healthcare professional.

Naproxen sodium is generally avoided during the third trimester of pregnancy because of potential risks to the fetus and prolonged labor. Use during the first two trimesters should only occur if the benefit outweighs the risk and under medical supervision. Limited data exist for breastfeeding, so a prescriber should evaluate safety before use.

To place an order, submit an enquiry on the product page at gnhindia.com, specifying the required quantity. GNH India works with hospitals, pharmacies and procurement teams worldwide, and will request verification of trade or institutional credentials. After confirmation, the team provides pricing, availability, shipping details (including any temperature requirements) and assists with import documentation.

Both naproxen and ibuprofen belong to the NSAID class and share similar mechanisms of COX inhibition. Naproxen has a longer half‑life, allowing twice‑daily dosing, whereas ibuprofen often requires three‑four times daily. Naproxen may provide more sustained pain control for chronic conditions, but individual response and safety profiles should guide selection.

Store the product at room temperature, preferably below 25 °C, in its original packaging to protect it from moisture and excessive heat. Keep the container tightly closed and out of reach of children. Do not expose the tablets to direct sunlight or humid environments, as this may affect stability.

Naproxen sodium is taken orally with a full glass of water. It may be taken with food or milk to lessen gastrointestinal discomfort, but absorption is not significantly affected. Swallow the tablet whole; do not crush or chew unless specifically instructed by a healthcare professional.

The most serious adverse events include gastrointestinal ulceration or bleeding, severe renal impairment, cardiovascular events such as heart attack or stroke, and life‑threatening skin reactions like Stevens‑Johnson syndrome. Patients should be monitored for signs of these conditions, especially if they have pre‑existing risk factors.

Naproxen sodium is contraindicated in individuals with known hypersensitivity to naproxen or other NSAIDs, active gastrointestinal ulcer or bleeding, severe heart failure, and in the third trimester of pregnancy. Caution is also advised for patients with uncontrolled hypertension, significant renal or hepatic disease, and those taking anticoagulants without close medical supervision.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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