Background pattern

Tioner 100 mg/ml solucion oral

About the medication

Introduction

Prospecto: information for the user

Tioner 100 mg/ml oral solution

Tramadol, hydrochloride

Read this prospect carefully before starting to take this medicine, as it contains important information for you.

  • Keep this prospect, as you may need to read it again.
  • If you have any doubts, consult your doctor or pharmacist.
  • This medicine has been prescribed only for you, and you must not give it to other people even if they have the same symptoms as you, as it may harm them.
  • If you experience any adverse effects, consult your doctor or pharmacist, even if they are not listed in this prospect. See section 4.

1.What Tioner is and for what it is used

2.What you need to know before starting to take Tioner

3.How to take Tioner

4.Possible adverse effects

5.Storage of Tioner

6.Contents of the package and additional information

1. What is Tioner and what is it used for

Tramadol, the active ingredient in this medication, is a pain reliever belonging to the opioid group that acts on the central nervous system.It relieves pain by acting on specific nerve cells in the spinal cord and brain.

Tioner is used in the treatment of moderate to severe pain.

2. What you need to know before starting to take Tioner

Do not take Tioner

  • if you are allergic to tramadol or any of the other ingredients of this medicine (listed in section 6);
  • in case of acute intoxications caused by alcohol, sleeping pills, painkillers, or other psychotropic drugs (medicines that act on mood and emotions);
  • if you are also taking MAO inhibitors (a certain type of medicine used to treat depression) or if you have taken them in the last 14 days before starting treatment with this medicine (see "Taking Tioner with other medicines");
  • if you have epilepsy and your seizures are not adequately controlled with treatment;
  • for the treatment of withdrawal syndrome.
  • in children under 3 years old.

Warnings and precautions

Consult your doctor before starting to take Tioner:

  • if you think you have dependence on other painkillers (opioids);
  • if you have consciousness disorders (if you think you are going to faint);
  • if you are in shock (a sign of this state can be cold sweat);
  • if you have increased intracranial pressure (for example after a head trauma or brain diseases);
  • if you have difficulty breathing;
  • if you are epileptic or have seizures, because the risk of seizures may increase;
  • if you have any liver or kidney disease;

if you suffer from depression and are taking antidepressants, as some may interact with tramadol (see "Other medicines and Tioner").

Tolerance, dependence, and addiction

This medicine contains tramadol, which is an opioid medicine. Repeated use of opioids can make the medicine less effective (the body gets used to it, which is known as pharmacological tolerance). Repeated use of Tioner 100 mg oral solution may also cause dependence, abuse, and addiction, which could lead to a potentially fatal overdose. The risk of these adverse effects may be higher with a higher dose and longer use.

Dependence or addiction may cause a feeling of lack of control over the amount of medicine you should use or over the frequency with which you should use it.

The risk of dependence or addiction varies from person to person. The risk of becoming dependent or addicted to Tioner 100 mg/mL oral solution may be higher if:

  • You or any member of your family have abused alcohol or experienced dependence on it, prescription medicines, or illegal drugs ("addiction").
  • You are a smoker
  • You have had any problems with mood (depression, anxiety, or personality disorder) or have followed treatment with a psychiatrist for other mental health conditions).

If you observe any of the following symptoms while using Tioner 100 mg/mL oral solution, it could be a sign of dependence or addiction:

  • You need to use the medicine for a longer time than indicated by your doctor
  • You need to use a higher dose than recommended
  • You are using the medicine for reasons other than those prescribed, for example "to feel calm" or "to help you sleep".
  • You have made repeated and unsuccessful attempts to stop using the medicine or control its use.
  • You feel unwell when you stop using the medicine, and you feel better once you take it again ("withdrawal symptoms").

If you notice any of these signs, consult your doctor to determine the best treatment for you, when it is appropriate to stop the medicine, and how to do it safely (see section 3, if you interrupt treatment with Tioner 100 mg/mL oral solution).

Respiratory disorders related to sleep

Tioner may cause respiratory disorders related to sleep, such as sleep apnea (pauses in breathing during sleep) and sleep-related hypoxemia (low oxygen levels in the blood). Among the symptoms may include pauses in breathing during sleep, nocturnal awakenings due to lack of breath, difficulty maintaining sleep, or excessive daytime somnolence. If you or someone else observes these symptoms, contact your doctor. Your doctor may consider reducing the dose.

Seizures have been reported in patients taking tramadol at the recommended dose. The risk may increase when the tramadol dose exceeds the recommended maximum daily dose (400 mg).

Be aware that this medicine may cause physical and psychological dependence. When used for a prolonged period, its effect may decrease, requiring the use of higher doses (development of tolerance). In patients with a tendency to abuse medicines or those with dependence on medicines, treatment with Tioner should only be carried out for short periods of time and under strict medical supervision.

Also inform your doctor if any of the following problems occur during treatment with this medicine or if they have occurred at any time:

Extreme fatigue, loss of appetite, severe abdominal pain, nausea, vomiting, or low blood pressure. They may be indicators of adrenal insufficiency (low cortisol levels). If you have these symptoms, contact your doctor, who will decide if you need to take hormone supplements.

Tramadol is metabolized in the liver by an enzyme. Some people have a variation of this enzyme, and this can affect each person differently. In some people, it may not be possible to achieve sufficient pain relief, while others may be more likely to experience severe adverse effects. If you notice any of the following adverse effects, stop taking this medicine and consult a doctor immediately: slow or shallow breathing, confusion, drowsiness, constricted pupils, general discomfort, or vomiting, constipation, loss of appetite.

There is a weak risk that you may experience a serotonin syndrome that can occur after taking tramadol in combination with certain antidepressants or tramadol alone. Consult your doctor immediately if you experience any of the symptoms linked to this severe syndrome (see section 4 "Possible adverse effects").

Use in athletes

This medicine contains tramadol, which can produce a positive result in doping control tests.

Other medicines and Tioner

Inform your doctor or pharmacist if you are taking, have taken recently, or may need to take any other medicine.

It is recommended to avoid simultaneous treatment of Tioner with MAO inhibitors (a certain type of medicine used to treat depression).

The effect and duration of pain relief produced by Tioner may be reduced if you take medicines that contain:

  • Carbamazepine (for epilepsy);
  • Ondansetron (to prevent nausea).

Your doctor will indicate if you should take this medicine and in what dose.

The risk of adverse effects increases,

  • if you are taking this medicine simultaneously with tranquilizers, sleeping pills, other painkillers such as morphine and codeine (even when used to treat cough) and alcohol. In these cases, you may feel drowsy or dizzy. If this happens, consult your doctor; The concomitant use of Tioner with sedatives or sleep-inducing medicines (such as benzodiazepines) increases the risk of drowsiness, respiratory difficulties (respiratory depression), coma, and may be potentially fatal. Therefore, only consider concomitant use when other treatment options are not possible.

However, if your doctor prescribes tramadol with sedatives, you should limit the dose and duration of concomitant treatment.

Inform your doctor about all sedatives you are taking and strictly follow your doctor's recommended dose. It may be helpful to inform your friends and family about the signs and symptoms mentioned above. Inform your doctor if you experience any of these symptoms;

  • if you are takingmedicines that facilitate or may cause seizures, such as certain antidepressants or antipsychotics. The risk of seizures increases if you take Tioner simultaneously with these medicines. Your doctor will tell you if Tioner is suitable for you;
  • if you are taking antidepressants, Tioner may interact with these medicines and you may experience a serotonin syndrome (see section 4 "Possible adverse effects");
  • if you are taking anticoagulant coumarins (medicines to thin the blood) such as warfarin, while takingTioner. The effect of these medicines on blood coagulationmay be affected and may causebleeding;
  • if you take medicines that can increase the accumulation of tramadol and therefore, its adverse effects (such as ritonavir, quinidine, paroxetine, fluoxetine, sertraline, amitriptyline, isoniazid, ketoconazole, and erythromycin).
  • Gabapentin or pregabalin to treat epilepsy or pain due to nerve problems (neuropathic pain).

Taking Tioner with food and alcohol

Do not consume alcohol during treatment with this medicine, as its effect may be intensified.

Food does not affect the effect of Tioner.

Children and adolescents

Use in children with respiratory problems:

Tramadol is not recommended for use in children with respiratory problems, as the symptoms of tramadol toxicity may worsen in these children.

In particular, the first administration of tramadol should be carried out under strict medical supervision in children.

Observe the child, especially during the first administration. If you notice any warning signs (such as altered consciousness, constricted pupils, vomiting, seizures, very slow breathing...), call a doctor immediately or consult an emergency service (see section "If you take more Tioner than you should").

Pregnancy, breastfeeding, and fertility

If you are pregnant or breastfeeding, or if you think you may be pregnant, consult your doctor or pharmacist before using this medicine.

There is very little information available on the safety of tramadol in pregnant women. Therefore, do not take this medicine if you are pregnant.

Long-term treatment during pregnancy may cause withdrawal syndrome in newborn babies after birth.

Tramadol is excreted in breast milk. Therefore, do not take this medicine more than once during breastfeeding, or if you take Tioner more than once, stop breastfeeding.

Based on human experience, it is not suggested that tramadol affects male and female fertility.

Driving and using machines

Ask your doctor if you can drive or use machines during treatment with this medicine. It is essential to observe how this medicine affects you before driving or using machines. Do not drive or use machines if you feel drowsy, dizzy, have blurred vision, or have difficulty concentrating. Be especially careful at the start of treatment, after increasing the dose, after changing the formulation, and/or when taking it with other medicines.

Tioner contains saccharose, hydroxyethylstearate, propylene glycol (E-1520), and sodium

This medicine contains saccharose. If your doctor has indicated that you have an intolerance to certain sugars, consult with them before taking this medicine. If Tioner is to be used chronically (e.g., for two weeks or more), it may cause tooth decay.

This medicine may cause stomach discomfort and diarrhea because it contains hydroxyethylstearate.

This medicine contains 150 mg of propylene glycol (E-1520) per 1 ml of solution.

This medicine contains less than 1 mmol of sodium (23 mg) per 1 ml of solution; this is essentially "sodium-free".

3. How to Take Tioner

Follow exactly the administration instructions of this medication as indicated by your doctor. If in doubt, consult your doctor or pharmacist again.

Before starting treatment and regularly during it, your doctor will also explain what you can expect from the use of Tioner 100 mg/mL oral solution, when and for how long you should use it, when you should contact your doctor, and when you should discontinue use (see also section 2).

The recommended dose is, unless your doctor has given you different instructions:

Adults and adolescents over 12 years old

Normally, the initial dose is 4-8 pulses from the Tioner pump (equivalent to 50-100 mg of tramadol hydrochloride). Depending on the pain, the effect of the medication may last between 4-6 hours.

The dose should be adjusted to the intensity of the pain and your individual sensitivity. Normally, the lowest effective dose that produces pain relief should be used.Do not take more than 32 pulses from the Tioner pump equivalent to 400 mg of tramadol hydrochloride per day, that is, 4 doses of 8 pulses in 24 hours, unless your doctor has indicated otherwise.

To adjust the dose in pulses, consult the following equivalence table:

Equivalence table of the number of pulses corresponding to the content in mg of tramadol hydrochloride

Number of pulses

Content of tramadol hydrochloride

1 pulse

12.5 mg

2 pulses

25 mg

3 pulses

37.5 mg

4 pulses

50 mg

5 pulses

62.5 mg

6 pulses

75 mg

7 pulses

87.5 mg

8 pulses

100 mg

Children

For children over 3 years of age, the recommended dose is 1 mg of tramadol hydrochloride per kg of body weight.

Do not exceed 2 mg of tramadol hydrochloride per kg of body weight per dose.

Approximately, the usual and maximum doses per dose, according to weight, are as follows:

Child's weight

Child's age (approximate)

Usual dose per child's weight and per dose (in pulses*)

Maximum dose per child's weight and per dose (in pulses*)

15 kg – 20 kg

3 – 5 years

1 pulse

2 pulses

20 kg – 25 kg

5 – 8 years

1 pulse

3 pulses

25 kg – 35 kg

8 – 11 years

2 pulses

4 pulses

35 kg – 37 kg

11 years

3 pulses

5 pulses

37 kg – 44 kg

11 – 13 years

3 pulses

6 pulses

44 kg – 45 kg

≥ 13 years

3 pulses

7 pulses

*Always round the number of pulses to the lower unit.

Use the lowest effective dose that produces pain relief. Do not exceed daily doses of 8 mg of tramadol hydrochloride per kg of body weight or 400 mg of tramadol hydrochloride, whichever is less.

Older adults

In older adults (over 75 years), tramadol elimination may be slow. If this is your case, your doctor may recommend prolonging the dosing intervals.

Patients with liver or kidney insufficiency/patients on dialysis

If you have severe liver or kidney disease, treatment with this medication is not recommended. If you have moderate liver or kidney disease, your doctor may prolong the dosing intervals.

How and when to take Tioner?

It is administered orally.

The solution can be dissolved in a sweet solution or with a little liquid.

You can take the medication with an empty stomach or with meals.

For how long should you take Tioner?

This medication should not be administered for longer than strictly necessary. If you require prolonged treatment, your doctor will monitor you at short and regular intervals (if necessary with interruptions in treatment) to see if you should continue treatment with this medication and at what dose.

If you estimate that the effect of this medication is too strong or too weak, inform your doctor or pharmacist.

Information on the management of Tioner 100 mg/mL oral solution, bottle with pump

Note on use

Before using the pump for the first time, actuate it several times until the oral solution appears (due to technical reasons, it is necessary for the pump mechanism to fill and the release of solution to be homogeneous).

Place the container (spoon, cup, etc.) under the dispenser opening and actuate the pump. One complete pulse releases an amount of oral solution equivalent to 5 drops and containing 12.5 mg of tramadol hydrochloride (for dosage instructions, see section 3.How to take Tioner”).

Note on the level of the contents of the container

Due to differences in the thickness of the glass walls and the bottom of the bottles, the liquid level may vary by a few millimeters from one bottle to another (even if they are originally filled with Tioner).

If you take more Tioner than you should

If you have taken an additional dose by mistake, generally there will be no negative effects. Take the next dose as prescribed.

After taking very high doses of tramadol, you may experience pupil constriction, vomiting, decreased blood pressure, increased heart rate, collapse, decreased level of consciousness to coma (deep unconsciousness), seizures, and difficulty breathing that may lead to respiratory arrest. In this case, call a doctor immediately!

In case of overdose or accidental ingestion, consult your doctor, pharmacist, or call the Toxicology Information Service, phone 91 562 04 20, indicating the medication and the amount taken. It is recommended to bring the medication package insert to the healthcare professional.

If you forget to take Tioner

If you forget to take the medication, it is likely that the pain will return. Do not take a double dose to compensate for the missed doses, simply continue taking Tioner as you have been doing until now.

If you interrupt treatment with Tioner

If you interrupt or discontinue treatment with this medication too soon, it is likely that the pain will return. If you want to interrupt treatment due to side effects, consult your doctor.

Do not stop taking this medication suddenly unless your doctor tells you to. If you want to stop taking your medication, talk to your doctor first, especially if you have been taking it for a long time. Your doctor will inform you when and how to discontinue it, which can be done by gradually reducing the dose to reduce the likelihood of unnecessary side effects (withdrawal symptoms).

Generally, there are no side effects when treatment is discontinued. However, in rare cases, people who have been taking this medication for some time may feel unwell if they discontinue treatment abruptly. They may feel agitated, anxious, nervous, or shaky. They may be hyperactive, have difficulty sleeping, or experience gastrointestinal and intestinal transit problems. Very few people may experience panic attacks, hallucinations, unusual perceptions such as itching, numbness, and tingling, and ringing in the ears (tinnitus). Very rarely, more unusual central nervous system symptoms such as confusion, delirium, change in perception of personality (derealization), and change in perception of reality (depersonalization) and delusions of persecution (paranoia) have been detected. If you experience any of these symptoms after discontinuing treatment with this medication, consult your doctor.

If you have any other questions about the use of this medication, ask your doctor or pharmacist.

4. Possible Adverse Effects

Like all medicines, this medicine can cause side effects, although not everyone will experience them.

You should consult your doctor immediately if you experience symptoms of an allergic reaction such as swelling of the face, tongue, and/or throat and/or difficulty swallowing and hives along with difficulty breathing.

The most common side effects during treatment with Tioner 100 mg/ml oral solution are nausea and dizziness, which occur in more than 1 in 10 people.

Very common: may affect more than 1 in 10 people

  • Dizziness.
  • Nausea.

Common: may affect 1 in 10 people

  • Headache, numbness.
  • Fatigue.
  • Constipation, dry mouth, vomiting.
  • Sweating (hyperhidrosis).

Uncommon: may affect 1 in 100 people

  • Effects on the heart and blood circulation (strong heartbeats and rapid heartbeats, sensation of dizziness or collapse). These side effects may occur particularly in patients who are lying down or who are engaging in physical effort.
  • Desire to vomit (retching), gastrointestinal discomfort (e.g. feeling of pressure in the stomach, swelling), diarrhea.
  • Dermatological reactions (e.g. itching, skin rash).

Rare: may affect 1 in 1,000 people

  • Allergic reactions (e.g. difficulty breathing, wheezing, skin swelling) and shock (sudden circulatory failure) have occurred in very rare cases.
  • Slow heart rate.
  • Increased blood pressure.
  • Abnormal sensations (e.g. itching, tingling, numbness), tremor, seizures, muscle cramps, uncoordinated movements, transient loss of consciousness (syncope), speech disorders.
  • Seizures occur mainly after the use of high doses of tramadol or when another medicine that may induce them is taken simultaneously.
  • Changes in appetite.
  • Hallucinations, confusion, sleep disturbances, delirium, anxiety, and nightmares.
  • Psychological changes may occur after treatment with Tioner 100mg/ml oral solution. Their intensity and nature may vary (depending on the patient's personality and the duration of treatment). These may appear in the form of mood changes (usually euphoria, occasionally irritability), changes in activity (usually decreased and occasionally increased) and decreased cognitive and sensory perception (alterations of the senses and perception that may lead to judgment errors).
  • This may cause dependence on the medicine. If Tioner 100mg/ml oral solution is taken for prolonged periods, it may produce dependence, although the risk is very low. When treatment is stopped abruptly, withdrawal syndrome (see "If you stop taking Tioner 100mg/ml oral solution") may occur.
  • Blurred vision, pupil constriction (miosis), excessive pupil dilation (midriasis).
  • Slow breathing, shortness of breath (dyspnea).
  • Cases of worsening asthma have been reported, however it has not been established if they were caused by tramadol. If the recommended doses are exceeded or if it is taken concomitantly with other medicines that depress brain function, a decrease in respiratory frequency may occur.
  • Muscle weakness.
  • Difficulty or pain urinating, decreased urine output (dysuria).

Very rare: may affect 1 in 10,000 people

  • Increased liver enzymes.

Frequency not known: frequency that cannot be estimated from available data

  • Decreased blood sugar levels.
  • Hypophagia.
  • Serotonin syndrome, which may manifest as changes in mental state (e.g. agitation, hallucinations, coma), and other effects, such as fever, increased heart rate, unstable blood pressure, involuntary muscle contractions, muscle rigidity, lack of coordination, and/or gastrointestinal symptoms (e.g. nausea, vomiting, diarrhea) (see section 2 "What you need to know before taking Tioner").

Reporting of side effects:

If you experience any type of side effect, consult your doctor or pharmacist, even if it is a possible side effect that does not appear in this leaflet. You can also report them directly through the Spanish System for the Pharmacovigilance of Medicines for Human Use:https://www.notificaram.es. By reporting side effects, you can contribute to providing more information on the safety of this medicine.

5. Preservation of Tioner

Keep this medication out of the sight and reach of children.

Store this medication in a safe and protected place, to which no one else can access. This medication can cause serious harm or even be fatal to people who have not been prescribed it.

Do not use this medication after the expiration date that appears on the packaging and on the label of the bottle after CAD. The expiration date is the last day of the month indicated.

Once the packaging is opened, the solution must be used within a maximum period of 12 months.

Keep the packaging well closed.

Medications should not be thrown away through drains or in the trash.Dispose of the packaging and medications you no longer need at the SIGRE collection point at the pharmacy. If in doubt, ask your pharmacist how to dispose of the packaging and medications you no longer need. In this way, you will help protect the environment.

6. Contents of the packaging and additional information

Composition of Tioner 100 mg/ml oral solution

The active ingredient is tramadol hydrochloride.

1 ml of Tioner contains 100 mg of tramadol hydrochloride (1 pump stroke releases a quantity of oral solution containing 12.5 mg of tramadol hydrochloride).

The other components are: glycerol (E-422), potassium sorbate (E-202), macrogolglycerol hydroxystearate, propylene glycol (E-1520), sodium cyclamate, sodium saccharin, saccharose (0.2 g/ml of solution), peppermint essence, anise flavor, and purified water.

Appearance of the product and contents of the packaging

Clear, colorless to slightly yellowish, and slightly viscous solution.

This medicine is packaged in brown glass bottles equipped with a pump dispenser containing 30 ml of oral solution.

Holder of the marketing authorization and manufacturer

Holder of the marketing authorization:

Aristo Pharma Iberia, S.L.

C/ Solana, 26

28850, Torrejón de Ardoz

Madrid. Spain

Manufacturer:

Grünenthal GmbH

Zieglerstrasse 6 - D-52078 Aachen (Germany)

Last review date of this leaflet: December 2024

Detailed and updated information on this medicine is available on the website of the Spanish Agency for Medicines and Medical Devices (AEMPS)http://www.aemps.gob.es/

Country of registration
Active substance
Prescription required
Yes
Composition
Ciclamato de sodio (10 mg mg), Glicerol (e 422) (150 mg mg), Propilenglicol (150 mg mg), Sacarosa (200 mg mg), Sorbato potasico (1,5 mg mg), Sacarina sodica dihidrato (5,0 mg mg), Macrogolglicerol, hidroxiestearato de (1,0 mg mg)
This information is for reference only and does not constitute medical advice. Always consult a licensed doctor before taking any medication. Oladoctor is not responsible for medical decisions based on this content.

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