Product image of Paracodin N (Dihydrocodeine Tartrate) supplied by GNH India

Paracodin N

Active Ingredient:
Dihydrocodeine Tartrate
Origin:
EU

Paracodin N (Dihydrocodeine Tartrate)

Dihydrocodeine tartrate, the active ingredient in Paracodin N, is an opioid analgesic presented as a tablet for oral use. It is employed in the management of moderate to severe pain where other analgesics may be insufficient, and it is prescribed for adult patients. GNH India supplies Paracodin N as a licensed, GDP‑compliant international pharmaceutical supplier serving hospitals, pharmacies and clinics worldwide.

GNH India supplies Paracodin N as a licensed, GDP‑compliant international pharmaceutical supplier serving hospitals, pharmacies and clinics worldwide.

Manufacturer / TM Owner

Teofarma S.R.L.

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Indications & Clinical Uses

Paracodin N contains dihydrocodeine tartrate, an opioid that acts on the central nervous system to relieve pain.

  • Acute postoperative pain: provides analgesia during the recovery period after surgery.
  • Cancer‑related pain: helps control moderate to severe pain associated with malignant disease.
  • Severe chronic non‑cancer pain: used when other analgesics are inadequate for persistent pain conditions.

How It Works

  • Dihydrocodeine tartrate binds to μ‑opioid receptors in the central nervous system, producing analgesia by inhibiting the transmission of nociceptive signals and altering pain perception. The drug also exerts mild activity at κ‑opioid receptors, contributing to its overall effect on pain modulation.

Side Effects

Paracodin N may cause a range of adverse reactions, most of which are dose‑dependent and reversible.

Common Side Effects

  • Nausea and vomiting: mild to moderate gastrointestinal upset.
  • Constipation: reduced bowel motility leading to hard stools.
  • Drowsiness or sedation: increased sleepiness or reduced alertness.
  • Dizziness: sensation of light‑headedness or imbalance.
  • Dry mouth: reduced salivation causing oral discomfort.

Serious or Rare Side Effects

  • Respiratory depression: slowed or shallow breathing that may be life‑threatening.
  • Severe hypotension: marked drop in blood pressure causing faintness.
  • Allergic reactions: rash, itching, swelling, or anaphylaxis.
  • Dependence or withdrawal: signs of physical dependence with abrupt discontinuation.
  • Confusion or hallucinations: altered mental status in susceptible individuals.
  • Urinary retention: difficulty initiating or maintaining urine flow.

Precautions & Warnings

When prescribing Paracodin N, clinicians should consider several safety aspects.

  • Assess pain severity and prior opioid exposure: ensure appropriate indication before initiating therapy.
  • Monitor for respiratory depression: especially in opioid‑naïve patients or those with pulmonary disease.
  • Evaluate liver and kidney function: adjust use in patients with significant hepatic or renal impairment.
  • Avoid concurrent CNS depressants: limit use with alcohol, benzodiazepines or other sedatives.
  • Educate patients on dependence risk: discuss safe use, storage and disposal.
  • Store at below 25°C: keep in the original packaging, protect from moisture and direct sunlight.

Avoid Interactions

Paracodin N can interact with other medicines, altering its efficacy or safety profile.

Major Interactions (Avoid)

  • Other opioids or strong CNS depressants: may cause additive respiratory depression.
  • Monoamine oxidase inhibitors (MAOIs): increase risk of serotonin syndrome.
  • CYP3A4 inhibitors (e.g., ketoconazole, erythromycin): raise dihydrocodeine plasma levels.

Moderate Interactions (Monitor Closely)

  • CYP2D6 inhibitors (e.g., fluoxetine, paroxetine): may reduce conversion to active metabolites.
  • Anticholinergic agents: can worsen constipation.
  • Diuretics: may enhance hypotensive effects.
  • Alcohol: potentiates sedation and respiratory depression.
  • Antihistamines: increase drowsiness.

Frequently Asked Questions

Paracodin N contains dihydrocodeine tartrate, an opioid analgesic that is prescribed to manage moderate to severe pain, including postoperative pain, cancer‑related pain, and chronic non‑cancer pain when other treatments are insufficient.

Dihydrocodeine tartrate binds to μ‑opioid receptors in the central nervous system, reducing the transmission of pain signals and altering the perception of pain. It also has mild activity at κ‑opioid receptors, contributing to its overall analgesic effect.

The appropriate dose of Paracodin N is determined by the prescribing clinician based on the patient’s pain severity, prior opioid exposure, age, weight, and overall health status. Dosage regimens are individualized and should follow local prescribing guidelines.

Opioid analgesics, including dihydrocodeine, are generally contraindicated during pregnancy because of potential fetal harm and neonatal respiratory depression. They are also not recommended while breastfeeding, as the drug can pass into breast milk and affect the infant.

To request Paracodin N, submit an enquiry on the product page at gnhindia.com with 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.

Paracodin N (dihydrocodeine) is a semi‑synthetic opioid that offers analgesia comparable to low‑dose morphine but with a slightly lower risk of severe respiratory depression. It is often chosen when a moderate‑strength opioid is needed and may have a more favorable side‑effect profile than stronger opioids such as oxycodone.

Paracodin N tablets should be stored at temperatures below 25 °C, in their original packaging, protected from moisture, heat and direct sunlight to maintain potency and stability.

Paracodin N is supplied as oral tablets and is taken by mouth with or without food, as directed by the prescribing healthcare professional. Swallow the tablet whole; do not crush or chew unless specifically instructed.

The most serious risks include respiratory depression, severe hypotension, dependence and potential for overdose. Patients should be monitored for signs of slowed breathing, extreme drowsiness, or any allergic reactions, and the medication should be used only as prescribed.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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