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Gabapentina kern pharma 800 mg comprimidos recubiertos con pelicula efg

About the medication

Introduction

Leaflet: information for the user

Gabapentin Kern Pharma 800 mg film-coated tablets EFG

Read this leaflet carefully before you start taking the medicine.

  • 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 and should not be given to others, even if they have the same symptoms, as it may harm them.
  • If you consider that any of the side effects you are experiencing are serious or if you notice any side effects not mentioned in this leaflet, inform your doctor or pharmacist. See section 4.

1. What is Gabapentin Kern Pharma 800 mg and what it is used for

2. Before taking Gabapentin Kern Pharma 800 mg

3. How to take Gabapentin Kern Pharma 800 mg

4. Possible side effects

5. Storage of Gabapentin Kern Pharma 800 mg

6. Contents of the pack and additional information

1. What is Gabapentina Kern Pharma 800 mg and what is it used for

Gabapentina Kern Pharma belongs to a group of medications used to treat epilepsy and peripheral neuropathic pain.

Epilepsy:Gabapentina is used to treat certain types of epilepsy (seizures initially limited to certain parts of the brain, whether the seizure spreads to other parts of the brain or not). Your doctor will prescribe this medication to help treat your epilepsy when your current treatment does not fully control the disease. You must take Gabapentina in addition to your current treatment unless otherwise instructed.

Gabapentina can also be administered as a single medication in the treatment of adults and children over 12 years old.

Peripheral neuropathic pain:Gabapentina is used to treat chronic pain caused by nerve damage. Various diseases can cause peripheral neuropathic pain (mainly in legs and/or arms), such as diabetes or herpes. The pain sensation could be described as heat, burning, pulsating pain, stabbing pain, sharp pain, acute pain, spasms, continuous pain, tingling, numbness, and pins and needles, etc.

2. Before taking Gabapentin Kern Pharma 800 mg

Do not take Gabapentina Kern Pharma

  • If you are allergic to gabapentin or any of the other components of this medication (listed in section 6).

Warnings and precautions

Consult your doctor or pharmacist before starting to take Gabapentina Kern Pharma.

Severe skin reactions associated with the use of gabapentin, including Stevens-Johnson syndrome, toxic epidermal necrolysis, and drug reaction with eosinophilia and systemic symptoms (DRESS), have been reported. Stop taking gabapentin and seek medical attention immediately if you notice any of the symptoms related to these severe skin reactions described in section 4.

Read the description of these symptoms in section 4 of this prospectus in “Call your doctor immediately if you experience any of the following symptoms after taking this medication, as they may be serious”.

Be especially careful with Gabapentina Kern Pharma:

  • If you have kidney problems.
  • If you develop persistent stomach pain, feel dizzy or nauseous, inform your doctor immediately.
  • If you have a nervous system disorder or a respiratory disorder or if you are over 65 years old, your doctor may prescribe a different dose.
  • Before taking this medication, inform your doctor if you have ever abused or had dependence on alcohol, prescribed medications, or illegal drugs; you may have a higher risk of developing dependence on Gabapentina Kern Pharma.

Dependence

Some people may develop dependence (need to continue taking the medication) on Gabapentina Kern Pharma. They may experience withdrawal symptoms when they stop taking Gabapentina Kern Pharma (see section 3, "How to take Gabapentina Kern Pharma" and "If you interrupt treatment with Gabapentina Kern Pharma"). If you are concerned about developing dependence on Gabapentina Kern Pharma, it is essential to consult your doctor.

If you experience any of the following signs while taking Gabapentina Kern Pharma, it may indicate that you have developed dependence.

  • You feel the need to take the medication for a longer time than prescribed.
  • You feel the need to take a higher dose than recommended.
  • You are taking the medication for reasons other than your prescription.
  • You have tried several times to stop taking the medication or control how you take it, without success.
  • You feel unwell when you stop taking the medication and feel better when you take it again.

If you notice any of the above, talk to your doctor to decide on the best course of treatment for you, including when it is appropriate to stop treatment and how to do it safely.

A small number of people who were treated with antiepileptic medications like Gabapentina have had thoughts of self-harm or suicide. If you ever have these thoughts, contact your doctor immediately.

Other medications and Gabapentina Kern Pharma

Inform your doctor or pharmacist if you are using, have used recently, or may need to take any other medication, including those purchased without a prescription.

Especially, inform your doctor (or pharmacist) if you are taking or have taken recently any medication for seizures, sleep disorders, depression, anxiety, or any other neurological or psychiatric problem.

If you are using any medication that contains morphine, inform your doctor or pharmacist as morphine may increase the effect of Gabapentina.

No interaction is expected between Gabapentina and other antiepileptic medications or oral contraceptive pills.

Gabapentina may interfere with some laboratory tests, so if you need a urine test, inform your doctor or the hospital that you are taking this medication.

If you take Gabapentina at the same time as antacids containing aluminum or magnesium, the absorption of Gabapentina in the stomach may be reduced. It is recommended that this medication be taken at least two hours after taking an antacid.

Taking Gabapentina Kern Pharma with food and drinks

This medication can be taken with or without food.

Pregnancy and breastfeeding

If you are pregnant or breastfeeding, think you may be pregnant, or plan to become pregnant, consult your doctor or pharmacist before using any medication.

Do not take Gabapentina during pregnancy, unless your doctor has told you to. Use an effective contraceptive method in women of childbearing age.

No specific studies have been conducted on the use of gabapentin in pregnant women, but in the case of other medications used to treat seizures, an increased risk of fetal damage has been reported, particularly when more than one medication is used to treat seizures at the same time. Therefore, whenever possible and only under the advice of your doctor, try to take only one medication for seizures during pregnancy.

Do not stop taking this medication abruptly as this may cause an anticipation of the seizure, which could have serious consequences for you and your baby.

If you take Gabapentina during pregnancy, it may cause withdrawal symptoms in newborns. This risk may be higher when Gabapentina is taken concomitantly with opioid analgesics (pain medications).

Contact your doctor immediately if you become pregnant, think you may be pregnant, or plan to become pregnant while taking this medication.

Gabapentin, the active ingredient in Gabapentina Kern Pharma, is excreted in breast milk. It is not recommended to breastfeed while taking this medication, as the effect on infants is unknown.

Driving and operating machinery

Gabapentina may cause symptoms such as drowsiness, dizziness, or visual disturbances, and may impair your ability to react. These effects, as well as the underlying condition, may make it difficult for you to drive vehicles or operate machinery. Therefore, do not drive, operate machinery, or engage in other activities that require special attention, until your doctor assesses your response to this medication.

Gabapentina Kern Pharma contains castor oil

This medication may cause stomach discomfort and diarrhea due to the presence of castor oil.

3. How to take Gabapentina Kern Pharma 800 mg

Follow exactly the administration instructions for Gabapentin as indicated by your doctor or pharmacist. In case of doubt, consult your doctor or pharmacist again. Do not take a higher dose of medication than prescribed.

Your doctor will determine the appropriate dose for you.

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

If you are an elderly patient (over 65 years old), take Gabapentin normally, except if you have kidney problems.

Your doctor may prescribe a different dosing regimen or dose if you have kidney problems.

Swallow the tablets with a sufficient amount of water.The tablets can be divided into two equal halves.

Continue takingthis medication until your doctor tells you to stop.

Peripheral neuropathic pain:

Take the number of tablets as indicated by your doctor. Normally, your doctor will gradually increase your dose. The initial dose will generally be between300 to900 mg per day. Therefore, the dose can be increased up to a maximum dose of 3600 mg per day, divided into three equal doses, for example, one in the morning, one at noon, and one at night.

Epilepsy:

Adults and adolescents:

Take the number of tablets as indicated by your doctor. Normally, your doctor will gradually increase your dose. The initial dose will generally be between300 to900 mg per day. Therefore, the dose can be increased up to a maximum dose of 3600 mg per day, divided into three equal doses, for example, one in the morning, one at noon, and one at night.

Children 6 years or older:

Your doctor will decide on the dose to be administered to your child based on the child's weight. Treatment will begin with a low initial dose that will be gradually increased over a period of approximately 3 days. The normal dose for controlling epilepsy is 25-35 mg/kg/day. The dose is normally administered by taking the tablets, divided into 3 equal doses per day, for example, one in the morning, one at noon, and one at night.

This medication is not recommended for children under 6 years old.

If you take more Gabapentin Kern Pharma than you should

Consult your doctor immediately or go to the nearest hospital emergency unit. Bring with you any remaining tablets, along with the packaging and the leafletso that the hospital can easily identify the medication you have taken.

You can also call the Toxicological Information Service, phone: 91 562 04 20.

If you forgot to take Gabapentin Kern Pharma

If you forgot to take a dose, take it as soon as you remember, unless it is time for the next dose.

Do not take a double dose to compensate for the missed doses.

If you interrupt treatment with Gabapentin Kern Pharma

Do not stop taking Gabapentin Kern Pharma suddenly. If you want to stop taking Gabapentin Kern Pharma, talk to your doctor first. Your doctor will tell you how to proceed. If you are going to stop treatment, this should be done gradually over a minimum of one week. You should know that you may experience certain adverse effects, called withdrawal syndrome, after interrupting a short or long-term treatment with Gabapentin Kern Pharma. These include seizures, anxiety, difficulty sleeping, feeling unwell (nausea), pain, sweating, tremors, headache, depression, abnormal sensation, dizziness, and general feeling of discomfort. These effects usually occur within the first 48 hours after stopping treatment with Gabapentin Kern Pharma. If you experience this withdrawal syndrome, contact your doctor.

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

4. Possible Adverse Effects

Stop taking Gabapentina Kern Pharma and seek immediate medical attention if you notice any of the following symptoms:

  • Flat, red patches with a target-like appearance or circular patches on the trunk, often with blisters in the center; skin peeling, mouth ulcers, throat, nose, genital, and eye ulcers. These severe skin eruptions may be preceded by fever and flu-like symptoms (Stevens-Johnson syndrome, toxic epidermal necrolysis).
  • Widespread rash, high body temperature, and enlarged lymph nodes (DRESS syndrome or drug hypersensitivity syndrome).

Like all medications, gabapentina may cause side effects, although not everyone will experience them.

Gabapentina can cause a severe or potentially fatal allergic reaction that can affect the skin or other parts of the body, such as the liver or blood cells. When this type of reaction occurs, it may or may not be accompanied by a rash. In the event of this type of allergic reaction, you may need to be hospitalized or stop taking this medication.

Inform your doctor immediately if you experience any of the following symptoms:

  • Rashes on the skin,
  • Hives,
  • Fever,
  • Swollen lymph nodes that do not subside,
  • Swelling of the lips and tongue,
  • Yellow discoloration of the skin or white of the eyes,
  • Unusual bleeding or bruising,
  • Severe fatigue or weakness,
  • Unexpected muscle pain,
  • Frequent infections,
  • Difficulty breathing that, if severe, may require emergency medical attention to breathe normally.

These symptoms may be the first signs of a severe reaction. Your doctor will examine you to decide whether you should continue taking gabapentina.

The very common side effects that may affect more than 1 in 10 people are:

  • Viral infection.
  • Drowsiness, dizziness, lack of coordination.
  • Feeling tired, fever.

The common side effects that may affect more than 1 in 100 people are:

  • Pneumonia, respiratory infection, urinary tract infection, infection, ear inflammation.
  • Low white blood cell count.
  • Loss of appetite, increased appetite.
  • Anger towards others, confusion, mood changes, depression, anxiety, nervousness, difficulty thinking.
  • Seizures, convulsions, difficulty speaking, memory loss, tremors, difficulty sleeping, headache, skin sensitivity, decreased sensations, coordination difficulties, unusual eye movements, increased, decreased, or absent reflexes.
  • Blurred vision, double vision.
  • Dizziness.
  • Increased blood pressure, redness or dilation of blood vessels.
  • Difficulty breathing, bronchitis, sore throat, cough, dry nose.
  • Vomiting (feeling dizzy), nausea (feeling dizzy), dental problems, inflamed gums, diarrhea, stomach pain, indigestion, constipation, dry mouth or throat, flatulence.
  • Swelling of the face, hives, rash, itching, acne.
  • Muscle pain, muscle cramps, back pain, spasms.
  • Incontinence.
  • Erectile dysfunction.
  • Swelling in the legs and arms or swelling that can affect the face, trunk, and extremities, difficulty walking, weakness, pain, feeling unwell, flu-like symptoms.
  • Decreased white blood cell count, weight gain.
  • Accidental injuries, fractures, bruises.

The uncommon side effects that may affect between 1 and 10 in every 1,000 patients are:

  • Agitation (a chronic state of restlessness and involuntary, purposeless movements).
  • Difficulty swallowing

The rare side effects that may affect fewer than 1 in 1,000 people are:

  • Decreased platelets (blood clotting cells).
  • Allergic reaction such as hives.
  • Hallucinations.
  • Abnormal movement problems such as contortions, convulsions, and rigidity.
  • Tinnitus (ringing in the ears).
  • Increased heart rate.
  • Pancreatitis (inflammation of the pancreas).
  • Hepatitis (inflammation of the liver), yellow discoloration of the skin and eyes.
  • Severe skin reactions that require immediate medical attention, swelling of the lips and face, rash, and redness, hair loss.
  • Acute kidney failure.
  • Side effects after abrupt discontinuation of gabapentina treatment (anxiety, difficulty sleeping, dizziness, pain, and sweating), chest pain.
  • Fluctuations in blood glucose in patients with diabetes, abnormal blood test results that may indicate liver problems.
  • Difficulty breathing, shallow breathing (respiratory depression).

Other possible side effects: their frequency cannot be estimated from available data:

You should know that you may experience certain side effects, called withdrawal syndrome, after stopping short-term or long-term treatment with Gabapentina Kern Pharma (see "If you stop taking Gabapentina Kern Pharma").

Additionally, in clinical trials in children, aggressive behavior and convulsions were reported as common side effects.

Reporting side effects:

If you experience any type of side effect, consult your doctor, pharmacist, or nurse, even if it is a possible side effect that does not appear in this prospectus. You can also report them directly through theSistema Español de Farmacovigilancia de Medicamentos de Uso Humano (Website:www.notificaram.es)Reporting side effects can help provide more information about the safety of this medication.

5. Conservation of Gabapentina Kern Pharma 800 mg

Keep out of the sight and reach of children.

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

Do not store at a temperature above30°C.

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

6. Contents of the packaging and additional information

Composition of Gabapentina Kern Pharma800 mg tablets

  • The active ingredient is gabapentin. Each film-coated tablet contains 800 mg of gabapentin.
  • The other components of this medication are: microcrystalline cellulose, hydroxypropyl cellulose, hydroxypropyl cellulose LH-21, hydrogenated castor oil, magnesium stearate, sodium lauryl sulfate, and Opadry II 85F18422 (partially hydrolyzed polyvinyl alcohol, titanium dioxide (E-171), macrogol, and talc).

Appearance of the product and contents of the packaging

Film-coated tablets. The tablets are oval (10 mm x 19 mm), white in color, scored on one face and “800” engraved on the other. The score serves to divide the tablet into two equal halves.

Each package contains 90 tablets.

Holder of the marketing authorization and responsible for manufacturing

Kern Pharma, S.L.

Venus, 72 – Pol. Ind. Colón II

08228 Terrassa - Barcelona

Spain

This prospectus was reviewed in January 2023

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/

Country of registration
Active substance
Prescription required
Yes
Manufacturer
Composition
Laurilsulfato de sodio (16 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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