Package Leaflet: Information for the User
ORACEA40mg modified-release hard capsules
Doxycycline
Read all of this leaflet carefully before you start taking this medicine because it contains important information for you.
Contents of the pack and other information:
Oracea is a medicine that contains the active substance doxycycline. It is used in adults to reduce the red bumps and spots on the face caused by a condition called rosacea.
Do not take Oracea
Oracea should not be given to babies or children under 12 years of age, as it may cause permanent tooth discolouration or affect tooth development.
Warnings and precautions
Oracea should not be used to treat bacterial infections.
Tell your doctor or pharmacist before taking Oracea if:
Oracea may cause permanent tooth discolouration.
Tell your doctor or pharmacist if you:
Take Oracea exactly as your doctor has told you. Taking more than the prescribed dose may increase the risk of bacteria in your gut becoming resistant to Oracea.
Taking Oracea with other medicines
Tell your doctor or pharmacist if you are taking, have recently taken or might take any other medicines.
Oracea and certain other medicines may not work properly if taken at the same time. Tell your doctor about any medicines you are taking or plan to take during treatment with Oracea
Taking Oracea with food and drink
Take Oracea with a full glass of water, while sitting or standing, to reduce the risk of irritation or ulcers in the throat or oesophagus.
Do not take milk or dairy products at the same time as Oracea, as they contain calcium which may reduce the effectiveness of Oracea. Wait for 2 to 3 hours after taking your daily dose of Oracea before drinking or eating dairy products.
Pregnancy, breast-feeding and fertility
Oracea should not be taken during pregnancy, as it may cause permanent tooth discolouration in the unborn child.
Oracea should not be taken for prolonged periods by breast-feeding mothers, as it may cause tooth discolouration and affect bone growth in the breast-fed child.
Driving and using machines
Oracea has no or negligible influence on the ability to drive and use machines.
Important information about some of the ingredients of Oracea
Oracea contains sucrose. If your doctor has told you that you have an intolerance to some sugars, consult with them before taking this medicine.
The ink used to print on the capsule contains aluminium lake red Allura AC (E129), which may cause allergic reactions. It can cause asthma, especially in patients allergic to acetylsalicylic acid.
Follow exactly the instructions of your doctor to take this medicine. If you are not sure, ask your doctor or pharmacist again.
The recommended dose is one Oracea capsule per day, in the morning, on an empty stomach, preferably at least one hour before or two hours after a meal. Swallow the capsule whole and do not chew it.
Take the Oracea capsule with a full glass of water, while sitting or standing, to avoid throat irritation.
If you take more Oracea than you should
If you take an overdose of Oracea, there is a risk of damage to the liver, kidneys or pancreas.
If you take more Oracea capsules than you should, contact your doctor immediately.
In case of overdose or accidental ingestion, contact your doctor or pharmacist immediately or call the Toxicology Information Service, telephone 91 562 04 20, indicating the medicine and the amount used.
If you forget to take Oracea
Do not take a double dose to make up for a forgotten dose.
If you stop taking Oracea
Continue to take Oracea until your doctor tells you to stop.
If you have any further questions on the use of this product, ask your doctor or pharmacist.
Like all medicines, this medicine can cause side effects, although not everybody gets them.
If any of the following side effects occur, contact your doctor as soon as possible:
Common side effects
The following side effects may occur frequently (affect 1 to 10 users in 100):
Uncommon side effects(frequency cannot be estimated from the available data).
The following side effects may occur:
Rare side effects
The following side effects may occur rarely (affect 1 to 10 users in 10,000):
Very rare side effects
The following side effects may occur very rarely (affect less than 1 user in 10,000):
Side effects of unknown frequency(cannot be estimated from the available data).
The following side effects may occur:
Reporting of side effects
If you experience any side effects, talk to your doctor or pharmacist. This includes any possible side effects not listed in this leaflet. You can also report side effects directly via the Spanish Medicines Information System: https://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.
Do not use this medicine after the expiry date which is stated on the carton after EXP:. The expiry date refers to the last day of that month.
Store in the original package to protect from light.
Medicines should not be disposed of via wastewater or household waste. Ask your pharmacist how to dispose of medicines no longer required. These measures will help protect the environment.
Composition of Oracea
The active substance is doxycycline. Each capsule contains 40 mg of doxycycline (as monohydrate).
The other ingredients are:
Hypromellose (E464), methacrylic acid-ethyl acrylate copolymer (1:1), triethyl citrate, talc (E553b), titanium dioxide (E171), macrogol 400, yellow iron oxide (E172), red iron oxide (E172), polysorbate 80 (E433), sugar spheres (maize starch, sucrose).
Capsules: gelatin, black iron oxide (E172), red iron oxide (E172), yellow iron oxide (E172), titanium dioxide (E171)
Printing ink: shellac, propylene glycol (E1520), black iron oxide (E172), aluminium lake red Allura AC (E129), aluminium lake blue brilliant FCF, aluminium lake yellow D & C No. 10
See the end of section 2 for information on sucrose and aluminium lake red Allura AC (E129).
Appearance and packaging of Oracea
Oracea is presented as modified-release hard capsules.
The capsules are beige and marked with “GLD 40”.
Oracea is available in packs of 56, 28 or 14 capsules.
Not all pack sizes may be marketed.
Marketing authorisation holder and manufacturer
Marketing authorisation holder:
Laboratorios Galderma, S.A.
Serrano Galvache, 56
28033 Madrid
Spain
Manufacturer:
LABORATOIRES GALDERMA Zone Industrielle - Montdesir (Alby Sur Cheran) - F-74540 – France
CATALENT UK SWINDON ZYDIS LTD.
Frankland Road. Blagrove, Swindon (Wiltshire) - SN5 8RU - United Kingdom
GALDERMA LABORATORIUM GMBH,
Toulouser Allee 23a
40211 Düsseldorf
Germany
PATHEON FRANCE
40 Boulevard de Champaret
38300 Bourgoin Jallieu
France
This medicine is authorised in the Member States of the European Economic Area under the following names:
Denmark, Greece, Finland, Iceland, Norway, Sweden: Oracea 40 mg modified release hard capsules
Austria, Germany: ORAYCEA 40 mg modified release hard capsules
Belgium, France, Ireland, Italy, Netherlands, Poland, Portugal, United Kingdom, Luxembourg: EFRACEA 40 mg modified release hard capsules
Spain: Oracea 40 mg modified-release hard capsules
This leaflet was approved in June 2019
Detailed and up-to-date information on this medicine is available on the website of the Spanish Agency for Medicines and Health Products (AEMPS) http://www.aemps.es