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Melodin Long

Melodin Long

About the medicine

How to use Melodin Long

Leaflet included in the packaging: patient information

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.

  • Keep this leaflet, you may need to read it again.
  • In case of any doubts, consult a doctor or pharmacist.
  • This medicine has been prescribed to you by a doctor for a specific reason. Do not pass it on to others. The medicine may harm another person, even if their symptoms are the same.
  • If the patient experiences any side effects, including any side effects not listed in this leaflet, they should tell their doctor or pharmacist. See section 4.

Table of contents of the leaflet

  • 1. What is Melodyn Long and what is it used for
  • 2. Important information before using Melodyn Long
  • 3. How to use Melodyn Long
  • 4. Possible side effects
  • 5. How to store Melodyn Long
  • 6. Contents of the packaging and other information

1. What is Melodyn Long and what is it used for

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).

2. Important information before using Melodyn Long

When not to use Melodyn Long:

  • In case of allergy to buprenorphine or any other component of the medicine (listed in section 6);
  • If the patient is addicted to strong painkillers (opioids);
  • If the patient has diseases that may cause severe breathing difficulties;
  • If the patient is taking monoamine oxidase inhibitors (MAOIs - certain medicines used to treat depression) or has taken them in the last two weeks (see "Melodyn Long and other medicines");
  • If the patient has myasthenia gravis (muscle weakness);
  • If the patient has delirium tremens (a state of confusion and tremors caused by sudden withdrawal of alcohol in people who drink excessively or during an episode of excessive alcohol consumption).

Melodyn Long must not be used to treat withdrawal symptoms in people addicted to drugs.

Warnings and precautions

Before using Melodyn Long, the patient should consult a doctor or pharmacist in the following cases:

  • After recent consumption of large amounts of alcohol;
  • If the patient has a history of seizures or convulsions;
  • If the patient has impaired consciousness (dizziness or fainting) for unknown reasons;
  • If the patient is in a state of withdrawal (a symptom of withdrawal may be cold sweats);
  • If the patient has increased intracranial pressure (e.g., after a head injury or due to a brain disease) and it is not possible to use artificial respiration;
  • If the patient has breathing difficulties or is taking other medicines that may cause weakness or slowing of respiratory function (see "Melodyn Long and other medicines");
  • If the patient has liver function disorders;
  • If the patient has a tendency to abuse drugs or narcotics;
  • If the patient has depression or other diseases treated with antidepressants; Using these medicines at the same time as Melodyn Long may lead to serotonin syndrome, a life-threatening condition (see "Melodyn Long and other medicines").

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:

  • In some people, long-term use of strong painkillers like Melodyn Long may lead to addiction. Stopping the use of these medicines may cause withdrawal reactions (see "Discontinuation of Melodyn Long").
  • Heat and the use of external heat sources may increase the dose of buprenorphine released into the blood. The use of external heat sources may cause the patch to adhere improperly to the skin. Therefore, do not use external heat sources (sauna, infrared lamp, electric blanket, hot water bottle). Consult a doctor if the patient has a fever.

Tolerance, dependence, and addiction

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:

  • The patient or a family member has a history of substance abuse or addiction;
  • The patient is a smoker;
  • The patient has a history of mood disorders (depression, anxiety, or personality disorders) or has been treated by a psychiatrist for other mental illnesses.

If the patient experiences any of the following symptoms while taking Melodyn Long, it may indicate addiction:

  • Need to take the medicine for a longer period than prescribed by the doctor
  • Need to take a higher dose than prescribed
  • Need to continue taking the medicine even if it does not relieve pain
  • Taking the medicine for reasons other than prescribed, such as "to calm down" or "to fall asleep"
  • Repeatedly attempting to stop or control the use of the medicine
  • Feeling unwell after stopping the medicine and feeling better after taking it again ("withdrawal symptoms")

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.

Children and adolescents

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.

Melodyn Long and other medicines

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.

  • Do not use Melodyn Long at the same time as monoamine oxidase inhibitors (MAOIs - certain medicines used to treat depression) or if the patient has taken these medicines in the last two weeks.
  • Melodyn Long may cause drowsiness, dizziness, or fainting, and may lead to slowed or weakened breathing. These side effects may be increased if the patient is taking other medicines with similar side effects. Such medicines include strong painkillers (opioids), certain sedatives, anesthetics, and medicines used to treat certain mental illnesses, such as sedatives, antidepressants, and antipsychotics.
  • Taking Melodyn Long at the same time as certain medicines may increase the effect of the transdermal system. These medicines include certain antibacterial and antifungal medicines (e.g., those containing erythromycin or ketoconazole) and medicines used to treat HIV infection (e.g., those containing ritonavir).
  • Taking Melodyn Long at the same time as certain medicines may decrease the effect of the transdermal system. These medicines include dexamethasone; medicines used to treat epilepsy (e.g., those containing carbamazepine or phenytoin); and medicines used to treat hyperthyroidism (e.g., rifampicin).

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:

  • Antidepressants, such as moclobemide, tranylcypromine, citalopram, escitalopram, fluoxetine, fluvoxamine, paroxetine, sertraline, duloxetine, venlafaxine, amitriptyline, doxepin, or trimipramine. These medicines may interact with Melodyn Long and cause symptoms such as involuntary, rhythmic muscle contractions, including those that control eye movements, agitation, hallucinations, sleepiness, excessive sweating, tremors, increased reflexes, increased muscle tension, and body temperature above 38°C. If the patient experiences these symptoms, they should consult their doctor.
  • Gabapentin or pregabalin used to treat epilepsy or nerve pain (neuropathic pain).
  • Medicines used to treat allergies, motion sickness, or nausea (antihistamines or antiemetics).
  • Medicines used to treat mental disorders (antipsychotics or neuroleptics).
  • Muscle relaxants.
  • Medicines used to treat Parkinson's disease.

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.

Melodyn Long with food, drink, and alcohol

While taking Melodyn Long, the patient should not consume alcohol. Alcohol may increase certain side effects and worsen the patient's condition.

Pregnancy, breastfeeding, and fertility

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.

Driving and using machines

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:

  • At the start of treatment;
  • When changing the dose;
  • When switching from another painkiller to Melodyn Long;
  • If other medicines that act on the central nervous system are used;
  • If alcohol is consumed.

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.

3. How to use Melodyn Long

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.

Use in children and adolescents

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.

Method of administration

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.

Application

Before applying the transdermal system

  • Choose an area of skin on the upper part of the body, preferably on the chest below the collarbone or on the upper back (see illustration), which is flat, clean, has no scars, and is hairless. The patient should ask for help if they cannot apply the patch themselves.
Front or Back or
Human silhouette with the area on the chest below the collarbone marked for patch application
Human silhouette with the area on the chest marked for patch application
Human silhouette with the area on the upper back marked for patch application
Human silhouette with the area on the back marked for patch application
  • If the chosen skin area has hair, the patient should cut the hair with scissors. Do not shave!
  • The patient should avoid applying the patch to skin that is red, irritated, or has wounds, such as large scars.
  • The chosen skin area must be clean and dry. If necessary, the patient should wash the skin with cold or lukewarm water. Do not use soap or other detergents. After a hot bath or shower, the patient should wait until the skin is completely dry and cool. Do not apply creams, lotions, or oils to the chosen skin area, as this may cause the patch to adhere poorly.

Applying the transdermal system

  • Step 1: Each patch is sealed in a pouch. Immediately before application, the patient should cut the pouch open with scissors. Remove the patch from the pouch.
Scissors cutting open the pouch with the patchHands removing the transparent protective film from the patch
  • Step 2: The adhesive side of the patch is covered with a transparent protective film. The patient should carefully remove one partof the film, trying not to touch the adhesive surface.
Hand applying the patch to the chest
  • Step 3: Apply the patch to the chosen skin area and remove the remaining film.
Hand pressing the patch onto the chest
  • Step 4: Press the patch onto the skin with the palm of the hand for about 30 to 60 seconds. The patient should make sure the patch adheres to the skin with its entire surface, especially at the edges.
  • Step 5: The patient should wash their hands thoroughly. Do not use soap.

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

  • Remove the patch.
  • Fold the patch in half, with the adhesive side inward.
  • Dispose of the used patch with caution, preferably by taking it to a pharmacy to dispose of it in a container for unused medicines.
  • Apply a new patch to a different area of skin (following the instructions above). The patient can apply a new patch to the same area of skin only after a week has passed.

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.

Using a higher dose of Melodyn Long than prescribed

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.

Missing a dose of Melodyn Long

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.

Discontinuation of Melodyn Long

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.

4. Possible side effects

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):

  • Nausea (vomiting),
  • Redness, sweating

Common(may affect up to 1 in 10 people):

  • Dizziness, headache,
  • Shallow breathing,
  • Vomiting, constipation,
  • Skin changes (generalized or recurrent rash), sweating,
  • Swelling (e.g., swelling of the legs), fatigue

Uncommon(may affect up to 1 in 100 people)

  • Confusion, sleep disorders, restlessness,
  • Various degrees of sedation (calmness) from fatigue to a feeling of fogginess in the head,
  • Circulatory disorders (such as low blood pressure or, less often, circulatory collapse),
  • Dry mouth,
  • Rash,
  • Urination disorders, urinary retention (passing less urine than usual),
  • Weakness

Rare(may affect up to 1 in 1,000 people)

  • Loss of appetite,
  • Hallucinations, anxiety, and nightmares, decreased libido, concentration disorders, speech disorders, feeling of fogginess in the head, balance disorders, abnormal skin sensations (tingling, prickling, burning),
  • Vision disorders, blurred vision, eyelid swelling,
  • Hot flashes,
  • Breathing difficulties (respiratory failure),
  • Heartburn,
  • Hives,
  • Erectile dysfunction,
  • Withdrawal symptoms (see below), reactions at the application site

Very rare(may affect up to 1 in 10,000 people)

  • Severe skin reactions (see below),
  • Addiction, mood changes,
  • Muscle tremors, taste disorders,
  • Pupil constriction,
  • Ear pain,
  • Accelerated breathing, hiccups,
  • Nausea,
  • Small blisters,
  • Chest pain

Unknown:frequency cannot be estimated from the available data

  • Contact dermatitis (skin rash with inflammation, which may include a burning sensation), skin discoloration

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.

Reporting side effects

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.

5. How to store Melodyn Long

  • The medicine should be kept out of sight and reach of children.
  • This medicine should be stored in a safe place, out of reach of other people. The medicine can cause serious harm or even death if taken accidentally or intentionally by someone who has not been prescribed it.
  • Do not use this medicine after the expiry date stated on the carton and pouch. The expiry date refers to the last day of the month.
  • This medicine does not require special storage conditions.
  • Used patches should be folded in half, with the adhesive side inward, placed in the original pouch, and disposed of safely, preferably by taking them to a pharmacy to dispose of them in a container for unused medicines.
  • Medicines should not be thrown away in drains or household waste. The patient should ask their pharmacist how to dispose of medicines that are no longer needed. This will help protect the environment.

6. Contents of the packaging and other information

What Melodyn Long contains

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.

Other ingredients are:

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

What Melodyn Long looks like and contents of the pack

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.

Marketing authorization holder

G.L. Pharma GmbH
Schloβplatz 1
A-8502 Lannach
Austria

Manufacturer

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

Date of last revision of the leaflet: 09.10.2024

  • Country of registration
  • Active substance
  • Prescription required
    Yes
  • Importer
    G.L. Pharma GmbH Labtec GmbH

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