Hydromorphone

Table of contents

  • Brand Names
  • Chemistry
  • Pharmacologic Category
  • Mechanism of Action
  • Therapeutic Use
  • Unlabeled Use
  • Pregnancy and Lactation Implications
  • Contraindications
  • Warnings and Precautions
  • Adverse Reactions
  • Toxicological Effects
  • Caution and personalized dose adjustment in patients with the following genotypes
  • Other genes that may be involved
  • Substrate of
  • Drug Interactions
  • Nutrition/Nutraceutical Interactions
  • Dosage
  • Pharmacokinetics and Pharmacodynamics
  • Special Considerations

Brand Names

Europe

Austria: Hydal, Jurnista; Belgium: Palladone; Denmark: Jurnista, Palladone; Estonia: Jurnista, Palladone-XL; Finland: Palladon; France: Sophidone; Germany: Jurnista, Palladon; Greece: Palladone; Hungary: Jurnista, Palladone; Ireland: Hydromorphone, Palladone; Italy: Jurnista; Luxembourg: Palladone; Netherlands: Palladon; Poland: Palladone; Portugal: Hidromorfona, Jurnista, Palladone; Slovakia: Jurnista, Palladone; Slovenia: Jurnista, Palladone; Spain: Jurnista; Sweden: Palladon; UK: Palladone.

North America

Canada: Dilaudid, Hydromorph, Hydromorphone; USA: Dilaudid, Exalgo, Hydromorphone, Palladone.

Latin America

Mexico: Liberaxim.

Drug combinations

Chemistry

Hydromorphone Hydrochloride: C~17~H~19~NO~3~ HCl. Mw: 321.80. (1) Morphinan-6-one, 4,5-epoxy-3-hydroxy-17-methyl-, hydrochloride, (5α)-; (2) 4,5 α-Epoxy-3-hydroxy-17-methylmorphinan-6-one hydrochloride. CAS-71-68-1; CAS-466-99-9 (hydromorphone).

Pharmacologic Category

Analgesics and Antipyretics; Opiate Agonists. Narcotic Analgesic. Opiate Analgesic. (ATC-Code: N02AA03).

Mechanism of action

Hydromorphone is a semisynthetic phenanthrene-derivative opiate agonist. Binds to opiate receptors in CNS, causing inhibition of ascending pain pathways, altering perception of and response to pain. Causes cough suppression by direct central action in medulla. Produces generalized CNS depression.

Therapeutic use

Hydromorphone is a strong analgesic used in relief of moderate to severe pain. For relief of malignant (cancer) pain and chronic nonmalignant pain.

Pregnancy and lactiation implications

Hydromorphone was teratogenic in some, but not all, animal studies. Maternal toxicity also reported. Hydromorphone crosses placenta. Chronic opioid use during pregnancy may lead to withdrawal syndrome in neonate. Use not recommended during lactation.

Unlabeled use

Antitussive.

Contraindications

Hypersensitivity to hydromorphone, or any component of the formulation. Acute or severe asthma, severe respiratory depression. Severe CNS depression. Pregnancy (prolonged use or high doses at term). Obstetrical analgesia.

Warnings and precautions

Might cause CNS depression. Risk of hypotension. Use with caution in hypersensitivity reactions to other phenanthrene derivative opioid agonists (codeine, hydrocodone, levorphanol, oxycodone, oxymorphone). Myoclonus and seizures reported with high doses. May obscure diagnosis or clinical course of acute abdominal conditions. Use with caution in adrenal insufficiency, including Addison’s disease. Use with caution in biliary tract dysfunction (acute pancreatitis may cause constriction of sphincter of Oddi). Use with caution in CNS depression or coma. Use with caution in history of drug abuse or acute alcoholism (potential for drug dependency). Use with extreme caution in head injury, intracranial lesions, or elevated intracranial pressure (exaggerated elevation of intracranial pressure might occur). Use with caution in hepatic impairment. Use with caution in morbidly obese patients. Use with caution in prostatic hyperplasia and/or urinary stricture. Use with caution in toxic psychoses. Use with caution in renal impairment. Use with caution in pre-existing respiratory compromise (hypoxia and/or hypercapnia), COPD or other obstructive pulmonary disease, and kyphoscoliosis or other skeletal disorder which may alter respiratory function. Use with caution in thyroid dysfunction. Effects may be potentiated when used with other sedative drugs or ethanol. Use with caution in debilitated patients (greater potential for critical respiratory depression), and in the elderly (might be more sensitive to adverse effects). Some dosage forms contain trace amounts of sodium metabisulfite which may cause allergic reactions in susceptible individuals. Abrupt discontinuation may lead to withdrawal symptoms.

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