Tramadol/paracetamol andromaco 37,5/325 mg comprimidos efervescentes efg

Leaflet: information for the user

Tramadol/Paracetamol Andrómaco 37,5/325 mg effervescent tablets EFG

Tramadol, hydrochloride/Paracetamol

Read this leaflet carefully before you start to take this medicine, because it contains important information for you.

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

This medicationis a combination of two analgesics, tramadol hydrochloride and paracetamol, which act together to relieve pain.

Tramadol/Paracetamol is used in the treatment of moderate to intense pain whenever your doctor believes that the combination of tramadol hydrochloride and paracetamol is necessary.

This medication should only be used by adults and adolescents over 12 years old.

Do not take Tramadol/Paracetamol Andrómaco

• if you are allergic to tramadol hydrochloride, paracetamol, or any of the other components of this medication (listed in section 6);
• if you have taken any medication for insomnia, analgesics, or psychotropic medications (medications that can alter mood and emotions) in case of acute alcohol intoxication;
• if you are also taking MAO inhibitors (certain medications used for the treatment of depression or Parkinson's disease) or if you have taken them in the last 14 days before treatment with Tramadol/Paracetamol;
• if you have severe liver disease;
• if you have uncontrolled epilepsy with your current treatment.

Warnings and precautions

Consult your doctor before starting to take Tramadol/Paracetamol Andrómaco, if

• you are taking other medications that contain paracetamol or tramadol hydrochloride;
• you have liver problems or liver disease or if you notice that your eyes or skin turn yellow. This may be indicative of jaundice or problems with your bile ducts;
• you have kidney problems;
• you have severe respiratory difficulties, for example asthma or severe lung problems;
• you are epileptic or have had seizures or convulsions;
• you suffer from depression and are taking antidepressants, as some may interact with tramadol (see "Other medications and Tramadol/Paracetamol Andrómaco");
• you have recently experienced head trauma, shock, or severe headaches associated with vomiting;
• you are dependent on any other medication used for pain relief, for example morphine;
• you are taking other pain medications that contain buprenorphine, nalbuphine, or pentazocine;
• you are to be anesthetized. Tell your doctor or dentist that you are taking this medication.

Tolerance, dependence, and addiction

This medication contains tramadol, which is an opioid medication. Repeated use of opioids can make the medication less effective (the body becomes accustomed to it, known as pharmacological tolerance). Repeated use of Tramadol/Paracetamol can 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 can cause a feeling of lack of control over the amount of medication you should use or 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 Tramadol/Paracetamol may be higher if:

- You or any family member have abused alcohol or experienced dependence on prescription medications 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 notice any of the following symptoms while using Tramadol/Paracetamol, it could be a sign of dependence or addiction:

– You need to use the medication for a longer period than indicated by your doctor.

– You need to use a higher dose than recommended.

– You are using the medication 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 medication or control its use.

– You feel unwell when you stop using the medication, 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 course of treatment for you, when it is appropriate to stop taking the medication, and how to do it safely (see section 3, if you interrupt treatment with Tramadol/Paracetamol).

Respiratory problems related to sleep

This medication contains an active ingredient that belongs to the opioid group. Opioids can cause respiratory problems related to sleep; for example, central sleep apnea (shallow breathing or pauses in breathing during sleep) and sleep-related hypoxemia (low oxygen levels in the blood).

The risk of experiencing central sleep apnea depends on the dose of opioids. Your doctor may consider reducing the total dose of opioids if you experience central sleep apnea.

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 associated with this severe syndrome (see section 4 "Possible adverse effects").

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 medication and consult your doctor immediately: slow or shallow breathing, confusion, drowsiness, constricted pupils, general discomfort, or vomiting, constipation, loss of appetite.

If you experience or have experienced any of these problems while taking Tramadol/Paracetamol, please inform your doctor. He will decide whether you should continue taking this medication.

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 can worsen in these children.

Inform your doctor if you experience any of the following symptoms while taking this medication:

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

Other medications and Tramadol/Paracetamol Andrómaco

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

Important: This medication contains paracetamol and tramadol hydrochloride. Inform your doctor if you are takingany other medication that contains paracetamol or tramadol hydrochloride,so as not to exceed the maximum daily dose.

Tramadol/Paracetamolshould not be takenwith monoamine oxidase inhibitors (MAOIs) (see "Do not take Tramadol/Paracetamol Andrómaco").

Tramadol/Paracetamol is not recommended for use if you are being treated with:

• Carbamazepine (a medication normally used to treat epilepsy or some types of pain, such as severe facial pain called trigeminal neuralgia).
• Buprenorphine, nalbuphine, or pentazocine (opioid analgesic). Pain relief may be reduced.

Inform your doctor or pharmacist if you are taking:

flucloxacillin (antibiotic), due to a severe risk of blood and fluid disorder (metabolic acidosis with high anion gap) that must be treated urgently and that may occur particularly in cases of severe kidney or liver disease, sepsis (when bacteria and their toxins circulate in the blood causing organ damage), malnutrition, chronic alcoholism, and if you are taking the maximum daily dose of paracetamol, especially if you are taking the maximum daily dose of paracetamol for a longer period. Metabolic acidosis with high anion gap is a serious disease that must have urgent treatment.

The risk of adverse effects increases if you are taking:

• triptans (for the treatment of migraine) or selective serotonin reuptake inhibitors, "SSRIs" (for the treatment of depression). If you experience confusion, agitation, fever, sweating, uncoordinated movements of the limbs or eyes, involuntary muscle contractions, or diarrhea, you should call your doctor.
• other analgesics such as morphine and codeine (also when used for cough treatment), baclofen (muscle relaxant), some medications to lower blood pressure, medications for allergy treatment. You may feel drowsy or dizzy. If this occurs, consult your doctor.

The concomitant use of Tramadol/Paracetamol and sedatives such as benzodiazepines or related medications increases the risk of drowsiness, respiratory difficulties (respiratory depression), coma, and may be potentially fatal. Therefore, concomitant use should only be considered when other treatment options are not possible. However, if your doctor prescribesyou this medicationwith sedatives, you should limit the dose and duration of concomitant treatment.

Inform your doctor about all sedatives you are taking and follow your doctor's dosage recommendation strictly. 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.

• medications that facilitate or may cause seizures, such as certain antidepressants or antipsychotics. The risk of seizures increases if you take Tramadol/Paracetamol simultaneously with these medications. Your doctor will tell you if Tramadol/Paracetamol is suitable for you.
• medications for depression treatment. Tramadol/Paracetamol may interact with these medications and may experience a serotonin syndrome (see section 4 "Possible adverse effects").
• warfarin or phenprocoumon (medication used to prevent blood clots). The effectiveness of these medications may be altered, with a risk of bleeding. You should inform your doctor immediately of any prolonged or unexpected bleeding.
• gabapentin or pregabalin for treating epilepsy or pain due to nervous system problems (neuropathic pain).

The effectiveness of this medication may be altered if you are also taking:

• metoclopramide, domperidone, or ondansetron (medications for nausea and vomiting treatment),
• cholestyramine (medication that reduces cholesterol in the blood).

Your doctor will know which medications are safe to use with Tramadol/Paracetamol.

Tramadol/Paracetamol Andrómaco with food and alcohol

This medication may make you feel drowsy. Alcohol may make you feel drowsy, so it is recommended not to drink alcohol while taking this medication.

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 medication.

Due to the fact that this medication contains tramadol hydrochloride, it is not recommended to take it during pregnancy or breastfeeding. If you become pregnant during treatment with Tramadol/Paracetamol, consult your doctor before taking the next tablet.

Breastfeeding

Tramadol is excreted in breast milk. Therefore, you should not take this medication more than once during breastfeeding or, if you take it more than once, you should stop breastfeeding.

Based on human experience, it is not suggested that tramadol affects male and female fertility. There are no available data on the combination of tramadol and paracetamol on fertility.

Driving and operating machines

Ask your doctor if you can drive or operate machines during treatment with Tramadol/Paracetamol. It is essential to observe how this medication affects you before driving or operating machines. Do not drive or operate machines if you feel drowsy, dizzy, have blurred vision, or double 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 medications.

Tramadol/Paracetamol Andrómaco contains yellow-orange colorant (E110), sodium, and sulfite.

This medication may cause allergic reactions because it contains yellow-orange colorant (E110). It may cause asthma, especially in patients allergic to acetylsalicylic acid.

This medicament contains 179.3 mg of sodium (main component of table salt/for cooking) in each effervescent tablet. This is equivalent to 9.0% of the maximum daily dietary intake of sodium recommended for an adult. Consult your doctor or pharmacist if you need 2 or more effervescent tablets daily for a prolonged period, especially if you have been recommended a low-sodium diet.

The orange flavoring of this medication contains small amounts of sulfite, which rarely may cause severe hypersensitivity reactions and bronchospasm.

Follow exactly the administration instructions of this medication indicated by your doctor. In case of doubt, consult your doctor or pharmacist again.

Your doctor will also explain to you what you can expect from the use of Tramadol/Paracetamol, 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).

You should take this medication for the shortest time possible.

This medication is not recommended for children under 12 years old.

The dose should be adjusted to the intensity of the pain and your individual sensitivity. Normally, the lowest dose possible that produces pain relief should be used.

Unless your doctor prescribes otherwise, the recommended starting dose for adults and adolescents over 12 years old is 2 effervescent tablets.

If necessary, you can increase the dose as recommended by your doctor. The shortest interval between doses should be at least 6 hours.

Do not take more than 8 effervescent tablets of Tramadol/Paracetamol per day.

Do not take this medication more frequently than your doctor has indicated.

Older patients

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

Patients with liver or kidney disease/patients on dialysis

If you have a 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.

Administration form

The effervescent tablets are administered orally.

The effervescent tablets are taken dissolved in a glass of water.

If you estimate that the effect of this medication is too strong (e.g. you feel very drowsy or have difficulty breathing) or too weak (e.g. you do not have adequate pain relief), inform your doctor.

If you take more Tramadol/Paracetamol Andrómaco than you should

If you have taken more Tramadol/Paracetamol than you should, even if you feel well, consult your doctor or pharmacist immediately, as there is a risk of severe liver damage that may only become apparent later.

In case of overdose or accidental ingestion, consult the Toxicological Information Service, telephone 91 562 04 20, indicating the medication and the amount ingested.

If you forget to take Tramadol/Paracetamol Andrómaco

If you forget to take a dose of the medication, it is likely that the pain will recur. Do not take a double dose to compensate for the missed doses, simply continue taking the effervescent tablets as usual.

If you interrupt treatment with Tramadol/Paracetamol Andrómaco

You should 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 stop it, which can be done by gradually reducing the dose to reduce the risk of unnecessary adverse effects (withdrawal symptoms).

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

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

Very common: may affect more than 1 in 10 people;

• nausea,
• dizziness, drowsiness.

Common: may affect 1 in 10 people;

• vomiting, digestive problems (constipation, flatulence, diarrhea), stomach pain, dry mouth,
• itching, increased sweating (hyperhidrosis),
• headache, agitation,
• confusion, sleep disorders, mood changes (anxiety, nervousness, euphoria - feeling "high" all the time).

Uncommon: may affect 1 in 100 people;

• increased heart rate or increased blood pressure, heart rhythm and frequency disorders,
• sensation of tingling, numbness, or pinching in the extremities, ear noises, involuntary muscle spasms,
• depression, nightmares, hallucinations (hearing, seeing, or perceiving something that does not exist in reality), memory loss,
• difficulty breathing,
• difficulty swallowing, blood in the stool,
• skin reactions (e.g. rashes, urticarial hives),
• increased liver enzyme values,
• presence of albumin in the urine, difficulty or pain urinating,
• chills, hot flashes, chest pain.

Rare: may affect 1 in 1,000 people;

• seizures, difficulty performing coordinated movements, transient loss of consciousness (syncope),
• dependence on the medication,
• delirium,
• blurred vision, pupil constriction (miosis),
• speech disorders,
• excessive pupil dilation (mydriasis).

Frequency not known:

• decreased blood sugar levels (hypoglycemia),
• 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 starting to take Tramadol/Paracetamol Andrómaco").

The following adverse effects recognized have been reported by people who have taken medications containing only hydrochloride tramadol or only paracetamol. However, if you experience any of these symptoms while taking Tramadol/Paracetamol, please tell your doctor:

• Dizziness when getting up after lying down or sitting, low heart rate, fainting, changes in appetite, muscle weakness, slower or weaker breathing, changes in mood, changes in activity, changes in perception, worsening of asthma.
• The use of paracetamol alone or when taken with the antibiotic flucloxacillin may induce an anomaly in the blood and fluids (metabolic acidosis with high anion gap) when there is an increase in plasma acidity.
• The use of this medication with anticoagulants (e.g. fenprocoumon, warfarin) may increase the risk of bleeding. Please inform your doctor immediately about any prolonged or unexpected bleeding.

• In rare cases, skin eruptions, indicating allergic reactions that may manifest as sudden swelling of the face and neck, shortness of breath, or low blood pressure and dizziness. If this happens, interrupt treatment and consult your doctor immediately. Do not take this medication again.

In rare cases, using a medication like hydrochloride tramadol may make you dependent on it, making it difficult to stop taking it.

In rare instances, people who have been taking hydrochloride tramadol for some time may feel unwell if they stop treatment abruptly. They may feel agitated, anxious, nervous, or shaky. They may be hyperactive, have difficulty sleeping, and experience gastrointestinal and intestinal disorders. Very few people may also experience panic attacks, hallucinations, unusual perceptions such as itching, tingling, and numbness, and ear noises (tinnitus). If you experience any of these symptoms after stopping treatment with Tramadol/Paracetamol, please consult your doctor.

Frequency not known: hiccups.

In exceptional cases, blood tests may reveal certain abnormalities, such as low platelet count, which may result in nasal or gum bleeding.

In very rare cases, severe skin reactions with paracetamol have been reported.

Rare cases of respiratory depression with tramadol have been reported.

Reporting of adverse effects

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

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

Store this medication in a safe and protected location, inaccessible to others. This medication may cause severe harm or even be fatal to individuals who have not been prescribed it.

Do not use this medication after the expiration date appearing on the box and the aluminum strip after CAD. The expiration date is the last day of the month indicated.

Do not store at a temperature above 25 °C.

Medications should not be disposed of through drains or trash. Dispose of packaging and unused medications at the SIGRE collection point at the pharmacy. If in doubt, ask your pharmacist how to dispose of unused packaging and medications. By doing so, you will help protect the environment.

Composition of Tramadol/Paracetamol Andrómaco

• The active principles are tramadol hydrochloride and paracetamol.

Each effervescent tablet contains 37.5 mg of tramadol hydrochloride and 325 mg of paracetamol.

• The other components (excipients) are:

Citric acid anhydrous, anhydrous citrate monosodium, Povidone K30, sodium hydrogen carbonate, Macrogol 6000, anhydrous colloidal silica, magnesium stearate, orange flavor (contains corn-derived maltodextrin, modified starch (E1450), natural and artificial flavors, sulfite), potassium acesulfame, sodium saccharin, yellow-orange colorant (E110).

Appearance of Tramadol/Paracetamol Andrómacoand content of the packaging

Round, flat, beveled-edge tablets, white to slightly pink, with speckles of color, packaged in aluminum-coated strips, and packaged in boxes of 20 and 100 effervescent tablets.

Only some packaging sizes may be commercially marketed.

Marketing authorization holder

Andrómaco Pharma, S.L.

Doctor Zamenhof, 36 – 28027 Madrid, Spain

Responsible for manufacturing

Grünenthal GmbH

Zieglerstrasse 6 – D – 52078 Aachen, Germany

Last review date of this leaflet: December 2024

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