50 mg film-coated tablets
naltrexone hydrochloride
What Naltrexone Accord is and what it is used for
The active substance, naltrexone hydrochloride, belongs to a group of medicines acting on the nervous system which are used in the treatment of addiction.
What Naltrexone Accord is used for
Naltrexone hydrochloride is used in combination with other medicines or treatments to help those who are addicted to drugs such as heroin ( opioids ) get out of their addiction.
It is used as a supportive adjunctive therapy in alcoholic patients to counteract withdrawal symptoms.
Naltrexone works by blocking receptors in the brain that block the effects of opioids. You will no longer feel the elation you once experienced after taking opioids.
Naltrexone hydrochloride contained in Naltrexone Accord may also be approved for the treatment of other conditions not mentioned in this product information. Ask your doctor, pharmacist, or other healthcare professionals if you have any further questions, and always follow their instructions.
What you need to know before using Naltrexone Accord
Do not use Naltrexone Accord
- if you are allergic to naltrexone hydrochloride or any of the other ingredients of this medicine (listed in section 6).
- if you are addicted to opioids or undergoing detoxification treatment, as withdrawal syndrome or an exacerbation of withdrawal syndrome may occur.
- if you are taking opioid-containing medicines, such as certain cough medicines, medicines to treat diarrhea (such as kaolin and morphine) and painkillers.
Note that naltrexone hydrochloride has no blocking effect on non- opioid analgesics (eg ibuprofen , paracetamol and acetylsalicylic acid ). - if you have an acute liver infection or if your liver function is impaired.
- if you have withdrawal symptoms after administration of naloxone hydrochloride.
- if you are taking methadone .
If you think any of these apply to you, do not take the tablets. Talk to your doctor first and follow your doctor’s advice.
Warnings and cautions
Talk to your doctor or pharmacist before taking Naltrexone Accord:
- If you have any liver or kidney disease. Patients taking Naltrexone Accord may still experience hypersensitivity reactions when taking opiate-containing medicines, even after use.
- Before starting treatment, your doctor may take a blood sample. Blood tests are also necessary during treatment, as Naltrexone Accord is metabolised by the liver and these tests show how well your liver is working.
- If a patient needs to be treated with opioids , e.g. painkillers or anesthesia during surgery in an emergency, a higher dose of opioid is required to achieve the treatment effect. In these cases, respiratory depression and circulatory effects will be deeper and longer lasting.
- Treatment with naltrexone should be started only when the opioid has not been used for a sufficiently long time (about 5 to 7 days for heroin and at least 10 days for methadone ).
- Abnormal results from liver function tests have been reported in obese and elderly patients taking naltrexone and who have no previous drug abuse.
- It is important to stop taking Naltrexone Accord immediately and tell your doctor if you get the following symptoms: persistent stomach pain, white stools, dark urine or if your eyes and / or skin turn yellow.
Consult a physician if any of the above warnings apply or have previously applied to you.
Older
There are insufficient data on the safety and efficacy of naltrexone in elderly patients.
Children and young people
Naltrexone should not be used in children and adolescents below 18 years of age due to a lack of clinical data in this age group. Safe use in children has not been ensured.
Other medicines and Naltrexone Accord
Tell your doctor or pharmacist if you are taking, have recently taken, or might take any other medicines.
- Concomitant use of Naltrexone Accord and opiate-containing drugs must be avoided. If you try to overcome the blocking effect of Naltrexone Accord with large amounts of opioids , you can get serious problems, which can lead to difficulty breathing, coma and even death.
- Concomitant use of Naltrexone Accord and thioridazine may cause drowsiness. No other adverse effects between Naltrexone Accord and other medicines are known.
- Drugs can affect or be affected by each other.
Naltrexone Accord with food and drink
Taking food and drink has no effect on your treatment with Naltrexone Accord.
Pregnancy and breastfeeding
The safety of Naltrexone Accord during pregnancy has not been established.
It is not known whether naltrexone is excreted in human milk. As the safety of naltrexone in neonates and infants has not been established, breastfeeding is discouraged when using Naltrexone Accord.
If you are pregnant or breastfeeding, think you may be pregnant, or are planning to have a baby, ask your doctor or pharmacist for advice before taking this medicine.
Driving and using machines
Naltrexone may impair the mental and/or physical ability required to perform potentially dangerous tasks such as driving or using machines.
You are responsible for assessing whether you are fit to drive a motor vehicle or perform work that requires sharpened attention. One of the factors that can affect your ability in these respects is the use of drugs due to their effects and/or side effects. Descriptions of these effects and side effects can be found in other sections. Read all the information in this leaflet for guidance. If you are not sure, talk to your doctor or pharmacist.
Naltrexone Accord contains lactose monohydrate
This medicine contains 192.85 mg of lactose. According to the dose recommendations, each dose contains up to 192.85 mg of lactose. If you have been told by your doctor that you have an intolerance to some sugars, contact your doctor before taking this medicine.
How to use Naltrexone Accord
Always take this medicine exactly as your doctor or pharmacist has told you. Ask your doctor or pharmacist if you are unsure.
The recommended dose is 1 tablet daily unless your doctor prescribes another dose.
- Naltrexone Accord is taken by mouth with a small amount of liquid.
- Before you start taking Naltrexone Accord, you must not have taken any other opioids for at least 7-10 days. Before starting treatment, your doctor may use a test to determine if you are free of these drugs. Treatment is usually started with a dose of half a tablet daily (25 mg), which is later increased to 1 tablet daily (50 mg).
- Naltrexone Accord should only be used for the condition prescribed by your doctor.
- It is important to carefully follow the dosage one prescribed by your doctor.
- It is important that you take Naltrexone Accord for as long as your doctor prescribes it. The treatment period is usually three months, but can last longer. Your doctor will decide how long you should be treated. Naltrexone Accord should be combined with other treatments.
If you notice that the effect of Naltrexone Accord is too strong or not strong enough, you should consult your doctor or pharmacist.
If you use more Naltrexone Accord than you should
If you have ingested too much medicine or if e.g. a child inadvertently ingested the medicine immediately contact a doctor or hospital for risk assessment and advice.
If you forget to use Naltrexone Accord
You can still take Naltrexone Accord when you remember.
Do not take a double dose to make up for a forgotten dose.
If you stop using Naltrexone Accord
If you are considering stopping before the end of the agreed treatment period, always discuss this with your doctor.
If you have any further questions on the use of this product, ask your doctor or pharmacist.
Possible side effects
Like all medicines, this medicine can cause side effects, although not everybody gets them. Naltrexone Accord may affect your liver function. Your doctor may take a blood sample before you start treatment and then at different times during treatment to check your liver function.
Stop taking Naltrexone Accord and contact your doctor immediately if you notice any of the following:
- abdominal pain lasting more than a few days
- white stools
- dark urine
- yellowing of the eyes
as this may be a sign that your liver is not working well
If you notice any of the following, contact your doctor immediately:
- swelling of the face, lips or tongue
- rash
- breathing difficulties
as this may be a sign of an allergic reaction.
Very common (may affect more than 1 user in 10)
- difficulty sleeping
- anxiety or nervousness
- abdominal cramps and abdominal pain
- malaise and / or nausea
- lack of energy or strength
- joint and / or muscle pain
- headache
- fast or irregular heartbeat
- restlessness
Common (may affect up to 1 in 10 people)
- irritation
- Mood swings
- increased energy
- Depression
- dizziness
- frostbite
- increased or profuse sweating
- dizziness
- increased tear production
- fast pulse
- palpitation
- ECG changes
- chest pain
- diarrhea
- constipation
- rash
- difficulty urinating ( urinary retention )
- delayed ejaculation
- difficulty getting an erection
- lack of appetite
- thirst
- feeling of increased energy
- overindulge
Uncommon (may affect up to 1 in 100 people)
- some infections (eg cold sores, tinea pedis )
- swollen / enlarged lymph nodes
- hallucinations
- confusion
- Depression
- paranoia
- disorientation
- nightmares
- indignation
- decreased sexual desire
- abnormal dreams
- tremors
- drowsiness
- dimsyn
- eye irritation
- hypersensitivity to light
- swelling of the eyes
- pain in the eyes
- strained eyes
- ear problems
- pain in the ears
- ringing in the ears
- dizziness
- blood pressure variations
- hot flashes
- nasal congestion and discomfort
- sneezing
- increased saliva volume
- sinus problems
- voice problems
- shortness of breath / difficulty breathing
- cough
- yawn
- Runny nose
- gas in the stomach
- hemorrhoids
- gastric ulcer
- dry mouth
- liver disease (including hepatitis)
- elevated liver enzymes
- oily skin
- itching
- acne
- hair loss
- groin pain
- increased urine output
- inflammation of the bladder
- increased appetite
- weight loss
- weight gain
- fever
- pain
- cold hands and feet
- feeling of warmth
Rare (may affect up to 1 in 1,000 people)
- suicidal thoughts
- suicide attempt
- bleeding disorder
- speech disorders
Very rare (may affect up to 1 in 10,000 people)
- euphoria (feeling of elation)
- rash
- skeletal muscle injury
How to store Naltrexone Accord
- Keep this medicine out of the sight and reach of children.
- Do not use this medicine after the expiry date which is stated on the carton after “EXP”. and on the blister after “EXP”. The expiration date is the last day of the specified month.
- There are no special storage instructions for this medicine.
- 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.
Contents of the pack and other information
Content declaration
The active substance is naltrexone hydrochloride.
One film-coated tablet contains 50 mg of naltrexone hydrochloride.
Other ingredients are:
Tablet core: lactose monohydrate, microcrystalline cellulose, crospovidone, colloidal anhydrous silica, magnesium stearate
Film coating: hypromellose (E464), macrogol 400, polysorbate 80 (E433), yellow iron oxide (E172), red iron oxide (E172), titanium dioxide (E171)
What the medicine looks like and contents of the pack
Naltrexone Accord is yellow, oval, biconvex, film-coated tablets with a scoreline on one side and flat on the other.
The tablet can be divided into two equal doses.
Naltrexone Accord is available in white, opaque PVC / PE / Aclar-Alu blister and Alu-Alu blister packs containing 7, 14, 28, 30, 50, and 56 tablets.
Not all pack sizes may be marketed.
Marketing Authorization Holder and Manufacturer
Marketing Authorisation Holder
Accord Healthcare BV
Winthontlaan 200
3526 kV Utrecht
Netherlands
Manufacturer
Accord Healthcare Polska Sp.z oo,
ul. Lutomierska 50,95-200 Pabianice, Poland
Accord Healthcare BV
Winthontlaan 200
3526 kV Utrecht
Netherlands