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APIDRA PACKAGE INSERT PDF

Apidra SoloStar Units/ml solution for injection in a pre-filled pen – Patient The Patient Information Leaflet (PIL) is the leaflet included in the pack with a. Apidra SoloStar Units/ml solution for injection in a pre-filled pen . SoloStar, the Instructions for use included in the Package leaflet must be read carefully. APIDRA [insulin glulisine injection (rDNA origin)] is a recombinant . package insert, and the pump manufacturer’s manual (see DOSAGE AND.

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Push them out with the plunger and withdraw the correct dose of insulin. Growth hormones, such as somatropin, may lackage insulin onsert, leading to glucose intolerance and loss of blood glucose control. Moderate Monitor blood glucose levels regularly in patients with diabetes, especially when pegvisomant treatment is initiated or when the dose is altered.

Possible side effects Like all medicines, this medicine can cause side effects, although not everybody gets them. Do not use injection sites that are thickened, red, or bumpy. Speak to a doctor immediately if you are not able to control the hypoglycaemia or if it recurs.

Check with your doctor or pharmacist if you are not sure. Children or thin individuals can use a short needle and a 45 degree angle to avoid intramuscular injection. Before use always attach a new needle, and perform a safety test. Optimizing glycemic control before conception and during pregnancy appears to improve fetal outcome; this should include the avoidance of episodes of hypoglycemia as the toxic effects of maternal hypoglycemia on the fetus have been well-documented.

Each pen contains multiple doses. Other side effects Common reported side effects may affect up to 1 in 10 people Skin and allergic reactions at the injection site Reactions at the injection site may occur such as reddening, unusually intense pain on injection, itching, hives, swelling or inflammation.

Insulin glulisine may be given via intravenous administration under proper packqge supervision in a clinical setting for glycemic control, although dosage, safety, and efficacy information for this route of administration is not available. Specific information for insulin glulisine should be followed for in-use time, frequency of changing infusion sets, or other details as the manufacturer of the pump’s or other insulin products’ information may differ see Administration section.

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Sign Up Log In Cancel. What Apidra is and what it is used for 2. What you need to know before you use Apidra Do not use Apidra If you are allergic to insulin glulisine or any of the other ingredients of this medicine listed in section 6.

Last updated on eMC: Serious side effects Hypoglycaemia low blood sugar can be very serious. Insulin requirements are highly variable and must be individualized based on patient-specific factors and type of insulin regimen. Moderate Systemic bexarotene may enhance the action of insulin, resulting in hypoglycemia. Because of differences in onset of action, sodium polystyrene sulfonate is often used with these agents. Individualize dosage based on blood glucose and other clinical parameters. There is no concern when glucagon is used to treat severe hypoglycemia.

Finally, insulin is involved in the regulation of protein metabolism inwert increasing protein synthesis and inhibiting proteolysis in muscle tissue. Moderate Monitor patients receiving insulin closely for changes in diabetic control when niacin, niacinamide is instituted or discontinued.

This helps prevent contamination, and potential needle blocks. Pump or infusion set malfunction or insulin degradation can lead to hyperglycemia and DKA or HHS in a short time because of the small subcutaneous depot of insulin.

Fast-Acting, Mealtime Insulin | Apidra® (insulin glulisine [rDNA origin] injection)

The volume of distribution of insulin glulisine after IV administration is 13 L, which is similar to the volume of distribution of regular insulin after IV administration 21 L. Apidra contains metacresol Apidra contains metacresol, which may cause allergic reactions. If you forget to use Apidra If you have missed a dose of Apidra or if inxert have not injected enough insulin, your blood sugar level may become inserh high hyperglycaemia. Apidra in a pre-filled pen is only suitable for injecting just under the skin.

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Storage of opened products: Changes in glycemic control can usually be corrected through modification of hypoglycemic therapy. These differences may be particularly relevant when patients are switched from multiple injection therapy or infusion with buffered regular insulin.

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Hypoglycemia has not been associated with bexarotene aipdra. Once removed from refrigeration, pens should be discarded within 28 days, even if they have not been opened and even if they still contain insulin.

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This effect may lead to hypoglycemia acutely, followed hyperglycemia with prolonged pentamidine therapy. There is insufficient clinical information on the use of Apidra in children younger than the age of 6 jnsert. Moderate Cyclosporine may cause hyperglycemia. If your injection is given by another person, or if you are giving an injection to another person, special caution must pavkage taken by this person when removing and disposing of the needle. Pull back the plunger of a disposable syringe to fill the syringe with an amount of air equal to your dose of insulin if your dose is 30 units, pull the plunger to the 30 unit mark.

Select an injection site on the stomach, arm, buttocks, or thigh, and clean with an alcohol wipe. Contents of the pack and pacage information. In diabetic patients, the metabolic effects of androgens may decrease blood glucose and, therefore, may decrease antidiabetic agent dosage requirements.

Moderate Propoxyphene may enhance the hypoglycemic action of antidiabetic agents.

Apidra SoloStar 100 Units/ml solution for injection in a pre-filled pen

If you are not sure whether you are taking one of those medicines ask your doctor or pharmacist. Patients pqckage risk include those with compromised renal function, those fasting for prolonged periods, those that are malnourished, and those receiving high or excessive doses of sulfonamides.

In addition, diuretics reduce the risk of stroke and cardiovascular disease in patients with diabetes.