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Subuphine

PACKAGE LEAFLET: INFORMATION FOR THE USER


Subuphine 0.4, 2 and 8 mg sublingual tablets


buprenorphine


Read all of this leaflet carefully before you start taking this medicine.


In this leaflet:

1. What Subuphineis and what it is used for

2. Before you take Subuphine

3. How to take Subuphine

4. Possible side effects

How to store Subuphine

6. Further information.



WHAT SUBUPHINE IS AND WHAT IT IS USED FOR


Subuphine is used:


if you are addicted to opioids, e. g. heroin or morphine, within a framework of medical, social and psychological treatment.


The treatment is prescribed and monitored by doctors specialized in treating drug addiction.



BEFORE YOU TAKE SUBUPHINE


Do not takeSubuphine if you:

  • - are allergic (hypersensitive) to buprenorphine or any of the other ingredients of Subuphine

  • - suffer from serious breathing difficulties

  • suffer from a seriously reduced liver function

  • suffer from alcoholism or delirium tremens.


Take special care with Subuphine if you:

  • -have taken morphine or heroin (opioids)less than 6 hours ago, as withdrawal symptoms can occur

  • have taken methadone less than 24 hours ago, as withdrawal symptoms can occur (if you use methadone your dose may have to be adjusted before you take buprenorphine, see section 3)

  • -suffer from asthma or breathing difficulties

  • -suffer from reduced function of the kidneys or the liver. If you suffer from serious liver insufficiency you must not take buprenorphine

  • -suffer from low bloodpressure

  • -have difficulty passing urine (because of an enlarged prostate gland or urethral stricture)

  • -suffer from a head injury and have an increased intracranial pressure


Observe that Subuphine may:

  • cause dependence

  • cause a positive reaction to ”anti doping tests”

  • cause your blood pressure to drop suddenly, causing you to feel dizzy and unwell if you get up too quickly from sitting or lying down

  • mask other diseases where pain is a symptom since buprenorphine has a pain relieving effect.



Taking other medicines

Buprenorphine may influence the efffect of other medicines and other medicines may influence the effect of buprenorphine.

It is therefore important you tell your doctor if you use any of the following medicines:

  • medicine used in the treatment of anxiety and disquiet and sleeping difficulties (benzodiazepines and anxiolytics other than benzodiazepines)

  • medicine used in the treatment of skin infection in the scalp (ketoconazole, itraconazole)

  • medicine used in the treatment of certain infections (rifampicin)

  • medicine used in the treatment of HIV (ritonavir, indinavir, nelfinavir)

  • some types of medicine used in the treatment of allergy

  • some types of medicine used in the treatment of depression

  • medicine used in the treatment of migraine, hot flushes and abstinences as a result of medicine abuse (clonidine)

  • cough medicine (dextromethorphan, noscapine)

  • painkillers (morphine and morphine-like substances)

  • medicine containing alcohol

  • medicine used in the treatment of epilepsy (phenobarbital, phenytoin, carbamazepine)

  • medicine used in the treatment of psychosis (neuroleptics)

  • medicine used as sedatives and to relieve convulsions (barbiturates).


Please tell your doctor or pharmacist if you are taking or have recently taken any other medicines, including medicines obtained without a prescription.


Taking Subuphine with food and drink

You can take Subuphine independently of a meal.


Alcohol

Do not drink alcohol when you are treated with Subuphine since alcohol will increase the sedative effect of buprenorphine.


Pregnancy and breast-feeding

Ask your doctor or pharmacist for advice before taking any medicine.


Pregnancy

You should not use buprenorphine during your pregnancy. But if your doctor finds it appropriate an exception can be made for the first 3 months of your prenancy.


Breast-feeding

Do not take buprenorphine if you are breast-feeding.


Driving and using machines

Subuphine can be sedating, cause fainting and dizziness, and therefore it can reduce the ability to drive and use machines.

Do not drive or use machines if you feel dizzy or drowsy. This usually occurs at the beginning of treatment and when the dose is increased.


Important information about some of the ingredients of Subuphine

Subuphine contains lactose.

If you have been told by your doctor that you have an intolerance to some sugars, contact your doctor before

taking this medicinal product


HOW TO TAKE SUBUPHINE


Always take Subuphine exactly as your doctor has told you. You should check with your doctor or pharmacist if you are not sure.


This is the way you take Subuphine

A sublingual tablet is a tablet that is taken under your tongue. Keep the tablet dose under your tungue until it dissolves – normally it takes 5-10 minutes. Do not swallow, crush or chew the tablet.


Usual dose if you are/have:

Adults or elderly:

Your initial dose will be between 0.8 to 4 mg (one tablet once daily). Your doctor will increase your dose according to your response to the treatment until you have a stabil dose, 16 mg daily is often sufficient. The maximum daily dose is 24 mg. Your doctor will then individually determine the length of your treatment and gradually reduce your dose. Do not change the treatment in any way or stop treatment without the agreement of the doctor who is treating you.


Children and adolescents (younger than 18 years):

Children and adolescents under the age of 18 must not use Subuphine.


Recuced kidney or liver function:

If you have problems with your kidneys or liver your dose may have to be reduced. Talk to your doctor. If you suffer from serious liver insufficiency you must not take buprenorphine.


Concomitant methadone treatment

Your dose of methadone has to be reduced to a maximum of 30 mg daily before starting treatment with Subuphine. Contact your doctor if you experience withdrawal symptoms (sweating, disquiet or restlessness).


If you take more Subuphine than you should

In case of overdose of buprenorphine, you must go or be taken immediately to an emergency centre or hospital for treatment.

Symptoms of an overdose is breathing difficulties, slowly breathing or heart symptoms.

Toxic poisoning has been observed after misuse (overdose or wrong administration) and in worst case it can result in stop of breathing/heart failure and/or liver damage.


If you forget to take Subuphine

Do not take a double dose to make up for a forgotten dose.


If you stop taking Subuphine

Do not stop the treatment yourself, but ask your doctor how to end the treatment.

A sudden interruption can cause withdrawal symptoms (sweating, disquiet and restlessness).


If you have any further questions on the use of this product, ask your doctor or pharmacist.



4. POSSIBLE SIDE EFFECTS


Like all medicines, Subuphine can cause side effects, although not everybody gets them.


You should stop taking Subuphine and see your doctor immediately if you experience symptoms of angioneurotic oedema, such as:

  • swollen face, tongue or pharynx

  • difficulty to swallow

  • hives and difficulties to breath


Addiction to Subuphine

Please observe that Subuphine may cause dependence.


Common side effects(occuring in more than 1 but less than 10 in 100 patients):

Headache, fainting, dizziness, obstipation, nausea, vomiting, insomnia, drowsiness, feeling of weakness, drop in blood pressure on changing position from sitting or lying down to standing, sweating.


In long term use of buprenorphine, the common undesirable effects diminish successively. However constipation and sweating often remain.


Rare side effects(occurring in more than 1 but less than 10 in 10,000 patients):

Hallucinations, respiratory depression, bronchial spasm, damage of the liver, hepatitis, anafylatic shock, angioneurotic oedema, urine retention.


If any of the side effects gets serious, or if you notice any side effects not listed in this leaflet, please tell your doctor or pharmacist.



5. HOW TO STORE SUBUPHINE


Keep out of the reach and sight of children.


Do not use Subuphine after the expiry date which is stated on the carton and on the blister after Exp.The expiry date refers to the last day of that month.


Does not require any special storage conditions.


Medicines should not be disposed of via wastewater or household waste. Ask your pharmacist how to dispose of medicines no longer required. These measures will help to protect the environment.



6. FURTHER INFORMATION


What Subuphine contains

  • The active substance is buprenorphine as buprenorphine hydrochloride. Each sublingual tablet contains 0.4 mg, 2 mg and 8 mg buprenorphine respectively.

  • The other ingredients are lactose monohydrate, mannitol (E421), maize starch, citric acid (E330), sodium citrate (E331), povidone (E1201), magnesium stearate (E470b).

  • The 0.4 mg sublingual tablets also contain: Talc (E553b) and colloidal anhydrous silica.


What Subuphine looks like and contents of the pack

Subuphine 0.4 mg is a round, biconvex and white sublingual tablet.

Subuphine 2 mg is an oval, biconvex and white sublingual tablet with “2” embossed on one side.

Subuphine 8 mg is an oval, biconvex and white sublingual tablet with “8” embossed on one side.


Subuphine is packed in blister packs of 7, 14 and 28 sublingual tablets. Not all pack sizes may be marketed.


Marketing Authorisation Holder

BMM Pharma AB

Blasieholmsgatan 2

SE-11148 Stockholm

Sweden


Manufacturer

DDSA Pharmaceuticals Ltd

310 Old Brompton Road

London SW5 9JQ

UK


Laboratorios Atral, S.A.

Rua da Estacao no.42

Vala do Carregado

Castanheira do Ribatejo

2600-726, Portugal

The manufacturer (Laboratorios Atral, S.A.) is only valid for the 2mg & 8mg Subuphine Sublingual Tablets.


This medicinal product is authorised in the Member States of the EEA under the following names:

< To be completed nationally >


This leaflet was last approved in 22 February 2016.



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