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Diclofenac Sodium EC contains the active ingredient diclofenac sodium, which is a type of medicine called a non-steroidal anti-inflammatory drug (NSAID). All the medicines in the NSAID group reduce inflammation caused by the body\'s own immune system and are effective painkillers. Diclofenac Sodium EC works by blocking the action of a substance in the body called cyclo-oxygenase. Cyclo-oxygenase is involved in the production of various chemicals in the body, some of which are known as prostaglandins. The body in response to injury and certain diseases produces prostaglandins and they go on to cause the pain, swelling and inflammation of these conditions. Arthritic conditions are one example of this. As Diclofenac Sodium EC ss the body producing these inflammatory prostaglandins, it relieves the associated pain and inflammation. Diclofenac Sodium EC is used to relieve pain and inflammation in a wide range of musculoskeletal conditions, including arthritis, gout, sprains, fractures, dislocations, back pain, tendinitis and frozen shoulder. Diclofenac Sodium EC is also used to relieve pain and inflammation following dental, orthopaedic (bone) and other minor surgery. swelling, weight gain, feeling short of breath;(IN-su-lin)

You may experience blurred vision, dizziness, or drowsiness due to extremely low or high blood sugar levels. Do not drive, use machinery, or do any activity that requires alertness or clear vision until you are sure you can perform such activities safely. ABILIFY Injection is available in single-dose vials as a ready-to-use, 9.75 mg/1.3 mL (7.5 mg/mL) clear, colorless, sterile, aqueous solution for intramuscular use only. Inactive ingredients for this solution include 199.5 mg of sulfobutylether b-cyclodextrin (SBECD), 10.4 mg of tartaric acid, qs to pH 4.3 of sodium hydroxide, and qs to 1.33 mL of water for injection.

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Elderly patients with dementia-related psychosis treated with antipsychotic drugs are at an increased risk of death. Analyses of seventeen placebo-controlled trials (modal duration of 10 weeks), largely in patients taking atypical antipsychotic drugs, revealed a risk of death in drug-treated patients of between 1.6 to 1.7 times the risk of death in placebo-treated patients. Over the course of a typical 10-week controlled trial, the rate of death in drug-treated patients was about 4.5%, compared to a rate of about 2.6% in the placebo group. Although the causes of death were varied, most of the deaths appeared to be either cardiovascular (e.g., heart failure, sudden death) or infectious (e.g., pneumonia) in nature. Observational studies suggest that, similar to atypical antipsychotic drugs, treatment with conventional antipsychotic drugs may increase mortality. The extent to which the findings of increased mortality in observational studies may be attributed to the antipsychotic drug as opposed to some characteristic(s) of the patients is not clear. GEODON (ziprasidone) is not approved for the treatment of patients with Dementia-Related Psychosis [see WARNINGS AND PRECAUTIONS]).

OVERDOSE: If overdose is suspected, contact your local poison control center or emergency room immediately. US residents can call the US national poison hotline at 1-800-222-1222. Canadian residents should call their local poison control center directly.(sye-klo-SPORE-een MY-crow-ee-MULL-shun)

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