Razor blade symptoms and conditions

I hate this thing and can not wait to have it removed!!! I'm 45 and thought this was a great choice for me with menopause on the horizon. NOT! I had the very painful insert on Aug 4th 09 and have been bleeding ever since. 2 weeks of bleeding straight, I'd rather give birth to a razor blade! Then spotted for two weeks. Went back to have a recheck on Sept. 3rd and have had a tampon in all day and night for a month! I 'm now worried about TSS and I'm now also 10 pounds heavier, have experienced tingling in my arms, pain across my shoulder blades and I cry, a lot! I called my Dr. and she said this was normal and would subside! WHAT? Sex is not even an issue because who wants to be down in the red zone! I'm having it expelled on Tues. the 6th and can't wait to lose the symptoms and be back to normal. I look forward to having sex again without towels down like I'm house training a puppy. Good Luck to all of us and yes I think we should sue!

I am a loving mother of a 5 1/2 year old boy. He has been on Singulair for over 3 years. In this past 3 years my son has suffered in an unspeakable amount. He came down with Rota Virus and was hospitalized at 2. He then came in contact with Pneumonia in the hospital while he was there. They automatically put him on Singulair, Zyrtec, Prednisone, and antibiotics to treat the pneumonia. Since that day, my son has gone though more tests than I have in my entire life. He has had asthma, sinusitis, leg cramping ( to the point he cannot walk for 2 years), IBS, Acid reflux,(they gave him laxatives for a year that made things worse and addicted to them also), stomach pain, constipation and diarrhea back and forth. He also got Erythema Mulitforme TWICE, while on this drug. All of which the doctors said could NOT be caused by Singulair. He has had several Upper GI's and CT scans. Along with Barium enemas, several hundreds of blood tests, and many many pokes and prodded that were not necessary. All since he has been on Singulair. He now has frequent bathroom trips, depression, confusion, and anger outbursts. He also has to go to the restroom every 5 minutes. He has had genital swelling, and many other aches and pains. None of which his "doctor" ever said could be a result of Singulair. I am 100% sure it was!!!! He currently has anxiety and emotional sporadic issues causing problems in school The teachers and counselors say that it is so strange because there is no TRIGGER and the outbursts are completely inconsistent. His preschool teacher and director are sure he has ADHD. Well, we had him tested and he does not have any part of it. He has no learning disability what-so-ever. So that brought me back to square one. He is in a positive loving enviroment. How could he be depressed and want to hurt everyone around him? He cannot sit still. He cries and says he is 'stupid" and "can't think" like the other boys. He has nightmares and cannot sleep alone. He is scared of everyone and everything. So, as I sit here crying, I realized that this has all been a reaction of his "medicine" Singulair. He never should have gone through all of those painful tests, only to prove they couldn't find anything. So many treatments and sound full advice speeches from his doctors. How could they be so naive and selfish in the life of my son?

When I called my pediatrician of 5 years, she told me that " parents that have children with behavioral problems will LOOK for something to blame their problems on." She also said "drug companies only put side effects on their labels to PROTECT the drug companies. (as she laughed at me) They are not always valid". Then she said "if you take you child off of Singulair you will be playing Russian Roulette in his life." Then she said that all children around 5 or 6 go though this emotional time in their lives." She told me that if I take my child off of Singulair that she would no longer be a part of his health regimen for his asthma. She told me to see a Pulmonologist for further treatment.
Who is paying who? This is my son's life???????? I decided to go with my mother-gut instinct and get him off of this medicine. No matter what. He has been a different person since. He is currently going though a lot of side effects and withdrawals (leg pain, insomnia, hic-ups, emotional distress) but every day is getting better. How can the drug companies say that this is a "wonder drug?" There are more reported side effected patients then clinical studied patients! How can a "medication" that stimulates the brain not be connected to other problems? This "medication" interferes with the bio synthesis and action of LTs and has been marketed as NOVEL medication against asthma and allergic rhinitis. Who the hell is playing God here??? The pocket books of Merck or our over PAID "doctors?" Who pays the price? Our children? Or us. Thank god I found this before it was too late. I would not be able to withstand the pain of losing my son due to their lack of scientific evidence. They are lucky I am one of the smart ones. I will not settle for less than Justice for the drug companies and their paid "doctors?" You all end up in the same place. HELL

There are 18 million people on this drug. Most of them are children. Please save a life if not your own child's life. Thank You

Hi my history started from last couple months when I realize my bp went up very high(160/100) so I started metoprolol succinate 25mg,for couple days i felt fine and my bp went down but I noticed some pain in my right side so i thought maybe is the liver problem and i started to get off.After a week i was suffered from withdrawal(first week i decreased dose to 12,5mg)then my bp was very high so i called doctor and he prescribed metoprolol 100 mg and lisinopril 25(i never used this one)and hydloxiazyde 12,5 and i felt better for couple weeks then I started to get heart palpitation and very low bp so I quit hydroxiazyde and now I'm on toprol xl (oryginal brand) and still have chest tightness (i switch metoprolol to toprol one day ago)and how you guys divide the tablets to get exact amount its hard

Hi, I started Yaz about 2 weeks ago. I am already on Zoloft for minor depression and anxiety. Stared Yaz the sunday I started my period. First the moodiness started, then the headaches. I thought I was getting sick with a cold because I had razor blade pain in my throat that I ended up attributing to Reflux. Went to the doctor to get meds to treat that. The pain went away then I got a metallic taste that I couldn't get rid of. Went to the dentist and nothing was wrong with my fillings. I thought I was going crazy because then I had vaginal itching and odor. I wasn't have a full period but I never stopped bleeding from my period when I started the pack. After finding this website I stopped mid cycle. This has scared the crap out of me. I know I haven't been on it for long, but can anyone tell me if they have stopped in the middle of the pack and how long it took for your period to be on a normal schedule again.

65 year-old female. Severe headache subsided after first day on macrobid; loss of appetite but despite 300-800 daily calories for 10 days, no weight loss (Still 168.5 lbs.); razor blade feeling in vagina is the worst symptom; weak legs; shortness of breath.
Urologist's PA put me on macrobid for 14 days when she saw cloudy urine. Following week uriinalysis revealed no infection. Dr. cancelled macrobid on day 13. That was a full week ago. Razor blades and shortness of breath persist. Years ago a GYN recommended inserting plain vanilla yogurt for razor blade feeling with yeast infection anti-biotics. It has given some relief, if you don't mind tiny bugs and little dogs following you around!
Only now did I research urine infection test strips to learn I could have bought them myself and learned whether I had an infection immediately. I'm allergie to every anti-biotic.(Can't breathe.) I've had good results with macrobid prescribed for a few days in the past. I never want to take it again.

Hi All, I am a 37 year old mother of 4, with a history of severe Hemiplegic migraines (up to 14 a month). I've been on Verapamil and Topamax for 7-8 months with a gradual increase of the Topamax to 150 mg a day. Before I start writing this I have to preface it with two things: First, Before Topamax I was one of those women my friends refer to as a "Supermom", I home school my kids and used to love it, we normally have a lot of fun and I have a successful, happy marriage. Second, on Topamax, I went from 14 migraines a month to 0. It didn't happen over night, they went away as we ramped up the dosage, but for the last few months I have had no migraines, I can feel it occasionally when my head is fighting one off, but nothing an Advil won't stop, and for those of us who've lived with trying to care for kids while having migraines (especially Hemiplegic) you may understand why I initially put up with the following: I started out with the tingling in my hands and feet (that went away in a couple of months), word finding difficulties (which never really went away, I just learned to accept it),occasional blurred vision which never lasts very long but which has been an issue the entire time I've been on the med, and weight loss ...I am 5'4" and was only 118 lbs to start with, and have nearly "disappeared" into a size 0 and 105 lbs, and it doesn't matter how much I eat, I've been trying 3 meals, snacks, cookies, candy, you name it, I can't gain weight. I was never nauseous, no diarrhea, I just don't get hungry... I had to start wearing a watch at one point to remind myself to feed the kids, because if they didn't ask, they weren't getting lunch until 2:00 because I wasn't getting hungry! Soda does taste like metal (fortunately I don't drink it normally anyway), and you do get loopy with one glass of anything alcoholic.
Then to add to the lovely appearance of skin and bones, my hair is falling out. Before Topamax I worked out regularly, I am even on commercials for my gym (recorded a year ago), since Topamax, I was so tired, depressed, and so afraid of losing weight that I stopped working out. Now a woman who has always made it a goal to set a good example for my daughters that a fit body is the goal, not a thin body, has her mother in law telling her that she looks "bulimic"! In August I noticed I was crying a lot, then I thought well, maybe it's the Topamax, so I started drinking more water and it went away... so I've been very careful to drink A LOT of water and only decaf tea while on this med, but apparently that wasn't enough, because a few weeks ago my husband pointed out that I stopped showering every day. I have been crying at the drop of a hat for a couple of months again, and I have never been someone to cry in public, I have even started crying in front of my daughters friends' mothers and near tears in front of her teacher over the littlest things... then last weekend I found myself with four hours to myself in my house for the first time in months and I was thinking about how I might be able to use it for unspeakable things like running away, or worse... if those aren't signs of a pretty severe depression I don't know what are, fortunately I recognized them and put them together with the memory problems, etc. As for the memory loss, there have been problems with that for months as well, my daughter has been telling me I "have a bad rememberer" , This weekend everything culminated and other people were recognizing the memory issues that I had been keeping private until now (including my husband). Before that, I would be in the kitchen cooking and forget what I was doing, I went to drive to a party this weekend and forgot where I was going, so I called a friends husband and he had to tell me four times where to go before I could retain it (at first he thought I was joking) and then I still couldn't remember the name of the place, only the # and street, I haven't been able to remember routes to places I used to drive... I'll find myself sitting at a light not sure where to go, and making mistakes with our money because I forgot whether I did or didn't pay a bill (something I've never done, we have always had excellent credit). On Topamax I went from feeling like an attractive, successful, good mom,with a happy family... to constantly stressed, even by things I had previously enjoyed doing, and a completely depressed failure... but I had no migraines. I have now been weaning off the Topamax for a few days. I was playing phone tag with my neurologist... so due to the urgency of the problem I took myself down to 100 mg a day. I have since spoken with my neurologist and I am going off of it completely... by the way don't ever discontinue this med without ramping off of it, doing so can cause a seizure. I am unbelievably grateful that I put 2 and 2 together the weekend I had time to myself and got lost going to the party and I already feel more awake, less tearful and depressed... I know that things will be ok anyway. I hope that anyone reading this who is having memory or emotional issues on Topamax and just brushing them aside (because they don't want to risk going back to the migraines or whatever), will get off this med. Please realize that this med could have cost me, my kids and my husband a lot more than my migraines ever will. I have never experienced depression before Topamax, and I can't say that I'm completely back to myself yet, but I hope that when I am off this med I will find normal again, and I pray it will be without migraines, but I know that I wouldn't wish these past few months that I've put myself and my family through on anyone. Now, I need to go take a shower :) , then I'm going to my neurologist to pick up some 25 mg samples to continue ramping off! Good luck to you all!

So far it has been a life saver for me. I have been able to get up and and do things I took for granted. There is a price ( side effects that I can sometimes live with). Two days ago my knees down went numb, pins and needles/razor blade feeling in the feet, my face, lips were numb like novacaine, that lasted 6 hours and scared me alittle. I have herniated/steniosis thorasic, cervical, lumbar, I take 2, 400 mg aday. I also am bipolar and recently were put on topomax 50 mg am 100 mg pm. Anyone? What do ya think? Recliner looking good again?
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