Lamotrigine
important information for the patient.
Epitrigine belongs to a group of medicines called antiepileptics. It is used to treat two conditions - epilepsy and bipolar affective disorders.
The action of Epitrigine in the treatment of epilepsyinvolves blocking impulses in the brain that cause epileptic seizures
in adults and children over 13 years of age, Epitrigine can be used alone
or in combination with other medicines to treat epilepsy. Epitrigine can also be used
in combination with other medicines to treat epileptic seizures associated with a condition called Lennox-Gastaut syndrome.
in children between 2 and 12 years of age, Epitrigine can be used in combination with other medicines
to treat these conditions. It can be used alone to treat a type of epilepsy called typical absence seizures.
Epitrigine is also used to treat bipolar affective disorders.
In patients with bipolar affective disorders (sometimes called manic-depressive psychosis), there are extreme mood swings with episodes of mania (excitement or euphoria) alternating with episodes of depression (deep sadness or despair). In adult patients over 18 years of age, Epitrigine can be used alone or in combination with other medicines to prevent depressive episodes occurring in bipolar affective disorders. It is not yet known how Epitrigine works in the brain to produce this effect.
if the patient is allergicto lamotrigine or any of the other ingredients of this medicine (listed in section 6).
In case of the above-mentioned case
if the patienthas ever had a rash after taking lamotrigine or other medicines used to treat bipolar affective disorders or epilepsy a rash has occurred
if the patient has had a rash or sunburn
due to exposure to sunlight or artificial light (e.g. in a solarium). The doctor will check the treatment the patient is taking and may advise avoiding sunlight or using sun protection (e.g. using a sunscreen or wearing protective clothing).
if the patient has ever had meningitis
after taking lamotrigine(see description of symptoms in section 4 of this leaflet
"Rare side effects").
if the patient is taking a medicine containing lamotrigine
if the patient has a condition called Brugada syndrome or other heart diseases.
Brugada syndrome is a genetically determined heart condition characterized by electrical disturbances in the heart. Abnormal ECG recordings are associated with arrhythmia (abnormal heart rhythm), which can be caused by taking lamotrigine.
In case of any of the above-mentioned cases
A small number of patients taking Epitrigine have a life-threatening allergic reaction or skin reaction, which can cause more serious symptoms if left untreated. These reactions include: Stevens-Johnson syndrome, toxic epidermal necrolysis, and drug rash with eosinophilia and systemic symptoms (DRESS syndrome). The patient should be aware of the symptoms to expect when taking Epitrigine. This risk may be associated with a genetic variant found in people of Asian descent (mainly Chinese Han and Thai). If the patient has such a background and has been previously tested for this genetic variant (HLA-B*1502), they should discuss it with their doctor before taking Epitrigine.
Rare but very serious reactions of the immune system have been reported in patients taking lamotrigine
Antiepileptic medicines are used to treat several conditions, including epilepsy and bipolar affective disorders.
In patients with bipolar affective disorders, thoughts of harming themselves or committing suicide may sometimes occur. If the patient has bipolar affective disorders, such thoughts may occur more frequently:
when starting treatment for the first time
if the patient has had thoughts of self-harm or suicide before
if the patient is under 25 years of age
If the patient experiences worrying thoughts or feelings or if they experience a worsening of their condition or new symptoms while taking Epitrigine
A small number of people taking antiepileptic medicines containing lamotrigine have thought about harming themselves or committing suicide. If such thoughts ever occur to the patient, they should contact their doctor immediately.
Seizures in some types of epilepsy may sometimes worsen or occur more frequently when taking Epitrigine. In some patients, severe seizures may occur, which can pose a serious risk to the patient's health. If the patient experiences more frequent seizures or a severe seizure while taking Epitrigine
in patients under 18 years of age.
Medicines used to treat depression or other mental disorders in children and adolescents under 18 years of age increase the risk of suicidal thoughts or behaviors.
currently or recently, and about medicines the patient plans to take, including herbal medicines or other medicines available without a prescription.
The doctor should know that the patient is taking the following medicines. This will allow the doctor to determine the correct dose of Epitrigine. These medicines include:
oxcarbazepine, felbamate, gabapentin, levetiracetam, lacosamide, perampanel,
pregabalin, topiramate, zonisamide, used to treat epilepsy
lithium, olanzapineor aripiprazole, used to treat mental disorders
bupropion, used to treat mental disordersor nicotine addiction
paracetamol, used to treat pain, fever
Some medicines interact with Epitrigine or increase the risk of side effects. These include:
The doctor may recommend using a specific type of hormonal contraceptive or another method of contraception, such as a condom, diaphragm, or intrauterine device. If the patient is using hormonal contraceptives, such as "the pill", the doctor may recommend blood tests to check the level of Epitrigine in the blood. If the patient is using or plans to use hormonal contraceptives
Epitrigine may also affect the action of hormonal contraceptives, although it is unlikely to reduce their effectiveness. If the patient is using hormonal contraceptives and notices any changes in their menstrual cycle, such as bleeding or spotting
they should consult their doctor or pharmacist before taking this medicine.
pharmacist before taking this medicine.
The active substance of Epitrigine passes into breast milk and may affect the baby. The doctor will discuss the risks and benefits of breastfeeding while taking Epitrigine and if the patient decides to breastfeed, they will periodically check the baby for excessive sleepiness, rash, or poor weight gain. If any of these symptoms occur in the baby, the doctor should be informed.
Epitrigine may cause dizziness and double vision
driving and using machines.
If the patient has been diagnosed with an intolerance to some sugars, they should contact their doctor before taking the medicine.
This medicine should always be taken as directed by the doctor or pharmacist. In case of doubts, consult a doctor or pharmacist.
Determining the correct dose of Epitrigine for the patient may take time. The dose taken by the patient depends on:
the patient's age
whether the patient is taking Epitrigine in combination with other medicines
whether the patient has any kidney or liver disease
The doctor will initially prescribe a small dose and then gradually increase it over several weeks
until the effective dose for the patient (called the maintenance dose) is reached.
Never take more than the dose recommended by the doctor.
Usually, the maintenance dose of Epitrigine for adults and children over 13 years of age is
between 100 mg and 400 mg per day.
For children between 2 and 12 years of age, the maintenance dose is dependent on body weight - usually between 1 mg and 15 mg per kilogram of body weight, up to a maximum maintenance dose of 200 mg per day.
Epitrigine is not recommended for children under 2 years of age.
The dose of Epitrigine should be taken once or twice a day, as directed by the doctor. Epitrigine can be taken with or without food.
The doctor may also recommend starting or stopping other medicines,
depending on the indication and the patient's response to treatment.
Swallow the tablets whole. Do not break, chew, or crush them.
Always take the entire doseprescribed by the doctor. Never take part of a tablet.
Taking too much Epitrigine can increase the risk of serious side effects, which can be fatal.
In a person who has taken too much Epitrigine, the following symptoms may occur:
rapid, involuntary eye movements (nystagmus)
clumsiness and lack of coordination (ataxia)
heart rhythm disturbances (detectable on an ECG)
loss of consciousness, seizures, or coma
take the next dose at the usual time.
Epitrigine. This is important for the patient.
Do not stop taking Epitrigine unless the doctor advises it.
Epitrigine should be taken for as long as the doctor recommends. Do not stop taking it unless the doctor advises it.
To stop taking Epitrigine, it is essential to gradually reduce the dose over about two weeks.
If Epitrigine is stopped suddenly, the patient's epilepsy symptoms may return or worsen.
It may take some time before the beneficial effect of Epitrigine occurs, so it is unlikely that an improvement will occur immediately. When stopping Epitrigine, there is no need to gradually reduce the dose. However, the patient should consult their doctor if they plan to stop taking Epitrigine.
Like all medicines, Epitrigine can cause side effects, although not everybody gets them.
A small number of patients taking Epitrigine have a life-threatening allergic reaction or skin reaction, which can worsen if left untreated. These symptoms may occur more frequently during the first few months of taking Epitrigine, especially if the patient has been given too high a dose, the dose has been increased too quickly, or the patient is taking Epitrigine in combination with another medicine called valproate. Some of these symptoms occur more frequently in children, so parents should pay particular attention to them.
The symptoms of these reactions include:
skin rashes or redness, which can worsen to severe skin reactions, including widespread rash with blisters and peeling of the skin, especially on the lips, nose, eyes, and genitals (Stevens-Johnson syndrome), widespread peeling of the skin (toxic epidermal necrolysis), or severe rash with symptoms from the liver, blood, and other organs (drug rash with eosinophilia and systemic symptoms, also known as DRESS syndrome)
ulcers in the mouth, throat, nose, or genitals
pain in the mouth or redness and swelling of the eyes(conjunctivitis)
high fever(fever), flu-like symptoms, or drowsiness
swelling of the faceor enlarged lymph nodes in the neck, armpits, and groin
unexplained bleeding or bruisingor blue discoloration of the fingers
sore throator more frequent infections (such as colds)
increased liver enzyme levels, which can be detected in blood tests
increased white blood cell count (eosinophilia)
enlarged lymph nodes
symptoms may also affect other parts of the body, such as the liver and kidneys
In many cases, these symptoms indicate less serious side effects. However, remember that they can be life-threatening and can develop into serious conditions,
such as organ failure, if left untreated. If any of these symptoms occur
Hemophagocytic lymphohistiocytosis (HLH)(see section 2 "Important information before taking Epitrigine")
May occur in more than 1 in 10patients:
headache
skin rash
May occur in up to 1 in 10patients:
aggression or irritability
drowsiness
dizziness
tremors
difficulty sleeping (insomnia)
feeling agitated
diarrhea
dry mouth
nausea or vomiting
feeling tired
back pain or joint pain, or pain in any other location
May occur in up to 1 in 100patients:
clumsiness and lack of coordination (ataxia)
double or blurred vision
unusual hair loss (alopecia)
skin rash or sunburn after exposure to sunlight or artificial light (photosensitivity)
May occur in up to 1 in 1,000patients:
life-threatening skin reaction (Stevens-Johnson syndrome) (also see information at the beginning of section 4)
rapid, involuntary eye movements (nystagmus)
itching eyes with discharge (conjunctivitis)
May occur in up to 1 in 10,000patients:
life-threatening skin reaction (toxic epidermal necrolysis) (also see information at the beginning of section 4)
drug rash with eosinophilia and systemic symptoms (DRESS syndrome) (also see information at the beginning of section 4)
high fever (fever) (also see information at the beginning of section 4)
swelling of the face or enlarged lymph nodes in the neck, armpits, and groin (generalized lymphadenopathy) (also see information at the beginning of section 4)
liver function changes, which can be detected in blood tests, or liver failure (also see information at the beginning of section 4)
severe blood clotting disorder, which can cause unexpected bleeding or bruising (disseminated intravascular coagulation) (also see information at the beginning of section 4)
hemophagocytic lymphohistiocytosis (HLH) (see section 2 "Important information before taking Epitrigine")
changes in blood test results, including decreased red blood cell count (anemia), decreased white blood cell count (leukopenia, neutropenia, agranulocytosis), decreased platelet count (thrombocytopenia), and decreased count of all blood cells (pancytopenia), as well as a bone marrow disorder called aplastic anemia
hallucinations (seeing or hearing things that are not real)
disorientation
feeling "unsteady" or lacking balance while moving
involuntary, repetitive movements of the body and/or sounds or words (tics), involuntary muscle contractions affecting the eyes, head, and trunk (choreoathetosis) or other unusual body movements, such as jerks, tremors, or stiffness
increased frequency of seizures in patients with previously diagnosed epilepsy
worsening of symptoms in patients with diagnosed Parkinson's disease
pseudolymphoma syndrome (symptoms may include back or joint pain, which may be accompanied by fever and/or general malaise)
Have been reported in a small number of people, but the frequency is unknown:
reports of bone disorders, including osteopenia and osteoporosis (weakening of bones), as well as fractures. If the patient is taking antiepileptic medicines for a long time, has previously had osteoporosis, or is taking steroids, they should discuss this with their doctor or pharmacist.
kidney inflammation (interstitial nephritis) or simultaneous kidney and eye inflammation (interstitial nephritis and uveitis)
nightmares
reduced immunity due to lower levels of antibodies in the blood, called immunoglobulins, which help protect the body against infections
red bumps or spots on the skin (pseudolymphoma)
If side effects occur, including any not listed in this leaflet, the patient should tell their doctor or pharmacist. Side effects can be reported directly to the Department of Drug Safety, Urząd Rejestracji Produktów Leczniczych, Wyrobów Medycznych i Produktów Biobójczych, Al. Jerozolimskie 181C, 02-222 Warszawa, tel.: +48 22 49 21 301, fax: +48 22 49 21 309, website: https://smz.ezdrowie.gov.pl
Side effects can also be reported to the marketing authorization holder.
Reporting side effects will help to gather more information on the safety of this medicine.
Keep the medicine out of sight and reach of children.
There are no special storage instructions for this medicine.
Do not take this medicine after the expiry date stated on the blister and carton after "EXP:". The expiry date refers to the last day of the month.
Medicines should not be disposed of via wastewater or household waste. Ask the pharmacist how to dispose of medicines that are no longer needed. This will help protect the environment.
Epitrigine 50 mg tablets are light yellow, round, flat, marked with the number 50, with a diameter of 8 mm.
Epitrigine 100 mg tablets are light yellow, round, flat, marked with the number 100, with a diameter of 10 mm.
Blister packs (aluminum/PVC) in a carton: 30 tablets.
+pharma arzneimittel gmbh
Hafnerstraße 211
A-8054 Graz
Austria
Actavis Group PTC ehf
Reykjavíkurvegur 76-78
220 Hafnarfjörður
Iceland
BALKANPHARMA – DUPNITSA AD
3 Samokovsko Shosse Str.
Dupnitsa 2600
Bulgaria
Tjoapack Netherlands B.V.
Nieuwe Donk 9
4879 AC Etten-Leur
Netherlands
PharmaPath S.A.
28is Oktovriou 1
Agia Varvara, 123 51
Greece
To obtain more detailed information on this medicine, contact the representative of the marketing authorization holder:
+pharma Polska sp. z o.o.
ul. Podgórska 34
31-536 Kraków, Poland
tel. +48 12 262 32 36
Date of last revision of the leaflet: November 2023
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