imipenem uses rocaltrol

Rocaltrol (calcitriol) is indicated in the management of secondary hyperparathyroidismand resultant metabolicbone disease in patients with moderate to severe chronic renal failure(Ccr 15 to 55 mL/min) not yet on dialysis. While this is usually reversible, it is important in such patients to pay careful attention to those factors which may lead to hypercalcemia.

6 and titanium dioxide; 0.5 mcg - FD&C Red No. Imipenem and cilastatin will not treat a Store unmixed medicine at room temperature, away from moisture and heat. There is evidence that maternal calcitriol may enter the fetal circulation. If the drug has passed through the stomach, the administration of mineral oil may promote its fecal elimination. Los estuches con viales de 100 ml contienen 1 vial.Puede que no estén comercializados todos los tamaños de envases.Titular de la autorización de comercialización y responsable de la fabricaciónResponsable de la fabricación (responsable de la liberación del lote en EEE)Este medicamento está autorizado en los estados miembros del Espacio Económico Europeo con los siguientes nombres:Austria: Imipenem/Cilastatin Pfizer 500 mg/500 mg Pulver zur Herstellung einer InfusionslösungCyprus: Imipenem/Cilastatin Hospira 500 mg/500 mg KGermany: Imipenem/Cilastatin Hospira 500 mg/500 mg Pulver zur Herstellung einer InfusionslösungGreece: Imipenem/Cilastatin Hospira 500 mg/500 mg KItaly: Imipenem/Cilastatina Pfizer 500 mg/500mg polvere per soluzione per infusioneLatvia: Imipenem/Cilastatin Hospira 500 mg/500mg pulveris infuziju škiduma pagatavošanaiLithuania: Imipenem/Cilastatin Hospira 500 mg/500 mg miltelaMalta: Imipenem/Cilastatin Hospira 500 mg/500mg Powder for Solution for InfusionPortugal: Imipenem + Cilastatina Pfizer, 500 mg + 500 mg pó para solução para perfusãoRomania: Imipenem/Cilastatin Hospira 500 mg/500mg, pulbere pentru solutie perfuzabilaSpain: Imipenem/Cilastatina Hospira 500 mg/500 mg polvo para solución para perfusión EFGUnited Kingdom: Imipenem/Cilastatin 500 mg/500mg Powder for Solution for Infusioninformación detallada y actualizada de este medicamento está disponible en la página Web de la Agencia Española de Medicamentos y Productos Sanitarios (AEMPS)--------------------------------------------------------------------------------------------------------------------Esta información está destinada únicamente a médicos o profesionales  sanitarios:El producto se suministra como un polvo seco estéril en viales que contienen el equivalente a 500 mg de imipenem y 500 mg de cilastatina.El medicamento está tamponado con hidrógeno carbonato sódico, para obtener un pH de la solución entre 6,5 – 8,5. Should, however, persistent and markedly elevated serum calcium levels occur, there are a variety of therapeutic alternatives which may be considered, depending on the patient's underlying condition. After mixing imipenem and cilastatin, you must use it within 4 hours.You may also store mixed medicine in the refrigerator for up to 24 hours. If treatment is switched from ergocalciferol (vitamin DCalcitriol increases inorganic phosphate levels in serum. If your symptoms do not improve or get worse, tell your doctor.Use imipenem, cilastatin, and relebactam injection until you finish the prescription, even if you feel better.

It is given by injection into a vein or muscle.

4.2 Posology and method of administration

It works by killing bacteria. Las reacciones adversas en el sistema nervioso central pueden ocurrir si la dosis no se ajusta a la función renal)cualquier trastorno del sistema nervioso central, como temblores localizados o crisis epilépticas (ataques)Puede desarrollar una prueba positiva (prueba de Coombs), que indica la presencia de anticuerpos que pueden destruir los glóbulos rojos. Hypercalcemia frequently resolves in 2 to 7 days. A healthcare provider will give your first dose and may teach you how to properly use the medication by yourself.Imipenem and cilastatin must be mixed with a liquid (diluent) before using it.

Antibacteriano sistémico. The number of treated patients with pseudohypoparathyroidism less than 6 years of age is too small to make dosage recommendations.Malabsorption is occasionally noted in patients with hypoparathyroidism; hence, larger doses of Rocaltrol may be needed.The recommended initial dosage of Rocaltrol is 0.25 mcg/day in adults and pediatric patients 3 years of age and older.

Rocaltrol contains a medicine called calcitriol.

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