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

Nefopam Viatris

Active Ingredient:
Nefopam Hydrochloride
Origin:
EU

Nefopam Viatris (Nefopam Hydrochloride)

Nefopam Hydrochloride, the active ingredient in Nefopam Viatris, is a central acting analgesic presented as an injectable solution for intramuscular and intravenous use. It provides relief from moderate acute pain and postoperative pain in adult patients, acting through multiple neurotransmitter pathways.

GNH India supplies Nefopam Viatris as a licensed, GDP‑compliant international pharmaceutical supplier serving hospitals, pharmacies and clinics worldwide, ensuring quality manufacturing and regulatory compliance across EU and global markets through robust quality systems and reliable logistics.

Manufacturer / TM Owner

Viatris Sante

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Indications & Clinical Uses

Nefopam Hydrochloride is indicated for pain management within the acute and postoperative pain pathways.

  • Moderate acute pain: provides effective analgesia for sudden, non‑chronic pain episodes, improving patient comfort and functional ability.
  • Postoperative pain: reduces pain intensity after surgical procedures, facilitating early mobilization and recovery in the postoperative period.
  • Trauma‑related pain: helps control pain following injuries such as fractures or soft‑tissue damage, supporting analgesic needs in emergency settings.

How It Works

  • Nefopam Hydrochloride exerts its central analgesic effect by inhibiting the reuptake of serotonin, norepinephrine and dopamine, thereby increasing synaptic concentrations of these neurotransmitters. It also blocks voltage‑gated sodium channels and reduces calcium influx in neuronal membranes, which diminishes neuronal excitability and pain signal transmission. The combined actions result in modulation of pain pathways without direct opioid receptor involvement.

Side Effects

Nefopam Hydrochloride may be associated with a range of adverse reactions, varying in frequency and severity.

Common Side Effects

  • Nausea: mild to moderate feeling of queasiness.
  • Sweating: increased perspiration without exertion.
  • Tachycardia: elevated heart rate.
  • Dry mouth: reduced salivation causing discomfort.

Serious or Rare Side Effects

  • Seizures: rare occurrence of convulsive episodes.
  • Severe hypotension: marked drop in blood pressure.
  • Allergic reactions: including rash, urticaria, or anaphylaxis.

Precautions & Warnings

When using Nefopam Hydrochloride, clinicians should observe specific precautions to ensure patient safety.

  • Cardiovascular monitoring: observe heart rate and blood pressure, especially in patients with pre‑existing cardiac conditions.
  • Seizure risk assessment: avoid use in individuals with a history of seizures or epilepsy.
  • Drug interactions: review concomitant medications that affect monoamine levels.
  • Renal/hepatic function: adjust use in patients with significant impairment.
  • Pregnancy and lactation: use only if potential benefit justifies potential risk, as safety data are limited.
  • Store at ambient temperature: keep vials below 25 °C, protect from light and moisture, and retain in original packaging.

Avoid Interactions

Nefopam Hydrochloride can interact with several medicines; awareness of major and moderate interactions helps prevent adverse events.

Major Interactions (Avoid)

  • MAO inhibitors: concurrent use may cause hypertensive crisis or serotonin syndrome.
  • Tricyclic antidepressants: increased risk of cardiovascular side effects and serotonin toxicity.
  • SSRIs/SNRIs: heightened potential for serotonin syndrome.

Moderate Interactions (Monitor Closely)

  • Antihypertensives: may enhance hypotensive effects.
  • Anticonvulsants: possible reduction in seizure threshold.
  • Diuretics: may increase risk of dehydration and electrolyte imbalance.

Frequently Asked Questions

Nefopam Viatris is used to relieve moderate acute pain and postoperative pain in adult patients. It is administered by injection and works as a non‑opioid central analgesic, helping to improve comfort after surgery or injury.

Nefopam Hydrochloride works by blocking the reuptake of serotonin, norepinephrine and dopamine, which raises their levels in the central nervous system. It also inhibits sodium channels and reduces calcium influx, decreasing neuronal excitability and pain signal transmission.

The appropriate dose of Nefopam Viatris is determined by the prescribing clinician based on the patient’s condition, age, weight, and response. Healthcare professionals adjust the dosage to achieve effective pain control while minimizing adverse effects.

Safety data for Nefopam Hydrochloride in pregnancy and lactation are limited, and the product is classified as having an unknown pregnancy category. It should only be used if the potential benefit justifies any potential risk to the fetus or infant, and under close medical supervision.

To order Nefopam Viatris, submit an enquiry on the product page at gnhindia.com with 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.

Nefopam is a non‑opioid central analgesic, whereas the most common alternatives for moderate pain are opioid analgesics such as morphine or tramadol. Compared with opioids, Nefopam does not cause respiratory depression and has a different side‑effect profile, but it may cause cardiovascular stimulation and carries a risk of seizures.

Nefopam Viatris should be stored at ambient temperature, preferably below 25 °C. Keep the vials in their original packaging, protect them from light and moisture, and avoid freezing. Follow standard aseptic handling procedures when preparing for injection.

Nefopam Viatris is administered by a healthcare professional as an intramuscular or intravenous injection. The route, rate, and volume are selected by the prescriber according to the clinical situation and patient characteristics.

Serious risks associated with Nefopam include seizures, severe hypotension, and allergic reactions such as rash, urticaria or anaphylaxis. Patients should be monitored for these events, especially if they have a history of epilepsy, cardiovascular disease, or known hypersensitivity.

Nefopam Viatris should be avoided in patients with known hypersensitivity to Nefopam or any excipients, those taking monoamine oxidase inhibitors, and individuals with uncontrolled hypertension, recent myocardial infarction, or a history of seizures unless the prescriber determines the benefits outweigh the risks.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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