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Voltaren Tablets
Diclofenac Sodium
$162.00
100mg · 9 × 10 tablets · 3 months supply
GenericGeneric medicine· By Dexxon
$54.00 per month
How long a supply?
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Annual cost
$666a year at this pack size
Prescription required
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FDA boxed warningRisk of serious cardiovascular and gastrointestinal events
Cardiovascular Thrombotic Events
WARNINGS ).
Diclofenac Sodium Extended-release Tablets are contraindicated in the setting of coronary artery bypass graft (CABG) surgery (see
CONTRAINDICATIONS
Gastrointestinal Bleeding, Ulceration, and Perforation
NSAIDs cause an increased risk of serious gastrointestinal (GI) 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 and patients with a prior history of peptic ulcer disease and/or GI bleeding are at greater risk for serious GI events (see
About Voltaren Tablets
Overview
Voltaren Tablets contain diclofenac sodium, a nonsteroidal anti-inflammatory drug (NSAID). They are used to relieve the signs and symptoms of osteoarthritis and rheumatoid arthritis. How diclofenac works is not fully understood, but it reduces the production of prostaglandins, substances involved in pain and inflammation.
What it treats
- Relief of the signs and symptoms of osteoarthritis - Relief of the signs and symptoms of rheumatoid arthritis
Safety information
Side effects
Commonly reported side effects include stomach pain, constipation, diarrhea, indigestion, gas, heartburn, nausea, vomiting, headache, dizziness, itching, rash and ringing in the ears. Swelling, anemia, changes in kidney function, raised liver enzymes and prolonged bleeding time are also reported. Contact a doctor promptly for serious side effects, including stomach or intestinal ulcers, bleeding or perforation; liver injury or failure; kidney injury or failure; high potassium levels; high blood pressure; heart failure; and blood disorders. Stomach or intestinal bleeding, ulcers and perforation were among the effects reported in approximately 1% to 10% of patients taking diclofenac extended-release tablets or other NSAIDs. Seek urgent medical help for vomiting blood, black stools or rectal bleeding, yellowing of the skin or eyes, markedly reduced urination, or difficulty breathing. Other serious reactions reported include heart attack, abnormal heart rhythms, severe allergic reactions with swelling, and severe skin reactions involving blistering or peeling.
FDA boxed warning
Risk of serious cardiovascular and gastrointestinal events
Cardiovascular Thrombotic Events
WARNINGS ).
Diclofenac Sodium Extended-release Tablets are contraindicated in the setting of coronary artery bypass graft (CABG) surgery (see
CONTRAINDICATIONS
Gastrointestinal Bleeding, Ulceration, and Perforation
NSAIDs cause an increased risk of serious gastrointestinal (GI) 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 and patients with a prior history of peptic ulcer disease and/or GI bleeding are at greater risk for serious GI events (see
A boxed warning is the strongest warning the US Food and Drug Administration requires on a medicine label. Text is taken from the official label, with internal section references removed.
When to call your doctor
If symptoms are severe or getting worse quickly, seek emergency care rather than waiting.
Before taking this medicine
Do not take diclofenac sodium tablets if you: • Are allergic to diclofenac or any ingredient in the tablets, including if you have had a severe allergic reaction or serious skin reaction. • Have had asthma, hives or an allergic-type reaction after taking aspirin or another nonsteroidal anti-inflammatory drug (NSAID). Severe, sometimes fatal allergic reactions have been reported in these patients. Diclofenac must not be used in the setting of coronary artery bypass graft (CABG) surgery.
Interactions
Diclofenac can interact with the following medicines: • Blood thinners such as warfarin, antiplatelet medicines such as aspirin, and SSRI or SNRI antidepressants can increase bleeding risk. Your doctor should monitor for signs of bleeding. • Aspirin used for pain relief, other NSAIDs and salicylates such as diflunisal or salsalate are generally not recommended with diclofenac. These combinations increase the risk of stomach or intestinal side effects, including bleeding, with little or no added benefit. Diclofenac does not replace aspirin prescribed for heart protection. • ACE inhibitors, angiotensin receptor blockers (ARBs) and beta-blockers may become less effective at lowering blood pressure. ACE inhibitors and ARBs can also increase the risk of kidney problems when taken with diclofenac, especially in older adults, people with reduced fluid levels or those with kidney impairment. Blood pressure and kidney monitoring may be needed. • Diuretics, including furosemide and thiazide diuretics, may work less effectively. Your doctor should check their effect and monitor kidney function. • Digoxin levels can rise, and its effects may last longer. Blood-level monitoring is recommended. • Lithium levels can rise, increasing the risk of lithium toxicity. Monitoring for toxicity is recommended. • Methotrexate toxicity may increase, including low white blood cell or platelet counts and kidney problems. Monitoring is recommended. • Cyclosporine may cause more kidney harm when taken with diclofenac. Kidney monitoring is recommended. • Pemetrexed can cause more bone marrow suppression, kidney problems and stomach or intestinal side effects when taken with diclofenac. Diclofenac should be avoided around pemetrexed treatment; ask your treating doctor when to pause it. • Medicines that affect the liver enzyme CYP2C9 can alter diclofenac’s effects. Voriconazole may increase diclofenac exposure and toxicity, while rifampin may reduce its effectiveness. Your prescriber may need to adjust treatment.
Using Voltaren Tablets
Dosing
Dosing is set by your prescriber. Each health care professional may prescribe medication differently according to a patient's medical history and condition, so follow the directions on your prescription label and speak to your doctor or pharmacist before changing anything.
Storage
Store below 25°C in a dry place, in the original pack, away from direct light and moisture. Do not keep it in a bathroom. Keep all medicines out of the sight and reach of children.
Clinical information on this page is summarised from the US FDA label DICLOFENAC SODIUM TABLET, FILM COATED, EXTENDED RELEASE [A-S MEDICATION SOLUTIONS] (DailyMed, retrieved 19 September 2026).
Patient information and references
Official and supporting information to read alongside advice from your prescriber or pharmacist.
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