


Ask a doctor about a prescription for ALMAGATO STADAPHARM 500 MG CHEWABLE TABLETS
Package Leaflet: Information for the User
Almagato Stadapharm 500 mg chewable tablets
Read this package leaflet carefully before starting to take this medicine, as it contains important information for you.
Follow the administration instructions of the medicine contained in this package leaflet or as indicated by your doctor, pharmacist, or nurse.
Contents of the Package Leaflet
Almagato Stadapharm belongs to a group of medicines called antacids, which are compounds that act by neutralizing excess stomach acid.
It is indicated for the relief and symptomatic treatment of heartburn and stomach acid in adults and adolescents.
You should consult a doctor if your symptoms worsen or do not improve after 14 days.
Do not take Almagato Stadapharm
Warnings and Precautions
Consult your doctor, pharmacist, or nurse before taking this medicine:
Tell your doctor if you experience any symptoms that may indicate digestive tract bleeding, such as vomiting blood or black stools.
Children and Adolescents
Antacids should not be given to children under 12 years old, as they may mask other existing diseases (e.g., appendicitis). In younger children, there is a risk of increased magnesium levels in the blood or aluminum toxicity, especially if they are dehydrated or have kidney disease.
Other Medicines and Almagato Stadapharm
Tell your doctor or pharmacist if you are taking, have recently taken, or may need to take any other medicine.
Antacids alter the absorption of many medicines, so, in general, the intake of Almagato Stadapharm 500 mg should be spaced out (2-3 hours) from the administration of any other medicine.
It is especially important to inform your doctor if you are taking any of the following medicines:
Anti-ulcer medicines (medicines for treating stomach ulcers or duodenal ulcers and heartburn, among others, e.g., cimetidine, famotidine, ranitidine)
Antipsychotics (medicines for treating behavioral disorders and psychiatric symptoms, e.g., chlorpromazine)
as this medicine may reduce the absorption of the aforementioned medicines due to changes in stomach conditions or the formation of poorly soluble complexes.
Consult your doctor if you are going to have a stomach composition analysis, as Almagato Stadapharm may alter the test results.
Pregnancy, Breastfeeding, and Fertility
If you are pregnant or breastfeeding, think you may be pregnant, or plan to become pregnant, consult your doctor or pharmacist before taking this medicine.
Pregnancy
Chronic or excessive use of Almagato Stadapharm should be avoided during pregnancy due to the risk of fetal/newborn disorders.
If you need prolonged treatment, consult your doctor, who will indicate the appropriate treatment.
If you are pregnant or think you may be pregnant, consult your doctor or pharmacist before taking any medicine. Taking medicines during pregnancy can be hazardous to the embryo or fetus and should be monitored by your doctor. |
Breastfeeding
Chronic or excessive use of medicines containing almagato should be avoided.
Although small amounts of aluminum and magnesium can be eliminated through breast milk in mothers treated with almagato, their concentration is not high enough to cause adverse effects in the infant.
Driving and Using Machines
Almagato Stadapharm does not affect your ability to drive or operate machinery.
Almagato Stadapharm 500 mg Chewable Tablets Contain Sulfites
This medicine may cause severe allergic reactions and bronchospasm (sudden feeling of suffocation) because it contains sulfites.
Follow the administration instructions of the medicine contained in this package leaflet or as indicated by your doctor, pharmacist, or nurse. If in doubt, ask your doctor or pharmacist or nurse.
Use in Adults and Adolescents:the recommended dose is 2 tablets (1 gram of almagato) three times a day, preferably 30 minutes to 1 hour after meals. If symptoms recur, another dose can be taken before bedtime.
Do not exceed 8 grams per day (16 tablets).
Use in Elderly Patients:no dose adjustment is necessary (see "Warnings and Precautions" section).
Use in Patients with Kidney Disease:if you have severe kidney failure, this medicine is not recommended (see "Warnings and Precautions" section).
If you have mild or moderate kidney disease, your doctor may recommend lower doses (see "Warnings and Precautions" section).
This medicine should be taken orally.
The tablets can be chewed or dissolved in the mouth.
If You Take More Almagato Stadapharm Than You Should
At the recommended doses, no intoxication with this medicine is expected. In patients with a low-phosphorus diet and/or prolonged treatment with high doses, a decrease in blood phosphate levels and insufficient bone mineralization may occur.
If you have taken more Almagato Stadapharm than you should, consult your doctor or pharmacist immediately, or call the Toxicology Information Service, phone 915 620 420, indicating the medicine and the amount taken.
If You Forget to Take Almagato Stadapharm
Do not take a double dose to make up for forgotten doses. Take the forgotten dose when you can if the time interval is small, or wait for the next dose, provided there are no symptoms, in which case you can take it before. Take the next doses with the indicated time interval between them.
If you have any other doubts about the use of this medicine, ask your doctor, pharmacist, or nurse.
Like all medicines, this medicine can cause side effects, although not everyone gets them.
Due to the low intestinal absorption, the side effects of almagato are rare. Occasionally (no data are available to estimate the frequency), diarrhea has been reported, which usually disappears after treatment is discontinued.
Reporting Side Effects
If you experience any side effects, consult your doctor, pharmacist, or nurse, even if they are not listed in this package leaflet. You can also report them directly through the Spanish Medicines Surveillance System for Human Use, Website: 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.
No special storage conditions are required.
Do not use this medicine after the expiration date stated on the package after CAD. The expiration date is the last day of the month indicated.
Medicines should not be disposed of through wastewater or household waste. Deposit the packages and medicines you no longer need in the pharmacy's SIGRE point. If in doubt, ask your pharmacist how to dispose of packages and medicines you no longer need. This will help protect the environment.
Composition of Almagato Stadapharm 500 mg Chewable Tablets
•The active ingredient is almagato. Each tablet contains 500 mg of almagato.
•The other ingredients are: mannitol (E-421), povidone (E-1201), potato starch, sodium saccharin, ammonium glycyrrhizate, magnesium stearate, and peppermint flavor (contains sulfites).
Appearance of the Product and Package Contents
Almagato Stadapharm is presented in the form of white, mint-flavored chewable tablets.
Each box contains 18, 24, 48, or 54 tablets.
Not all 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
GALENICUM HEALTH, S.L.U.
Sant Gabriel, 50
08950 Esplugues de Llobregat (Barcelona), Spain
or
SAG MANUFACTURING, S.L.U.
Ctra. N-I, km 36
28750 San Agustín de Guadalix, Madrid
Spain
Date of the Last Revision of this Package Leaflet:June 2024
Detailed information about 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 ALMAGATO STADAPHARM 500 MG CHEWABLE TABLETS – subject to medical assessment and local rules.