Oxycodone hydrochloride
Oxydolor Fast is a strong pain reliever belonging to the opioid group.
Oxydolor Fast is used in adults and adolescents aged 12 years and older for the treatment of
severe pain that can only be adequately managed with opioid analgesics.
Oxydolor Fast may cause respiratory depression during sleep, such as sleep apnea (pauses in breathing during sleep) and associated hypoxemia (low oxygen level in the blood).
Symptoms may include pauses in breathing during sleep, nighttime awakenings due to shortness of breath, difficulty staying asleep, or excessive daytime sleepiness. If the patient or another person observes these symptoms, they should contact a doctor. The doctor may consider reducing the dose.
The most serious risk associated with opioid overdose is shallow and slow breathing (respiratory depression). This most often occurs in the elderly and frail. It can also cause a decrease in oxygen levels in the blood, which can lead to fainting.
Tolerance, dependence, and addiction
This medicine contains oxycodone, which is an opioid. It can cause dependence and (or) addiction.
If Oxydolor Fast is used for long-term treatment, tolerance to the medicine may develop. This means that in order to control the pain, there may be a need for gradual dose escalation. The dose should not be changed without consulting a doctor.
This medicine contains oxycodone, which is an opioid medicine. Repeated use of opioid analgesics can lead to a decrease in their effectiveness (the patient's body gets used to it, which is called tolerance). Repeated use of Oxydolor Fast can lead to dependence, abuse, and addiction, which can lead to life-threatening overdose. The risk of these side effects may be higher when using higher doses for a longer period.
If the patient notices any of the following symptoms while taking Oxydolor Fast, it may indicate that they are developing dependence or addiction.
If the patient observes any of these symptoms, they should contact their doctor to discuss the best treatment plan, including the right time and safe way to stop treatment (see section 3 "Stopping Oxydolor Fast").
Oxydolor Fast has addictive properties. If treatment is stopped suddenly, withdrawal symptoms may occur, such as yawning, dilated pupils, lacrimation, rhinorrhea, sneezing, gooseflesh, sweating, anxiety, agitation, tremors, insomnia, or muscle pain. If the use of the medicine is no longer necessary, the doctor will gradually reduce the dose.
The doctor will assess the possible risk compared to the benefits of using this medicine.
You should consult your doctor if you have any additional questions about this.
The safety and efficacy of Oxydolor Fast in children under 12 years of age have not been established. Therefore, the use of Oxydolor Fast in this age group is not recommended.
Athletes should be aware that this medicine can cause a positive result in doping tests.
Taking Oxydolor Fast as a doping agent can be a risk to health.
You should tell your doctor or pharmacist about all medicines you are taking, have recently taken, or plan to take.
Concomitant use of Oxydolor Fast and sedating medicines, such as benzodiazepines or related drugs, increases the risk of sedation, respiratory depression, coma, and may be life-threatening. Therefore, concomitant use should only be considered when other treatment options are not possible.
If the doctor prescribes Oxydolor Fast with sedating medicines, the dose and duration of concomitant use should be limited by the doctor.
You should inform your doctor about all sedating medicines and strictly follow the doctor's instructions regarding dosage. It may be helpful to inform friends or relatives to be aware of the signs and symptoms listed above. In case of such symptoms, you should contact a doctor.
The side effects of Oxydolor Fast may occur more frequently or be more severe if it is used concomitantly with medicines that affect brain activity or with medicines used to treat allergies, motion sickness, or vomiting. Side effects may include shallow and slow breathing (respiratory depression), constipation, dry mouth, or urinary retention.
The risk of side effects increases if you take antidepressant medicines (such as citalopram, duloxetine, escitalopram, fluoxetine, fluvoxamine, paroxetine, sertraline, venlafaxine). These medicines may interact with oxycodone, which can cause the patient to experience the following symptoms: involuntary, rhythmic muscle contractions, including muscles that control eye movements, agitation, excessive sweating, tremors, increased reflexes, muscle stiffness, and elevated body temperature above 38°C. In case of these symptoms, you should contact a doctor.
You should inform your doctor or pharmacist if you are taking any of the following medicines:
You should not take Oxydolor Fast with alcohol. Consuming alcohol may increase the side effects of oxycodone, such as sedation, drowsiness, and slow and shallow breathing.
You should avoid taking Oxydolor Fast if you currently or have previously abused alcohol or drugs.
Grapefruit juice may increase the level of oxycodone in the blood. You should discuss this with your doctor if you regularly drink grapefruit juice.
If you are pregnant, breastfeeding, think you may be pregnant, or plan to have a child, you should consult your doctor or pharmacist before taking this medicine.
Pregnancy
It is recommended to avoidtaking Oxydolor Fast during pregnancy.
Use ofoxycodone during pregnancyfor a prolonged period may causewithdrawal symptomsin the newborn. If oxycodone is given during delivery, the baby may experience respiratory depression (shallow breathing).
Breastfeeding
You should stopbreastfeeding while taking Oxydolor Fast. Oxycodone hydrochloride passes into breast milk and may cause sedation, shallow and slow breathing (respiratory depression) in the breastfed child. Therefore, it cannot be ruled out that there is a risk to the breastfed child, especially after taking multiple doses of Oxydolor Fast.
Oxydolor Fast may impair your ability to drive and use machines.
You should expect this, especially when starting treatment with Oxydolor Fast, after dose escalation, or when switching treatment, as well as when Oxydolor Fast interacts with alcohol or medicines that affect brain activity. In the case of stabilized therapy, it is not necessary to introduce a general ban on driving. The treating doctor must assess the individual situation of the patient.
Oxydolor Fast contains lactose. If you have been told by your doctor that you have an intolerance to some sugars, you should contact your doctor before taking this medicine.
Oxydolor Fast contains soy. If you are allergic to peanuts or soy, you should not take this medicine.
Oxydolor Fast, 5 mg, coated tablets contain the colorant Sunset Yellow FCF (E 110), aluminum lake, which may cause allergic reactions.
This medicine should always be taken exactly as prescribed by your doctor. In case of doubt, you should consult your doctor or pharmacist.
Before starting treatment and regularly during treatment, your doctor will discuss with you what to expect from the use of Oxydolor Fast, when and how long to take it, when to contact the doctor, and when to stop taking it (see also "Stopping Oxydolor Fast").
For doses that cannot be achieved with this strength, other strengths of this medicine are available.
The doctor will determinethe dose based on the intensity of the pain and individual response to treatment.
Do not changethe dosage without consulting your doctor.
You should take the smallest effective dose necessary to relieve the pain.
If you have previously been treated with opioids, your doctor may start treatment with a higher dose.
It may be necessary to gradually increase the dose if pain relief is inadequate or if the pain worsens.
You should inform your doctor if the effect of Oxydolor Fast is too strong or too weak.
Patients who have previously taken other strong pain relievers(opioids) may be prescribed a higher starting dose by their doctor.
The doctor will decide on the daily dose and how to divide it into individual doses.
The doctor will also decide on any dose changes during treatment.
If you experience pain between doses of Oxydolor Fast, it may mean that you need higher doses of the medicine. In this case, you should consult your doctor.
If you require long-term treatment for severe pain, you should switch to a prolonged-release formulation of oxycodone hydrochloride.
Oral use
The medicine should be taken with a sufficient amount of liquid(e.g., ½ glass of water) every 4-6 hours, as prescribed by the doctor. The medicine can be taken with or without food.
Your doctor will inform you how long to take Oxydolor Fast.
You should not stop taking Oxydolor Fast without consulting your doctor (see "Stopping Oxydolor Fast").
In the case of long-term use of Oxydolor Fast, you should regularly review your treatment with your doctor. This is necessary to achieve the best possible pain relief, i.e., to enable early treatment of any side effects and to decide on dose adjustment and continuation of treatment.
You should consult your doctor or pharmacist if you feel that the effect of Oxydolor Fast is too strong or too weak.
This medicine is in a pack that is protected against opening by children. You should press the tablet firmly to remove it from the blister pack.
In case of overdose, you should immediately contact a doctor.
Overdose may cause:
In severe cases, it may lead to loss of consciousness (coma), fluid accumulation in the lungs, and circulatory failure, potentially ending in death.
Under no circumstances should you expose yourself to situations that require increased concentration, such as driving a vehicle.
If you take a lower dose of Oxydolor Fast than prescribed or miss a dose,
pain relief may not be achieved.
If you forget to take a dose, you can take it as soon as you remember.
You should remember that this medicine should be taken at intervals of 4-6 hours.
You should not take a double dose to make up for a missed dose.
You should not stop taking Oxydolor Fast without consulting your doctor.
Stopping Oxydolor Fast may cause withdrawal symptoms (such as yawning, dilated pupils, lacrimation, rhinorrhea, sneezing, gooseflesh, sweating, anxiety, agitation, tremors, insomnia, or muscle pain). Therefore, it may be recommended that the doctor gradually reduce the dose.
In case of any further doubts related to the use of this medicine, you should consult 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
Frequency not known:cannot be estimated from the available data
If you experience any side effects, including those not listed in this leaflet, you should tell your doctor or pharmacist. Side effects can be reported directly to:
Department for Monitoring of Adverse Reactions to Medicinal Products, Office for Registration of Medicinal Products, Medical Devices, and Biocidal Products, Al. Jerozolimskie 181C, 02-222 Warsaw, tel.: +48 22 49 21 301, fax: +48 22 49 21 309, website: https://smz.ezdrowie.gov.pl
Side effects can also be reported to the marketing authorization holder.
By reporting side effects, you can help provide more information on the safety of this medicine.
The medicine should be kept out of the sight and reach of children. This medicine should be stored in a closed and secure place, to which other people do not have access. It can be very harmful and may cause death in a person for whom it has not been prescribed.
Do not use this medicine after the expiry date stated on the blister pack and carton after EXP.
The expiry date refers to the last day of the month stated.
This medicine does not require any special storage conditions.
Medicines should not be disposed of via wastewater or household waste. You should ask your pharmacist how to dispose of medicines that are no longer needed. This will help protect the environment.
The active substanceis oxycodone hydrochloride.
Each coated tablet contains 5 mg of oxycodone hydrochloride, which corresponds to 4.48 mg of oxycodone.
Each coated tablet contains 10 mg of oxycodone hydrochloride, which corresponds to 8.97 mg of oxycodone.
Each coated tablet contains 20 mg of oxycodone hydrochloride, which corresponds to 17.93 mg of oxycodone.
Tablet core:
Sodium carboxymethylcellulose (type A)
Lactose monohydrate
Microcrystalline cellulose
Silica, colloidal, anhydrous
Magnesium stearate
Tablet coating:
Polyvinyl alcohol
Talc
Titanium dioxide (E 171)
Macrogol 3350
Soybean lecithin (E 322)
Indigo carmine, aluminum lake (E 132)
Sunset Yellow FCF, aluminum lake (E 110) (for 5 mg coated tablets)
Yellow iron oxide (E 172) (for 20 mg coated tablets)
Dark blue, round, biconvex coated tablets.
Blue, convex, oblong coated tablets with a dividing line on both sides.
The tablet can be divided into two equal doses.
Light blue, convex, oblong coated tablets with a dividing line on both sides.
Length: 12.1 mm, thickness: 3.5 mm, width: 5.2 mm.
The tablet can be divided into two equal doses.
Oxydolor Fast is available in blister packs of 10, 20, 30, 56, or 60 coated tablets.
Not all pack sizes may be marketed.
G.L. Pharma GmbH
Schloβplatz 1
8502 Lannach
Austria
G.L. PHARMA POLAND Sp. z o.o.
Al. Jana Pawła II 61/313
01-031 Warsaw, Poland
Phone: 022/636 52 23; 636 53 02
biuro@gl-pharma.pl
Germany: Oxycodon G.L. 5/10/20 mg Filmtabletten
Hungary: Codoxy Rapid 10mg filmtabletta
Poland: Oxydolor Fast
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