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Most Important Fact about Diclofenac Sodium EC You should have frequent checkups with your doctor if you take Diclofenac Sodium EC regularly. Ulcers or internal bleeding can occur without warning. Diclofenac Sodium EC precautions if you are pregnant or breastfeeding Do not take Diclofenac Sodium EC late in your pregnancy; it could harm the baby. Check with your doctor before taking Diclofenac Sodium EC early in pregnancy; it should be used only if necessary. Diclofenac Sodium EC does appear in breast milk and could affect a nursing infant. If Diclofenac Sodium EC is essential to your health, your doctor may advise you to discontinue breastfeeding until your treatment with it is finished. Special warnings about Diclofenac Sodium EC Diclofenac Sodium EC may cause dizziness and so may affect your ability to drive or operate machinery safely. Do not drive or operate machinery until you know how Diclofenac Sodium EC affects you and you are sure it won\'t affect your performance. People with impaired kidney, liver or heart function who are taking Diclofenac Sodium EC should have their kidney function monitored. During long-term treatment, routine blood tests are recommended to monitor kidney function, liver function and levels of blood components, particularly in the elderly. Diclofenac Sodium EC may mask the signs and symptoms of infection. This may make you think mistakenly that an infection is getting better when it isn\'t, or that an infection is less serious than it is. For this reason you should tell your doctor if you get an infection while you are taking Diclofenac Sodium EC. It is important that people with a history of disorders affecting the stomach or intestines are closely monitored by a doctor while taking Diclofenac Sodium EC, particularly if elderly. Consult your doctor immediately if you experience side effects such as stomach pain, indigestion, heartburn or signs of bleeding in the stomach or intestines, eg blood in the stools, while taking Diclofenac Sodium EC. Close medical supervision is important in people suffering from severe impairment of liver function. SIDE EFFECTS: Injection site reactions (such as pain, redness, irritation) may occur. If any of these effects persist or worsen, tell your doctor or pharmacist promptly. Remember that your doctor has prescribed this medication because he or she has judged that the benefit to you is greater than the risk of side effects. Many people using this medication do not have serious side effects. Tell your doctor right away if you have any serious side effects, including: signs of low potassium level in the blood (such as muscle cramps, weakness, irregular heartbeat). This medication can cause low blood sugar (hypoglycemia). This may occur if you do not consume enough calories from food or if you do unusually heavy exercise. Symptoms of low blood sugar include sudden sweating, shaking, fast heartbeat, hunger, blurred vision, dizziness, or tingling hands/feet. It is a good habit to carry glucose tablets or gel to treat low blood sugar. If you don't have these reliable forms of glucose, rapidly raise your blood sugar by eating a quick source of sugar such as table sugar, honey, or candy, or drink fruit juice or non-diet soda. Tell your doctor immediately about the reaction and the use of this product. To help prevent low blood sugar, eat meals on a regular schedule, and do not skip meals. Check with your doctor or pharmacist to find out what you should do if you miss a meal. Symptoms of high blood sugar (hyperglycemia) include thirst, increased urination, confusion, drowsiness, flushing, rapid breathing, and fruity breath odor. If these symptoms occur, tell your doctor immediately. Your dosage may need to be increased. A very serious allergic reaction to this drug is rare. However, get medical help right away if you notice any symptoms of a serious allergic reaction, including: rash, itching/swelling (especially of the face/tongue/throat), severe dizziness, fast heartbeat, sweating, trouble breathing. This is not a complete list of possible side effects. If you notice other effects not listed above, contact your doctor or pharmacist. In the US - Call your doctor for medical advice about side effects. You may report side effects to FDA at 1-800-FDA-1088. In Canada - Call your doctor for medical advice about side effects. You may report side effects to Health Canada at 1-866-234-2345.

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MEDICAL ALERT: Your condition can cause complications in a medical emergency. For enrollment information call MedicAlert at 1-800-854-1166 (USA) or 1-800-668-1507 (Canada).slow heart rate, weak pulse, fainting, slow breathing (breathing may s);All dose strengths contain: crospovidone, hydroxypropyl cellulose, hypromellose, magnesium stearate, microcrystalline cellulose, polyethylene glycol, silicon dioxide, titanium dioxide. Dose strength-specific ingredients include: 5 mg—ferric oxide yellow, lactose monohydrate; 30 mg—lactose monohydrate; 35 mg—ferric oxide red, ferric oxide yellow, lactose monohydrate; 75 mg—ferric oxide red; 150 mg—FD&C blue #2 aluminum lake.

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25 mM L-arginine hydrochlorideGEODON (ziprasidone HCl) Structural Formula Illustration

REMICADE is supplied as a sterile, white, lyophilized powder for intravenous infusion. Following reconstitution with 10 mL of Sterile Water for Injection, USP, the resulting pH is approximately 7.2. Each single-use vial contains 100 mg infliximab, 500 mg sucrose, 0.5 mg polysorbate 80, 2.2 mg monobasic sodium phosphate, monohydrate, and 6.1 mg dibasic sodium phosphate, dihydrate. No preservatives are present.

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