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I am a former college administrator who is now the adoptive parent of 12 children, most of whom...
US Food and Drug Administration
The FDA is responsible for protecting the public health by assuring the safety, efficacy, and...
New York, New York
Barbara Ficarra RN, BSN, MPA is an award-winning journalist, media broadcaster, media...
i am 62and have been a diabetic for 30 years insulin dependant for about 15years i have been in...
Fitness and health were not always part of my life. After college, I found myself overweight, ill...
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Medtronic MiniMed Paradigm
Infusion Sets: Class 1 Recall - Potential for Over or Under Delivery of
professionals to inform them of the potential for over or under delivery of
or other fluids... Medical Device Safety Notification to all Paradigm
pump users and distributors to inform...
Mannkind Submits Afresa –Inhaled
Device/Drug to the FDA
levels within 12-14 minutes of
, which more closely mimics the natural release... It’s been a while since we heard about
that can be inhaled, as Pfizer abandoned their drug...
Medtronic Gets FDA Approval of the MiniMed® 530G
Pump With Enlite® Using Artificial Pancreas Technology
, which automatically stops
delivery when sensor glucose levels reach a preset low level. The Enlite sensor... if needed to cut down on transit times. UPS pharmacists fill 4,000 orders a day for
Pump Problems and Recalls – FDA Get Those Tags Out There So Consumers Can Identify Them Easily with Cell Phones
said Wednesday it has seen an increasing number of hardware and software problems with
pumps, tiny devices worn by thousands of diabetics to deliver
. "Device problems...
FDA Approves Roche Accu-Chek Combo
System With 2 Way Wireless Bluetooth Technology From the Pump to the Meter
(FDA) for the Accu-Chek Combo system for
pump therapy. The Accu-Chek Combo system seamlessly combines a blood glucose meter with an
pump, which are able to exchange data...
V-Go™ Disposable No-Needle
Delivery Device Receives FDA 510(k) Clearance to use Valeritas Drug
to 40 units of
over a 24 hour period. Separate prescriptions are needed for the
... for use with the V-Go™ Disposable
Delivery Device BRIDGEWATER, N.J., March 1, 2011 /PRNewswire...
Does It Ever Stop–Johnson and Johnson Recall of
Cartridges And an FDA Warning Letter on the Cordis Stents
There have been adverse events reported but luckily no deaths on the
cartridges. If you have one of their
pumps from the Animas unit, check it out and they truly are the big post child...
Asante Solutions Gets FDA Approval for “Pearl Cartridge
has granted 510(k) clearance for the company's Pearl
Pump. Last month, the Pearl...
use easier with using a pre-filled
cartridge and I would also guess that of course...
MannKind Corp Waiting for FDA Approval of Inhaled
–Afrezza-An Army of Inhaler Manufacturers Awaits With Products fo
This is a video with the owner of Mannkind who has been developing the inhaled
product... Dr. Alfred Mann, CEO of Mannkind Corp has developed an inhaled form of
, which the FDA...
From the FDA: Lantus (
glargine) and Cancer
about. Lantus (
glargine) Audience - Diabetes health care professionals, patients FDA notified... that looked at the use of Lantus (
glargine) and possible risk for cancer in patients with diabetes...
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Type 1 diabetes mellitus
... have for type 1 diabetes are detailed below.
treatment As type 1 diabetes occurs be ...
» Read on
... re is a possibility that you may also need, or eventually need,
treatment or other medicines for your condition. This is ...
» Read on
›› View Wellpedia for Type 1 diabetes mellitus
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