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

Nefopam Panpharma

Active Ingredient:
Nefopam Hydrochloride
Origin:
EU

Nefopam Panpharma (Nefopam Hydrochloride)

Nefopam Hydrochloride, the active ingredient in Nefopam Panpharma, is a non‑opioid analgesic presented as an oral formulation for oral use. It is employed to manage moderate acute pain, post‑operative discomfort, and musculoskeletal pain in adult patients requiring central analgesic therapy and is commonly prescribed when opioid alternatives are unsuitable for the patient.

GNH India supplies Nefopam Panpharma as a licensed, GDP‑compliant international pharmaceutical supplier serving hospitals, pharmacies and clinics worldwide. The company ensures consistent quality and regulatory compliance across all shipments.

Manufacturer / TM Owner

Laboratoire Cevidra

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Indications & Clinical Uses

Nefopam acts as a central analgesic for various pain conditions, providing relief through neurotransmitter modulation.

  • Moderate acute pain: reduces intensity of sudden, severe pain episodes in adults.
  • Post‑operative pain: facilitates recovery by alleviating surgical site discomfort.
  • Musculoskeletal pain: eases chronic strain‑related discomfort in joints and muscles.

How It Works

  • Nefopam inhibits the reuptake of serotonin, norepinephrine and dopamine, increasing their synaptic concentrations, while also blocking voltage‑gated sodium and calcium channels in central neurons. This combined action diminishes neuronal excitability and modulates pain pathways, producing analgesia without engaging opioid receptors. The drug’s effect on monoamine levels enhances descending inhibitory pathways, and the ion‑channel blockade stabilizes neuronal membranes, together contributing to its central analgesic profile.

Side Effects

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

Common Side Effects

  • Nausea: mild to moderate feeling of stomach upset.
  • Dry mouth: reduced salivation causing throat discomfort.
  • Sweating: increased perspiration without exertion.
  • Dizziness: transient light‑headedness, especially when standing quickly.

Serious or Rare Side Effects

  • Seizures: convulsive episodes requiring immediate medical attention.
  • Severe hypotension: sudden drop in blood pressure that may cause fainting.
  • Allergic reactions: rash, itching, swelling, or anaphylaxis.
  • Stevens‑Johnson syndrome: rare skin disorder with blistering and mucosal involvement.

Precautions & Warnings

When prescribing nefopam, clinicians should evaluate patient history and monitor for specific safety concerns.

  • Cardiovascular assessment: monitor heart rate and blood pressure for tachycardia or hypotension.
  • Seizure risk: avoid use in patients with a history of epilepsy or convulsive disorders.
  • Hepatic impairment: adjust therapy and observe liver function tests in patients with liver disease.
  • Concomitant serotonergic agents: do not combine with MAO inhibitors, SSRIs, or SNRIs due to serotonin syndrome risk.
  • Pregnancy and lactation: use only if the potential benefit justifies the potential risk; consult obstetric guidance.
  • Store at room temperature: keep in the original container, protect from moisture and direct sunlight.

Avoid Interactions

Nefopam can interact with other medicines, altering its efficacy or increasing toxicity.

Major Interactions (Avoid)

  • MAO inhibitors: concurrent use may precipitate severe serotonin syndrome.
  • SSRIs, SNRIs, or tricyclic antidepressants: increase risk of serotonin toxicity.
  • Anticholinergic drugs: may exacerbate dry mouth and urinary retention.

Moderate Interactions (Monitor Closely)

  • Antihypertensive agents: nefopam may enhance blood‑pressure‑lowering effects, requiring dose adjustment.
  • Anticholinergic medications: monitor for additive anticholinergic burden.
  • CNS depressants: may potentiate dizziness or sedation, necessitating observation.

Frequently Asked Questions

Nefopam Panpharma contains nefopam hydrochloride, a non‑opioid analgesic indicated for the relief of moderate acute pain, post‑operative discomfort, and musculoskeletal pain in adult patients when opioid therapy is not appropriate.

Nefopam works by inhibiting the reuptake of serotonin, norepinephrine and dopamine, which raises their levels in the central nervous system, and by blocking voltage‑gated sodium and calcium channels. These actions reduce neuronal excitability and enhance descending pain‑inhibitory pathways, providing analgesia without opioid receptor activation.

The appropriate dose of Nefopam Panpharma is determined by the prescribing healthcare professional based on the patient’s condition, severity of pain, and individual response. Dosage instructions are provided on the prescription label and should be followed exactly as directed.

Safety data for nefopam in pregnancy and lactation are limited. It should only be used if the potential benefit to the mother outweighs any possible risk to the fetus or infant, and only under the guidance of a qualified obstetric or pediatric specialist.

To place an order, submit an enquiry on the product page at gnhindia.com, specifying the required quantity. GNH India supplies hospitals, pharmacies and procurement teams worldwide, and will request verification of trade or institutional credentials before providing pricing, availability, shipping details and any necessary import documentation.

Unlike opioids, nefopam does not act on opioid receptors, reducing the risk of dependence, respiratory depression and typical opioid‑related side effects. Its analgesic effect is achieved through monoamine reuptake inhibition and ion‑channel blockade, making it a useful alternative for patients who cannot tolerate or should avoid opioids.

Nefopam Panpharma should be stored at room temperature, below 25 °C, in its original packaging. Keep the product away from excess moisture, direct sunlight and heat sources to maintain its stability and potency.

The medication is administered orally, typically as a tablet or capsule, and should be taken with a full glass of water. It may be taken with or without food, but patients should follow the specific instructions provided by their healthcare provider.

Serious adverse reactions, although rare, include seizures, severe hypotension, and hypersensitivity reactions such as anaphylaxis or Stevens‑Johnson syndrome. Patients should seek immediate medical attention if they experience convulsions, a sudden drop in blood pressure, or any signs of a severe allergic response.

Nefopam should be avoided in patients with a known hypersensitivity to nefopam or any of its excipients, those with uncontrolled epilepsy, severe cardiovascular disease, or those currently taking monoamine oxidase inhibitors, selective serotonin reuptake inhibitors, or other serotonergic agents due to the risk of serotonin syndrome.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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