Product image of Hydromorphon Retard Hexal (Hydromorphone Hydrochloride) supplied by GNH India

Hydromorphon Retard Hexal

Active Ingredient:
Hydromorphone Hydrochloride
Origin:
EU

Hydromorphon Retard Hexal (Hydromorphone Hydrochloride)

Hydromorphone, the active ingredient in Hydromorphon Retard Hexal, is an opioid analgesic presented as an extended‑release oral tablet for oral use. It is indicated for the management of moderate to severe acute pain, postoperative pain, and cancer‑related pain in adult patients. The formulation provides prolonged plasma concentrations, allowing twice‑daily dosing in many treatment protocols.

GNH India supplies Hydromorphon Retard Hexal as a licensed, GDP‑compliant international pharmaceutical supplier serving hospitals, oncology centres and pharmacies worldwide.

Manufacturer / TM Owner

Hexal Ag

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Indications & Clinical Uses

Hydromorphon Retard Hexal, an opioid analgesic, is used in pain pathways that involve central mu‑opioid receptors.

  • Moderate to severe acute pain: provides sustained relief for intense short‑term pain episodes.
  • Postoperative pain: helps control pain after major surgical procedures.
  • Cancer pain: offers continuous analgesia for persistent malignant pain.

How It Works

  • Hydromorphone hydrochloride acts as a high‑affinity agonist at the mu‑opioid receptors in the central nervous system. Activation of these receptors inhibits the release of neurotransmitters involved in nociceptive transmission, leading to reduced perception of pain and increased pain threshold. The extended‑release formulation allows gradual drug absorption, maintaining therapeutic plasma levels over an extended period.

Side Effects

Hydromorphon Retard Hexal may cause a range of adverse reactions, which are grouped by frequency and severity.

Common Side Effects

  • Constipation: reduced gastrointestinal motility.
  • Nausea: mild to moderate upset stomach.
  • Drowsiness: increased sedation.
  • Dry mouth: decreased salivation.
  • Sweating: excessive perspiration.
  • Itching: mild pruritus.

Serious or Rare Side Effects

  • Respiratory depression: slowed breathing, potentially life‑threatening.
  • Severe hypotension: marked drop in blood pressure.
  • Dependence or addiction: risk of misuse with prolonged use.
  • Allergic reactions: rash, angioedema, or anaphylaxis.
  • QT prolongation: cardiac conduction abnormalities.
  • Withdrawal syndrome: symptoms upon abrupt discontinuation after prolonged therapy.

Precautions & Warnings

When prescribing Hydromorphon Retard Hexal, clinicians should consider several safety measures.

  • Assess pain severity: confirm that opioid therapy is appropriate for the level of pain.
  • Evaluate respiratory function: avoid use in patients with compromised breathing.
  • Monitor for signs of dependence: watch for misuse or addiction behaviors.
  • Adjust for renal/hepatic impairment: dose may need modification in organ dysfunction.
  • Avoid concurrent CNS depressants: limit use with benzodiazepines or alcohol.
  • Store at ambient temperature: keep below 25 °C in the original container, protect from moisture and light.

Avoid Interactions

Hydromorphon Retard Hexal can interact with other medicines, altering its efficacy or safety.

Major Interactions (Avoid)

  • Other opioids: additive respiratory depression.
  • Benzodiazepines: heightened sedation and respiratory risk.
  • MAO inhibitors: potential for severe hypotension.
  • CNS depressants (e.g., antihistamines, muscle relaxants): increased drowsiness.

Moderate Interactions (Monitor Closely)

  • CYP3A4 inhibitors (e.g., ketoconazole): may raise hydromorphone levels.
  • CYP3A4 inducers (e.g., rifampin): may reduce analgesic effect.
  • Anticholinergics: may exacerbate constipation.
  • Diuretics: can enhance orthostatic hypotension.
  • Serotonergic agents: risk of serotonin syndrome when combined with high‑dose opioids.

Frequently Asked Questions

Hydromorphon Retard Hexal is an extended‑release oral tablet containing hydromorphone. It is prescribed to manage moderate to severe acute pain, postoperative pain after major surgery, and persistent cancer‑related pain in adult patients.

Hydromorphone binds selectively to mu‑opioid receptors in the brain and spinal cord. This binding inhibits the release of pain‑transmitting neurotransmitters, reduces neuronal excitability, and raises the pain threshold, resulting in analgesia.

The specific dose and dosing interval are determined by the prescribing clinician based on the patient’s pain severity, prior opioid exposure, and individual health factors. Dosing should follow the prescriber’s instructions and local regulatory guidelines.

Safety data for hydromorphone in pregnancy and lactation are limited. The drug should be used only if the potential benefit justifies the potential risk to the fetus or infant, and it is generally avoided unless absolutely necessary.

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 required import documentation.

Hydromorphon Retard Hexal offers an extended‑release formulation of hydromorphone, providing longer‑lasting analgesia compared with immediate‑release opioids such as morphine tablets. Its potency is higher than morphine on a milligram‑per‑milligram basis, allowing lower dose requirements for equivalent pain control.

Store the tablets at ambient temperature, preferably below 25 °C. Keep them in the original blister pack, protect from moisture, heat and direct sunlight, and keep out of reach of children.

The medication is taken orally, usually with a full glass of water. It is designed for once‑ or twice‑daily dosing, depending on the prescriber’s regimen, and should be swallowed whole; crushing or chewing can alter the release profile.

The most serious risks include respiratory depression, severe hypotension, profound sedation, dependence or addiction, and the potential for overdose. Patients should be monitored closely, especially during initiation, dose escalation, or when combined with other CNS depressants.

Hydromorphon Retard Hexal is contraindicated in patients with known hypersensitivity to hydromorphone or any component of the tablet, in those with severe respiratory insufficiency, acute or severe bronchial asthma, and in individuals who are actively abusing opioids.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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