avandia fda panel

Daily visits to selected websites, subscriptions to selected scientific and medical podcast as well as my monthly magazines such as Nature, Scientific American, Physics Today, Science Magazine and Science Readers. respirate just convinced me to add the FDA website into my dailies. What is good with technology these days is that you can be very selective regarding the kind of information you want to get and newspapers make me angry for some reasons that are totally personal.

See this link for FDA issued warnings on Actos and Avandia http://diabetes.niddk.nih.gov/dm/pubs/medicines_ez/insert_J.aspx Kinda makes you wonder if it's time to leave the sinking ship.

Also, Avandia is the other drug that falls into this classification. The FDA warns not to use Avandia for first time users, in fact, the FDA severely restricts its use. You can read about the different oral diabetes medication classifications and drugs that fall into each class here. http://tinyurl.com/type2-diabetes-drug-classes Always ask your doctor why he/she is Rx a drug vs others on the market.

org/wiki/Thiazolidinedione this drug is same family as Rosiglitazone (Avandia) which has been foud active on hbsag and hbvdna, question is does TZD lower hbsag since decrease of hbsag inibits cancer growth too and if lowered to und eradicate hbv?

She is gaining weight, has trouble breathing, and has been experiencing some chest pains lately (Dr. gave nitro). She is on avandia and I would like to know if this could be the cause of her recent decline in health?

I use Actos, but for some reason my fingers typed Avandia. Our FDA went through the same review on Avandia recently, and reluctantly left it on the shelf; however, it is used only when patients are found refractory to other, similar drugs, I believe. FlGuy, although I was down to 185 pounds at one point during treatment, I’m currently the lankiest 6’ 0” 250 pounder you’ve ever seen :o). I’ve always led an active lifestyle, so I don’t fit the sedentary profile of typical DM II patients.

Actos belongs in class of diabetes medications called thiazolidinediones. In this class are Avandia and a combination drug Avandamet [Avandia and Metformin]. Rezulin is in this class but not much known about it.

Also go on the websites of the manufactures, sometimes they have coupons for a % off your bill. When I joint the avandia program I got a couple months free avandia, plus they send coupons at times. Also ask your md for samples. I use to work at a doctors office and we got enough samples to open a pharmacy. Another thing, if your job offers a flexible spending account, I find that is nice as well. it reduces your taxes and you can contribute up to 3000 a year to them. good luck.

The advisory panel voted unanimously for approval yesterday. The FDA meeting is in few weeks.

s briefing document in advance of the panel review this coming Friday 10/25. Evidently the govt. shutdown did not affect the timeline for approval. The PDUFA decision date for sofosbuvir is December 8 or 9 depending on where you look. The overall tone of this document is very encouraging for a swift approval. As a genotype 2 hoping for the all oral treatment ASAP this is very good news. http://www.fda.

You stated "prior partial responders 57% and 15%" - seems like a wide range, was there different classifications for partial responders to make the range so wide?

This is our week. April 27 the US FDA advisory panel meets to review bocerprevir. The next day, April 28, the same panel meets to review telaprevir. The FDA is supposed to publish a reveiw of both on Monday, April 25, posted to their website: http://www.fda.gov/AdvisoryCommittees/CommitteesMeetingMaterials/Drugs/AntiviralDrugsAdvisoryCommittee/ucm247236.htm These panels should show us what questions or concerns are being raised by the FDA.

This level of bureaucratic quagmire is ludicrous. The data has been accumulating for years, There's no reasonable reason that partial reviews could not have been undertaken so the FDA panel was ready to roll once formal submission was made. 6 mos to make a decision? What's that about - diffuculty scheduling around golf vacations? Jesus!!!

Yes, i was put on Avandia for Type 2 abt 5 years ago. Since then my #'s have improved with diet and exercise to the point that a new Dr. said she saw no reason for me to be on Avandia and i have since stopped useing it. It was never vy high, around 159 or so when it was diagnosed. If i am not careful of my diet it can jump up to the 130's to 140's. Am also on diovan for HBP which is usually under good control with the 1 med.

http://www.medhelp.org/posts/Fibromyalgia---CFS/FDA-Reviews-use-of-pain-meds-vs-risks-for-treatment-of-chronic-pain/show/974188 An advisory panel has recommended a ban on the following pain medications to the FDA: Percocet Vicodin Darvon Darvocet http://supersaiyan.newsvine.com/_news/2009/06/30/2985607-panel-recommends-ban-on-2-popular-painkillers http://cbs13.com/health/fda.food.and.2.922915.html These are just the few that I found so far...

Can I take Evening Primrose and Femara together? I'm also taking Avandia. Any thoughts would be great!

After retirement from my civilian job in 2003, my docotr placed me on low dosage Avandia. That brought my blood sugar reading down. I lost a few pounds and after three years of "normal" glucose and glycohemoglobin readings, he took me off Avandia. For the past four years my glucose reading has been fluctuating between 110-140 (fasting) and averages 150 (non-fasting). My glycohemoglobin readings were consistently below 6.5 and my urine read "normal" for blood sugar.

Avandia fda panel

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