


Ask a doctor about a prescription for TRAZODONE STADAFARMA 100 mg TABLETS
Package Leaflet: Information for the Patient
Trazodone Stadafarma 50 mg Tablets EFG
Trazodone Stadafarma 100 mg Tablets EFG
Trazodone Stadafarma 150 mg Tablets EFG
Trazodone Hydrochloride
Read all of this leaflet carefully before you start taking this medicine because it contains important information for you.
Contents of the pack
This medicine contains the active ingredient trazodone hydrochloride. It belongs to a group of medicines called antidepressants.
Trazodone is used to treat symptoms of depression (major depressive episodes) in adults.
Do not take Trazodone Stadafarma if
Warnings and precautions
Suicidal thoughts and worsening of your depression
If you are depressed, you may sometimes have thoughts of harming or killing yourself. These may increase when you first start taking antidepressants, as all these medicines take time to work, usually around two weeks, but sometimes longer.
You are more likely to think this way if:
If you have thoughts of harming or killing yourself at any time, contact your doctor or go to a hospital immediately.
It may be helpful to tell a relative or close friend that you are depressed and ask them to read this leaflet. You might ask them to tell you if they think your depression or anxiety is getting worse, or if they are worried about changes in your behavior.
Liver problems
Severe liver disorders have been reported with the use of trazodone. If you experience any of the following symptoms, you should contact your doctor immediately:
Consult your doctor or pharmacist before taking trazodona if you:
Severe liver disorders have been reported with the use of trazodone, with a possible fatal outcome.
Stop taking trazodone and talk to your doctor immediately if you experience yellowing of the skin or the whites of your eyes (jaundice) or signs such as asthenia, anorexia, nausea, vomiting, abdominal pain (see section 4 "Possible side effects").
If you have schizophrenia or other psychotic disorders, the administration of antidepressants may result in a possible worsening of psychotic symptoms. Paranoid thoughts may intensify. During therapy with trazodone, a depressive phase may change from a manic-depressive psychosis to a manic phase. In that case, the use of trazodone should be discontinued.
If you have a sore throat, fever or flu-like symptoms while taking trazodone, you should talk to your doctor immediately. In these cases, it is recommended to check your blood as agranulocytosis, a blood disorder, may be revealed clinically with these symptoms.
Caution is recommended when using trazodone with other medicines known to prolong the QT interval or increase the risk of serotonin syndrome/neuroleptic malignant syndrome (see "Other medicines and Trazodone Stadafarma" and section 4 "Possible side effects").
Elderly patients
If you are elderly, you may experience dizziness and lightheadedness when standing up or stretching. You may also feel more sleepy or drowsy than usual.
Greater caution is advised if you suffer from other diseases and are taking medicines to treat them, along with taking trazodone.
Children and adolescents
Trazodone should not be used in children and adolescents under 18 years of age.
Other medicines and Trazodone Stadafarma
Tell your doctor or pharmacist if you are taking, have recently taken or might take any other medicines. This includes medicines that you buy without a prescription, including herbal medicines. This is because trazodone can affect the way other medicines work and vice versa.
Tell your doctor if you are taking any of the following medicines:
Anesthetics
If you are going to be given an anesthetic (for an operation), tell your doctor or dentist that you are taking trazodone.
Taking Trazodone Stadafarma with alcohol
You should avoid drinking alcohol while taking trazodone.
Pregnancy and breastfeeding
Pregnancy
If you are pregnant, think you may be pregnant or are planning to have a baby, ask your doctor for advice before taking this medicine.
Trazodone should not be taken during the first 3 months of pregnancy. Taking trazodone in the later stages of pregnancy may cause your baby to have withdrawal symptoms when born. In that case, your newborn will be monitored by a doctor.
Breastfeeding
If you are breastfeeding or plan to breastfeed, talk to your doctor or pharmacist before taking this medicine.
Driving and using machines
Trazodone may make you feel drowsy or dizzy. This can affect your eyesight and cause confusion. If this happens, do not drive or use tools or machines.
Trazodone Stadafarma contains sodium
This medicine contains less than 23 mg of sodium (1 mmol) per tablet; this is, essentially “sodium-free”.
Always take trazodone exactly as your doctor has told you. Check with your doctor or pharmacist if you are not sure.
Adults
Depression
Elderly patients
In elderly or fragile patients, the initial dose will usually be 100 mg per day.
Children and adolescents
Trazodone should not be used in children and adolescents under 18 years of age.
Taking this medicine
Trazodone Stadafarma 50 mg Tablets EFG
The score line is not intended for breaking the tablet.
Trazodone Stadafarma 100 mg/ 150 mg Tablets EFG
The tablet can be divided into equal doses.
Duration of treatment
It will usually take 2 to 4 weeks before you start to feel better.
Your doctor will regularly reassess your dose depending on your condition and determine the need for continued maintenance treatment.
If you take more Trazodone Stadafarma than you should
In case of overdose or accidental ingestion, consult your doctor or pharmacist immediately or call the Toxicology Information Service, telephone 91 562 04 20, indicating the medicine and the amount ingested. You can also go to the emergency department of the nearest hospital. Bring the package so that the doctor knows what you have taken.
The following effects may occur: feeling sick or being sick, feeling drowsy, dizzy or faint, fits (seizures), confusion, breathing or heart problems.
If you forget to take Trazodone Stadafarma
If you forget to take a dose, take it as soon as you remember. However, if it is almost time for the next dose, do not take the missed dose. Do not take a double dose to make up for forgotten doses.
If you stop taking Trazodone Stadafarma
Continue taking trazodone until your doctor tells you to stop. Do not stop taking trazodone just because you feel better. When your doctor tells you that you can stop taking this medicine, they will help you gradually reduce the dose to avoid the risk of withdrawal symptoms, such as agitation, sleep disturbances, feeling sick, headache and feeling unwell.
If you have any further questions on the use of this product, ask your doctor or pharmacist.
Like all medicines, trazodone can cause side effects, although not everybody gets them.
Stop taking trazodone and consult a doctor or go to a hospital immediately if you experience any of the following side effects:
Frequency not known: cannot be estimated from the available data
Talk to your doctor immediately if you notice any of the following side effects:
Frequency not known: cannot be estimated from the available data
Other side effects:
Frequency not known: cannot be estimated from the available data
Reporting of side effects:
If you experience any side effects, talk to your doctor or pharmacist. This includes any possible side effects not listed in this leaflet. You can also report side effects directly to the Spanish Medicines Agency's Pharmacovigilance System for Human Use: https://www.notificaram.es. By reporting side effects, you can help provide more information on the safety of this medicine.
Keep this medicine out of the sight and reach of children.
Do not use this medicine after the expiry date which is stated on the carton and blister after “EXP”. The expiry date is the last day of the month stated.
This medicine does not require any special storage conditions.
Store in the original package to protect from light.
Medicines should not be disposed of via wastewater or household waste. Return any unused medicine to your pharmacist. Ask your pharmacist how to dispose of medicines no longer required. This will help to protect the environment.
Composition of Trazodona Stadafarma
Each Trazodona Stadafarma 50 mg tablet contains 50 mg of trazodone hydrochloride.
Each Trazodona Stadafarma 100 mg tablet contains 100 mg of trazodone hydrochloride.
Each Trazodona Stadafarma 150 mg tablet contains 150 mg of trazodone hydrochloride.
Microcrystalline cellulose
Sodium carboxymethyl starch (type A)
Pregelatinized corn starch
Anhydrous colloidal silica
Magnesium stearate
Product Appearance and Package Contents
Trazodona Stadafarma 50 mg tablets are white to off-white, round, biconvex tablets, 7.14 mm in diameter, engraved with "IT" and "I" on either side of the score line and smooth on the other side. The score line should not be used to divide the tablet.
Trazodona Stadafarma 100 mg tablets are white to off-white, round, biconvex tablets, 9.52 mm in diameter, engraved with "IT" and "II" on either side of the score line and smooth on the other side. The tablet can be divided into equal doses.
Trazodona Stadafarma 150 mg tablets are white to off-white, oval, flat tablets with beveled edges, 16.90 mm in length and 8.40 mm in width, engraved with "IT" and "III" on either side of the score line and smooth on the other side. The tablet can be divided into equal doses.
Packaging of 20, 30, 50, 60, 100 tablets and packaging of 20x1, 30x1, 50x1, 60x1, 100x1 tablets.
Only some package sizes may be marketed.
Marketing Authorization Holder and Manufacturer
Marketing Authorization Holder
Laboratorio STADA, S.L.
Frederic Mompou, 5
08960 Sant Just Desvern (Barcelona)
Spain
Manufacturer
Laboratori Fundació DAU
C/ C, 12-14, Pol. Ind. Zona Franca,
08040 Barcelona,
Spain
or
STADA Arzneimittel AG
Stadastrasse 2 – 18
61118 Bad Vilbel
Germany
This medicinal product is authorized in the Member States of the European Economic Area under the following names:
Germany: Trazodon STADA 50 mg Tabletten
Trazodon STADA 100 mg Tabletten
Trazodon STADA 150 mg Tabletten
Spain: Trazodona STADAFARMA 50 mg tablets EFG
Trazodona STADAFARMA 100 mg tablets EFG
Trazodona STADAFARMA 150 mg tablets EFG
Date of the last revision of this leaflet:June 2025
Detailed information on this medicinal product is available on the website of the Spanish Agency for Medicines and Health Products (AEMPS) (http://www.aemps.gob.es/)
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