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

Nefopam Hydrochloride Dawa

Active Ingredient:
Nefopam Hydrochloride
Origin:
EU

Nefopam Hydrochloride Dawa (Nefopam Hydrochloride)

Nefopam Hydrochloride, the active ingredient in Nefopam Hydrochloride Dawa, is a non‑opioid analgesic presented as an oral formulation for oral use. It is used to treat moderate to severe acute pain, including post‑operative pain, in adult patients.
GNH India supplies Nefopam Hydrochloride Dawa as a licensed, GDP‑compliant international pharmaceutical supplier serving hospitals, pharmacies and clinics worldwide.

Manufacturer / TM Owner

Dawa Limited

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Indications & Clinical Uses

Nefopam Hydrochloride is a centrally acting analgesic used for pain conditions where non‑opioid therapy is indicated.

  • Moderate to severe acute pain: provides effective relief without opioid‑related side effects.
  • Post‑operative pain: helps control pain after surgical procedures, facilitating recovery.

How It Works

  • Nefopam Hydrochloride inhibits the reuptake of norepinephrine, serotonin and dopamine in the central nervous system, increasing the synaptic concentrations of these neurotransmitters. This multimodal action produces analgesia by modulating pain pathways without engaging opioid receptors, resulting in central analgesic effects.

Side Effects

Nefopam Hydrochloride may cause a range of adverse reactions, most of which are dose‑related and reversible.

Common Side Effects

  • Nausea: mild to moderate stomach upset.
  • Dizziness: transient light‑headedness.
  • Dry mouth: reduced salivation.
  • Sweating: increased perspiration.
  • Constipation: reduced bowel movements.
  • Blurred vision: temporary visual disturbance.

Serious or Rare Side Effects

  • Tachycardia: rapid heart rate requiring monitoring.
  • Seizures: rare convulsive episodes, especially in predisposed individuals.
  • Severe hypotension: marked drop in blood pressure.
  • Allergic reactions: rash, itching, or anaphylaxis.
  • Hepatic dysfunction: abnormal liver enzymes or jaundice.

Precautions & Warnings

Before prescribing Nefopam Hydrochloride, clinicians should consider several safety aspects.

  • Renal function assessment: adjust use in patients with impaired kidney function.
  • Cardiovascular monitoring: observe for tachycardia or hypertension.
  • Seizure history: avoid in patients with uncontrolled epilepsy.
  • Concomitant serotonergic drugs: evaluate risk of serotonin syndrome.
  • Discontinuation: taper gradually to prevent withdrawal symptoms.
  • Store at room temperature: keep in the original container, protect from moisture and direct sunlight.

Avoid Interactions

Nefopam Hydrochloride can interact with several medication classes, influencing efficacy or safety.

Major Interactions (Avoid)

  • Monoamine oxidase inhibitors (MAOIs): risk of severe serotonin syndrome.
  • Selective serotonin reuptake inhibitors (SSRIs): increased serotonergic activity.
  • Tricyclic antidepressants (TCAs): heightened risk of cardiovascular side effects.

Moderate Interactions (Monitor Closely)

  • Antihypertensive agents: possible additive blood pressure reduction.
  • Anticholinergic drugs: may exacerbate dry mouth and constipation.
  • Central nervous system depressants: enhanced sedation or dizziness.

Frequently Asked Questions

Nefopam Hydrochloride Dawa is a prescription, non‑opioid analgesic indicated for the management of moderate to severe acute pain, including pain following surgical procedures. It provides central pain relief without the risks associated with opioid therapy.

The drug blocks the reuptake of the neurotransmitters norepinephrine, serotonin and dopamine in the central nervous system. By increasing the levels of these chemicals, it modulates pain pathways and produces analgesia without activating opioid receptors.

The appropriate dose is determined by the prescribing healthcare professional based on the patient’s condition, severity of pain, and individual response. Dosage regimens are individualized and should follow the prescriber’s instructions.

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

Enquiries can be submitted via the product page on 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.

Compared with opioid analgesics, Nefopam offers effective pain relief without opioid‑related dependence or respiratory depression. It differs from NSAIDs by lacking significant anti‑inflammatory activity and gastrointestinal risk, making it an alternative for patients who cannot tolerate those classes.

Store the product at room temperature, below 25 °C, in its original packaging. Protect it from moisture, excessive heat and direct sunlight to maintain stability and potency.

The medication is taken orally, usually in tablet or capsule form, as directed by the prescriber. It should be swallowed with water and taken with or without food according to the healthcare professional’s guidance.

Serious adverse events, though rare, include tachycardia, severe hypotension, seizures, allergic reactions such as anaphylaxis, and hepatic dysfunction. Patients should seek immediate medical attention if any of these symptoms occur.

Individuals with known hypersensitivity to nefopam, uncontrolled epilepsy, recent myocardial infarction, or those taking monoamine oxidase inhibitors should avoid this medication. A thorough medical review is essential before initiating therapy.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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