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buproprion (Wellbutrin)Very common (10% or more): Pain (included flank and back pain; up to 13%)If you notice any changes in your vision while taking this drug, call your doctor or health care professional as soon as possible. S using this medicine and call your health care provider right away if you have a loss of sight in one or both eyes.Why Diclofenac Sodium EC should not be prescribed Diclofenac Sodium EC should not be used by people in whom aspirin or other NSAIDs, eg ibuprofen, cause allergic reactions such as asthma attacks, itchy rash (urticaria), nasal inflammation (rhinitis) or swelling of the lips, tongue and throat (angioedema) Diclofenac Sodium EC should not be used if you have a history of bleeding from the stomach or intestines. Diclofenac Sodium EC should not be used if suspect or have a history of Peptic ulcer. Diclofenac Sodium EC should not be used if you are allergic to one or any of its ingredients. Please inform your doctor or pharmacist if you have previously experienced such an allergy. If you feel you have experienced an allergic reaction, s using Diclofenac Sodium EC and inform your doctor or pharmacist immediately. Possible Diclofenac Sodium EC Side effects More common side effects of Diclofenac Sodium EC may include: abdominal pain or cramps, constipation, diarrhea, headache, indigestion, nausea Less common side effects of Diclofenac Sodium EC may include: abdominal bleeding, abdominal swelling, dizziness, fluid retention, gas, itching, peptic ulcers, rash, ringing in the ears Rare side effects of Diclofenac Sodium EC may include: anaphylaxis (severe allergic reaction), anemia, anxiety, appetite change, asthma, black stools, blood disorders, bloody diarrhea, blurred vision, changes in taste, colitis, congestive heart failure, convulsions, decrease in white blood cells, decreased urine production, depression, double vision, drowsiness, dry mouth and mucous membranes, hair loss, hearing loss, hepatitis, high blood pressure, hives, inability to sleep, inflammation of the colon, inflammation of mouth, inflammation of the pancreas, irritability, kidney failure, liver disease, low blood pressure, nosebleed, red or purple skin discoloration and itching, sensitivity to light, skin eruptions and inflammation, scaling or peeling, sores in the gullet, Stevens-Johnson syndrome (a severe form of skin eruption), swelling of eyelids, lips, and tongue, swelling of the throat due to fluid retention, vague feeling of illness, vision changes, vomiting, yellow eyes and skin

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The manufacturing process was also investigated for its capacity to decrease the infectivity of an experimental agent of TSE, considered a model for CJD and its variant vCJD.16 Several of the production steps have been shown to decrease TSE infectivity of an experimental model agent. TSE reduction steps include octanoic acid fractionation (≥ 6.4 log10), depth filtration (2.6 log10), and virus filtration (≥ 5.8 log10). These studies provide reasonable assurance that low levels of vCJD/CJD agent infectivity, if present in the starting material, would be removed.stroke

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Lymphoma and other malignancies, some fatal, have been reported in children and adolescent patients treated with TNF blockers, including Enbrel.vaginal yeast infection, iramate (amax)

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