Oxymorphone (oral)
Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]; Associate Editor(s)-in-Chief: Chetan Lokhande, M.B.B.S [2]
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Overview
Oxymorphone (oral) is an analgesic opioid that is FDA approved for the {{{indicationType}}} of Anesthesia; AdjunctView additional information.
Anxiety, Due to dyspnea associated with pulmonary edema caused by acute left ventricular dysfunctionView additional information.
Obstetric pain
Pain, acute (Moderate to Severe)
Pain, chronic (Severe), in patients requiring daily long-term around-the-clock opioid analgesic
Premedication for anesthetic procedure - Surgical procedure.. Common adverse reactions include Cardiovascular: Hypotension (less than 10% )
Dermatologic: Pruritus (less than or equal to 15.2% ), Sweating symptom (1% to less than 10% )
Gastrointestinal: Abdominal pain (1% to less than 10% ), Constipation (4.1% to 27.6% ), Nausea (2.9% to 33.1% ), Vomiting (less than or equal to 15.6% ), Xerostomia (1% to less than 10% )
Neurologic: Confusion (1% to less than 10% ), Dizziness (5% to 17% ), Headache (4% to 12% ), Somnolence (2% to 19% )
Respiratory: Dyspnea (1% to less than 10% ), Hypoxia (less than 10% )
Other: Fatigue (1% to less than 10% ), Fever (1% to 14.2% ).
Adult Indications and Dosage
FDA-Labeled Indications and Dosage (Adult)
be aware oxymorphone 5 mg and 10 mg tablets are available as both immediate- and extended-release formulations [1]. do not discontinue abruptly in the physically dependent patient [2] oral oxymorphone is approximately 10% bioavailable; to convert to parenteral therapy, administer one-tenth the patient's total daily oral oxymorphone dose as the total daily injection dose divided in 4 to 6 doses per day [2] Anesthesia; Adjunct: initially, 1 to 1.5 mg IM or subQ repeated every 4 to 6 hours as needed OR 0.5 mg IV [2] Anxiety, Due to dyspnea associated with pulmonary edema caused by acute left ventricular dysfunction: initially, 1 to 1.5 mg IM or subQ repeated every 4 to 6 hours as needed OR 0.5 mg IV [2] Obstetric pain: 0.5 to 1 mg IM during labor [2] Pain, acute (Moderate to Severe): (immediate release), initially, 5 to 20 mg ORALLY every 4 to 6 hours; MAX initial: 20 mg/dose; titrate based on patient response [3] Pain, acute (Moderate to Severe): initially, 1 to 1.5 mg IM or subQ repeated every 4 to 6 hours as needed OR 0.5 mg IV [2] Pain, chronic (Severe), in patients requiring daily long-term around-the-clock opioid analgesic: initial dose selection must take into account patient's prior analgesic treatment experience and risk factors for addiction, abuse, and misuse [1] Pain, chronic (Severe), in patients requiring daily long-term around-the-clock opioid analgesic: (extended-release) as first opioid analgesic and in patients who are not opioid-tolerant: initiate at 5 mg extended-release ORALLY every 12 hours [1] Pain, chronic (Severe), in patients requiring daily long-term around-the-clock opioid analgesic: (conversion from oral immediate-release oxymorphone) administer one-half total daily immediate-release dose ORALLY every 12 hours [1] Pain, chronic (Severe), in patients requiring daily long-term around-the-clock opioid analgesic: (conversion from parenteral oxymorphone) administer 5 times the patient's total daily parenteral dose ORALLY every 12 hours and monitor closely due to patient variability [1] Pain, chronic (Severe), in patients requiring daily long-term around-the-clock opioid analgesic: (conversion from other oral opioids) underestimate patient's 24-hour oral oxymorphone dose and administer one-half ORALLY every 12 hours while providing rescue medication as needed [1] Pain, chronic (Severe), in patients requiring daily long-term around-the-clock opioid analgesic: (extended-release) maintenance: adjust dose of extended-release tablets in increments of 5 to 10 mg ORALLY every 12 hours every 3 to 7 days [1] Premedication for anesthetic procedure - Surgical procedure: initially, 1 to 1.5 mg IM or subQ repeated every 4 to 6 hours as needed OR 0.5 mg IV [2]
Off-Label Use and Dosage (Adult)
Guideline-Supported Use
There is limited information about Off-Label Guideline-Supported Use of Oxymorphone in adult patients.
Non–Guideline-Supported Use
There is limited information about Off-Label Non–Guideline-Supported Use of Oxymorphone in adult patients.
Pediatric Indications and Dosage
FDA-Labeled Indications and Dosage (Pediatric)
safety and efficacy have not been established in pediatric patients younger than 18 years
Off-Label Use and Dosage (Pediatric)
Guideline-Supported Use
There is limited information about Off-Label Guideline-Supported Use of Oxymorphone in pediatric patients.
Non–Guideline-Supported Use
There is limited information about Off-Label Non–Guideline-Supported Use of Oxymorphone in pediatric patients.
Contraindications
Oxymorphone hydrochloride tablets are contraindicated in patients with a known hypersensitivity to oxymorphone or to any of the other ingredients in oxymorphone hydrochloride tablets, or with known hypersensitivity to morphine analogs such as codeine.
Oxymorphone hydrochloride tablets are contraindicated in patients with respiratory depression, except in monitored settings and in the presence of resuscitative equipment. Oxymorphone hydrochloride tablets are contraindicated in patients with acute or severe bronchial asthma or hypercarbia. Oxymorphone hydrochloride tablets are contraindicated in any patient who has or is suspected of having paralytic ileus [see Warnings and Precautions (5.8)]. Oxymorphone hydrochloride tablets are contraindicated in patients with moderate or severe hepatic impairment [see Warnings and Precautions (5.6)].
Warnings
Respiratory Depression
Respiratory depression is the chief hazard of oxymorphone hydrochloride. Respiratory depression may occur more frequently in elderly or debilitated patients as well as in those suffering from conditions accompanied by hypoxia or hypercapnia, when even moderate therapeutic doses may dangerously decrease pulmonary ventilation.
Administer oxymorphone hydrochloride with extreme caution to patients with conditions accompanied by hypoxia, hypercapnia, or decreased respiratory reserve such as: asthma, chronic obstructive pulmonary disease or cor pulmonale, severe obesity, sleep apnea syndrome, myxedema, kyphoscoliosis, CNS depression, or coma. In these patients, even usual therapeutic doses of oxymorphone may decrease respiratory drive while simultaneously increasing airway resistance to the point of apnea. Consider alternative non-opioid analgesics and use oxymorphone hydrochloride only under careful medical supervision at the lowest effective dose in such patients.
5.2 Misuse, Abuse, and Diversion of Opioids
Oxymorphone hydrochloride tablets contain oxymorphone, a mu opioid agonist and a Schedule II controlled substance with an abuse liability similar to morphine. Opioid agonists are sought by drug abusers and people with addiction disorders and are subject to criminal diversion.
Oxymorphone can be abused in a manner similar to other opioid agonists, legal or illicit. This issue should be considered when prescribing or dispensing oxymorphone in situations where the physician or pharmacist is concerned about an increased risk of misuse, abuse, or diversion.
Oxymorphone hydrochloride tablets may be abused by crushing, chewing, snorting, or injecting the product. These practices pose a significant risk to the abuser that could result in overdose and death [see Drug Abuse and Dependence (9)].
Oxymorphone hydrochloride tablets may be targeted for theft and diversion. Healthcare professionals should contact their State Medical Board, State Board of Pharmacy, or State Control Board for information on how to detect or prevent diversion of this product, and security requirements for storing and handling of oxymorphone hydrochloride tablets.
Healthcare professionals should advise patients to store oxymorphone hydrochloride tablets in a secure place, preferably locked and out of the reach of children and other non-caregivers.
Concerns about abuse, misuse, diversion and addiction should not prevent the proper management of pain.
5.3 Additive CNS Depressant Effects
The concomitant use of other CNS depressants including other opioids, general anesthetics, phenothiazines, other tranquilizers, sedatives, hypnotics, and alcohol with oxymorphone may produce increased depressant effects including hypoventilation, hypotension, profound sedation, coma and death [see Drug Interactions (7.1)].
5.4 Use in Patients With Head Injury and Increased Intracranial Pressure
In the presence of head injury, intracranial lesions or a preexisting increase in intracranial pressure, the respiratory depressant effects of opioid analgesics and their potential to elevate cerebrospinal fluid pressure (resulting from vasodilation following CO2 retention) may be markedly exaggerated. Furthermore, opioid analgesics can produce effects on papillary response and consciousness, which may obscure neurologic signs of further increases in intracranial pressure in patients with head injuries.
Administer oxymorphone hydrochloride with extreme caution in patients who may be particularly susceptible to the intracranial effects of CO2 retention, such as those with evidence of increased intracranial pressure or impaired consciousness. Opioids may obscure the clinical course of a patient with a head injury and should be used only if clinically warranted.
5.5 Hypotensive Effect
Oxymorphone hydrochloride, like all opioid analgesics, may cause severe hypotension in a patient whose ability to maintain blood pressure has been compromised by a depleted blood volume, or after concurrent administration with drugs such as phenothiazines or other agents that compromise vasomotor tone. Administer oxymorphone hydrochloride with caution to patients in circulatory shock, since vasodilation produced by the drug may further reduce cardiac output and blood pressure.
5.6 Hepatic Impairment
A study of extended-release oxymorphone tablets in patients with hepatic disease indicated greater plasma concentrations than in those with normal hepatic function [see Clinical Pharmacology (12.3)]. Use oxymorphone hydrochloride with caution in patients with mild impairment, starting with the lowest dose and titrating slowly while carefully monitoring for side effects [see Dosage and Administration (2.2, 2.5)]. Oxymorphone hydrochloride is contraindicated in patients with moderate or severe hepatic impairment.
5.7 Special Risk Groups
Use oxymorphone hydrochloride with caution in the following conditions: adrenocortical insufficiency (e.g., Addison’s disease), prostatic hypertrophy or urethral stricture, severe impairment of pulmonary or renal function, and toxic psychosis.
Opioids may aggravate convulsions in patients with convulsive disorders, and may induce or aggravate seizures in some clinical settings.
5.8 Gastrointestinal Effects
Opioids diminish propulsive peristaltic waves in the gastrointestinal tract. Monitor for decreased bowel motility in post-operative patients receiving opioids. The administration of oxymorphone hydrochloride may obscure the diagnosis or clinical course in patients with acute abdominal conditions. Oxymorphone hydrochloride is contraindicated in patients with paralytic ileus.
5.9 Use in Pancreatic/Biliary Tract Disease
Oxymorphone hydrochloride, like other opioids, may cause spasm of the sphincter of Oddi and should be used with caution in patients with biliary tract disease, including acute pancreatitis.
5.10 Driving and Operating Machinery
Opioid analgesics impair the mental and physical abilities needed to perform potentially hazardous activities such as driving a car or operating machinery.
Adverse Reactions
Clinical Trials Experience
The following serious adverse reactions are discussed elsewhere in the labeling:
Respiratory depression [see Warnings and Precautions (5.1)] Misuse and abuse [see Warnings and Precautions (5.2) and Drug Abuse and Dependence (9)] CNS depressant effects [see Warnings and Precautions (5.3)]
Because clinical trials are conducted under widely varying conditions, adverse reaction rates observed in the clinical trials of a drug cannot be directly compared to rates in the clinical trials of another drug and may not reflect the rates observed in clinical practice.
6.1 Clinical Trials Experience
A total of 591 patients were treated with oxymorphone hydrochloride in controlled clinical trials. The clinical trials consisted of patients with acute post-operative pain (n = 557) and cancer pain (n = 34) trials.
The following table lists adverse reactions that were reported in at least 2% of patients receiving oxymorphone hydrochloride in placebo-controlled trials (acute post-operative pain (N = 557)).
The common (≥ 1% to < 10%) adverse drug reactions reported at least once by patients treated with oxymorphone hydrochloride in the clinical trials organized by MedDRA’s (Medical Dictionary for Regulatory Activities) System Organ Class were and not represented in Table 1:
Cardiac disorders: tachycardia Gastrointestinal disorders: dry mouth, abdominal distention, and flatulence General disorders and administration site conditions: sweating increased Nervous system disorders: anxiety and sedation Respiratory, thoracic and mediastinal disorders: hypoxia Vascular disorders: hypotension
Other less common adverse reactions known with opioid treatment that were seen < 1% in the oxymorphone hydrochloride trials include the following:
Abdominal pain, ileus, diarrhea, agitation, disorientation, restlessness, feeling jittery, hypersensitivity, allergic reactions, bradycardia, central nervous system depression, depressed level of consciousness, lethargy, mental impairment, mental status changes, fatigue, depression, clamminess, flushing, hot flashes, dehydration, dermatitis, dyspepsia, dysphoria, edema, euphoric mood, hallucination, hypertension, insomnia, miosis, nervousness, palpitation, postural hypotension, syncope, dyspnea, respiratory depression, respiratory distress, respiratory rate decreased, oxygen saturation decreased, difficult micturition, urinary retention, urticaria, vision blurred, visual disturbances, weakness, appetite decreased, and weight decreased.
Postmarketing Experience
The following adverse reactions have been identified during post approval use of oxymorphone hydrochloride. Because these reactions are reported voluntarily from a population of uncertain size, it is not always possible to reliably estimate their frequency or establish a causal relationship to drug exposure.
Nervous system disorder: amnesia, convulsion, memory impairment
Drug Interactions
Use With CNS Depressants
The concomitant use of other CNS depressants including sedatives, hypnotics, tranquilizers, general anesthetics, phenothiazines, other opioids, and alcohol may produce additive CNS depressant effects. Oxymorphone hydrochloride, like all opioid analgesics, should be started at 1/3 to 1/2 of the usual dose in patients who are concurrently receiving other central nervous system depressants because respiratory depression, hypotension, and profound sedation, coma and death may result and titrated slowly as necessary for adequate pain relief.
When combined therapy with any of the above medications is considered, the dose of one or both agents should be reduced [see Dosage and Administration (2.7) and Warnings and Precautions (5.3)].
7.2 Interactions With Mixed Agonist/Antagonist Opioid Analgesics
Agonist/antagonist analgesics (i.e., pentazocine, nalbuphine, butorphanol, and buprenorphine) should be administered with caution to a patient who has received or is receiving a course of therapy with a pure opioid agonist analgesic such as oxymorphone. In this situation, mixed agonist/antagonist analgesics may reduce the analgesic effect of oxymorphone and/or may precipitate withdrawal symptoms in these patients.
7.3 Cimetidine
CNS side effects have been reported (e.g., confusion, disorientation, respiratory depression, apnea, seizures) following coadministration of cimetidine with opioid analgesics; a causal relationship has not been established.
7.4 Anticholinergics
Anticholinergics or other medications with anticholinergic activity when used concurrently with opioid analgesics may result in increased risk of urinary retention and/or severe constipation, which may lead to paralytic ileus.
7.5 MAO Inhibitors
Oxymorphone hydrochloride is not recommended for use in patients who have received MAO inhibitors within 14 days, because severe and unpredictable potentiation by MAO inhibitors has been reported with opioid analgesics. No specific interaction between oxymorphone and monoamine oxidase inhibitors has been observed, but caution in the use of any opioid in patients taking this class of drugs is appropriate.
Use in Specific Populations
Pregnancy
Pregnancy Category (FDA):
There is no FDA guidance on usage of Oxymorphone (oral) in women who are pregnant.
Pregnancy Category (AUS):
There is no Australian Drug Evaluation Committee (ADEC) guidance on usage of Oxymorphone (oral) in women who are pregnant.
Labor and Delivery
There is no FDA guidance on use of Oxymorphone (oral) during labor and delivery.
Nursing Mothers
There is no FDA guidance on the use of Oxymorphone (oral) in women who are nursing.
Pediatric Use
There is no FDA guidance on the use of Oxymorphone (oral) in pediatric settings.
Geriatic Use
There is no FDA guidance on the use of Oxymorphone (oral) in geriatric settings.
Gender
There is no FDA guidance on the use of Oxymorphone (oral) with respect to specific gender populations.
Race
There is no FDA guidance on the use of Oxymorphone (oral) with respect to specific racial populations.
Renal Impairment
There is no FDA guidance on the use of Oxymorphone (oral) in patients with renal impairment.
Hepatic Impairment
There is no FDA guidance on the use of Oxymorphone (oral) in patients with hepatic impairment.
Females of Reproductive Potential and Males
There is no FDA guidance on the use of Oxymorphone (oral) in women of reproductive potentials and males.
Immunocompromised Patients
There is no FDA guidance one the use of Oxymorphone (oral) in patients who are immunocompromised.
Administration and Monitoring
Administration
There is limited information regarding Oxymorphone (oral) Administration in the drug label.
Monitoring
There is limited information regarding Oxymorphone (oral) Monitoring in the drug label.
IV Compatibility
There is limited information regarding the compatibility of Oxymorphone (oral) and IV administrations.
Overdosage
There is limited information regarding Oxymorphone (oral) overdosage. If you suspect drug poisoning or overdose, please contact the National Poison Help hotline (1-800-222-1222) immediately.
Pharmacology
There is limited information regarding Oxymorphone (oral) Pharmacology in the drug label.
Mechanism of Action
There is limited information regarding Oxymorphone (oral) Mechanism of Action in the drug label.
Structure
There is limited information regarding Oxymorphone (oral) Structure in the drug label.
Pharmacodynamics
There is limited information regarding Oxymorphone (oral) Pharmacodynamics in the drug label.
Pharmacokinetics
There is limited information regarding Oxymorphone (oral) Pharmacokinetics in the drug label.
Nonclinical Toxicology
There is limited information regarding Oxymorphone (oral) Nonclinical Toxicology in the drug label.
Clinical Studies
There is limited information regarding Oxymorphone (oral) Clinical Studies in the drug label.
How Supplied
There is limited information regarding Oxymorphone (oral) How Supplied in the drug label.
Storage
There is limited information regarding Oxymorphone (oral) Storage in the drug label.
Images
Drug Images
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Package and Label Display Panel
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Patient Counseling Information
There is limited information regarding Oxymorphone (oral) Patient Counseling Information in the drug label.
Precautions with Alcohol
Alcohol-Oxymorphone interaction has not been established. Talk to your doctor about the effects of taking alcohol with this medication.
Brand Names
There is limited information regarding Oxymorphone (oral) Brand Names in the drug label.
Look-Alike Drug Names
There is limited information regarding Oxymorphone (oral) Look-Alike Drug Names in the drug label.
Drug Shortage Status
Price
References
The contents of this FDA label are provided by the National Library of Medicine.