Product image of Palladone-Sr (Hydromorphone Hydrochloride) supplied by GNH India

Palladone-Sr

Active Ingredient:
Hydromorphone Hydrochloride
Origin:
EU

Palladone-Sr (Hydromorphone Hydrochloride)

Hydromorphone hydrochloride, the active ingredient in Palladone‑Sr, is an opioid analgesic presented as a sterile injectable solution for intravenous use. It is employed in the management of moderate to severe pain, particularly in postoperative settings and in patients with cancer‑related pain.
GNH India supplies Palladone‑Sr as a licensed, GDP‑compliant international pharmaceutical supplier serving hospitals and clinics worldwide.

Manufacturer / TM Owner

Napp Pharmaceuticals Ltd

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Indications & Clinical Uses

Hydromorphone hydrochloride acts on the central nervous system to provide analgesia for several painful conditions.

  • Post‑operative pain: delivers rapid relief of acute pain following surgery.
  • Cancer‑related pain: helps control persistent severe pain in oncology patients.
  • Severe chronic pain: used when other opioids are insufficient for managing chronic nociceptive pain.

How It Works

  • Hydromorphone hydrochloride is a full agonist at the µ‑opioid receptors in the central nervous system. Binding activates inhibitory G‑protein pathways, reducing neuronal excitability, decreasing the perception of pain, and altering pain‑modulating neurotransmitter release.

Side Effects

Adverse reactions may occur with hydromorphone use and should be monitored.

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.
  • Pruritus: itching without rash.
  • Dry mouth: reduced salivation causing oral discomfort.

Serious or Rare Side Effects

  • Respiratory depression: slowed or shallow breathing that can be life‑threatening.
  • Severe hypotension: marked drop in blood pressure.
  • Cardiac arrhythmias: abnormal heart rhythms.
  • Anaphylaxis: acute allergic reaction with hives, swelling, and airway compromise.
  • Dependence and withdrawal: physical dependence with withdrawal symptoms on abrupt cessation.

Precautions & Warnings

Hydromorphone should be prescribed and monitored carefully to minimise risks.

  • Assess pain severity: confirm that opioid therapy is appropriate for the level of pain.
  • Evaluate respiratory function: monitor for signs of respiratory depression, especially after dose changes.
  • Review patient history: consider prior opioid use, substance abuse, or tolerance.
  • Adjust for organ impairment: modify dosing in renal or hepatic dysfunction.
  • Educate on side‑effects: inform patients about constipation, sedation and the need to avoid driving if impaired.
  • Store at ambient temperature: keep in original container, protect from light and moisture.

Avoid Interactions

Hydromorphone may interact with other medications, altering its safety or effectiveness.

Major Interactions (Avoid)

  • CNS depressants: concurrent use with benzodiazepines or barbiturates can cause profound respiratory depression.
  • MAO inhibitors: may precipitate severe hypertension or serotonin syndrome.
  • Opioid antagonists: naloxone or naltrexone can reverse analgesia and precipitate withdrawal.

Moderate Interactions (Monitor Closely)

  • CYP3A4 inhibitors: ketoconazole, erythromycin may increase hydromorphone plasma levels.
  • CYP3A4 inducers: rifampicin, carbamazepine may reduce effectiveness.
  • Anticholinergics: may worsen constipation.
  • Diuretics: can enhance hypotensive effects.
  • Alcohol: additive central nervous system depression.

Frequently Asked Questions

Palladone‑Sr contains hydromorphone hydrochloride, an opioid analgesic used to treat moderate to severe acute or chronic pain, such as post‑operative pain, cancer‑related pain, or pain that has not responded adequately to other opioids.

Hydromorphone binds as a full agonist to µ‑opioid receptors in the brain and spinal cord, activating inhibitory G‑protein pathways that lower neuronal excitability and reduce the transmission of pain signals, producing analgesia.

The dose of Palladone‑Sr is individualized; a qualified prescriber determines the appropriate amount, route, and frequency based on the patient’s pain severity, prior opioid exposure, and clinical condition.

Opioids, including hydromorphone, are generally contraindicated during pregnancy and lactation because they may cause fetal respiratory depression or neonatal sedation. Use only if the potential benefit justifies the risk and under strict medical supervision.

To 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 necessary import documentation.

Hydromorphone is more potent on a milligram‑per‑milligram basis than morphine, offering rapid onset of analgesia with a shorter duration. It is often chosen when stronger pain control is needed, but it shares similar safety considerations and monitoring requirements as other strong opioids.

Store the injectable solution at controlled room temperature, below 25 °C, in its original packaging. Protect it from direct light, moisture and extreme temperature fluctuations to maintain potency.

Palladone‑Sr is supplied as a sterile solution for intravenous injection. It should be administered by a qualified healthcare professional using aseptic technique, with dosing adjusted according to the patient’s response and clinical guidelines.

The most serious risks include respiratory depression, severe hypotension, profound sedation, dependence, and the potential for overdose. Continuous monitoring of respiratory function and vital signs is essential, especially after dose initiation or escalation.

Patients with known hypersensitivity to hydromorphone or any component of the formulation, those with severe respiratory insufficiency, acute or severe asthma, and individuals taking monoamine oxidase inhibitors should avoid using Palladone‑Sr.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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