Trade Names:Dilaudid- Tablets 2 mg- Tablets 4 mg- Tablets 8 mg- Injection 1 mg/mL- Injection 2 mg/mL- Injection 4 mg/mL- Suppositories 3 mg- Oral liquid 1 mg/mL
Trade Names:Dilaudid-HP- Injection 10 mg/mL- Powder for Injection, lyophilized 250 mgDilaudid-HP Plus (Canada)Dilaudid Sterile Powder (Canada)Dilaudid-XP (Canada)Hydromorph Contin (Canada)Hydromorphone HP 10 (Canada)Hydromorphone HP 20 (Canada)Hydromorphone HP 50 (Canada)Hydromorphone HP Forte (Canada)PMS-Hydromorphone (Canada)
Relieves pain by stimulating opiate receptors in CNS; also causes respiratory depression, inhibition of cough reflex, peripheral vasodilation, inhibition of intestinal peristalsis, sphincter of Oddi spasm, stimulation of chemoreceptors that cause vomiting, and increased bladder tone.
Rapidly absorbed after oral administration. C max is 5.5 mg, T max is 0.74 h, and AUC is 23.7 ng•h/mL (8 mg tablet).
8% to 19% bound to plasma proteins. Vd at steady state is 302.9 L (IV bolus).
Hydromorphone is metabolized in the liver as glucuronidated conjugate (major metabolite) and 6-hydroxy (minor metabolite).
Systemic clearance is approximately 1.96 L/min. Terminal elimination t ½ is 2.3 h (IV). The mean t ½ is approximately 2.64 h. Hydromorphone is excreted primarily as the glucuronidated conjugate.
Onset of hydromorphone is 15 min (parenterally) and 30 min (oral).
Time to peak effect is 0.5 to 1 h.
Duration is longer than 5 h.
C max and AUC 0-48 is increased 2-fold in patients with moderate (CrCl 40 to 60 mL/min) and 3-fold in patients with severe (CrCl less than 30 mL/min) renal function impairment.Hepatic Function Impairment
C max and AUC 0-t is increased 4-fold in patients with moderate (Child-Pugh group B) hepatic function impairment.Gender
Women appear to have a 25% higher C max than men.
Relief of moderate to severe pain in opioid-tolerant patients such as because of biliary colic, burns, cancer, MI, renal colic, surgery, or trauma of soft tissue and bone.
Hypersensitivity to similar compounds; depressed ventilatory function; acute asthma; patients not already receiving large amounts of parenteral narcotics; patients with respiratory depression without access to resuscitative equipment; labor.
PO Usual starting dosage is 2 mg every 4 to 6 h as needed. For more severe pain, give 4 mg every 4 to 6 h. If the pain increases in severity, analgesia is not adequate, or tolerance occurs, a gradual increase in dosage may be necessary.Oral liquid
Usual dosage is 2.5 to 10 mg (2.5 to 10 mL) every 3 to 6 h, depending on the clinical situation. A gradual increase in dose may be required if analgesia is inadequate, tolerance develops, or pain severity increases.Adults
Suppositories One inserted rectally every 6 to 8 h.Adults
IM / Subcutaneous Usual starting dosage is 1 to 2 mg every 4 to 6 h as needed. Adjust dose according to severity of pain, underlying disease, age, and size of the patient.Adults
IV Administer slowly, over at least 2 to 3 min. A gradual increase in dose may be necessary if analgesia is inadequate, tolerance occurs, or pain severity increases. Note concentration and do not confuse with other standard, less concentrated formulations.
Store at 59° to 86°F. Protect from light.Suppositories
Store in refrigerator between 36° and 46°F.
Additive CNS and respiratory depression.Neuromuscular blocking agents
Pharmacologic effects may be enhanced, producing increased respiratory depression.Opioid agonist/antagonist analgesics (eg, buprenorphine, butorphanol, nalbuphine, pentazocine)
Use with caution; analgesic effect of hydromorphone may be reduced and withdrawal symptoms may be precipitated.
Bradycardia; cardiac arrest; circulatory depression; faintness; flushing of the face; hypertension; hypotension; orthostatic hypotension; palpitations; peripheral circulatory collapse; shock; syncope; tachycardia.
Agitation; anxiety; disorientation; dizziness; drowsiness; dysphoria; euphoria; fear; hallucination; headache; impaired physical performance; increased intracranial pressure; insomnia; lethargy; light-headedness; mental clouding; mental impairment; mood change (including apprehension, depression, dreams, floating feeling, nervousness); muscle rigidity; muscle tremor; paresthesia; psychic dependence; sedation; tremor; uncoordinated muscle movement; weakness.
Pruritus; rash; sweating; urticaria.
Blurred vision; diplopia; miosis; nystagmus; visual disturbances.
Anorexia; biliary tract spasm; constipation; cramps; diarrhea; dry mouth; ileus; nausea; taste alterations; vomiting.
Antidiuretic effect; spasm of vesical sphincters; ureteral spasm; urinary hesitancy; urinary retention.
Pain at injection site; wheal and flare over the vein with IV injection.
Apnea; bronchospasm; irregular and periodic breathing; laryngospasm; respiratory depression; respiratory arrest.
Hydromorphone injection is available as a highly concentrated solution (10 mg/mL) intended for use in narcotic-tolerant patients. Do not confuse with other standard, less concentrated formulations. Overdose and death could occur.Abuse
Hydromorphone is a potent opioid agonist with a high potential for abuse and risk of producing respiratory depression.
During dose titration, closely monitor patients with hepatic or renal function impairment.
Category C .
Excreted in breast milk.
Safety and efficacy not established.
Use with caution, usually starting at the low end of the dosage range, because of the greater frequency of decreased hepatic, renal, or cardiac function, and concomitant diseases or other drug therapy.
May need to reduce dose.
May need to reduce dose.
Use with caution in the elderly or debilitated and those with severe impairment of hepatic, pulmonary, or renal function; myxedema or hypothyroidism; adrenocortical insufficiency (eg, Addisons disease); CNS depression or coma; toxic psychosis; circulatory shock; prostatic hypertrophy or urethral stricture; gall bladder disease; pulmonary disease; acute alcoholism; delirium tremens; kyphoscoliosis; or following surgery.
Use with caution in patients known to be sensitive to sulfites, as some products contain bisulfites.
Diagnosis and clinical course may be obscured.
Use with caution in patients undergoing biliary tract surgery since drug may cause spasm of the sphincter of Oddi.
Cerebrospinal fluid pressure may be markedly exaggerated in the presence of head injury, other intracranial lesions, or preexisting increase in intracranial pressure.
Severe hypotension may occur; orthostatic hypotension may occur in ambulatory patients.
The 500 mg per 50 mL single-use vial contains rubber latex.
Respiratory depression is the chief hazard of hydromorphone injection. It occurs more frequently in elderly patients, in debilitated patients, and in patients suffering from hypoxia or hypercapnia. Even therapeutic doses may dangerously decrease pulmonary ventilation. Use with extreme caution in patients with COPD or cor pulmonale, decreased respiratory reserve, hypoxia, hypercapnia, or preexisting respiratory depression.
Mild to severe seizures and myoclonus may occur.
Both tolerance and physical dependence may occur.
Apnea; bradycardia; cardiopulmonary arrest; circulatory collapse; cold, clammy skin; constricted pupils; death; hypotension; respiratory depression; skeletal muscle flaccidity; somnolence progressing to stupor or coma.
Copyright © 2009 Wolters Kluwer Health.