Morphine Sulfate Generic Name & Formulations
Legal Class
General Description
Pharmacological Class
See Also
How Supplied
Contact supplier
Manufacturer
Mechanism of Action
Morphine Sulfate Indications
Indications
Limitations of Use
Due to risks of addiction, abuse, and misuse with opioids (can occur at any dosage or duration), reserve for use in patients for whom alternative treatment options (eg, non-opioid analgesics, opioid combination products) are not tolerated or inadequate to provide analgesia. Should not be used for an extended period of time unless the pain remains severe enough to require an opioid analgesic and for which alternative treatment options continue to be inadequate.
Morphine Sulfate Dosage and Administration
Adult
Children
Morphine Sulfate Contraindications
Contraindications
Morphine Sulfate Boxed Warnings
Boxed Warning
Serious and life-threatening risks from use of Morphine Sulfate: Addiction, abuse, and misuse; Life-threatening respiratory depression; Accidental ingestion; Risks from concomitant use with benzodiazepines or other CNS depressants; Neonatal opioid withdrawal syndrome; Opioid analgesic risk evaluation and mitigation strategy (REMS).
Morphine Sulfate Warnings/Precautions
Warnings/Precautions
Assess the potential need for access to naloxone when initiating and renewing therapy. Consider prescribing naloxone based on risk factors for overdose (eg, history of opioid use disorder, prior opioid overdose, household members or other close contacts at risk for accidental ingestion or overdose). Abuse potential (monitor). Life-threatening respiratory depression esp. during initiation or following dose increases. Accidental exposure may cause fatal overdose (esp. in children). Sleep-related breathing disorders (including central sleep apnea (CSA), sleep-related hypoxemia); consider dose reduction if CSA develops. Opioid-induced hyperalgesia (OIH) and allodynia; consider decreasing dose of current opioid or opioid rotation if OIH is suspected. COPD, cor pulmonale, decreased respiratory reserve, hypoxia, hypercapnia, or pre-existing respiratory depression; monitor and consider non-opioid analgesics. Adrenal insufficiency. Monitor for signs of hypotension when initiating or titrating dose. Head injury. Increased intracranial pressure, brain tumors; monitor. Seizure disorders. CNS depression. Impaired consciousness, coma, shock; avoid. Biliary tract disease. Acute pancreatitis. Drug abusers. Renal or hepatic impairment; initiate lower doses and titrate slowly. Reevaluate periodically. Avoid abrupt cessation. Elderly. Cachectic. Debilitated. Pregnancy; potential neonatal opioid withdrawal syndrome during prolonged use. Labor & delivery: not recommended. Nursing mothers: monitor infants.
REMS
Morphine Sulfate Pharmacokinetics
Absorption
Oral bioavailability: <40%. Maximum analgesic effect occurs 60 minutes post-administration.
Distribution
Volume of distribution: ~1–6 L/kg. Plasma protein bound: 20–35%.
Elimination
Renal (primary), fecal (7–10%). Half-life: ~2 hours (after IV admin). Plasma clearance: ~20–30 mL/min/kg (adult).
Morphine Sulfate Interactions
Interactions
Morphine Sulfate Adverse Reactions
Adverse Reactions
Constipation, nausea, somnolence, lightheadedness, dizziness, sedation, vomiting, sweating; respiratory depression, orthostatic hypotension, syncope, OIH and allodynia.
Morphine Sulfate Clinical Trials
See Literature
Morphine Sulfate Note
Not Applicable
Morphine Sulfate Patient Counseling
See Literature