Product image of Nefopam Chlorhydrate Eg Labo (Nefopam Hydrochloride) supplied by GNH India

Nefopam Chlorhydrate Eg Labo

Active Ingredient:
Nefopam Hydrochloride
Origin:
EU

Nefopam Chlorhydrate Eg Labo (Nefopam Hydrochloride)

Nefopam Hydrochloride, the active ingredient in Nefopam Chlorhydrate Eg Labo, is a non‑opioid analgesic presented as a sterile injectable for intramuscular and intravenous use. It is employed to manage moderate acute pain, including postoperative pain, in adult patients.

GNH India supplies Nefopam Chlorhydrate Eg Labo as a licensed, GDP‑compliant international pharmaceutical supplier serving hospitals, pharmacies and clinics worldwide.

Manufacturer / TM Owner

Eg Labo Laboratoires Eurogenerics

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Indications & Clinical Uses

Nefopam Hydrochloride is used to treat pain conditions that involve central pain pathways.

  • Moderate acute pain: provides analgesia for sudden, short‑term pain episodes such as injury or trauma.
  • Post‑operative pain: helps control pain following surgical procedures.
  • Pain after major trauma: reduces discomfort associated with severe tissue injury.

How It Works

  • Nefopam inhibits the reuptake of norepinephrine, serotonin and dopamine in the central nervous system, thereby enhancing descending inhibitory pain pathways. This multimodal neurotransmitter modulation reduces the perception of pain without acting on opioid receptors, offering analgesia while avoiding typical opioid‑related effects.

Side Effects

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

Common Side Effects

  • Nausea: mild to moderate upset stomach.
  • Sweating: increased perspiration without exertion.
  • Dry mouth: reduced salivation.
  • Dizziness: light‑headed sensation.
  • Tachycardia: faster than normal heart rate.
  • Blurred vision: temporary visual disturbance.

Serious or Rare Side Effects

  • Seizures: convulsive episodes, especially in predisposed individuals.
  • Severe hypotension: marked drop in blood pressure.
  • Allergic reactions: rash, itching, or anaphylaxis.
  • Cardiac arrhythmia: irregular heart rhythm.
  • Hepatic dysfunction: abnormal liver enzyme elevations.
  • Neuropsychiatric effects: agitation or confusion.

Precautions & Warnings

Before initiating therapy, clinicians should evaluate patient‑specific risk factors and monitor for adverse events.

  • Cardiovascular assessment: check blood pressure and heart rate before use.
  • Seizure risk: avoid in patients with a history of epilepsy.
  • Hepatic/renal function: adjust use if liver or kidney impairment is present.
  • Glaucoma caution: monitor intra‑ocular pressure in susceptible patients.
  • Discontinuation: taper gradually to prevent withdrawal phenomena.
  • Store below 25°C: keep in the original container, protect from light and moisture.

Avoid Interactions

Nefopam can interact with several drug classes; awareness of these interactions helps prevent adverse outcomes.

Major Interactions (Avoid)

  • Monoamine oxidase inhibitors (MAOIs): risk of severe hypertension or serotonin syndrome.
  • Selective serotonin reuptake inhibitors (SSRIs): increased serotonin toxicity.
  • Tricyclic antidepressants: heightened seizure risk.
  • Antihypertensive agents: additive hypotensive effect.

Moderate Interactions (Monitor Closely)

  • CYP450 inhibitors (e.g., fluoxetine): may raise nefopam plasma levels.
  • CYP450 inducers (e.g., carbamazepine): may reduce efficacy.
  • Non‑steroidal anti‑inflammatory drugs (NSAIDs): combined gastrointestinal irritation.
  • Anticholinergic drugs: may exacerbate dry mouth.
  • Diuretics: potential electrolyte disturbances.

Frequently Asked Questions

Nefopam Chlorhydrate Eg Labo contains nefopam hydrochloride, a non‑opioid analgesic indicated for the relief of moderate acute pain, including pain after surgery or trauma. It works by modulating central neurotransmitters to reduce the perception of pain in adult patients.

Nefopam blocks the reuptake of norepinephrine, serotonin and dopamine in the central nervous system. By increasing the levels of these neurotransmitters, it enhances descending inhibitory pathways that dampen pain signals, providing analgesia without engaging opioid receptors.

The specific dose of nefopam is determined by the prescribing clinician based on the patient’s condition, weight, and response. Dosing regimens are individualized and should follow the prescriber’s instructions and local regulatory guidelines.

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

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 (including any cold‑chain requirements) and necessary import documentation.

Unlike opioid analgesics, nefopam does not act on μ‑opioid receptors, reducing the risk of respiratory depression and dependence. Compared with NSAIDs, it does not inhibit cyclo‑oxygenase enzymes, so it carries a lower risk of gastrointestinal bleeding but may cause cardiovascular or central nervous system effects.

Nefopam Chlorhydrate Eg Labo should be stored below 25 °C in its original packaging, protected from light and moisture. Avoid freezing and keep the vial or ampoule sealed until use to maintain sterility.

The medication is supplied as a sterile injectable solution for intramuscular or intravenous administration. It is given by a qualified healthcare professional, typically as a slow IV infusion or IM injection, according to the prescriber’s dosing instructions.

Serious adverse events include seizures, severe hypotension, allergic reactions such as anaphylaxis, cardiac arrhythmias, and hepatic dysfunction. Patients should be monitored closely for these signs, especially if they have pre‑existing risk factors.

Nefopam is contraindicated in patients with known hypersensitivity to the drug, those taking monoamine oxidase inhibitors, and individuals with uncontrolled epilepsy or severe cardiovascular instability. Clinicians should also avoid use in patients with significant hepatic or renal impairment unless benefits outweigh risks.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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