Package Insert: Information for the Patient
Serdolect 16 mg Film-Coated Tablets
Sertindol
Read this entire package insert carefully before starting to use this medication, as it contains important information for you.
1. What is Serdolect and for what it is used
2. What you need to know before starting to take Serdolect
3. How to take Serdolect
4. Possible adverse effects
5. Storage of Serdolect
6. Contents of the package and additional information
Serdolect contains the active ingredient sertindol and belongs to a group of medicines called antipsychotics. These act on nerve pathways in specific areas of the brain and help by correcting certain chemical imbalances in the brain that cause their symptoms.
Serdolect is indicated for treating schizophrenia in cases where another medicine is not effective.
Do not take Serdolect :
if you are/ have
?allergy to sertindol or any of the other components of
?low levels of potassium or magnesium in the blood that have not been treated
?significant heart disease
-heart failure with swelling caused by excess fluid
-enlargement of the heart
-irregular or slow heartbeats
?you have been born or have had an episode ofprolonged ventricular cardiac activity, measured on an ECG, or someone in your family has this abnormal heart rhythm
?severely reduced liver function
?you are taking medications that prolong the time of ventricular cardiac activity or affect liver function. See the first two points in the section “Other medications and Serdolect” in section 2
Warnings and precautions
Consult your doctor before starting to take Serdolect if you are/ have:
•vomiting or diarrhea during treatment with Serdolect
•decreased liver function
•Parkinson's disease
•diabetes or risk factors for developing diabetes
•risk factors for stroke, such as high blood pressure, previous stroke or heart attack, diabetes, high cholesterol, dementia, smoker
•65 years of age or older
•history of blood clots in the veins or family history of blood clots in the veins, as medications for the treatment of schizophrenia have been associated with the formation of blood clots.
•seizures
•unusual movement of the mouth and tongue, which may be early signs of a nervous system disorder called tardive dyskinesia
•high fever, muscle stiffness, and changes in consciousness, especially if accompanied by sweating and rapid heartbeats. These may be signs of a rare but serious condition called neuroleptic malignant syndrome
When starting treatment with Serdolect, you may feel dizzy when getting up from bed or standing up. Your doctor may reduce this risk by starting with a low dose, gradually increasing it over several weeks. This feeling usually disappears when you have taken Serdolect for a while.
Monitoring before and during treatment
Before and during your treatment with Serdolect, your doctor may perform certain tests, such as:
•an electrocardiogram of your ventricular cardiac activity to check if there is prolongation of the QT interval
This test is repeated after 3 weeks of treatment or when you reach a daily dose of 16 mg of sertindol. During maintenance treatment, it is done every 3 months. In addition, an ECG is done before and after increasing the dose. This is also done if you change the dose of another medication you take that may affect the level of sertindol in the blood.
•potassium and magnesium level test in the blood
If potassium or magnesium levels decrease, your doctor will start treatment to correct it. Do not take Serdolect if you have untreated low levels of potassium or magnesium in the blood.
Contact your doctor if you have vomiting, diarrhea, electrolyte disturbances, or take medications to increase urine production. Your doctor may measure the amount of potassium in your blood.
•blood pressure monitoring
Children under 18 years
Serdolect should not be used in this age group as there are no available data.
Taking Serdolect with other medications
Inform your doctor or pharmacist if you are taking, have taken recently, or may need to take any other medication.
Serdolectshould not be usedwhen the following medications are used:
•medications that affect liver function, such as:
Other medications that may affect or be affected by Serdolect are:
•medications used to treat Parkinson's disease called dopamine agonists
•some medications used to treat depression and anxiety disorders, such as fluoxetine, paroxetine
•rifampicin: medication for tuberculosis or other infections
•carbamazepine, phenytoin, phenobarbital: medications for epilepsy
•medications to increase urine production, which decreases potassium levels in the blood
Taking Serdolect with food and drinks
Avoid alcoholduring treatment with Serdolect, although no influence is expected from alcohol.
Pregnancy, breastfeeding, and fertility
Serdolectis not recommendedduring pregnancy.
The following symptoms may appear in newborns of mothers who have taken Serdolect during the last trimester (the last three months of pregnancy):
Contact your doctor if your baby shows any of these symptoms.
Serdolectshould not be usedduring breastfeeding unless your doctor says it is absolutely necessary. Considerinterrupting breastfeedingif treatment is necessary, as Serdolect is excreted in breast milk.
•Fertility
Serdolect may have adverse effects that may affect your sexual activity and fertility. These are reversible. Please talk to your doctor about any problems related to your sexual activity.
Driving and using machines
Do not drive or use machinery until you know how Serdolect affects you, although it does not cause drowsiness.
Serdolect contains lactose
If your doctor has told you that you have an intolerance to certain sugars, consult with him before taking this medication.
Serdolect contains sodium
This medication contains less than 1 mmol sodium (23mg) per tablet; it is essentially “sodium-free”.
Follow exactly the administration instructions of this medication indicated by your doctor or pharmacist. In case of doubt, consult your doctor or pharmacist again.
The recommended dose is:
Alternatively, the maximum dose can be reached by taking 1 tablet of 20 mg of Serdolect plus 1 tablet of 4 mg of Serdolect.
Patients over 65 years old
It is very likely that your doctor will increase the dose of Serdolect over a longer period of time than usual. Your doctor may also prescribe a lower maintenance dose than normally recommended.
Patients with reduced liver function
Your doctor may monitor you more closely and increase your dose over a long period if you have mildly or moderately reduced liver function. Your doctor may also prescribe a lower maintenance dose than normally recommended.
Serdolect should not be used in patients with severely reduced liver function.
Patients with reduced renal function
Serdolect can be administered to patients with reduced renal function at the usual doses.
Administration
Take the whole tablets with a glass of water, every day at the same time. The tablets can be taken with or without food.
Treatment duration
Take the tablets for the recommended time by your doctor.
Never change the medication dose without consulting your doctor first.
If you want to stop using the medication, please note the information in the section 3 “If you interrupt Serdolect treatment”.
If you take more Serdolect than you should
If this occurs, contact your doctor or nearest hospital immediately. Do it even if you do not have any signs of discomfort.
The symptoms of overdose are:
In case of overdose or accidental ingestion, consult your doctor or pharmacist immediately or call the Toxicological Information Service, phone 91 562 04 20, indicating the medication and the amount ingested. Do it even when you do not observe any discomfort or signs of intoxication. Bring the Serdolect package with you if you go to the doctor or hospital.
If you forgot to take Serdolect
Do not take a double dose to compensate for the missed doses.
If you forget to take your daily dose, contact your doctor. Your doctor will indicate how to continue your treatment correctly.
If you interrupt Serdolect treatment
Do not stop taking Serdolect without your doctor's permission, even if you start feeling better. The underlying disease may persist for a long time. If you interrupt your treatment too soon, your symptoms may return and involuntary movements may also occur.
Your doctor will advise you on how and when to stop your treatment to avoid the unpleasant symptoms that may occur. If you stop taking Serdolect abruptly, you may experience discontinuation symptoms such as:
If you have any other doubts 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.
Contact your doctor or hospital immediately if you have any of the side effects mentioned in the following 4 points:
Rare: may affect up to 1 in 100 people
These symptoms may indicate life-threatening irregular heartbeats.
This could indicate a nervous system disorder called tardive dyskinesia
Uncommon: may affect up to 1 in 1,000 people
These symptoms may indicate a life-threatening nervous disorder called neuroleptic malignant syndrome.
Unknown: the frequency cannot be estimated from available data
Other possible side effects that may occur with the following frequencies are:
Very common: may affect more than 1 in 10 people
Common: may affect up to 1 in 10 people
Rare:may affect up to 1 in 100 people:
In elderly patients with dementia, a small increase in the number of deaths in patients taking antipsychotics has been reported, compared to those not taking them.
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 Pharmacovigilance of Medicines for Human Use: http;//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.
Store in the original packaging to protect it from light.
Medications should not be disposed of through drains or trash. Dispose of 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 unused packaging and medications. By doing so, you will help protect the environment.
Composition of Serdolect
The active ingredient is sertindol.
Each film-coated tablet contains 16 mg of sertindol.
The other components are:
Appearance of the product and contents of the package
Serdolect 16 mg is presented in the form of film-coated tablets.
The tablets are dark pink, oval, rounded on the upper and lower faces, marked with the letters “S16” on one face.
Serdolect 16 mg is presented in packages of 7, 10, 14, 20, 28, 30, 50, 98 or 100 tablets
Only some package sizes may be commercially available.
Holder of the marketing authorization and responsible for manufacturing
H. Lundbeck A/S
Ottilliavej, 9
2500 Valby
Denmark
Phone: +45 3630 1311
You can request more information about this medication by contacting the local representative of the marketing authorization holder:
Local Representative:
Lundbeck España, S.A.
Av. Diagonal, 605
08028 Barcelona
(Spain)
This medication is authorized in the following member states of the EU/European
Economic Area with the following names:
Member state name | Medication name |
Austria | Serdolect |
Belgium | Serdolect |
Bulgaria | Serdolect |
Czech Republic | Serdolect |
Croatia | Serdolect |
Denmark | Serdolect |
Estonia | Serdolect |
Finland | Serdolect |
Germany | Serdolect |
Greece | Serdolect |
Hungary | Serdolect |
Iceland | Serdolect |
Latvia | Serdolect |
Luxembourg | Serdolect |
Netherlands | Serdolect |
Norway | Serdolect |
Poland | Serdolect |
Romania | Serdolect |
Slovakia | Serdolect |
Spain | Serdolect |
Sweden | Serdolect |
This leaflet was approved in April 2021
For detailed and updated information about this medication, please visit the website of the Spanish Agency for Medicines and Medical Devices (AEMPS)http://www.aemps.gob.es.
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