Melodyn Long, 35 micrograms/hour, transdermal system, patch
Melodyn Long, 52.5 micrograms/hour, transdermal system, patch
Melodyn Long, 70 micrograms/hour, transdermal system, patch
Buprenorphine
Read the leaflet carefully before using the medicine, as it contains important information for the patient.
The active substance of Melodyn Long is buprenorphine.
Melodyn Long is a pain-relieving medicine (analgesic) used to treat moderate to severe pain in cancer patients and severe pain that does not respond to other types of painkillers. Melodyn Long works through the skin. Buprenorphine is an opioid (strong pain reliever) that reduces pain by acting on the central nervous system (specialized nerve cells in the spinal cord and brain). The effect of the transdermal system lasts for up to 4 days. Melodyn Long is not intended for the treatment of acute pain (short-term).
Melodyn Long must not be used to treat withdrawal symptoms in people addicted to drugs.
Before using Melodyn Long, the patient should consult a doctor or pharmacist in the following cases:
Respiratory disorders associated with sleep
Melodyn Long may cause respiratory disorders associated with sleep, such as sleep apnea (pauses in breathing during sleep) and sleep-related hypoxemia (low oxygen levels in the blood). Symptoms may include pauses in breathing during sleep, nighttime awakenings due to shortness of breath, difficulty maintaining sleep, or excessive daytime sleepiness. If the patient or another person notices these symptoms, they should consult a doctor. The doctor may consider reducing the dose.
Also, pay attention to the following warnings:
This medicine contains buprenorphine, which is an opioid. Repeated use of opioids can lead to tolerance (the medicine becomes less effective). Long-term use of Melodyn Long may also lead to dependence and addiction, which can result in life-threatening overdose. The risk of these side effects may increase with higher doses and longer treatment duration.
Dependence or addiction can cause the patient to lose control over the amount of medicine taken and the frequency of use.
The risk of addiction to Melodyn Long varies from person to person. The risk of addiction to Melodyn Long may be higher if:
If the patient experiences any of the following symptoms while taking Melodyn Long, it may indicate addiction:
If any of these symptoms occur, the patient should talk to their doctor to discuss the best treatment option, including when to stop taking the medicine and how to do it safely (see "Discontinuation of Melodyn Long").
It is also important to inform athletes that this medicine may cause positive doping test results.
Melodyn Long should not be used in people under 18 years of age, as there is no experience with the use of this medicine in this age group.
The patient should tell their doctor or pharmacist about all medicines they are currently taking or have recently taken, as well as any medicines they plan to take.
Certain medicines may increase the side effects of Melodyn Long and sometimes cause very severe reactions. While taking Melodyn Long, the patient should not take other medicines without consulting their doctor first, especially:
Taking Melodyn Long at the same time as sedatives, such as benzodiazepines or related medicines, increases the risk of drowsiness, breathing difficulties (respiratory depression), sleepiness, and may be life-threatening. Therefore, taking these medicines at the same time should only be considered when other treatment options are not possible.
If the doctor prescribes Melodyn Long together with a sedative, the dose and duration of concurrent use should be limited.
The patient should inform their doctor about all sedatives they are taking and follow the doctor's instructions for dosing. It may be helpful to inform friends or family members to be aware of the above symptoms. If these symptoms occur, the patient should consult their doctor.
While taking Melodyn Long, the patient should not consume alcohol. Alcohol may increase certain side effects and worsen the patient's condition.
If the patient is pregnant, breastfeeding, or thinks they may be pregnant, they should consult their doctor or pharmacist before using Melodyn Long.
There is limited experience with the use of Melodyn Long in pregnant women.
Therefore, Melodyn Long should not be used in pregnant women or if the woman may become pregnant during treatment.
Buprenorphine, the active substance in the transdermal system, inhibits milk production and passes into breast milk. Therefore, Melodyn Long should not be used during breastfeeding.
Melodyn Long may cause dizziness, drowsiness, and blurred or double vision, which may affect the patient's reactions to the extent that they may not react properly or quickly enough in unexpected or emergency situations. This is especially true:
In such cases, the patient should not drive or operate machines while taking Melodyn Long. This also applies to the period after stopping Melodyn Long. The patient should not drive or operate machines for at least 24 hours after removing the patch.
In case of doubts or questions, the patient should consult their doctor or pharmacist.
This medicine should always be used exactly as prescribed by the doctor or pharmacist. In case of doubts, the patient should consult their doctor or pharmacist.
Before starting treatment and regularly during treatment, the doctor will discuss with the patient what to expect from Melodyn Long, when and for how long to take it, when to consult the doctor, and when to stop taking the medicine (see also "Discontinuation of Melodyn Long").
Melodyn Long is available in three strengths: Melodyn Long 35 micrograms/hour, transdermal system, Melodyn Long 52.5 micrograms/hour, transdermal system, and Melodyn Long 70 micrograms/hour, transdermal system.
The doctor will choose the most suitable strength of Melodyn Long for the patient. If necessary, the doctor will decide to change the strength during treatment.
Usually, the recommended dose is:
Adults
If the doctor does not prescribe otherwise, the patient should apply one Melodyn Long patch (as described below)
and change it at least every 4 days. To make it easier to remember, the patient can change the patches twice a week, on the same days, e.g., always on Monday morning and Thursday evening. To remember when to change the patch, the patient should write the date on the calendar on the outer packaging. If the doctor prescribes additional painkillers, the patient should follow the doctor's instructions carefully. Otherwise, the patient may not get the full benefit of using Melodyn Long.
Elderly patients
There is no need to adjust the dose in elderly patients.
Patients with kidney or liver function disorders
There is no need to adjust the dose in patients with kidney disorders or those undergoing dialysis.
Patients with liver function disorders.
In patients with liver function disorders, the effect and duration of action of Melodyn Long may be changed. The doctor will monitor these patients more closely.
Melodyn Long should not be used in people under 18 years of age, as there is no experience with the use of this medicine in this age group.
The patch is intended for use on the skin.
After applying the patch to the skin, the active substance, buprenorphine, passes through the skin into the blood.
Before applying the transdermal system
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Applying the transdermal system
Wearing the transdermal system
The patient can wear the applied patch for up to 4 days. If the patch is applied correctly, the risk of it coming off on its own is low. The patient can take a normal shower, bathe, or swim. However, the patient should not expose the patch to excessive heat (e.g., sauna, infrared radiation, electric blanket, hot water bottle).
If the patch comes off prematurely (which is unlikely), the patient should not reuse it. Instead, they should apply a new transdermal system (see "Changing the transdermal system" below).
Changing the transdermal system
Duration of treatment
The doctor will inform the patient how long to use Melodyn Long. The patient should not stop using Melodyn Long on their own, as this may cause the pain to return and worsen their condition (see also "Discontinuation of Melodyn Long").
If the patient feels that the effect of Melodyn Long is too strong or too weak, they should consult their doctor or pharmacist.
If the patient uses a higher dose of Melodyn Long than prescribed, they may experience symptoms of buprenorphine overdose. An overdose may lead to an increase in buprenorphine's side effects, such as drowsiness, nausea, and vomiting. The patient may have pinpoint pupils, and their breathing may slow down or become shallow. They may also experience circulatory collapse.
If the patient realizes they have used more patches than necessary, they should remove the extra patch and consult their doctor or pharmacist immediately.
If the patient forgets to apply a patch, they should do so as soon as they remember. In this case, the patient will need to change their patch application schedule, e.g., if they usually change patches on Mondays and Thursdays, but now they apply a new patch on Wednesday, they will need to change patches on Wednesdays and Saturdays from then on. The patient should write the new patch change days on the calendar on the outer packaging.
If the patient changes the patch too late, their pain may return. In this case, the patient should consult their doctor.
The patient should never take a double dose to make up for a missed dose.
If the patient stops using or ends the use of Melodyn Long, their pain may return.
If the patient wants to stop using Melodyn Long due to unpleasant side effects, they should first consult their doctor, who will inform them how to stop the treatment safely and whether they need to use other medicines.
In some patients, after long-term use of strong painkillers, withdrawal symptoms may occur. The risk of withdrawal symptoms after stopping Melodyn Long is very low. However, if the patient experiences agitation, anxiety, nervousness, or tremors, and is overactive and has difficulty sleeping or digestive disorders after stopping the treatment, they should consult their doctor.
In case of any further doubts or questions about using this medicine, the patient should consult their doctor or pharmacist.
Like all medicines, Melodyn Long can cause side effects, although not everybody gets them.
If the patient experiences any of the following symptoms: swelling of the face, lips, tongue, or throat, which may cause difficulty swallowing or breathing, hives, fainting, yellowing of the skin and eyes (jaundice), they should remove the transdermal system and consult their doctor or seek emergency help at the nearest hospital. These may be symptoms of a severe allergic reaction.
The following side effects have been reported:
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)
Unknown:frequency cannot be estimated from the available data
If the patient experiences any of the side effects listed above, they should consult their doctor immediately.
In some cases, delayed allergic reactions may occur with visible symptoms of inflammation. In such cases, the patient should stop using Melodyn Long after consulting their doctor.
In some patients, after long-term use of strong painkillers, withdrawal symptoms may occur. The risk of withdrawal symptoms after stopping Melodyn Long is low. However, if the patient experiences any of the following symptoms: agitation, anxiety, nervousness, or tremors, and is overactive and has difficulty sleeping or digestive disorders, they should inform their doctor.
If the patient experiences any side effects, including any side effects not listed in the leaflet, they should tell their doctor or pharmacist. Side effects can be reported directly to the Department of Drug Safety Monitoring, Office for Registration of Medicinal Products, Medical Devices, and Biocidal Products
Al. Jerozolimskie 181 C
02-222 Warsaw
Phone: +48 22 49 21 301
Fax: +48 22 49 21 309
email: ndl@urpl.gov.pl
Side effects can also be reported to the marketing authorization holder.
Reporting side effects helps to gather more information on the safety of the medicine.
The active substance is buprenorphine
Melodyn Long, 35 micrograms/hour, transdermal system, patch
Each transdermal system with a surface area of 25 cm contains 20 mg of buprenorphine and releases 35 micrograms of buprenorphine per hour.
Melodyn Long, 52.5 micrograms/hour, transdermal system, patch
Each transdermal system with a surface area of 37.5 cm contains 30 mg of buprenorphine and releases 52.5 micrograms of buprenorphine per hour.
Melodyn Long, 70 micrograms/hour, transdermal system, patch
Each transdermal system with a surface area of 50 cm contains 40 mg of buprenorphine and releases 70 micrograms of buprenorphine per hour.
Povidone K90
Levulinic acid
Oleic acid oleate
Copolymer of 2-ethylhexyl acrylate, butyl acrylate, acrylic acid, and vinyl acetate (75:15:5:5)
The adhesive matrix does not contain the active substance:
Copolymer of 2-ethylhexyl acrylate, vinyl acetate, 2-hydroxyethyl acrylate, and glycidyl methacrylate (68:27:5:0.15)
Protective layer:
Siliconized polyethylene terephthalate
Separating foil:
Polyethylene terephthalate
Outer layer:
Polyester
Blue ink
Each transdermal system is a rectangular patch with rounded edges, beige in color, with the inscription:
Melodyn Long 35 micrograms/hour "Buprenorphin" and "35µg/h".
Melodyn Long 52.5 micrograms/hour "Buprenorphin" and "52.5µg/h".
Melodyn Long 70 micrograms/hour "Buprenorphin" and "70µg/h".
Each transdermal system is packaged in a separate child-resistant pouch.
The following pack sizes are available: 4, 5, 8, 10, 16, or 24 patches.
Not all pack sizes may be marketed.
G.L. Pharma GmbH
Schloβplatz 1
A-8502 Lannach
Austria
G.L. Pharma GmbH
Schloβplatz 1
A-8502 Lannach
Austria
Labtec GmbH
Heykenaukamp 10
21147 Hamburg
Germany
To obtain more detailed information and information on the names of the medicinal product in other EU member states, the patient should contact the representative of the marketing authorization holder:
G.L. Pharma GmbH Sp. z o.o. Oddział w Polsce
Al. Jana Pawła II 61
01-031 Warsaw
Poland
Phone: 022/636 52 23; 636 53 02
Fax: 022/636 50 76
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