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The product code(s) for this leaflet is: PL 21597/0044.
Oxycodone Hydrochloride G.L. Pharma 10mg/ml Solution for Injection/Infusion
Oxycodone Hydrochloride G.L. Pharma 10 mg/ml solution for injection/infusion
oxycodone hydrochloride
1. What Oxycodone Hydrochloride G.L. Pharma is and what it is used for
2. What you need to know before you are treated with Oxycodone Hydrochloride G.L. Pharma
3. How you are given Oxycodone Hydrochloride G.L. Pharma
4. Possible side effects
5. How to store Oxycodone Hydrochloride G.L. Pharma
6. Contents of the pack and other information
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
Talk to your doctor or pharmacist before using Oxycodone Hydrochloride G.L. Pharma
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).
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:
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.
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.
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.
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:
Please tell your doctor or pharmacist if you are taking any of the medicines from the following list:
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.
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.
The medicine can affect your ability to drive as it may make you sleepy or dizzy.
Talk to your doctor or pharmacist if you are not sure whether it is safe for you to drive while taking this medicine.
This medicinal product contains less than 1 mmol sodium (23 mg) per ampoule, i.e. essentially ‘sodium- free’.
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.
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.
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.
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.
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:
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 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.
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.
Like all medicines, this medicine can cause side effects, although not everybody gets them.
Very common: may affect more than 1 in 10 people
Common: may affect up to 1 in 10 people
Uncommon: may affect up to 1 in 100 people
Rare: may affect up to 1 in 1,000 people
Very rare: may affect up to 1 in 10,000 people
Not known: frequency cannot be estimated from the available data
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
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.
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.
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 Number
PL 21597/0044
This leaflet was last revised in April 2024.