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

Hydromorphon Stada

Active Ingredient:
Hydromorphone Hydrochloride
Origin:
EU

Hydromorphon Stada (Hydromorphone Hydrochloride)

Hydromorphone, the active ingredient in Hydromorphon Stada, is an opioid analgesic presented as an oral formulation for oral use. It is prescribed for the management of moderate to severe pain in adult patients when other analgesics are insufficient. The drug acts centrally on the nervous system to provide effective analgesia and sedation, and is classified under the ATC code N02AA02.

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

Manufacturer / TM Owner

Stada Arzneimittel Gmbh

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Indications & Clinical Uses

  • Hydromorphone is an opioid analgesic used in the management of pain.
  • Acute postoperative pain: provides rapid relief after surgical procedures.
  • Cancer‑related pain: helps control severe pain associated with malignant disease.
  • Chronic non‑cancer pain: employed when other analgesics are inadequate for long‑term severe pain.

How It Works

  • Hydromorphone binds as an agonist to the μ‑opioid receptors in the central nervous system. Activation of these receptors inhibits the release of neurotransmitters involved in pain transmission, leading to decreased perception of pain and increased analgesic effect. The drug also produces sedation by modulating neuronal activity in brain regions that regulate arousal.

Side Effects

Hydromorphone may cause a range of adverse reactions, from mild to serious. Patients should be informed of common and less frequent side effects.

Common Side Effects

  • Nausea: feeling of sickness or urge to vomit.
  • Constipation: reduced bowel movements and hard stools.
  • Drowsiness: increased sleepiness or fatigue.
  • Dizziness: sensation of light‑headedness or unsteadiness.
  • Dry mouth: reduced salivation leading to a parched feeling.
  • Vomiting: expulsion of stomach contents.

Serious or Rare Side Effects

  • Respiratory depression: slowed or shallow breathing that can be life‑threatening.
  • Severe hypotension: marked drop in blood pressure causing faintness.
  • Addiction or dependence: potential for misuse and physical dependence.
  • Adrenal insufficiency: impaired cortisol production.
  • Seizures: rare occurrence of convulsive episodes.

Precautions & Warnings

When prescribing or dispensing Hydromorphone, several safety considerations are essential.

  • Assess pain level: confirm that opioid therapy is appropriate for the intensity of pain.
  • Screen for respiratory disorders: avoid use in patients with severe asthma or COPD.
  • Evaluate hepatic and renal function: dose adjustments may be required in impairment.
  • Avoid concomitant CNS depressants: limit use with benzodiazepines or alcohol.
  • Monitor for signs of dependence: watch for cravings, tolerance, or withdrawal.
  • Store at ambient temperature: keep in the original container, protect from moisture and light.

Avoid Interactions

Hydromorphone can interact with other medicines, altering its safety or effectiveness.

Major Interactions (Avoid)

  • Other opioids: additive respiratory depression.
  • Benzodiazepines: increased risk of profound sedation and respiratory compromise.
  • MAO inhibitors: potential for severe hypertension or serotonin syndrome.

Moderate Interactions (Monitor Closely)

  • Anticholinergics: may worsen constipation and urinary retention.
  • SSRIs or SNRIs: possible serotonin syndrome when combined.
  • Alcohol: enhances CNS depression and impairs judgment.

Frequently Asked Questions

Hydromorphon Stada contains hydromorphone, an opioid analgesic indicated for the relief of moderate to severe pain, including postoperative pain, cancer‑related pain, and chronic pain that is not adequately controlled by non‑opioid medications.

Hydromorphone acts as an agonist at the μ‑opioid receptors in the brain and spinal cord. By activating these receptors, it reduces the transmission of pain signals and alters the perception of pain, while also producing sedation.

The appropriate dose of Hydromorphon Stada is determined by the prescribing clinician based on the patient’s pain severity, prior opioid exposure, age, organ function, and other individual factors. Only a qualified health professional should set the dosing regimen.

Safety of hydromorphone in pregnancy or lactation has not been fully established. It should only be used if the potential benefit justifies the potential risk to the fetus or infant, and this 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 required import documentation.

Hydromorphone is more potent on a milligram‑per‑milligram basis than morphine, offering strong analgesia with a relatively shorter onset of action. Compared with codeine or tramadol, it provides more reliable pain control for severe pain but carries a higher risk of typical opioid‑related adverse effects.

Hydromorphon Stada should be stored at ambient temperature, below 25 °C, in its original packaging to protect it from moisture, light and accidental ingestion. Keep the product out of reach of children and unauthorized personnel.

The medication is formulated for oral administration. It is taken by mouth with or without food, as directed by the prescriber. Swallow tablets or capsules whole; do not crush or chew unless specifically instructed.

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

Hydromorphon Stada is contraindicated in patients with known hypersensitivity to hydromorphone or any component of the formulation, in those with significant respiratory depression, acute or severe asthma, or in individuals who have taken monoamine‑oxidase inhibitors within the past 14 days.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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