Etodolac Tablets USP 400mg Taj Pharma

Etodolac Tablets USP 400mg Taj Pharma

1. Name of the medicinal product

Etodolac Tablets USP 300mg Taj Pharma
Etodolac Tablets USP 400mg Taj Pharma

2. Qualitative and quantitative composition

Each tablet contains
Etodolac USP                                    300mg
Excipient                                             q.s

Each tablet contains
Etodolac USP                                      400mg
Excipient                                             q.s
For the full list of excipients, see section 6.1.

3. Pharmaceutical form

Film Coated tablet.

4. Clinical particulars

4.1 Therapeutic indications

Etodolac is indicated for acute or long-term use in rheumatoid arthritis and osteoarthritis.

4.2 Posology and method of administration

Posology

Adults

One tablet daily, taken with a glass of water.

Etodolac must be swallowed whole.

The safety of doses in excess of 300mg/400mg per day has not been established.

No occurrence of tolerance or tachyphylaxis has been reported.

Elderly

No change in initial dosage is generally required in the elderly (see section 4.4). The elderly are at increased risk of the serious consequences of adverse reactions. If an NSAID is considered necessary, the lowest effective dose should be used and for the shortest possible duration. The patient should be monitored regularly for GI bleeding during NSAID therapy.

Paediatric population

Use in children is not recommended.

Method of administration

For oral administration.

To be taken preferably with or after food.

Undesirable effects may be minimised by using the lowest effective dose for the shortest duration necessary to control symptoms (see section 4.4).

4.3 Contraindications

Hypersensitivity to the active substance or to any of the excipients listed in section 6.1.

NSAIDs are contraindicated in patients who have previously shown hypersensitivity reactions (e.g. asthma, rhinitis, angioedema or urticaria) during therapy with ibuprofen, aspirin, or other non-steroidal anti-inflammatory drugs.

History of gastrointestinal bleeding or perforation, related to previous NSAIDs therapy.

Active or history of recurrent peptic ulceration or a history of peptic ulcer disease (with two or more distinct episodes of proven ulceration or bleeding).

Severe heart failure, hepatic failure and renal failure (see section 4.4).

During the last trimester of pregnancy (see section 4.6).

4.4 Special warnings and precautions for use

Undesirable effects may be minimized by using the lowest effective dose for the shortest duration necessary to control symptoms (see section 4.2, and GI and cardiovascular risks below).

The use of etodolac with concomitant NSAIDs including cyclooxygenase-2-selective inhibitors should be avoided (see section 4.5).

Elderly

The elderly have an increased frequency of adverse reactions to NSAIDs especially gastrointestinal bleeding and perforation, which may be fatal (see section 4.2).

Platelets

Although non-steroidal anti-inflammatory drugs do not have the same direct effects on platelets as does aspirin, all drugs which inhibit the biosynthesis of prostaglandins may interfere, to some extent, with platelet function. Patients receiving etodolac who may be adversely affected by such actions should be carefully observed.

Cardiovascular, renal and hepatic impairment

In patients with renal, cardiac or hepatic impairment especially those taking diuretics and the elderly, renal function should be monitored in these patients (see also section 4.3). Caution is required since the use of NSAIDs may result in a dose dependent reduction in prostaglandin formation and precipitate renal failure. The dose should be kept as low as possible. However, impairment of renal or hepatic functions due to other causes may alter drug metabolism; patients receiving concomitant long-term therapy, especially the elderly, should be observed for potential side effects and their drug doses adjusted as needed, or the drug discontinued.

Patients on long-term treatment with etodolac should be regularly reviewed as a precautionary measure e.g. for changes in renal function, haematological parameters, or hepatic function.

Cardiovascular and cerebrovascular effects

Appropriate monitoring and advice are required for patients with a history of hypertension and/or mild to moderate congestive heart failure as fluid retention and oedema have been reported in association with NSAID therapy.

Clinical trial and epidemiological data suggest that use of some NSAIDs (particularly at high doses and in long term treatment) may be associated with a small increased risk of arterial thrombotic events (for example myocardial infarction or stroke). There are insufficient data to exclude such a risk for etodolac.

Patients with uncontrolled hypertension, congestive heart failure, established ischaemic heart disease, peripheral arterial disease, and/or cerebrovascular disease should only be treated with etodolac after careful consideration. Similar consideration should be made before initiating longer-term treatment of patients with risk factors for cardiovascular disease (e.g. hypertension, hyperlipidaemia, diabetes mellitus, smoking).

Dermatological

Serious skin reactions, some of them fatal, including exfoliative dermatitis, Stevens-Johnson syndrome, and toxic epidermal necrolysis have been reported very rarely in association with the use of NSAIDs (see section 4.8). Patients appear to be at highest risk for these reactions early in the course of therapy: the onset of the reaction occurring in the majority of cases within the first month of treatment. Etodolac should be discontinued at the first appearance of the skin rash, mucosal lesions, or any other sign of hypersensitivity.

Respiratory disorders

Caution is required if etodolac is administered to patients suffering from, or with a previous history of, bronchial asthma since NSAIDs have been reported to precipitate bronchospasm in such patients.

SLE and mixed connective tissue disease

In patients with systemic lupus erythematous (SLE) and mixed connective tissue disorders there may be an increased risk of aseptic meningitis (see section 4.8)

Impaired female fertility

The use of etodolac may impair female fertility and is not recommended in woman attempting to conceive. In women who have difficulties conceiving or who are undergoing investigation of infertility, withdrawal of etodolac should be considered.

Gastrointestinal bleeding, ulceration and perforation

Serious gastrointestinal adverse effects such as bleeding, ulceration and perforation, which can be fatal, has been reported with all NSAIDs at any time during treatment, with or without warning symptoms or a previous history of serious GI events. If any sign of gastrointestinal bleeding occurs, etodolac should be stopped immediately.

The risk of GI bleeding, ulceration or perforation is higher with increasing NSAID doses, in patients with a history of ulcer, particularly if complicated with haemorrhage or perforation (see section 4.3), and in the elderly. These patients should commence treatment on the lowest dose available. Combination therapy with protective agents (e.g. misoprostol or proton pump inhibitors) should be considered for these patients, and also for patients requiring concomitant low dose aspirin or other drugs likely to increase gastrointestinal risk (see section 4.5)

Patients with a history of GI toxicity, particularly when elderly, should report any unusual abdominal symptoms (especially GI bleeding) particularly in the initial stages of treatment.

Caution should be advised in patients receiving concomitant medications which could increase the risk of ulceration or bleeding, such as oral corticosteroids, anticoagulants such as warfarin, selective serotonin-reuptake inhibitors or anti-platelet agents such as aspirin (see section 4.5)

When GI bleeding or ulceration occurs in patients receiving etodolac, the treatment should be withdrawn.

NSAIDs should be given with care to patients with a history of gastrointestinal disease (ulcerative colitis, Crohn’s disease) as these conditions may be exacerbated (see section 4.8).

Patients with rare hereditary problems or galactose intolerance, the Lap lactase deficiency or glucose-galactose malabsorption should not take this medicine.

4.5 Interaction with other medicinal products and other forms of interaction

Corticosteroids: increased risk of gastrointestinal ulceration or bleeding (see section 4.4)

Anti-coagulants: NSAIDs may enhance the effects of anti-coagulants, such as warfarin (see section 4.4).

Since etodolac is extensively protein-bound, it may be necessary to modify the dosage of other highly protein-bound drugs.

Bilirubin tests can give a false positive result due to the presence of phenolic metabolites of etodolac in the urine.

Anti-hypertensives: Reduced anti-hypertensive effect.

Mifepristone: NSAIDs should not be used for 8 – 12 days after mifepristone administration as NSAIDs can reduce the effect of mifepristone.

Other analgesics including cyclooxygenase-2 selective inhibitor: Avoid concomitant use of two or more NSAIDs (including aspirin) as this may increase the risk of adverse effects (see section 4.4).

Quinolone antibiotics: Animal data indicate that NSAIDs can increase the risk of convulsions associated with quinolone antibiotics. Patients taking NSAIDs and quinolones may have an increased risk of developing convulsions.

Diuretics: Reduced diuretic effect. Diuretics can increase the risk of nephrotoxicity of NSAIDs.

Cardiac glycosides: NSAIDs may exacerbate cardiac failure, reduce GFR and increase plasma glycoside levels.

Lithium: Decreased elimination of lithium.

Methotrexate: Decreased elimination of methotrexate.

Ciclosporin: Increased risk of nephrotoxicity.

Anti-platelet agents and selective serotonin reuptake inhibitors (SSRIs): Increased risk of gastrointestinal bleeding (see section 4.4).

Tacrolimus: Possible increased risk of nephrotoxicity when NSAIDs are given with tacrolimus.

Zidovudine: Increased risk of haematological toxicity when NSAIDs are given with zidovudine. There is a evidence of an increased risk of haemarthroses and haematoma in HIV(+) haemophiliacs receiving concurrent treatment with zidovudine and ibuprofen.

4.6 Fertility, pregnancy and lactation

Pregnancy

Drugs which inhibit prostaglandin biosynthesis may cause dystocia and delayed parturition as evidenced by studies in pregnant animals.

Congenital abnormalities have been reported in association with NSAID administration in man; however, these are low in frequency and do not appear to follow any discernible pattern. In view of the known effects of NSAIDs on the foetal cardiovascular system, some inhibitors of prostaglandin biosynthesis have been shown to interfere with the risk of closure of the ductus arteriosus, use in the last trimester of pregnancy is contraindicated. The onset of labour may be delayed and the duration increased with an increased bleeding tendency in both mother and child (see section 4.3). NSAIDs should not be used during the first two trimesters of pregnancy or labour unless the potential benefit to the patient outweighs the potential risk to the foetus.

Breast-feeding

In limited studies so far available, NSAIDs can appear in breast milk in very low concentrations. NSAIDs should, if possible, be avoided when breastfeeding.

See section 4.4 Special warnings and precautions for use, regarding female fertility.

4.7 Effects on ability to drive and use machines

Etodolac can cause dizziness, drowsiness, fatigue or abnormal vision. Patients need to be aware of how they react to this medicine before driving or operating machines.

4.8 Undesirable effects

Gastrointestinal

The most commonly observed adverse events are gastrointestinal in nature. Peptic ulcers, perforation or GI bleeding, sometimes fatal, particularly in the elderly, may occur (see section 4.4). Nausea, vomiting, diarrhoea, epigastric pain, flatulence, constipation, dyspepsia, abdominal pain, melaena, haematemesis, ulcerative stomatitis, exacerbation of colitis and Crohn’s disease (see section 4.4), indigestion, heartburn, rectal bleeding have been reported following administration. Less frequently, gastritis has been observed. Pancreatitis has been reported very rarely.

Reported side effects include vasculitis, palpitations, anaphylactoid reaction, have been reported following administration.

Hypersensitivity

Hypersensitivity reactions have been reported following treatment with NSAIDs. These may consist of (a) non-specific allergic reactions and anaphylaxis (b) respiratory tract reactivity comprising asthma, aggravated asthma, bronchospasm or dyspnoea, or (c) assorted skin disorders, including rashes of various types, pruritus, urticaria, purpura, angioedema and more rarely exfoliative and bullous dermatoses (including epidermal necrolysis and erythema multiforme).

Cardiovascular and cerebrovascular

Oedema, hypertension and cardiac failure have been reported in association with NSAID treatment.

Clinical trial and epidemiological data suggest that use of some NSAIDs (particularly at high doses and in long term treatment) may be associated with an increased risk of arterial thrombotic events (for example myocardial infarction of stroke) (see section 4.4).

Other adverse reactions reported less commonly include:

Endocrine disorders

Oedema, pyrexia

Musculoskeletal connective tissue and bone disorders

Weakness/malaise

Respiratory, thoracic and mediastinal disorders

Dyspnoea

Neurological and special senses

Visual disturbances, optic neuritis, headaches, paraesthesia, reports of aseptic meningitis (especially in patients with existing auto-immune disorders, such as systemic lupus erythematosus, mixed connective tissue disease), with symptoms such as stiff neck, headache, nausea, vomiting, fever or disorientation (see section 4.4), depression, confusion, hallucinations, tinnitus, vertigo, dizziness, malaise, fatigue, tremor, insomnia, and drowsiness.

Dermatological

Bullous reactions including Stevens-Johnson syndrome, and Toxic Epidermal Necrolysis (very rare). Photosensitivity.

Haematological

Thrombocytopenia, neutropenia, agranulocytosis, aplastic anaemia and haemolytic anaemia.

Hepatic

Abnormal liver function, hepatitis and jaundice.

Renal

Bilirubinuria, urinary frequency, dysuria, Nephrotoxicity in various forms including interstitial nephritis, nephrotic syndrome and renal failure.

Reporting of suspected adverse reactions

Reporting suspected adverse reactions after authorisation of the medicinal product is important. It allows continued monitoring of the benefit/risk balance of the medicinal product.

4.9 Overdose

1. a) Symptoms

Symptoms include headache, nausea, vomiting, epigastric pain, gastrointestinal bleeding, rarely diarrhoea, disorientation, excitation, coma, drowsiness, dizziness, tinnitus, fainting, occasionally convulsions. In cases of significant poisoning acute renal failure and liver damage are possible.

1. b) Therapeutic measure

Patients should be treated symptomatically as required.

Within one hour of ingestion of a potentially toxic amount, activated charcoal should be considered. Alternatively, in adults, gastric lavage should be considered within one hour of indigestion of a potentially life-threatening overdose.

Good urine output should be ensured.

Renal and liver function should be closely monitored.

Patients should be observed for at least four hours after ingestion of potentially toxic amounts.

Frequent or prolonged convulsions should be treated with intravenous diazepam.

Other measures may be indicated by the patient’s clinical condition.

The standard practices of gastric lavage, activated charcoal administration and general supportive therapy should be undertaken.

5. Pharmacological properties

5.1 Pharmacodynamic properties

Pharmacotherapeutic group: anti-inflammatory and anti-rheumatic products, non-steroids, acetic acid derivatives and related substances,

Inhibition of prostaglandin synthesis and COX-2 selectivity

All non-steroidal anti-inflammatory drugs (NSAIDs) have been shown to inhibit the formation of prostaglandins. It is this action which is responsible both for their therapeutic effects and some of their side-effects. The inhibition of prostaglandin synthesis observed with etodolac differs from that of other NSAIDs. In an animal model at an established anti-inflammatory dose, cytoprotective PGE concentration in the gastric mucosa have been shown to be reduced to a lesser degree and for a shorter period than other NSAIDs. This finding is consistent with subsequent in-vitro studies which have found etodolac to be selective for induced cyclo-oxygenase 2 (COX-2, associated with inflammation) over COX-1 (cytoprotective).

Furthermore, studies in human cell models have confirmed that etodolac is selective for the inhibition of COX-2.

The clinical benefit of preferential COX-2 inhibition over COX-1 has yet to be proven.

Anti-inflammatory effects

Experiments have shown etodolac to have marked anti-inflammatory activity, being more potent than several clinically established NSAIDs.

5.2 Pharmacokinetic properties

In man, etodolac is well absorbed following oral administration.

Etodolac is highly bound to serum proteins.

The elimination half-life averages seven hours in man. The primary route of excretion is in the urine, mostly in the form of metabolites.

In subjects receiving daily doses of etodolac 400mg or 300mg/400mg to steady state levels over a three day period, the peak plasma concentrations were 7.5 μg/ml at 7.9 hours and 11.9 μg/ml at 7.8 hours.

5.3 Preclinical safety data

Preclinical data reveal no special hazard based on conventional studies of safety, pharmacology, repeated dose toxicity, genotoxicity and carcinogenic potential.

6. Pharmaceutical particulars

6.1 List of excipients

Tablet Core

Microcrystalline cellulose, Povidone, Methyl hydroxypropyl cellulose, Lactose anhydrous, Magnesium stearate

Tablet Coat

Hypromellose, Polydextrose, Macrogol, Triacetin, Titanium dioxide, Indigo Carmine Lake, Orange Yellow, Allura Red, Black iron oxide, Yellow iron oxide

6.2 Incompatibilities

Not applicable

6.3 Shelf life

2 years

6.4 Special precautions for storage

Keep out of the sight and reach of children.

Do not use after the expiry date printed on the carton.

6.5 Nature and contents of container

PVC/PVDC/Aluminium blister packs in outer cardboard cartons.

PVC/PE/Aclar/Aluminium blister packs in outer cardboard cartons.

White round HDPE container with PP safety cap with aluminium foil inner seal and purified cotton fill.

Available in pack sizes of 30 and 100 tablets.

Not all packs may be marketed.

6.6 Special precautions for disposal and other handling

No special requirements.

7. Manufactured By:
   Taj Pharmaceuticals Ltd.
   at: Plot. No. 220, Mahagujarat
   Industrial Estate, At & Post-Moraiya,
   Tal-Sanand, Dist- Ahmedabad Gujarat (India)

Etodolac  300mg/400mg   tablets USP

Package leaflet: Information for the user

Etodolac  300mg tablets USP Taj Pharma
Etodolac  400mg tablets USP Taj Pharma

etodolac

Read all of this leaflet carefully before you start taking this medicine because it contains important information for you.

• Keep this leaflet. You may need to read it again.
• If you have any further questions, ask your doctor or your pharmacist.
• This medicine has been prescribed for you only. Do not pass it on to others. It may harm them, even if their signs of illness are the same as yours.
• If you get any side effects, talk to your doctor or pharmacist. This includes any possible side effects not listed in this leaflet. See section 4.

What is in this leaflet

1. What Etodolac is and what it is used for
   2. What you need to know before you take Etodolac
   3. How to take Etodolac
   4. Possible side effects
   5. How to store Etodolac
   6. Contents of the pack and other information
2. What Etodolac is and what it is used for

Etodolac  is used to treat the symptoms of rheumatoid arthritis and osteoarthritis by reducing inflammation, swelling, stiffness and joint pain. This medicine is released slowly which means that you only have to take one tablet each day.

Etodolac  is one of a group of medicines called “non-steroidal anti-inflammatory drugs” (NSAIDs) which are usually taken to relieve pain, inflammation and stiffness often caused by osteoarthritis or rheumatoid arthritis.

2. What you need to know before you take Etodolac

Do not take Etodolac

• if you are allergic to etodolac or any of the other ingredients of this medicine (listed in section 6)
• if you have had an allergic reaction to other non-steroidal anti-inflammatory drugs such as aspirin or ibuprofen
• if you have experienced shortness of breath, rhinitis (blocked or runny nose) or urticaria (allergic skin reaction) when taking aspirin, ibuprofen or another non-steroidal anti-inflammatory drug
• if you have experienced gastrointestinal bleeding or perforation due to another non-steroidal anti-inflammatory drug
• if you have a peptic ulcer (ulcer in your stomach or duodenum) or have had two or more episodes of peptic ulcers, stomach bleeding or perforation
• if you have severe heart failure, liver failure or kidney failure
• if you are in your last trimester of pregnancy.

Warnings and precautions

Talk to your doctor or pharmacist before taking Etodolac

• if you have problems with your heart, liver or kidneys or suffer from a blood disorder
• if you have a mixed connective tissue disorder such as lupus (SLE)
• if you suffer from or have had asthma or breathing difficulties
• if you suffer from fluid retention, (swelling of legs ankles and feet)
• if you suffer from heart failure or high blood pressure
• if you are taking long term-therapy with a medicine other than Etodolac , as your doctor will want to arrange regular check-ups, especially if you are elderly
• if you have disease that affects your digestion such as ulcerative colitis or Crohn’s disease
• if you have heart problems, previous stroke or think that you might be at risk of these conditions (for example if you have high blood pressure, diabetes or high cholesterol or are a smoker)
• your doctor may carry out a number of blood, kidney function and liver function tests whilst you take Etodolac
• if you are currently taking “water-pills” (diuretics)
• if any signs of gastrointestinal bleeding.

Medicines such as Etodolac  may be associated with a small increased risk of heart attack (myocardial infarction) or stroke. Any risk is more likely with high doses and prolonged treatment. Do not exceed the recommended dose or duration of treatment.

Children

Etodolac  is not recommended for use in children.

Other medicines and Etodolac

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

Etodolac  can react with some medicines, which can cause unwanted effects or prevent the medicines from working properly

• drugs used to treat high blood pressure
• drugs used to thin the blood e.g. warfarin
• drugs called cardiac glycosides such as digoxin (used to treat heart problems)
• ciclosporin or tacrolimus (used after an organ transplant)
• methotrexate (used to treat rheumatoid arthritis or psoriasis)
• lithium (used to treat mental illness)
• mifepristone (used for the medical termination of pregnancy)
• other non-steroidal anti-inflammatory drugs e.g. aspirin, ibuprofen
• corticosteroids such as prednisolone
• quinolone antibiotics (e.g. ciprofloxacin, levofloxacin, ofloxacin)
• antidepressants called SSRIs
• drugs used to stop blood clotting called antiplatelet agents (e.g. aspirin, dipyridamole, clopidogrel)
• diuretics (‘water-pills’)
• zidovudine (used to treat HIV infection).

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.

Etodolac  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 becoming pregnant.

Do not use Etodolac  in the last trimester of pregnancy.

Etodolac  should not be used during the first two trimesters of pregnancy unless your doctor advises you otherwise.

Etodolac  have not been established as safe for use in breast-feeding mothers.

Driving and using machines

Etodolac  may cause drowsiness, tiredness, dizziness and abnormal vision. Do not drive or operate machinery if you experience any of these symptoms.

Etodolac  contains lactose and sunset yellow

Lactose is an ingredient in Etodolac . If you have been told that you have an intolerance to some sugars, contact your doctor before taking this medicinal product.

Etodolac  contains orange yellow S E110. This may cause allergic reactions.

3. How to take Etodolac

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

The recommended dose is one tablet taken daily.

If you are elderly, your doctor will make sure you take the lowest dose for the shortest time, as you may be more likely to have the serious side effects.

Take with or after food. Swallow the tablet whole with water, do not crush or chew the tablets.

Use in children

Etodolac  is not recommended for use in children.

If you take more Etodolac  than you should

If you or anybody else take(s) too many tablets call your doctor or contact your nearest hospital immediately. Symptoms of an overdose include headache, feeling and being sick, pain in the upper abdomen (above the navel), vomiting blood, disorientation, excitation, coma, drowsiness, dizziness, ringing in the ears (tinnitus), fainting and occasionally convulsions.

If you forget to take Etodolac

If you forget to take a dose at the right time, take it as soon as you remember, unless it is nearly time for the next dose. Do not take a double dose to make up for a forgotten dose. Do not take more than one tablet in a single day.

If you stop taking Etodolac

Do not stop taking Etodolac  without your doctor’s permission.

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.

Stop taking and seek immediate medicinal attention if you experience any of the following

• epigastric pain (upper abdomen), vomiting blood, bloody stools, bleeding from the anus, inflammation of the colon, ulcers of mouth
• heartburn, indigestion abdominal pain
• allergic reactions such as rash, itching, blistering of skin, discolouration, swelling, wheezing or shortness of breath
• aseptic meningitis (stiff neck, headache, feeling or being sick, fever, disorientation) has been reported particularly in patients with lupus (SLE) or other mixed connective tissue disease
• very rarely, Stevens-Johnson syndrome, inflammation or blistering of the skin, mouth or tongue and/or inflammation of the eyes with increased sensitivity to sunlight. These may be severe and be accompanied by feeling generally unwell.

Other side effects

• feeling or being sick, vomiting, diarrhoea, flatulence, constipation, worsening of colitis or Crohn’s disease
• less frequently, gastritis (inflammation of the stomach lining)
• very rarely, inflammation of the pancreas (pancreatitis)
• swelling, high blood pressure and heart failure
• fever, weakness, feeling unwell, shortness of breath, abnormal vision, headache, unusual sensations such as burning or tingling in the hands or feet, depression, confusion hallucinations, ringing in the ears (tinnitus), dizziness (including vertigo), tiredness, tremor, sleep difficulties (insomnia), drowsiness.
• anaemia, sore throat, fever, unexpected bleeding.
• yellowing of the skin or whites of the eyes
• increased need to urinate, difficulty passing urine or discolouration of urine
• changes in liver function and changes in the blood can only be detected by blood tests
• inflammation of blood vessels (vasculitis)
• feelings of having rapid, fluttering or pounding heart (palpitations)
• small increased risk of heart attack (“myocardial infarction”) or stroke.

Reporting of side effects

If you get any side effects, talk to your doctor, pharmacist or nurse. This includes any possible side effects not listed in this leaflet.

5. How to store Etodolac

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 label. The expiry date refers to the last date of that month.

Do not throw away any medicines via wastewater or house hold waste. Ask your pharmacist how to throw away medicines you no longer use. These measures will help with the environment.

6. Contents of the pack and other information

What Etodolac  contains

• The active substance is etodolac
• The other ingredients are:
  tablet core:microcrystalline cellulose, povidone, methyl hydroxypropyl cellulose, lactose anhydrous, magnesium stearate
  tablet coat: hypromellose, polydextrose, macrogol, triacetin, titanium dioxide, indigo carmine lake, orange yellow, allura red AC lake, black iron oxide and yellow iron oxide.

What Etodolac  looks like and contents of the pack

The tablets are supplied in blister packs of 30 or 100 tablets.

Not all pack sizes may be marketed.

7. Manufactured By:
   Taj Pharmaceuticals Ltd.
   at: Plot. No. 220, Mahagujarat
   Industrial Estate, At & Post-Moraiya,
   Tal-Sanand, Dist- Ahmedabad Gujarat (India)