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

Nefopam Arrow

Active Ingredient:
Nefopam Hydrochloride
Origin:
EU

Nefopam Arrow (Nefopam Hydrochloride)

Nefopam Hydrochloride, the active ingredient in Nefopam Arrow, is a non‑opioid central analgesic presented as an injectable solution for intramuscular and intravenous use. It is employed to manage acute, postoperative and musculoskeletal pain in adult patients requiring rapid analgesia.

GNH India supplies Nefopam Arrow as a licensed, GDP‑compliant international pharmaceutical supplier serving hospitals, pharmacies and clinics worldwide. The company adheres to stringent quality standards and provides regulatory documentation for global distribution. Our network ensures timely delivery and support for clinical procurement needs.

Manufacturer / TM Owner

Eugia Pharma (Malta) Ltd

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Indications & Clinical Uses

  • Nefopam Arrow is indicated for pain conditions that involve central sensitization and musculoskeletal injury.
  • Acute pain: provides rapid analgesia for short‑term severe pain.
  • Postoperative pain: reduces need for opioid rescue medication after surgery.
  • Musculoskeletal pain: alleviates pain associated with sprains, strains and soft‑tissue injuries.

How It Works

  • Nefopam inhibits the reuptake of norepinephrine, serotonin and dopamine in the central nervous system, thereby enhancing descending inhibitory pathways. It also blocks voltage‑sensitive sodium channels, which reduces neuronal excitability. These actions produce analgesic effects within minutes after intravenous administration and sustain relief for several hours.

Side Effects

Nefopam Arrow may be associated with a range of adverse reactions, varying from mild to severe.

Common Side Effects

  • Nausea: mild to moderate gastrointestinal upset, often transient.
  • Sweating: increased perspiration, usually temporary and dose‑related.
  • Tachycardia: elevated heart rate without underlying cardiac disease, may be self‑limiting.
  • Dizziness: sensation of light‑headedness or imbalance, often occurring shortly after dosing.

Serious or Rare Side Effects

  • Seizures: rare convulsive episodes, more likely with high plasma concentrations or pre‑existing seizure disorders.
  • Severe hypotension: marked drop in blood pressure that may require medical intervention.
  • Allergic reactions: skin rash, urticaria or anaphylaxis indicating hypersensitivity.

Precautions & Warnings

When prescribing Nefopam Arrow, clinicians should consider several precautionary measures to ensure safe use.

  • Assess cardiac history: evaluate for arrhythmias or uncontrolled hypertension before initiation.
  • Review seizure risk: avoid in patients with epilepsy or a history of convulsions.
  • Monitor blood pressure: observe for hypotension, especially after rapid intravenous administration.
  • Use caution in hepatic impairment: adjust therapy if liver function is compromised.
  • Avoid concomitant MAO inhibitors: increased risk of serotonin syndrome when combined.
  • Store at 2-8°C: keep refrigerated, protect from light, do not freeze or shake.

Avoid Interactions

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

Major Interactions (Avoid)

  • MAO inhibitors: risk of severe serotonin syndrome; concurrent use is contraindicated.
  • Tricyclic antidepressants: additive anticholinergic effects and heightened cardiovascular stimulation.
  • Anticonvulsants that lower seizure threshold: may increase seizure risk.

Moderate Interactions (Monitor Closely)

  • SSRIs and SNRIs: possible enhancement of serotonergic activity, monitor for serotonin syndrome.
  • Beta‑blockers: may blunt tachycardia response, observe heart rate.
  • Diuretics: potential for additive hypotensive effects, check blood pressure regularly.

Frequently Asked Questions

Nefopam Arrow is a prescription‑only injectable analgesic used to treat acute pain, postoperative pain, and musculoskeletal pain. It provides rapid, non‑opioid relief by acting on central pain pathways, making it suitable for short‑term management of moderate to severe pain in adult patients.

Nefopam Hydrochloride works by inhibiting the reuptake of norepinephrine, serotonin and dopamine, which enhances descending inhibitory pain pathways in the central nervous system. It also blocks voltage‑sensitive sodium channels, reducing neuronal excitability and thereby diminishing the transmission of pain signals.

The appropriate dose of Nefopam Arrow is determined by the prescribing clinician based on the patient’s condition, severity of pain, and route of administration. Healthcare professionals adjust the regimen to achieve effective analgesia while minimizing adverse effects.

Safety data for Nefopam Arrow 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 order Nefopam Arrow, submit an enquiry on the product page at gnhindia.com, specifying the required quantity. GNH India supplies hospitals, pharmacies and procurement teams worldwide, verifies trade or institutional credentials, and then provides pricing, availability, shipping details (including cold‑chain if needed) and import documentation.

Unlike opioids, Nefopam does not act on opioid receptors, reducing the risk of dependence, respiratory depression and constipation. It provides effective analgesia for many acute pain scenarios, but may cause different side‑effects such as tachycardia or sweating. Choice of therapy depends on patient factors and clinical judgment.

Nefopam Arrow should be stored at 2‑8 °C, kept refrigerated, protected from light, and never frozen or shaken. The product must be handled in a clean environment, and any unused portion should be discarded according to local regulations after the recommended storage period.

Nefopam Arrow is supplied as an injectable solution for intramuscular or intravenous administration. The route, rate of infusion, and total daily dose are determined by the prescribing clinician, who may adjust the regimen according to the patient’s response and tolerability.

Serious risks include seizures, severe hypotension, and allergic reactions such as anaphylaxis. Patients should be monitored for signs of convulsion, sudden drops in blood pressure, or any hypersensitivity symptoms, and medical attention should be sought immediately if these occur.

Nefopam Arrow should be avoided in patients with a known hypersensitivity to Nefopam or any excipients, those taking monoamine oxidase inhibitors, individuals with uncontrolled hypertension or significant cardiac arrhythmias, and patients with a history of seizures unless the benefits outweigh the risks.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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