Product image of Naofid (Nimesulide) supplied by GNH India

Naofid

Active Ingredient:
Nimesulide
Origin:
EU

Naofid (Nimesulide)

Nimesulide, the active ingredient in Naofid, is a non‑steroidal anti‑inflammatory drug (NSAID) presented as an oral tablet for oral use. It provides analgesic and anti‑inflammatory effects for mild to moderate pain and inflammatory conditions such as osteoarthritis and dysmenorrhea in adult patients, and is marketed in the European Union.

GNH India supplies Naofid as a licensed, GDP‑compliant international pharmaceutical supplier serving hospitals, pharmacies, clinics and procurement teams worldwide. Our distribution network ensures consistent quality and regulatory compliance across multiple regions.

Manufacturer / TM Owner

Velka Hellas S.A.

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Indications & Clinical Uses

Nimesulide is an NSAID used to manage pain and inflammation in several clinical settings.

  • Mild to moderate pain: reduces pain intensity in conditions such as headache, dental pain, or postoperative discomfort.
  • Osteoarthritis: alleviates joint pain and improves functional mobility.
  • Dysmenorrhea: relieves menstrual cramps and associated discomfort.

How It Works

  • Nimesulide selectively inhibits cyclo‑oxygenase‑2 (COX‑2), decreasing the conversion of arachidonic acid to prostaglandins that mediate pain, fever and inflammation. By sparing COX‑1 activity, it aims to preserve gastric mucosal protection while providing anti‑inflammatory and analgesic effects. The drug is rapidly absorbed after oral administration, reaches peak plasma concentrations within 1–2 hours, and is metabolized primarily in the liver to inactive metabolites that are excreted in urine.

Side Effects

Nimesulide may cause a range of adverse reactions, varying from mild to serious.

Common Side Effects

  • Gastrointestinal discomfort: nausea, dyspepsia, abdominal pain or loss of appetite.
  • Headache: mild to moderate intensity, often transient.
  • Dizziness: transient sensation of light‑headedness or vertigo.
  • Skin rash: mild erythema, pruritus or localized urticaria.

Serious or Rare Side Effects

  • Hepatotoxicity: significant elevation of liver enzymes, hepatitis or liver failure.
  • Severe skin reactions: Stevens‑Johnson syndrome, toxic epidermal necrolysis or widespread bullous eruptions.
  • Renal impairment: reduced kidney function, acute interstitial nephritis or renal failure.
  • Allergic anaphylaxis: sudden swelling, bronchospasm, hypotension or shock.

Precautions & Warnings

When prescribing Nimesulide, clinicians should consider several precautionary measures to minimize risk.

  • Indication limitation: use only for short‑term treatment of mild to moderate pain or inflammation.
  • Hepatic monitoring: assess liver function before initiating therapy and periodically during use.
  • Renal caution: avoid in patients with existing kidney disease or dehydration.
  • Gastro‑intestinal risk: use with caution in individuals with a history of ulcers or bleeding.
  • Drug interactions: review concomitant medications that may increase bleeding or affect liver enzymes.
  • Pregnancy and lactation: avoid use during pregnancy and breastfeeding due to unknown safety.
  • Store at ambient temperature: keep below 25°C in the original packaging, protected from moisture.

Avoid Interactions

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

Major Interactions (Avoid)

  • Anticoagulants (e.g., warfarin): increased risk of bleeding.
  • Other NSAIDs or COX‑2 inhibitors: additive gastrointestinal toxicity.
  • Hepatotoxic drugs (e.g., isoniazid, methotrexate): heightened liver injury risk.

Moderate Interactions (Monitor Closely)

  • ACE inhibitors or diuretics: possible reduction in renal function.
  • Lithium: increased serum lithium levels.
  • Corticosteroids: enhanced risk of ulceration.
  • Antihypertensives: potential attenuation of blood pressure control.

Frequently Asked Questions

Naofid contains Nimesulide, an NSAID indicated for short‑term relief of mild to moderate pain, osteoarthritis‑related joint discomfort, and dysmenorrhea. It is prescribed to reduce inflammation and provide analgesia in adult patients when other treatments are insufficient.

Nimesulide works by selectively inhibiting the cyclo‑oxygenase‑2 (COX‑2) enzyme, which reduces the synthesis of prostaglandins responsible for pain, fever, and inflammation. This COX‑2 selectivity aims to maintain gastric protection while delivering anti‑inflammatory and analgesic effects.

The dosage of Naofid is determined by the prescribing clinician based on the patient’s specific condition, severity of symptoms, and relevant clinical guidelines. Patients should follow the prescribed regimen and any instructions on the medication label.

Safety of Nimesulide during pregnancy and lactation has not been established. It is generally avoided in pregnant or nursing women unless the potential therapeutic benefit justifies the potential risk, and only under close medical supervision.

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.

Compared with non‑selective NSAIDs, Nimesulide’s COX‑2 selectivity may lower the risk of gastric irritation but it still carries potential hepatic and renal adverse effects. Choice of NSAID depends on individual patient risk factors, therapeutic goals and clinician judgment.

Naofid should be stored at ambient temperature below 25 °C, in its original packaging, protected from moisture and direct sunlight. Proper storage helps maintain the tablet’s stability and potency throughout its shelf life.

Naofid is taken orally, usually with a full glass of water. It may be taken with or without food as directed by the prescriber, and patients should adhere to the dosing schedule indicated on the prescription label.

The most serious adverse events linked to Naofid include hepatotoxicity (elevated liver enzymes, hepatitis, or liver failure), severe skin reactions such as Stevens‑Johnson syndrome or toxic epidermal necrolysis, and significant renal impairment. Prompt medical attention is required if any of these symptoms appear.

Naofid should be avoided in individuals with known hypersensitivity to Nimesulide or other NSAIDs, patients with severe hepatic or renal disease, active peptic ulcer disease, and those who are pregnant or breastfeeding unless a clear benefit outweighs the risk.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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