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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.

The flexible container is fabricated from a specially formulated non-plasticized, thermoplastic copolyester (CR3). The amount of water that can permeate from the container into the overwrap is insufficient to affect the solution significantly. Solutions in contact with the flexible container can leach out certain of the container's chemical components in very small amounts within the expiration period. The suitability of the container material has been confirmed by tests in animals according to USP biological tests for plastic containers.TEMODAR 250 mg: lactose anhydrous (154.3 mg), colloidal silicon dioxide (0.7 mg), sodium starch glycolate (22.5 mg), tartaric acid (9 mg), and stearic acid (13.5 mg).Read All Potential Side Effects and See Pictures of Temodar The inactive ingredients in ADDERALL XR capsules include: gelatin capsules, hydroxypropyl methylcellulose, methacrylic acid copolymer, opadry beige, sugar spheres, talc, and triethyl citrate. Gelatin capsules contain edible inks, kosher gelatin, and titanium dioxide. The 5 mg, 10 mg, and 15 mg capsules also contain FD&C Blue #2. The 20 mg, 25 mg, and 30 mg capsules also contain red iron oxide and yellow iron oxide.

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