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Jeff Browning/Apidra® Story


Jeff

Meet Jeff Browning:
Loving husband, good father, and Apidra® patient

I was diagnosed with diabetes in August 2002 when I was 36 years old. While diabetes may be present without symptoms, the truth is, I knew in my heart that I had diabetes long before I received my formal diagnosis. With my health care background, I understood the symptoms of diabetes, and I knew I had them: unquenchable thirst, frequent trips to the bathroom, and just feeling sick and tired all the time.

When I was finally diagnosed, I was told I had Type 1. This came as a surprise because I knew Type 1 normally struck children. The news scared me. I was married and the father of two young children. I had an active lifestyle and was not terribly overweight. But my disease changed my relationships with everyone.

Basically, it was like my wife now had three kids instead of two. She constantly had to ask me if I checked my blood sugar. She watched what I ate. I was really concerned about the burden I was putting on my family. I felt like I couldn't be a Daddy and a husband because of the diabetes.

So I started making some changes. The first change I made was to eliminate snacks like candy and soda from my diet, replacing them with whole grains and diet soda instead. I took a nutrition class and even a personal health class. Fear was my motivator; I didn't want to end up like my former neighbor, a man who suffered complications from diabetes.

Three months after I was diagnosed, I found my fear had been replaced with anger. One day it hit me that I was going to be sticking myself with needles for the rest of my life. My anger and unhappiness were apparent to everyone around me. Finally, a friend took me aside and asked me what I was going to do with my diabetes.

In that moment, I realized that I truly had to learn how to take control of this disease, rather than continue allowing it to control me. I knew complications happened when you don't take care of your problems, and I wasn't taking care of mine.

Since then, I've taken control. I watch what I eat, get plenty of exercise, check my blood sugar eight to ten times a day, and take my insulin religiously. And the tools I have to help me are getting better and better all the time. I urge you to work with your healthcare provider who is the best source of information to help you develop a treatment plan that works for you.

In March 2005, I added Apidra® to my insulin regimen. Because it is a rapid-acting, "mealtime" insulin, I inject it just before I eat a meal or a carbohydrate snack. It helps to eliminate the post-meal blood sugar spike I used to get, and it is out of my system within two or three hours.

Apidra® is also flexible. I can take it within 15 minutes before eating or up to 20 minutes after starting a meal. That flexibility really helps when I go out to eat at a restaurant. Once I get my meal, I can sample it and figure out how much I am actually going to eat before injecting the appropriate amount of Apidra®. As a result, I no longer worry that I might be forced to eat a whole plate of food I don't care for just because I have already taken my insulin.

Apidra® has been a great addition to my treatment plan for other reasons as well. In the first eight months I was on it, it helped decrease my A1C.

Testing my blood sugar and taking insulin have become a normal part of my life. I have accepted diabetes as a positive force in my life, which has led me to make healthier choices.

Important Safety Information for Apidra®

Do not use Apidra® during a low blood sugar reaction (hypoglycemia) or if you are allergic to any of the ingredients in Apidra®.

You must test your blood sugar levels while using insulin, such as Apidra®. Do not make any changes to your dose or type of insulin without talking to your healthcare provider. Any change of insulin should be made cautiously and only under medical supervision. Apidra® must only be used if the solution is clear and colorless with no particles visible. Do not share needles, insulin pens or syringes with others.

Apidra®, when given by injection under the skin, should not be mixed with insulins other than NPH. Do not mix Apidra® with any insulin when used in the pump or for intravenous administration.

The most common side effect of insulin, including Apidra®, is low blood sugar (hypoglycemia), which may be serious. Some people may experience symptoms such as shaking, sweating, fast heartbeat, and blurred vision. Severe hypoglycemia can be dangerous and can cause harm to your heart or brain. It may cause unconsciousness, seizures, or death. Other possible side effects may include low blood potassium, injection site reactions, such as changes in fat tissue at the injection site, and allergic reactions, such as itching and rash. Less common, but potentially more serious or life-threatening, is generalized allergy to insulin, including anaphylactic reactions.

Tell your doctor about other medicines and supplements you are taking because they can change the way insulin works. Before starting Apidra®, tell your doctor about all your medical conditions including if you have liver or kidney problems, are pregnant or planning to become pregnant, or are breast-feeding or planning to breast-feed.

If the pump or infusion set does not work right, you may not receive the right amount of insulin. Hypoglycemia, hyperglycemia, or ketosis can happen. Problems should be identified and corrected as quickly as possible. Change the Apidra® in the pump reservoir every 48 hours.

Indications and Usage

Prescription Apidra® is for adults with type 2 diabetes or adults and children (4 years and older) with type 1 diabetes to improve blood sugar control. Apidra® is usually used with a longer-acting insulin. When used as a mealtime insulin, Apidra® should be given within 15 minutes before or within 20 minutes after starting a meal.

Apidra® may be infused subcutaneously by external insulin infusion pumps.

Apidra® SoloSTAR® is a disposable prefilled insulin pen.

Click here for additional important information for Apidra®.

Important Safety Information for Lantus® (insulin glargine [rDNA origin] injection)

Do not take Lantus® if you are allergic to insulin or any of the inactive ingredients in Lantus®.

You must test your blood sugar levels while using insulin, such as Lantus®. Do not make any changes to your dose or type of insulin without talking to your healthcare provider. Any change of insulin should be made cautiously and only under medical supervision.

Do NOT dilute or mix Lantus® with any other insulin or solution. It will not work as intended and you may lose blood sugar control, which could be serious. Lantus® must only be used if the solution is clear and colorless with no particles visible. Do not share needles, insulin pens or syringes with others.

The most common side effect of insulin, including Lantus®, is low blood sugar (hypoglycemia), which may be serious. Some people may experience symptoms such as shaking, sweating, fast heartbeat, and blurred vision. Severe hypoglycemia can be dangerous and can cause harm to your heart or brain. It may cause unconsciousness, seizures, or death. Other possible side effects may include injection site reactions, including changes in fat tissue at the injection site, and allergic reactions, including itching and rash. In rare cases, some allergic reactions may be life threatening.

Tell your doctor about other medicines and supplements you are taking because they can change the way insulin works. Before starting Lantus®, tell your doctor about all your medical conditions including if you have liver or kidney problems, are pregnant or planning to become pregnant, or are breast-feeding or planning to breast-feed.

Indications and Usage

Prescription Lantus® is a long-acting insulin used to treat adults with type 2 diabetes and adults and children (6 years and older) with type 1 diabetes for the control of high blood sugar. It should be taken once a day at the same time each day to lower blood glucose.

Do not use Lantus® to treat diabetic ketoacidosis.

Click here for additional important information for Lantus®.

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• Offer is not valid for patients participating in Medicare, Medicaid, or any other federal- or state funded benefit programs. Offer not valid in MA (except for cash-paying patients). Void where prohibited by law.

The health information contained herein is provided for general educational purposes only. Your healthcare professional is the single best source of information regarding your health. Please consult your healthcare professional if you have any questions about your health or treatment.