Relanium

Package leaflet: Information for the patient

Warning! Keep this leaflet. The information on the immediate packaging is in a foreign language.
Relanium
5 mg, tablets
Diazepamum
Please read this leaflet carefully before using the medicine, as it contains
important information for the patient.

• Keep this leaflet for future reference.
• Consult your doctor or pharmacist if you have any questions.
• This medicine has been prescribed for a specific individual. Do not give it to others. The medicine may harm another person, even if their symptoms are the same.
• If you experience any adverse effects, including any not listed in this leaflet, inform your doctor, pharmacist, or nurse. See section 4.

Table of contents of the leaflet:

1. What Relanium is and what it is used for
2. Important information before taking Relanium
3. How to take Relanium
4. Possible side effects
5. How to store Relanium
6. Contents of the pack and other information

1. What Relanium is and what it is used for

Relanium contains the active substance diazepam, which belongs to a group of medicines called benzodiazepine derivatives.
Relanium has anxiolytic, sedative, hypnotic, and anticonvulsant properties. It also reduces skeletal muscle tension.
Indications:

• Treatment of anxiety states.
• Treatment of insomnia associated with anxiety (only in cases of severe disturbances that impair normal daily functioning, or that cause extreme discomfort to the patient).
• Control of muscle spasms, including those related to increased central origin muscle tension.
• Pharmacological preparation of patients prior to minor surgical procedures (premedication).
• Treatment of symptoms of acute alcohol withdrawal.

2. Important information before using Relanium

When not to use Relanium

• if the patient is allergic (hypersensitive) to the active substance, other benzodiazepines, or any of the other ingredients of the medicine (listed in section 6),
• if the patient has excessive muscle weakness (called muscle fatigue – myasthenia gravis),
• if the patient has severe respiratory insufficiency,
• if the patient has sleep apnoea syndrome (repeated breathing pauses during sleep causing hypoxia),
• if the patient has severe hepatic insufficiency.

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Warnings and precautions

Before starting treatment with Relanium, discuss this with your doctor.

• Diazepam is not recommended for the treatment of chronic psychoses or conditions with phobias or obsessions.
• Do not take Relanium together with alcohol, sleeping medicines, or sedatives, as Relanium may enhance their effects (see section: Relanium with other medicines).
• If the patient is dependent on alcohol or drugs, avoid using Relanium. This does not apply to the treatment of acute withdrawal symptoms. In such cases, the doctor will regularly monitor the patient and recommend using the lowest effective dose.
• If the patient has previously abused alcohol or drugs, Relanium should be used with particular caution.
• If Relanium is used for several weeks, tolerance to the medicine may develop (reduced effectiveness).
• Long-term use of Relanium, especially in high doses, may lead to physical and psychological dependence. The risk of dependence increases with dose and duration of treatment. It is higher in patients who have previously abused alcohol or drugs, and in patients with personality disorders.
• If the patient is dependent on Relanium, sudden discontinuation may cause withdrawal symptoms such as: headache, muscle pain, extreme anxiety, tension, restlessness, confusion, irritability. In more severe cases, the following may occur: loss of reality perception, personality disturbances, numbness and tingling of limbs, hallucinations, seizures, hypersensitivity to light, sound, or touch.
• Withdrawal symptoms may also occur when switching from Relanium to benzodiazepines with a short duration of action.
• During or after discontinuation of Relanium, a temporary worsening of the symptoms that led to treatment may occur. To prevent this, the medicine should be discontinued gradually, strictly according to the doctor's instructions (see section: Discontinuing Relanium).
• Relanium may cause anterograde amnesia (inability to learn and remember new information, see section 4: Possible side effects). To reduce the risk of anterograde amnesia, it is important that the patient has uninterrupted sleep for 7 to 8 hours.
• In children and elderly patients, there is an increased risk of undesirable and paradoxical psychological reactions (see section 4: Possible side effects).
• In elderly and debilitated patients, the doctor may prescribe a lower dose (see section 3: How to take Relanium). The medicine reduces muscle tone, increasing the risk of falls and consequently hip fractures in elderly patients.
• In patients with chronic respiratory insufficiency, the doctor may prescribe a lower dose, as breathing disturbances may occur.
• Caution is required when using Relanium in patients with heart failure.
• In patients with epilepsy, abrupt discontinuation of treatment should be avoided due to the risk of seizures.
• If the patient has severe hepatic insufficiency, Relanium should not be used due to the risk of neurological dysfunction (hepatic encephalopathy).
• In patients with impaired liver and/or kidney function, the doctor will decide whether to reduce the dose. During long-term treatment with Relanium, the doctor may order blood tests to closely monitor blood cell counts and liver function.
• If the patient has psychotic disorders (e.g. schizophrenia), Relanium should not be used.
• If the patient has depression or anxiety associated with depression, Relanium should not be used as the sole treatment, as it may increase the risk of suicide.
• Use of Relanium in individuals experiencing grief (after loss of loved ones) does not improve well-being. Page 2 of 8

Children and adolescents
Use of Relanium in children: the doctor will determine the dose and duration of treatment (see section 3: How to take Relanium).
Use of Relanium for the treatment of anxiety states and insomnia in children is not recommended.
Relanium should not be used in children under 6 years of age, as the safety and efficacy of the medicine have not been established in this age group. Only when alternative treatments cannot be used, may the doctor decide to administer Relanium, but only under strict supervision by a specialist (paediatrician, neurologist, psychiatrist, anaesthesiologist, or intensive care specialist), who will determine the dose.

Relanium with other medicines
Inform your doctor or pharmacist about all medicines currently taken, recently taken, or planned to be taken.
In particular, inform your doctor about the following medicines, as they may enhance the effects of Relanium:

• atazanavir and ritonavir – used in the treatment of HIV infection and hepatitis C,
• cimetidine – a medicine used to treat peptic ulcer disease,
• ketoconazole – a medicine used to treat fungal infections,
• medicines used to treat depression, e.g. fluvoxamine, fluoxetine,
• omeprazole – a medicine that reduces gastric acid secretion,
• cisapride – a medicine used in gastro-oesophageal reflux disease,
• disulfiram – a medicine used in the treatment of alcoholism,
• isoniazid – a medicine used to treat tuberculosis,
• propranolol – a medicine used to treat high blood pressure and irregular heartbeat,
• rifampicin – a medicine used to treat bacterial infections,
• antipsychotic medicines,
• anxiolytic and sedative medicines,
• sleeping medicines,
• medicines used to treat epilepsy,
• medicines used for general anaesthesia,
• sedative antihistamines – used, for example, to treat allergies,
• opioid analgesics.

Concomitant use of Relanium and opioids (strong painkillers, medicines used in substitution therapy for addiction, and some cough medicines) increases the risk of drowsiness, breathing difficulties (respiratory depression), coma, and may be life-threatening. Therefore, concomitant use of these medicines should only be considered when no other treatment options are available. If your doctor prescribes Relanium together with opioids, the dose and duration of combination therapy should be minimized. Inform your doctor about all opioid medicines you are taking and strictly follow dosing instructions. It may be helpful to inform family members or friends so they are aware of the above-mentioned symptoms. If such symptoms occur, contact your doctor immediately.

Relanium may affect the action of phenytoin used as an antiepileptic medicine.
Theophylline – a medicine used to treat asthma – may reduce the effect of benzodiazepines.
Concomitant use of buprenorphine with Relanium (or other benzodiazepines) should be avoided, as it may result in death due to respiratory centre depression.
Concomitant use of valproic acid increases the risk of psychosis.

Relanium with food, drink and alcohol
Do not consume any alcoholic beverages while taking this medicine. Alcohol enhances the sedative effect of Relanium.

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Pregnancy and breastfeeding
If the patient is pregnant or breastfeeding, suspects she may be pregnant, or is planning a pregnancy, she should consult her doctor before using this medicine.
Relanium should not be used during pregnancy, especially in the first and third trimesters.
Use of Relanium during pregnancy is acceptable only if the doctor considers it absolutely necessary and will closely monitor the patient.
If a woman takes Relanium during the last three months of pregnancy or during delivery, the newborn may experience low body temperature, reduced muscle tone, irregular heartbeat, difficulty sucking, and breathing disturbances.
In infants of mothers who have taken diazepam long-term during late pregnancy, physical dependence may develop, and there is a risk of neonatal withdrawal syndrome after birth.
The medicine passes into breast milk; therefore, it should not be used during breastfeeding.
If the patient is breastfeeding, she must consult her doctor before starting treatment with Relanium.

Driving and operating machinery
Relanium may impair psychomotor performance. Do not drive motor vehicles or operate machinery while taking this medicine.

Relanium contains monohydrate lactose.
If the patient has previously been diagnosed with intolerance to certain sugars, the patient should consult a doctor before taking the medicine.

Relanium contains sodium (present in quinoline yellow (E 104)).
The medicine contains less than 1 mmol (23 mg) of sodium per tablet, meaning the medicine is considered "sodium-free".

Relanium contains the colouring agent quinoline yellow (E 104).
Due to the presence of quinoline yellow, the medicine may cause allergic reactions.

3. How to use Relanium

Relanium must always be used as directed by the physician. In case of doubt, consult your doctor or pharmacist.
Treatment with diazepam should be as short as possible and should not exceed 4 weeks in the case of insomnia or 8–12 weeks in the case of anxiety disorders, including the time needed for gradual withdrawal of the drug. Do not extend treatment beyond the times indicated above without a re-evaluation of the patient's condition by the physician.

Dosage in adults

• Anxiety disorders and insomnia
  • Anxiety disorders: the usual dose is 2 mg three times daily; the maximum dose used in the treatment of anxiety disorders is 30 mg per day in divided doses.
  • Insomnia associated with anxiety: 5 mg to 15 mg per day, taken before bedtime. The physician will recommend the lowest dose that controls symptoms.
• Conditions related to muscle spasms
  • Muscle spasms: 2 mg to 15 mg per day in divided doses.
  • Control of increased muscle tension of central origin: 2 mg to 60 mg per day in divided doses.
• Premedication prior to general anesthesia
  • 5 mg to 20 mg.
• Treatment of symptoms of acute alcohol withdrawal
  • Usually 10 mg, 3 to 4 times during the first 24 hours; thereafter, the physician may reduce the dose to 5 mg, 3 to 4 times daily.

Dosage in children

• Anxiety disorders and insomnia
  • Relanium is not recommended for the treatment of anxiety disorders or insomnia in children.
• Conditions related to muscle spasms
  • For control of irritability and increased muscle tension of central origin: 5 mg to 40 mg per day in divided doses.
  • Children aged 6 to 12 years: initial dose is 5 mg twice daily.
  • Children aged 12 to 18 years: initial dose is 10 mg twice daily; maximum dose is 40 mg per day.
• Premedication prior to general anesthesia
  • Children aged 6 to 18 years: 2 mg to 10 mg.

Dosage in children under 6 years of age
Relanium tablets are not intended for use in children under 6 years of age.

Dosage in elderly or debilitated patients
Do not exceed half the dose usually used in adults.

Patients with renal and/or hepatic impairment
In patients with impaired kidney and/or liver function, the physician will decide whether to reduce the dose.

Method of administration

• The medicine should be taken orally.
• Do not use for longer than 4 weeks in the case of insomnia or 8 to 12 weeks in the case of anxiety disorders (including the time required for gradual withdrawal of the medicine).

Use of a higher than recommended dose of Relanium
If a higher than recommended dose of Relanium is taken, seek immediate medical help from a doctor or the nearest hospital.
Overdose with Relanium is rarely life-threatening if the drug was taken alone.
The following symptoms of overdose may occur: drowsiness, ataxia (impaired coordination), slurred speech, nystagmus, areflexia (loss of reflexes), apnea, hypotension, circulatory and respiratory depression, and coma.
Coma, if it occurs, usually lasts several hours but may last longer and may recur periodically, especially in elderly patients.

Missed dose of Relanium
If a dose of the medicine is missed, take it as soon as possible. If it is almost time for the next dose, skip the missed dose. Take the next dose at the regular time as directed by the physician. Do not take a double dose to make up for a missed dose.

Discontinuation of Relanium
The medicine should be discontinued gradually. Abrupt discontinuation of Relanium may temporarily worsen the symptoms of the condition for which the medicine was prescribed. Other symptoms may also occur, such as: headache, muscle pain, extreme anxiety, tension, agitation, confusion, irritability, mood changes, sleep disturbances, and restlessness. In more severe cases, the following symptoms may occur: loss of reality, personality changes, hypersensitivity to sound, numbness and tingling of the extremities, hypersensitivity to light, noise and touch, hallucinations, and epileptic seizures.
Always follow the physician's instructions. In case of any doubts regarding the use of the medicine, consult your doctor or pharmacist.
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4. Possible adverse effects

Like all medicines, this medicine can cause adverse effects, although not everyone will experience them.
Most commonly occurring adverse effects are:

• fatigue,
• drowsiness,
• muscle weakness. These effects occur particularly at the beginning of treatment and diminish after repeated administration.

Frequency unknown (cannot be estimated from the available data):

• paradoxical reactions: anxiety, excitement, irritability, aggressive behaviour, anger, rage, delusions,
• nightmares, hallucinations, psychoses,
• behavioural changes, including inappropriate behaviour,
• thought disturbances, disturbances in orientation with regard to time, place, situation or self (confusion),
• emotional blunting (emotional flattening),
• reduced alertness,
• depression,
• decreased or increased sexual drive (libido),
• motor incoordination (difficulty maintaining balance) – may lead to falls and dangerous bone fractures, especially in elderly individuals,
• slurred speech, unclear speech,
• headache, dizziness,
• tremor,
• inability to learn and remember new information (so-called anterograde amnesia); to prevent this, the patient should have uninterrupted 7–8 hours of sleep,
• double vision, blurred vision,
• heart failure, cardiac arrest, irregular heartbeat,
• low blood pressure, slowed heart rate,
• slowed and shallow breathing, apnoea,
• nausea, constipation, gastrointestinal disturbances (e.g. bloating),
• dry mouth or excessive salivation,
• jaundice (yellowing of the skin and whites of the eyes), increased liver enzyme activity (aminotransferases and alkaline phosphatase) in blood,
• skin reactions,
• urinary incontinence or inability to urinate (strong urge to urinate, lower abdominal pain),
• blood morphology disorders (dyscrasia). Long-term use (even at therapeutic doses) may lead to physical dependence; abrupt discontinuation of the medicinal product may result in withdrawal symptoms or rebound phenomena (see section Warnings and precautions). Psychological dependence may occur. Cases of benzodiazepine abuse have been reported.

Reporting of adverse effects
If any adverse effects occur, including any adverse effects not listed
in this leaflet, tell your doctor, pharmacist or nurse. Adverse effects
can be reported directly to the Department of Monitoring Adverse Drug Reactions, Office for Registration of Medicinal Products, Medical Devices and Biocidal Products, Al. Jerozolimskie 181C, 02-222 Warsaw, tel.: +48 22 49 21 301, fax: +48 22 49 21 309, website: https://smz.ezdrowie.gov.pl
By reporting adverse effects, additional information on the safety of this medicine can be collected.
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5. How to store Relanium

Keep this medicine out of sight and reach of children.
Do not store above 25°C. Store in the original packaging to protect from light and moisture.
Do not use this medicine after the expiry date stated on the packaging. The expiry date refers to the last day of the stated month.
Medicines must not be disposed of via wastewater or household waste. Ask your pharmacist how to dispose of medicines no longer in use. Such measures help protect the environment.

6. Contents of the pack and other information

What Relanium contains
The active substance is diazepam. One tablet contains 5 mg of diazepam.
The other ingredients are: monohydrate lactose, potato starch, talc, magnesium stearate,
anhydrous colloidal silicon dioxide, quinoline yellow (E 104).

What Relanium 5 mg tablets look like and contents of the pack
Relanium tablets are yellow, round, biconvex, with a smooth surface.
The pack contains 20 tablets.

How to remove the tablet from the blister
These tablets are supplied in special child-resistant packaging. Each blister section containing one tablet is numbered. Tablets should be taken sequentially according to the numbering, starting from number 1.

1. Separating the tablet: To separate the blister section containing one tablet, tear the blister along the perforated lines.

2. Removing the outer layer: Starting from the corner, lift and tear off the outer layer from the separated blister section.

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3. Removing the tablet: Gently push the tablet through the foil layer.

For more detailed information, please contact the responsible party or the parallel importer.

Responsible party in Lithuania, country of export:
GlaxoSmithKline Trading Services Limited, 12 Riverwalk, Citywest Business Campus, Dublin 24, Ireland

Manufacturer:
Delpharm Poznań Spółka Akcyjna, ul. Grunwaldzka 189, 60-322 Poznań

Parallel importer:
Delfarma Sp. z o.o., ul. Św. Teresy od Dzieciątka Jezus 111, 91-222 Łódź

Repackaged in:
Delfarma Sp. z o.o., ul. Św. Teresy od Dzieciątka Jezus 111, 91-222 Łódź
Polfarmex S.A., ul. Józefów 9, 99-300 Kutno

Lithuania, country of export marketing authorisation number: LT/1/94/1933/001
LT/1/94/1933/002

Parallel import authorisation number: 23/15
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