Product image of Nefalgic (Nefopam Hydrochloride) supplied by GNH India

Nefalgic

Active Ingredient:
Nefopam Hydrochloride
Origin:
EU

Nefalgic (Nefopam Hydrochloride)

Nefopam Hydrochloride, the active ingredient in Nefalgic, is a non‑opioid central acting analgesic presented as an injectable solution for intramuscular and intravenous use. It is indicated for the management of moderate pain, including post‑operative pain, in adult patients.
GNH India supplies Nefalgic as a licensed, GDP‑compliant international pharmaceutical supplier serving hospitals, pharmacies and clinics worldwide.

Manufacturer / TM Owner

Medis Adria D.O.O.

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Indications & Clinical Uses

Nefopam, a non‑opioid central acting analgesic, is employed in the treatment of moderate pain conditions, particularly after surgery.

  • Moderate acute pain: provides effective analgesia without opioid‑related side effects.
  • Post‑operative pain: reduces the need for additional opioid rescue medication following surgical procedures.
  • Procedural pain: helps control discomfort during minor surgical or diagnostic interventions.

How It Works

  • Nefopam inhibits the reuptake of serotonin, norepinephrine, and dopamine, while also blocking sodium channels and modulating NMDA receptors. This multimodal action reduces neuronal excitability and pain signal transmission in the central nervous system, resulting in analgesic effects without engaging opioid pathways.

Side Effects

Nefopam may cause a range of adverse reactions, most of which are mild and transient.

Common Side Effects

  • Nausea: mild to moderate gastrointestinal upset.
  • Dry mouth: reduced salivation leading to throat discomfort.
  • Sweating: increased perspiration, especially during the first doses.
  • Dizziness: transient light‑headedness or vertigo.
  • Tachycardia: elevated heart rate without significant hemodynamic compromise.
  • Constipation: reduced bowel motility in some patients.

Serious or Rare Side Effects

  • Seizures: rare occurrence, particularly in patients with a seizure history.
  • Severe hypotension: marked drop in blood pressure requiring medical attention.
  • Anaphylactic reaction: acute allergic response with rash, bronchospasm, or angioedema.
  • Agranulocytosis: very rare hematologic abnormality with risk of infection.

Precautions & Warnings

When prescribing Nefopam, clinicians should consider several safety aspects.

  • Renal impairment: monitor renal function and adjust therapy if needed.
  • Hepatic impairment: use cautiously and observe liver enzyme levels.
  • Cardiovascular disease: watch for tachycardia or arrhythmias during treatment.
  • Seizure disorder: avoid or use with heightened vigilance due to seizure risk.
  • Concomitant MAO inhibitors: contraindicated because of potential hypertensive crisis.
  • Store at room temperature: keep in the original container, protect from moisture and light.

Avoid Interactions

Nefopam can interact with several drug classes, requiring attention to avoid adverse outcomes.

Major Interactions (Avoid)

  • MAO inhibitors: may precipitate hypertensive crisis.
  • SSRIs or SNRIs: increased risk of serotonin syndrome.
  • Anticholinergic agents: additive anticholinergic burden leading to severe dryness and urinary retention.

Moderate Interactions (Monitor Closely)

  • Beta‑blockers: may mask tachycardia induced by Nefopam.
  • Diuretics: potential electrolyte disturbances when combined.
  • General anesthetics: additive central nervous system effects requiring dose adjustment.

Frequently Asked Questions

Nefalgic contains nefopam hydrochloride, a non‑opioid central acting analgesic indicated for the relief of moderate pain, especially pain that follows surgical procedures. It is used in adult patients when opioid therapy is not required or as an adjunct to reduce opioid consumption.

Nefopam works by inhibiting the reuptake of serotonin, norepinephrine, and dopamine, while also blocking sodium channels and modulating NMDA receptors. This combination reduces neuronal excitability and pain signal transmission in the central nervous system, providing analgesia without engaging opioid receptors.

The specific dose and administration schedule of Nefalgic are determined by the prescribing clinician based on the patient’s condition, severity of pain, and clinical response. Healthcare professionals adjust the regimen according to individual therapeutic needs.

Safety data for nefopam hydrochloride in pregnancy and lactation are limited. It should only be used if the potential benefit justifies any potential risk to the fetus or infant, and the decision must be made by a qualified healthcare provider.

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.

Unlike opioids, nefopam does not act on opioid receptors, reducing the risk of respiratory depression, dependence, and constipation. It provides comparable analgesia for moderate pain but may cause different side effects such as sweating or tachycardia, which should be considered when selecting therapy.

Nefalgic should be stored at room temperature, below 25 °C, in its original packaging. Protect the product from moisture and direct light to maintain stability and potency throughout its shelf life.

Nefalgic is supplied as an injectable solution for intramuscular or intravenous administration. The route, injection site, and infusion rate are determined by the prescribing clinician, who follows standard aseptic techniques and monitors the patient during and after administration.

Serious risks, though rare, include seizures, severe hypotension, anaphylactic reactions, and agranulocytosis. Patients should be monitored for neurological changes, sudden drops in blood pressure, signs of allergic reaction, and any unexplained infections, especially during the initial treatment period.

Nefalgic is contraindicated in patients with known hypersensitivity to nefopam or any formulation components, those taking monoamine oxidase inhibitors, or individuals with a history of seizures unless benefits outweigh risks. Clinicians should also avoid use in patients with uncontrolled cardiovascular disease without careful monitoring.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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