Ask a doctor about a prescription for ONDANSETRON ARISTO 4 mg ORALLY DISINTEGRATING TABLETS
PACKAGE LEAFLET: INFORMATION FOR THE USER
Ondansetron Aristo 4 mg oral lyophilisates EFG
Read all of this leaflet carefully before you start taking this medicine because it contains important information for you.Keep this leaflet, you may need to read it again.
-If you have any further questions, ask your doctor or pharmacist.
-This medicine has been prescribed for you only. Do not pass it on to others. It may harm them, even if their signs of illness are the same as yours.
-If you experience any side effects, talk to your doctor or pharmacist. This includes any possible side effects not listed in this leaflet.
Contents of the pack:
1 What is Ondansetron Aristo and what is it used for
2 What you need to know before you take Ondansetron Aristo
3 How to take Ondansetron Aristo
4 Possible side effects
5 Storing Ondansetron Aristo
6 Contents of the pack and other information
This medicine contains ondansetron, which belongs to a group of medicines called antiemetics that help improve the feeling of nausea and vomiting.
Ondansetron is used to treat nausea (feeling of discomfort) and vomiting (discomfort) caused by some medical treatments for cancer, such as chemotherapy (in adults and children), or radiotherapy (adults).
It is also used to prevent nausea and vomiting in patients after an operation (adults).
Do not take Ondansetron Aristo:
If you are allergic to Ondansetron or any of the other ingredients of this medicine (listed in section 6).
If you have had any allergic reaction (hypersensitivity) to other antiemetics (e.g. granisetron or dolasetron).
Warnings and precautions:
Be especially careful with Ondansetron Aristo:
IF YOU ARE GOING TO HAVE ANY DIAGNOSTIC TEST (INCLUDING BLOOD, URINE, SKIN TESTS THAT USE ALLERGENS, ETC.), TELL YOUR DOCTOR THAT YOU ARE TAKING THIS MEDICINE, AS IT MAY ALTER THE RESULTS.
Talk to your doctor if any of the above circumstances apply to you before starting treatment with Ondansetron Aristo.
Using Ondansetron Aristo with other medicines:
Ondansetron Aristo may have some effect on other medicines and other medicines may have some effect on ondansetron.
Tell your doctor or pharmacist if you are using, or have recently used, any other medicines, including those obtained without a prescription.
In particular, it is important to inform your doctor if you are taking any of the following medicines, as it may be necessary to adjust the dose:
Pregnancy and breastfeeding
Pregnancy:
Ondansetron Aristo should not be used during the first trimester of pregnancy. This is because Ondansetron Aristo may slightly increase the risk of a baby being born with a cleft lip and/or cleft palate (openings or gaps in the upper lip or palate). If you are already pregnant, think you may be pregnant, or are planning to become pregnant, tell your doctor before taking Ondansetron Aristo. If you are a woman of childbearing age, you are advised to use an effective contraceptive method.
Breastfeeding:
You should not breastfeed your child while being treated with ondansetron.
Ask your doctor or pharmacist for advice before taking any medicine.
Driving and using machines
Ondansetron is unlikely to affect your ability to drive or use machines.
Important information about some of the ingredients of Ondansetron Aristo:
This medicine contains sorbitol. If your doctor has told you that you have an intolerance to some sugars, consult them before taking this medicine.
This medicine may be harmful to people with phenylketonuria because it contains aspartame, which is a source of phenylalanine.
This medicine may cause severe allergic reactions and bronchospasm (sudden feeling of suffocation) because it contains sulfur dioxide.
Follow the instructions for administration of this medicine exactly as indicated by your doctor. If in doubt, ask your doctor or pharmacist.
Ondansetron oral lyophilisates should be taken orally. The tablet dissolves quickly in the mouth and can then be swallowed in the usual way. Drink a glass of water afterwards.
Important: Do not remove Ondansetron oral lyophilisates from the blister or aluminum until you are ready to take it.
Treatment of nausea and vomiting (nausea and vomiting) in patients who are going to receive chemotherapy or
radiotherapy:
Adults (including elderly)
The usual dose is 8 mg of Ondansetron 1-2 hours before chemotherapy or radiotherapy, followed by 8 mg of ondansetron 12 hours later. In order to protect against delayed nausea, or additional nausea, treatment may be continued with a dose of 8 mg of Ondansetron twice a day for 5 days after treatment.
Treatment of nausea and vomiting (nausea and vomiting) in patients who are going to receive chemotherapy:
Children (6 months or older) and adolescents (under 18 years):
Your doctor will decide what dose of Ondansetron is suitable. This will depend on the size and weight of the child.
To prevent nausea and vomiting after surgery:
Adults: The usual dose is 16 mg before surgery or one 8 mg tablet one hour before surgery. And then, another 8 mg tablet eight hours after the first dose and another 8 mg tablet eight hours after the second dose.
The effect of the ondansetron oral lyophilisates starts one to two hours after taking the corresponding dose.
If you vomit during the hour after taking the 8 mg dose: take another 8 mg tablet, but do not take more ondansetron oral lyophilisates than indicated in this leaflet.
Patients with liver problems: The total daily dose should not be more than 8 mg.
If you take more Ondansetron Aristo than you should:
If you or your child take more ondansetron than you should, talk to a doctor or go to the nearest hospital immediately. Bring the medicine with you.
If you have taken Ondansetron Aristo more than you should, consult your doctor or pharmacist or the Toxicology Information Service, telephone 915620420, indicating the medicine and the amount taken.
In case of overdose, the symptoms that may appear are: vision problems, low blood pressure (which can cause dizziness or fainting) and palpitations (irregular or rapid heartbeat).
If you forget to take Ondansetron Aristo:
If you forget a dose, take it when you remember, unless it is almost time for the next dose. Do not take a double dose to make up for forgotten doses.
If you stop taking Ondansetron Aristo
Do not stop taking ondansetron without talking to your doctor, even if you feel better. If you have any further questions on the use of this product, ask your doctor or pharmacist.
Like all medicines, Ondansetron Aristo can cause side effects, although not everybody gets them.
If any of the following symptoms appear soon after taking Ondansetron Aristo, stop taking the medicine and inform your doctor immediately.
Ondansetron side effects:
If you are unsure about the side effects, talk to your doctor. If you think any side effect is serious or have noticed any side effects not mentioned in this leaflet, tell your doctor or pharmacist.
Very common side effects: in more than 1 in 10 patients treated
Common side effects: up to 1 in 10 patients treated:
Uncommon side effects: up to 1 in 100 patients treated
Rare side effects: up to 1 in 1,000 patients treated
Very rare side effects: less than 1 in 10,000 patients treated
Frequency not known: cannot be estimated from the available data
If you think any side effect is serious or have noticed any side effects not mentioned in this leaflet, tell your doctor or pharmacist.
Keep this medicine out of the sight and reach of children.
Store in the original package
Do not use this medicine after the expiry date which is stated on the carton. The expiry date is the last day of the month stated.
Medicines should not be disposed of via wastewater or household waste. Ask your pharmacist how to dispose of medicines no longer required. This will help protect the environment.
Composition of Ondansetron Aristo
The active substance is Ondansetron. Each tablet contains 4 mg of ondansetron.
The other ingredients are: PharmaburstTM C1 (a compound of mannitol, sorbitol, crospovidone, and colloidal silicon dioxide), Microcrystalline cellulose, Crospovidone type B, Aspartame, Strawberry flavor (a compound of identical natural flavoring substances, natural flavoring substances, natural flavoring preparations, corn starch dextrin, maltodextrin, Gum arabic E414, Sulfur dioxide E220, Flavor), Fumaric acid and sodium, Magnesium stearate.
Appearance of the product and contents of the pack
Ondansetron Aristo are white, flat, round, and beveled oral lyophilisates.
Ondansetron Aristo 4 mg is presented in aluminum/aluminum blisters. It is presented in packs containing 10 and 500 oral lyophilisates.
Not all pack sizes may be marketed.
Marketing authorization holder and manufacturer
Marketing authorization holder:
Aristo Pharma Iberia, S.L.
C/ Solana, 26
28850, Torrejón de Ardoz
Madrid – Spain
Manufacturer:
Sofarimex Industria Química e Farmaceutica Lda
Av. Indústrias, Alto do Colaride, Agualva-2735-213, Cacém
Portugal
or
MPF B.V.
Applehof 13, 8465 RX, Heerenveen (Ouderhaske)
Netherlands
or
Laboratorios de Medicamentos Internacionales, S.A. (Medinsa)
c/ Solana, 26
28850 – Torrejón de Ardoz, Madrid
Spain
Date of last revision of this leaflet: February 2022
Detailed and updated information on this medicine is available on the website of the Spanish Agency for Medicines and Health Products (AEMPS) http://www.aemps.gob.es/
Discuss dosage, side effects, interactions, contraindications, and prescription renewal for ONDANSETRON ARISTO 4 mg ORALLY DISINTEGRATING TABLETS – subject to medical assessment and local rules.