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Arcoxia 60 mg film-coated tablets – patient leaflet, side effects, dosage

Last updated: · Text from the MHRA, as of · About this document

Medicine status: Prescription only (POM) Details

Medicine strength:
60 mg
Contains active substance:
ATC code:
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Patient leaflet - Arcoxia 60 mg film-coated tablets

1. WHAT ARCOXIA® IS AND WHAT IT IS USED FOR

What is Arcoxia®?

  • Arcoxia® contains the active substance etoricoxib. Arcoxia® is one of a group of medicines called selective COX-2 inhibitors. These belong to a family of medicines called non-steroidal anti-inflammatory drugs (NSAIDs).

What is Arcoxia® used for?

  • Arcoxia® helps to reduce the pain and swelling (inflammation) in the joints and muscles of people 16 years of age and older with osteoarthritis, rheumatoid arthritis, ankylosing spondylitis and gout.
  • Arcoxia® is also used for the short-term treatment of moderate pain after dental surgery in people 16 years of age and older.

What is osteoarthritis?

Osteoarthritis is a disease of the joints. It results from the gradual breakdown of cartilage that cushions the ends of the bones. This causes swelling (inflammation), pain, tenderness, stiffness and disability.

What is rheumatoid arthritis?

Rheumatoid arthritis is a long-term inflammatory disease of the joints. It causes pain, stiffness, swelling, and increasing loss of movement in the joints it affects. It may also cause inflammation in other areas of the body.

What is gout?

Gout is a disease of sudden, recurring attacks of very painful inflammation and redness in the joints. It is caused by deposits of mineral crystals in the joint.

What is ankylosing spondylitis?

Ankylosing spondylitis is an inflammatory disease of the spine and large joints.

2. WHAT YOU NEED TO KNOW BEFORE YOU TAKE ARCOXIA®

Do not take Arcoxia®

  • if you are allergic (hypersensitive) to etoricoxib or any of the other ingredients of this medicine (listed in section 6)
  • if you are allergic to non-steroidal anti-inflammatory drugs (NSAIDs), including aspirin and COX-2 inhibitors (see Possible side effects, section 4)
  • if you have a current stomach ulcer or bleeding in your stomach or intestines
  • if you have serious liver disease
  • if you have serious kidney disease
  • if you are or could be pregnant or are breast-feeding (see ‘Pregnancy, breast-feeding, and fertility’)

    • if you are under 16 years of age
    • if you have inflammatory bowel disease, such as Crohn’s Disease, Ulcerative Colitis, or Colitis
    • if you have high blood pressure that has not been controlled by treatment (check with your doctor or nurse if you are not sure whether your blood pressure is adequately controlled)
    • if your doctor has diagnosed heart problems including heart failure (moderate or severe types), angina (chest pain)
    • if you have had a heart attack, bypass surgery, peripheral arterial disease (poor circulation in legs or feet due to narrow or blocked arteries)
    • if you have had any kind of stroke (including mini-stroke, transient ischaemic attack or TIA). Etoricoxib may slightly increase your risk of heart attack and stroke and this is why it should not be used in those who have already had heart problems or stroke.

If you think any of these are relevant to you, do not take the tablets until you have consulted your doctor.

Warnings and precautions

Talk to your doctor or pharmacist before taking Arcoxia® if:

  • You have a history of stomach bleeding or ulcers.
  • You are dehydrated, for example by a prolonged bout of vomiting or diarrhoea.
  • You have swelling due to fluid retention.
  • You have a history of heart failure, or any other form of heart disease.
  • You have a history of high blood pressure. Arcoxia® can increase blood pressure in some people, especially in high doses, and your doctor will want to check your blood pressure from time to time.
  • You have any history of liver or kidney disease.
  • You are being treated for an infection. Arcoxia® can mask or hide a fever, which is a sign of infection.
  • You have diabetes, high cholesterol, or are a smoker. These can increase your risk of heart disease.
  • You are a woman trying to become pregnant.
  • You are over 65 years of age.

If you are not sure if any of the above apply to you, talk to your doctor before taking Arcoxia® to see if this medicine is suitable for you. Arcoxia® works equally well in older and younger adult patients. If you are over 65 years of age, your doctor will want to appropriately keep a check on you. No dosage adjustment is necessary for patients over 65 years of age.

Children and adolescents

Do not give this medicine to children and adolescents under 16 years of age.

Other medicines and Arcoxia®

Tell your doctor or pharmacist if you are taking, have recently taken or might take any other medicines, including medicines obtained without a prescription.

In particular if you are taking any of the following medicines, your doctor may want to monitor you to check that your medicines are working properly, once you start taking Arcoxia®:

  • medicines that thin your blood (anticoagulants), such as warfarin
  • rifampicin (an antibiotic)
  • methotrexate (a drug used for suppressing the immune system, and often used in rheumatoid arthritis)
  • ciclosporin or tacrolimus (drugs used for suppressing the immune system)
  • lithium (a medicine used to treat some types of depression)
  • medicines used to help control high blood pressure and heart failure called ACE inhibitors and angiotensin receptor blockers, examples include enalapril and ramipril, and losartan and valsartan
  • diuretics (water tablets)
  • digoxin (a medicine for heart failure and irregular heart rhythm)
  • minoxidil (a drug used to treat high blood pressure)
  • salbutamol tablets or oral solution (a medicine for asthma)
  • birth control pills (the combination may increase your risk of side effects)
  • hormone replacement therapy (the combination may increase your risk of side effects)
  • aspirin, the risk of stomach ulcers is greater if you take Arcoxia® with aspirin.
  • aspirin for prevention of heart attacks or stroke:

    Arcoxia® can be taken with low-dose aspirin. If you are currently taking low-dose aspirin to prevent heart attacks or stroke, you should not stop taking aspirin until you talk to your doctor

  • aspirin and other non-steroidal anti-inflammatory drugs (NSAIDs): do not take high dose aspirin or other anti-inflammatory medicines while taking Arcoxia®.

Arcoxia® with food and drink

The onset of the effect of Arcoxia® may be faster when taken without food.

Pregnancy, breast-feeding and fertility

Pregnancy

Arcoxia® tablets must not be taken during pregnancy. If you are pregnant or think you could be pregnant, or if you are planning to become pregnant, do not take the tablets. If you become pregnant, stop taking the tablets and consult your doctor. Consult your doctor if you are unsure or need more advice.

Breast-feeding

It is not known if Arcoxia® is excreted in human milk. If you are breast-feeding, or planning to breast-feed, consult your doctor before taking Arcoxia®. If you are using Arcoxia®, you must not breast-feed.

Fertility

Arcoxia® is not recommended in women attempting to become pregnant.

Driving and using machines

Dizziness and sleepiness have been reported in some patients taking Arcoxia®.

Do not drive if you experience dizziness or sleepiness. Do not use any tools or machines if you experience dizziness or sleepiness.

Arcoxia® contains lactose

If you have been told by your doctor that you have an intolerance to some sugars, contact your doctor before taking this medicine.

Arcoxia® contains sodium

This medicine contains less than 1 mmol sodium (23 mg) per film-coated tablet, that is to say essentially ‘sodium-free’.

3. HOW TO TAKE ARCOXIA®

Always take this medicine exactly as your doctor has told you. You should check with your doctor or pharmacist if you are not sure. Do not take more than the recommended dose for your condition. Your doctor will want to discuss your treatment from time to time. It is important that you use the lowest dose that controls your pain and you should not take Arcoxia® for longer than necessary. This is because the risk of heart attacks and strokes might increase after prolonged treatment, especially with high doses.

There are different strengths available for this medicinal product and depending on your disease your doctor will prescribe the tablet strength that is appropriate for you.

The recommended dose is:

Osteoarthritis

The recommended dose is 30 mg once a day, increase to a maximum of 60 mg once a day if needed.

Rheumatoid arthritis

The recommended dose is 60 mg once a day, increased to a maximum of 90 mg once a day if needed.

Ankylosing spondylitis

The recommended dose is 60 mg once a day, increased to a maximum of 90 mg once a day if needed.

Acute pain conditions

Etoricoxib should be used only for the acute painful period.

Gout

The recommended dose is 120 mg once a day which should only be used for the acute painful period, limited to a maximum of 8 days treatment.

Postoperative dental surgery pain

The recommended dose is 90 mg once daily, limited to a maximum of 3 days treatment.

People with liver problems

  • If you have mild liver disease, you should not take more than 60 mg a day.
  • If you have moderate liver disease, you should not take more than 30 mg a day.

Use in children and adolescents

Arcoxia® tablets should not be taken by children or adolescents under 16 years of age.

Elderly

No dose adjustment is necessary for elderly patients. As with other medicines, caution should be exercised in elderly patients. Method of administration

Arcoxia® is for oral use. Take the tablets once a day. Arcoxia® can be taken with or without food.

If you take more Arcoxia® than you should

You should never take more tablets than the doctor recommends. If you do take too many Arcoxia® tablets, you should seek medical attention immediately.

If you forget to take Arcoxia®

It is important to take Arcoxia® as your doctor has prescribed. If you miss a dose, just resume your usual schedule the following day. Do not take a double dose to make up for the forgotten tablet.

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

4. POSSIBLE SIDE EFFECTS

Like all medicines, this medicine can cause side effects, although not everybody gets them.

If you develop any of these signs you should stop Arcoxia® and talk to your doctor immediately (see What you need to know before you take Arcoxia® section 2):

  • shortness of breath, chest pains, or ankle swelling appear or if they get worse
  • yellowing of the skin and eyes (jaundice) – these are signs of liver problems
  • severe or continual stomach pain or your stools become black
  • an allergic reaction- which can include skin problems such as ulcers or blistering, or swelling of the face, lips, tongue, or throat which may cause difficulty in breathing

The frequency of possible side effects listed below is defined using the following convention:

Very common (affects more than 1 user in 10)

Common (affects 1 to 10 users in 100)

Uncommon (affects 1 to 10 users in 1,000)

Rare (affects 1 to 10 users in 10,000)

Very rare (affects less than 1 user in 10,000).

The following side effects can occur during treatment with Arcoxia®:

Very Common:

  • stomach pain

Common:

  • dry socket (inflammation and pain after a tooth extraction)
  • swelling of the legs and/or feet due to fluid retention (oedema)
  • dizziness, headache
  • palpitations (fast or irregular heartbeat), irregular heart rhythm (arrhythmia)
  • increased blood pressure
  • wheezing or shortness of breath (bronchospasms)
  • constipation, wind (excessive gas), gastritis (inflammation of the lining of the stomach), heartburn, diarrhoea, indigestion (dyspepsia)/stomach discomfort, nausea, being sick (vomiting), inflammation of the oesophagus, mouth ulcers
  • changes in blood tests related to your liver
  • bruising

    • weakness and fatigue, flu-like illness

Uncommon:

  • gastroenteritis (inflammation of the gastrointestinal tract that involves both the stomach and small intestine/stomach flu), upper respiratory infection, urinary tract infection
  • changes in laboratory values (decreased number of red blood cells, decreased number of white blood cells, platelets decreased)
  • hypersensitivity (an allergic reaction including hives which may be serious enough to require immediate medical attention)
  • appetite increases or decreases, weight gain
  • anxiety, depression, decreases in mental sharpness; seeing, feeling or hearing things that are not there (hallucinations)
  • taste alteration, inability to sleep, numbness or tingling, sleepiness
  • blurred vision, eye irritation and redness
  • ringing in the ears, vertigo (sensation of spinning while remaining still)
  • abnormal heart rhythm (atrial fibrillation), fast heart rate, heart failure, feeling of tightness, pressure or heaviness in the chest (angina pectoris), heart attack
  • flushing, stroke, mini-stroke (transient ischaemic attack), severe increase in blood pressure, inflammation of the blood vessels
  • cough, breathlessness, nose bleed
  • stomach or bowel bloating, changes in your bowel habits, dry mouth, stomach ulcer, inflammation of the stomach lining that can become serious and may lead to bleeding, irritable bowel syndrome, inflammation of the pancreas
  • swelling of the face, skin rash or itchy skin, redness of the skin
  • muscle cramp/spasm, muscle pain/stiffness
  • high levels of potassium in your blood, changes in blood or urine tests relating to your kidney, serious kidney problems
  • chest pain

Rare:

  • angioedema (an allergic reaction with swelling of the face, lips, tongue and/or throat which may cause difficulty in breathing or swallowing, which may be serious enough to require immediate medical attention)/anaphylactic/anaphylactoid reactions including shock (a serious allergic reaction that requires immediate medical attention)
  • confusion, restlessness
  • liver problems (hepatitis)
  • low blood levels of sodium
  • liver failure, yellowing of the skin and/or eyes (jaundice)
  • severe skin reactions

Reporting of side effects

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 at:

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.

5. HOW TO STORE ARCOXIA®

  • Keep out of the sight and reach of children.
  • Do not use this medicine after the expiry date which is stated on the carton. The expiry date refers to the last day of that month.
  • Store in the original package in order to protect from moisture.
  • If the tablets become discoloured or show any other signs of deterioration, you should seek the advice of your pharmacist who will tell you what to do.
  • 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.

6. CONTENTS OF THE PACK AND OTHER INFORMATION

What Arcoxia® contains

The active substance is etoricoxib. Each film coated tablet contains 60 mg of etoricoxib.

The other ingredients are:

Core: calcium hydrogen phosphate anhydrous, croscarmellose sodium, magnesium stearate, microcrystalline cellulose.

Tablet coating: carnauba wax, lactose monohydrate, hypromellose, titanium dioxide (E171), triacetin, yellow ferric oxide (E172) and indigo carmine lake (E132).

What Arcoxia® looks like and contents of the pack

Arcoxia® tablets are dark green, apple-shaped, biconvex film coated tablets marked ‘ARCOXIA 60’ on one side and ‘200’ on the other. Arcoxia® tablets are available as blister packs of 30 tablets.

Manufacturer

Organon Heist bv, Industriepark 30, 2220 Heist-op-den-Berg, Belgium.

Schering-Plough Labo NV, Industriepark 30, Heist-op-den-Berg, 2220, Belgium.

Procured from within the EU and repackaged by the Product Licence Holder Beachcourse Ltd., Unit 2-3, Townsend Industrial Estate, Waxlow Road, London, NW10 7NU.

PL 16378/1205 POM

Revision date: 13.12.2024

Arcoxia® is a registered trademark of N.V. Organon.

Blind or partially sighted? Is this leaflet hard to see or read? Phone Beachcourse,

Tel: 020 8896 9054 for help. Ref. number: 1205/V2

About this document

Source: MHRA - Medicines and Healthcare products Regulatory Agency (products.mhra.gov.uk) · Marketing authorisation: PLPI 16378/1205

Last revision stated in the text: 13 December 2024 · MHRA data as of 13 October 2026

Found a mistake? Tell us on the contact page.

The information on this site does not replace the advice of a doctor or pharmacist.

Facts about Arcoxia 60 mg film-coated tablets

Prescription needed? Yes, prescription-only medicine (POM)
Active substance Etoricoxib
Strength 60 mg
Pharmaceutical form Oral tablet
30 mg tablets: Blue-green, apple-shaped biconvex tablets debossed ‘101’ on one side and ‘ACX 30’ on the other side.
60 mg tablets: Dark green, apple-shaped, biconvex tablets debossed ‘200’ on one side and ‘ARCOXIA 60’ on the other side.
90 mg tablets: White, apple-shaped, biconvex tablets debossed ‘202’ on one side and ‘ARCOXIA 90’ on the other side.
120 mg tablets: Pale-green, apple-shaped, biconvex tablets debossed ‘204’ on one side and ‘ARCOXIA 120’ on the other side.
How is it taken Oral
Excipients Calcium hydrogen phosphate (anhydrous), Croscarmellose sodium, Magnesium stearate, Microcrystalline cellulose, Carnauba wax, Lactose monohydrate, Hypromellose, Titanium dioxide (E171), Triacetin, The 30-, 60- and 120-mg tablets also contain indigo carmine lake (E132) and yellow ferric oxide (E172).
Pack sizes 28 tablet
Is it available? Listed as available (NHS Dictionary of Medicines and Devices – not a record of current supplies)
Shelf life 3 years.
Storage Bottles: Keep the container tightly closed in order to protect from moisture.
Blisters: Store in the original package in order to protect from moisture.
Drug group (ATC) Anti-inflammatory and antirheumatic products, non-steroids, coxibs
  1. M Musculo-skeletal system drugs
    1. M01 Antiinflammatory and antirheumatic products
      1. M01A Antiinflammatory and antirheumatic products, non-steroids
        1. M01AH Coxibs
          1. M01AH05 etoricoxib
Marketing authorisation PL 00025/0642 (first authorised 13 February 2012), PLPI 16378/1205
Marketing authorisation holder Organon Pharma (UK) Limited
Codes GTIN 0840164525144 · BNF 10010100

Sources: the MHRA product information (products.mhra.gov.uk) and the NHS Dictionary of Medicines and Devices (dm+d), release 10.2.0 of 19 October 2026, NHS Business Services Authority. Contains public sector information licensed under the Open Government Licence v3.0.