Product image of Nurofen (Ibuprofen, Codeine Phosphate Hemihydrate) supplied by GNH India

Nurofen

Active Ingredient:
Ibuprofen, Codeine Phosphate Hemihydrate
Origin:
EU

Nurofen (Ibuprofen, Codeine Phosphate Hemihydrate)

Ibuprofen and Codeine Phosphate Hemihydrate, the active ingredients in Nurofen, are a nonsteroidal anti‑inflammatory drug (NSAID) and an opioid analgesic presented as an oral combination tablet for oral use. It treats mild to moderate pain, fever and related discomfort in adult patients.
GNH India supplies Nurofen as a licensed, GDP‑compliant international pharmaceutical supplier serving hospitals, pharmacies and clinics worldwide.

Manufacturer / TM Owner

Reckitt Benckiser Healthcare (Uk) Ltd

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Indications & Clinical Uses

Nurofen, a combination NSAID and opioid analgesic, is indicated for conditions that involve pain and fever.

  • Mild to moderate pain: provides effective analgesia for acute pain such as injury or postoperative discomfort.
  • Fever: reduces elevated body temperature associated with infection or inflammation.
  • Headache: alleviates tension‑type and migraine‑related head pain.
  • Dental pain: eases pain after dental procedures or toothache.
  • Musculoskeletal pain: relieves pain from strains, sprains and arthritis flares.
  • Menstrual pain: diminishes dysmenorrhea and associated cramps.

How It Works

  • Ibuprofen inhibits cyclooxygenase‑1 and cyclooxygenase‑2 enzymes, decreasing prostaglandin synthesis and thereby reducing inflammation, pain, and fever. Codeine phosphate hemihydrate acts as a mu‑opioid receptor agonist in the central nervous system, modulating pain perception and providing additional analgesic effect.

Side Effects

Adverse reactions may vary in frequency and severity.

Common Side Effects

  • Nausea: mild to moderate stomach upset.
  • Constipation: reduced bowel movements.
  • Dizziness: transient light‑headedness.
  • Drowsiness: increased sleepiness.
  • Stomach upset: dyspepsia or heartburn.
  • Headache: occasional mild headache.

Serious or Rare Side Effects

  • Gastrointestinal bleeding or ulceration: potentially life‑threatening.
  • Renal impairment: reduced kidney function.
  • Hepatic injury: elevated liver enzymes.
  • Respiratory depression: especially with high opioid exposure.
  • Severe allergic reactions: rash, swelling, anaphylaxis.
  • Seizures: rare neurologic events.

Precautions & Warnings

Before prescribing Nurofen, clinicians should consider several safety factors.

  • Assess renal function: avoid in patients with severe kidney disease.
  • Evaluate gastrointestinal risk: avoid in active peptic ulcer disease or history of GI bleeding.
  • Use cautiously with other CNS depressants: increased sedation and respiratory risk.
  • Monitor for signs of dependence: codeine may cause addiction with prolonged use.
  • Do not use in children under 12 without specialist guidance: safety data limited.
  • Store at room temperature: keep in the original pack, protect from moisture.

Avoid Interactions

Nurofen can interact with several drug classes, requiring careful management.

Major Interactions (Avoid)

  • Concurrent opioid analgesics: heightened risk of respiratory depression.
  • Additional NSAIDs or aspirin: increased gastrointestinal bleeding.
  • Anticoagulants (e.g., warfarin): amplified anticoagulant effect and bleeding.

Moderate Interactions (Monitor Closely)

  • Alcohol: may potentiate sedation and GI irritation.
  • CYP2D6 inhibitors (e.g., fluoxetine): can raise codeine plasma levels.
  • Diuretics: may affect renal clearance of ibuprofen.
  • ACE inhibitors or ARBs: combined use may reduce renal perfusion.

Frequently Asked Questions

Nurofen is a prescription oral tablet that combines ibuprofen and codeine phosphate hemihydrate. It is used to relieve mild to moderate pain such as headache, dental pain, musculoskeletal discomfort, menstrual cramps, and to reduce fever associated with infections or inflammatory conditions.

Ibuprofen blocks cyclooxygenase‑1 and‑2 enzymes, lowering prostaglandin production and thereby reducing inflammation, pain, and fever. Codeine acts on central mu‑opioid receptors, altering pain signal transmission in the brain and spinal cord to provide additional analgesia.

The specific dose and dosing schedule for Nurofen are determined by the prescribing clinician based on the patient’s age, weight, severity of pain, and medical history. Patients should follow the prescriber’s instructions and not exceed the recommended amount.

Safety of Nurofen in pregnancy or lactation has not been fully established. It should only be used if the potential benefit justifies the possible risk to the fetus or infant, and this decision must be made by a qualified healthcare professional.

To order Nurofen, 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 single‑ingredient NSAIDs, Nurofen adds codeine, offering stronger analgesia for moderate pain. Unlike pure opioid preparations, the ibuprofen component also reduces inflammation and fever, potentially allowing lower opioid doses and limiting opioid‑related side effects.

Nurofen tablets should be stored at room temperature, below 25 °C, in the original packaging to protect them from moisture and light. Keep the product out of reach of children and do not use after the expiry date.

Nurofen is taken orally with a full glass of water. It may be taken with or without food, although taking it with food can reduce stomach irritation. Swallow the tablet whole; do not crush or chew it.

Serious risks include gastrointestinal bleeding or ulceration, renal impairment, hepatic injury, severe allergic reactions, and respiratory depression, especially when combined with other CNS depressants or taken in excess.

Nurofen should be avoided in patients with known hypersensitivity to ibuprofen, codeine, or any component of the formulation, those with active peptic ulcer disease, severe renal or hepatic impairment, and in children under 12 years unless directed by a specialist.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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