PATIENT INFORMATION LEAFLET
Plantaben3,5 geffervescent powder
seed coat ofPlantago ovata(ispaghula husk)
Read this leaflet carefully before you start taking this medicinebecause it contains important information for you
Follow exactly the administration instructions contained in this leaflet or those given by your doctor or pharmacist or nurse.
- Ifyou experience any side effects, consult your doctor, pharmacist or nurse,even if they are not listed in this leaflet. See section 4.
Contents of the pack and additional information
Plantabenbelongs to a group of medications called:volume-forming laxatives. The active ingredient is the cuticles of the seeds of a plant called Plantago Ovata. These cuticles have a great capacity to retain liquid, increasing the volume of the fecal mass and giving it an adequate consistency to regulate intestinal transit.
Plantabenis used:
You should consult a doctor if it worsens or does not improve after 3 days.
Do not takePlantaben
Warnings and precautions
Consult your doctor, pharmacist, or nurse before starting to take Plantaben.
If you are a healthcare professional or caregiver who has handled products with Plantago ovata powder for a prolonged period, you may have become allergic to these products due to continuous inhalation. If symptoms (listed in section 4) are confirmed to be due to an allergic reaction, do not use this product (see section “Do not take Plantaben”).
During treatment, you should drink 1-2 liters of water per day. Ingestion of this product without adequate liquid may cause a blockage in the throat or esophagus.
This preparation should not be taken and then immediately laid down.
If abdominal pain, nausea, or vomiting occur, treatment will be interrupted and a doctor will be consulted.
Children and adolescents
It is not recommended for use in children under 6 years old.
Other medications and Plantaben
Inform your doctor or pharmacist that you are using, have used recently, or may need to use any other medication.
TakingPlantabenwith food and drinks and alcohol
The fiber can be taken before or after meals. If taken 30 minutes before meals, it may reduce appetite.
Pregnancy and lactation and fertility
If you are pregnant or breastfeeding, or think you may be pregnant, consult your doctor or pharmacist before using this medication.
The soluble fiber absorbs organic, inorganic, and mineral substances, so to avoid the risk of excessive elimination of these substances during pregnancy, it is recommended not to exceed the recommended doses in this prospectus or prescribed by your doctor.
Driving and operating machinery
No effects have been described that would affect the ability to drive or use hazardous machinery.
Plantaben contains sodium saccharin, sodium bicarbonate, and yellow-orange S (E-110) dye
This medication contains 178.36 mg of sodium (main component of table salt/for cooking) in each sachet. This is equivalent to 26.7% of the maximum daily sodium intake recommended for an adult.
Consult your doctor or pharmacist if you need Plantaben daily or for a prolonged period, especially if you have been advised to follow a low-sodium diet.
This medication may cause allergic reactions because it contains yellow-orange S (E-110) dye. It may cause asthma, especially in patients allergic to acetylsalicylic acid.
Follow exactly the administration instructions of themedication contained in this leaflet or thoseindicated by your doctor or pharmacist or nurse.In case of doubt, ask your doctor or pharmacist or nurse..
Plantaben is administered orally.
The recommended dose is:
Use in adults, elderly patients, and children over 12 years old:
2 to 3 sachets per day (equivalent to 7 –11 gof Ispaghula husk per day), as needed and response.
Use in children from6 to 12 years old:
1 to 2 sachets per day (equivalent to 3 –8 gof Ispaghula husk per day), as needed and response.
To ensure correct administration, it is recommended to empty the contents of the sachet into a glass of cold water or any other liquid (200 cc), shake the mixture until it is uniform, and drink immediately. It is recommended to drink another glass of liquid afterwards. Additionally, it is recommended to drinkfrom1 to 2 litersof water per day during treatment.
It should be taken in an upright position.
Do not take the preparation and lie down immediately afterwards
During the preparation of the product for administration, try to avoid inhaling the powder.
Remember to take your medicine.
Use in children and adolescents
It is not recommended for use in children under 6 years old.
If you take morePlantabenthan you should
In case of overdose or accidental ingestion, consult your doctor or pharmacist immediately or call the Toxicological Information Service, phone91 562 04 20indicating the medication and the amount ingested.
No symptoms of intoxication by overdose have been described, since the active components of this preparation are not absorbed.
However, in case of massive ingestion, symptomatic treatment will be performed. Overdose with Ispaghula may cause abdominal discomfort and flatulence and even intestinal obstruction. Adequate liquid intake should be maintained.
If you forgot to takePlantaben
Do not take a double dose to compensate for the missed doses.
If you have any other questions about the use of this medication, ask your doctor or pharmacist or nurse.
Like all medications, Plantaben may cause adverse effects, although not everyone will experience them.
The seeds of Plantago ovata contain substances that may cause allergic reactions after taking the medication orally, after contact with the skin, or, in the case of powder formulations, after inhalation.
Allergic symptoms may include nasal congestion, eye redness, difficulty breathing, skin reactions, itching, and in some cases, anaphylaxis (sudden and generalized allergic reaction that can cause life-threatening shock). People who frequently handle the powder formulations of the product are more prone to experiencing these reactions (See Section 2).
At the beginning of treatment and, depending on the dose, some discomforts such as flatulence (gas) and a feeling of fullness may appear, which disappear in a few days without the need to discontinue the medication.
In some cases, abdominal distension may appear.
If ingested without sufficient liquid, there may be a risk of intestinal or esophageal obstruction or fecal impaction (accumulation of hardened feces).
Reporting Adverse Effects
If you experience any type of adverse effect, consult your doctor, pharmacist, or nurse, even if it is a possible adverse 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 adverse effects, you can contribute to providing more information on the safety of this medication.
Keep this medication out of the sight and reach of children.
Do not usethis medicationafter the expiration date that appears on the packaging after CAD or EXP. The expiration date is the last day of the month indicated.
Medicinesshould not be thrownaway through the drains or in the trash. Dispose of thepackagingand themedicinesthat you no longer need at the SIGRE Pointof the pharmacy. If in doubt, ask your pharmacist how to dispose of thepackagingand themedicinesthat you no longer need. In this way, you will help to protect the environment.environment.
Composition ofPlantaben
The active principle is the seed coat ofPlantago ovata.Each sachet contains3.5 gof seed coat ofPlantago ovata.
The other components are: sodium saccharin, sodium bicarbonate, tartaric acid powder, orange essence, yellow-orange S (E-110) dye.
Appearance of the product and contents of the packaging
Plantaben is presented in boxes containing 30 sachets with5 gof effervescent powder, beige in color and orange-scented, for oral administration, once dispersed in water.
Holder of the marketing authorization
Cooper Consumer Health B.V.
Verrijn Stuartweg 60,
1112 AX Diemen,
Netherlands
Manufacturer responsible for the medicinal product
Rottapharm Ltd.
Damastown, Ind. Park, Mulhuddart, Dublin 15, Ireland.
You can request more information about this medicinal product by contacting the local representative of the marketing authorization holder:
Vemedia Pharma Hispania, S.A.
C/ Aragón, 182, 5th floor
08011 - Barcelona
Spain
Date of the last review of this leaflet: April 2023
The detailed information about this medicinal product is available on the website of the Spanish Agency for Medicines and Medical Devices (AEMPS) https://www.aemps.gob.es/
Have questions about this medication or your symptoms? Connect with a licensed doctor for guidance and personalized care.