Package Insert: Information for the Patient
Omeprazol Sandoz Care 20 mg Hard Gastroresistant Capsules
Read this package insert carefully before starting to take this medicine, as it contains important information for you.
Follow exactly the administration instructions for the medicine contained in this package insert or those indicated by your doctor or pharmacist.
6. Contents of the pack and additional information
Omeprazol Sandoz Care hard-gastrorresistant capsules contain omeprazole as the active ingredient. It belongs to a group of medicines called "proton pump inhibitors". These medicines act by reducing the amount of acid produced by the stomach.
Omeprazole is indicated in adults for the short-term treatment of symptoms of reflux (for example, heartburn, acid regurgitation).
Reflux is the backflow of acid from the stomach into the esophagus, which can become inflamed and painful. This can cause symptoms such as a burning sensation in the chest that rises up to the throat (heartburn) and a sour taste in the mouth (acid regurgitation).
You may need to take the capsules for 2-3 consecutive days to achieve an improvement in symptoms.
You should consult a doctor if symptoms worsen or do not improve after 14 days.
Do not take Omeprazol Sandoz Care
Do not take this medicine if you are in any of the above situations. If you are unsure, talk to your doctor or pharmacist before taking Omeprazol Sandoz Care.
Warnings and precautions
Consult your doctor or pharmacist before starting to take omeprazole.
Do not take omeprazole for more than 14 days without consulting your doctor. If you do not experience relief, or if you feel that your symptoms are worsening, consult your doctor.
Severe skin reactions, including Stevens-Johnson syndrome, toxic epidermal necrolysis, drug reaction with eosinophilia and systemic symptoms (DRESS), and acute generalized pustular psoriasis (AGPP), have been reported in association with omeprazole treatment. Stop taking omeprazole and consult your doctor immediately if you experience any of these symptoms related to severe skin reactions described in section 4.
Omeprazole may mask the symptoms of other diseases. Therefore, consult your doctor immediately if you experience any of the following symptoms before starting to take omeprazole or during treatment:
If you experience a skin rash, especially in sun-exposed areas, consult your doctor as soon as possible, as it may be necessary to interrupt omeprazole treatment. Remember to mention any other symptoms you may notice, such as joint pain.
Omeprazole may cause kidney inflammation. Signs and symptoms may include decreased urine volume or blood in the urine and/or hypersensitivity reactions such as fever, skin rash, and joint stiffness. Inform your doctor of these signs.
Patients should not take omeprazole as preventive medication.
Other medicines and Omeprazol Sandoz Care
Inform your doctor or pharmacist if you are taking, have taken recently, or may need to take any other medicine, including those purchased without a prescription. Omeprazole may affect the mechanism of action of some medicines and some medicines may affect omeprazole.
Do not take omeprazole if you are taking a medicine withnelfinavir(used to treat HIV infection).
Inform your doctor or pharmacist if you are taking any of the following medicines:
Omeprazol Sandoz Care with food and drinks
See section 3.
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 using this medicine.
Omeprazole passes into breast milk but is unlikely to affect the baby when used in therapeutic doses. Your doctor will decideif you can take omeprazole if you arebreastfeeding.
Driving and operating machinery
Omeprazole is unlikely to affect your ability to drive or use tools or machines.
Severe side effects such as dizziness and visual disturbances (see section 4) may occur. If they do, you should not drive or use machines.
Omeprazol Sandoz Care contains saccharose and sodium
If your doctor has told you that you have an intolerance to certain sugars, consult with them before taking this medicine.
This medicine contains less than1 mmolof sodium (23 mg) per capsule; it is essentially “sodium-free”.
Follow exactly the medication administration instructions contained in this leaflet or those indicated by your doctor or pharmacist.In case of doubt, ask your doctor or pharmacist.
The recommended dose is one 20 mg capsule once a day for 14 days. Contact your doctor if symptoms do not disappear after this time.
You may need to take the capsules for 2-3 consecutive days to achieve an improvement in symptoms.
How to take this medication
What to do if you have difficulty swallowing the capsules
What to do if you take more Omeprazol Sandoz Care than you should
In case of overdose or accidental ingestion, consult your doctor or pharmacist immediately or call the Toxicological Information Service, phone: 91 562 04 20, indicating the medication and the amount ingested.
What to do if you forget to take Omeprazol Sandoz Care
If you forget to take a dose, take it as soon as you remember. However, if there is little time left for the next dose, skip the missed dose. Do not take a double dose to compensate for the missed doses.
What to do if you interrupt treatment with Omeprazol Sandoz Care
Do not stop treatment with omeprazole without first speaking with your doctor or pharmacist.
If you have any other doubts about the use of this medication, ask your doctor or pharmacist.
If you experience any of the following rare (may affect up to 1 in 1,000 people) or very rare (may affect up to 1 in 10,000 people) but serious side effects, stop taking omeprazole and consult your doctor immediately:
Other side effects are:
Frequent side effects (may affect up to 1 in 10 people):
Less frequent side effects (may affect up to 1 in 100 people):
Rare side effects (may affect up to 1 in 1,000 patients/people):
Very rare side effects (may affect up to 1 in 10,000 patients/people):
Side effects of unknown frequency (cannot be estimated from available data):
In very rare casesomeprazolemay affect white blood cells in the blood and cause
immunodeficiency. If you experience an infection with symptoms such as fever with a verypoorgeneral condition or fever with local infection symptoms, such as neck pain, throat pain, or mouth pain ordifficulty urinating, you should consult your doctor as soon as possible to perform a blood test and rule out a lack of white blood cells (agranulocytosis). It is essential that at thatmoment you provide information about the medication you are taking.
Do not worry about this list of possible side effects. You may not experience any of them. Ifyou consider any of the side effects you are experiencing to be serious or if you experience any side effectsnot mentioned in this prospectus, inform your doctor or pharmacist.
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 the Pharmacovigilance of Medicinal Products for Human Use:http://www.notificaram.es. By reporting side effects, you can contribute to providing more information about the safety of this medication.
Keep this medication out of the sight and reach of children.
Do not use this medication after the expiration date that appears on the packaging after CAD/EXP. The expiration date is the last day of the month indicated.
BlisterAluminum/Aluminum:
Store in the original packaging to protect it from moisture.
Store below 30 °C.
HDPE plastic containerwith screw cap and silica gel desiccant:
Store below 25 °C.
Keep the container perfectly closed to protect it from moisture.
After opening the containeruse within the first 3 months.
Medicines should not be disposed of through drains or in the trash.
Deposit the containers and medicines you no longer need at the SIGREpoint of your usual pharmacy. Ask your pharmacist how to dispose of the containers and medicines you no longer need. By doing so, you will help protect the environment.
Composition of Omeprazol Sandoz Care
Appearance of the product and contents of the packaging
Yellow opaque hard gastro-resistant capsulecontaining white to cream-colored spherical microgranules.
Alu/Alu blister: 7, 14 capsules.
HDPE container with desiccant gel in the polypropylene lid: 7, 14 capsules.
Only some packaging sizes may be commercially marketed.
Marketing authorization holder and responsible manufacturer
Marketing authorization holder:
Sandoz Farmacéutica, S.A.
Centro Empresarial Parque Norte
Edificio Roble
C/ Serrano Galvache, 56
28033 Madrid
Spain
Responsible manufacturer:
Laboratorio Liconsa, S.A
Av. Miralcampo nº7,
Polígono Industrial Miralcampo
19200 Azuqueca de henares (Guadalajara)
Spain
Last review date of this leaflet:July 2024
The detailed information of this medicine is available on the website of the Spanish Agency for Medicines and Medical Devices (AEMPS) http://www.aemps.gobes
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