APIDRA PI PDF

PI & CMI Trade Names and Active Ingredients containing insulin glulisine. 1 Documents available. Need more information on a Apidra, CMIPI, Insulin glulisine. PI & CMI Trade Names and Active Ingredients containing insulin. 42 Documents Actrapid, PI, Insulin – human (human insulin) Apidra, CMIPI, Insulin glulisine. Apidra PI MKT. #v Page 1. PRODUCT INFORMATION. APIDRA APIDRA [insulin glulisine injection {rDNA origin}] is a recombinant human insulin .

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There are no documented safety concerns with insulin glulisine use in children in a subcutaneous basal-bolus regimen. Pre-filled pens that are first carried as a spare for a while must also be discarded 28 days after being removed from the refrigerator.

Do NOT reuse needles. MediKidz Comic Explains Type 1. Alcohol, diet, exercise and your general health all affect the control of your diabetes. Glulisine has not been approved by the Food Drug Administration for use in children or adults via CSII, but two clinical 2627 and two in vitro studies have investigated its use.

Rapid Acting Mealtime Insulin |Apidra® (insulin glulisine [rDNA origin] injection)

apirda If you are experiencing low blood sugar levels hypoglycaemia – a “hypo”. NovoLog savings card information. In solution, insulin molecules exist in equilibrium between monomers, dimers, tetramers, hexamers, and higher-order aggregates.

You and your doctor should design an insulin plan for those times when you are sick. Macquarie Park, NSW Draw air into the syringe equal to your dose of Apidra and inject it into the Apidra vial but do not withdraw the needle. An Ovid Medline search of the published literature found a limited number of articles on the use of glulisine among pediatric patients.

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Contact your doctor immediately if your blood sugar level apidrz very high or you experience any of the following symptoms. Tell your doctor if your diet changes.

Each country you visit will need to see this letter, so you apixra take several copies. The second clinical study, which included adolescents and adults, was a crossover trial looking at timing of meal-related glulisine bolus administration via CSII in 23 subjects.

Insulin analogs were first available for clinical use ina major advantage being reduced po episodes compared with regular human insulin RHI; Figure 1. Apidra is supplied in New Zealand by:.

It does not contain all the available information. Make sure that you tell every doctor, dentist, pharmacist or other healthcare professional who is treating you that you have diabetes and are using Apjdra.

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Efficacy and safety of insulin glulisne in japanese patients with type 1 diabetes mellitus; using glargine as basal insulin [Abstract Number PO] Diabetes.

If you have not told your doctor about any of the above, tell them before you start using Apidra. Tell your doctor if appidra are breastfeeding or plan to breastfeed. The Diabetes Control and Complications Trial.

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The role of insulin glulisine to improve glycemic control in children with diabetes mellitus

Heise T, Heinemann L. Tell your doctor if you drink alcohol.

Tell your doctor if you often have hypoglycaemia or if you have ever become unconscious after using Apidra. Closely monitor blood glucose in all patients treated with insulin.

Visit your apdra for regular checks of your eyes, feet, kidneys, heart, circulation, blood apidar blood pressure. Safety of insulin glulisine when given by continuous subcutaneous infusion using an apixra pump in patients with type 1 diabetes.

Self association properties of monomeric insulin analogs under formulation conditions. Apidra SoloStar is a pre-filled disposable pen containing a 3mL cartridge of Apidra.

Freecall helpline Do not be alarmed by the following lists of side effects. There were no trials comparing the efficacy of glulisine with aspart in pediatric patients. Pre-filled disposable pens Apidra SoloStar disposable pens are pre-filled and ready for use. Rapid and long-acting insulin analogues as an aproach to improve insulin therapy: Other than urticaria in a patient on RHI, details of the adverse reactions were not provided.