Ask a doctor about a prescription for SUBOXONE 8 mg/2 mg SUBLINGUAL TABLETS
Package Leaflet: Information for the User
Suboxone 8 mg/2 mg sublingual tablets
buprenorphine/naloxone
Read all of this leaflet carefully before you start taking this medicine because it contains important information for you.
Contents of the pack
Suboxone is used to treat opioid dependence (addiction to narcotic drugs such as heroin or morphine) in adults and adolescents over 15 years of age who have agreed to be treated for their addiction. Suboxone is used in conjunction with medical, social, and psychological support.
Do not take Suboxone
Warnings and precautions
Tell your doctor before you start taking Suboxone if you have:
Important things to bear in mind:
If you are over 65 years old, your doctor may monitor you more closely.
This medicine may be targeted by people who abuse prescription medicines and must be kept in a safe place to protect it from theft (see section 5). Do not give this medicine to anyone else. It may cause them to die or have other serious problems.
Some people have died from respiratory failure (inability to breathe) because they have misused buprenorphine or taken it with other central nervous system depressants, such as alcohol, benzodiazepines (tranquilizers), or other opioids.
This medicine can cause severe, potentially life-threatening respiratory depression in children and non-dependent persons if it is taken accidentally or intentionally.
This medicine can cause dependence.
This medicine can cause opioid withdrawal symptoms if taken too soon after using opioids. You should wait at least 6 hours after using a short-acting opioid (e.g. morphine, heroin) or at least 24 hours after using a long-acting opioid, such as methadone.
This medicine can also cause withdrawal symptoms if you stop taking it suddenly. See section 3 "If you stop treatment".
There have been reports of liver damage after taking Suboxone, especially when the medicine is misused. It may also be due to viral infections (e.g. chronic hepatitis C), alcohol abuse, anorexia, or the use of other medicines that can damage the liver (see section 4). Your doctor may perform regular blood tests to monitor your liver function. Inform your doctor if you have any liver problems before starting treatment with Suboxone.
This medicine can cause a sudden drop in blood pressure, making you feel dizzy if you get up too quickly after sitting or lying down.
This medicine may mask the symptoms of pain that could help in the diagnosis of some diseases. You should inform your doctor that you are taking this medicine.
Children and adolescents
Do not give this medicine to children under 15 years of age. If you are between 15 and 18 years old, your doctor may monitor you more closely during treatment due to the lack of data in this age group.
Other medicines and Suboxone
Tell your doctor if you are taking, have recently taken or might take any other medicines.
Some medicines may increase the adverse effects of Suboxone, and may be severe. Do not take other medicines at the same time as Suboxone without consulting your doctor first, especially:
Using Suboxone with food, drinks and alcohol
Do not drink alcoholwhile you are being treated with this medicine. Alcohol may increase drowsiness and the risk of respiratory failure if taken with Suboxone. Do not swallow or consume food or drinks until the tablet has dissolved completely.
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 for advice before taking this medicine. The risks of using Suboxone in pregnant women are not known. Your doctor will decide whether you should continue your treatment with another medicine.
When taken during pregnancy, especially in the last months, medicines like Suboxone may cause withdrawal symptoms in the newborn, including respiratory problems. This may occur several days after birth.
Do not breast-feed while you are taking this medicine, as buprenorphine is excreted in breast milk.
Driving and using machines
Do not drive or ride a bike, do not use tools or machines, or engage in hazardous activities until you know how this medicine affects you. Suboxone may cause drowsiness, dizziness or altered thinking. This may occur more frequently in the first few weeks of treatment, when the dose is being changed, but may also occur if you drink alcohol or take other sedative medicines at the same time as you take Suboxone.
Suboxone contains lactose and sodium.
This medicine contains lactose. If your doctor has told you that you have an intolerance to some sugars, consult them before taking this medicine.
This medicine contains less than 1 mmol of sodium (23 mg) per tablet; this is essentially "sodium-free".
Follow exactly the administration instructions of this medicine given by your doctor or pharmacist. If you are unsure, consult your doctor or pharmacist again.
Treatment is prescribed and supervised by doctors with experience in the treatment of drug addiction.
Your doctor will determine the best dose for you. During treatment, your doctor may adjust your dose based on your response to treatment.
Starting treatment
The recommended initial dose in adults and adolescents over 15 years of age is normally two Suboxone 2 mg/0.5 mg sublingual tablets.
This dose may be repeated on Day 1, depending on your needs.
Before taking your first dose of Suboxone, you must have clear signs of withdrawal. Your doctor will tell you when to take your first dose.
If you are dependent on heroin or a short-acting opioid, the first dose should be taken when withdrawal signs appear, at least 6 hours after the last time you used opioids.
If you have been taking methadone or a long-acting opioid, it is recommended to reduce the methadone dose to less than 30 mg/day before starting treatment with Suboxone. The first dose of Suboxone should be taken when withdrawal signs appear and at least 24 hours after the last time you used methadone.
How to take Suboxone
Do not consume food or drinks until the tablets have dissolved completely.
How to remove the tablet from the blister pack
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If the blister pack is damaged, discard the tablet.
Dose adjustment and maintenance treatment:
During the days following the start of treatment, your doctor may increase the dose of Suboxone you take according to your needs. If you think the effect of Suboxone is too strong or too weak, inform your doctor or pharmacist. The maximum daily dose is 24 mg of buprenorphine.
After a period of satisfactory treatment, you may agree with your doctor to gradually reduce the dose to a lower maintenance dose.
Stopping treatment
Depending on your condition, the dose of Suboxone may be gradually decreased under close medical supervision until it can be finally stopped.
Do not change the treatment in any way or stop it without the authorization of the doctor who is treating you.
If you take more Suboxone than you should
If you or someone else takes too much of this medicine, go or be taken immediately to the emergency department or hospital for treatment, as an overdose of Suboxone can cause serious, potentially life-threatening breathing problems.
Symptoms of overdose may include drowsiness and disorientation with slow reflexes, blurred vision and/or difficulty speaking. You may not be able to think clearly and may breathe more slowly than usual.
If you forget to take Suboxone
If you forget to take a dose, inform your doctor as soon as possible.
If you stop treatment with Suboxone
Do not change the treatment in any way or stop it without the authorization of the doctor who is treating you. Sudden stopping of treatment may cause withdrawal symptoms.
If you have any further questions on the use of this medicine, ask your doctor or pharmacist.
Like all medicines, this medicine can cause adverse effects, although not all people suffer from them.
Report immediately to your doctor or seek urgent medical attentionif you experience adverse effects such as:
Also, report immediately to your doctorif you experience adverse effects such as:
Adverse Effects Reported with Suboxone
Very Common Adverse Effects (may affect more than 1 in 10 people): |
Insomnia (inability to sleep), constipation, nausea, excessive sweating, headache, drug withdrawal syndrome. |
Common Adverse Effects (may affect up to 1 in 10 people): |
Weight loss, swelling of hands and feet, drowsiness, anxiety, nervousness, tingling, depression, decreased sexual desire, increased muscle tension, abnormal thinking, increased tear production (tearful eyes) or other tear disorders, blurred vision, hot flashes, increased blood pressure, migraines, runny nose, sore throat and difficulty swallowing, increased cough, stomach discomfort or other stomach problems, diarrhea, liver function abnormalities, flatulence, vomiting, skin rash, itching, hives, pain, joint pain, muscle pain, leg cramps (muscle spasms), difficulty achieving or maintaining an erection, urinary abnormalities, abdominal pain, back pain, weakness, infection, chills, chest pain, flu-like symptoms, general feeling of discomfort, accidental injury due to loss of alertness or coordination, fainting, and dizziness. |
Uncommon Adverse Effects (may affect up to 1 in 100 people): |
Inflamed glands (lymph nodes), agitation, tremors, abnormal dreams, excessive muscle activity, depersonalization (feeling not like oneself), drug dependence, amnesia (memory disorder), loss of interest, exaggerated sense of well-being, convulsions (epileptic seizures), speech disorders, small pupils, difficulty urinating, eye inflammation or infection, rapid or slow heartbeat, low blood pressure, palpitations, heart attack, chest tightness, shortness of breath, asthma, yawning, mouth pain and sores, tongue discoloration, acne, skin nodules, hair loss, dry or scaly skin, joint inflammation, urinary tract infection, abnormal blood tests, blood in the urine, abnormal ejaculation, menstrual or vaginal problems, kidney stones, protein in the urine, pain or difficulty urinating, sensitivity to heat or cold, heat stroke, loss of appetite, feelings of hostility. |
Frequency Not Known (cannot be estimated from the available data): |
Sudden withdrawal syndrome caused by taking Suboxone too soon after consuming illegal opioids, drug withdrawal syndrome in newborns, slow or difficult breathing, liver damage with or without jaundice, hallucinations, swelling of the face and throat or potentially life-threatening allergic reactions, drop in blood pressure when changing from a sitting or lying position to standing. |
Misuse of this medicine by injection can cause withdrawal symptoms, infections, other skin reactions, and potentially serious liver problems (see "Warnings and Precautions").
Reporting of Adverse Effects
If you experience any type of adverse effect, consult your doctor or pharmacist, even if it is an adverse effect not listed in this leaflet. You can also report them directly through the national reporting system included in Appendix V. By reporting adverse effects, you can contribute to providing more information on the safety of this medicine.
Keep this medicine out of sight and reach of children and other family members.
Do not use this medicine after the expiration date shown on the box. The expiration date is the last day of the month indicated.
This medicine does not require special storage conditions. However, Suboxone can be a target for people who abuse prescription medicines. Keep this medicine in a safe place to protect it from theft.
Store the blister pack safely.
Never open the blister pack before its time.
Never take this medicine in front of children.
In case of accidental ingestion or suspected ingestion, contact an emergency unit immediately.
Medicines should not be disposed of via wastewater or household waste. Ask your pharmacist how to dispose of the packaging and any unused medicines. This will help protect the environment.
Composition of Suboxone
Each 8 mg/2 mg sublingual tablet contains 8 mg of buprenorphine (as hydrochloride) and 2 mg of naloxone (as hydrochloride dihydrate).
Appearance of the Product and Package Contents
Suboxone 8 mg/2 mg sublingual tablets are white, hexagonal, and biconvex
Packaged in packs of 7 and 28 tablets.
Only certain pack sizes may be marketed.
Marketing Authorization Holder
Indivior Europe Limited
27 Windsor Place
Dublin 2
Ireland
Manufacturer
Reckitt Benckiser Healthcare (UK) Ltd,
Dansom Lane,
Hull,
East Yorkshire HU8 7DS,
United Kingdom
Or
Indivior Europe Limited
27 Windsor Place
Dublin 2
Ireland
You can request more information about this medicine by contacting the local representative of the marketing authorization holder:
België/Belgique/Belgien Indivior Europe Limited Tel: 0800 780 41 e-mail: PatientSafetyRow@indivior.com | Lietuva Indivior Europe Limited Tel: 880030793 e-mail: PatientSafetyRoW@indivior.com |
???????? Indivior Europe Limited Tel: 00800 110 4104 e-mail: PatientSafetyRoW@indivior.com | Luxembourg/Luxemburg Indivior Europe Limited Tel: 800 245 43 e-mail: PatientSafetyRow@indivior.com |
Ceská republika Indivior Europe Limited Tel: 800 143 737 e-mail: PatientSafetyRoW@indivior.com | Magyarország Indivior Europe Limited Tel: 6800 19301 e-mail: PatientSafetyRoW@indivior.com |
Danmark Indivior Europe Limited Tlf: 80826653 e-mail: PatientSafetyRoW@indivior.com | Malta Indivior Europe Limited Tel: 80062185 e-mail: PatientSafetyRoW@indivior.com |
Deutschland Indivior Europe Limited Tel: 800 181 3799 e-mail: PatientSafetyRoW@indivior.com | Nederland Indivior Europe Limited Tel: 0800 022 87 83 e-mail: PatientSafetyRow@indivior.com |
Eesti Indivior Europe Limited Tel: 8000041004 e-mail: PatientSafetyRoW@indivior.com | Norge Indivior Europe Limited Tlf: 80016773 e-mail: PatientSafetyRoW@indivior.com |
Ελλ?δα Indivior Europe Limited Τηλ: 800 270 81 901 e-mail: PatientSafetyRoW@indivior.com | Österreich Indivior Europe Limited Tel: 800 296551 e-mail: PatientSafetyRoW@indivior.com |
España Indivior Europe Limited Tel: 900 994 121 e-mail: PatientSafetyRoW@indivior.com | Polska Indivior Europe Limited Tel: 0800 4111237 e-mail: PatientSafetyRoW@indivior.com |
France Indivior Europe Limited Tél:0800 909 972 e-mail: PatientSafetyFrance@indivior.com | Portugal Indivior Europe Limited Tel: 800 841 042 e-mail: PatientSafetyRoW@indivior.com |
Hrvatska Indivior Europe Limited Tel: + +0800 222 899 e-mail: PatientSafetyRoW@indivior.com | România Indivior Europe Limited Tel: 800 477 029 e-mail: PatientSafetyRoW@indivior.com |
Ireland Indivior Europe Limited Tel: 1800554156 e-mail: PatientSafetyRoW@indivior.com | Slovenija Indivior Europe Limited Tel: 080080715 e-mail: PatientSafetyRoW@indivior.com |
Ísland Indivior Europe Limited Sími: 8009875 Netfang: PatientSafetyRoW@indivior.com | Slovenská republika Indivior Europe Limited Tel: 800110286 e-mail: PatientSafetyRoW@indivior.com |
Italia Indivior Europe Limited Tel: 800 789 822 e-mail: PatientSafetyRoW@indivior.com | Suomi/Finland Indivior Europe Limited Puh/Tel: 0800417489 e-mail: PatientSafetyRoW@indivior.com |
Κ?προς Indivior Europe Limited Τηλ: 800 270 81 901 e-mail: PatientSafetyRoW@indivior.com | Sverige Indivior Europe Limited Tel: 020791680 e-mail: PatientSafetyRoW@indivior.com |
Latvija Indivior Europe Limited Tel: 800 05612 e-mail: PatientSafetyRoW@indivior.com | United Kingdom Indivior Europe Limited Tel: 0808 234 9243 e-mail: PatientSafetyRoW@indivior.com |
Date of the Last Revision of this Leaflet:
Detailed information on this medicine is available on the European Medicines Agency website: http://www.ema.europa.eu/.
Discuss dosage, side effects, interactions, contraindications, and prescription renewal for SUBOXONE 8 mg/2 mg SUBLINGUAL TABLETS – subject to medical assessment and local rules.