Guest guest Posted July 18, 2008 Report Share Posted July 18, 2008 That is interesting Chris. I don't suppose anyone knows if the Eltroxin problem reported in New Zealand is affecting the UK Eltroxin? My eyes are absolutely fine now. In fact today is the first day I've noticed the swelling has practically gone. My cheek bones and jawline are back too, so the facial swelling which worsened with the Teva brand is now sorted out. Tracey > > Hi Tracey > My FT4 is consistently 32.6 on 200 mcg Activis/Alpharma, but on > Eltroxin it was 30.8, only a drop of less than 2 but by golly did I > feel it even though it turned out that FT3 was exactly the same at 7. > According to the chemist the only Brand name is Eltroxin and this is > the only one allowed to be named on a prescription, otherwise it is > levothyroxine of whatever they have in at the time. > > Chris > > My 1st and current pills are actavis branded. In > > between I was prescribed Teva brand and coincidentally developed > > sore itchy swollen eyes and burning skin plus allergic sneezing. > > This appeared to improve with the actavis (which I started, having > > set aside the last pills in my teva pack). Yesterday I took the > last > > teva pills to see whether I genuinely had a problem with them. > My > > eyes are VERY itchy this morning and my skin hurts. I'm going to > > avoid that brand in future, travelling from chemist to chemist if > I > > have to - so a result of sorts! Strange thing is the filler > > ingredients are the same for both brands. Quote Link to comment Share on other sites More sharing options...
Guest guest Posted July 18, 2008 Report Share Posted July 18, 2008 Hi Tracey This was only after taking Eltroxin for 2 weeks. I could not take it any longer, it gave me chest pain and immediate tiredness from the onset. It felt very week and I wonder if the FT4 would have dropped some more had I been able to take it a bit longer. Chris > > > > Hi Tracey > > > My FT4 is consistently 32.6 on 200 mcg Activis/Alpharma, but on > > Eltroxin it was 30.8, only a drop of less than 2 but by golly did > I > > feel it even though it turned out that FT3 was exactly the same at > 7. > > > According to the chemist the only Brand name is Eltroxin and this > is > > the only one allowed to be named on a prescription, otherwise it > is > > levothyroxine of whatever they have in at the time. > > > > Chris > > > > > My 1st and current pills are actavis branded. In > > > between I was prescribed Teva brand and coincidentally developed > > > sore itchy swollen eyes and burning skin plus allergic sneezing. > > > This appeared to improve with the actavis (which I started, > having > > > set aside the last pills in my teva pack). Yesterday I took the > > last > > > teva pills to see whether I genuinely had a problem with them. > > My > > > eyes are VERY itchy this morning and my skin hurts. I'm going to > > > avoid that brand in future, travelling from chemist to chemist > if > > I > > > have to - so a result of sorts! Strange thing is the filler > > > ingredients are the same for both brands. > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted July 18, 2008 Report Share Posted July 18, 2008 Hi Tracey that's interesting:- http://www.forbes.com/feeds/ap/2008/07/18/ap5230927.html Teva to buy Barr Pharma for more than $7 billion By LINDA A. JOHNSON 07.18.08, 3:09 PM ET is this coincidence?? Bob > > That is interesting Chris. I don't suppose anyone knows if the > Eltroxin problem reported in New Zealand is affecting the UK > Eltroxin? Quote Link to comment Share on other sites More sharing options...
Guest guest Posted July 19, 2008 Report Share Posted July 19, 2008 I don't see what they have to gain by producing drug fillers which are more likely cause their clients to suffer adverse reactions, than their rivals' pills do. I suppose the less competition there is, the less the drug company needs to take patients' experiences into account as the patients have limited choice by then. I do hope our choices don't end up as take it or leave it! Hang on, what am I doing talking about choice! I'm an NHS patient and get what I'm given ;0) - though I do have the option of cycling around town and getting the prescription done where the pharmacist doesn't have Teva levothyroxine. Tracey > > Hi Tracey > > that's interesting:- > > http://www.forbes.com/feeds/ap/2008/07/18/ap5230927.html > > Teva to buy Barr Pharma for more than $7 billion > By LINDA A. JOHNSON 07.18.08, 3:09 PM ET > > is this coincidence?? > > Bob Quote Link to comment Share on other sites More sharing options...
Guest guest Posted July 19, 2008 Report Share Posted July 19, 2008 Hi Tracey I came across a little bit of information and made a phone call on Friday. Your local area should have what's called an LPC (Local Pharmaceutical Committee): it'll be in the phone book under your county name + LPC in words. I called ours and a lady called me back (answerphone); THE SUBSTANCE OF THE PHONE CALL WAS RELATED TO PSYCHIATRIC DRUG PRESCRIBING AND I ASKED HER A RELEVANT PHARMACEUTICAL QUESTION. Whilst she understood what I was saying, to some extent, she did explain that her role (and that of her committee), was a somewhat political one. hhmmmm?? and she suggested I call our area hospital-based drug information unit (Salisbury Hospital for us). A local pharmaceutical committee with a political role??? Maybe you can find some answers in other areas (political or pharmaceutical)? Equally relevant to Dawn's position. I doubt the fillers in drugs would cause a 'political' intervention.. but very expensive patented drugs may be different, and that might very well involve a political, not medical, decision. So who decides where the money gets spent (on medical grounds; NICE/The government/your doctor/a local committee with a pharmaceutical/political mandate....? best wishes Bob > I don't see what they have to gain by producing drug fillers which are more likely cause their clients to suffer adverse reactions, than their rivals' pills do. I suppose the less competition there is, the Quote Link to comment Share on other sites More sharing options...
Guest guest Posted July 19, 2008 Report Share Posted July 19, 2008 Hi (again) Tracey, Another legitimate question one might ask is:- do the suppliers test their generics on homegeneous populations with an inherent genetic risk of adverse reaction to some fillers but not others?? as opposed to tests carried out on a heterogeneous population ?? best wishes Bob > I don't see what they have to gain by producing drug fillers which are more likely cause their clients to suffer adverse reactions, than their rivals' pills do. I suppose the less competition there is, the Quote Link to comment Share on other sites More sharing options...
Guest guest Posted July 19, 2008 Report Share Posted July 19, 2008 Bob, I had wondered that too. How DO Japanese people with their racial genetic tendency to lactose intolerance cope with lactose in most western pills? Does their soy-based diet predispose them to thyroid failure, considering the general advice to avoid excessive soy consumption if you have a wobbly thyroid? I understand that many drugs have been tested more thoroughly on men than women and, considering how differently our bodies function, have often thought there should be male and female versions of pills. As a chemist you may have come across the studies which expand on that theme? Tracey > > > I don't see what they have to gain by producing drug fillers which are > more likely cause their clients to suffer adverse reactions, than > their rivals' pills do. I suppose the less competition there is, Quote Link to comment Share on other sites More sharing options...
Guest guest Posted July 22, 2008 Report Share Posted July 22, 2008 Hi , Folk seem to have less problems with Eltroxin that other brands ( it’s the original T4 and much more expensive) APS seems to have a bad rep for side effects. You can only tell by reading the label if you have known sensitivities, or by the old fashioned trial and error. The problems seem to occur with the different fillers. Same applies to natural thyroid. I’m taking Nature-Throid at the moment and for me is is not as good as Armour ,it does have different fillers. I have no known allergies to any of the ingredients, but Armour makes me feel better- not logical maybe, but a lot thyroid isn’t too logical. Subject: Re: Re: What causes differences in generic levothyroxine? How do you know which brand of thyroxine suits you best? None of them have made me feel that great and really wouldnt know which brand was better for me or not. I have been given several different brands since I was first diagnosed. I think my time for armour is fast approaching From: cassiecfc <cassiecfc@...> Subject: Re: What causes differences in generic levothyroxine? thyroid treatment Date: Friday, 11 July, 2008, 1:50 PM Oh blimey...I just checked mine...I have 3 different brands! > > I think what is being referred to Tracey is the 'potency' difference between different brands of thyroxine - not a difference in potency of one particular brand. It is well known that different brands of thyroxine should be avoided and you should make your doctor write the particular brand name of the thyroxine that is best for you. Your pharmacist should give you the brand on the prescription and should not change this for any other brand. > > Luv - Sheila > > > > > But I don't understand how the potency of levothyroxine can vary > from batch to batch. It is synthetic so I would have thought its > potency would be controllable. I also don't understand how the > inconsistent- potency argument is used against prescribing animal- > sourced thyoxine but NOT against synthetic levothyroxine. What > causes the potency variations anyway? > > Tracey > > > > > No virus found in this incoming message. > Checked by AVG - http://www.avg. com > Version: 8.0.138 / Virus Database: 270.4.7/1545 - Release Date: 10/07/2008 18:43 > Not happy with your email address? Get the one you really want - millions of new email addresses available now at Quote Link to comment Share on other sites More sharing options...
Guest guest Posted July 22, 2008 Report Share Posted July 22, 2008 Hi Sheila Dr B phoned me today. He said that it did sound as though I was slightly over-medicated now. He advised me to stay at 100mcg T4 which I had reduced down from 125 myself and to try 10mcg T3 as opposed to 20mcg. He has said that if I still have hyper symptoms with that dose to drop the T4 further to 75mcg. He has also said that if my hypo symptoms come back when my T4 reduction has had time to settle I can try going back to T3 20 mcg if I feel I need to. He is going to arrange for a blood test mid August when I am back from my holidays and will phone me to discuss the results. He was very nice and treated me with respect. He never mentioned my query about Armour but I will bring it up next time if I am still suffering from these horrible leg cramps when my dose has stabilised. Love Lizzie > Keep battling on Lizzie, and inundate the secretary with emails until you DO get a response. This is YOUR life and Dr B not responding is just not helping you enjoy it at all. I would also keep trying to telephone, there must be a time when he is in his office, able to take calls. > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted July 23, 2008 Report Share Posted July 23, 2008 HI Lizzie I am so pleased he has phoned you (at last!!!) but I am still not sure why he is insisting on you keep taking 100 mcgs T4 and reducing your T3. Most people need T3 - NOT T4 (which is an inactive hormone). I would be very tempted if this was me to stop the L-thyroxine completely and just have a trial of T3 only and see what happened...but that is only my personal thoughts about this. Why wait to cut your T4 to 75mcgs??? This is just delaying things and meanwhile, you are suffering. Anyway, DO remember to stop ALL your thyroid hormone replacement for at least 24 hours before your blood test - and longer if that is at all possible, because otherwise, the reading could be wrong and your Free T3 could show high ion the range, probably making Dr B decide to lower your dose yet again, because it might look you are going hyperthyroid. However, haviong said that, as Dr B does treat with T3 and Armour, he should know that anyway. Luv - Sheila Hi SheilaDr B phoned me today. He said that it did sound as though I wasslightly over-medicated now. He advised me to stay at 100mcg T4 whichI had reduced down from 125 myself and to try 10mcg T3 as opposed to20mcg. He has said that if I still have hyper symptoms with that doseto drop the T4 further to 75mcg. He has also said that if my hyposymptoms come back when my T4 reduction has had time to settle I cantry going back to T3 20 mcg if I feel I need to. He is going toarrange for a blood test mid August when I am back from my holidaysand will phone me to discuss the results. He was very nice and treatedme with respect. He never mentioned my query about Armour but I willbring it up next time if I am still suffering from these horrible legcramps when my dose has stabilised.Love Lizzie> .. No virus found in this incoming message. Checked by AVG - http://www.avg.com Version: 8.0.138 / Virus Database: 270.5.4/1566 - Release Date: 22/07/2008 06:00 Quote Link to comment Share on other sites More sharing options...
Guest guest Posted July 30, 2008 Report Share Posted July 30, 2008 Hi michelle, You can get pill cutters which some find useful- try ebay if the chemist doesn't have them. Now I find I can bite them into quarters quite accurately- I have to take 3/4 per day! Remember if one bit is a bit bigger that you should take the big bit in the am, then the smaller bit for the next dose later- will balance itself out without too many ups and downs. Subject: Re: What causes differences in generic levothyroxine? Oh ok, Thanks Sheila I now have in my possesion Liothyronine sodium? 20 mcg, I have 20 because the chemist that got it said it did not come in any smaller dose and that I had to cut it into 4, what!!!! have you seen how small this tablet is? so off to get back to work I rang the hospital and spoke to the doctors secretary who took all the details and rang me later and said the doctor said to up the dose and now take 10mcg which means cutting the pill in half, (what a farce eh?) and I also have 50 mcg of the levo I dont exactly understand what any of them do but will try the levo at night and the lio in the morning maybe when I get to work? Michele __________________________________________________________ Not happy with your email address?. Get the one you really want - millions of new email addresses available now at http://uk.docs./ymail/new.html ------------------------------------ TPA is not medically qualified. Consult with a qualified medical practitioner before changing medication. Quote Link to comment Share on other sites More sharing options...
Recommended Posts
Join the conversation
You are posting as a guest. If you have an account, sign in now to post with your account.
Note: Your post will require moderator approval before it will be visible.