Generically available as Tolmetin Sodium 400mg capsules and 600mg tablets

Resources

PATIENT ASSISTANCE PROGRAM

The manufacturers of Tolectin^® offer a Patient Assistance Program (PAP) and convenient Dispensing Pharmacy Solution to ensure patients can get their prescription hassle-free and affordably. The Patient Assistance Program includes up to $150 copay assistance for commercially insured patients, so that patients may pay as little as $0 for their prescription. Patients that are uninsured or underinsured will be offered a cash pay alternative of $45 when using the Tolectin^® dispensing pharmacy.*

*Certain restrictions apply based upon eligibility requirements.

The Dispensing Pharmacy Solution offers patients:

Free pharmacist consultation
Lowest price on cash prescriptions*
Applied manufacturer coupons
Priority mail delivery

*The cost of medication cannot be guaranteed outside the dispensing pharmacy network.

Contact our GaltDirect™ Help Desk to learn more:

1-855-965-2783 | galtdirect@galtrx.com

Important Safety Information for Tolectin^® (Tolmetin Sodium) ▲ expand ▼ collapse

Cardiovascular Risk:

NSAIDs may cause an increased risk of serious cardiovascular thrombotic events, myocardial infarction, and stroke, which can be fatal. This risk may increase with duration of use. Patients with cardiovascular disease or risk factors for cardiovascular disease may be at greater risk.
TOLECTIN^® is contraindicated for the treatment of peri-operative pain in the setting of coronary artery bypass graft (CABG) surgery

Gastrointestinal Risk:

NSAIDs cause an increased risk of serious gastrointestinal adverse events including bleeding, ulceration, and perforation of the stomach or intestines, which can be fatal. These events can occur at any time during use and without warning symptoms. Elderly patients are at greater risk for serious gastrointestinal events.

Indications and Usage:

Carefully consider the potential benefits and risks of TOLECTIN^® and other treatment options before deciding to use TOLECTIN^®. Use the lowest effective dose for the shortest duration consistent with individual patient treatment goals.
TOLECTIN^® is indicated for the relief of signs and symptoms of rheumatoid arthritis and osteoarthritis. TOLECTIN^® is indicated in the treatment of acute flares and the long-term management of the chronic disease.
TOLECTIN^® is also indicated for treatment of juvenile rheumatoid arthritis. The safety and effectiveness of TOLECTIN^® have not been established in pediatric patients under 2 years of age.

Contraindications:

TOLECTIN^® is contraindicated in patients with known hypersensitivity to TOLECTIN^® or any components of the formulation.
TOLECTIN^® 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^® should not be used for the treatment of peri-operative pain in the setting of coronary artery bypass graft (CABG) surgery.

Warnings and Precautions:

Cardiovascular Thrombotic Events: TOLECTIN^®, like other NSAIDs, may cause an increased risk of serious cardiovascular thrombotic events, myocardial infarction, and stroke, which can be fatal. Patients with cardiovascular disease or risk factors for cardiovascular disease may be at greater risk.

Hypertension - NSAIDs, including TOLECTIN^®, can lead to onset of new hypertension or worsening of preexisting hypertension, either of which may contribute to the increased incidence of CV events. Blood pressure (BP) should be monitored closely during the initiation of NSAID treatment and throughout the course of therapy.

Congestive Heart Failure - Fluid retention and edema have been observed in some patients taking NSAIDs. TOLECTIN^® should be used with caution in patients with fluid retention or heart failure.

Gastrointestinal Bleeding, Ulceration, and Perforation: TOLECTIN^® can cause serious gastrointestinal adverse events, including bleeding, ulceration, and perforation of the stomach or intestines, which can be fatal. These events may occur at any time during treatment, with or without warning symptoms. Elderly patients and those with a history of gastrointestinal ulcers or bleeding are at increased risk.

Hepatotoxicity: TOLECTIN^® may cause elevations in liver enzymes and liver injury. Severe hepatic reactions, including jaundice and fatal fulminant hepatitis, have occurred. Patients with preexisting liver disease or those taking other hepatotoxic medications may be at increased risk.

Renal Toxicity: NSAIDs, including TOLECTIN^®, can cause renal adverse reactions, including acute renal failure, which may be reversible upon discontinuation of the drug. Patients with preexisting renal dysfunction, heart failure, dehydration, or those taking diuretics are at increased risk.

Hematologic Effects: TOLECTIN^® may inhibit platelet aggregation and prolong bleeding time. Patients taking anticoagulants or those with bleeding disorders may be at increased risk of bleeding complications.

Anaphylactic Reactions: TOLECTIN^® can cause severe allergic reactions, including anaphylaxis, which may be fatal. Patients with a history of allergic reactions to NSAIDs should avoid TOLECTIN^®.

Serious Skin Reactions: TOLECTIN^® can cause serious skin reactions, including Stevens-Johnson syndrome and toxic epidermal necrolysis, which may be fatal. These reactions can occur without warning. Patients should discontinue TOLECTIN^® at the first appearance of rash or skin lesions.

Pregnancy and Lactation:

TOLECTIN^® should be avoided in the third trimester of pregnancy due to the risk of premature closure of the ductus arteriosus.
TOLECTIN^® is not recommended during breastfeeding, as it may be excreted in breast milk.

Adverse Reactions:

The most common adverse reactions (≥1%) reported with Tolectin^® include gastrointestinal disturbances (e.g., abdominal pain, dyspepsia, nausea, diarrhea), dizziness, headache, and rash.
Other adverse reactions may include gastrointestinal ulceration, hepatotoxicity, renal toxicity, anemia, hypertension, and edema.

Drug Interactions:

TOLECTIN^® may interact with other medications, including but not limited to anticoagulants, antiplatelet agents, diuretics, lithium, methotrexate, SSRIs, and ACE inhibitors. Patients should inform their healthcare provider of all medications they are taking.

Overdosage:

In case of overdose, seek immediate medical attention. Symptoms of overdose may include nausea, vomiting, epigastric pain, gastrointestinal bleeding, dizziness, headache, tinnitus, confusion, and in severe cases, metabolic acidosis, coma, and respiratory depression.

Reporting Adverse Events:

Healthcare professionals and patients should report any adverse events associated with TOLECTIN^® to the FDA's MedWatch program at 1-800-FDA-1088 or www.fda.gov/medwatch.

For additional information about Tolectin^®, please refer to the full Prescribing Information.

Book a Telehealth Consultation Today

If you’re unable to access your own healthcare provider or don’t have one, you can schedule a telehealth consultation today from the comfort of your own home. Access a third-party healthcare professional online who can help determine if you are an appropriate candidate to receive treatment for mild to moderate acute muscle aches and pain.

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Resources

PATIENT ASSISTANCE PROGRAM

Contact our GaltDirect™ Help Desk to learn more: 1-855-965-2783 | galtdirect@galtrx.com

Important Safety Information for Tolectin® (Tolmetin Sodium) ▲ expand ▼ collapse

Book a Telehealth Consultation Today

Contact our GaltDirect™ Help Desk to learn more:

1-855-965-2783 | galtdirect@galtrx.com

Important Safety Information for Tolectin^® (Tolmetin Sodium) ▲ expand ▼ collapse