Morphine Sulfate 100 MG Extended Release Oral Tablet
Generic Name: MORPHINE SULFATE
Brand Name: morphine sulfate extended release
- Substance Name(s):
- MORPHINE SULFATE
DRUG INTERACTIONS
7 Mixed agonist/antagonist opioid analgesics: Avoid use with morphine sulfate extended-release tablets because they may reduce analgesic effect of morphine sulfate extended-release tablets or precipitate withdrawal symptoms.
(5.11, 7.2) Muscle relaxants: Avoid use with morphine sulfate extended-release tablets because of increased risk of respiratory depression.
(7.3) Monoamine oxidase inhibitors (MAOIs): Avoid morphine sulfate extended-release tablets in patients taking MAOIs or within 14 days of stopping such treatment.
(7.4) 7.1 CNS Depressants Concurrent use of morphine sulfate extended-release tablets and other central nervous system (CNS) depressants including sedatives or hypnotics, general anesthetics, phenothiazines, tranquilizers, and alcohol can increase the risk of respiratory depression, hypotension, profound sedation or coma.
Monitor patients receiving CNS depressants and morphine sulfate extended-release tablets for signs of respiratory depression and hypotension.
When such combined therapy is contemplated, reduce the initial dose of one or both agents.
7.2 Mixed Agonists/Antagonist Opioid Analgesics Mixed agonist/antagonist analgesics (i.e., pentazocine, nalbuphine, butorphanol) may reduce the analgesic effect of morphine sulfate extended-release tablets or may precipitate withdrawal symptoms in these patients.
Avoid the use of agonist/antagonist analgesics in patients receiving morphine sulfate extended-release tablets.
7.3 Muscle Relaxants Morphine may enhance the neuromuscular blocking action of skeletal muscle relaxants and produce an increased degree of respiratory depression.
Monitor patients receiving muscle relaxants and morphine sulfate extended-release tablets for signs of respiratory depression that may be greater than otherwise expected.
7.4 Monoamine Oxidase Inhibitors (MAOIs) The effects of morphine may be potentiated by MAOIs.
Monitor patients on concurrent therapy with an MAOI and morphine sulfate extended-release tablets for increased respiratory and central nervous system depression.
MAOIs have been reported to potentiate the effects of morphine anxiety, confusion, and significant depression of respiration or coma.
Morphine sulfate extended-release tablets should not be used in patients taking MAOIs or within 14 days of stopping such treatment.
7.5 Cimetidine Cimetidine can potentiate morphine-induced respiratory depression.
There is a report of confusion and severe respiratory depression when a patient undergoing hemodialysis was concurrently administered morphine and cimetidine.
Monitor patients for respiratory depression when morphine sulfate extended-release tablets and cimetidine are used concurrently.
7.6 Diuretics Morphine can reduce the efficacy of diuretics by inducing the release of antidiuretic hormone.
Morphine may also lead to acute retention of urine by causing spasm of the sphincter of the bladder, particularly in men with enlarged prostates.
7.7 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.
Monitor patients for signs of urinary retention or reduced gastric motility when morphine sulfate extended-release tablets are used concurrently with anticholinergic drugs.
7.8 P-Glycoprotein (PGP) Inhibitors PGP-inhibitors (e.g., quinidine) may increase the absorption/exposure of morphine sulfate by about two-fold.
Therefore, monitor patients for signs of respiratory and central nervous system depression when morphine sulfate extended-release tablets are used concurrently with PGP inhibitors.
OVERDOSAGE
10 Clinical Presentation Acute overdosage with morphine is manifested by respiratory depression, somnolence progressing to stupor or coma, skeletal muscle flaccidity, cold and clammy skin, constricted pupils, and, in some cases, pulmonary edema, bradycardia, hypotension, and death.
Marked mydriasis rather than miosis may be seen due to severe hypoxia in overdose situations.
Treatment of Overdose In case of overdose, priorities are the reestablishment of a patent and protected airway and institution of assisted or controlled ventilation if needed.
Employ other supportive measures (including oxygen, vasopressors) in the management of circulatory shock and pulmonary edema as indicated.
Cardiac arrest or arrhythmias will require advanced life support techniques.
The opioid antagonists, naloxone or nalmefene, are specific antidotes to respiratory depression resulting from opioid overdose.
Opioid antagonists should not be administered in the absence of clinically significant respiratory or circulatory depression secondary to morphine overdose.
Such agents should be administered cautiously to persons who are known, or suspected to be physically dependent on morphine sulfate extended-release tablets.
In such cases, an abrupt or complete reversal of opioid effects may precipitate an acute withdrawal syndrome.
Because the duration of reversal would be expected to be less than the duration of action of morphine in morphine sulfate extended-release tablets, carefully monitor the patient until spontaneous respiration is reliably reestablished.
Morphine sulfate extended-release tablets will continue to release morphine and add to the morphine load for 24 to 48 hours or longer following ingestion necessitating prolonged monitoring.
If the response to opioid antagonists is suboptimal or not sustained, additional antagonist should be administered as directed in the product’s prescribing information.
In an individual physically dependent on opioids, administration of the usual dose of the antagonist will precipitate an acute withdrawal syndrome.
The severity of the withdrawal symptoms experienced will depend on the degree of physical dependence and the dose of the antagonist administered.
If a decision is made to treat serious respiratory depression in the physically dependent patient, administration of the antagonist should be begun with care and by titration with smaller than usual doses of the antagonist.
DESCRIPTION
11 Morphine Sulfate Extended-Release Tablets are for oral use and contain morphine sulfate, an agonist at the mu-opioid receptor.
Each tablet contains the following inactive ingredients common to all strengths: cetostearyl alcohol, hydroxyethyl cellulose, hypromellose, magnesium stearate, polyethylene glycol, talc and titanium dioxide.
The tablet strengths describe the amount of morphine per tablet as the pentahydrated sulfate salt (morphine sulfate).
The 15 mg tablets also contain: FD&C Blue No.
2, lactose monohydrate, polysorbate 80 The 30 mg tablets also contain: D&C Red No.
7, FD&C Blue No.
1, lactose monohydrate, polysorbate 80 The 60 mg tablets also contain: D&C Red No.
30, D&C Yellow No.
10, hydroxypropyl cellulose, lactose monohydrate The 100 mg tablets also contain: black iron oxide The 200 mg tablets also contain: D&C Yellow No.
10, FD&C Blue No.
1, hydroxypropyl cellulose Morphine sulfate is an odorless, white, crystalline powder with a bitter taste.
It has a solubility of 1 in 21 parts of water and 1 in 1000 parts of alcohol, but is practically insoluble in chloroform or ether.
The octanol: water partition coefficient of morphine is 1.42 at physiologic pH and the pKb is 7.9 for the tertiary nitrogen (mostly ionized at pH 7.4).
Its structural formula is: Structure
HOW SUPPLIED
16 /STORAGE AND HANDLING EXTENDED-RELEASE, ROUND, GRAY-COLORED, FILM-COATED TABLETS BEARING THE SYMBOL ABG OH ONE SIDE AND 100 ON THE OTHER
RECENT MAJOR CHANGES
Boxed Warning 2/2012 Indications and Usage (1) 2/2012 Dosage and Administration (2) 2/2012 Contraindications (4) 2/2012 Warnings and Precautions (5) 2/2012
DOSAGE FORMS AND STRENGTHS
3 DOSAGE FORMS & STRENGTHS Morphine sulfate extended-release tablets 15 mg Round, blue-colored, film-coated tablets bearing the symbol ABG on one side and 15 on the other Morphine sulfate extended-release tablets 30 mg Round, lavender-colored, film-coated tablets bearing the symbol ABG on one side and 30 on the other Morphine sulfate extended-release tablets 60 mg Round, orange-colored, film-coated tablets bearing the symbol ABG on one side and 60 on the other Morphine sulfate extended-release tablets 100 mg* Round, gray-colored, film-coated tablets bearing the symbol ABG on one side and 100 on the other Morphine sulfate extended-release tablets 200 mg* Capsule-shaped, green-colored, film-coated tablets bearing the symbol ABG on one side and 200 on the other *100 mg and 200 mg tablets are for use in opioid-tolerant patients only Tablets (morphine sulfate): 15 mg, 30 mg, 60 mg, 100 mg, 200 mg (3)
MECHANISM OF ACTION
12.1 Mechanism of Action Morphine sulfate, an opioid agonist, is relatively selective for the mu receptor, although it can interact with other opioid receptors at higher doses.
In addition to analgesia, the widely diverse effects of morphine sulfate include analgesia, dysphoria, euphoria, somnolence, respiratory depression, diminished gastrointestinal motility, altered circulatory dynamics, histamine release, physical dependence, and alterations of the endocrine and autonomic nervous systems.
Morphine produces both its therapeutic and its adverse effects by interaction with one or more classes of specific opioid receptors located throughout the body.
Morphine acts as a full agonist, binding with and activating opioid receptors at sites in the peri-aqueductal and peri-ventricular grey matter, the ventro-medial medulla and the spinal cord to produce analgesia.
Effects on the Central Nervous System The principal actions of therapeutic value of morphine are analgesia and sedation.
Specific CNS opiate receptors for endogenous compounds with opioid-like activity have been identified throughout the brain and spinal cord and are likely to play a role in the expression of analgesic effects.
Morphine produces respiratory depression by direct action on brainstem respiratory centers.
The mechanism of respiratory depression involves a reduction in the responsiveness of the brainstem respiratory centers to increases in carbon dioxide tension, and to electrical stimulation.
Morphine depresses the cough reflex by direct effect on the cough center in the medulla.
Morphine causes miosis, even in total darkness.
Pinpoint pupils are a sign of narcotic overdose but are not pathognomonic (e.g., pontine lesions of hemorrhagic or ischemic origins may produce similar findings).
Marked mydriasis rather than miosis may be seen with worsening hypoxia.
Effects on the Gastrointestinal Tract and Other Smooth Muscle Morphine causes a reduction in motility associated with an increase in smooth muscle tone in the antrum of the stomach and in the duodenum.
Digestion of food is delayed in the small intestine and propulsive contractions are decreased.
Propulsive peristaltic waves in the colon are decreased, while tone may be increased to the point of spasm.
The end result is constipation.
Morphine can cause a marked reduction in gastric, biliary and pancreatic secretions, spasm of the sphincter of Oddi, and transient elevations in serum amylase.
Effects on the Cardiovascular System Morphine produces peripheral vasodilation which may result in orthostatic hypotension.
Release of histamine can occur and may contribute to opioid-induced hypotension.
Manifestations of histamine release and/or peripheral vasodilation may include pruritus, flushing, red eyes, and sweating.
Effects on the Endocrine System Opioids inhibit the secretion of ACTH, cortisol, testosterone, and luteinizing hormone (LH) in humans.
They also stimulate prolactin, growth hormone (GH) secretion, and pancreatic secretion of insulin and glucagon.
Effects on the Immune System Opioids have been shown to have a variety of effects on components of the immune system in in vitro and animal models.
The clinical significance of these findings is unknown.
Overall, the effects of opioids appear to be modestly immunosuppressive.
INDICATIONS AND USAGE
1 INDICATIONS & USAGE Morphine Sulfate Extended-Release Tablets are indicated for the management of moderate to severe pain when a continuous, around-the-clock opioid analgesic is needed for an extended period of time.
Limitations of Use Morphine sulfate extended-release tablets are not for use: As an as-needed (prn) analgesic.
For pain that is mild or not expected to persist for an extended period of time For acute pain In the immediate postoperative period (the first 24 hours following surgery) for patients not previously taking the drug, because its safety in this setting has not been established.
For postoperative pain unless the patient is already receiving chronic opioid therapy prior to surgery or if the postoperative pain is expected to be moderate to severe and persist for an extended period of time.
Morphine sulfate extended-release 100 mg and 200 mg tablets are only for patients in whom tolerance to an opioid of comparable potency is established.
Patients considered opioid-tolerant are those taking at least 60 mg of morphine daily, at least 30 mg of oral oxycodone daily, at least 8 mg of oral hydromorphone daily, or an equianalgesic dose of another opioid for a week or longer.
Morphine sulfate extended-release tablets are an opioid agonist product indicated for the management of moderate to severe pain when a continuous, around-the-clock opioid analgesic is needed for an extended period of time.
(1) Limitations of Use Morphine sulfate extended-release tablets are not for use: As an as-needed (prn) analgesic (1) For pain that is mild or not expected to persist for an extended period of time (1) For acute pain (1) In the immediate postoperative period (1) For postoperative pain, unless the patient is already receiving chronic opioid therapy prior to surgery, or if the postoperative pain is expected to be moderate to severe and persist for an extended period of time (1) Morphine sulfate extended-release 100 mg and 200 mg tablets are only for patients in whom tolerance to an opioid of comparable potency is established.
(1)
PEDIATRIC USE
8.4 Pediatric Use The safety and effectiveness in pediatric patients below the age of 18 have not been established.
PREGNANCY
8.1 Pregnancy Teratogenic Effects (Pregnancy Category C) No formal studies to assess the teratogenic effects of morphine in animals have been conducted.
It is also not known whether morphine can cause fetal harm when administered to a pregnant woman or can affect reproductive capacity.
Morphine should be given to a pregnant woman only if clearly needed.
In humans, the frequency of congenital anomalies has been reported to be no greater than expected among the children of 70 women who were treated with morphine during the first four months of pregnancy or in 448 women treated with morphine anytime during pregnancy.
Furthermore, no malformations were observed in the infant of a woman who attempted suicide by taking an overdose of morphine and other medication during the first trimester of pregnancy.
Several literature reports indicate that morphine administered subcutaneously during the early gestational period in mice and hamsters produced neurological, soft tissue and skeletal abnormalities.
With one exception, the effects that have been reported were following doses that were maternally toxic and the abnormalities noted were characteristic of those observed when maternal toxicity is present.
In one study, following subcutaneous infusion of doses greater than or equal to 0.15 mg/kg to mice, exencephaly, hydronephrosis, intestinal hemorrhage, split supraoccipital, malformed sternebrae, and malformed xiphoid were noted in the absence of maternal toxicity.
In the hamster, morphine sulfate given subcutaneously on gestation day 8 produced exencephaly and cranioschisis.
In rats treated with subcutaneous infusions of morphine during the period of organogenesis, no teratogenicity was observed.
No maternal toxicity was observed in this study; however, increased mortality and growth retardation were seen in the offspring.
In two studies performed in the rabbit, no evidence of teratogenicity was reported at subcutaneous doses up to 100 mg/kg.
Non-Teratogenic Effects Infants born to mothers who have taken opioids chronically may exhibit neonatal withdrawal syndrome [see Use in Specific Populations ( 8.6 )], reversible reduction in brain volume, small size, decreased ventilatory response to CO2 and increased risk of sudden infant death syndrome.
Morphine sulfate should be used by a pregnant woman only if the need for opioid analgesia clearly outweighs the potential risks to the fetus.
Controlled studies of chronic in utero morphine exposure in pregnant women have not been conducted.
Published literature has reported that exposure to morphine during pregnancy in animals is associated with reduction in growth and a host of behavioral abnormalities in the offspring.
Morphine treatment during gestational periods of organogenesis in rats, hamsters, guinea pigs and rabbits resulted in the following treatment-related embryotoxicity and neonatal toxicity in one or more studies: decreased litter size, embryo-fetal viability, fetal and neonatal body weights, absolute brain and cerebellar weights, delayed motor and sexual maturation, and increased neonatal mortality, cyanosis and hypothermia.
Decreased fertility in female offspring, and decreased plasma and testicular levels of luteinizing hormone and testosterone, decreased testes weights, seminiferous tubule shrinkage, germinal cell aplasia, and decreased spermatogenesis in male offspring were also observed.
Decreased litter size and viability were observed in the offspring of male rats administered morphine (25 mg/kg, IP) for 1 day prior to mating.
Behavioral abnormalities resulting from chronic morphine exposure of fetal animals included altered reflex and motor skill development, mild withdrawal, and altered responsiveness to morphine persisting into adulthood.
NUSRING MOTHERS
8.3 Nursing Mothers Morphine is excreted in breast milk, with a milk to plasma morphine AUC ratio of approximately 2.5:1.
The amount of morphine received by the infant varies depending on the maternal plasma concentration, the amount of milk ingested by the infant, and the extent of first pass metabolism.
Withdrawal signs can occur in breast-feeding infants when maternal administration of morphine is stopped.
Because of the potential for adverse reactions in nursing infants from morphine sulfate extended-release tablets, a decision should be made whether to discontinue nursing or discontinue the drug, taking into account the importance of the drug to the mother.
BOXED WARNING
WARNING: ABUSE POTENTIAL, LIFE-THREATENING RESPIRATORY DEPRESSION, and ACCIDENTAL EXPOSURE Abuse Potential Morphine sulfate extended-release tablets contain morphine; an opioid agonist and Schedule II controlled substance with an abuse liability similar to other opioid agonists, legal or illicit [see Warnings and Precautions ( 5.1 )] .
Assess each patient’s risk for opioid abuse or addiction prior to prescribing morphine sulfate extended-release tablets.
The risk for opioid abuse is increased in patients with a personal or family history of substance abuse (including drug or alcohol abuse or addiction) or mental illness (e.g., major depressive disorder).
Routinely monitor all patients receiving morphine sulfate extended-release tablets for signs of misuse, abuse, and addiction during treatment [see Drug Abuse and Dependence ( 9 )].
Life-Threatening Respiratory Depression Respiratory depression, including fatal cases, may occur with use of morphine sulfate extended-release tablets, even when the drug has been used as recommended and not misused or abused [see Warnings and Precautions ( 5.2 )] .
Proper dosing and titration are essential and morphine sulfate extended-release tablets should only be prescribed by healthcare professionals who are knowledgeable in the use of potent opioids for the management of chronic pain.
Monitor for respiratory depression, especially during initiation of morphine sulfate extended-release tablets or following a dose increase .
Instruct patients to swallow morphine sulfate extended-release tablets whole.
Crushing, dissolving, or chewing the tablet can cause rapid release and absorption of a potentially fatal dose of morphine.
Accidental Exposure Accidental ingestion of morphine sulfate extended-release tablets, especially in children, can result in a fatal overdose of morphine [see Warnings and Precautions ( 5.3 )] .
WARNING: ABUSE POTENTIAL, LIFE-THREATENING RESPIRATORY DEPRESSION, and ACCIDENTAL EXPOSURE See full prescribing information for complete boxed warning .
Morphine sulfate extended-release tablets contain morphine sulfate, a Schedule II controlled substance.
Monitor for signs of misuse, abuse, and addiction during morphine sulfate extended-release tablet therapy (5.1, 9).
Fatal respiratory depression may occur, with highest risk at initiation and with dose increases.
Instruct patients on proper administration of morphine sulfate extended-release tablets to reduce the risk (5.2).
Accidental ingestion of morphine sulfate extended-release tablets can result in fatal overdose of morphine, especially in children (5.3).
WARNING AND CAUTIONS
5 WARNINGS AND PRECAUTIONS Elderly, cachectic, and debilitated patients, and patients with chronic pulmonary disease: Monitor closely because of increased risk of respiratory depression.
(5.4, 5.5) Interaction with CNS depressants: Consider dose reduction of one or both drugs because of additive effects.
(5.6, 7.1) Hypotensive effect: Monitor during dose initiation and titration (5.7) Patients with head injury or increased intracranial pressure: Monitor for sedation and respiratory depression.
Avoid use of morphine sulfate extended-release tablets in patients with impaired consciousness or coma susceptible to intracranial effects of CO2 retention.
(5.8) 5.1 Abuse Potential Morphine sulfate extended-release tablets contain morphine, an opioid agonist and a Schedule II controlled substance.
Morphine can be abused in a manner similar to other opioid agonists, legal or illicit.
Opioid agonists are sought by drug abusers and people with addiction disorders and are subject to criminal diversion.
Consider these risks when prescribing or dispensing morphine sulfate extended-release tablets in situations where there is concern about increased risks of misuse, abuse, or diversion.
Concerns about abuse, addiction, and diversion should not, however, prevent the proper management of pain.
Assess each patient’s risk for opioid abuse or addiction prior to prescribing morphine sulfate extended-release tablets.
The risk for opioid abuse is increased in patients with a personal or family history of substance abuse (including drug or alcohol abuse or addiction) or mental illness (e.g., major depression).
Patients at increased risk may still be appropriately treated with modified-release opioid formulations; however these patients will require intensive monitoring for signs of misuse, abuse, or addiction.
Routinely monitor all patients receiving opioids for signs of misuse, abuse, and addiction because these drugs carry a risk for addiction even under appropriate medical use.
Misuse or abuse of morphine sulfate extended-release tablets by crushing, chewing, snorting, or injecting the dissolved product will result in the uncontrolled delivery of the opioid and pose a significant risk that could result in overdose and death [see Overdosage ( 10 )].
Contact local state professional licensing board or state controlled substances authority for information on how to prevent and detect abuse or diversion of this product.
5.2 Life-Threatening Respiratory Depression Respiratory depression is the chief hazard of opioid agonists, including morphine sulfate extended-release tablets.
Respiratory depression if not immediately recognized and treated, may lead to respiratory arrest and death.
Respiratory depression from opioids is manifested by a reduced urge to breathe and a decreased rate of respiration, often associated with a “sighing” pattern of breathing (deep breaths separated by abnormally long pauses).
Carbon dioxide (CO2) retention from opioid-induced respiratory depression can exacerbate the sedating effects of opioids.
Management of respiratory depression may include close observation, supportive measures, and use of opioid antagonists, depending on the patient’s clinical status [see Overdosage ( 10 )].
While serious, life-threatening, or fatal respiratory depression can occur at any time during the use of morphine sulfate extended-release tablets, the risk is greatest during the initiation of therapy or following a dose increase.
Closely monitor patients for respiratory depression when initiating therapy with morphine sulfate extended-release tablets and following dose increases.
Instruct patients against use by individuals other than the patient for whom morphine sulfate extended-release tablets were prescribed and to keep morphine sulfate extended-release tablets out of the reach of children, as such inappropriate use may result in fatal respiratory depression.
To reduce the risk of respiratory depression, proper dosing and titration of morphine sulfate extended-release tablets are essential [see Dosage and Administration ( 2 )].
Overestimating the morphine sulfate extended-release tablets dose when converting patients from another opioid product can result in fatal overdose with the first dose.
Respiratory depression has also been reported with use of modified-release opioids when used as recommended and not misused or abused.
To further reduce the risk of respiratory depression, consider the following: •Proper dosing and titration are essential and morphine sulfate extended-release tablets should only be prescribed by healthcare professionals who are knowledgeable in the use of potent opioids for the management of chronic pain.
Morphine sulfate extended-release 100 mg and 200 mg tablets are for use in opioid-tolerant patients only.
Ingestion of these strengths of morphine sulfate extended-release tablets may cause fatal respiratory depression when administered to patients not already tolerant to high doses of opioids.
•Instruct patients to swallow morphine sulfate extended-release tablets intact.
The tablets are not to be crushed, dissolved, or chewed.
The resulting morphine dose may be fatal, particularly in opioid-naïve individuals.
•Morphine sulfate extended-release tablets are contraindicated in patients with respiratory depression and in patients with conditions that increase the risk of life-threatening respiratory depression [see Contraindications (4)].
5.3 Accidental Exposure Accidental consumption of morphine sulfate extended-release tablets, especially in children, can result in a fatal overdose of morphine.
5.4 Elderly, Cachectic, and Debilitated Patients Respiratory depression is more likely to occur in elderly, cachectic, or debilitated patients as they may have altered pharmacokinetics or altered clearance compared to younger, healthier patients.
Therefore, monitor such patients closely, particularly when initiating and titrating morphine sulfate extended-release tablets and when morphine sulfate extended-release tablets are given concomitantly with other drugs that depress respiration [see Warnings and Precautions ( 5.2 )].
5.5 Use in Patients with Chronic Pulmonary Disease Monitor patients with significant chronic obstructive pulmonary disease or cor pulmonale, and patients having a substantially decreased respiratory reserve, hypoxia, hypercapnia, or pre-existing respiratory depression for respiratory depression, particularly when initiating therapy and titrating with morphine sulfate extended-release tablets, as in these patients, even usual therapeutic doses of morphine sulfate extended-release tablets may decrease respiratory drive to the point of apnea [see Warnings and Precautions ( 5.2 )].
Consider the use of alternative non-opioid analgesics in these patients if possible.
5.6 Interactions with Alcohol, CNS Depressants, and Illicit Drugs Hypotension, and profound sedation, coma or respiratory depression may result if morphine sulfate extended-release tablets are used concomitantly with other CNS depressants (e.g., sedatives, anxiolytics, hypnotics, neuroleptics, muscle relaxants, other opioids).
When considering the use of morphine sulfate extended-release tablets in a patient taking a CNS depressant, assess the duration of use of the CNS depressant and the patient’s response, including the degree of tolerance that has developed to CNS depression.
Additionally, consider the patient’s use, if any, of alcohol and/or illicit drugs that can cause CNS depression.
If morphine sulfate extended-release tablet therapy is to be initiated in a patient taking a CNS depressant, start with a lower morphine sulfate extended-release tablet dose than usual and monitor patients for signs of sedation and respiratory depression and consider using a lower dose of the concomitant CNS depressant [see Drug Interactions ( 7.1 )].
5.7 Hypotensive Effects Morphine sulfate extended-release tablets may cause severe hypotension including orthostatic hypotension and syncope in ambulatory patients.
There is an increased risk in patients whose ability to maintain blood pressure has already been compromised by a reduced blood volume or concurrent administration of certain CNS depressant drugs (e.g., phenothiazines or general anesthetics) [see Drug Interactions ( 7.1 )].
Monitor these patients for signs of hypotension after initiating or titrating the dose of morphine sulfate extended-release tablets.
In patients with circulatory shock, morphine sulfate extended-release tablets may cause vasodilation that can further reduce cardiac output and blood pressure.
Avoid the use of morphine sulfate extended-release tablets in patients with circulatory shock.
5.8 Use in Patients with Head Injury or Increased Intracranial Pressure Monitor patients taking morphine sulfate extended-release tablets that may be susceptible to the intracranial effects of CO2 retention (e.g., those with evidence of increased intracranial pressure or brain tumors) for signs of sedation and respiratory depression, particularly when initiating therapy with morphine sulfate extended-release tablets.
Morphine sulfate extended-release tablets may reduce respiratory drive, and the resultant CO2 retention can further increase intracranial pressure.
Opioids may also obscure the clinical course in a patient with a head injury.
Avoid the use of morphine sulfate extended-release tablets in patients with impaired consciousness or coma.
5.9 Use in Patients with Gastrointestinal Conditions Morphine sulfate extended-release tablets are contraindicated in patients with paralytic ileus.
Avoid the use of morphine sulfate extended-release tablets in patients with other GI obstruction.
The morphine in morphine sulfate extended-release tablets may cause spasm of the sphincter of Oddi.
Monitor patients with biliary tract disease, including acute pancreatitis, for worsening symptoms.
Opioids may cause increases in the serum amylase.
5.10 Use in Patients with Convulsive or Seizure Disorders The morphine in morphine sulfate extended-release tablets may aggravate convulsions in patients with convulsive disorders, and may induce or aggravate seizures in some clinical settings.
Monitor patients with a history of seizure disorders for worsened seizure control during morphine sulfate extended-release tablet therapy.
5.11 Avoidance of Withdrawal Avoid the use of mixed agonist/antagonist analgesics (i.e., pentazocine, nalbuphine, and butorphanol) in patients who have received or are receiving a course of therapy with a full opioid agonist analgesic, including morphine sulfate extended-release tablets.
In these patients, mixed agonists/antagonists analgesics may reduce the analgesic effect and/or may precipitate withdrawal symptoms.
When discontinuing morphine sulfate extended-release tablets, gradually taper the dose [see Dosage and Administration ( 2.3 )].
Do not abruptly discontinue morphine sulfate extended-release tablets.
5.12 Driving and Operating Machinery Morphine sulfate extended-release tablets may impair the mental or physical abilities needed to perform potentially hazardous activities such as driving a car or operating machinery.
Warn patients not to drive or operate dangerous machinery unless they are tolerant to the effects of morphine sulfate extended-release tablets and know how they will react to the medication.
INFORMATION FOR PATIENTS
17 See FDA-approved patient labeling (Medication Guide) Abuse Potential Inform patients that morphine sulfate extended-release tablets contain morphine, a Schedule II controlled substance that is subject to abuse.
Instruct patients not to share morphine sulfate extended-release tablets with others and to take steps to protect morphine sulfate extended-release tablets from theft or misuse.
Life-Threatening Respiratory Depression Discuss the risk of respiratory depression with patients, explaining that the risk is greatest when starting morphine sulfate extended-release tablets or when the dose is increased.
Advise patients how to recognize respiratory depression and to seek medical attention if they are experiencing breathing difficulties.
Accidental Exposure Instruct patients to take steps to store morphine sulfate extended-release tablets securely.
Accidental exposure, especially in children, may result in serious harm or death.
Advise patients to dispose of unused morphine sulfate extended-release tablets by flushing the tablets down the toilet.
Risks from Concomitant Use of Alcohol and other CNS Depressants Inform patients that the concomitant use of alcohol with morphine sulfate extended-release tablets can increase the risk of life-threatening respiratory depression.
Instruct patients not to consume alcoholic beverages, as well as prescription and over-the-counter drug products that contain alcohol, during treatment with morphine sulfate extended-release tablets.
Inform patients that potentially serious additive effects may occur if morphine sulfate extended-release tablets are used with other CNS depressants, and not to use such drugs unless supervised by a health care provider.
Important Administration Instructions Instruct patients how to properly take morphine sulfate extended-release tablets, including the following: Swallowing morphine sulfate extended-release tablets whole Not crushing, chewing, or dissolving the tablets Using morphine sulfate extended-release tablets exactly as prescribed to reduce the risk of life-threatening adverse reactions (e.g., respiratory depression) Not discontinuing morphine sulfate extended-release tablets without first discussing the need for a tapering regimen with the prescriber Hypotension Inform patients that morphine sulfate extended-release tablets may cause orthostatic hypotension and syncope.
Instruct patients how to recognize symptoms of low blood pressure and how to reduce the risk of serious consequences should hypotension occur (e.g., sit or lie down, carefully rise from a sitting or lying position).
Driving or Operating Heavy Machinery Inform patients that morphine sulfate extended-release tablets may impair the ability to perform potentially hazardous activities such as driving a car or operating heavy machinery.
Advise patients not to perform such tasks until they know how they will react to the medication.
Constipation Advise patients of the potential for severe constipation, including management instructions and when to seek medical attention.
Anaphylaxis Inform patients that anaphylaxis has been reported with ingredients contained in morphine sulfate extended-release tablets.
Advise patients how to recognize such a reaction and when to seek medical attention.
Pregnancy Advise female patients that morphine sulfate extended-release tablets can cause fetal harm and to inform the prescriber if they are pregnant or plan to become pregnant.
Healthcare professionals can telephone Rhodes Pharmaceuticals L.P.
(1-888-827-0616) for information on this product.
Marketed by: Rhodes Pharmaceuticals L.P.
Coventry, RI 02816 Manufactured by: Purdue Pharmaceuticals, L.P.
Wilson, NC 27893 302567-0A Rev.
05/12
DOSAGE AND ADMINISTRATION
2 DOSAGE & ADMINISTRATION Individualize dosing based on patient’s prior analgesic treatment experience, and titrate as needed to provide adequate analgesia and minimize adverse reactions.
(2.1, 2.2) Do not abruptly discontinue morphine sulfate extended-release tablets in a physically dependent patient.
(2.3) Instruct patients to swallow morphine sulfate extended-release tablets intact.
(2.4) 2.1 Initial Dosing Initiate the dosing regimen for each patient individually, taking into account the patient’s prior analgesic treatment experience.
Monitor patients closely for respiratory depression, especially within the first 24 to 72 hours of initiating therapy with morphine sulfate extended-release tablets [see Warnings and Precautions ( 5.2 )].
Consider the following factors when selecting an initial dose of morphine sulfate extended-release tablets: Total daily dose, potency, and any prior opioid the patient has been taking previously; Reliability of the relative potency estimate used to calculate the equivalent dose of morphine needed (Note: potency estimates may vary with the route of administration); Patient’s degree of opioid experience and opioid tolerance; General condition and medical status of the patient; Concurrent medication; Type and severity of the patient’s pain.
Morphine sulfate extended-release tablets are administered at a frequency of twice daily (every 12 hours) or three times daily (every 8 hours).
Use of Morphine Sulfate Extended-Release Tablets as the First Opioid Analgesic There has been no systematic evaluation of morphine sulfate extended-release tablets as an initial opioid analgesic in the management of pain.
Because it may be more difficult to titrate a patient using controlled-release morphine, it is ordinarily advisable to begin treatment using an immediate-release formulation.
Conversion from Other Oral Morphine to Morphine Sulfate Extended-Release Tablets Patients receiving other oral morphine formulations may be converted to morphine sulfate extended-release tablets by administering one-half of the patient’s 24-hour requirement as morphine sulfate extended-release tablets on an every-12-hour schedule or by administering one-third of the patient’s daily requirement as morphine sulfate extended-release tablets on an every-8-hour schedule.
Conversion from Parenteral Morphine or Other Opioids (Parenteral or Oral) to Morphine Sulfate Extended-Release Tablets While there are useful tables of oral and parenteral equivalents, there is substantial inter-patient variability in the relative potency of different opioid drugs and formulations.
As such, it is safer to underestimate a patient’s 24-hour oral morphine dose and provide rescue medication (e.g., immediate-release morphine) than to overestimate the 24-hour oral morphine dose and manage an adverse reaction.
Consider the following general points: Parenteral to oral morphine ratio: Between 2 to 6 mg of oral morphine may be required to provide analgesia equivalent to 1 mg of parenteral morphine.
Typically, a dose of morphine that is approximately three times the previous daily parenteral morphine requirement is sufficient.
Other parenteral or oral non-morphine opioids to oral morphine sulfate: Specific recommendations are not available because of a lack of systematic evidence for these types of analgesic substitutions.
Published relative potency data are available, but such ratios are approximations.
In general, begin with half of the estimated daily morphine requirement as the initial dose, managing inadequate analgesia by supplementation with immediate-release morphine.
The first dose of morphine sulfate extended-release tablets may be taken with the last dose of any immediate-release opioid medication due to the extended-release characteristics of the morphine sulfate extended-release tablets formulation.
2.2 Titration and Maintenance of Therapy Individually titrate morphine sulfate extended-release tablets to a dose that provides adequate analgesia and minimizes adverse reactions.
Continually reevaluate patients receiving morphine sulfate extended-release tablets to assess the maintenance of pain control and the relative incidence of adverse reactions.
During chronic therapy, especially for non-cancer-related pain (or pain associated with other terminal illnesses), periodically reassess the continued need for the use of opioid analgesics.
If the level of pain increases, attempt to identify the source of increased pain, while adjusting the morphine sulfate extended-release tablets dose to decrease the level of pain.
Because steady-state plasma concentrations are approximated in 1 day, morphine sulfate extended-release tablets dosage adjustments may be done every 1 to 2 days.
Patients who experience breakthrough pain may require dosage adjustment or rescue medication with an appropriate dose of an immediate-release opioid and non-opioid medication.
If signs of excessive opioid-related adverse reactions are observed, the next dose may be reduced.
Adjust the dose to obtain an appropriate balance between management of pain and opioid-related adverse reactions.
During chronic, around-the-clock opioid therapy, especially for non-cancer pain syndromes, the continued need for around-the-clock opioid therapy should be reassessed periodically (e.g., every 6 to 12 months) as appropriate.
2.3 Discontinuation of Morphine Sulfate Extended-Release Tablets When the patient no longer requires therapy with morphine sulfate extended-release tablets, use a gradual downward titration of the dose to prevent signs and symptoms of withdrawal in the physically-dependent patient.
Do not abruptly discontinue morphine sulfate extended-release tablets.
2.4 Administration of Morphine Sulfate Extended-Release Tablets Instruct patients to swallow morphine sulfate extended-release tablets intact.
The tablets are not to be crushed, dissolved, or chewed due to the risk of rapid release and absorption of a potentially fatal dose of morphine [see Warnings and Precautions ( 5.2 )].