Tolectin DS

Tolectin DS Uses, Dosage, Side Effects, Food Interaction and all others data.

The mode of action of tolmetin is not clearly known. However, studies in laboratory animals and man have demonstrated that the anti-inflammatory action of tolmetin is not due to pituitary-adrenal stimulation. Tolectin DS inhibits prostaglandin synthetase in vitro and lowers the plasma level of prostaglandin E in man. This reduction in prostaglandin synthesis may be responsible for the anti-inflammatory action. Tolectin DS does not appear to alter the course of the underlying disease in man.

Tolectin DS is a nonsteroidal anti-inflammatory agent. Studies in animals have shown tolmetin to possess anti-inflammatory, analgesic and antipyretic activity. In the rat, tolmetin prevents the development of experimentally induced polyarthritis and also decreases established inflammation. In patients with either rheumatoid arthritis or osteaoarthritis, tolmetin is as effective as aspirin and indomethacin in controlling disease activity, but the frequency of the milder gastrointestinal adverse effects and tinnitus was less than in aspirin-treated patients, and the incidence of central nervous system adverse effects was less than in indomethacin-treated patients. In patients with juvenile rheumatoid arthritis, tolmetin is as effective as aspirin in controlling disease activity, with a similar incidence of adverse reactions. tolmetin has produced additional therapeutic benefit when added to a regimen of gold salts and, to a lesser extent, with corticosteroids. Tolectin DS should not be used in conjunction with salicylates since greater benefit from the combination is not likely, but the potential for adverse reactions is increased.

Trade Name Tolectin DS
Availability Prescription only
Generic Tolmetin
Tolmetin Other Names Tolmetin, Tolmetina, Tolmétine, Tolmetino, Tolmetinum
Related Drugs Humira, Buprenex, aspirin, prednisone, ibuprofen, acetaminophen, tramadol, meloxicam, duloxetine, cyclobenzaprine
Weight 400mg, , 600mg
Type Capsule, Oral, Oral Capsule, Oral Tablet
Formula C15H15NO3
Weight Average: 257.2845
Monoisotopic: 257.105193351
Groups Approved
Therapeutic Class Drugs for Osteoarthritis, Drugs used for Rheumatoid Arthritis, Non-steroidal Anti-inflammatory Drugs (NSAIDs)
Manufacturer Sanofi Bangladesh LTD,
Available Country Bangladesh, United States,
Last Updated: September 19, 2023 at 7:00 am
Tolectin DS
Tolectin DS

Uses

Carefully consider the potential benefits and risks of Tolectin DS and other treatment options before deciding to use Tolectin DS. Use the lowest effective dose for the shortest duration consistent with individual patient treatment goals.

Tolectin DS is used for the relief of signs and symptoms of rheumatoid arthritis and osteoarthritis. Tolectin DS is used for the treatment of acute flares and the long-term management of the chronic disease.

Tolectin DS is also used for treatment of juvenile rheumatoid arthritis. The safety and effectiveness of Tolectin DS have not been established in pediatric patients under 2 years of age

Tolectin DS is also used to associated treatment for these conditions: Ankylosing Spondylitis (AS), Osteoarthritis (OA), Pain, Rheumatoid Arthritis, Rheumatoid Arthritis, Juvenile, Rheumatoid arthritis flare up, Adhesive capsulitis shoulder, Radiohumeral bursitis

How Tolectin DS works

The mode of action of tolmetin is not known. However, studies in laboratory animals and man have demonstrated that the anti-inflammatory action of tolmetin is not due to pituitary-adrenal stimulation. Tolectin DS inhibits prostaglandin synthetase in vitro and lowers the plasma level of prostaglandin E in man. This reduction in prostaglandin synthesis may be responsible for the anti-inflammatory action. Tolectin DS does not appear to alter the course of the underlying disease in man.

Dosage

Tolectin DS dosage

Carefully consider the potential benefits and risks of Tolectin DS and other treatment options before deciding to use Tolectin DS. Use the lowest effective dose for the shortest duration consistent with individual patient treatment goals.

After observing the response to initial therapy with Tolectin DS, the dose and frequency should be adjusted to suit an individual patient's needs.

For the relief of rheumatoidarthritisor osteoarthritis:the recommended starting dose for adults is 400 mg three times daily (1200 mg daily), preferably including a dose on arising and a dose at bedtime. To achieve optimal therapeutic effect the dose should be adjusted according to the patient's response after one or two weeks. Control is usually achieved at doses of 600-1800 mg daily in divided doses (generally t.i.d.). Doses larger than 1800 mg/day have not been studied and are not recommended.

For the relief of juvenile rheumatoid arthritis:the recommended starting dose for pediatric patients (2 years and older) is 20 mg/kg/day in divided doses (t.i.d. or q.i.d.). When control has been achieved, the usual dose ranges from 15 to 30 mg/kg/day. Doses higher than 30 mg/kg/day have not been studied, and, therefore, are not recommended.

A therapeutic response to Tolectin DS can be expected in a few days to a week. Progressive improvement can be anticipated during succeeding weeks of therapy. If gastrointestinal symptoms occur, Tolectin DS can be administered with antacids other than sodium bicarbonate. Tolectin DS bioavailability and pharmacokinetics are not significantly affected by acute or chronic administration of magnesium and aluminum hydroxides; however, bioavailability is affected by food or milk

Side Effects

Nausea, dyspepsia, diarrhoea, flatuence, vomiting, headache, GI bleed, hypersensitivity reactions, asthenia, hypertension, oedema, dizziness, weight gain, weight loss, visual disturbances, tinnitus, abnormal liver function. Erosive oesophagitis, interstitial nephritis and nephrotic syndrome.

Toxicity

Symptoms of overdose include lethargy, drowsiness, nausea, vomiting, and epigastric pain.

Precaution

Lactation, elderly. Impaired renal and hepatic function. CV diseases, fluid retention, heart failure, history of GI bleed or gastric ulcer, dehydration, hypertension. Monitor renal function regularly.

Interaction

Decreases the efficacy of mifepristone. Increased risk of bleeding with anticoagulants, other NSAIDs, antiplatelets, LMWH. Increased risk of convulsions with quinolones. Decreased antihypertensive response to loop diuretics, β-blockers and ACE inhibitors. Coadmin increased plasma concentrations of lithium, methotrexate and cardiac glycosides. Increased risk of nephrotoxicity with ACE inhibitors, penicillamine, ciclosporin, tacrolimus or diuretics.

Food Interaction

  • Avoid alcohol. Ingesting alcohol may increase the risk of developing an ulcer, or gastrointestinal bleed.
  • Take with or without food. Food (or milk) can decrease oral bioavailability by 16%. Tolectin DS may be taken with food to reduce gastrointestinal upset, but it may reduce tolmetin serum levels by 50%.

Tolectin DS Alcohol interaction

[Moderate] GENERALLY AVOID:

The concurrent use of aspirin or nonsteroidal anti-inflammatory drugs (NSAIDs) and ethanol may lead to gastrointestinal (GI) blood loss.

The mechanism may be due to a combined local effect as well as inhibition of prostaglandins leading to decreased integrity of the GI lining.



Patients should be counseled on this potential interaction and advised to refrain from alcohol consumption while taking aspirin or NSAIDs.

Tolectin DS Hypertension interaction

[Major] Fluid retention and edema have been reported in association with the use of nonsteroidal anti-inflammatory drugs (NSAIDs).

Therapy with NSAIDs should be administered cautiously in patients with preexisting fluid retention, hypertension, or a history of heart failure.

Blood pressure and cardiovascular status should be monitored closely during the initiation of NSAID treatment and throughout the course of therapy.

Hypertension interaction

[Moderate] Nonsteroidal anti-inflammatory drugs (NSAIDs), including topicals, can lead to new onset of hypertension or worsening of preexisting hypertension, either of which can contribute to the increased incidence of cardiovascular events.

NSAIDs should be used with caution in patients with hypertension.

Blood pressure should be monitored closely during the initiation of NSAID therapy and throughout the course of therapy.

Elimination Route

Rapidly and almost completely absorbed with peak plasma levels being reached within 30-60 minutes after an oral therapeutic dose.

Half Life

Biphasic elimination from the plasma consisting of a rapid phase with a half-life of one to 2 hours followed by a slower phase with a half-life of about 5 hours.

Pregnancy & Breastfeeding use

Pregnancy Category C. Reproduction studies in rats and rabbits at doses up to 50 mg/kg (1.5 times the maximum clinical dose based on a body weight of 60 kg) revealed no evidence of teratogenesis or impaired fertility due to Tolectin DS. However, animal reproduction studies are not always predictive of human response. There are no adequate and well-controlled studies in pregnant women. Tolectin DS should be used in pregnancy only if the potential benefit justifies the potential risk to the fetus.

Nonteratogenic Effects: Because of the known effects of NSAIDs on the fetal cardiovascular system (closure of ductus arteriosus), use during pregnancy (particularly late pregnancy) should be avoided.

Labor and Delivery: In rat studies with NSAIDs, as with other drugs known to inhibit prostaglandin synthesis, an increased incidence of dystocia, delayed parturition, and decreased pup survival occurred. The effects of Tolectin DS on labor and delivery in pregnant women are unknown.

Nursing Mothers: Tolectin DS sodium has been shown to be secreted in human milk. Because of the potential for serious adverse reactions in nursing infants from tolmetin sodium, a decision should be made whether to discontinue nursing or to discontinue the drug, taking into account the importance of the drug to the mother.

Contraindication

Tolectin DS is contraindicated in patients with known hypersensitivity to tolmetin sodium.

Tolectin DS should not be given to patients who have experienced asthma, urticaria or allergic-type reactions after taking aspirin or other NSAIDs. Severe, rarely fatal, anaphylactic-like reactions to NSAIDs have been reported in such patients Tolectin DS is contraindicated for the treatment of peri-operative pain in the setting of coronary artery bypass graft (CABG) surgery is contraindicated in patients with known hypersensitivity to tolmetin sodium.

Tolectin DS should not be given to patients who have experienced asthma, urticaria or allergic-type reactions after taking aspirin or other NSAIDs. Severe, rarely fatal, anaphylactic- like reactions to NSAIDs have been reported in such patients

Tolectin DS is contraindicated for the treatment of peri-operative pain in the setting of coronary artery bypass graft (CABG) surgery

Special Warning

Pediatric Use: Safety and effectiveness in pediatric patients below the age of 2 years have not been established.

Geriatric Use: As with any NSAIDs, caution should be exercised in treating the elderly (65 years and older).

Acute Overdose

In the event of overdosage, the stomach should be emptied by inducing vomiting or by gastric lavage followed by the administration of activated charcoal.

Storage Condition

Oral: Store at 20-25°C

Innovators Monograph

You find simplified version here Tolectin DS

FAQ

What is Tolectin DS used for?

Tolectin DS is used to relieve pain, tenderness, swelling, and stiffness caused by osteoarthritis (arthritis caused by a breakdown of the lining of the joints) and rheumatoid arthritis (arthritis caused by swelling of the lining of the joints).

How safe is Tolectin DS?

Tolectin DS may raise your risk of having a heart attack or stroke. This is more likely in people who already have heart disease. People who use this medicine for a long time might also have a higher risk. This medicine may cause bleeding in your stomach or intestines.

What are the common side effects of Tolectin DS?

The most common side effects of Tolectin DS include:

  • indigestion,
  • stomach pain,
  • nausea,
  • vomiting,
  • diarrhea,
  • gas,
  • headache,
  • dizziness,
  • weakness, and
  • changes in weight

Is Tolectin DS safe during pregnancy?

There are no controlled data in human pregnancy. potential benefits may warrant use of the drug in pregnant women despite potential risks.

Is Tolectin DS safe during breastfeeding?

The manufacturer recommends to discontinue breastfeeding or discontinue the drug, taking into account the importance of the drug to the mother.

Can I drink alcohol with Tolectin DS?

Avoid drinking alcohol. It may increase your risk of stomach bleeding.

Can I drive after taking Tolectin DS?

Ulcers and bleeding can happen without warning symptoms and can cause death. You may get drowsy or dizzy. Do not drive, use machinery, or do anything that needs mental alertness until you know how this medicine affects you.

Is Tolectin DS an NSAID?

Tolectin DS is in a class of medications called NSAIDs. It works by stopping the body's production of a substance that causes pain, fever, and inflammation.

How long take Tolectin DS?

Your symptoms may improve within one week after you start to take Tolectin DS, but it may take several weeks or longer for you to feel the full benefit of the medication

How to use Tolectin DS?

Take this medication by mouth, usually 3 times a day with a full glass of water  or as directed by your doctor. Do not lie down for at least 10 minutes after taking this drug. If stomach upset occurs, take this medication with food, milk, or an antacid

Who sould not take Tolectin DS?

Tolectin DS should not be given to patients who have experienced asthma, urticaria or allergic-type reactions after taking aspiri.

What happens if I miss a dose?

Take the medicine as soon as you can, but skip the missed dose if it is almost time for your next dose. Do not take two doses at one time.

Does Tolectin DS affect my heart?

Tolectin DS can increase your risk of fatal heart attack or stroke. Do not use tolmetin just before or after heart bypass surgery.Tolectin DS may also cause stomach or intestinal bleeding, which can be fatal.

*** Taking medicines without doctor's advice can cause long-term problems.
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