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Lormetazepam Tablets 1mg

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Document: leaflet MAH GENERIC_PL 17225-0013 change

TEXT FOR NON-MARKETED PACK GENUS PHARMACEUTICALS LTD - GENERIC

PACKAGE LEAFLET: INFORMATION FOR THE USER

Lormetazepam Tablets 0.5 mg and 1 mg

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

-    Keep this leaflet. You may need to read it again.

-    If you have any further questions, ask your doctor or pharmacist.

-    This medicine has been prescribed for you only. Do not pass it on to others. It may harm them, even if their signs of illness are the same as yours.

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

In this leaflet

1.    What Lormetazepam Tablets are and what they are used for

2.    Before you take Lormetazepam Tablets

3.    How to take Lormetazepam Tablets

4.    Possible side -effects

5.    How to store Lormetazepam Tablets

6.    Further information

1.    WHAT LORMETAZEPAM TABLETS ARE AND WHAT THEY ARE USED FOR

The name of your medicine is Lormetazepam Tablets. Lormetazepam is a member of a group of medicines called benzodiazepines. Lormetazepam is used for short-term therapy to help with sleeping difficulties which are significantly affecting your normal daily life.

2.    BEFORE YOU TAKE LORMETAZEPAM TABLETS Do not take Lormetazepam Tablets:

-    if you have severe breathing or chest problems;

-    if you are allergic to benzodiazepines or any of the other ingredients in Lormetazepam Tablets (see list under ‘What Lormetazepam Tablets contain’)

-    if you have myasthenia gravis (very weak or tired muscles)

-    if you have serious liver problems

-    if you suffer from sleep apnoea (breathing problems when you are asleep)

-    if you are breast-feeding, since the drug may pass into breast milk.

Take special care with Lormetazepam Tablets:

-    if you are pregnant, or trying to become pregnant (see below)

-    if you abuse or have in the past abused drugs or alcohol

-    if you have a personality disorder. If so, you have a greater chance of becoming dependant on lormetazepam

-    if you have any kidney or liver problems

-    if you are suffering from depression, since lormetazepam may increase any suicidal feelings which you may have

-    if you have suffered from depression before, since it could re-occur during treatment with lormetazepam

-    if you suffer from breathing problems

-    if you are suffering from an eye problem called glaucoma.

Taking other medicines

Tell your doctor or pharmacist if you are taking lormetazepam before taking any other Medicines or if you enter hospital for treatment, or if you are taking any other medicines, including those which have not been prescribed by the doctor, since they may affect the way Lormetazepam Tablets work.

Lormetazepam Tablets may also affect the way other drugs work. In particular, you should tell your doctor if you are taking any other sedatives, ant-anxiety drugs, anti-depressants, anti-hypertensives, strong pain-killers (e.g. methadone), drugs for epilepsy, drugs to help breathing, drugs which stop liver enzymes working; anaesthetics; antihistamines or drugs for mood or mental disorders (e.g. chlorpromazine). The dose of these drugs may need to be reduced before you can take lormetazepam.

Pregnancy and breast-feeding Pregnancy

Do not take this medicine if you are pregnant, or might become pregnant, without consulting your doctor. Benzodiazepines, including lormetazepam, may cause damage to the foetus if taken during early pregnancy.

If you take this medicine during late pregnancy or during labour, your baby, when born, may be less active than other babies, have a low body temperature, be floppy, or have breathing of feeding difficulties for a while. Your baby’s response to the cold might be temporarily impaired. If this medicine is taken regularly in late pregnancy, your baby may develop withdrawal symptoms after birth.

Breast-feeding

Do not take this medicine if you are breast-feeding, since the drug may pass into breast milk, and may cause the baby to be less active and unable to suckle.

Driving and using machines

Lormetazepam may make you feel dizzy or sleepy during the day, or may affect your concentration. This may affect your performance at skilled tasks such as driving and operating machinery..

You should avoid alcohol while you are taking lormetazepam, since this may make you very drowsy and seriously affect your ability to drive or use machines.

This medicine can affect your ability to drive as it may make you sleepy or dizzy . Do not drive while taking this medicine until you know how it affects you . It is an offence to drive if this medicine affects your ability to drive . However, you would not be committing an offence if: o The medicine has been prescribed to treat a medical or dental problem and o You have taken it according to the instructions given by the prescriber or the information provided with the medicine and it was not affecting your ability to drive safely.

Talk to your doctor or pharmacist if you are not sure whether it is safe for you to drive while taking this medicine.

Important Information about some of the ingredients of Lormetazepam Tablets

If you have been told by your doctor that you have an intolerance to some sugars, contact your doctor before taking this medicinal product.

Always take Lormetazepam Tablets exactly as your doctor has told you. The label on your medicine should also tell you. You should check with your doctor or pharmacist if you are not sure.

The usual adult dose of Lormetazepam Tablets is 0.5mg to 1.5mg. For patients with mild to moderate difficulties in breathing or patients with liver impairment a dose reduction should be considered.

You should swallow your tablets with water just before you go to bed at night. Make sure you can have 7 or 8 hours of uninterrupted sleep before taking Lormetazepam Tablets.

Elderly: Elderly patients may respond to half the usual adult dose or less. The label on your medicine will tell you how many tablets to take and how often. If it does not, or you are not sure, ask your doctor or pharmacist.

Treatment usually lasts from a few days to 2 weeks. It should not usually last longer than 4 weeks including a dose reduction at the end. This reduces the risk of becoming dependant on Lormetazepam Tablets, of suffering unpleasant side effects when you stop taking it (See ‘If you stop taking Lormetazepam Tablets’ section). The beneficial effect of Lormetazepam Tablets may be less apparent after several weeks of use. If you are given lormetazepam for more than 4 weeks, your doctor might want to take blood samples occasionally to check your blood and liver, since drugs like lormetazepam have occasionally affected liver function.

If you take more Lormetazepam Tablets than you should

Do not take more tablets than stated on the label of your medicine. If you take too many tablets you should seek medical attention immediately, either by calling your doctor, or going to the nearest casualty department. Always take the labelled medicine container with you, even if there are no tablets left.

If you forget to take Lormetazepam Tablets

If you forget to take a dose, don’t worry, just take your next tablet when it is due. Do not Take a double dose to make up for a forgotten tablet.

If you stop taking Lormetazepam Tablets

-    After you have finished your prescribed treatment with lormetazepam, your doctor will decide if you need further treatment.

-    The number of Lormetazepam Tablets and how often you take them should always be reduced slowly before stopping them. This allows your body to get used to being without your tablets, and reduces the risk of unpleasant effects when you stop taking them. Your doctor will tell you how to do this.

-    On stopping lormetazepam, you may experience symptoms such as headaches, muscle pain, anxiety, tension, depression, restlessness, sweating, confusion or irritability. Your original sleeplessness may also return. If you suffer from any of these symptoms, ask your doctor for advice.

-    Do not stop taking your tablets suddenly. This could lead to more serious symptoms such as loss of sense of reality, feeling unreal or detached from life and unable to feel emotion. Some patients have also experienced numbness or tingling of the arms or legs, tinnitus (ringing sounds in the ears), oversensitivity to light, sound and touch, uncontrolled or overactive movements, twitching, shaking, feeling sick, being sick, stomach upsets or stomach pain, loss of appetite, agitation, abnormally fast heartbeats, panic attacks, dizziness or feeling that you are about to fall, memory loss,

hallucinations, feeling stiff and unable to move easily, feeling very warm, convulsions (sudden uncontrollable shaking or jerking of the body).

- Patients taking anti-depressants and patients with seizure disorders may be more likely to experience convulsions.

If you suffer from any of these symptoms, ask your doctor for advice immediately.

4.    POSSIBLE SIDE-EFFECTS

Like all medicines, this medicine can cause side effects, although not everybody gets them. These are usually not serious and do not last long.

If you experience any of the following more rare unwanted effects, you should tell your doctor immediately:

Confusion, depression, numbed emotions, difficulty controlling urges and impulses to speak, act or show emotions, a feeling of well being for no reason, allergic reaction, changes in appetite, sleep problems,changes in sex drive, sexual problems, headaches, reduced alertness, speech problems, memory loss or forgetfulness, problems with vision, worsening of sleep apnoea, difficulty breathing, feeling sick, stomach upsets, changes in the amount of saliva in the mouth, yellowing of the skin and eyes, skin problems such as rash, dependence to Lormetazepam Tablets, suicidal thoughts or plans, hypersensitivity including anaphylaxis, twitching or shaking, feeling worried or stressed, slow thoughts, coma, feeling very cold, worsening of original sleeplessness and related symptoms such as : restlessness, agitation, irritability, aggressiveness, loss of sense of reality, intense anger, nightmares, hallucinations and inappropriate behaviour.

Other rare unwanted effects include blood or liver function changes, or low blood pressure. However, you should tell your doctor if any of the following symptoms are severe or become troublesome:

Daytime drowsiness, feeling calm and sleepy, dizziness, muscle weakness, poor muscle control and unsteady movements, general weakness, feeling tired.

Reporting of side effects

If you get any side effects, talk to your doctor, pharmacist or nurse. This includes any possible side effects not listed in this leaflet. You can also report side effects directly via the Yellow Card Scheme at: www.mhra.gov.uk/yellowcard.

By reporting side effects you can help provide more information on the safety of this medicine.

5.    HOW TO STORE LORMETAZEPAM TABLETS Keep this medicine out of the sight and reach of children

Do not take Lormetazepam Tablets after the expiry date shown on the carton after EXP. The expiry date refers to the last day of the month.

Lormetazepam Tablets should be kept in a cool, dry place. Return any unused tablets to your pharmacist. Only keep them if your doctor tells you to. 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 protect the environment.

6.    FURTHER INFORMATION What Lormetazepam Tablets contain

The active ingredient in 0.5mg and 1mg tablets is lormetazepam

The other ingredients are lactose, maize starch, polyvinylpyrrolidone and magnesium stearate.

What Lormetazepam Tablets look like and contents of the pack

Lormetazepam Tablets are round, white tablets, plain on one side, and with either ‘GP036’ (0.5mg tablets) or with ‘GP037’ (1mg tablets) on the other.

Each pack contains 30 tablets.

POM

PL 17225/0012 Lormetazepam Tablets 0.5 mg PL 17225/0013 Lormetazepam Tablets 1 mg

Marketing Authorisation Holder

Genus Pharmaceuticals, Linthwaite, Huddersfield, HD7 5QH, UK.

Manufacturer

Haupt Pharma Munster GmbH, Schleebruggenkamp 15, 48159 Munster, Germany.

This leaflet was last revised in December 2014