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Teva-Diclofenac: Uses, Side Effects and Dosage

Updated:
Facts
Status:
Prescription (Rx) Current status: Cancelled Post Market
Strength:
100 mg, 50 mg
Active ingredient:
ATC code:

Patient Medication Information: uses, side effects, how to take - Teva-Diclofenac

ABOUT THIS MEDICATION

What the Medication is used for:

Your health care provider has prescribed TEVA-DICLOFENAC EC or TEVA-DICLOFENAC SR or TEVA-DICLOFENAC for you to relieve pain and swelling in rheumatoid arthritis and osteoarthritis, including degenerative joint disease of the hip.

What it does:

TEVA-DICLOFENAC EC, TEVA-DICLOFENAC SR and TEVA-DICLOFENAC (diclofenac sodium), as nonsteroidal anti-inflammatory drugs (NSAIDs), can reduce the chemicals prostaglandins produced by your body which cause pain and swelling.

TEVA-DICLOFENAC EC, TEVA-DICLOFENAC SR and TEVA-DICLOFENAC, as nonsteroidal anti-inflammatory drugs (NSAIDs) do NOT cure your illness or prevent it from getting worse. TEVA-DICLOFENAC EC or TEVA-DICLOFENAC SR or TEVA-DICLOFENAC can only relieve pain and reduce swelling as long as you continue to take it.

When it should not be used:

DO NOT TAKE TEVA-DICLOFENAC EC or TEVA-DICLOFENAC SR or TEVA-DICLOFENAC if you have any of the following conditions:

  • Heart bypass surgery (planning to have or recently had)
  • Severe, uncontrolled heart failure
  • Bleeding in the brain or other bleeding disorders
  • Current pregnancy (after 28 weeks of pregnancy)

    • Currently breastfeeding (or planning to

      breastfeed)

    • Allergy (hypersensitivity) to diclofenac sodium, or ASA (Acetylsalicylic Acid) or other NSAIDs (Nonsteroidal Anti- Inflammatory Drugs), or any of the nonmedicinal ingredients in TEVA-DICLOFENAC EC or TEVA-DICLOFENAC SR or TEVA-DICLOFENAC
    • Ulcer (active)
    • Bleeding or perforation from the stomach or gut (active)
    • Inflammatory bowel disease (Crohn’s Disease

      or Ulcerative Colitis)

    • Liver disease (active or severe)
    • Kidney disease (severe or worsening)
    • High potassium in the blood

Do not use TEVA-DICLOFENAC suppositories if you have inflammation of the rectum or anus or have a recent history of bleeding from the rectum or anus.

Patients who took a drug in the same class as TEVA-DICLOFENAC EC, TEVA-DICLOFENAC SR and TEVA-DICLOFENAC after a type of heart surgery (coronary artery bypass grafting (CABG)) were more likely to have heart attacks, strokes, blood clots in the leg(s) or lung(s), and infections or other complications than those who did NOT take that drug.

TEVA-DICLOFENAC EC, TEVA-DICLOFENAC SR and TEVA-DICLOFENAC should NOT be used in patients under 16 years of age since the safety and effectiveness have NOT been established.

What the medicinal ingredient is:

diclofenac sodium.

What the non-medicinal ingredients are:

TEVA-DICLOFENAC EC (diclofenac sodium) 25 mg and 50 mg enteric coated tablets:

Each tablet contains the medicinal ingredient diclofenac sodium and non-medicinal ingredients: magnesium stearate, microcrystalline cellulose, povidone, pregelatinized starch, silicon dioxide, sodium lauryl sulfate and sodium starch glycolate.

The film coating contains (25mg): D&C Yellow # 10, hypromellose, iron oxide red, iron oxide yellow, maltodextrin, methacrylic acid, polyethylene glycol, talc, titanium dioxide, triethyl citrate

The film coating contains (50mg): hypromellose, iron oxide black, iron oxide red, iron oxide yellow, maltodextrin, methacrylic acid, polyethylene glycol, talc, titanium dioxide, triethyl citrate

Printing ink contains: black iron oxide, lecithin, shellac glaze, simethicone

TEVA-DICLOFENAC SR (diclofenac sodium) 75 mg and 100 mg slow release tablets:

Each tablet contains the medicinal ingredient diclofenac sodium and non-medicinal ingredients: colloidal silicon dioxide, lactose monohydrate, magnesium stearate and povidone.

The film coating contains: aquacoat ECD-30, dibutyl sebacate, FD&C Blue #2, FD&C Red #40, FD&C Yellow #6, hypromellose, polyethylene glycol, polysorbate and titanium dioxide.

TEVA-DICLOFENAC (diclofenac sodium) 50 mg and 100 mg suppositories:

Each rectal suppository contains the medicinal ingredient diclofenac sodium and non-medicinal ingredients: diglyceride, monoglyceridem free glycerin, free fatty acids and triglycerides.

What dosage forms it comes in:

TEVA-DICLOFENAC EC (diclofenac sodium) 25 mg: Yellowish, tan coloured, round, bi-convex , enteric film coated tablets, printed with black ink modified N/25 on one side and plain on the reverse.

TEVA-DICLOFENAC EC (diclofenac sodium) 50 mg: Tan coloured, round, bi-convex, enteric film coated tablets, printed with black ink modified N/50 on one side and plain on the reverse.

TEVA-DICLOFENAC SR (diclofenac sodium) 75 mg: Light pink triangular standard bi-convex bevel-edged film coated slow release tablets. Printed with black ink N on one side and SR /75 on the reverse.

TEVA-DICLOFENAC SR (diclofenac sodium) 100mg: Pink round bi-convex bevel-edged film coated slow release tablets. Printed N on one side and SR/100 on the reverse.

TEVA-DICLOFENAC (diclofenac sodium) 50mg: Yellowish-white coloured, smooth, torpedo-shaped suppositories.

TEVA-DICLOFENAC (diclofenac sodium) 100mg: Yellowish-white coloured, smooth, torpedo-shaped suppositories.

Check with your pharmacist if the identifying markings or colour appear different.

WARNINGS AND PRECAUTIONS

If you have, or previously had, any of the following conditions, see your health care provider to discuss treatment options other than TEVA-DICLOFENAC EC or TEVA-DICLOFENAC SR or TEVA-DICLOFENAC:

  • Heart Attack or Angina
  • Stroke or Mini-stroke
  • Loss of Vision
  • Current Pregnancy (less than 28 weeks)
  • Congestive Heart Failure
  • High blood pressure
  • Diabetes
  • High levels of fats in your blood
  • Smoking

It is important to take the lowest dose of TEVA-DICLOFENAC EC, TEVA-DICLOFENAC SR and TEVA-DICLOFENAC that relieves your pain and/or swelling and for the shortest time possible in order to keep your risk of side effects on the heart and blood vessels as small as possible.

Use of NSAIDS, such as TEVA-DICLOFENAC EC, TEVA-DICLOFENAC SR and TEVA-DICLOFENAC can result in increased blood pressure and /or worsening of congestive heart failure.

Use of NSAIDs, such as TEVA-DICLOFENAC EC, TEVA-DCLOFENAC SR and TEVA-DICLOFENAC, may cause stomach and bowel problems (such as ulceration, perforation, obstruction and bleeding).

Before taking this medication, tell your health care provider if you have any of the following:

  • Disease of the heart or blood vessels (also called cardiovascular disease, including uncontrolled high blood pressure, congestive heart failure, established ischemic heart disease, or peripheral arterial disease), as treatment with TEVA-DICLOFENAC,TEVA-DICLOFENAC SR and TEVA-DICLOFENAC in these cases is not recommended.
  • Risk factors for cardiovascular disease (see above) such as high blood pressure, abnormally high levels of fat (cholesterol, triglycerides) in your blood, diabetes, or if you smoke.
  • Diabetes mellitus or on a low sugar diet
  • Atherosclerosis
  • Poor circulation to your extremities
  • Kidney disease or urine problems
  • Previous ulcer or bleeding from the stomach or gut
  • Previous bleeding in the brain
  • Bleeding problems
  • Family history of allergy to NSAIDs, such as acetylsalicylic acid (ASA), celecoxib, diclofenac, diflunisal, etodolac, fenoprofen, flurbiprofen, ibuprofen, indomethacin, ketoprofen, ketorolac, mefenamic acid, meloxicam, nabumetone, naproxen, oxaprozin, piroxicam, rofecoxib, sulindac, tenoxicam, tiaprofenic acid, tolmetin, or valdecoxib (NOT a complete list)
  • Family history of asthma, nasal polyps, long- term swelling of the sinus (chronic sinusitis) or hives

Also, before taking this medication, tell your health care provider if you are pregnant or you are planning to get pregnant.

While taking this medication:

  • Tell any other doctor, dentist, pharmacist or other health care professional that you see, that you are taking this medication, especially if you are planning to have heart surgery;
  • Do NOT drink alcoholic beverages while taking this medication because you would be more likely to develop stomach problems;
  • Fertility may be decreased. The use of TEVA-DICLOFENAC EC or TEVA-DICLOFENAC SR or TEVA-DICLOFENAC is not recommended in women trying to get pregnant. In women who have difficulty conceiving, stopping TEVA-DICLOFENAC EC or TEVA-DICLOFENAC SR or TEVA-DICLOFENAC should be considered.
  • If you have cardiovascular disease or risks for cardiovascular disease, your doctor will periodically re-evaluate whether you should continue treatment with TEVA-DICLOFENAC EC or TEVA-DICLOFENAC SR or TEVA-DICLOFENAC.
  • Your doctor will monitor your kidney function, your liver function and your blood count to decide if TEVA-DICLOFENAC EC or TEVA-DICLOFENAC SR or TEVA-DICLOFENAC needs to be discontinued or if the dose needs to be changed.

    If, at any time while taking TEVA-DICLOFENAC or TEVA-DICLOFENAC SR or TEVA-DICLOFENAC you experience any signs or symptoms of problems with your heart or blood vessels such as chest pain, shortness of breath, weakness, or slurring of speech, contact your doctor immediately.

    Long-term use of TEVA-DICLOFENAC EC or TEVA-DICLOFENAC SR or TEVA-DICLOFENAC might increase the risk of heart attacks or strokes.

    TEVA-DICLOFENAC EC or TEVA-DICLOFENAC SR or TEVA-DICLOFENAC is NOT recommended for use in patients under 16 years of age since safety and effectiveness have NOT been established.

INTERACTIONS WITH THIS MEDICATION

What About Taking Other Drugs At The Same

Time?

See your health care provider and pharmacist if you are taking any other medication (prescription or non- prescription) such as any of the following (NOT a complete list):

  • Acetaminophen
  • Acetylsalicylic Acid (ASA) or other NSAIDs e.g. ASA, celecoxib, diclofenac, ibuprofen, indomethacin, ketorolac, meloxicam, naproxen
  • Alcohol
  • Antacids
  • Anti-depressants
  • Selective Serotonin Reuptake Inhibitors (SSRIs)

    e.g. citalopram, fluoxetine, paroxetine, sertraline

  • Blood pressure medications

    • ACE (angiotensin converting enzyme)

inhibitors

e.g. enalapril, lisinopril, perindopril, ramipril

  • ARBs (angiotensin II receptor blockers)

e.g. candesartan, irbesartan, losartan, valsartan

  • Beta-blockers e.g. metoprolol
  • Blood thinners (medicine used to prevent blood- clotting)

    e.g. warfarin, ASA, clopidogrel

  • Corticosteroids (including glucocorticoids) (medicines used to provide relief for inflamed areas of the body)

    e.g. prednisone

  • Cyclosporin (a medicine primarily used in patients who have received organ transplants)
  • Digoxin (a medicine used for heart problems)
  • Diuretics (medicines used to increase the amount of urine)

    e.g. furosemide, hydrochlorothiazide

  • Lithium
  • Methotrexate (a medicine used to treat some kinds of cancer or arthritis)
  • Oral hypoglycemics (diabetes medications such as metformin)
  • Phenytoin (a medicine used to treat seizures).
  • Probenecid
  • Quinolone antibacterials (medicines used against infection)
  • Rifampin (an antibiotic medicine used to treat bacterial infections)
  • Sulfinpyrazone (a medicine used to treat gout)
  • Tacrolimus (a medicine primarily used in patients who have received organ transplants)
  • Trimethroprim (a medicine used to prevent or treat urinary tract infection)
  • Voriconazole (a medicine used to treat fungal infections)

Your health care provider may prescribe low dose ASA (acetylsalicylic acid) as a blood thinner to reduce your risk of having a heart attack or stroke) while you are taking TEVA-DICLOFENAC EC or TEVA-DICLOFENAC SR or TEVA-DICLOFENAC. Take only the amount of ASA prescribed by your health care provider. You are more likely to upset or damage your stomach if you take both TEVA-DICLOFENAC EC or TEVA-DICLOFENAC SR or TEVA-DICLOFENAC and ASA than if you took TEVA-DICLOFENAC EC or TEVA-DICLOFENAC SR or TEVA-DICLOFENAC alone.

PROPER USE OF THIS MEDICATION

TEVA-DICLOFENAC EC, TEVA-DICLOFENAC is used for maintenance therapy only.

Usual Dose for patients 16 years of age and older:

Medical ConditionStarting Dose (per day)
TEVA-DICLOFENAC EC 25 mg enteric-coated tablets
Rheumatoid Arthritis25 mg 3 times a day.
Osteoarthritis25 mg 3 times a day.

Medical

Condition

Maintenance Dose

Maximum Dose

(per day)

TEVA-DICLOFENAC EC 50 mg enteric-coated tablets
Rheumatoid Arthritis50 mg twice daily100 mg
Osteoarthritis50 mg twice daily100 mg
TEVA-DICLOFENAC SR 75 & 100 mg slow-release tablets
Rheumatoid Arthritis75 mg once daily100 mg
Osteoarthritis75 mg once daily100 mg
TEVA-DICLOFENAC 50 mg and 100 mg suppositories
Rheumatoid Arthritis50 mg once daily100 mg
Osteoarthritis50 mg once daily100 mg

Take TEVA-DICLOFENAC EC or TEVA-DICLOFENAC SR or TEVA-DICLOFENAC only as directed by your health care provider. Do NOT take more of it, do NOT take it more often and do NOT take it for a longer period of time than your health care provider recommended. If possible, you should take the lowest dose of this medication for the shortest time period. Taking too much TEVA-DICLOFENAC EC or TEVA-DICLOFENAC SR or TEVA-DICLOFENAC may increase your chances of unwanted and sometimes dangerous side effects, especially if you are elderly and frail or if you have a low body weight, have other diseases or take other medications.

If you will be using TEVA-DICLOFENAC EC or TEVA-DICLOFENAC SR or TEVA-DICLOFENAC for more than 7 days, see your health care provider regularly to discuss whether this medicine is working for you and if it is causing you any unwanted effects.

Swallow the tablet whole with water, do not chew or divide the tablet. It is best to take your dose at the same time each day.

To help reduce the possibility of stomach upset you should take TEVA-DICLOFENAC EC or TEVA-DICLOFENAC SR or TEVA-DICLOFENAC immediately after a meal or with food or milk. Also, you should remain standing or sitting upright (i.e. do not lie down) for about 15-30 minutes after taking the medicine. This helps to prevent irritation that may lead to trouble swallowing. If stomach upset (indigestion, nausea, vomiting, stomach pain or diarrhea) occurs and continues, contact your doctor.

Using Suppositories

TEVA-DICLOFENAC suppositories (50 and 100 mg) are wrapped in a plastic film. Make sure that the plastic wrapping is fully removed before inserting the suppository into the rectum. It is best to take the suppositories after emptying your bowels.

Do not take suppositories by mouth.

This medication has been prescribed specifically for you. Do NOT give it to anyone else. It may harm them, even if their symptoms seem to be similar to yours.

Missed dose:

If you forget to take your scheduled dose, you should not double the next scheduled dose to make up for the missed dose.

Overdose:

If you have accidentally taken more than the prescribed dose of TEVA-DICLOFENAC EC, TEVA-DICLOFENAC or TEVA-DICLOFENAC SR, contact your doctor, pharmacist or poison control centre immediately or go to the hospital emergency unit at once. You may require medical attention.

SIDE EFFECTS AND WHAT TO DO ABOUT THEM

TEVA-DICLOFENAC EC or TEVA-DICLOFENAC SR or TEVA-DICLOFENAC may cause some side effects, especially when used for a long time or in large doses. When these side effects occur, you may require medical attention. Report all symptoms or side effects to your health care provider

TEVA-DICLOFENAC EC or TEVA-DICLOFENAC SR or TEVA-DICLOFENAC may cause you to become drowsy or tired. Be careful about driving or participating in activities that require you to be alert. If you become drowsy, dizzy or light-headed after taking TEVA-DICLOFENAC EC or TEVA-DICLOFENAC SR or TEVA-DICLOFENAC, do NOT drive or operate machinery.

TEVA-DICLOFENAC EC or TEVA-DICLOFENAC SR or TEVA-DICLOFENAC may cause you to become more sensitive to sunlight. Any exposure to sunlight or sunlamps may cause sunburn, skin blisters, skin rash, redness, itching or discolouration, or vision changes. If you have a reaction from the sun, check with your health care provider.

Check with your health care provider IMMEDIATELY if you develop chills, fever, muscle aches or pains, or other flu-like symptoms, especially if they occur before or together with a skin rash. These symptoms may be the first signs of a SERIOUS ALLERGIC REACTION to this medication.

SERIOUS SIDE EFFECTS AND WHAT TO DO

ABOUT THEM

Symptom

STOP taking

TEVA-DICLOFENAC EC or

TEVA-DICLOFENAC SR or TEVA-DICLOFENAC and get emergency medical attention IMMEDIATELY

STOP taking

TEVA-DICLOFENA C-EC or

TEVA-DICLOFENA C SR or TEVA-DICLOFENA C and talk to your physician or pharmacist

Bloody or black tarry stools, vomiting blood√

SERIOUS SIDE EFFECTS AND WHAT TO DO

ABOUT THEM

Spontaneous bleeding or bruising (signs of thrombocytopenia)√
Shortness of breath, wheezing, any trouble breathing or chest tightness√
Skin rash, hives, swelling or itching√

Skin rash with flacking or peeling

(signs of dermatitis exfoliative).

√

Purple skin patches (signs of purpura or

Henoch-Schonlein purpura if caused by an allergy).

√
Blurred vision, or any visual disturbance√
Any change in the amount or colour of your urine (red or brown)√
Any pain or difficulty experienced while urinating√

Swelling of the feet, lower legs;

weight gain

√
Swelling mainly of the face and throat (signs of angioedema)√
Vomiting or persistent indigestion, nausea, stomach pain or diarrhea√
Yellow discolouration of the skin or eyes (signs of liver failure), with or without itchy skin skin√

Malaise, fatigue, loss of appetite or

« flu-like »

symptoms

√

SERIOUS SIDE EFFECTS AND WHAT TO DO

ABOUT THEM

Headaches, stiff

neck, fever, nausea, vomiting (signs of aseptic meningitis)

√

Mental confusion,

depression

√

Dizziness,

lightheadedness

√
Hearing problems√

Rectal itching or

bleeding

√

Right upper

abdominal discomfort or pain

√

This is NOT a complete list of side effects. If you develop any other symptoms while taking TEVA-DICLOFENAC EC and/or TEVA-DICLOFENAC SR and/or TEVA-DICLOFENAC, see your health care provider.

HOW TO STORE IT

Store between 15°-30°C. Unit dose strips should be stored between 15°-25°C and protected from high humidity.

Do NOT keep outdated medicine or medicine no longer needed. Any outdated or unused medicine should be returned to your pharmacist.

Keep this and all medication out of the reach of children.

REPORTING SUSPECTED SIDE EFFECTS

Reporting Side Effects

You can help improve the safe use of health products for Canadians by reporting serious and unexpected side effects to Health Canada. Your report may help to identify new side effects and change the product safety information.

3 ways to report:

  • Online at MedEffect (http://hc-sc.gc.ca/dhp-mps/medeff/index-eng.php);
  • By calling 1-866-234-2345 (toll-free);
  • By completing a Consumer Side Effect Reporting Form and sending it by:

    • Fax to 1-866-678-6789 (toll-free), or
    • Mail to: Canada Vigilance Program

      Health Canada

      Postal Locator 0701E

      Ottawa, ON

      K1A 0K9

Postage paid labels and the Consumer Side Effect Reporting Form are available at MedEffect (http://hc-sc.gc.ca/dhp-mps/medeff/index-eng.php).

NOTE: Contact your health professional if you need information about how to manage your side effects. The Canada Vigilance Program does not provide medical advice.

MORE INFORMATION

This document plus the full product monograph, prepared for health professionals can be found by contacting Teva Canada Limited by:

Phone: 1-800-268-4127 ext. 3;

Email: druginfo@tevacanada.com; or

Fax: 1-416-335-4472

Teva Canada Limited

30 Novopharm Court

Toronto, Ontario

Canada, M1B 2K9

www.tevacanada.com

Last revised: August 15, 2016

About this document

Source: Health Canada – Drug Product Database (DPD) and product monographs · DIN (Drug Identification Number): 02174685

Revision date stated in the text: August 15, 2016

Found a mistake? Write to us via the contact page.

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

Drug information for Teva-Diclofenac

Rx or OTC
Prescription (Rx)?
DIN 02174685, 02174677
Schedule(s) PRESCRIPTION
Active ingredient(s) Diclofenac sodium
Dosage form(s) Suppository
Route(s) of administration Rectal
Drug class (WHO ATC)
  1. M Musculo-skeletal system drugs
    1. M01 Antiinflammatory and antirheumatic products
      1. M01A Antiinflammatory and antirheumatic products, non-steroids
        1. M01AB Acetic acid derivatives and related substances
          1. M01AB05 Diclofenac
Company TEVA CANADA LIMITED
Current status Cancelled Post Market
Current status date June 15, 2018
Strengths and forms
DIN Strength Dosage form(s) Current status
02174685 100 MG Suppository Cancelled Post Market June 15, 2018
02174677 50 MG Suppository Cancelled Post Market June 15, 2018

Source: Health Canada – Drug Product Database (DPD) and product monographs, data as of November 1, 2026. Data from the Health Canada Drug Product Database, as published there. Not a substitute for the advice of a doctor or pharmacist.