Background pattern

Zolmitriptan flas teva-ratio 2,5 mg comprimidos bucodispersables efg

About the medication

Introduction

Leaflet: information for the user

Zolmitriptán Flas Teva-ratio 2.5 mg orally disintegrating tablets EFG

Zolmitriptán

Read this leaflet carefully before you start taking this medicine, because it contains important information for you.

-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 only, and you must not give it to others even if they have the same symptoms as you, as it may harm them.

-If you experience any side effects, consult your doctor or pharmacist, even if they are not listed in this leaflet. See section 4.

1. What is Zolmitriptán Flas Teva-ratio and what is it used for

Zolmitriptán Flas Teva-ratio belongs to a group of medicines called triptans.

Zolmitriptán Flas Teva-ratio is used to treat migraine headache.

  • The symptoms of a migraine may be caused by a dilation (widening) of the blood vessels in the head. Zolmitriptán Flas Teva-ratio reduces the dilation of these blood vessels. This helps the disappearance of the headache pain and other symptoms of a migraine attack, such as nausea, vomiting, and sensitivity to light and sound.
  • Zolmitriptán Flas Teva-ratio will not prevent a migraine attack from occurring, it is only effective when a migraine attack has started.

2. What you need to know before starting to take Zolmitriptán Flas Teva-ratio

Do not take Zolmitriptán Flas Teva-ratio

  • if you are allergic (hypersensitive) to the active ingredient zolmitriptán or to any of the other components of this medicine(listed in section 6)
  • if you have high blood pressure.
  • if you have had any heart problems, including heart attack, angina (chest pain caused by exercise or effort), Prinzmetal's angina (chest pain that occurs at rest) or have experienced symptoms that may be related to the heart such as shortness of breath or pressure on the chest.
  • if you have had a stroke (cerebrovascular accident) or symptoms of short duration similar to a stroke (transient ischemic attack or TIA).
  • if you have severe kidney problems.
  • if you are already taking other medicines for migraine (for example ergotamine or ergot-type medicines such as dihydroergotamine and methysergide) or other medicines for migraine in the same group as zolmitriptán. For additional information, see the next section: “Use of other medicines”.

If you are unsure whether any of this applies to you, consult your doctor or pharmacist.

Warnings and precautions

Before starting treatment with Zolmitriptán Flas Teva-ratio, inform your doctor:

  • if you are at risk of suffering from ischemic heart disease (insufficient blood flow to the heart arteries). The risk is higher if you smoke, have high blood pressure, high cholesterol levels, diabetes or if a family member has ischemic heart disease.
  • if you have been told that you have Wolff-Parkinson-White syndrome (a type of abnormal heart rhythm).
  • if you have ever had liver problems.
  • if you have headaches other than your usual migraine headache.
  • if you are taking any medicine for depression.

If you go to a hospital, you must inform your doctor or healthcare staff that you are taking Zolmitriptán Flas Teva-ratio.

Zolmitriptán Flas Teva-ratio is not recommended for people under 18 years or over 65 years.

Like other treatments for migraine, excessive use of Zolmitriptán Flas Teva-ratio may cause daily headaches or worsening of your migraine headaches. Consult your doctor if you think this is the case. You may need to stop using Zolmitriptán Flas Teva-ratio to correct the problem.

Use of Zolmitriptán Flas Teva-ratio with other medicines

Inform your doctor or pharmacist if you are taking, have taken recently or may need to take any other medicine. This includes herbal remedies and medicines that you buy without a prescription.

Especially inform your doctor if you are taking any of the following medicines:

Migraine medicines

  • Other triptans, different from zolmitriptán: leave 24 hours before taking Zolmitriptán Flas Teva-ratio
  • Ergotamine or ergot-type medicines (such as dihydroergotamine or methysergide):

- Leave 24 hours before taking Zolmitriptán Flas Teva-ratio after taking ergotamine or ergot-type medicines.

- Leave 6 hours before taking ergotamine or ergot-type medicines after taking Zolmitriptán Flas Teva-ratio

Depression medicines

  • Moclobemide or fluvoxamine.
  • Medicines called SSRIs (selective serotonin reuptake inhibitors) such as paroxetine or citalopram.
  • Medicines called SNRIs (serotonin and norepinephrine reuptake inhibitors) such as venlafaxine, duloxetine.

Other medicines

  • Cimetidine (for indigestion or stomach ulcers).
  • Antibiotics in the quinolone group (such as ciprofloxacin).

If you are using herbal remedies that contain St. John's Wort (Hypericum perforatum), you may increase the risk of adverse effects of Zolmitriptán Flas Teva-ratio

Use of Zolmitriptán Flas Teva-ratio with food and drinks

You can take Zolmitriptán Flas Teva-ratio with or without food. This does not affect how Zolmitriptán Flas Teva-ratio works.

Pregnancy and breastfeeding

If you are pregnant or breastfeeding, consult your doctor or pharmacist before using this medicine.

We do not know if taking Zolmitriptán Flas Teva-ratio during pregnancy is harmful. Inform your doctor if you are pregnant or trying to become pregnant.

Avoid breastfeeding within 24 hours of taking zolmitriptán.

Driving and operating machinery

This medicine, like migraine, can cause drowsiness. If you experience these effects, avoid driving or operating machinery as it may be hazardous.

During a migraine crisis, your reactions may be slower than usual. Take this into account when driving or using tools or machinery.

Zolmitriptán Flas Teva-ratio contains aspartame (E 951)

This medicine contains 0.90 mg of aspartate in each buccal tablet.

Aspartame contains a source of phenylalanine that may be harmful in the case of phenylketonuria (PKU), a rare genetic disease in which phenylalanine accumulates because the body is unable to eliminate it correctly.

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3. How to Take Zolmitriptán Flas Teva-ratio

Follow exactly the administration instructions for this medication as indicated by your doctor or pharmacist. If in doubt, consult your doctor or pharmacist again.

You can take Zolmitriptán Flas Teva-ratio as soon as the migraine headache or migraine crisis begins. You can also take it once the crisis has started.

The usual dose is one tablet (2.5 mg).

- Separate the aluminum foil and carefully remove the tablet. Do not push the tablet through the aluminum foil.

- Place the tablet on the tongue, where it will dissolve, and swallow it with saliva. It is not necessary to drink water to swallow the tablet.

- You can take another tablet after two hours if the migraine still persists or if it reappears within 24 hours.

If the tablets do not provide sufficient relief for your migraine, inform your doctor. Your doctor may increase the dose to 5 mg or change your treatment. Do not use more than the dose prescribed.

Do not use more than two doses in a day. If you have been prescribed the 2.5 mg tablet, the maximum daily dose is 5 mg.

If you take more Zolmitriptán Flas Teva-ratio than you should

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.

Like other migraine treatments, excessive use of Zolmitriptán Flas Teva-ratio may cause daily headaches or worsening of migraine headaches. Consult your doctor if you think this is the case. You may need to stop taking Zolmitriptán Flas Teva-ratio to correct the problem.

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

4. Possible Adverse Effects

Like all medicines, Zolmitriptán Flas Teva-ratio may cause side effects, although not everyone will experience them.

Some of the side effects listed below may be symptoms of the migraine itself.

Frequent side effects (may affect up to 1 in 10 people)

  • Abnormal tactile sensations, such as tingling in the fingers of the hands and feet or sensitive skin.
  • Sensation of drowsiness, dizziness, or heat.
  • Headache.
  • Irregular heartbeat.
  • Nausea, vomiting.
  • Stomach pain.
  • Dry mouth.
  • Muscle weakness or muscle pain.
  • Sensation of weakness.
  • Weight, tension, pain, or pressure in the throat, neck, arms, and legs, or chest.
  • Difficulty swallowing.

Less frequent side effects (may affect up to 1 in 100 people)

  • Very rapid heartbeat.
  • Slightly higher blood pressure.
  • Increased urine production or the number of times you need to urinate.

Rare side effects (may affect up to 1 in 1,000 people)

  • Allergic reactions (hypersensitivity), including hives and swelling of the face, lips, mouth, tongue, and throat. If you think Zolmitriptán Flas Teva-ratio is causing an allergic reaction,stop taking it and contact your doctorimmediatelywith your doctor.

Very rare side effects (may affect up to 1 in 10,000 people)

  • Angina (chest pain, often caused by exercise), heart attack, or coronary artery spasm. If you experience chest pain or difficulty breathing after taking Zolmitriptán Flas Teva-ratio,stop taking it and contact your doctor.
  • Intestinal vessel spasm that may damage your intestine. You may experience stomach pain or bloody diarrhea. If this occurs,contact your doctor and do not take any more Zolmitriptán Flas Teva-ratio.

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 prospectus. You can also report them directly through the Spanish System for Pharmacovigilance of Medicines for Human Use: https://www.notificaram.es. By reporting side effects, you can contribute to providing more information on the safety of this medicine.

5. Conservation of Zolmitriptán Flas Teva-ratio

Keep this medication out of the sight and reach of children.

Do not useZolmitriptán Flas Teva-ratioafter the expiration date that appears on the packaging. The expiration date is the last day of the month indicated.

Do not store at a temperature above30°C. Store in the original packaging.

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

6. Content of the container and additional information

Composition of Zolmitriptán Flas Teva-ratio

The active ingredient is zolmitriptan. Each buccal dispersible tablet contains 2.5 mg of active ingredient.

The other components are: mannitol (E-421), crospovidone, calcium silicate, aspartame (E-951), orange aroma, strawberry aroma, citric acid monohydrate, and magnesium stearate.

Appearance of Zolmitriptán Flas Teva-ratio and content of the container

The buccal dispersible tablets of Zolmitriptán Flas Teva-ratio are white, flat-faced, and round.

Zolmitriptán Flas Teva-ratio is available in aluminum blister packs containing 2, 6, or 12 (6x2) buccal dispersible tablets.

Only some container sizes may be marketed.

Other presentations

Zolmitriptán Flas Teva-ratio 5 mg buccal dispersible tablets: containers of 2, 6, or 12 (6 x2) tablets.

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.

28108 Alcobendas (Madrid)

Responsible for manufacturing

Neuraxpharm Pharmaceuticals, S.L.

Avda. Barcelona 69

08970 Sant Joan Despí

Barcelona – Spain

Last review date of this leaflet: December 2021

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/)

You can access detailed and updated information about this medicine by scanning the QR code included in the carton with your smartphone. You can also access this information at the following internet address: https://cima.aemps.es/cima/dochtml/p/74379/P_74379.html

Country of registration
Active substance
Prescription required
Yes
Manufacturer
Composition
Manitol (e-421) (72,80 mg mg), Aspartamo (e-951) (0,90 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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