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SODIUM VALPROATE ZENTIVA 200MG/5ML LIQUID

Active substance(s): SODIUM VALPROATE

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PATIENT INFORMATION LEAFLET
SODIUM VALPROATE ZENTIVA 200MG/5ML LIQUID

▼This medicine is subject to additional monitoring. This will allow quick identification of
new safety information. You can help by reporting any side effects you may get. See the end of
section 4 for how to report side effects.
Warning
Valproate can cause birth defects and problems with early development of the child if it is taken
during pregnancy. If you are a female of childbearing age you should use an effective method of
contraception throughout your treatment.
Your doctor will discuss this with you but you should also follow the advice in section 2 of this
leaflet. Tell your doctor at once if you become pregnant or think you might be pregnant.
Read all of this leaflet carefully before you start taking this medicine because it contains
important information for you.
• Keep this leaflet. You may need to read it again.
• If you have further questions, please ask your doctor or pharmacist.
• This medicine has been prescribed for you only. Do not pass it onto others. It may harm
them even if their symptoms are the same as yours.
• If you get any side effects, talk to your doctor or pharmacist. This includes any possible side
effects not listed in this leaflet. See section 4.
What is in this leaflet
1. What sodium valproate is and what is it used for
2. What you need to know before you take sodium valproate
3. How to take sodium valproate
4. Possible side effects
5. How to store sodium valproate
6. Contents of the pack and other information

1.

WHAT SODIUM VALPROATE IS AND WHAT IT IS USED FOR

The name of your medicine is Sodium Valproate Zentiva 200mg/5ml Liquid (called sodium
valproate throughout this leaflet). This belongs to a group of medicines called anti-convulsants or
anti-epileptic agents. It works by controlling the activity of the brain which causes fits or seizures.
It is used to treat epilepsy (fits) in adults and children.

2.

WHAT YOU NEED TO KNOW BEFORE YOU TAKE SODIUM
VALPROATE

Do not take sodium valproate and tell your doctor if:
• You are allergic (hypersensitive) to sodium valproate or any of the other ingredients of this
medicine (listed in section 6).
Signs of an allergic reaction include: a rash, swallowing or breathing problems, swelling of
your lips, face, throat or tongue.
• You have liver problems or a family history of liver problems.





You have a rare illness called porphyria which affects your metabolism.
You have a known metabolic disorder i.e. a urea cycle disorder.
You have a genetic problem caused by a mitochondrial disorder (e.g. Alpers-Huttenlocher
syndrome).

Talk to your doctor or pharmacist before taking sodium valproate if:

You have diabetes. This medicine may affect the results of urine tests.
• You have a carnitine palmitoyltransferase type II deficiency.
• You have kidney problems – you may need a lower dose.
• You have a ‘urea cycle disorder’ – where too much ammonia builds up in the body.
• You have an illness called “lupus” – a disease of the immune system which affects the skin,
bones, joints, lungs and kidneys.
• You know that there is a genetic problem caused by a mitochondrial disorder in your family.
Talk to your doctor or pharmacist before taking sodium valproate if you have these conditions.
Do this even if you no longer have them, but have had them in the past.
Sodium valproate can increase your appetite and may make you put on weight. Talk to your
doctor about how this will affect you.
Your doctor may wish to do blood tests before you start taking sodium valproate and during the
first six months of treatment.
Warnings and precautions
• A small number of people being treated with anti-epileptics such as sodium valproate have
had thoughts of harming or killing themselves. If at any time you have these thoughts,
immediately contact your doctor.
• As with other antiepileptic drugs, convulsions may become worse or happen more frequently
whilst taking this medicine. If this happens contact your doctor immediately.
Other medicines and sodium valproate
Please tell your doctor or pharmacist if you are taking or have recently taken any other medicines,
including medicines obtained without a prescription. This includes herbal medicines. This is
because sodium valproate can affect the way some other medicines work. Also some medicines
can affect the way sodium valproate works.
In particular, check with your doctor or pharmacist if you are taking any of the following medicines:
• Anti-psychotic agents such as quetiapine and olanzapine – for mental health problems. Sodium
valproate may increase the effects of these drugs. In particular, when taken with the medicine
olanzapine the following effects occur: neutropenia (a blood problem which reduces the chance
of fighting infection), tremor, dry mouth, increased appetite and weight gain, problems with
speech, sleepiness or extreme tiredness.
• Medicines for depression – including monoamine oxidase inhibitors (MAOI) such as
moclobemide.
• Benzodiazepines (such as diazepam) – used as sleeping tablets and for anxiety.
• Some medicines for epilepsy such as phenytoin, carbamazepine, rufinamide, topiramate,
acetazolamide, phenobarbital, lamotrigine, primidone, felbamate.
• Medicines for thinning the blood such as warfarin.
• Salicylates such as aspirin.
• Cholestyramine – for high blood lipid (fat) levels.
• Cimetidine – for stomach ulcers.








Carbapenem agents (antibiotics used to treat bacterial infections) such as imipenem,
meropenem, rifampicin and erythromycin. The combination of sodium valproate and
carbapenems should be avoided because it may decrease the effect of your medicine.
Mefloquine and chloroquine – used to prevent and treat malaria. Taking these with sodium
valproate may increase the chance of a fit. Before travelling to a malaria area, ask your doctor or
pharmacist about the best malaria prevention tablets for you.
Zidovudine and protease inhibitors such as lopinavir and ritonavir – for HIV and AIDS.
Temozolomide – for cancer.
Nimodipine.
Propofol – used for anaesthesia.

Taking sodium valproate with food and drink
Take sodium valproate with or after food. This will help to stop the feelings of sickness that may
happen after taking the medicine.
Alcohol intake is not recommended during treatment.
Pregnancy, breast feeding and fertility
Important advice for women
• Valproate can be harmful to unborn children when taken by a woman during pregnancy.
• Whether taken on its own or with another epilepsy medicine, valproate seems to carry a
higher risk if taken during pregnancy than other epilepsy medicines. The higher the dose, the
higher the risks but all doses carry a risk.
• It can cause serious birth defects and can affect the way in which the child develops as it
grows. Birth defects which have been reported include spina bifida (where the bones of the
spine are not properly developed); facial and skull malformations; heart, kidney, urinary tract
and sexual organ malformations; limb defects.
• If you take valproate during pregnancy you have a higher risk than other women of having a
child with birth defects that require medical treatment. Because valproate has been used for
many years we know that in women who take valproate around 10 babies in every 100 will
have birth defects. This compares to 2-3 babies in every 100 born to women who don’t have
epilepsy.
• It is estimated that up to 30-40% of preschool children whose mothers took valproate during
pregnancy may have problems with early childhood development. Children affected can be
slow to walk and talk, intellectually less able than other children, and have difficulty with
language and memory.
• Autistic spectrum disorders are more often diagnosed in children exposed to valproate and
there is some evidence children may be more likely to develop symptoms of Attention
Deficit Hyperactivity Disorder (ADHD).
• If you are a woman capable of becoming pregnant your doctor should only prescribe
valproate for you if nothing else works for you.
• Before prescribing this medicine to you, your doctor will have explained what might happen
to your baby if you become pregnant whilst taking valproate. If you decide later you want to
have a child you should not stop taking your medicine until you have discussed this with
your doctor and agreed a plan for switching you onto another product if this is possible.
• Ask your doctor about taking folic acid when trying for a baby. Folic acid can lower the
general risk of spina bifida and early miscarriage that exists with all pregnancies. However,
it is unlikely that it will reduce the risk of birth defects associated with valproate use.
FIRST PRESCRIPTION

If this is the first time you have been prescribed valproate your doctor will have explained the
risks to an unborn child if you become pregnant. Once you are of childbearing age, you will need
to make sure you use an effective method of contraception throughout your treatment. Talk to
your doctor or family planning clinic if you need advice on contraception.
Key messages:
• Make sure you are using an effective method of contraception.
• Tell your doctor at once if you are pregnant or think you might be pregnant.
CONTINUING TREATMENT AND NOT TRYING FOR A BABY
If you are continuing treatment with valproate but you don’t plan to have a baby make sure you
are using an effective method of contraception. Talk to your doctor or family planning clinic if
you need advice on contraception.
Key messages:
• Make sure you are using an effective method of contraception
• Tell your doctor at once if you are pregnant or think you might be pregnant.
CONTINUING TREATMENT AND CONSIDERING TRYING FOR A BABY
If you are continuing treatment with valproate and you are now thinking of trying for a baby you
must not stop taking either your valproate or your contraceptive medicine until you have
discussed this with your prescriber. You should talk to your doctor well before you become
pregnant so that you can put several actions in place so that your pregnancy goes as smoothly as
possible and any risks to you and your unborn child are reduced as much as possible.
Your doctor may decide to change the dose of valproate or switch you to another medicine before
you start trying for a baby.
If you do become pregnant you will be monitored very closely both for the management of your
underlying condition and to check how your unborn child is developing.
Ask your doctor about taking folic acid when trying for a baby. Folic acid can lower the general
risk of spina bifida and early miscarriage that exists with all pregnancies. However, it is unlikely
that it will reduce the risk of birth defects associated with valproate use.
Key messages:
• Do not stop using your contraception before you have talked to your doctor and worked
together on a plan to ensure your epilepsy is controlled and the risks to your baby are reduced.
• Tell your doctor at once when you know or think you might be pregnant.
UNPLANNED PREGNANCY WHILST CONTINUING TREATMENT
Babies born to mothers who have been on valproate are at serious risk of birth defects and
problems with development which can be seriously debilitating. If you are taking valproate and
you think you are pregnant or might be pregnant contact your doctor at once. Do not stop taking
your medicine until your doctor tells you to.
Ask your doctor about taking folic acid. Folic acid can lower the general risk of spina bifida and
early miscarriage that exists with all pregnancies. However, it is unlikely that it will reduce the
risk of birth defects associated with valproate use.
Key messages:
• Tell your doctor at once if you know you are pregnant or think you might be pregnant.
• Do not stop taking valproate unless your doctor tells you to.

Make sure you read the patient booklet and sign the Acknowledgement of Risk form which
should be given to you and discussed with you by your doctor or pharmacist.
Breast-feeding
Very little sodium valproate gets into the breast milk. However, talk to your doctor about whether
you should breastfeed your baby. Ask your doctor or pharmacist for advice before taking any
medicine.
Driving and using machines
You may feel sleepy:
• When you first start taking sodium valproate.
• If you are taking it with other medicines, such as other antiepileptic drugs or
benzodiazepines.
If this happens to you, do not drive or use any tools or machines.
Important information about some of the ingredients of sodium valproate
This liquid contains:
• A colour called ‘ponceau 4R aluminium lake (E124)’: This may cause allergic reactions
including asthma in some people. You are more likely to have an allergy if you are also
allergic to aspirin.
• Sodium methyl hydroxybenzoate and sodium propyl hydroxybenzoate: This may cause
allergic reactions (these may not happen straight away).
• Sorbitol: This is a type of sugar. If you have been told by your doctor that you cannot
tolerate some sugars, talk to your doctor before taking the liquid.

3.

HOW TO TAKE SODIUM VALPROATE

Always take sodium valproate exactly as your doctor has told you. You should check with your
doctor or pharmacist if you are not sure.
Sodium valproate treatment must be started and supervised by a doctor specialised in the
treatment of epilepsy.
Taking this medicine
• Sodium valproate should be swallowed with or after food. This will help reduce the chances
of getting certain side effects such as nausea or upset stomach.
• You will be able to measure the dose in the measuring cup supplied with the liquid.
• The marks of the cup show you how to measure between 5ml (200mg) and 15ml (600mg)
• If the dose is less than 5ml (200mg), talk to your doctor or pharmacist about how to measure
the dose.
• Do not mix sodium valproate with any other liquids. Do not dilute this medicine.
How much to take
Adults
• The usual dose of sodium valproate is between 1000mg and 2000mg each day.
• This may be increased to 2500mg each day.
• Take this in 2 separate doses – half in the morning and half in the evening.
Children over 20kg:
• The dose of sodium valproate is based on the child’s weight.





The usual dose is between 20 and 30mg for each kg of body weight.
This may be increased to 35mg for each kg of body weight each day.
Take this in 2 separate doses – half in the morning and half in the evening.

Children under 20kg:
• The usual dose of sodium valproate is based on the child’s weight
• The usual dose is 20mg for each kg of body weight.
• Give in 2 separate doses – half in the morning and half in the evening.
People with kidney problems
If you or your child have kidney disease, your doctor may prescribe a lower dose.
Do not change the dose you have been prescribed without first discussing with your doctor.
When treatment is first started
At first you may be prescribed a lower dose. This is because some patients need less sodium
valproate than others to control their fits. Your doctor will then increase the dosage until your
condition is controlled.
• Because of this it is very important that you follow your doctor’s instructions about how
much to take.
• Blood tests may be needed to check how well the medicine is working.
• You may be taking other medicines for epilepsy at the same time as sodium valproate. If so,
your doctor may increase the dose of sodium valproate by 5 to 10mg for each kg of body
weight each day.
Appointments
Make sure you keep your regular appointments for a check-up. They are very important as your
dose may need to be changed. If you go into hospital or visit another doctor or a dentist, tell them
you are taking sodium valproate.
If you take more sodium valproate than you should
An overdose of this medicine may be dangerous. If you think you may have taken more sodium
valproate than you should (or someone else has taken some), talk to a doctor, pharmacist or go to
the nearest hospital casualty department straight away. Take the medicine bottle with you.
The following effects may happen: feeling sick or being sick, pupils of the eye become smaller,
dizziness, loss of consciousness, weak muscles and poor reflexes, breathing problems, headaches,
fits (seizures), confusion, memory loss and unusual or inappropriate behaviour.
If you forget to take sodium valproate
If you forget to take a dose at the right time, take it as soon as you remember. Then go on as
before. Do not take a double dose to make up for a forgotten dose.
If you stop taking sodium valproate
Do not stop taking sodium valproate without first discussing this with your doctor, even if you
feel better. This is because stopping suddenly may lead to your fits coming back.
If you have any further questions on the use of this product, ask your doctor or pharmacist.

4.

POSSIBLE SIDE EFFECTS

Like all medicines, sodium valproate can cause side effects, although not everybody gets them.
Usually they are not serious, and may stop if you change to another medicine.
Stop taking sodium valproate and see a doctor or go to a hospital straight away if:
• You get swelling of the face, lips or throat which may cause difficulty in swallowing or
breathing. Hands, feet or genitals may also be affected. More severe allergic reactions can
lead to lymph node enlargement and possible impairment of other organs.You could also
notice an itchy, lumpy rash (hives), nettle rash (urticaria), joint pain or fever (systemic lupus
erythematosus). This may mean you are having an allergic reaction to sodium valproate.
Tell your doctor straight away if you notice any of the following serious side effects – you
may need urgent medical treatment.
• Liver problems and problems of the pancreas may show as a sudden illness which may
happen in the first six months of treatment. This is a common side effect in people taking
sodium valproate. It includes feeling and being sick many times, being very tired, sleepy and
weak, stomach pain including very bad upper stomach pain, jaundice (yellowing of the skin
or whites of the eyes), leg swelling, worsening of your epilepsy or a general feeling of being
unwell. Your doctor may tell you to stop taking sodium valproate if you have these
symptoms.
Uncommon side effects (may affect up to 1 in 100 people)
• Breathing difficulty and pain due to inflammation of lungs (pleural effusion).
• An increase in the number and severity of convulsions.
Rare side effects (may affect up to 1 in 1,000 people)
• You have a skin rash or skin lesions with a pink/red ring and a pale centre which may be
itchy, scaly or filled with fluid. The rash may appear especially on the palms or soles of
your feet. These could be signs of a serious allergy to the medicine called ‘erythema
multiforme’ Blistering or bleeding of the skin around the lips, eyes, mouth, nose and
genitals. Also flu-like symptoms and fever. This may be something called ‘StevensJohnson syndrome’.
• Severe blistering rash where layers of the skin peel off to leave large areas of raw exposed
skin over the body. Also a feeling of being generally unwell, fever, chills and aching
muscles. This may be something called ‘Toxic epidermal necrolysis’.
• Bruising more easily and getting more infections than usual. This could be a blood problem
called ‘thrombocytopenia.’ It can also be due to a fall in the number of white blood cells,
bone marrow depression or another condition that affects red blood cells, white blood cells
and platelets (pantocytopenia).
• Blood problems such as blood clotting problems (bleeding for longer than normal), bruising
or bleeding for no reason or getting infections more easily than usual. These blood problems
could include bone marrow depression or how the blood clots.
• Changes in mood, loss of memory, lack of concentration and deep loss of consciousness
(coma).
• Underactive thyroid gland, which may cause tiredness or weight gain (hypothyroidism).
Tell your doctor as soon as possible if you have any of the following side effects:









Very unusual behaviour including being very alert, and sometimes also aggressive, hyperactive and showing bad behaviour. This can be associated with more frequent or severe fits,
and loss of drive. This is more likely if phenobarbital and topiramate is taken at the same
time or if the sodium valproate dose has been suddenly increased.
Sleepy or unsteady when walking or jerky muscle movements. This is a common side effect
(may affect up to 1 in 10 people).
Feeling tired, confused, with loss of consciousness (coma) sometimes accompanied by
hallucinations or fits. This is a common side effect (may affect up to 1 in 10 people).
Rapid, uncontrollable movement of the eyes. This is a common side effect (may affect up to
1 in 10 people).
Blisters with the skin flaking away. This is a rare side effect (may affect up to 1 in 10,000
people).
Changes in the amount of ammonia in the blood. Symptoms of this condition are being sick,
problems with balance and co-ordination, feeling lethargic or less alert. This is a rare side
effect (may affect up to 1 in 10,000 people).

Tell your doctor or pharmacist if any of the following side effects get serious or lasts longer
than a few days, or if you notice any side effects not listed in this leaflet:
Very common side effects (may affect more than 1 in 10 people)
• Feeling sick (nausea) especially when starting treatment. Feeling sick may be made better
by taking the liquid with or after food.
• Feeling shaky (tremor)
Common (may affect up to 1 in 10 people)
• Being sick (vomiting), stomach ache or diarrhoea, especially when starting treatment.
• Swelling of gums or sore mouth
• Hearing problems
• Nail and nail bed disorders
• Loss of hair which is usually temporary. When it grows back it may be more curly than
before.
• Weight gain – as your appetitie may be increased
• Headache
• Seeing or hearing things that are not there (hallucinations)
• Aggression, agitation and disturbance in attention
• Painful periods
Uncommon side effects (may affect up to 1 in 100 people)
• Feeling tired, confused, having hallucinations or changes in mood and loss of consciousness
(coma).
• Inflamed blood vessels (vasculitis) – you may notice pain, redness or itching
• Changes in women’s periods absence of periods
• Swelling of the feet and legs (oedema)
• Severe stomach pain which may reach through to your back. This could be a sign of
pancreatitis.
• Tingling or numbness in the hands and feet
• Hair disorders (changes in texture, colour or growth)
• Increased levels of some hormones (androgens), which may lead to increased hair growth on
the face, breasts or chest, acne or thinning hair.




Kidney disease
Lowering of normal body temperature

Rare side effects (may affect up to 1 in 1,000 people)
• Abnormal blood clotting factors
• Abnormal behaviour, restlessness/hyperactivity and learning disorder
• Kidney problems, bedwetting or increased need to pass urine
• Blood in the urine
• Skin problems such as rashes. These happen rarely, but more often in people also taking
lamotrigine.
• Muscle pain and weakness (rhabdomyolysis)
• Male infertility, polycystic ovaries
• Obesity
Very rare side effects (may affect up to 1 in 10,000 people)
• Increased breast growth in men
Frequency unknown (cannot be estimated from available data)
• Fainting
These effects usually get better when you stop taking sodium valproate.
Bone disorders
There have been reports of bone disorders including osteopenia and osteoporosis (thinning of the
bone) and fractures. Check with your doctor or pharmacist if you are on long-term antiepileptic
medication, have a history of osteoporosis, or take steroids.
Sodium valproate may decrease blood sodium. This can make you feel tired, weak, dizzy or faint.
You may also feel or be sick and have muscle cramps.
Less commonly you may be bloated with swelling and tightness of the hands and feet, feel
confused and have fits. Sometimes it can cause changes in the blood. Here you may notice
unusual bleeding or bruising more easily, severe stomach pains, feeling shaky or problems with
balance.
Male fertility
Taking sodium valproate can be a contributing factor in male infertility.
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 or search for MHRA Yellow Card in the Google Play
or Apple App Store.
By reporting side effects you can help provide more information on the safety of this medicine.

5.



HOW TO STORE SODIUM VALPROATE
Keep out of the sight and reach of children.
Do not take this medicine after the expiry date shown on the pack.





6.

Store this medicine below 25ºC and away from direct sunlight.
Store this medicine in the original container.
Ask your pharmacist how to dispose of medicines no longer required. Do not dispose of
medicines by flushing down a toilet or sink or by throwing out with your normal household
rubbish. This will help to protect the environment.

CONTENTS OF THE PACK AND OTHER INFORMATION

What sodium valproate contains
Each 5ml of Sodium Valproate Liquid contains 200mg of sodium valproate.
The liquid also contains sorbitol (E420), hydroxyethylcellulose, sodium methyl hydroxybenzoate
(E219), sodium propyl hydroxybenzoate (E217), saccharin sodium, anhydrous citric acid, water,
Ponceau 4R (E124, a colourant) and cherry flavour.
What Sodium Valproate 200mg/5ml Liquid looks like and contents of the pack
Sodium valproate is a red, cherry flavoured liquid. It is supplied in bottles of 300ml.
The Marketing Authorisation Holder is: Winthrop Pharmaceuticals, PO Box 611, Guildford,
Surrey, GU1 4YS, UK.
Or
Zentiva, One Onslow Street, Guildford, Surrey, GU1 4YS, UK.
The Manufacturer is: Unither Liquid Manufacturing, Zone industrielle, d’En Sigal, 1-3 allee de
la Neste, 31770 Colomiers, France.
This leaflet was last revised in March 2018.
© 2018 Winthrop Pharmaceuticals
Or
© 2018 Zentiva.
There are two organisations that will also be happy to try and answer any general questions on
epilepsy.
They can be contacted at:
Epilepsy Action, New Anstey House, Gate Way Drive, Yeadon, Leeds, LS19 7XY
Telephone: 0808 800 5050
Website: www.epilepsy.org.uk
National Society for Epilepsy (NSE), Chesham Lane, Chalfont St Peter, Bucks, SL9 0RJ
Telephone: 01494 601400
Website: www.epilepsynse.org.uk

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