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Celebrex_100mg_200mg_30_60 – patient leaflet, side effects, dosage

Text from the MHRA, as of · About this document

Medicine status: Prescription only (POM) Details

Medicine strength:
200 mg
Contains active substance:
ATC code:

Patient leaflet - Celebrex 200 mg capsules

1. What Celebrex is and what it is used for

Celebrex belongs to a group of medicines called nonsteroidal anti-inflammatory drugs (NSAID), and specifically a sub-group known as cyclooxygenase-2 (COX-2) inhibitors. Your body makes prostaglandins that may cause pain and inflammation. In conditions such as rheumatoid arthritis and osteoarthritis your body

makes more of these. Celebrex acts by reducing the production of prostaglandins, thereby reducing the pain and inflammation.

Celebrex is used in adults for the relief of signs and symptoms of rheumatoid arthritis, osteoarthritis and ankylosing spondylitis.

You should expect your medicine to start working within hours of taking the first dose, but you may not experience a full effect for several days.

2. What you need to know before you take Celebrex

You have been prescribed Celebrex by your doctor. The following information will help you get the best results with Celebrex. If you have any further questions please ask your doctor or pharmacist. Do not take Celebrex

Tell your doctor if any of the following are true for you as patients with these conditions should not take Celebrex.

  • if you are allergic to celecoxib or

    any of the other ingredients of this medicine (listed in section 6)

  • if you have had an allergic reaction

    to a group of medicines called “sulfonamides” (e.g. some antibiotics used to treat infections)

  • if you currently have an ulcer in your

    stomach or intestines, or bleeding in your stomach or intestines

  • if as a result of taking acetylsalicylic

    acid or any other anti-inflammatory and pain-relieving medicine (NSAID) you have had asthma, nose polyps, severe nose congestion, or an allergic reaction such as an itchy skin rash, swelling of the face, lips, tongue or throat, breathing difficulties or wheezing

  • if you are pregnant. If you can

    become pregnant during ongoing

    treatment you should discuss methods of contraception with your doctor

    • if you are breast-feeding
    • if you have severe liver disease
    • if you have severe kidney disease
    • if you have an inflammatory disease

      of the intestines such as ulcerative colitis or Crohn’s disease

    • if you have heart failure, established

      ischaemic heart disease, or cerebrovascular disease, e.g. you have been diagnosed with a heart attack, stroke, or transient ischaemic attack (temporary reduction of blood flow to the brain; also known as “mini-stroke”), angina, or blockages of blood vessels to the heart or brain

    • if you have or have had problems

      with your blood circulation

      (peripheral arterial disease) or if you have had surgery on the arteries of your legs

Warnings and precautions

Talk to your doctor or pharmacist before taking Celebrex:

  • if you have previously had an ulcer

    or bleeding in your stomach or intestines. (Do not take Celebrex if you currently have an ulcer or bleeding in your stomach or intestine)

  • if you are taking acetylsalicylic acid

    (even at low dose for heart protective purposes)

  • if you are taking antiplatelet

    therapies

  • if you use medicines to reduce blood

    clotting (e.g. warfarin/warfarin like anticoagulants or novel oral anti-clotting medicines, e.g. apixaban)

  • if you use medicines called

    corticosteroids (e.g. prednisone)

  • if you are using Celebrex at the same

    time as other non-acetylsalicylic NSAIDs such as ibuprofen or

    diclofenac. The use of these medicines together should be avoided

    • if you smoke, have diabetes, raised

      blood pressure or raised cholesterol

    • if your heart, liver or kidneys are not

      working well your doctor may want to keep a regular check on you

    • if you have fluid retention (such as

      swollen ankles and feet)

    • if you are dehydrated, for instance

      due to sickness, diarrhoea or the use of diuretics (used to treat excess fluid in the body)

    • if you have had a serious allergic

      reaction or a serious skin reaction to any medicines

    • if you feel ill due to an infection

      or think you have an infection, as Celebrex may mask a fever or other signs of infection and inflammation

    • if you are over 65 years of age your

      doctor will want to monitor you regularly

    • the consumption of alcohol and

      NSAIDs may increase the risk of gastrointestinal problems

As with other NSAIDs (e.g. ibuprofen or diclofenac) this medicine may lead to an increase in blood pressure, and so your doctor may ask to monitor your blood pressure on a regular basis. Some cases of severe liver reactions, including severe liver inflammation, liver damage, liver failure (some with fatal outcome or requiring liver transplant), have been reported with celecoxib. Of the cases that reported time to onset, most severe liver reactions occurred within one month of start of treatment. Serious skin reactions have been reported in association with Celebrex treatment. Stop using Celebrex and seek medical attention immediately if you notice any of the symptoms of serious skin reactions described in section 4, Possible side effects.

Celebrex may make it more difficult to become pregnant. You should inform your doctor if you are planning to become pregnant or if you have problems to become pregnant (see section on Pregnancy and breast-feeding). Other medicines and Celebrex

Tell your doctor or pharmacist if you are taking, have recently taken or might take any other medicines:

  • Dextromethorphan (used to treat

    coughs)

  • ACE inhibitors, angiotensin II

    antagonists, beta blockers and diuretics (used for high blood pressure and heart failure)

  • Fluconazole and rifampicin (used to

    treat fungal and bacterial infections)

  • Warfarin or other warfarin like

    medicines (“blood-thinning” agents that reduce blood clotting) including newer medicines like apixaban

  • Lithium (used to treat some types of

    depression)

  • Other medicines to treat depression,

    sleep disorders, high blood pressure or an irregular heartbeat

  • Neuroleptics (used to treat some

    mental disorders)

  • Methotrexate (used to treat rheumatoid

    arthritis, psoriasis and leukaemia)

  • Carbamazepine (used to treat

    epilepsy/seizures and some forms of pain or depression)

  • Barbiturates (used to treat epilepsy/

    seizures and some sleep disorders)

  • Ciclosporin and tacrolimus (used for

    immune system suppression e.g. after transplants)

Celebrex can be taken with low dose acetylsalicylic acid (75 mg or less daily). Ask your doctor for advice before taking both medicines together. Pregnancy, breast-feeding and fertility

If you are pregnant or breast-feeding, think you may be pregnant or are

planning to have a baby, ask your doctor or pharmacist for advice before taking this medicine.

Pregnancy

Celebrex must not be used by women who are pregnant or can become pregnant (i.e. women of child bearing potential who are not using adequate contraception) during ongoing treatment. If you become pregnant during treatment with Celebrex you should discontinue the treatment and contact your doctor for alternative treatment.

Breast-feeding

Celebrex must not be used during breast-feeding.

Fertility

NSAIDs, including Celebrex, may make it more difficult to become pregnant. You should tell your doctor if you are planning to become pregnant or if you have problems becoming pregnant. Driving and using machines

You should be aware of how you react to Celebrex before you drive or operate machinery. If you feel dizzy or drowsy after taking Celebrex, do not drive or operate machinery until these effects wear off.

Celebrex contains lactose

Celebrex contains lactose (a type of sugar). If you have been told by your doctor that you have an intolerance to some sugars, contact your doctor before taking this medicinal product. Celebrex contains sodium

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

3. How to take Celebrex

Always take this medicine exactly as your doctor or pharmacist has told you. Check with your doctor or pharmacist if you are not sure. If you think or feel that

the effect of Celebrex is too strong or too weak, talk to your doctor or pharmacist. Your doctor will tell you what dose you should take. As the risk of side effects associated with heart problems may increase with dose and duration of use, it is important that you use the lowest dose that controls your pain and you should not take Celebrex for longer than necessary to control symptoms. Method of administration

Celebrex is for oral use. The capsules can be taken at any time of the day, with or without food. However, try to take each dose of Celebrex at the same time each day.

If you have difficulty swallowing capsules: The entire capsule contents can be sprinkled onto a level teaspoon of semi-solid food (such as cool or room temperature applesauce, rice gruel, yogurt or mashed banana) and swallowed immediately with a drink approximately 240 ml of water. To open the capsule, hold upright to contain the granules at the bottom then gently squeeze the top and twist to remove, taking care not to spill the contents. Do not chew or crush the granules.

Contact your doctor within two weeks of starting treatment if you do not experience any benefit.

The recommended dose is

For osteoarthritis the recommended dose is 200 mg each day, increased by your doctor to a maximum of 400 mg, if needed.

The dose is usually:

one 200 mg capsule once a day; or one 100 mg capsule twice a day. For rheumatoid arthritis the

recommended dose is 200 mg each day, increased by your doctor to a maximum of 400 mg, if needed.

The dose is usually:

one 100 mg capsule twice a day. For ankylosing spondylitis the recommended dose is 200 mg each day, increased by your doctor to a maximum of 400 mg, if needed. The dose is usually:

one 200 mg capsule once a day; or one 100 mg capsule twice a day. Kidney or liver problems: make sure your doctor knows if you have liver or kidney problems as you may need a lower dose.

The elderly, especially those with a weight less than 50 kg: if you are over 65 years of age and especially if you weigh less than 50 kg, your doctor may want to monitor you more closely. You should not take more than 400 mg per day.

Use in children

Celebrex is for adults only, it is not for use in children.

If you take more Celebrex than you should

You should not take more capsules than your doctor tells you to. If you take too many capsules contact your doctor, pharmacist or hospital and take your medicine with you.

If you forget to take Celebrex

If you forget to take a capsule, take it as soon as you remember. Do not take a double dose to make up for a forgotten dose.

If you stop taking Celebrex

Suddenly stopping your treatment with Celebrex may lead to your symptoms getting worse. Do not stop taking Celebrex unless your doctor tells you to. Your doctor may tell you to reduce the dose over a few days before stopping completely.

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Date: Time:

DescriptionCelebrex_100mg_200mg_30_60
LeafletSite Barcode/ DataMatrixFront 6433 Back 6434No. of colours2Page Count
3989268Viatris SAP No.400566736;400566478
ART-40363-03122524660/0020
39892681
MA No.United Kingdomwith
Supplier SAP No.N/A
New Supplier Code6001039043D Render IDN/AMain FontHelvetica Neue LT W1G9 pt
600102583200 x 510 mm9 pt
Klocke Verpackungs-Service GmbH (Weingarten - DE)Keyline/Drawing No.N/A

14:25 27-NOV-2025

PL 46302/0273; PL 46302/0274
N/A
GTIN/PCN/A

Sign-offs

Notes

N/A
N/A
V6 APR 2025

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.

The side effects listed below were observed in arthritis patients who took Celebrex. Side effects marked

with an asterisk (*) are listed below at the higher frequencies that occurred in patients who took Celebrex to

prevent colon polyps. Patients in these studies took Celebrex at high doses and for a long duration. If any of the following happen, stop

taking Celebrex and tell your doctor immediately:

If you have:

  • an allergic reaction such as skin

    rash, swelling of the face, wheezing or difficulty breathing

  • heart problems such as pain in the

    chest

  • severe stomach pain or any sign of

    bleeding in the stomach or intestines, such as passing black or bloodstained stools, or vomiting blood

  • a skin reaction such as rash,

    blistering or peeling of the skin

  • liver failure (symptoms may include

    nausea (feeling sick), diarrhoea, jaundice (your skin or the whites of your eyes look yellow)).

Very common: may affect more than

1 in 10 people

  • High blood pressure, including

    worsening of existing high blood pressure *

Common: may affect up to 1 in

10 people

  • Heart attack*

    • Fluid build up with swollen ankles,

      legs and/or hands

    • Urinary infections
    • Shortness of breath*, sinusitis

      (sinus inflammation, sinus infection, blocked or painful sinuses), blocked or runny nose, sore throat, coughs, colds, flu-like symptoms

    • Dizziness, difficulty sleeping
    • Vomiting*, stomach ache, diarrhoea,

      indigestion, wind

    • Rash, itching
    • Muscle stiffness
    • Difficulty swallowing*
    • Headache
    • Nausea (feeling sick)
    • Painful joints
    • Worsening of existing allergies
    • Accidental injury

Uncommon: may affect up to 1 in

100 people

  • Stroke*
  • Heart failure, palpitations (awareness

    of heart beat), fast heart rate

  • Abnormalities in liver-related blood

    tests

  • Abnormalities in kidney-related

    blood tests

  • Anaemia (changes in red blood

    cells that can cause fatigue and breathlessness)

  • Anxiety, depression, tiredness,

    drowsiness, tingling sensations (pins and needles)

  • High levels of potassium in blood

    test results (can cause nausea (feeling sick), fatigue, muscle weakness or palpitations)

  • Impaired or blurred vision, ringing

    in the ears, mouth pain and sores, difficulty hearing*

  • Constipation, burping, stomach

    inflammation (indigestion, stomach ache or vomiting), worsening of inflammation of the stomach or intestine

    • Leg cramps
    • Raised itchy rash (hives)
    • Eye inflammation
    • Difficulty breathing
    • Skin discolouration (bruising)
    • Chest pain (generalised pain not

      related to the heart)

    • Face swelling

Rare: may affect up to 1 in

1,000 people

  • Ulcers (bleeding) in the stomach,

    gullet or intestines; or rupture of the intestine (can cause stomach ache, fever, nausea, vomiting, intestinal blockage), dark or black stools, inflammation of the pancreas (can lead to stomach pain), inflammation of the gullet (oesophagus)

  • Low levels of sodium in the blood (a

    condition known as hyponatraemia)

  • Reduced number of white blood

    cells (which help to protect the body from infection) or blood platelets (increased chance of bleeding or bruising)

  • Difficulty coordinating muscular

    movements

  • Feeling confused, changes in the

    way things taste

  • Increased sensitivity to light
  • Loss of hair
  • Hallucinations
  • Bleeding in the eye
  • Acute reaction that may lead to lung

    inflammation

  • Irregular heartbeat
  • Flushing
  • Blood clot in the blood vessels in

    the lungs. Symptoms may include sudden breathlessness, sharp pains when you breathe or collapse

  • Bleeding of the stomach or

    intestines (can lead to bloody stools or vomiting), inflammation of the intestine or colon

  • Severe liver inflammation (hepatitis).

    Symptoms may include nausea (feeling sick), diarrhoea, jaundice

    (yellow discolouration of the skin or eyes), dark urine, pale stools, bleeding easily, itching or chills

    • Acute kidney failure
    • Menstrual disturbances
    • Swelling of the face, lips, mouth,

      tongue or throat, or difficulty swallowing

Very rare: may affect up to 1 in

10,000 people

  • Serious allergic reactions (including

    potentially fatal anaphylactic shock)

  • Serious skin conditions such

    as Stevens-Johnson syndrome, exfoliative dermatitis and toxic epidermal necrolysis (can cause rash, blistering or peeling of the skin) and acute generalised exanthematous pustulosis

    (symptoms include the skin becoming red with swollen areas covered in numerous small pustules)

  • A delayed allergic reaction with

    possible symptoms such as rash, swelling of the face, fever, swollen glands, and abnormal test results (e.g., liver, blood cell (eosinophilia, a type of raised white blood cell count))

  • Bleeding within the brain causing

    death

  • Meningitis (inflammation of the

    membrane around the brain and spinal cord)

  • Liver failure, liver damage and

    severe liver inflammation (fulminant hepatitis) (sometimes fatal or requiring liver transplant). Symptoms may include nausea (feeling sick), diarrhoea, jaundice (yellow discolouration of the skin or eyes), dark urine, pale stools, bleeding easily, itching or chills

  • Liver problems (such as cholestasis

    and cholestatic hepatitis, which may be accompanied by symptoms such

    as discoloured stools, nausea and yellowing of the skin or eyes)

    • Inflammation of the kidneys and

      other kidney problems (such as nephrotic syndrome and minimal change disease, which may be accompanied by symptoms such as water retention (oedema), foamy urine, fatigue and a loss of appetite)

    • Worsening of epilepsy (possible

      more frequent and/or severe seizures)

    • Blockage of an artery or vein in the

      eye leading to partial or complete loss of vision

    • Inflamed blood vessels (can cause

      fever, aches, purple blotches on the skin)

    • A reduction in the number of red

      and white blood cells and platelets (may cause tiredness, easy bruising, frequent nose bleeds and increased risk of infections)

    • Muscle pain and weakness
    • Impaired sense of smell
    • Loss of taste

Not known: frequency cannot be estimated from the available data

  • Decreased fertility in females,

    which is usually reversible on discontinuation of the medicine

  • Other serious skin conditions such

    as fixed drug eruption (a distinctive cutaneous allergic reaction that usually recurs at the same site(s) on re-exposure to the medication and may look like round or oval patches of redness and swelling of the skin, blistering (hives), itching) and generalised bullous fixed drug eruption (can involve widespread skin reactions)

In clinical studies not associated with arthritis or other arthritic conditions, where Celebrex was

taken at doses of 400 mg per day for up to 3 years, the following additional side effects have been observed: Common: may affect up to 1 in

10 people

  • Heart problems: angina (chest pain)
  • Stomach problems: irritable bowel

    syndrome (can include stomach ache, diarrhoea, indigestion, wind)

  • Kidney stones (which may lead to

    stomach or back pain, blood in urine), difficulty passing urine

  • Weight gain

Uncommon: may affect up to 1 in

100 people

  • Deep vein thrombosis (blood clot

    usually in the leg, which may cause pain, swelling or redness of the calf or breathing problems)

  • Stomach problems: stomach

    infection (which can cause irritation and ulcers of the stomach and intestines)

  • Lower limb fracture
  • Shingles, skin infection, eczema

    (dry itchy rash), pneumonia (chest infection (possible cough, fever, difficulty breathing))

  • Floaters in the eye causing blurred

    or impaired vision, vertigo due to inner ear troubles, sore, inflamed or bleeding gums, mouth sores

  • Excessive urination at night,

    bleeding from piles/ haemorrhoids, frequent bowel movements

  • Fatty lumps in skin or elsewhere,

    ganglion cyst (harmless swellings on or around joints and tendons in the hand or foot), difficulty speaking, abnormal or very heavy bleeding from the vagina, breast pain

  • High levels of sodium in blood test

    results

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 (see details below). By reporting side effects you can help provide more information on the safety of this medicine.

United Kingdom

Yellow Card Scheme website: www.mhra.gov.uk/yellowcard or search for MHRA Yellow Card in the Google Play or Apple App Store.

5. How to store Celebrex

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 blister and carton. The expiry date refers to the last day of that month. Do not store Celebrex above 30 oC. 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 Celebrex contains

  • The active substance is celecoxib.

    Each capsule contains 100 mg or 200 mg celecoxib.

  • The other ingredients are Lactose

    monohydrate, sodium laurilsulfate, povidone, croscarmellose sodium, magnesium stearate. Capsule shells contain gelatin, titanium dioxide E171, sodium laurilsulfate and sorbitan monolaurate. Printing ink contains shellac, propylene glycol, indigotine E132 (100 mg capsule), iron oxide E172 (200 mg capsule).

    What Celebrex looks like and contents of the pack

    Celebrex is available as capsules. Opaque, white with two blue bands marked 7767 and 100 (Celebrex 100 mg). Opaque, white with two gold bands marked 7767 and 200 (Celebrex 200 mg). The capsules are packaged in clear or opaque PVC/aluminium blisters. Celebrex is contained in packs of 2, 5, 6, 10, 20, 30, 40, 50, 60, 100, 10x10, 10x30, 10x50, 1x50 unit dose, 1x100 unit dose, 5x(10x10).

    Not all pack sizes may be marketed. Marketing Authorisation Holder and

    Manufacturer

    Marketing Authorisation Holder United Kingdom

    Viatris Products Limited,

    Station Close,

    Potters Bar,

    EN6 1TL,

    United Kingdom.

    Manufacturer

    Pfizer Manufacturing Deutschland GmbH

    Mooswaldallee 1,

    79108 Freiburg Im Breisgau

    Germany or

    Klocke Verpackungs-Service GmbH Max-Becker-Str. 6

    76356 Weingarten (Baden)

    Germany

    This leaflet was last revised in

    600103904 3989268

About this document

Source: MHRA - Medicines and Healthcare products Regulatory Agency (products.mhra.gov.uk) · Marketing authorisation: PL 46302/0274

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 Celebrex 200 mg capsules

Prescription needed? Yes, prescription-only medicine (POM)
Active substance Celecoxib
Strength 200 mg
Pharmaceutical form Oral capsule
Opaque, white with two gold bands marked 7767 and 200.
How is it taken Oral
Excipients Lactose monohydrate, Sodium laurilsulfate, Povidone, Croscarmellose sodium, Magnesium stearate, Gelatin, Titanium dioxide E171, Sorbitan monolaurate, Iron oxide E172, Shellac, Propylene glycol
Pack sizes 30 capsule
Is it available? Listed as available (NHS Dictionary of Medicines and Devices – not a record of current supplies)
Shelf life 3 years
Storage Do not store above 30 °C.
Drug group (ATC) Non-steroidal anti-inflammatory and antirheumatic drugs, NSAIDs, 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. M01AH01 celecoxib
Marketing authorisation PL 46302/0274 (first authorised 3 December 2009)
Marketing authorisation holder Viatris Products Limited
Codes GTIN 1210001140820 · 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.