Gabapentin may cause withdrawal symptoms in newborns if taken during pregnancy. This risk may be higher when gabapentin 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 Gabapentina ratiopharm. Do not stop taking this medication abruptly, as this may cause an anticipation of seizures, which could have serious consequences for both you and your baby.
Breastfeeding
Gabapentin, the active ingredient in Gabapentina ratiopharm, passes into breast milk. It is not recommended to breastfeed while taking Gabapentina ratiopharm, as its effect on the baby is unknown.
Fertility
There are no effects on fertility in animal studies.
Driving and operating machinery
Gabapentina ratiopharm may cause dizziness, drowsiness, and fatigue. Do not drive, operate heavy machinery, or engage in other potentially hazardous activities until you know if this medication affects your ability to perform these activities.
Gabapentina ratiopharm 400 mg hard capsules contain lactose.
This medication contains lactose. If your doctor has told you that you have a lactose intolerance, consult with them before taking this medication.
Follow exactly the administration instructions of this medication as indicated by your doctor. 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.
Epilepsy, the recommended dose is
Adults and adolescents
Take the number of capsules as indicated by your doctor. Normally, your doctor will gradually increase your dose. The initial dose will generally be 300 to 900 mg per day. From there, the dose can be increased, as indicated by your doctor, up to a maximum dose of 3,600 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 through ingestion of the capsules, divided into 3 equal doses per day, normally one in the morning, one at noon, and one at night.
This medication is not recommended for use in children under 6 years of age..
Peripheral neuropathic pain, the recommended dose is
Adults
Take the number of capsules as indicated by your doctor. Normally, your doctor will gradually increase your dose. The initial dose will generally be 300 to 900 mg per day. From there, the dose can be increased, as indicated by your doctor, up to a maximum dose of 3,600 mg per day, divided into three equal doses, for example, one in the morning, one at noon, and one at night.
If you have kidney problems or are receiving hemodialysis treatment
Your doctor may prescribe a different dosing regimen and/or dose if you have kidney problems or are receiving hemodialysis treatment.
If you are an elderly patient (over 65 years of age)
You should take the normal dose of this medication, except if you have kidney problems. Your doctor may prescribe a different dosing regimen or dose if you have kidney problems.
If you consider that the effect of Gabapentina ratiopharm is too strong or too weak, inform your doctor or pharmacist as soon as possible.
Method of administration
This medication is administered orally. Swallow the capsules whole with a sufficient amount of water.
Continue takingGabapentina ratiopharm until your doctor tells you to stop.
If you take more Gabapentina ratiopharm than you should
Doses higher than recommended may cause an increase in adverse effects, including loss of consciousness, dizziness, double vision, slurred speech, numbness, and diarrhea. In case of overdose or accidental ingestion, consult your doctor, pharmacist, or call the Toxicological Information Service, phone 91 562 04 20, indicating the medication and the amount ingested, or go to the emergency department of the nearest hospital if you take more Gabapentina ratiopharm than your doctor prescribed. Bring any capsules you have not taken, along with the packaging and the leaflet, so that the hospital can easily identify the medication you have taken.
If you forget to take Gabapentina ratiopharm
If you forget 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 Gabapentina ratiopharm
Do not stop taking this medication suddenly. If you want to stop taking Gabapentina ratiopharm, talk to your doctor first. Your doctor will indicate 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 this medication. These include seizures, anxiety, difficulty sleeping, feeling unwell (nausea), pain, sweating, tremors, headache, depression, abnormal sensation, dizziness, and general feeling of unwellness. These effects usually occur within the first 48 hours after stopping treatment with this medication. If you experience this withdrawal syndrome, contact your doctor.
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.
Stop taking gabapentin and seek medical attention immediately if you notice any of the following symptoms:
Contact your doctor immediately if you experience any of the following symptoms after taking this medicine, as they may be serious:
Contact your doctor immediately if you have any of the following symptoms after taking this medicine, as they may be serious:
These symptoms may be the first signs of a severe reaction. You should have a doctor examine you to decide if you should continue taking Gabapentin ratiopharm.
Other side effects include:
Very common: (may affect more than 1 in 10 people)
Common: (may affect up to 1 in 10 people)
Additionally, in clinical trials in children, aggressive behavior and spasmodic movements were reported as common side effects.
Uncommon: (may affect up to 1 in 100 people)
Rare: (may affect up to 1 in 1000 people)
After the marketing of Gabapentin ratiopharm, the following side effects have been reported:
You should know that you may experience certain side effects, called withdrawal syndrome, after interrupting a short or long-term treatment with Gabapentin ratiopharm (see "If you stop taking Gabapentin ratiopharm").
Reporting 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 Vigilance of Medicinal Products for Human Use: https://www.notificaram.es. By reporting side effects, you can contribute to providing more information on the safety of this medicine.
Keep this medication 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 above 25°C.
Medications should not be disposed of through drains or trash. Dispose of packaging and medications you no longer need at the SIGRE point of your pharmacy. If in doubt, ask your pharmacist how to dispose of medications you no longer need. By doing so, you will help protect the environment.
Composition of Gabapentina ratiopharm
The active ingredient is gabapentin. Each hard capsule contains 400 mg of gabapentin.
The other components (excipients) are: lactose, cornstarch and talc (E553b).See section 2Gabapentina ratiopharm 400 mg hard capsules contain lactose.
The excipients of the cap/ body are: titanium dioxide (E171), yellow iron oxide (E172), red iron oxide (E172) and gelatin.
Printing ink: shellac, black iron oxide (E 172), propylene glycol, potassium hydroxide (E525) and ammonium solution.
Appearance of the product and contents of the packaging
Gabapentina ratiopharm 400 mg are hard gelatin capsules of orange color, with “400” and “G” engraved on the cap and body of the capsule respectively.
Each package contains 90 capsules and each capsule contains 400 mg of gabapentin.
Holder of the marketing authorization and responsible for manufacturing
Holder of the marketing authorization
Teva Pharma, S.L.U.
C/Anabel Segura 11, Edificio Albatros B, 1st floor,
Alcobendas, 28108 Madrid
Responsible for manufacturing
Merckle GmbH
Ludwig-Merckle-Strasse 3
89143-Blaubeuren
Germany
or
Merckle GmbH
Graf Arco Strasse 3
89079 Ulm
Germany
or
Teva Operations Poland SP.Z.O.O.
Ul. Mogilska 80,
31-546 Cracovia
Poland
Last review date of this leaflet:July 2024
Other sources of information:
The detailed information of this medicine is available on the website of the Spanish Agency for Medicines and Medical Devices (AEMPS) http://www.aemps.gob.es/
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