• Keep this leaflet. You may need to read it again.
• If you have any further questions, ask your doctor, pharmacist or nurse .
• This medicine has been precribed for you only. Do not pass it onto others. It may harm them, even if their signs of illness 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.

1. What Chloral Hydrate Oral Solution is and what it is used for
2. What do you need to know before you take Chloral Hydrate Oral Solution
3. How to take Chloral Hydrate Oral Solution
4. Possible side effects
5. How to store Chloral Hydrate Oral Solution
6. Contents of the pack and other information

• are allergic to chloral hydrate or any of the other ingredients of this medicine (see section 6)
• have severe liver or kidney problems
• have severe heart problems
• suffer from porphyria (an inherited blood disorder)
• have active inflammation of the stomach or gullet (gastritis or oesophagitis), a stomach or gut ulcer or perforation of the stomach or gut wall
• are pregnant or breast feeding.

Do not give to a child under 2 years of age.

Talk to your doctor, pharmacist or nurse before taking Chloral Hydrate Oral Solution:

• if you are elderly or frail (weak),
• if you have mild or moderate kidney impairment,
• if you have mild or moderate liver impairment,
• if you suffer from alcoholism or drug addiction problems,
• if you have dependency to sleep medications,
• if you have had inflammation of the stomach or gullet (gastritis or oesophagitis), an ulcer in the stomach or the gut (gastric or duodenal ulcer) or perforation of the stomach or gut wall in the past,
• if you have heart disease or heart rhythm abnormalities (including so called QT prolongation seen with ECG monitoring),
• if you have low potassium or magnesium levels.

Tell your doctor or pharmacist if you are taking or have recently taken or might take any other medicines.:

It is important to tell your doctor if you are taking any of the following:

• sleep medication and tranquilisers (sedatives, hypnotics),
• medicines to thin your blood (such as Warfarin),
• medicines for depression or nervous disorders,
• medicines intended to reduce muscle spasms,
• medicines that affect the heart rhythm, such as medicines for heart rhythm abnormalities, medicines against malaria, some medicines against allergies (antihistamines), medicines to treat certain mental health disorders (antipsychotics) and medicines that lower potassium or magnesium levels (diuretics).

Alcohol can increase the sedative effect of chloral hydrate. Alcohol should therefore be avoided whilst taking this medicine. Chloral Hydrate Oral Solution should be taken with water or milk.

Chloral Hydrate Oral Solution should not be taken if you are pregnant or trying to become pregnant or you are breast feeding.

Please note that your ability to drive or operate hazardous machinery may be impaired by drowsiness as a result of taking Chloral Hydrate Oral Solution. Ask your doctor whether you may drive or operate machines.

Chloral Hydrate Oral Solution contains the following:

• Glycerol which may cause headache, stomach upset and diarrhoea.
• This medicine contains 23.17 g glucose per dose. This should be taken into account in patients with diabetes mellitus.
• This medicine contains 6.3 mg of Sodium Benzoate in each 5 mL, which is equivalent to 1.26 mg /mL
• This medicine contains 18.39 mg propylene glycol in each 5 ml which is equivalent to 3.678 mg/ ml. If your child is less than 5 years old, talk to your doctor or pharmacist before giving them this medicine, in particular if they use other medicines that contain propylene glycol or alcohol.
• This medicine contains less than 1 mmol sodium (23 mg) per 5 ml, which is to say it is essentially ‘sodium-free’.

If you are having blood tests for your thyroid, tell your doctor or nurse that you are taking this medicine, as chloral hydrate may interfere with these tests.

Adults and Children aged 12 years and over and the Elderly:

The usual starting dose in 430-860 mg (15-30 ml of the 143mg/5ml strength).

In the frail elderly or patients with liver problems, a smaller dose may be required.

Not more than 70 ml of the 143mg/5ml strength Chloral Hydrate Oral Solution (equivalent to 2 g of Chloral Hydrate) should be taken in any one day.

Children 2 - 11 years:

The use of Chloral Hydrate Oral Solution in children and adolescents is not generally recommended and if used should be under the supervision of a medical specialist. The dose will be calculated by your doctor or pharmacist based on the weight of the child. You should follow their instructions. Not more than 35 ml of the 143mg/5ml strength Chloral Hydrate Oral Solution (equivalent to 1 g of Chloral Hydrate) should be taken in any one day.

If you are unsure about how to take your medicine, ask your doctor or pharmacist.

Chloral Hydrate Oral Solution is usually prescribed for the short-term treatment of sleeping problems when other non-medication treatments (e.g. behavioural therapy and sleep hygiene) have failed, for a maximum treatment period of 2 weeks.

Repeat courses of Chloral Hydrate Oral Solution are not recommended and can only be administered following medical specialist re-assessment, because there is a risk of abuse and dependence.

If you take Chloral Hydrate Oral Solution over a long period of time, you may find that the medicine takes longer to work and the effect does not last for as long. This is called “tolerance” to the chloral hydrate ingredient. If you find you are becoming “tolerant” to Chloral Hydrate Oral Solution, do not increase the amount you take. Speak to your doctor.

Following prolonged treatment with Chloral Hydrate Oral Solution the dose should be slowly reduced before discontinuation, because there is a risk of withdrawal symptoms. Suddenly stopping Chloral Hydrate Oral Solution may cause delirium (severe confusion). Contact your doctor before you stop taking the medicine, as they will advise you how to stop.

In the event of an accidental overdose, contact your nearest hospital casualty department or tell your doctor immediately. It is advisable to have the medicine in its original packaging available for the doctor or hospital. Signs of an overdose include, vomiting, breathing problems, abnormal heartbeat, abnormally low body temperature, pin point pupils, low blood pressure or coma.

If you have missed one dose, this dose should be omitted, and the next dose should be taken at the usual time. Do not take a double dose to make up for a forgotten dose.

• Headache
• Mental side effects such as anxiety, restlessness, excitation or confusion
• Loss of coordination of muscle movements (ataxia)
• Stomach and intestinal problems such as abdominal pain, distension of the abdomen, flatulence, nausea and vomiting (as these might reflect serious problems such as stomach irritation, gastric necrosis, gastric perforation or gut swelling)
• Long-term use of this medication leading to tolerance (usual doses not producing the desired effect)
• Dependence on the medication and its abuse
• Chronic intoxication with mental symptoms or any other symptoms described here
• Withdrawal symptoms which may be severe and include hallucinations and delirium
• Ketonuria (a condition in which ketone bodies are present in the urine) detected by tests as advised by your doctor

If you are elderly you may be more susceptible to confusion and co-ordination problems which may lead to falls and injury.

In new-borns and children <2 years of age, there is an increased risk of side effects. Do not give to a child under 2 years of age.

If any of the symptoms become troublesome, or if you notice anything else not mentioned here, please go and see your doctor. He/she may want to adjust the dose or give you a different medicine.

If you get any side effects, talk to your doctor, nurse or pharmacist. 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 the side effects you can help provide more information on the safety of this medicine.

The active substance in Chloral Hydrate Oral Solution is chloral hydrate. Chloral Hydrate Oral Solution also contains glycerol (E 422), liquid glucose, sodium benzoate (E 211), sodium citrate (E 331), citric acid monohydrate (E 330), saccharin sodium (E 954), essence of passion fruit (containing natural flavouring, artificial flavouring, propylene glycol (E1520)), and purified water.

Chloral Hydrate Oral Solution is a clear solution with a fruity odour containing 143.3 mg chloral hydrate per 5 ml. A pack size of 150 ml is available.

The Product Licence number is PL 23138/0016.

For information in large print tape, CD or Braille, telephone 01279 406759