Product image of Nefopam Hydrochloride Brown & Burk Uk (Nefopam Hydrochloride) supplied by GNH India

Nefopam Hydrochloride Brown & Burk Uk

Active Ingredient:
Nefopam Hydrochloride
Origin:
EU

Nefopam Hydrochloride Brown & Burk Uk (Nefopam Hydrochloride)

Nefopam Hydrochloride, the active ingredient in Nefopam Hydrochloride Brown & Burk Uk, is a non‑opioid central acting analgesic presented as an oral tablet for oral administration. It is indicated for the management of moderate acute pain and postoperative pain in adult patients.

GNH India supplies Nefopam Hydrochloride Brown & Burk Uk as a licensed, GDP‑compliant international pharmaceutical supplier, providing the product to hospitals, pharmacies and clinics worldwide, originating from the EU market.

Manufacturer / TM Owner

Brown & Burk Uk Limited

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Indications & Clinical Uses

Nefopam Hydrochloride is employed to relieve pain conditions that involve central nociceptive pathways.

  • Moderate acute pain: provides analgesia for short‑term severe pain episodes.
  • Post‑operative pain: reduces pain following surgical procedures.
  • Traumatic injury pain: helps control pain after physical injuries.

How It Works

  • Nefopam Hydrochloride exerts its analgesic effect by inhibiting the reuptake of the monoamines norepinephrine, serotonin and dopamine within the central nervous system. This increase in synaptic concentrations modulates pain transmission pathways and produces antispasmodic activity, resulting in reduced perception of pain without acting on opioid receptors. The drug does not bind to opioid receptors and therefore avoids typical opioid‑related tolerance.

Side Effects

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

Common Side Effects

  • Nausea: mild to moderate feeling of sickness.
  • Dry mouth: reduced salivation causing throat discomfort.
  • Sweating: increased perspiration without exertion.
  • Dizziness: transient light‑headedness.
  • Constipation: reduced bowel movements.
  • Blurred vision: temporary visual disturbances.

Serious or Rare Side Effects

  • Tachycardia: rapid heart rate that may require monitoring.
  • Seizures: convulsive episodes, especially in predisposed individuals.
  • Severe hypotension: marked drop in blood pressure.
  • Allergic reactions: rash, itching, or anaphylaxis.
  • Agranulocytosis: rare drop in white blood cells.

Precautions & Warnings

When prescribing Nefopam Hydrochloride, clinicians should consider several safety precautions to minimize risk.

  • Assess renal function: adjust use in patients with severe renal impairment.
  • Monitor hepatic function: use with caution in liver disease.
  • Avoid in uncontrolled hypertension: drug may increase blood pressure.
  • Use cautiously in seizure disorders: may lower seizure threshold.
  • Pregnancy and lactation: safety not established; avoid unless benefit outweighs risk.
  • Store at ambient temperature: keep in original packaging, protect from moisture and light.

Avoid Interactions

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

Major Interactions (Avoid)

  • MAO inhibitors: risk of serotonin syndrome.
  • SSRIs or SNRIs: combined use may precipitate serotonin toxicity.
  • Tricyclic antidepressants: increased risk of cardiovascular side effects.

Moderate Interactions (Monitor Closely)

  • Antihypertensive agents: may reduce blood‑pressure‑lowering effect.
  • Anticholinergic drugs: additive dry‑mouth and constipation.
  • CYP450 inhibitors: possible increase in nefopam plasma levels.

Frequently Asked Questions

Nefopam Hydrochloride is a prescription‑only, non‑opioid central acting analgesic indicated for the relief of moderate acute pain and for managing pain after surgical procedures. It works by modulating neurotransmitter activity in the central nervous system, providing analgesia without engaging opioid receptors.

The drug inhibits the reuptake of three key monoamines—norepinephrine, serotonin and dopamine—thereby increasing their concentrations at synaptic sites in the brain and spinal cord. This elevation modifies pain signal transmission and produces antispasmodic effects, resulting in reduced perception of pain.

The appropriate dose of Nefopam Hydrochloride is determined by the prescribing clinician based on the patient’s condition, age, weight, renal and hepatic function, and other individual factors. Dosage regimens are not standardized in this description and should follow the prescriber’s instructions and local labeling.

The safety of Nefopam Hydrochloride during pregnancy and lactation has not been established. It is classified as pregnancy category unknown, and use is generally avoided unless the potential benefit justifies the potential risk to the fetus or infant. Breastfeeding mothers should consult their healthcare provider.

To place an order, visit the product page on gnhindia.com, enter the required quantity, and submit the enquiry form. 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 opioid analgesics, Nefopam provides pain relief without the risk of opioid‑related dependence, respiratory depression or constipation. Unlike NSAIDs, it does not inhibit cyclo‑oxygenase enzymes, so it lacks typical gastrointestinal or platelet‑related side effects. Its unique monoamine‑reuptake inhibition offers an alternative mechanism for moderate pain control.

Nefopam Hydrochloride tablets should be stored at ambient temperature, preferably below 25 °C, in the original packaging to protect them from moisture, light and humidity. Keep the product out of reach of children and do not store in areas with excessive heat or direct sunlight.

The medication is supplied as an oral tablet and is taken by mouth with

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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