Patient leaflets and SmPCs, drug interaction checker, official dosages and NHS pharmacy opening hours — all in one place.
Patient leaflets and SmPCs, drug interaction checker, official dosages and NHS pharmacy opening hours — all in one place.
The electronic medicines compendium (emc) no longer publishes a Summary of Product Characteristics for this product, which usually means it is no longer marketed in the UK. The patient leaflet below is kept for reference, but the product may not be available.
If you were prescribed this medicine, other products containing Morphine sulfate may still be available. Do not stop your treatment — ask your pharmacist or GP what to use instead.
for Morphine is one of a group of medicines called opioid analgesics, which are used to relieve moderate to severe pain. Morphine is used for the relief of severe pain and it is also used to treat breathlessness caused by fluid in the lungs and as a pre-medication before operations in adults.
Morphine sulfate Do not use Morphine sulfate if you:
these side effects can increase with a higher dose and longer duration of use. Dependence or addiction can make you feel that you are no longer in control of how much medicine you need to take or how often you need to take it. The risk of becoming dependent or addicted varies from person to person. You may have a greater risk of becoming dependent on or addicted to Morphine sulfate if:
Read all of this leaflet carefully before you start using this medicine because it contains important information for you.
If you notice any of these signs, speak to your doctor to discuss the best treatment pathway for you, including when it is appropriate to stop and how to stop safely (see section 3, If you stop using Morphine sulfate). Acute generalized exanthematous pustulosis (AGEP) Acute generalized exanthematous pustulosis (AGEP) has been reported in association with Morphine sulfate treatment. Symptoms usually occur within the first 10 days of treatment. Tell your doctor if you have ever developed a severe skin rash or skin peeling, blistering and/or mouth sores after taking Morphine sulfate or other opioids. Stop using Morphine sulfate and seek medical attention immediately, if you notice any of the following symptoms: blistering, widespread scaly skin or pus-filled spots together with fever. Sleep-related breathing disorders Morphine sulfate can cause sleep-related breathing disorders such as sleep apnoea (breathing pauses during sleep) and sleep related hypoxemia (low oxygen level in the blood). The symptoms can include breathing pauses during sleep, night awakening due to shortness of breath, difficulties to maintain sleep or excessive drowsiness during the day. If you or another person observe these symptoms, contact your doctor. A dose reduction may be considered by your doctor.
Children Morphine sulfate is never given to patients in This medicine is not recommended for use in a coma. If any of the above applies to you, do not use this children. medicine and talk to your doctor or nurse. Other medicines and Morphine sulfate Tell your doctor if you are taking have recently Warnings and precautions taken or might take any other medicines. In Talk to your doctor or nurse before you are particular, tell your doctor if you are taking any given Morphine sulfate if you: of the following:
Pregnancy and breast-feeding If you are pregnant, in labour or breastfeeding, Morphine sulfate will only be given to you if your doctor considers the benefit of treatment outweighs the risk to the infant foetus or new-born baby. Morphine may reduce contractions during labour, cause breathing problems to the infant
The following information is intended for healthcare professionals only:
about the risks and signs of OUD. If these signs occur, patients should be advised to contact their physician. Patients will require monitoring for signs of drug-seeking behaviour (e.g. too early requests for refills). This includes the review of concomitant opioids and psycho-active drugs (like benzodiazepines). For patients with signs and symptoms of OUD, consultation with an addiction specialist should be considered.
1. NAME OF THE MEDICINAL PRODUCT Morphine sulfate 10 mg/ml solution for injection Morphine sulfate 15 mg/ml solution for injection Morphine sulfate 30 mg/ml solution for injection 4.
CLINICAL PARTICULARS
4.1 Therapeutic indications Morphine is used for the symptomatic relief of severe pain; relief of dyspnoea of left ventricular failure and pulmonary oedema of cardiogenic origin; pre-operative use in adults. 4.2 Posology and method of administration Posology Adults The dosage should be based on the severity of the pain and the response and tolerance of the patient. The usual adult subcutaneous or intramuscular dose is 10 mg every 4 hours, if necessary, but may range from 5 mg to 20 mg. The usual adult intravenous dose is 2.5 mg to 15 mg not more than 4-hourly, where necessary, but dosage and dosing interval must be titrated against the patient's response and adjustments made until analgesia is achieved. Elderly Because of the depressant effect on respiration, caution is necessary when giving morphine to the elderly and reduced doses may be required.
Withdrawal (abstinence) syndrome The risk of withdrawal syndrome increases with the time the drug is used, and with higher doses. Symptoms can be minimised with adjustments of dose or dosage form, and gradual withdrawal of morphine. For individual symptoms, see section 4.8. Hyperalgesia Hyperalgesia that does not respond to a further dose increase of morphine may occur in particular in high doses. A morphine dose reduction or change in opioid may be required. Gastrointestinal disorders An unexplained increase in abdominal pain associated with disturbed intestinal motility, symptoms of constipation, bloating, abdominal distension and increased gastroesophageal reflux during treatment with morphine sulfate, may indicate the development of opioid-induced bowel dysfunction or narcotic bowel syndrome. In such situations consider the use of alternative analgesics and a morphine detoxification.
Risk from concomitant use of sedative medicines such as benzodiazepines or related drugs Concomitant use of Morphine sulfate and sedative medicines such as benzodiazepines or Hepatic impairment related drugs may result in sedation, respiratory A reduction in dosage should be considered in depression, coma and death. Because of these hepatic impairment. risks, concomitant prescribing with these sedative medicines should be reserved for Renal impairment patients for whom alternative treatment options The dosage should be reduced in moderate to are not possible. If a decision is made to severe renal impairment. prescribe Morphine sulfate concomitantly with For concomitant illnesses/conditions where dose sedative medicines, the lowest effective dose reduction may be appropriate, see 4.4. should be used, and the duration of treatment should be as short as possible. Method of administration The patients should be followed closely for signs The injection may be given by the intravenous, and symptoms of respiratory depression and intramuscular or subcutaneous route. sedation. In this respect, it is strongly The subcutaneous route is not suitable for recommended to inform patients and their oedematous patients. caregivers to be aware of these symptoms (see section 4.5). Treatment goals and discontinuation Before initiating treatment with Morphine Oral P2Y12 inhibitor antiplatelet therapy sulfate, a treatment strategy including treatment Within the first day of concomitant P2Y12 duration and treatment goals, and a plan for end inhibitor and morphine treatment, reduced of the treatment, should be agreed together with efficacy of P2Y12 inhibitor treatment has been the patient, in accordance with pain management observed (see section 4.5). guidelines. During treatment, there should be frequent contact between the physician and the Palliative care patient to evaluate the need for continued In the control of pain in terminal illness, these treatment, consider discontinuation and to adjust conditions should not necessarily be a deterrent dosages if needed. When a patient no longer to use. requires therapy with Morphine sulfate, it may be advisable to taper the dose gradually to Acute chest syndrome (ACS) in patients with prevent symptoms of withdrawal. In absence of sickle cell disease (SCD) adequate pain control, the possibility of Due to a possible association between ACS and hyperalgesia, tolerance and progression of morphine use in SCD patients treated with underlying disease should be considered morphine during a vaso-occlusive crisis, close (see section 4.4). monitoring for ACS symptoms is warranted. Paediatric population Use in children is not recommended.
Hepatobiliary disorders Opioids such as morphine should either be avoided in patients with biliary disorders or they should be given with an antispasmodic. Morphine may cause dysfunction and spasm of the sphincter of Oddi, thus raising intrabiliary pressure and increasing the risk of biliary tract symptoms and pancreatitis. Therefore, in patients with biliary tract disorders morphine may exacerbate pain (use in biliary colic is a contraindication, see section 4.3). In patients given morphine after cholecystectomy, biliary pain has been induced.
Ritonavir: Although there are no pharmacokinetic data available for concomitant use of ritonavir with morphine, ritonavir induces the hepatic enzymes responsible for the glucuronidation of morphine, and may possibly decrease plasma concentrations of morphine.
Oral P2Y12 inhibitors: A delayed and decreased exposure to oral P2Y12 inhibitor antiplatelet therapy has been observed in patients with acute coronary syndrome treated with morphine. This interaction may be related to reduced gastrointestinal motility and apply to other opioids. The clinical relevance is Opioid Use Disorder (abuse and dependence) unknown, but data indicate the potential for Tolerance and physical and/or psychological reduced P2Y12 inhibitor efficacy in patients dependence may develop upon repeated co-administered morphine and a P2Y12 inhibitor administration of opioids such Morphine sulfate. (see section 4.4). In patients with acute coronary Repeated use of Morphine sulfate can lead to syndrome, in whom morphine cannot be Opioid Use Disorder (OUD). A higher dose and withheld and fast P2Y12 inhibition is deemed longer duration of opioid treatment, can increase crucial, the use of a parenteral P2Y12 inhibitor the risk of developing OUD. Abuse or may be considered. intentional misuse of Morphine sulfate may result in overdose and/or death. The risk of 4.6 Fertility, pregnancy and lactation developing OUD is increased in patients with a personal or a family history (parents or siblings) Pregnancy of substance use disorders (including alcohol use Since morphine rapidly crosses the placental disorder), in current tobacco users or in patients barrier, it is not advised to administer morphine with a personal history of other mental health during pregnancy and labour. It may reduce disorders (e.g. major depression, anxiety and uterine contractions, cause respiratory personality disorders). depression in the foetus and new-born infant, Before initiating treatment with Morphine and may have significant effects on foetal heart sulfate and during the treatment, treatment goals rate. New-borns whose mothers received opioid and a discontinuation plan should be agreed with analgesics during pregnancy should be the patient (see section 4.2). Before and during monitored for signs of neonatal withdrawal treatment the patient should also be informed (abstinence) syndrome. Treatment may include
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Duration of treatment Adrenal insufficiency Morphine sulfate should not be used longer than Opioid analgesics may cause reversible adrenal necessary. insufficiency requiring monitoring and glucocorticoid replacement therapy. Symptoms of adrenal insufficiency may include e.g. nausea, 4.3 Contraindications vomiting, loss of appetite, fatigue, weakness, dizziness, or low blood pressure. Hypersensitivity to the active substance or to any of the excipients listed in section 6.1. Acute Decreased Sex Hormones and increased respiratory depression. Obstructive airways prolactin disease. Concurrent treatment with monoamine Long-term use of opioid analgesics may be oxidase inhibitors or within two weeks of their associated with decreased sex hormone levels discontinuation of treatment with them. Cerebral and increased prolactin. Symptoms include oedema. Head injuries. Coma. Convulsive decreased libido, impotence or amenorrhea. disorders. Raised intracranial pressure. Biliary colic. Acute alcoholism. Antibiotic induced Excipients pseudomembranous colitis. Ulcerative colitis This medicinal product contains less than because of the risk of toxic megacolon. 1 mmol sodium (23 mg) per ml of solution, that Phaeochromocytoma. Paralytic ileus. Acute is to say essentially 'sodium-free'. diarrhoea caused by poisoning or invasive pathogens. 4.5 Interaction with other medicinal products and other forms of interaction 4.4 Special warnings and precautions for use Alcohol: enhanced sedative and hypotensive Morphine is a potent medicine but with effects. considerable potential for harmful effect, including addiction. It should be used only if Anti-arrhythmics: There may be delayed other drugs with fewer hazards are inadequate, absorption of mexiletine. and with the recognition that it may possibly mask significant manifestations of disease which Antibacterials: The opioid analgesic should be identified for proper diagnosis and papaveretum has been shown to reduce plasma treatment. ciprofloxacin concentration. The manufacturer of ciprofloxacin advises that premedication with Use with caution or reduced doses opioid analgesics be avoided. Morphine should be given in reduced doses or with caution to patients with asthma or Antidepressants, anxiolytics, hypnotics: a reduced respiratory reserve (including Severe CNS excitation or depression emphysema, chronic cor pulmonale, (hypertension or hypotension) has been reported kyphoscoliosis, excessive obesity and sleep with the concurrent use of pethidine and apnoea). Avoid use during an acute asthma monoamine oxidase inhibitors (MAOIs) attack (see section 4.3). including selegiline, moclobemide and linezolid. Opioid analgesics in general should be As it is possible that a similar interaction may administered with caution or in reduced doses occur with other opioid analgesics, morphine to patients with hypotension, hypothyroidism, should be used with caution and consideration adrenocortical insufficiency, impaired kidney given to a reduction in dosage in patients or liver function, prostatic hypertrophy, receiving MAOIs. urethral stricture, shock, inflammatory or The sedative effects of morphine (opioid obstructive bowel disorders, or convulsive analgesics) are enhanced when used with disorders. depressants of the central nervous system such as gabapentin or pregabalin, hypnotics, Caution is advised when giving morphine to anxiolytics, tricyclic antidepressants and patients with impaired liver function due to its sedating antihistamines. hepatic metabolism (see section 4.2). Antipsychotics: possible enhanced sedative and Severe and prolonged respiratory depression has hypotensive effect. occurred in patients with renal impairment who have been given morphine (see section 4.2). Antidiarrhoeal and antiperistaltic agents (such as loperamide and kaolin): concurrent Dosage should be reduced in elderly and use may increase the risk of severe constipation. debilitated patients. Antimuscarinics: agents such as atropine Plasma concentrations of morphine may be antagonise morphine-induced respiratory reduced by rifampicin. The analgesic effect of depression and can partially reverse biliary morphine should be monitored and doses of spasm but are additive to the gastrointestinal and morphine adjusted during and after treatment urinary tract effects. Consequently, severe with rifampicin. constipation and urinary retention may occur during intensive antimuscarinic analgesic Sleep-related breathing disorders therapy. Opioids can cause sleep-related breathing disorders including central sleep apnoea (CSA) Metoclopramide and domperidone: There and sleep-related hypoxemia. Opioid use may be antagonism of the gastrointestinal effects increases the risk of CSA in a dose-dependent of metoclopramide and domperidone. fashion. In patients who present with CSA, consider decreasing the total opioid dosage. Sedative medicines such as benzodiazepines or related drugs: The concomitant use of Severe cutaneous adverse reactions (SCARs) opioids with sedative medicines such as Acute generalized exanthematous pustulosis benzodiazepines or related drugs increases the (AGEP), which can be life-threatening or fatal, risk of sedation, respiratory depression, coma has been reported in association with morphine and death because of additive CNS depressant treatment. Most of these reactions occurred effect. The dose and duration of concomitant use within the first 10 days of treatment. Patients should be limited (see section 4.4). should be informed about the signs and symptoms of AGEP and advised to seek medical Cimetidine: inhibits the metabolism of care if they experience such symptoms. morphine. If signs and symptoms suggestive of these skin reactions appear, morphine should be withdrawn Rifampicin: Plasma concentrations of morphine and an alternative treatment considered. may be reduced by rifampicin.
foetus or new-born baby and affect the heart rate The other side effects which have been reported are: of the foetus. If Morphine sulfate is used for Very common (may affect more than 1 in a long time during pregnancy, there is 10 people): a risk of the new-born child having drug withdrawal (abstinence) symptoms which should – Seeing or hearing things that are not there (hallucinations) be treated by a doctor.
to you – Increased sensitivity to pain
Like all medicines, this medicine can cause side effects, although not everybody gets them. Seek immediate medical help if you have any of the following symptoms:
Morphine sulfate Keep this medicine out of the sight and reach of children. Keep the ampoules in the outer carton in order to protect from light. Product containing visible particles should not be used. Do not use this medicine after the expiry date which is stated on the carton after EXP. The expiry date refers to the last day of that month. Do not throw away any medicines via wastewater or household waste. Ask your pharmacist how to throw away medicines you no longer use. These measures will help protect the environment.
What Morphine sulfate contains
Place for AS Kalceks internal code
05.06.2024 MUK/I/0/1
4.9 Overdose an opioid and supportive care. As with all drugs it is not advisable to administer Symptoms: respiratory depression, pin-point morphine during pregnancy. pupils, pneumonia aspiration and coma. In addition, shock, reduced body temperature and Breastfeeding The amount of morphine secreted in breast milk hypotension may occur. In mild overdose, symptoms include nausea and vomiting, tremor, after a single-dose administration seems to be compatible with breast feeding and insufficient miosis, dysphoria, hypothermia, hypotension, confusion and sedation. In cases of severe to cause major problems or dependence. However long-term treatment with morphine in poisoning, hypotension with circulatory failure, rhabdomyolysis progressing to renal failure, high doses may cause significant plasma concentration. That is why caution is advised on respiratory collapse may occur. Death may occur the use of morphine in breast-feeding patient and from respiratory failure. the benefit must outweigh the risk to the infant. If breast feeding is continued, the infant should Treatment: the patient must be given both respiratory and cardiovascular support and the be observed for possible adverse effects. specific antagonist, naloxone, should be administered using one of the recommended Fertility Animal studies have shown that morphine may dosage regimens. Fluid and electrolyte levels reduce fertility (see section 5.3). should be maintained. 4.7 Effects on ability to drive and use machines Morphine has major influence on the ability to drive and use machines. It may cause drowsiness so patients should avoid driving or operating machinery. When prescribing this medicine, patients should be told:
5.
PHARMACOLOGICAL PROPERTIES
5.1 Pharmacodynamic properties Pharmacotherapeutic group: Natural opium alkaloids, ATC code: N02AA01. Morphine is a narcotic analgesic obtained from opium, which acts mainly on the central nervous system and smooth muscle. 5.2 Pharmacokinetic properties Absorption Variably absorbed after oral administration; rapidly absorbed after subcutaneous or intramuscular administration. Blood concentration After an oral dose of 10 mg as the sulfate, peak serum concentrations of free morphine of about 10 ng/ml are attained in 15 to 60 minutes. After an intramuscular dose of 10 mg, peak serum concentrations of 70 to 80 ng/ml are attained in 10 to 20 minutes. After an intravenous dose of 10 mg, serum concentrations of about 60 ng/ml are obtained in 15 minutes falling to 30 ng/ml after 30 minutes and to 10 ng/ml after three hours. Subcutaneous doses give similar concentrations to intramuscular doses at 15 minutes but remain slightly higher during the following 3 hours; serum concentrations measured soon after administration correlate closely with the ages of the subjects studied and are increased in the elderly. Half-life Serum half-life in the period 10 minutes to 6 hours following intravenous administration, 2 to 3 hours; serum half-life in the period 6 hours onwards, 10 to 44 hours. Distribution Widely distributed throughout the body, mainly in the kidneys, liver, lungs and spleen; lower concentrations appear in the brain and muscles. Morphine crosses the placenta and traces are secreted in sweat and milk. Protein binding, about 35% bound to albumin and to immunoglobulins at concentrations within the therapeutic range.
Psychiatric disorders: Very common: Confusional state, hallucinations, physical and psychological dependence. Decreased libido, mood swings, Common: Biotransformation restlessness. Mainly glucuronic acid conjugation to form morphine-3 and 6-glucuronides, with sulfate Eye disorders: conjugation. N-demethylation, O-methylation Blurred vision, miosis, Common: and N-oxide glucuronide formation occurs in the nystagmus. intestinal mucosa and liver; N-demethylation Respiratory, thoracic and mediastinal disorders: occurs to a greater extent after oral than parental administration; the O-methylation pathway to Very common: Respiratory depression. form codeine has been challenged and codeine Bronchospasm, pulmonary Common: and norcodeine metabolites in urine may be oedema, which can lead to formed from codeine impurities in the morphine death. Respiratory failure, which also sample studied. Not known: can lead to death, central sleep Elimination apnoea syndrome. After an oral dose, about 60% is excreted in the urine in 24 hours, with about 3% excreted as free Cardiac disorders: Bradycardia, circulatory failure, morphine in 48 hours. Common: After a parental dose, about 90% is excreted in tachycardia. 24 hours, with about 10% as free morphine, Palpitations. Uncommon: 65 to 70% as conjugated morphine, 1% as normorphine and 3% as normorphine Vascular disorders: glucuronide. Hypotension, orthostatic Common: After administration of large doses to addicts hypotension. about 0.1% of a dose is excreted as norcodeine. Urinary excretion of morphine appears to be pH Gastrointestinal disorders: Very common: Constipation, nausea, vomiting. dependent to some extent; as the urine becomes more acidic more free morphine is excreted and Dry mouth, paralytic ileus. Common: as the urine becomes more alkaline more of the Intestinal functional disorder, Not known: glucuronide conjugate is excreted; up to 10% of narcotic bowel syndrome, a dose may be excreted in the bile. pancreatitis. 5.3 Preclinical safety data Hepatobiliary disorders: Biliary spasm. Common: Non-clinical data based on conventional studies Hepatic enzyme increase. Uncommon: Spasm of the sphincter of Oddi. of safety pharmacology, repeated dose toxicity, Not known: genotoxicity, carcinogenic potential reveal no special hazard additional to the known safety Reproductive system and breast disorders: profile of morphine in humans. In male rats, Erectile dysfunction. Common: reduced fertility and chromosomal damage in gametes have been reported. Renal and urinary disorders: Urinary retention. Common: Urethral spasm. Uncommon: 6. PHARMACEUTICAL PARTICULARS Renal failure. Not known: Immune system disorders: Anaphylactic reaction, Uncommon: hypersensitivity. Anaphylactoid reactions Not known:
6.1 List of excipients Sodium chloride Hydrochloric acid (for pH adjustment) Water for injections
General disorders and administration site 2 years. conditions: Very common: Drug tolerance 6.4 Special precautions for storage Fatigue, facial flushing, Common: hypothermia, injection site pain, Keep the ampoules in the outer carton in order to injection site irritation, drug protect from light. withdrawal (abstinence) syndrome (babies born to 6.5 Nature and contents of container opioid-dependent mothers also at risk to present withdrawal Type I amber glass ampoules of 1 ml with white syndrome). open point cut. The ampoules are packed in transparent polyvinylchloride film liners. The Drug dependence and withdrawal (abstinence) liners together with leaflets are packed in syndrome cartons. Use of opioid analgesics may be associated with the development of physical and/or Pack size: 5 or 10 ampoules. psychological dependence or tolerance. Repeated use of Morphine sulfate can lead to Not all pack sizes may be marketed. drug dependence, even at therapeutic doses. The risk of drug dependence may vary depending on 6.6 Special precautions for disposal and a patient's individual risk factors, dosage, and other handling duration of opioid treatment (see section 4.4). An abstinence syndrome may be precipitated The medicinal product is for single use only; when opioid administration is suddenly discard any remaining contents after use. discontinued or opioid antagonists administered, or can sometimes be experienced between doses. The required volume should be calculated based For management, see section 4.4. on the prescribed dose. Physiological withdrawal symptoms include: Any unused medicinal product or waste material Body aches, tremors, restless legs syndrome, should be disposed of in accordance with local diarrhoea, abdominal colic, nausea, flu-like requirements. symptoms, tachycardia and mydriasis. Psychological symptoms include dysphoric MARKETING AUTHORISATION mood, anxiety and irritability. In drug HOLDER dependence, "drug craving" is often involved. AS KALCEKS, Krustpils iela 71E, Rīga, LV-1057, Latvia, Tel.: +371 67083320, E-mail: Reporting of suspected adverse reactions [email protected] Reporting suspected adverse reactions after authorisation of the medicinal product is MARKETING AUTHORISATION important. It allows continued monitoring of the NUMBER(S) benefit/risk balance of the medicinal product. Morphine Sulfate 10 mg/ml solution for injection Healthcare professionals are asked to report any PL 47015/0003 suspected adverse reactions via: Morphine Sulfate 15 mg/ml solution for injection Yellow Card Scheme, Website: PL 47015/0004 www.mhra.gov.uk/yellowcard or search for Morphine Sulfate 30 mg/ml solution for injection MHRA Yellow Card in the Google Play or PL 47015/0005 Apple App Store.
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Musculoskeletal and connective tissue disorders: Muscle rigidity, Not known: 6.2 Incompatibilities rhabdomyolysis. Morphine salts may be precipitated in alkaline Skin and subcutaneous tissue disorders: solution. Morphine sulfate is incompatible with Very common: Pruritus. oxidizing agents. Angioedema, contact Common: Physicochemical incompatibility (formation of dermatitis, rash, urticaria. precipitates) has been demonstrated between Not known: Acute generalised solutions of morphine sulfate and 5-fluorouracil. exanthematous pustulosis (AGEP). 6.3 Shelf life
Morphine sulfate 15 mg/ml solution for injection comes as injection containing 15mg/ml. Always follow the dose your doctor or pharmacist has given you, and read the leaflet that comes with the medicine.
The active substance in Morphine sulfate 15 mg/ml solution for injection is morphine sulfate.
Medicines with the same active substance, strength and form include: Morphine Sulfate 15mg/ml Solution for Injection. They are interchangeable only if your prescriber or pharmacist says so.
This leaflet reproduces the patient information leaflet approved for Morphine sulfate 15 mg/ml solution for injection, as published on the electronic medicines compendium (emc). The version printed inside your medicine’s packaging is the one that applies to you.
Whether a medicine is available over the counter or on prescription only depends on its licence. Check the leaflet, or ask your pharmacist — they can tell you straight away.
The text above reproduces the patient information leaflet approved for this medicine, restructured for easier reading.
Morphine is used for the symptomatic relief of severe pain; relief of dyspnoea of left ventricular failure and pulmonary oedema of cardiogenic origin; pre-operative use in adults.
Posology
Adults
The dosage should be based on the severity of the pain and the response and tolerance of the patient. The usual adult subcutaneous or intramuscular dose is 10 mg every 4 hours, if necessary, but may range from 5 mg to 20 mg.
The usual adult intravenous dose is 2.5 mg to 15 mg not more than 4-hourly, where necessary, but dosage and dosing interval must be titrated against the patient's response and adjustments made until analgesia is achieved.
Elderly
Because of the depressant effect on respiration, caution is necessary when giving morphine to the elderly and reduced doses may be required.
Paediatric population
Use in children is not recommended.
Hepatic impairment
A reduction in dosage should be considered in hepatic impairment.
Renal impairment
The dosage should be reduced in moderate to severe renal impairment.
For concomitant illnesses/conditions where dose reduction may be appropriate, see section 4.4.
Method of administration
The injection may be given by the intravenous, intramuscular or subcutaneous route.
The subcutaneous route is not suitable for oedematous patients.
Treatment goals and discontinuation
Before initiating treatment with Morphine sulfate, a treatment strategy including treatment duration and treatment goals, and a plan for end of the treatment, should be agreed together with the patient, in accordance with pain management guidelines. During treatment, there should be frequent contact between the physician and the patient to evaluate the need for continued treatment, consider discontinuation and to adjust dosages if needed. When a patient no longer requires therapy with Morphine sulfate, it may be advisable to taper the dose gradually to prevent symptoms of withdrawal. In absence of adequate pain control, the possibility of hyperalgesia, tolerance and progression of underlying disease should be considered (see section 4.4).
Duration of treatment
Morphine sulfate should not be used longer than necessary.
- Hypersensitivity to the active substance or to any of the excipients listed in section 6.1.
- Acute respiratory depression
- Obstructive airways disease
- Concurrent treatment with monoamine oxidase inhibitors or within two weeks of their discontinuation of treatment with them
- Cerebral oedema
- Head injuries
- Coma
- Convulsive disorders
- Raised intracranial pressure
- Biliary colic
- Acute alcoholism
- Antibiotic induced pseudomembranous colitis
- Ulcerative colitis because of the risk of toxic megacolon
- Phaeochromocytoma
- Paralytic ileus
- Acute diarrhoea caused by poisoning or invasive pathogens.
Morphine is a potent medicine but with considerable potential for harmful effect, including addiction. It should be used only if other drugs with fewer hazards are inadequate, and with the recognition that it may possibly mask significant manifestations of disease which should be identified for proper diagnosis and treatment.
Use with caution or reduced doses
Morphine should be given in reduced doses or with caution to patients with asthma or a reduced respiratory reserve (including emphysema, chronic cor pulmonale, kyphoscoliosis, excessive obesity and sleep apnoea). Avoid use during an acute asthma attack (see section 4.3).
Opioid analgesics in general should be administered with caution or in reduced doses to patients with hypotension, hypothyroidism, adrenocortical insufficiency, impaired kidney or liver function, prostatic hypertrophy, urethral stricture, shock, inflammatory or obstructive bowel disorders, or convulsive disorders.
Caution is advised when giving morphine to patients with impaired liver function due to its hepatic metabolism (see section 4.2).
Severe and prolonged respiratory depression has occurred in patients with renal impairment who have been given morphine (see section 4.2).
Dosage should be reduced in elderly and debilitated patients.
Plasma concentrations of morphine may be reduced by rifampicin. The analgesic effect of morphine should be monitored and doses of morphine adjusted during and after treatment with rifampicin.
Sleep-related breathing disorders
Opioids can cause sleep-related breathing disorders including central sleep apnoea (CSA) and sleep-related hypoxemia. Opioid use increases the risk of CSA in a dose-dependent fashion. In patients who present with CSA, consider decreasing the total opioid dosage.
Severe cutaneous adverse reactions (SCARs)
Acute generalized exanthematous pustulosis (AGEP), which can be life-threatening or fatal, has been reported in association with morphine treatment. Most of these reactions occurred within the first 10 days of treatment. Patients should be informed about the signs and symptoms of AGEP and advised to seek medical care if they experience such symptoms.
If signs and symptoms suggestive of these skin reactions appear, morphine should be withdrawn and an alternative treatment considered.
Hepatobiliary disorders
Opioids such as morphine should either be avoided in patients with biliary disorders or they should be given with an antispasmodic.
Morphine may cause dysfunction and spasm of the sphincter of Oddi, thus raising intrabiliary pressure and increasing the risk of biliary tract symptoms and pancreatitis. Therefore, in patients with biliary tract disorders morphine may exacerbate pain (use in biliary colic is a contraindication, see section 4.3). In patients given morphine after cholecystectomy, biliary pain has been induced.
Opioid Use Disorder (abuse and dependence)
Tolerance and physical and/or psychological dependence may develop upon repeated administration of opioids such Morphine sulfate.
Repeated use of Morphine sulfate can lead to Opioid Use Disorder (OUD). A higher dose and longer duration of opioid treatment, can increase the risk of developing OUD. Abuse or intentional misuse of Morphine sulfate may result in overdose and/or death. The risk of developing OUD is increased in patients with a personal or a family history (parents or siblings) of substance use disorders (including alcohol use disorder), in current tobacco users or in patients with a personal history of other mental health disorders (e.g. major depression, anxiety and personality disorders).
Before initiating treatment with Morphine sulfate and during the treatment, treatment goals and a discontinuation plan should be agreed with the patient (see section 4.2). Before and during treatment the patient should also be informed about the risks and signs of OUD. If these signs occur, patients should be advised to contact their physician.
Patients will require monitoring for signs of drug-seeking behaviour (e.g. too early requests for refills). This includes the review of concomitant opioids and psycho-active drugs (like benzodiazepines). For patients with signs and symptoms of OUD, consultation with an addiction specialist should be considered.
Withdrawal (abstinence) syndrome
The risk of withdrawal syndrome increases with the time the drug is used, and with higher doses. Symptoms can be minimised with adjustments of dose or dosage form, and gradual withdrawal of morphine. For individual symptoms, see section 4.8.
Hyperalgesia
Hyperalgesia that does not respond to a further dose increase of morphine may occur in particular in high doses. A morphine dose reduction or change in opioid may be required.
Gastrointestinal disorders
An unexplained increase in abdominal pain associated with disturbed intestinal motility, symptoms of constipation, bloating, abdominal distension and increased gastroesophageal reflux during treatment with morphine sulfate, may indicate the development of opioid-induced bowel dysfunction or narcotic bowel syndrome. In such situations consider the use of alternative analgesics and a morphine detoxification.
Risk from concomitant use of sedative medicines such as benzodiazepines or related drugs
Concomitant use of Morphine sulfate and sedative medicines such as benzodiazepines or related drugs may result in sedation, respiratory depression, coma and death. Because of these risks, concomitant prescribing with these sedative medicines should be reserved for patients for whom alternative treatment options are not possible. If a decision is made to prescribe Morphine sulfate concomitantly with sedative medicines, the lowest effective dose should be used, and the duration of treatment should be as short as possible.
The patients should be followed closely for signs and symptoms of respiratory depression and sedation. In this respect, it is strongly recommended to inform patients and their caregivers to be aware of these symptoms (see section 4.5).
Oral P2Y12 inhibitor antiplatelet therapy
Within the first day of concomitant P2Y12 inhibitor and morphine treatment, reduced efficacy of P2Y12 inhibitor treatment has been observed (see section 4.5).
Palliative care
In the control of pain in terminal illness, these conditions should not necessarily be a deterrent to use.
Acute chest syndrome (ACS) in patients with sickle cell disease (SCD)
Due to a possible association between ACS and morphine use in SCD patients treated with morphine during a vaso-occlusive crisis, close monitoring for ACS symptoms is warranted.
Adrenal insufficiency
Opioid analgesics may cause reversible adrenal insufficiency requiring monitoring and glucocorticoid replacement therapy. Symptoms of adrenal insufficiency may include e.g. nausea, vomiting, loss of appetite, fatigue, weakness, dizziness, or low blood pressure.
Decreased Sex Hormones and increased prolactin
Long-term use of opioid analgesics may be associated with decreased sex hormone levels and increased prolactin. Symptoms include decreased libido, impotence or amenorrhea.
Excipients
This medicinal product contains less than 1 mmol sodium (23 mg) per ml of solution, that is to say essentially 'sodium-free'.
Alcohol: enhanced sedative and hypotensive effects.
Anti-arrhythmics: There may be delayed absorption of mexiletine.
Antibacterials: The opioid analgesic papaveretum has been shown to reduce plasma ciprofloxacin concentration. The manufacturer of ciprofloxacin advises that premedication with opioid analgesics be avoided.
Antidepressants, anxiolytics, hypnotics: Severe CNS excitation or depression (hypertension or hypotension) has been reported with the concurrent use of pethidine and monoamine oxidase inhibitors (MAOIs) including selegiline, moclobemide and linezolid. As it is possible that a similar interaction may occur with other opioid analgesics, morphine should be used with caution and consideration given to a reduction in dosage in patients receiving MAOIs.
The sedative effects of morphine (opioid analgesics) are enhanced when used with depressants of the central nervous system such as gabapentin or pregabalin, hypnotics, anxiolytics, tricyclic antidepressants and sedating antihistamines.
Antipsychotics: possible enhanced sedative and hypotensive effect.
Antidiarrhoeal and antiperistaltic agents (such as loperamide and kaolin): concurrent use may increase the risk of severe constipation.
Antimuscarinics: agents such as atropine antagonise morphine-induced respiratory depression and can partially reverse biliary spasm but are additive to the gastrointestinal and urinary tract effects. Consequently, severe constipation and urinary retention may occur during intensive antimuscarinicanalgesic therapy.
Metoclopramide and domperidone: There may be antagonism of the gastrointestinal effects of metoclopramide and domperidone.
Sedative medicines such as benzodiazepines or related drugs: The concomitant use of opioids with sedative medicines such as benzodiazepines or related drugs increases the risk of sedation, respiratory depression, coma and death because of additive CNS depressant effect. The dose and duration of concomitant use should be limited (see section 4.4).
Cimetidine: inhibits the metabolism of morphine.
Rifampicin: Plasma concentrations of morphine may be reduced by rifampicin.
Ritonavir: Although there are no pharmacokinetic data available for concomitant use of ritonavir with morphine, ritonavir induces the hepatic enzymes responsible for the glucuronidation of morphine, and may possibly decrease plasma concentrations of morphine.
Oral P2Y12 inhibitors: A delayed and decreased exposure to oral P2Y12 inhibitor antiplatelet therapy has been observed in patients with acute coronary syndrome treated with morphine. This interaction may be related to reduced gastrointestinal motility and apply to other opioids. The clinical relevance is unknown, but data indicate the potential for reduced P2Y12 inhibitor efficacy in patients co administered morphine and a P2Y12 inhibitor (see section 4.4). In patients with acute coronary syndrome, in whom morphine cannot be withheld and fast P2Y12 inhibition is deemed crucial, the use of a parenteral P2Y12 inhibitor may be considered.
Pregnancy
Since morphine rapidly crosses the placental barrier, it is not advised to administer morphine during pregnancy and labour. It may reduce uterine contractions, cause respiratory depression in the foetus and new-born infant, and may have significant effects on foetal heart rate. New-borns whose mothers received opioid analgesics during pregnancy should be monitored for signs of neonatal withdrawal (abstinence) syndrome. Treatment may include an opioid and supportive care.
As with all drugs it is not advisable to administer morphine during pregnancy.
Breastfeeding
The amount of morphine secreted in breast milk after a single-dose administration seems to be compatible with breast feeding and insufficient to cause major problems or dependence. However long-term treatment with morphine in high doses may cause significant plasma concentration. That is why caution is advised on the use of morphine in breast-feeding patient and the benefit must outweigh the risk to the infant. If breast feeding is continued, the infant should be observed for possible adverse effects.
Fertility
Animal studies have shown that morphine may reduce fertility (see section 5.3).
Morphine has major influence on the ability to drive and use machines. It may cause drowsiness so patients should avoid driving or operating machinery.
This medicine can impair cognitive function and can affect a patient's ability to drive safely. This class of medicine is in the list of drugs included in regulations under 5a of the Road Traffic Act 1988. When prescribing this medicine, patients should be told:
• The medicine is likely to affect your ability to drive
• Do not drive until you know how the medicine affects you
• It is an offence to drive while under the influence of this medicine
• However, you would not be committing an offence (called 'statutory defence') if:
o The medicine has been prescribed to treat a medical or dental problem and
o You have taken it according to the instructions given by the prescriber and in the information provided with the medicine and
o It was not affecting your ability to drive safely
Adverse effects can be listed in terms of their frequency of occurrence: very common (≥1/10), common (≥1/100 to <1/10), uncommon (≥1/1,000 to <1/100), not known (cannot be estimated from the available data).
Morphine may cause the following adverse events:
Nervous system disorders:
Very common:
Drowsiness, hyperhidrosis.
Common:
Convulsion, headache, increased intracranial pressure, myoclonus; opioid-induced hyperalgesia (or hyperaesthesia) (see section 4.4), vertigo.
Not known:
Allodynia (see section 4.4), coma.
Psychiatric disorders:
Very common:
Confusional state, hallucinations, physical and psychological dependence.
Common:
Decreased libido, mood swings, restlessness.
Eye disorders:
Common:
Blurred vision, miosis, nystagmus.
Respiratory, thoracic and mediastinal disorders:
Very common:
Respiratory depression.
Common:
Bronchospasm, pulmonary oedema, which can lead to death.
Not known:
Respiratory failure, which also can lead to death, central sleep apnoea syndrome.
Cardiac disorders:
Common:
Bradycardia, circulatory failure, tachycardia.
Uncommon:
Palpitations.
Vascular disorders:
Common:
Hypotension, orthostatic hypotension.
Gastrointestinal disorders:
Very common:
Constipation, nausea, vomiting.
Common:
Dry mouth, paralytic ileus.
Not known:
Intestinal functional disorder, narcotic bowel syndrome, pancreatitis.
Hepatobiliary disorders:
Common:
Biliary spasm.
Uncommon:
Hepatic enzyme increase.
Not known:
Spasm of the sphincter of Oddi.
Reproductive system and breast disorders:
Common:
Erectile dysfunction.
Renal and urinary disorders:
Common:
Urinary retention.
Uncommon:
Urethral spasm.
Not known:
Renal failure.
Immune system disorders:
Uncommon:
Anaphylactic reaction, hypersensitivity.
Not known:
Anaphylactoid reactions
Musculoskeletal and connective tissue disorders:
Not known:
Muscle rigidity, rhabdomyolysis.
Skin and subcutaneous tissue disorders:
Very common:
Pruritus.
Common:
Angioedema, contact dermatitis, rash, urticaria.
Not known:
Acute generalised exanthematous pustulosis (AGEP).
General disorders and administration site conditions:
Very common:
Drug tolerance
Common:
Fatigue, facial flushing, hypothermia, injection site pain, injection site irritation, drug withdrawal (abstinence) syndrome (babies born to opioid-dependent mothers also at risk to present withdrawal syndrome).
Drug dependence and withdrawal (abstinence) syndrome
Use of opioid analgesics may be associated with the development of physical and/or psychological dependence or tolerance. Repeated use of Morphine sulfate can lead to drug dependence, even at therapeutic doses. The risk of drug dependence may vary depending on a patient's individual risk factors, dosage, and duration of opioid treatment (see section 4.4).
An abstinence syndrome may be precipitated when opioid administration is suddenly discontinued or opioid antagonists administered, or can sometimes be experienced between doses. For management, see section 4.4.
Physiological withdrawal symptoms include: Body aches, tremors, restless legs syndrome, diarrhoea, abdominal colic, nausea, flu-like symptoms, tachycardia and mydriasis. Psychological symptoms include dysphoric mood, anxiety and irritability. In drug dependence, “drug craving” is often involved.
Reporting of suspected adverse reactions
Reporting suspected adverse reactions after authorisation of the medicinal product is important. It allows continued monitoring of the benefit/risk balance of the medicinal product. Healthcare professionals are asked to report any suspected adverse reactions via the Yellow Card Scheme, Website: www.mhra.gov.uk/yellowcard or search for MHRA Yellow Card in the Google Play or Apple App Store.
Symptoms: respiratory depression, pin-point pupils, pneumonia aspiration and coma. In addition, shock, reduced body temperature and hypotension may occur. In mild overdose, symptoms include nausea and vomiting, tremor, miosis, dysphoria, hypothermia, hypotension, confusion and sedation. In cases of severe poisoning, hypotension with circulatory failure, rhabdomyolysis progressing to renal failure, respiratory collapse may occur. Death may occur from respiratory failure.
Treatment: the patient must be given both respiratory and cardiovascular support and the specific antagonist, naloxone, should be administered using one of the recommended dosage regimens. Fluid and electrolyte levels should be maintained.
Ask anything about Morphine sulfate 15 mg/ml solution for injection. The assistant answers only from this leaflet — if the leaflet does not cover it, it will say so. It does not give medical advice.
Answers come from the patient leaflet published on the electronic medicines compendium (emc). They are not medical advice. Ask a pharmacist or your GP if you are unsure. For urgent help call NHS 111, or 999 in an emergency.
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