Product image of Naproxene Sodique Teva (Naproxen Sodium) supplied by GNH India

Naproxene Sodique Teva

Active Ingredient:
Naproxen Sodium
Origin:
EU

Naproxene Sodique Teva (Naproxen Sodium)

Naproxen sodium, the active ingredient in Naproxene Sodique Teva, is a nonsteroidal anti‑inflammatory drug (NSAID) presented as an oral dosage form for oral use. It is employed to relieve pain, reduce fever, and diminish inflammation in adult patients with conditions such as osteoarthritis, rheumatoid arthritis, and dysmenorrhea.

GNH India supplies Naproxene Sodique Teva as a licensed, GDP‑compliant international pharmaceutical supplier serving hospitals, pharmacies and clinics worldwide, with a focus on quality assurance, regulatory compliance and reliable logistics and on‑time delivery.

Manufacturer / TM Owner

Teva Santé

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Indications & Clinical Uses

Naproxen sodium is an NSAID that reduces inflammation and pain in several musculoskeletal and systemic conditions.

  • Pain: provides relief from mild to moderate acute or chronic pain.
  • Fever: lowers elevated body temperature associated with inflammatory states.
  • Inflammation: decreases swelling and tenderness in inflamed tissues.
  • Osteoarthritis: improves joint function and reduces discomfort.
  • Rheumatoid arthritis: helps control disease‑related pain and stiffness.
  • Dysmenorrhea: alleviates menstrual‑related cramping and pain.

How It Works

  • Naproxen sodium reversibly inhibits cyclooxygenase‑1 (COX‑1) and cyclooxygenase‑2 (COX‑2) enzymes, which blocks the conversion of arachidonic acid to prostaglandins. By lowering prostaglandin synthesis, it reduces the inflammatory response, diminishes peripheral sensitization to pain, and lowers fever through central thermoregulatory pathways.

Side Effects

Adverse reactions may occur with naproxen sodium use.

Common Side Effects

  • Gastrointestinal upset: dyspepsia, nausea, or abdominal discomfort.
  • Headache: mild to moderate intensity.
  • Dizziness or vertigo.
  • Skin rash or pruritus.
  • Elevated liver enzymes.

Serious or Rare Side Effects

  • Gastrointestinal bleeding or ulcer perforation.
  • Renal impairment or acute kidney injury.
  • Cardiovascular events such as myocardial infarction or stroke.
  • Severe skin reactions (e.g., Stevens‑Johnson syndrome).
  • Hepatotoxicity or severe liver injury.

Precautions & Warnings

Before initiating therapy, consider the following safety measures.

  • Assess renal function: avoid or adjust use in patients with significant renal impairment.
  • Evaluate gastrointestinal risk: contraindicated in active peptic ulcer disease or history of GI bleeding.
  • Monitor cardiovascular status: use cautiously in patients with established heart disease or risk factors.
  • Review concomitant medications: avoid combined use with other NSAIDs or anticoagulants without supervision.
  • Pregnancy and lactation: consult a healthcare professional before use during pregnancy or breastfeeding.
  • Store at ambient temperature: keep in the original container, protect from moisture and direct sunlight.

Avoid Interactions

Naproxen sodium can interact with several drug classes; some require avoidance while others need close monitoring.

Major Interactions (Avoid)

  • Anticoagulants (e.g., warfarin): increased risk of serious bleeding.
  • Antiplatelet agents (e.g., clopidogrel): heightened bleeding tendency.
  • Selective serotonin reuptake inhibitors (SSRIs): additive risk of gastrointestinal hemorrhage.

Moderate Interactions (Monitor Closely)

  • ACE inhibitors or ARBs: may reduce renal perfusion and function.
  • Diuretics: potential for electrolyte disturbances and reduced efficacy.
  • Lithium: naproxen can raise lithium serum concentrations, requiring level checks.

Frequently Asked Questions

Naproxene Sodique Teva contains naproxen sodium, an NSAID indicated for the relief of mild to moderate pain, reduction of fever, and control of inflammation associated with conditions such as osteoarthritis, rheumatoid arthritis, and dysmenorrhea.

Naproxen sodium blocks the cyclooxygenase‑1 and cyclooxygenase‑2 enzymes, preventing the formation of prostaglandins that mediate pain, fever, and inflammation. This inhibition reduces the sensitization of nerve endings and lowers the body’s temperature set‑point during febrile states.

The appropriate dose is determined by the prescribing healthcare professional based on the patient’s condition, age, renal function, and other individual factors. Dosage instructions are provided on the prescription label and should be followed exactly as directed.

Use of naproxen sodium during pregnancy, especially in the third trimester, may pose risks to the fetus and should only be considered when clearly needed and prescribed by a qualified clinician. Breastfeeding mothers should consult their physician, as the drug can be excreted in breast milk.

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, verifies trade or institutional credentials, and then provides pricing, availability, shipping details and any necessary import documentation.

Both naproxen and ibuprofen belong to the NSAID class and share similar mechanisms of COX inhibition. Naproxen generally has a longer half‑life, allowing less frequent dosing, while ibuprofen may have a slightly faster onset. Safety profiles are comparable, but individual patient factors dictate the preferred choice.

Store the product at ambient temperature, below 25 °C, in the original packaging to protect it from moisture and light. Keep it out of reach of children and do not use after the expiration date printed on the label.

The medication is taken orally, usually with a full glass of water. It may be taken with food or milk to lessen gastrointestinal discomfort, but it should be swallowed whole and not crushed or chewed unless the prescriber advises otherwise.

Serious adverse events include gastrointestinal bleeding or ulcer perforation, cardiovascular complications such as heart attack or stroke, and renal impairment that can lead to acute kidney injury. Patients should be monitored for signs of these conditions and seek immediate medical attention if they occur.

Individuals with a known hypersensitivity to naproxen or other NSAIDs, active peptic ulcer disease, severe heart failure, uncontrolled hypertension, or significant renal or hepatic impairment should avoid using this medication unless directed by a healthcare professional.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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