Patient Leaflet Updated 05-Apr-2024 | Dr. Reddy's Laboratories (UK) Ltd
Rivaroxaban 2.5 mg Film-Coated Tablets
Rivaroxaban Dr. Reddy’s 2.5 mg Film-Coated Tablets
1. What Rivaroxaban is and what it is used for
2. What you need to know before you take Rivaroxaban
3. How to take Rivaroxaban
4. Possible side effects
5. How to store Rivaroxaban
6. Contents of the pack and other information
You have been given Rivaroxaban because
or
Rivaroxaban contains the active substance rivaroxaban and belongs to a group of medicines called antithrombotic agents. It works by blocking a blood clotting factor (factor Xa) and thus reducing the tendency of the blood to form clots.
Do not take Rivaroxaban and tell your doctor if any of these apply to you.
Talk to your doctor or pharmacist before taking rivaroxaban.
Rivaroxaban should not be used in combination with certain other medicines which reduce blood clotting such as prasugrel or ticagrelor other than acetylsalicylic acid and clopidogrel/ticlopidine.
Take special care with Rivaroxaban
If any of the above apply to you, tell your doctor before you take Rivaroxaban. Your doctor will decide, if you should be treated with this medicine and if you should be kept under closer observation.
Rivaroxaban is not recommended for people under 18 years of age. There is not enough information on their use in children and adolescents.
Tell your doctor or pharmacist if you are taking, have recently taken or might take any other medicines, including medicines obtained without a prescription.
If you are taking:
If any of the above apply to you, tell your doctor before taking rivaroxaban, because the effect of Rivaroxaban may be increased. Your doctor will decide, if you should be treated with this medicine and if you should be kept under closer observation.
If your doctor thinks that you are at increased risk of developing stomach or bowel ulcers, he may also use a preventative ulcer treatment.
If you are taking:
If any of the above apply to you, tell your doctor before taking rivaroxaban, because the effect of rivaroxaban may be reduced. Your doctor will decide, if you should be treated with rivaroxaban and if you should be kept under closer observation.
Do not take rivaroxaban if you are pregnant or breastfeeding. If there is a chance that you could become pregnant, use a reliable contraceptive while you are taking rivaroxaban. If you become pregnant while you are taking this medicine, tell your doctor immediately, who will decide how you should be treated.
Rivaroxaban Tablets may cause dizziness (common side effect) or fainting (uncommon side effect) (see section 4, “Possible side effects”). You should not drive, ride a bicycle or use any tools or machines if you are affected by these symptoms.
If you have been told by your doctor that you have an intolerance to some sugars, contact your doctor before taking this medicine.
This medicine contains less than 1 mmol sodium (23 mg) per tablet, that is to say essentially ‘sodium-free’.
Always take this medicine exactly as your doctor has told you. Check with your doctor or pharmacist if you are not sure.
The recommended dose is one 2.5 mg tablet twice a day. Take rivaroxaban around the same time every day (for example, one tablet in the morning and one in the evening). This medicine can be taken with or without food.
If you have difficulty swallowing the tablet whole, talk to your doctor about other ways to take rivaroxaban. The tablet may be crushed and mixed with water or apple puree immediately before you take it.
If necessary, your doctor may also give you the crushed rivaroxaban tablet through a stomach tube.
Rivaroxaban will not be given to you on its own. Your doctor will also tell you to take acetylsalicylic acid. If you get Rivaroxaban after an acute coronary syndrome, your doctor may tell you to also take clopidogrel or ticlopidine.
If you get rivaroxaban after a procedure to open a narrowed or closed artery of your leg to restore blood flow, your doctor may also prescribe clopidogrel for you to take in addition to acetylsalicylic acid for a short while.
Your doctor will tell you how much of these to take (usually between 75 to 100 mg acetylsalicylic acid daily or a daily dose of 75 to 100 mg acetylsalicylic acid plus a daily dose of either 75 mg clopidogrel or a standard daily dose of ticlopidine).
Treatment with rivaroxaban after an acute coronary syndrome should be started as soon as possible after stabilisation of the acute coronary syndrome, at the earliest 24 hours after admission to hospital and at the time when parenteral (via injection) anticoagulation therapy would normally be stopped. Your doctor will tell you when to start treatment with Rivaroxaban if you have been diagnosed with coronary artery disease or peripheral artery disease. Your doctor will decide how long you must continue treatment.
Contact your doctor immediately if you have taken too many rivaroxaban tablets. Taking too much rivaroxaban increases the risk of bleeding.
Do not take a double dose to make up for a missed dose. If you miss a dose, take your next dose at the usual time.
Take rivaroxaban on a regular basis and for as long as your doctor keeps prescribing it.
Do not stop taking rivaroxaban without talking to your doctor first. If you stop taking this medicine, it may increase your risk of having another heart attack or stroke or dying from a disease related to your heart or your blood vessels.
If you have any further questions on the use of this medicine, ask your doctor or pharmacist.
Like all medicines, this medicine can cause side effects, although not everybody gets them.
Like other similar medicines, to reduce the formation of blood clots, rivaroxaban may cause bleeding which may potentially be life threatening. Excessive bleeding may lead to a sudden drop in blood pressure (shock). In some cases the bleeding may not be obvious.
Tell your doctor immediately if you experience any of the following side effects:
Signs of bleeding
Your doctor may decide to keep you under closer observation or change the treatment.
Signs of severe skin reactions:
The frequency of these side effects is very rare (up to 1 in 10,000 people)
Signs of severe allergic reactions
The frequencies of these severe allergic reactions are very rare (anaphylactic reactions, including anaphylactic shock; may affect up to 1 in 10,000 people) and uncommon (angioedema and allergic oedema; may affect up to 1 in 100 people).
Common (may affect up to 1 in 10 people):
Uncommon (may affect up to 1 in 100 people):
Rare (may affect up to 1 in 1,000 people):
Not known (frequency cannot be estimated from the available data):
If you get 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 Yellow Card Scheme website www.mhra.gov.uk/yellowcard or search for MHRA Yellow Card in the Google Play or Apple App Store. 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 and on each blister after EXP. The expiry date refers to the last day of that month.
This medicine does not require any special storage conditions.
Do not throw away any medicines via wastewater or household waste. Ask your pharmacist how to throw away medicines you no longer use. These measures will help protect the environment.
The active substance is rivaroxaban. Each tablet contains 2.5 mg of rivaroxaban.
The other ingredients are:
Tablet core: microcrystalline cellulose, lactose monohydrate, croscarmellose sodium, hypromellose, sodium laurilsulfate, magnesium stearate. See section 2 “Rivaroxaban contains lactose and sodium”.
Tablet film coat: macrogol, hypromellose, titanium dioxide (E 171), iron oxide yellow (E 172).
Light yellow, round biconvex tablets (approx.6 mm diameter) marked with "2.5" on one side
Pack sizes of 10, 14, 28, 30, 56, 100 or 196 film-coated tablets.
Not all pack sizes may be marketed.
This leaflet was last revised in 10/2023.
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