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Titular de la autorizaci n de comercializaci n y responsable de la fabricaci n Este medicamento est autorizado en los estados miembros del Espacio Econ mico Europeo con los siguientes nombres: La informaci n detallada y actualizada de este medicamento est disponible en la p gina web de la Agencia Espa ola de Medicamentos y Productos Sanitarios AEMPS ww.

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  • Pantoprazole 40 mg what is it for Epub 2013 Oct 29. Jiao HW, Sun LN, Li YQ, Yu L, Zhang HW, Wang MF, Yu LY, Abnormalities ZQ, Xie LJ, Chen J, Meng L, Zhang XH, Wang YQ. Eur J Clin Pharmacol. 2018 Mar; (3) 257-265.
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Keep pantoprazole sodium delayed-release tabletsand all medicines out of the reach of children. Medicines are sometimes prescribed for purposes other than those listed in a Medication Guide.613-9.

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In patients with severe renal impairment, pharmacokinetic parameters for pantoprazole were similar to those of healthy subjects. No dosage adjustment is necessary in patients with renal impairment or in patients undergoing hemodialysis.f you are taking the granules, take your dose 30 minutes before a meal. To take it by mouth, open the packet and mix the granules in applesauce or pantoprazole er 40 mg juice.

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Table 4: Clinically Relevant Interactions Affecting Drugs Co-Administered with Pantoprazole sodium and Interactions with Diagnostics The effect of PPIs on antiretroviral drugs is variable. The clinical importance and the mechanisms behind these interactions are not always known.The relative dose to the infant was estimated to be 7.

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It can be harmful for people to take this medication if their doctor has not prescribed it. Each yellow, oval, biconvex, enteric-coated tablet, plain on one side and 96 printed with brown ink on the other side, contains 20 mg of pantoprazole.The diluted solution may be stored at room temperature but must be used within 24 hours after initial reconstitution.

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In a population pharmacokinetic analysis, the systemic exposure was higher in patients less than 1 year of age with GERD compared to adults who received a single 40 mg dose geometric mean AUC was 103% higher in preterm infants and neonates receiving single dose of 2. mg of PROTONIX, and 23% higher in infants 1 through 11 months of age receiving a single dose of approximately 1.2555.

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