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

Nalgesin

Active Ingredient:
Naproxen Sodium
Origin:
EU

Nalgesin (Naproxen Sodium)

Naproxen sodium, the active ingredient in Nalgesin, is a nonsteroidal anti-inflammatory drug presented as an oral dosage form for oral use. It is employed to relieve mild to moderate pain, reduce inflammation, and lower fever in adult patients.
GNH India supplies Nalgesin as a licensed, GDP‑compliant international pharmaceutical supplier serving hospitals, pharmacies and clinics worldwide.

Manufacturer / TM Owner

Krka, D.D., Novo Mesto

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Indications & Clinical Uses

Nalgesin (naproxen sodium) acts on inflammatory pathways to provide analgesic and antipyretic effects.

  • Mild to moderate pain: alleviates headache, dental pain, and postoperative discomfort.
  • Osteoarthritis: reduces joint swelling and improves mobility.
  • Rheumatoid arthritis: helps control chronic inflammation and pain.
  • Musculoskeletal pain: eases strain, sprain, and backache symptoms.
  • Dysmenorrhea: lessens menstrual cramps and associated discomfort.
  • Fever: lowers elevated body temperature in acute febrile states.

How It Works

  • Naproxen sodium non‑selectively inhibits cyclooxygenase‑1 and cyclooxygenase‑2 enzymes, decreasing the conversion of arachidonic acid to prostaglandins. The reduced prostaglandin synthesis diminishes inflammation, pain signaling, and fever generation at peripheral and central sites.

Side Effects

Adverse reactions may vary in frequency and severity.

Common Side Effects

  • Gastrointestinal upset: nausea, dyspepsia, or abdominal pain.
  • Headache or dizziness.
  • Mild skin rash or itching.
  • Diarrhea or constipation.
  • Elevated blood pressure in some patients.

Serious or Rare Side Effects

  • Gastrointestinal bleeding, ulceration, or perforation.
  • Cardiovascular events such as myocardial infarction or stroke.
  • Acute renal impairment or worsening of chronic kidney disease.
  • Severe skin reactions (e.g., Stevens‑Johnson syndrome).
  • Hepatic dysfunction with elevated liver enzymes.
  • Anaphylaxis or severe hypersensitivity reactions.

Precautions & Warnings

When prescribing Nalgesin, clinicians should consider individual risk factors and monitor for complications.

  • Assess gastrointestinal risk: avoid in patients with active ulcers or a history of GI bleeding.
  • Evaluate cardiovascular profile: use caution in those with heart disease or hypertension.
  • Monitor renal function: adjust use in patients with impaired kidney function.
  • Use the lowest effective dose for the shortest duration needed.
  • Avoid in individuals with known hypersensitivity to naproxen or other NSAIDs.
  • Store at ambient temperature: keep in the original container, protect from moisture and direct sunlight.

Avoid Interactions

Naproxen sodium can alter the effects of several co‑administered medicines.

Major Interactions (Avoid)

  • Anticoagulants (e.g., warfarin): increased risk of serious bleeding.
  • Other NSAIDs or aspirin: heightened gastrointestinal toxicity.
  • Selective serotonin reuptake inhibitors (SSRIs): amplified bleeding tendency.

Moderate Interactions (Monitor Closely):\n- ACE inhibitors or ARBs: possible reduction in antihypertensive effect and renal function.

  • Diuretics: may diminish diuretic efficacy and affect kidney function.
  • Lithium: naproxen can raise lithium serum concentrations, requiring close monitoring.

Frequently Asked Questions

Nalgesin, containing naproxen sodium, is indicated for relief of mild to moderate pain, reduction of inflammation in osteoarthritis and rheumatoid arthritis, management of musculoskeletal aches, treatment of dysmenorrhea, and lowering of fever associated with acute illnesses.

Naproxen sodium blocks the activity of cyclooxygenase‑1 and cyclooxygenase‑2 enzymes, which are essential for producing prostaglandins. By lowering prostaglandin levels, it reduces inflammation, diminishes pain signals, and helps bring down elevated body temperature.

The appropriate dose of Nalgesin is determined by the prescribing healthcare professional based on the patient’s condition, age, weight, and overall health status. Patients should follow the prescriber’s instructions and not adjust the dose on their own.

Safety of naproxen sodium during pregnancy and lactation has not been fully established. It should only be used if the potential benefit outweighs the risk, and under direct medical supervision. Breastfeeding mothers should consult their doctor 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, verifies trade or institutional credentials, and then provides pricing, availability, shipping details, and any necessary import documentation.

Nalgesin (naproxen sodium) generally has a longer half‑life than ibuprofen, allowing for less frequent dosing. Both belong to the NSAID class and share similar mechanisms, but naproxen may provide more sustained pain control, while ibuprofen often has a quicker onset. Choice depends on clinical judgment and patient tolerance.

Nalgesin should be stored at ambient temperature, preferably below 25 °C. Keep the tablets in their original packaging, protect them from moisture, heat, and direct sunlight to maintain potency throughout the shelf life.

Nalgesin is taken orally, usually with a full glass of water. It can be taken with food or milk to lessen possible stomach irritation, but patients should follow the specific instructions given by their healthcare provider.

The most serious risks include gastrointestinal bleeding or ulceration, cardiovascular events such as heart attack or stroke, severe kidney injury, and rare but life‑threatening skin reactions. Patients should be monitored for signs of these conditions and seek immediate medical attention if they occur.

Nalgesin should be avoided in individuals with known hypersensitivity to naproxen or other NSAIDs, active gastrointestinal ulcers, recent major cardiovascular events, severe renal or hepatic impairment, and in patients who are currently taking anticoagulants without medical supervision.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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