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Narutis (Clopidogrel)
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Clopidogrel

Narutis is used to prevent blood clots if you have chest pain, peripheral artery disease (poor circulation in your legs), a heart attack, or stroke. This drug may be used as part of a combination therapy. That means you may need to take it with other drugs. Your doctor will decide if you should use this drug with other drugs, such as aspirin.

Other names for this medication:
Clopidogrel, Plavix, Anclog, Anlet, Antiplar, Artevil, Clavix, Clopicard, Clopilet, Clopivas, Deplatt, Diloxol, Duoplavin, Expansia, Farcet, Globel, Grepid, Iscover, Karum, Klopidogrel, Nabratin, Narutis, Nefazan, Noklot, Pidocar, Pidogrel, Pladex, Plagerine, Planor, Tisten, Troken, Trombex, Vaclo, Zyllt,

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Anazol, Clovate, Noprilam, Bicapain, Ginkan, Tensen, Parizac, Tagremin, Aldactazide, Strom, Procor, Dicloabak, Salivia, Diklofenak, Amoxinject, Fulcro, Carbatrol, Amitron, Almacin, Maxalt, Clarimax, Esomac, Zolnite, Candistat, Biger,

Narutis comes as a tablet to take by mouth. It is usually taken once a day with or without food. Take Narutis at around the same time every day. Follow the directions on your prescription label carefully, and ask your doctor or pharmacist to explain any part you do not understand. Take Narutis exactly as directed. Do not take more or less of it or take it more often than prescribed by your doctor.

Narutis will help prevent serious problems with your heart and blood vessels only as long as you take the medication. Continue to take Narutis even if you feel well. Do not stop taking Narutis without talking to your doctor. If you stop taking Narutis, there is a higher risk that you may have a heart attack or stroke. If you have a stent, there is also a higher risk that you could develop a blood clot in the stent if you stop taking Narutis too soon.

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Applying PCR-based differential display, we have identified four novel JH-responsive cDNAS, that is, three repressible (JR-1, 2 and 3) and one inducible (JI-1). Recombinant human erythropoietin in the prevention of chemotherapy-induced anaemia in children with malignant solid tumours. Spectroscopic studies on the interaction of pradimicin BMY-28864 with mannose derivatives. Here we report that group-living pigtail macaque females increased their rate of interaction with infants in the last weeks of pregnancy in correspondence with an increase in plasma levels of estradiol and progesterone.

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A study of the micromovement of pegged and keeled glenoid components compared using radiostereometric analysis. Tumorigenicity of simian virus 40-transformed human cells and mouse--human hybrids in nude mice. Within the past 10 years sufficient data have been collected to establish the accumulation of new/enlarging T2 lesions and gadolinium enhancing lesions, T2 lesion load, T1-hypointense lesions, and brain volume changes as reasonably well-defined markers of disease processes, which may serve to monitor treatment efficacy. We know little about factors associated with job satisfaction and dissatisfaction for nursing home workers. The same number of electrodes was inserted on average for both groups, with comparable numbers of electrodes in use.

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Prosthetic rehabilitation in patients with malignant tumors of the soft palate. In Canarian women, VDR genotype is not associated with changes in biochemical markers of bone remodelling or in bone mass or with the presence of osteoporosis or osteoporotic fractures. Establishing an account at EBSCO further allows a nurse to save references and searches and to receive e-mail alerts when new articles on a topic of interest are published. With the technique of radioimmunodiffusion and indirect FA staining, IgA antibody to measles, mumps, rubella, and polio-1 were determined in serum and middle ear fluid (MEF) of 103 patients with otitis media. This has raised interest in a more detailed knowledge of the mechanisms leading to DVT, and the correct employment of the latest equipment which enable diagnosis to be made and daily monitoring of the disease during its evolution.

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