What it is and what it is used for

for

Oxycodone Hydrochloride G.L. Pharma contains the active substance oxycodone hydrochloride which belongs to a group of medicines called opioids and has a strong analgesic (painkilling) effect. Oxycodone Hydrochloride G.L. Pharma is indicated in adults and adolescents (from 12 years and older) for the treatment of severe pain, which can be adequately managed only with opioid analgesics 2.

What you need to know before you are treated with Oxycodone Hydrochloride G.L. Pharma

You must not be treated with Oxycodone Hydrochloride G.L. Pharma if you are allergic to oxycodone hydrochloride or any of the other ingredients of this medicine (listed in section 6). if you have breathing problems, such as breathing more slowly or more weakly than expected (respiratory depression), low amount of oxygen or too much carbon dioxide in your blood. if you have a severe chronic lung disease associated with narrowing of the airways (COPD = chronic obstructive pulmonary disease). if you have a certain heart condition after long-term lung disease known as cor pulmonale. if you have severe bronchial asthma. if you have a type of bowel obstruction called paralytic ileus. Warnings and precautions Talk to your doctor or pharmacist before using Oxycodone Hydrochloride G.L. Pharma if you are elderly or debilitated (weak). if your lung, liver or kidney function is impaired. if you have an impaired function of the thyroid gland (hypothyroidism or myxoedema).

• if you have poor adrenal gland function (your adrenal gland is not working properly) for example Addinson's disease. if you have a mental disorder as a result of intoxication with another substance or alcohol.

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if you have delirium tremens due to alcohol withdrawal causing severe confusion, hallucinations and shaking. if you have enlargement of the prostate. if you have an inflammation of the pancreas (pancreatitis). if you have problems with your gall bladder or urinary tract, including difficulty or pain passing urine. if your doctor suspects you have intestinal paralysis (a condition where the bowel has stopped working) if you have inflammatory bowel disease. if your brain pressure is increased e.g. as a result of a head injury. if you have low blood pressure or if you have a reduced blood volume. if you have impaired consciousness if you are also taking a type of medicine known as take so called MAO inhibitors (generally used to for the treatment of depression or Parkinson's disease) or if you have been taking them within the last 2 weeks (see "other medicines" below).

The most severe risk of opioid overdose is very slow or weak breathing (respiratory depression), which is most common in the elderly or frail patients. Opioids may also cause a sudden, severe drop in blood pressure in people with an increased risk of this phenomenon. This may lead to fainting, for example (please see also Section 3 and 4). Sleep-related breathing disorders Oxycodone Hydrochloride G.L. Pharma can cause sleep-related breathing disorders such as sleep apnea (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. Tolerance, dependence and addiction When Oxycodone Hydrochloride G.L. Pharma is used for long-time treatment, tolerance to the medicine may occur. This means, that you may need a higher dose to achieve the desired pain relief. Do not change the dosage without consulting your doctor. This medicine contains oxycodone which is an opioid medicine. Repeated use of opioid painkillers can result in the drug being less effective (you become accustomed to it, known as tolerance). Repeated use of Oxycodone Hydrochloride G.L. Pharma may lead to dependence, abuse, and addiction, which may result in life-threatening overdose. The risk of 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. You might feel that you need to carry on taking your medicine, even when it doesn't help to relieve your pain. The risk of becoming dependent or addicted varies from person to person. You may have a greater risk of becoming dependent or addicted on Oxycodone Hydrochloride G.L. Pharma if: you or anyone in your family have ever abused or been dependent on alcohol, prescription medicines or illegal drugs ("addiction"). you are a smoker. you have ever had problems with your mood (depression, anxiety or a personality disorder) or have been treated by a psychiatrist for other mental illnesses. If you notice any of the following signs whilst taking Oxycodone Hydrochloride G.L. Pharma, it could be a sign that you have become dependent or addicted.

• You need to take the medicine for longer than advised by your doctor
• You need to take more than the recommended dose

• You are using the medicine for reasons other than prescribed, for instance, 'to stay calm' or 'help you sleep'
• You have made repeated, unsuccessful attempts to quit or control the use of the medicine
• When you stop taking the medicine you feel unwell, and you feel better once taking the medicine again ('withdrawal effects') 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 taking Oxycodone Hydrochloride G.L. Pharma). Oxycodone Hydrochloride G.L. Pharma has a dependence potential. If the treatment is stopped too suddenly, withdrawal symptoms such as yawning, dilted pupils, tearing, runny nose, tremors, sweating, chills, anxiety, restlessness, feeling your heartbeat or muscle pain may occur. . Other symptoms also may develop, including irritability, backache, joint pain, weakness, abdominal cramps, insomnia, nausea, loss of appetite, vomiting, diarrhoea, or increased blood pressure, respiratory rate or heart rate. If you no longer need treatment, your doctor will gradually reduce your daily dose. Your doctor will weigh the possible risks against the expected and needs to be evaluated in relation to the benefit. Ask your doctor if you have any questions about this. The active ingredient oxycodone hydrochloride, like other highly effective opioids (strong pain killers), has potential for abuse. The development of psychological addiction is possible. Oxycodone Hydrochloride G.L. Pharma should only be used with particular caution if there has been a history of alcohol, drug or drug abuse. Particularly in high doses, increased sensitivity to pain (hyperalgesia) can occur, which does not respond to a further increase in the dose of Oxycodone Hydrochloride G.L. Pharma. Your doctor will then decide whether to reduce the dose or switch to another strong pain reliever (opioid). If you need to have an operation, please tell your doctor that you are taking Oxycodone Hydrochloride G.L. Pharma. Contact your doctor if you experience severe upper abdominal pain possibly radiating to the back, nausea, vomiting or fever as this could be symptoms associated with inflammation of the pancreas (pancreatitis) and the biliary tract system. Similar to other opioids, oxycodone can affect the body's normal production of hormones (such as cortisol and sex hormones). Symptoms may be severe abdominal pain, nausea and vomiting, low blood pressure, extreme fatigue, lack of appetite and weight loss. If you have these symptoms, contact your doctor, who will decide if you need to take hormone supplement. Anti-Doping Warning Athletes must be aware that this medicine may cause a positive reaction to "anti-doping" tests. Use of Oxycodone Hydrochloride G.L. Pharma as a doping agent may become a health hazard. Other medicines and Oxycodone Hydrochloride G.L. Pharma Tell your doctor or pharmacist if you are taking, have recently taken or might take any other medicines. Concomitant use of Oxycodone Hydrochloride G.L. Pharma and sedative medicines such as benzodiazepines or related drugs increases the risk of drowsiness, difficulties in breathing (respiratory depression), coma and may be life-threatening. Because of this, concomitant use should only be considered when other treatment options are not possible.

However if your doctor does prescribe Oxycodone Hydrochloride G.L. Pharma together with sedative medicines the dose and duration of concomitant treatment should be limited by your doctor. Please tell your doctor about all sedative medicines you are taking, and follow your doctor's dose recommendation closely. It could be helpful to inform friends or relatives to be aware of the signs and symptoms stated above. Contact your doctor when experiencing such symptoms. The risk of side effects increases, if you use antidepressants (such as citalopram, duloxetine, escitalopram, fluoxetine, fluvoxamine, paroxetine, sertraline, venlafaxine). These medicines may interact with oxycodone and you may experience symptoms such as involuntary, rhythmic contractions of muscles, including the muscles that control movement of the eye, agitation, excessive sweating, tremor, exaggeration of reflexes, increased muscle tension, body temperature above 38°C. Contact your doctor when experiencing such symptoms. The risk of side effects is increased if Oxycodone Hydrochloride G.L. Pharma is used at the same time as medicines that can affect brain function. Medicines that affect the way the brain works include:

• sleeping pills or sedatives (e.g. hypnotics or sedatives, including benzodiazepines)
• medicines for depression (e.g. paroxetine or amitriptyline), including those belonging to a group of MAOIs (please see also section "Warnings and precautions"),
• medicines for allergies, motion sickness or vomiting (antihistamines, antiemetics),
• medicines for psychological or mental disorders (such as psychotropic drugs, phenothiazines or neuroleptics),
• Medicines used to treat epilepsy, pain and anxiety such as e.g. gabapentin and pregabalin. Please tell your doctor or pharmacist if you are taking any of the medicines from the following list: –

muscle relaxants used to treat muscle spasms medicines used to treat Parkinson's disease, other strong pain relievers (opioids), cimetidine (a medicine for stomach ulcers, indigestion or heartburn), medicines for fungal infections (such as ketoconazole, voriconazole, itraconazole or posaconazole), medicines for bacterial infections (such as clarithromycin, erythromycin or telithromycin), medicines from the group of protease inhibitors to treat HIV infection (e.g. boceprevir, ritonavir, indinavir, nelfinavir or saquinavir), rifampicin for tuberculosis, carbamazepine (a medicine for epilepsy or seizures and for certain types of pain), phenytoin (a medicine for epilepsy or seizures), the medicinal plant St. John's wort (also known as Hypericum perforatum), quinidine (a medicine for irregular heartbeat), certain medicines to prevent blood clotting or to thin the blood (such as coumarin medicines).

Oxycodone Hydrochloride G.L. Pharma with drink and alcohol Oxycodone Hydrochloride G.L. Pharma should not be taken with alcohol. Alcohol use could increase serious side-effects of oxycodone, such as sleepiness and drowsiness and slow and shallow breathing. Grapefruit juice may increase the levels of Oxycodone Hydrochloride G.L. Pharma in your blood. Check with your doctor if you drink grapefruit juice regularly. Pregnancy and breast-feeding If you are pregnant or breast-feeding, think you may be pregnant or are planning to have a baby, ask your doctor or pharmacist for advice before taking this medicine.

Pregnancy The use of Oxycodone Hydrochloride G.L. Pharma should be avoided to the extent possible during pregnancy. Prolonged use of oxycodone during pregnancy can cause withdrawal symptoms in newborns. If oxycodone is given during childbirth it may cause berathing difficulties (respiratory depression) in the newborn. Breast-feeding Do not take this medicine if you are breast-feeding. Oxycodone passes into breast milk and may cause shallow and slow breathing (respiratory depression) in the breast-fed child. Driving and using machines The medicine can affect your ability to drive as it may make you sleepy or dizzy.

• Do not drive while taking this medicine until you know how it affects you.
• It is an offence to drive if this medicine affects your ability to drive.
• However, you would not be committing an offence if:
• The medicine has been prescribed to treat a medical or dental problem and
• You have taken it according to the instructions given by the prescriber or in the information provided with the medicine and
• It was not affecting your ability to drive safely Talk to your doctor or pharmacist if you are not sure whether it is safe for you to drive while taking this medicine. Oxycodone Hydrochloride G.L. Pharma contains sodium chloride This medicinal product contains less than 1 mmol sodium (23 mg) per ampoule, i.e. essentially 'sodium- free'. 3.

How to take Oxycodone Hydrochloride G.L. Pharma

Always use this medicine exactly as your doctor has told you. Check with your doctor or pharmacist if you are not sure. Do not change the dosage without consulting your doctor. You should be given the lowest effective dose sufficient to relieve your pain. If you have previously been treated with opioids, your doctor may start your therapy with a higher dose. It may be necessary to increase the dose gradually if the pain relief is insufficient or if the pain becomes worse. A doctor or nurse will usually prepare and administer the injection for you. Adults and adolescents (from 12 years and older) Your doctor will adjust your dosage according to pain intensity and to your individual needs. If you have been treated with other strong pain killers (opioids) before, the doctor may adjust your dose taking into account your previous dose. If you experience pain between doses of Oxycodone Hydrochloride G.L. Pharma you may require higher doses of Oxycodone Hydrochloride G.L. Pharma. Please talk to your doctor if you have this problem. You should not be given Oxycodone Hydrochloride G.L. Pharma for longer than necessary. Use in children (below 12 years):

Safety and efficacy of Oxycodone Hydrochloride G.L. Pharma have not been tested sufficiently in children under 12 years of age. Therefore, treatment with Oxycodone Hydrochloride G.L. Pharma is not recommended in children under 12 years of age.

How to take it

to you Oxycodone Hydrochloride G.L. Pharma is given as a single injection or slow infusion into vein or under the skin. It is given by a healthcare professional. In special cases Oxycodone Hydrochloride G.L. Pharma can be given by patient controlled analgesia. In such cases the doctor will instruct you how much and when to take Oxycodone Hydrochloride G.L. Pharma. If you use more Oxycodone Hydrochloride G.L. Pharma than you should Oxycodone Hydrochloride G.L. Pharma is given to you by a doctor or nurse and is it not likely that you get too much. However if you believe you have gotten an too high dose, inform the hospital staff immediately. In special cases Oxycodone Hydrochloride G.L. Pharma may be given by yourself or a carer: if you think you have gotten too much of Oxycodone Hydrochloride G.L. Pharma or if someone else has taken it by mistake, immediately contact a doctor, hospital or your local poison control center. Members of the public seeking specific information on poisons should contact: In England and Wales: NHS 111 – dial 111 In Scotland: NHS 24 – dial 111 www.npis.org Overdosing can cause:

• constriction of the pupils,
• very slow and weak breathing (respiratory depression),
• drowsiness up to absent-mindedness (narcosis-like state),
• decreased tension in the skeletal muscles,
• slowing your pulse,
• drop in blood pressure
• a brain disorder (known as toxic leukoencephalopathy). In more severe cases, unconsciousness (coma), water retention in the lungs and circulatory failure can occur. Abuse of high doses of strong opioids such as oxycodone can be fatal. If you forget to take Oxycodone Hydrochloride G.L. Pharma If you get a smaller dose of Oxycodone Hydrochloride G.L. Pharma than prescribed, or if you miss a dose, adequate pain relief will probably not be achieved. In special cases Oxycodone Hydrochloride G.L. Pharma may be given by yourself or a carer: If you forget to take one dose, you can take the forgotten dose as soon as you remember it. Doses should not be administered more frequently than every 4 hours. Do not take a double dose to make up for a forgotten dose. If you stop taking Oxycodone Hydrochloride G.L. Pharma Do not stop treatment without first speaking with your doctor. If you stop taking Oxycodone Hydrochloride G.L. Pharma , after a long period of treatment, withdrawal symptoms such as restlessness, anxiety, insomnia, involuntary muscle contractions, tremors and gastrointestinal problems may occur. Your doctor will tell you how to stop treatment to reduce the risk of withdrawal symptoms, usually by gradually reducing the dose. If you have any further questions on the use of this medicine, ask your doctor or pharmacist. 4.

Possible side effects

Like all medicines, this medicine can cause side effects, although not everybody gets them. Contact a doctor immediately if the following symptom occurs: Very slow or weak breathing (respiratory depression). This is the most most serious risk in connection with medicines such as Oxycodone Hydrochloride G.L. Pharma (opioids), and may even be fatal after high doses of this medicine. Other side effects that may occur: Very common: may affect more than 1 in 10 people Sleepiness to drowsiness, dizziness, headache Constipation, feeling or being sick. Your doctor will prescribe an appropriate medicine to treat these symptoms. Itching Common: may affect up to 1 in 10 people Changes in mood (anxiety, confusion, depression, nervousness, sleep disorders, abnormal thoughts or dreams) Trembling Lowering of blood pressure, rarely accompanied by symptoms such as feeling your heartbeat, fainting or difficulty in breathing or wheezing Difficulty in breathing or wheezing, airway spasm Dry mouth, rarely accompanied by thirst and difficulty swallowing, general symptoms of indigestion such as stomachache, diarrhoea, heartburn, decreased appetite Rash Sweating, sometimes heavily Weakness Uncommon: may affect up to 1 in 100 people Allergic reactions Increase in the amount of a certain hormone (ADH = antidiuretic hormone) in the blood. Lack of water in the body (dehydration) Restlessness, mood swings, hallucinations, euphoric mood, decreased libido, drug dependence Amnesia Tingling or numbness (e.g. in the hands or feet) Convulsions, increased or decreased muscle tension, or uncontrollled movements Reduced sensitivity to pain or touch Changes in taste Difficult speeking Visual impairment, reduction in the size of the pupils Fainting or feeling of spinning or whirling (vertigo) Unpleasant sensation of irregular and/or forceful beating of the heart (in the context of withdrawal), increased pulse rate, low blood pressure Widening of the blood vessels causing low blood pressure Shortness of breath, increased coughing, sore throat, runny nose, voice changes Difficulty swallowing, mouth ulcers, inflammation of the gum or mouth causing sore gums/mouth, flatulence (excessive gas in the stomach or bowel), belching, obstruction of the bowel (ileus) Increased blood levels of certain hepatic enzymes (seen in blood tests) Dry skin Problems passing urine, frequent urination Disturbances of sexual function, impotence

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Chills, feeling sick, injuries due to accidents resulting from decreased alertness, pain (e.g. chest pain), fluid retention (oedema), migraine, thirst, physical dependence with withdrawal symptoms, tolerance

Rare: may affect up to 1 in 1,000 people Lymph node disease Seizures (fits), in particular in patients having epilepsy or with a tendency to seizures Low blood pressure, fall in blood pressure on standing up which causes dizziness, lightheadedness or fainting Bleeding gums Increased appetite Dark-coloured stools Itchy rash, blisters on the skin and mucosa (cold sores or herpes simplex), increased sensitivity to light Blood in urine Changes in body weight (loss or rise) Painful infection of the skin (cellulitis) Very rare: may affect up to 1 in 10,000 people Scaly rash Not known: frequency cannot be estimated from the available data Sleep apnoea (breathing pauses during sleep) Severe allergic reactions (which may cause difficulty in breathing, dizziness, skin rashes, fever) Aggression Increased sensitivity to pain Cavities or tooth decay Painful conditions where bile cannot flow from the liver to the duodenum (cholestasis) or stomach pain due to a gallstone temporarily blocking the bile duct (biliary colic) Absence of menstrual bleeding Long term use of Oxycodone Hydrochloride G.L. Pharma during pregnancy may cause lifethreatening withdrawal symptoms in the new-born. Symptoms to look for in the baby include irritability, hyperactivity and abnormal sleep pattern, high pitched cry, shaking, being sick, diarrhoea and not putting on weight. A problem affecting a valve in the intestines that may cause severe upper abdominal pain (sphincter of Oddi dysfunction). Reporting of side effects If you get any side effects, talk to your doctor, pharmacist or nurse. This includes any possible side effects not listed in this leaflet. You can also report side effects directly 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. By reporting side effects, you can help provide more information on the safety of this medicine. 5.

How to store it

Oxycodone Hydrochloride G.L. Pharma

Keep this medicine out of the sight and reach of children. Store this medicine in a locked safe and secure storage space, where other people cannot access it. It can cause serious harm and be fatal to people when it has not been prescribed for them. Do not use this medicine after the expiry date which is stated on the label and the carton after EXP. The expiry date refers to the last day of that month. Do not freeze.

Once the ampoule is opened the solution for injection/infusion should be used immediately. Any unused solution should be discarded. Chemical and physical in-use stability has been demonstrated for 48 hours/days at room temperature. This medicinal product is for single use only. Only clear solution free from particles and discoloration should be used. Do not throw away 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. 6.

Contents of the pack and other information

What Oxycodone Hydrochloride G.L. Pharma contains –

The active substance is oxycodone hydrochloride. Each ml contains 10 mg oxycodone hydrochloride. The other ingredients are sodium chloride, citric acid monohydrate, sodium hydroxide (for pHadjusting), hydrochloric acid (for pH-adjusting), water for injections.

What Oxycodone Hydrochloride G.L. Pharma looks like and contents of the pack Oxycodone Hydrochloride G.L. Pharma is a clear, colourless to slightly yellowish solution. Oxycodone Hydrochloride G.L. Pharma is available in clear, colourless glass ampoules of 1 ml or 2 ml with OPC (one point cut) breaking system. Oxycodone Hydrochloride G.L. Pharma is packed in card board fold boxes containing 1, 3, 5 or 10 ampoules per pack. Not all pack sizes may be marketed. Marketing Authorisation Holder and Manufacturer G.L. Pharma GmbH, Schlossplatz 1, 8502 Lannach, Austria Marketing Authorisation Number PL 21597/0044 This leaflet was last revised in April 2024. __________________________________________________________________________ The following information is intended for healthcare professionals only: Posology The dosage depends on the pain intensity, the total condition of the patient, previous or concurrent medication, and the patient's individual susceptibility to the treatment. The following general dosage recommendations apply:

The following starting doses are recommended. A gradual increase in dose may be required if analgesia is inadequate or if pain severity increases. If an immediate release opioid formulation is used as rescue medication in addition to prolongedrelease, the need for more than two "rescues" per day could be an indication that the prolonged-release dosage requires upward titration. Adults and adolescents (from 12 years and older) i.v. (Bolus): Administer a bolus dose of 1 to 10 mg slowly over 1-2 minutes to opioid-naïve patients. Doses should not be administered more frequently than every 4 hours. A maximum bolus dose of 5 mg is recommended in adolescents (from 12 years and older). i.v. (Infusion): A starting dose of 2 mg/hour is recommended in opioid-naïve patients. i.v. (PCA): Bolus doses of 0.03 mg/kg should be administered with a minimum lock-out time of 5 minutes to opioid-naïve patients. s.c. (Bolus): Use as 10 mg/ml concentration. A starting dose of 5 mg is recommended, repeated at 4hourly intervals in opioid-naïve patients as required. s.c. (Infusion): A starting dose of 7.5 mg/day is recommended in opioid naïve patients, titrating gradually according to symptom control. A starting dose of 5 mg/day is recommended in adolescents (from 12 years and older), titrating gradually according to symptom control. Cancer patients transferring from oral oxycodone may require much higher doses (see below) Transferring patients between oral and parenteral oxycodone The dose should be based on the following ratio: 2 mg of oral oxycodone is equivalent to 1 mg of parenteral oxycodone, if only a few doses have been given. In case of shift in choice of opioid to a patient, who has been in long-term opioid-treatment (opioidrotation), it should be emphasised that the above mentioned equipotent doses are guidance only. Often it is necessary to administer less a decreased dose as equipotency recommend. Based on this and the patients interindividual variability a shift requires that the dosing is titrated carefully for every single patient. This medicinal product is for single use only, any unused solution should be discarded. For intravenous use Oxycodone Hydrochloride G.L. Pharma concentrate for solution for infusion should be diluted to a concentration of 1 mg/ml oxycodone hydrochloride. Oxycodone Hydrochloride G.L. Pharma 10 mg/ml solution for injection/infusion and Oxycodone Hydrochloride G.L. Pharma 20 mg/2 ml solution for injection/infusion may be diluted with Water for injections Sodium chloride 9 mg/mL (0.9%) solution for injection Glucose 50 mg/mL (5%) solution for injection Ringer's solution for injection Sodium chloride and Glucose solution for injection (Sodium chloride 0.18% w/v and Glucose 4% w/v) Lactated Ringer's solution for injection (Ringer Lactate solution and 5% Glucose solution). Oxycodone hydrochloride, that was used undiluted or diluted to 1 mg/ml in various studies with different infusion solutions and under the use of representative brands of polypropylene or

polycarbonate syringes, polyethylene or PVC tubing and PVC or EVA infusion bags, does not have to be protected against light. Shelf-life 5 years. After dilution: Chemical and physical in-use stability has been demonstrated for 48 hours/days at room temperature. From a microbiological point of view, the product should be used immediately. If not used immediately, in-use storage times and conditions prior to are the responsibility of the user and would normally not be longer than 24 hours at 2 to 8 °C, unless reconstitution, dilution has taken place in controlled and validated aseptic conditions.