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Atripla (Tenofovir)
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Tenofovir

Atripla disoproxil fumarate (Atripla DF) is a prescription medicine approved by the U.S. Food and Drug Administration (FDA) for the treatment of HIV infection in adults and children 2 years of age and older who weigh at least 22 lb (10 kg). Atripla DF is always used in combination with other HIV medicines. Atripla DF belongs to a group of HIV drugs called nucleoside reverse transcriptase inhibitors (NRTIs). NRTIs block an HIV enzyme called reverse transcriptase. By blocking reverse transcriptase, NRTIs prevent HIV from multiplying and can reduce the amount of HIV in the body. HIV medicines can't cure HIV/AIDS, but taking a combination of HIV medicines (called an HIV treatment regimen) every day helps people with HIV live longer, healthier lives. HIV medicines also reduce the risk of HIV transmission. If you are taking HIV medicines, including Atripla DF, don't cut down on, skip, or stop taking them unless your health care provider tells you to. Atripla DF is also approved by FDA for the treatment of chronic hepatitis B virus infection (HBV) in adults and children 2 years of age and older who weigh at least 22 lb (10 kg). For information on the use of Atripla DF in people with HIV and HBV, please refer to the HBV section of the Guidelines for the Prevention and Treatment of Opportunistic Infections in HIV-Infected Adults and Adolescents.

Other names for this medication:
Tenofovir, Atripla, Tenvir, Trioday, Truvada, Viraday, Viread,

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We examined the effects of sodium arsenite preadministration on the parameters of cerulein-induced pancreatitis in rats and then monitored the effects of preincubating pancreatic acini with sodium arsenite in vitro. A suggestion is put forward that these rhythmic processes are transformed during subsequent development in circum-hour rhythms of some biochemical, physiological and biophysical processes discovered in the cells and organs of adult organism. The present study sought to determine if echo-Doppler-derived pulmonary vascular resistance (PVR echo), net-atrioventricular compliance (Cn) and tricuspid peak systolic annular velocity (Sa), as parameters of right ventricular function, have value in predicting exercise capacity in patients with mitral stenosis (MS).

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