Product image of Nefopam Hydrochloride Teva Uk (Nefopam Hydrochloride) supplied by GNH India

Nefopam Hydrochloride Teva Uk

Active Ingredient:
Nefopam Hydrochloride
Origin:
EU

Nefopam Hydrochloride Teva Uk (Nefopam Hydrochloride)

Nefopam Hydrochloride, the active ingredient in Nefopam Hydrochloride Teva Uk, is a non‑opioid centrally acting analgesic presented as a tablet for oral use. It treats moderate acute pain, post‑operative pain and musculoskeletal pain in adult patients.

GNH India supplies Nefopam Hydrochloride Teva Uk as a licensed, GDP‑compliant international pharmaceutical supplier serving hospitals, pharmacies and clinics worldwide.

Manufacturer / TM Owner

Teva Uk Limited

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Indications & Clinical Uses

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

  • Moderate acute pain: provides analgesia for short‑term severe pain episodes.
  • Post‑operative pain: helps control pain after surgical procedures.
  • Musculoskeletal pain: relieves pain associated with strains, sprains and other musculoskeletal injuries.

How It Works

  • Nefopam Hydrochloride inhibits the reuptake of norepinephrine, serotonin and dopamine while also blocking voltage‑sensitive sodium channels. This combined action reduces neuronal excitability in the central nervous system, producing analgesia without engaging opioid receptors.

Side Effects

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

Common Side Effects

  • Dry mouth: reduced salivary flow.
  • Sweating: increased perspiration.
  • Nausea: mild gastrointestinal upset.
  • Dizziness: transient light‑headedness.
  • Blurred vision: temporary visual disturbances.
  • Constipation: reduced bowel motility.

Serious or Rare Side Effects

  • Tachycardia: rapid heart rate requiring monitoring.
  • Seizures: rare occurrence, especially at high doses.
  • Severe hypotension: significant drop in blood pressure.
  • Allergic reactions: rash, urticaria or angioedema.
  • Hepatic dysfunction: elevated liver enzymes.
  • Psychotic symptoms: hallucinations or agitation.

Precautions & Warnings

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

  • Cardiovascular disease: monitor heart rate and blood pressure.
  • Seizure disorders: avoid in patients with a history of epilepsy.
  • Liver impairment: use with caution and assess hepatic function.
  • Renal impairment: adjust use if significant kidney dysfunction is present.
  • Concomitant MAO inhibitors: avoid due to risk of hypertensive crisis.
  • Store at ambient temperature: keep below 25 °C, retain in original packaging, protect from moisture and direct sunlight.

Avoid Interactions

Nefopam Hydrochloride can interact with other medicines, altering its safety profile.

Major Interactions (Avoid)

  • Monoamine oxidase inhibitors (MAOIs): risk of severe hypertension.
  • Tricyclic antidepressants: increased serotonergic activity.
  • Antihypertensive agents: additive blood pressure lowering.

Moderate Interactions (Monitor Closely)

  • Other serotonergic drugs (SSRIs, SNRIs): monitor for serotonin syndrome.
  • Anticholinergic medications: may exacerbate dry mouth.
  • CYP450 substrates: potential alteration of plasma levels, requiring dose adjustment.

Frequently Asked Questions

Nefopam Hydrochloride is a prescription analgesic indicated for the relief of moderate acute pain, post‑operative pain and musculoskeletal pain. It is used in adult patients when non‑opioid pain control is preferred.

The drug blocks the reuptake of norepinephrine, serotonin and dopamine and also inhibits voltage‑sensitive sodium channels in the central nervous system. This combination reduces neuronal excitability and produces analgesia without engaging opioid pathways.

The dosage of Nefopam Hydrochloride is determined by the prescribing clinician based on the patient’s condition, severity of pain, age, renal and hepatic function, and other individual factors. No fixed regimen is provided here.

Safety data for Nefopam Hydrochloride in pregnancy and lactation are limited. It should only be used if the potential benefit justifies the potential risk to the fetus or infant, and the decision must be made by the treating physician.

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 and any necessary import documentation.

Unlike opioid analgesics, Nefopam provides pain relief without acting on opioid receptors, reducing the risk of dependence and respiratory depression. Compared with NSAIDs, it does not inhibit cyclo‑oxygenase enzymes, so it has a different safety profile regarding gastrointestinal and renal effects.

Store the oral tablets at ambient temperature, preferably below 25 °C. Keep them in the original container, protect from moisture and direct sunlight, and ensure they are out of reach of children.

Nefopam Hydrochloride is administered orally, typically as a tablet taken with water. The exact dosing schedule and any required food considerations are determined by the prescribing healthcare professional.

Serious adverse events, although rare, include tachycardia, severe hypotension, seizures, hepatic dysfunction and allergic reactions such as rash or angioedema. Patients should be monitored for these signs, especially when higher doses or interacting drugs are used.

Nefopam is contraindicated in patients with known hypersensitivity to the drug, those taking monoamine oxidase inhibitors, and individuals with uncontrolled severe cardiovascular disease or a history of seizures. Clinicians should assess each patient’s medical history before prescribing.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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