Omeprazole Davur 10 mg gastro-resistant hard capsules

Spain
Brand name Omeprazole Davur 10 mg gastro-resistant hard capsules
Form capsules, hard, enteric-coated
Active substance / Dosage
OMEPRAZOLE · 10,00 mg
Prescription type Prescription Only Medicine
Registration number 65519
Omeprazole Davur 10 mg gastro-resistant hard capsules capsules, hard, enteric-coated

Package leaflet: Information for the user

Introduction

Package leaflet: information for the user

Omeprazol Davur 10 mg gastro-resistant hard capsules

Read the entire 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, ask your doctor or pharmacist.
  • This medicine has been prescribed for you only, and you should not give it to other people, even if they have the same symptoms as you, because it may harm them.
  • If you experience any adverse effects, consult your doctor or pharmacist, even if they are adverse effects not listed in this leaflet. See section 4.

Leaflet contents

  1. What Omeprazol Davur 10 mg is and what it is used for
  2. What you need to know before taking Omeprazol Davur 10 mg
  3. How to take Omeprazol Davur 10 mg
  4. Possible side effects
  5. How to store Omeprazol Davur 10 mg
  6. Contents of the pack and other information

1. What Omeprazol Davur 10 mg is and what it is used for

Omeprazol Davur contains the active substance omeprazole. It belongs to a group of medicines known as "proton pump inhibitors". These medicines work by reducing the amount of acid produced by the stomach.

Omeprazol Davur is used to treat the following conditions:

In adults:

  • Gastroesophageal reflux disease (GERD). In this disorder, stomach acid flows back into the esophagus (the tube connecting the throat to the stomach), causing pain, inflammation, and heartburn.
  • Ulcers in the upper part of the intestine (duodenal ulcer) or in the stomach (gastric ulcer).
  • Ulcers infected with a bacterium called "Helicobacter pylori". If you have this condition, your doctor may also prescribe antibiotics to treat the infection and allow the ulcer to heal.
  • Ulcers caused by a group of medicines called NSAIDs (non-steroidal anti-inflammatory drugs). Omeprazole may also be used to prevent the formation of ulcers if you are taking NSAIDs.
  • Excess stomach acid caused by a tumor in the pancreas (Zollinger-Ellison syndrome).

In children:

Children over 1 year of age and = 10 kg

  • Gastroesophageal reflux disease (GERD). In this disorder, stomach acid flows back into the esophagus (the tube connecting the throat to the stomach), causing pain, inflammation, and heartburn.

In children, symptoms of the disease may include regurgitation of stomach contents into the mouth, vomiting, and poor weight gain.

Children over 4 years of age and adolescents

Ulcers infected with a bacterium called "Helicobacter pylori". If your child has this condition, your doctor may also prescribe antibiotics to treat the infection and allow the ulcer to heal.

2. What you need to know before taking Omeprazol Davur 10 mg

Do not take Omeprazol Davur

  • if you are allergic to omeprazole or to any of the other components of this medicine (listed in section 6).
  • if you are allergic to medicines containing proton pump inhibitors (e.g. pantoprazole, lansoprazole, rabeprazole, esomeprazole).
  • if you are taking a medicine containing nelfinavir (used for HIV infection).

If you are unsure, talk to your doctor or pharmacist before taking omeprazole.

Warnings and precautions

Talk to your doctor or pharmacist before taking omeprazole.

Omeprazole may mask symptoms of other diseases. Therefore, if you experience any of the following conditions before starting omeprazole or during treatment, consult your doctor immediately:

  • You lose weight significantly without reason and have difficulty swallowing.
  • You have stomach pain or indigestion.
  • You start vomiting food or vomiting blood.
  • Your bowel movements are black (blood-stained stools).
  • You have severe or persistent diarrhoea, as omeprazole has been associated with a slight increase in infectious diarrhoea.
  • You have severe liver problems.
  • If you have ever had a skin reaction after treatment with a medicine similar to omeprazole used to reduce stomach acid.
  • If you develop a skin rash, especially in areas of skin exposed to sunlight, consult your doctor as soon as possible, as it may be necessary to stop treatment with omeprazole. Remember to mention any other symptoms you may notice, such as joint pain.
  • You are scheduled to have a specific blood test (chromogranin A).

When taking omeprazole, kidney inflammation may occur. 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. You should report these signs to your treating doctor.

If you take omeprazole for a long period (more than 1 year), your doctor will likely perform periodic check-ups. You should report any new or unusual symptoms or circumstances during visits to your doctor.

If you are taking proton pump inhibitors such as omeprazole, especially for more than one year, there may be a slight increase in the risk of fractures of the hip, wrist, and spine. Inform your doctor if you have osteoporosis or are taking corticosteroids (which may increase the risk of osteoporosis).

Omeprazole may interfere with certain diagnostic tests (chromogranin A). To avoid such interference, omeprazole treatment should be discontinued at least five days before measurement.

This medicine may affect how your body absorbs vitamin B12, especially if you need to take it for a long time. Contact your doctor if you notice any of the following symptoms, which could indicate low vitamin B12 levels:

  • Extreme tiredness or lack of energy
  • Tingling sensations
  • Tongue pain or red, sore tongue, mouth ulcers
  • Muscle weakness
  • Vision changes
  • Memory problems, confusion, depression

Taking Omeprazol Davur with other medicines

Tell your doctor or pharmacist if you are using, have recently used, or might need to use any other medicines. Omeprazole may affect how some medicines work, and some medicines may affect omeprazole.

Do not take omeprazole if you are taking a medicine containing nelfinavir (used to treat HIV infection).

Inform your doctor or pharmacist if you are taking any of the following medicines:

  • Ketoconazole, itraconazole, posaconazole, or voriconazole (used to treat fungal infections)
  • Digoxin (used to treat heart problems)
  • Diazepam (used to treat anxiety, relax muscles, or in epilepsy)
  • Phenytoin (used in epilepsy). If you are taking phenytoin, your doctor will need to monitor you when starting or stopping omeprazole treatment
  • Medicines used to prevent blood clots, such as warfarin or other vitamin K antagonists. Your doctor will need to monitor you when starting or stopping omeprazole treatment
  • Rifampicin (used to treat tuberculosis)
  • Atazanavir (used to treat HIV infection)
  • Tacrolimus (used in organ transplantation)
  • St. John’s wort (Hypericum perforatum) (used to treat mild depression)
  • Cilostazol (used to treat intermittent claudication)
  • Saquinavir (used to treat HIV infection)
  • Clopidogrel (used to prevent blood clots (thrombi))
  • Erlotinib (used to treat cancer)
  • Methotrexate (a chemotherapy medicine used in high doses to treat cancer). If you are taking a high dose of methotrexate, your doctor will need to temporarily stop omeprazole treatment.

If your doctor has prescribed you antibiotics amoxicillin and clarithromycin in addition to omeprazole to treat ulcers caused by Helicobacter pylori infection, it is very important that you inform them about any other medicines you are taking.

Taking Omeprazol Davur with food and drinks

You may take your capsules with food or on an empty stomach.

Fertility, pregnancy and breastfeeding

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. Your doctor will decide whether you can take omeprazole during this time.

Omeprazole passes into breast milk, but is unlikely to affect the infant when therapeutic doses are used. Your doctor will decide whether you can take omeprazole while breastfeeding.

Driving and using machines

Omeprazole is unlikely to affect your ability to drive or use tools or machines. However, adverse effects such as dizziness and visual disturbances may occur (see section 4). If these occur, you should not drive or use machines.

Omeprazol Davur contains sucrose and sodium

This medicine contains sucrose. If your doctor has told you that you have an intolerance to certain sugars, consult with him before taking this medicine.

This medicine contains less than 1 mmol of sodium (23 mg) per capsule; this is essentially “sodium-free”.

3. How to take Omeprazol Davur 10 mg

Follow exactly the instructions for use of this medicine as given by your doctor or pharmacist. If in doubt, consult your doctor or pharmacist again.

Your doctor will tell you how many capsules to take and for how long. This will depend on your condition and your age.

The usual doses are indicated below.

Use in adults:

Treatment of GERD symptoms, such as heartburn and acid regurgitation:

  • If your doctor confirms you have mild esophageal damage, the usual dose is 20 mg once daily for 4–8 weeks. Your doctor may prescribe a dose of 40 mg for another 8 weeks if the esophagus has not yet healed.
  • Once the esophagus has healed, the usual dose is 10 mg once daily.
  • If you do not have esophageal damage, the usual dose is 10 mg once daily.

Treatment of ulcers in the upper intestine (duodenal ulcer):

  • The usual dose is 20 mg once daily for 2 weeks. Your doctor may prescribe the same dose for another 2 weeks if the ulcer has not yet healed.
  • If the ulcer does not heal completely, the dose may be increased to 40 mg once daily for 4 weeks.

Treatment of stomach ulcers (gastric ulcer):

  • The usual dose is 20 mg once daily for 4 weeks. Your doctor may prescribe the same dose for another 4 weeks if the ulcer has not yet healed.
  • If the ulcer does not heal completely, the dose may be increased to 40 mg once daily for 8 weeks.

Prevention of recurrence of stomach and duodenal ulcers:

  • The usual dose is 10 mg or 20 mg once daily. Your doctor may increase the dose to 40 mg once daily.

Treatment of stomach and duodenal ulcers caused by NSAIDs (non-steroidal anti-inflammatory drugs):

  • The usual dose is 20 mg once daily for 4–8 weeks.

Prevention of stomach and duodenal ulcers during NSAID treatment:

  • The usual dose is 20 mg once daily.

Treatment of ulcers caused by Helicobacter pylori infection and prevention of their recurrence:

  • The usual dose is 20 mg of omeprazole twice daily for one week.
  • Your doctor will also instruct you to take two antibiotics from the following: amoxicillin, clarithromycin, and metronidazole.

Treatment of excess stomach acid caused by a pancreatic tumor (Zollinger-Ellison syndrome):

  • The usual dose is 60 mg per day.
  • Your doctor will adjust the dose according to your needs and will also decide how long you need to take the medicine.

Use in children and adolescents:

Treatment of GERD symptoms, such as heartburn and acid regurgitation:

  • Children over one year of age weighing more than 10 kg may take omeprazole. The dose for children is based on body weight, and the doctor will determine the correct dose.

Treatment of ulcers caused by Helicobacter pylori infection and prevention of their recurrence:

  • Children over 4 years of age may take omeprazole. The dose for children is based on body weight, and the doctor will determine the correct dose.
  • Your doctor will also prescribe two antibiotics for your child: amoxicillin and clarithromycin.

How to take this medicine

  • It is recommended to take the capsules in the morning.
  • You may take your capsules with food or on an empty stomach.
  • Swallow the capsules whole with half a glass of water. Do not chew or crush the capsules, as they contain coated granules that prevent the medicine from breaking down due to stomach acid. It is important not to damage the granules.

What to do if you or your child have difficulty swallowing the capsules

  • If you or your child have difficulty swallowing the capsules:
    • Open the capsule and swallow the contents directly with half a glass of water, or pour the contents into a glass of still water, acidic fruit juice (e.g., apple, orange, or pineapple), or apple sauce.
    • Always shake the mixture well just before drinking (the mixture will not be clear). Then drink the mixture immediately or within 30 minutes.
    • To ensure you have taken all the medicine, fill the glass halfway with water, swirl well, and drink the water. The solid particles contain the medicine; do not chew or crush them.

If you take more Omeprazol Davur than you should

If you have taken more Omeprazol Davur than prescribed by your doctor, contact your doctor or pharmacist immediately. You may also call the Toxicology Information Service at telephone number 91 562 04 20, stating the medicine and the amount ingested.

If you forget to take Omeprazol Davur

If you forget to take a dose, take it as soon as you remember. However, if it is almost time for your next dose, skip the missed dose. Do not take a double dose to make up for forgotten doses.

If you stop treatment with Omeprazol Davur

Do not stop treatment with omeprazole without first talking to your doctor or pharmacist.

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

4. Possible adverse effects

Like all medicines, this medicine can cause adverse effects, although not everyone will experience them.

If you experience any of the following adverse effects, contact your doctor or go to hospital immediately:

  • Sudden wheezing, swelling of the lips, tongue, throat or body, skin rash, fainting or difficulty swallowing (severe allergic reaction). (rare)
  • Reddening of the skin with blistering or peeling. Severe blisters and bleeding in the lips, eyes, mouth, nose and genitals may also occur. This could be “Stevens-Johnson syndrome” or “toxic epidermal necrolysis”. (very rare)
  • Widespread rash, high temperature and swollen lymph nodes (DRESS syndrome or drug hypersensitivity syndrome). (rare)
  • A widespread red, scaly rash with bumps under the skin and blisters, accompanied by fever. Symptoms usually appear at the beginning of treatment (acute generalized exanthematous pustulosis). (rare)
  • Yellowing of the skin, dark urine and fatigue, which may be symptoms of liver problems. (rare)

Other adverse effects include:

Common adverse effects (may affect up to 1 in 10 people)

  • Headache
  • Stomach or intestinal problems: diarrhoea, stomach pain, constipation and gas (flatulence)
  • Nausea or vomiting
  • Benign stomach polyps

Uncommon adverse effects (may affect up to 1 in 100 people)

  • Swelling of the feet and ankles
  • Sleep disorders (insomnia)
  • Dizziness, tingling sensation, drowsiness
  • Sensation of spinning (vertigo)
  • Abnormalities in blood tests used to monitor liver function
  • Skin rash, hives and itching
  • General feeling of discomfort and lack of energy
  • Wrist, hip or spine fracture

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

  • Blood problems, such as a decrease in white blood cells or platelets. This may cause weakness or bruising and increase the likelihood of developing infections.
  • Allergic reactions, sometimes severe, including swelling of the lips, tongue and throat, fever and wheezing.
  • Low sodium levels in the blood. This may cause weakness, vomiting and cramps.
  • Restlessness, confusion or depression.
  • Taste disturbances.
  • Vision problems, such as blurred vision.
  • Sudden sensation of difficulty breathing (bronchospasm).
  • Dry mouth.
  • Inflammation inside the mouth.
  • Fungal infection called “candidiasis” affecting the intestine.
  • Liver problems, such as jaundice, which may cause yellowing of the skin, dark urine and fatigue.
  • Hair loss (alopecia).
  • Skin rash upon exposure to sunlight.
  • Joint pain (arthralgia) or muscle pain (myalgia).
  • Serious kidney problems (interstitial nephritis).
  • Increased sweating.

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

  • Blood count abnormalities, such as agranulocytosis (lack of white blood cells). Aggressiveness.
  • Seeing, feeling or hearing things that are not real (hallucinations).
  • Serious liver problems leading to liver failure and brain inflammation.
  • Erythema multiforme.
  • Muscle weakness.
  • Enlargement of the breasts in men.

In very rare cases, omeprazole may affect the white blood cells and cause immunodeficiency. If you develop an infection with symptoms such as fever accompanied by a severely unwell general condition, or fever with signs of local infection such as neck, throat or mouth pain, or difficulty urinating, you should consult your doctor as soon as possible for a blood test to rule out a deficiency in white blood cells (agranulocytosis). It is important that you inform your doctor about any medicines you are taking at this time.

Frequency not known (cannot be estimated from available data)

  • Inflammation in the intestine (causing diarrhoea).

  • If you are taking omeprazole for more than three months, magnesium levels in the blood may decrease. Low magnesium levels can cause fatigue, involuntary muscle contractions, disorientation, seizures, dizziness, and increased heart rate. If you experience any of these symptoms, consult your doctor immediately. Low magnesium levels may also lead to decreased levels of potassium and calcium in the blood. Your doctor may decide to perform periodic blood tests to monitor magnesium levels.

  • Skin rash, possibly with joint pain

Reporting of adverse effects:

If you experience any adverse effect, talk to your doctor or pharmacist, even if it is not listed in this leaflet. You can also report them directly via the Spanish Pharmacovigilance System for Human Medicines: http://www.notificaram.es. By reporting adverse effects, you can help provide more information on the safety of this medicine.

5. Storage of Omeprazole Davur 10 mg

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

Do not use this medicine after the expiry date stated on the container after EXP. The expiry date is the last day of the month indicated.

Store below 30°C.

Keep the bottle tightly closed to protect it from moisture.

Keep the blister pack in the original packaging to protect it from moisture.

Medicines should not be disposed of via wastewater or household waste. Dispose of unused medicines and their containers at the SIGRE Point at your pharmacy. If you are unsure, ask your pharmacist how to dispose of medicines and containers you no longer need. This will help protect the environment.

6. Contents of the pack and other information

Composition of Omeprazol Davur 20 mg gastro-resistant hard capsules EFG

  • The active substance is omeprazole. Each capsule contains 20 mg of omeprazole.
  • The other components (excipients) are: sugar spheres (sucrose and maize starch), sodium carboxymethylstarch type A (from potato), sodium lauryl sulfate, povidone, trisodium phosphate dodecahydrate, hypromellose, methacrylic acid-ethyl acrylate copolymer (1:1), triethyl citrate, titanium dioxide (E171), talc, sodium hydroxide.

The capsule shell consists of: erythrosine (E127), indigo carmine (E132), titanium dioxide (E171), gelatin, quinoline yellow (E104).

Printing ink: Shellac, propylene glycol (E1520), sodium hydroxide, polyvinylpyrrolidone, titanium dioxide (E171).

Appearance of the product and contents of the container

Omeprazol Davur 20 mg capsules consist of an orange body marked with a "20" and a blue cap marked with "O", containing white-beige omeprazole microgranules.

Pack sizes:

HDPE bottles containing 14, 28 and 56 capsules.

Blister packs containing 14, 28 and 56 capsules.

Only certain pack sizes may be commercially available.

Marketing Authorization Holder and Manufacturer

Marketing Authorization Holder

Teva Pharma, S.L.U.

C/Anabel Segura 11, Edificio Albatros B, 1st floor,

Alcobendas, 28108 Madrid (Spain)

Manufacturer

Teva Pharma, S.L.U.

Polígono Malpica, Calle C nº 4.

50016 Zaragoza, Spain

Date of the most recent review of this leaflet: December 2023

Detailed information on this medicine is available on the website of the Spanish Agency for Medicines and Health Products (AEMPS): http://www.aemps.gob.es