Does anyone know what to take for an alternative to Aggrenox? I had a TIA almost 4 years ago and was put on Aggrenox, well, my husband will be losing his job in a week due to the economy which also means we will be losing our health insurance as well. I asked my doctor if he could take me off it and put me on something else and all he said was he would prefer I stayed on Aggrenox. I don't think we can afford it because it is $305 for a month supply!
Aggrenox does have aspirin in it. It is recommended for strokes, as you already know. I'm not sure why the Dr has taken away the Aggrenox. Maybe he feels that taking aspirin is equivalent with less side effects? Aspirin does work well to help prevent stokes and heart attacks. So, there was no reason given for the change?
I was put on Aggrenox/Aspirin after my stroke about 2 months ago. Does anyone on the same treatment take any kind of Vitamins/Herbs with this medication?
In June '08 I was sitting watching TV when my left side from my head down to my leg became stiff and numb. Went to the ER and checked by 5 neuronogists, had scans, MRI & other tests. Their consensus was a brain event in the rt. thalemus. For 2 & 1/2 yrs I was living with a 5 out of 10 sensation but last Dec. '10 as I was having dinner, the sensation became worse like an 8 out of 10 and I'm having increased trouble moving my whole left side.
Since the strokes, the migraines are almost a daily occurrence (although he does take propranolol as a preventative med for them), he cannot tolerate the CPAP( we have had additional sleep studies and made changes to the CPAP without any improvement).
I've found that Aggrenox seems to work without side effects. It's primarily baby aspirin, but also contains a drug that prevents platelets from sticking together. I've taken it twice a day since my stroke, and it appears to work, but who ever knows?
to Mayo and with all saying the same its still not sinking into this head... there is no fix... He has been sent home on a blood thinner (aggrenox) as to not thin the blood to much... With a healthy heart pumping against a 20% opening (when last tested)... So at night he is on oxgen to slow down the heart at night, for the heart pumps harder as ones breathing slows as we sleep... We live 30 mins from the closest hospital which isn't set up to handle this so life fight is another step...
I take 16 or 17 medications including the all inclusive plavix. a 3.25 aspiriin. AGGRENOX,Zocor,and a host of others.I watch my diet and exercise until it hurts to prove to my Dr. that I'm not just lying around. With your "scientific ' MINDS can you help?
Hello Chiari world!
I was diagnosed with Chiari in May. Now two of my cousins, my mom and brother have all be diagnosed with it as well. We are joining a genetics study and are curious if any of you others out there have joined any studies. We would like to know what the Pro's and Con's were/are. We feel that since so many of us have been diagnosed in the last three months that our family may be able to help future families and our future generations by joining the study.
I was wondering if anyone knows of any free syringoma studies being conducted in southern california. Your help is greatly appreciated.
It remains unclear whether hepatitis B virus (HBV) genotype has an influence on treatment response -- as is the case for hepatitis C virus (HCV) -- due to inconsistencies across studies and failure to account for differences in race/ethnicity, according to a report in the March 2010 Journal of Hepatology.
It is well known that viral genotype has a major impact on response to interferon-based therapy for hepatitis C, but it is unclear whether this is also true for hepatitis B.
I have been recently working on some clinical studies on anxiety and I was wondering if anybody knew of any clinical support services? I have looked into a few and came across some that sound pretty good. I was wondering if anybody has ever worked with TransPerfect Trial Interactive before? I checked out their website, TrialInteractive, and they seem pretty solid but I would like to hear other people's take on it. What do you guys think? or does anybody have any other suggestions?
Hi, I'm in Knoxville Tn, and I'm looking for information on the trail studies for Hep C treatment for my mom. Does anyone have any suggestions on where to start?
Does anyone have any information on current or recent studies on this disease? I was recently diagnosed and would welcome any information. My T3 and T4 are normal but microsomal antibodies are 192(high). Thinning hair and weight gain are my concerns.
you MUST contact your prescribing dr to get approval to stop this medication. Aggrenox, Plavix, and Aspirin must be discontinued for 7 days prior to injection and Ticlid 14 days prior to injection. Coumadin should be discontinued 3-4 days prior to injection and you will need to have blood work completed within 24 hours prior to procedure.
drink 1-2 full cups water 60 minutes prior to injection. eat a LIGHT meal.
About 1-1/2 months ago he started experiencing mild itching on his legs and has now become chronic all over his body. Most of his meds have rash and itching side effects. Aggrenox was just changed to Plavix, but the itching has not stopped. 325mg of aspirin is also a future consideration as a blood thinner. He was given Ativan 0.5mg two days ago to stop the itching. The first night he practically scratched two wholes in his paralyzed arm.
m on both of those meds, along with aggrenox, But I got caught up in looking for numbness when so many people died in my family, it's my own fault. It's my own wicked web I weave. I'm originally from Mich
I'm just afraid of what he will say I like & respect him a lot & he did not overprescribe, so I'm already anxious tapering.
The husband idea is an absolute no go unfortunately.
Very complicated.
Thank you for taking the time, and taking care of Michigan!.
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