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Can Voltaren Cause Diarrhea

author
Paul Gonzalez
• Thursday, 19 November, 2020
• 8 min read

Round, pink, imprinted with Voltaren XR, 100 The phase IV clinical study is created by health based on reports of 44,627 people who have side effects when taking Voltaren from the FDA, and is updated regularly.

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(Source: www.verywellhealth.com)

Contents

EHealthMe makes it possible for everyone to run personal clinical trial. The phase IV trial will monitor drug safety outcomes that are personalized to your gender and age (0-99+).

44,627 people reported to have side effects when taking Voltaren. Voltaren has active ingredients of diclofenac sodium.

Diarrhea has been reported by people with high blood pressure, rheumatoid arthritis, multiple sclerosis, psoriasis, Crohn's disease. Most likely your drugs were not studied in clinical trials based on patients like you.

By design, clinical trials use only a small and selected set of people, and are conducted in a highly controlled environment. On health, our answer is simple: run your own phase IV clinical trial.

Patients can bring a copy of the report to their healthcare provider to ensure that all drug risks and benefits are fully discussed and understood. It is recommended that patients use the information presented as a part of a broader decision-making process.

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(Source: nationsre.com)

Note: This document contains side effect information about diclofenac topical. Some dosage forms listed on this page may not apply to the brand name Voltaren Gel.

Topical application route (Patch, Extended Release) NSAIDs cause an increased risk of serious cardiovascular thrombotic events, including myocardial infarction and stroke, which can be fatal.

Diclofenac examine is contraindicated in the setting of coronary artery bypass graft surgery. 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.

NSAIDs cause an increased risk of serious cardiovascular thrombotic events, including myocardial infarction and stroke, which can be fatal. Diclofenac sodium is contraindicated in the setting of coronary artery bypass graft surgery.

Blood in the urine chest pain cough dry, itching, or burning eyes eye pain headaches, including migraines increased sensitivity of the skin to sunlight pain or tenderness around the eyes and cheekbones redness of the skin redness or swelling of the eyes runny or stuffy nose skin rash other than at the application site sore throat tightness in the chest troubled breathing ulcers or sores on the skin, other than at the application site Some side effects of diclofenac topical may occur that usually do not need medical attention.

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(Source: www.self.com)

These side effects may go away during treatment as your body adjusts to the medicine. Also, your health care professional may be able to tell you about ways to prevent or reduce some of these side effects.

Solarize (diclofenac topical)” SkyePharma, San Diego, CA. Always consult your healthcare provider to ensure the information displayed on this page applies to your personal circumstances.

Note: This document contains side effect information about diclofenac. NSAIDs cause an increased risk of serious cardiovascular thrombotic events, including myocardial infarction and stroke, which can be fatal.

NSAIDs also cause an increased risk of serious gastrointestinal (GI) adverse events, including bleeding, ulceration, and perforation of the stomach or intestines, which can be fatal. NSAIDs cause an increased risk of serious cardiovascular thrombotic events, including myocardial infarction and stroke, which can be fatal.

Diclofenac sodium is contraindicated in the setting of coronary artery bypass graft surgery. 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.

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(Source: getcollagen.co.za)

Oral route (Tablet; Capsule, Liquid Filled; Powder for Solution) NSAIDs cause an increased risk of serious cardiovascular thrombotic events, including myocardial infarction and stroke, which can be fatal.

Diclofenac is contraindicated in the setting of coronary artery bypass graft surgery. 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.

Agitation blurred vision change in consciousness change in the ability to see colors, especially blue or yellow confusion depression difficult or troubled breathing hives hostility irregular, fast or slow, or shallow breathing irritability loss of consciousness muscle twitching nervousness pain or discomfort in the chest, upper stomach, or throat pale or blue lips, fingernails, or skin puffiness or swelling of the eyelids or around the eyes, face, lips, or tongue rapid weight gain seizures sleepiness slow or fast heartbeat stupor swelling of the face, ankles, or hands tightness in the chest trouble sleeping unusual drowsiness, dullness, or feeling of sluggishness Some side effects of diclofenac may occur that usually do not need medical attention.

Continuing ringing or buzzing or other unexplained noise in the ears excess air or gas in the stomach or intestines hearing loss lack or loss of strength passing gas NSAIDs including this drug, can cause serious gastrointestinal (GI) events which can occur at any time, with or without warning.

Patients with a prior history of peptic ulcer disease and/or GI bleeding had a greater than 10-fold increased risk for developing a GI bleed than patients with neither of these risk factors. Elevations to greater than 3 x URN of AST occurred in about 2% (n=5700) of patients at some point during treatment.

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(Source: www.verywellhealth.com)

NSAIDs inhibit platelet aggregation and have been shown to prolong bleeding time in some patients. Unlike aspirin, the NSAID effect on platelet function is quantitatively less, of shorter duration, and reversible.

Frequency not reported : Confusion, drowsiness, insomnia, paresthesia, tremors Clinical trials of several cyclooxygenase (COX)-2 selective and nonselective NSAIDs of up to 3 years duration have shown an increased risk of serious cardiovascular thrombotic events, myocardial infarction, and stroke, which can be fatal.

Pharmacoepidemiological data reveal an increased risk of arteriothrombotic events associated with diclofenac (the active ingredient contained in Voltaren) use, particularly at a high dose and during long-term treatment. In a meta-analysis of long-term treatment with diclofenac 150 mg/day, compared with placebo use of this drug resulted in approximately 3 additional major vascular events per 1000 participants.

Always consult your healthcare provider to ensure the information displayed on this page applies to your personal circumstances.

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