Recovery time symptoms and conditions

Glad I stumbled on this website. I started NR in April. All seemed well. I spotted most of the 1st month pretty heavily but that's not unusual for me starting BC. A number of vague symptoms began creeping up on me and I decided to stop it last week to see if it could be related to NR since many of the symptoms appeared or worsened after starting it. Sudden hot flashes that lead to panic attacks, feeling like I was as close to fainting you can get without hitting the floor. At first that was once a month but then became more frequent until lately it's been everyday! No fun to say the least! vision changes, waves of severe nausea and dizziness in the past week...I've had it. And it's even been out for a week. I hope the effects wear off ASAP. appreciate all the comments on this forum. makes me feel less alone

I need laparascopic surgery to have my mirena removed from my abdomen as it perforated my uterus - can anyone tell me what to expect? I have a family of wee ones to take care of and am wondering what kind of pain or recovery time may be needed? thanks!

I have not heard what the FDA's findings were regarding their recent investigation. I think it is an outrage that so many people have suffered from this drug. My 4 year old child too was a victim of this nasty drug. No child especially young children should have to suffer. My doctor had no clue as with the pharmacist that singulair changed their pamphlets. It just inferiorates me. Merck stated that they were committed to safety and had communicated that information of changing the pamplets. Funny how so many doctors missed that!

I used to receive a Kenalog injection once a year to treat my skin. It worked great. Best drug, nothing compares to it. After a few years it worked so great that I didn't have to receive the shot anymore.

This drug is far too helpful in the medical field for it to be removed because of its side effects. Never had a problem with getting a hole "in my butt" either... Not that I let A LOT of people look at my butt anyway. There's a reason why you're told what the side effects could be, if you don't like them then tell the doctor you don't want to take the medicine.

If you're a model, then have it photoshopped out... We know now that's what they do anyway. You give young girls bad impressions thinking they have to be perfect, when you're not.

Seems like I'm in the same boat as a lot of people here. My dr. started me on Lipitor 40mg last year then raised it to 80mg. I started getting slight buring type chest pains with some sharp pains on the upper right side on my chest. The sharp pains increased when he raised me to 80mg. In Feb. 2008, I started to complain. He blew me off at first and then I ended up in the hospital for 2 days taking tests in March 2008. All the tests came back fine and my dr. explained the pains as "spasms" caused by "low flow" and told me to ignore then because it wasn't my heart...WHAT?? He gave me 2 other meds for the spasms. In Nov 2008, the sharp pains were daily and throughout the whole day. I started to research chest pains with lipitor and could believe the stories I read. It was as if I wrote them myself. I stopped taking lipitor on Dec 2, 2008 and within 2 weeks the sharp pains are almost by gone. I'm still having the slight burning feeling sometimes and was wondering how long this will last take to completely go away.

I took Levaquin 750 for 10 days for a sinus infection. I took first 5 doses, went to see my doctor again 6 days later because I was still sick. She prescribed again 5 does of Levanquin 750. I am still coughing and I feel very tired. It did not help at all. I am still sick and I have muscle pains in my two calves and stress Achille tendon. I am a runner and I have sometimes problems with my calf: I have been not running too much recently and I was wondering how come suddenly I had those muscle pains in both my calves. I am not sure if it is related to Levaquin, but when I read all those comments, I am worried. Why I have been prescribed this antibiotics if it is obviously dangerous?

After 12 weeks of using 2.5 mg per day of Lisinopril I developed meniscus pain and painful hamstring and glute muscles in my right leg. I quit using the drug and am losing my patience waiting for the pain to stop. Are there stats out there that can give me an idea about the length of recovery time? I a 59 years old and have never suffered from knee pain of any kind. Are there any class action suits against Lisinopril manufacturers?

This is my second post on this subject. The short story is I had a stroke at 43 years old, doctor prescribed Zocor to me, 90 percent of side affects posted here.

I went back to the doctors afraid I was going to get the treatment from mmy doctor that most others got "your crazy, and it's psycholog". To my surprise the doctor knew exactly what I was going through with the only information that I was on Zocor.

The doctor was aware of the undocumented side affects and told me stop taking it immediately. She prescribed Lipitor and so far so good.

Most of the side affects have gone, the foggy head totally gone. The doctor said I was lucky to be recovering so quickly as most take months and some times years from the damage of Zocor. The longer you take it the longer the recovery time which makes sense. The doctor said that Zocor is cheap and highly dangerous.

I urge anyone coming across this website to see your doctor for a medication change ASAP.

I will post again in six months and give an update.

I have been reading about the side effects of lipitor for several days now and am scared silly! I have been taking it for nearly 5 years now. My doc warned me about the muscle weakness/pain when I began taking it, but I didn't have any problems and it definitely provided good results for my cholesterol level. During the past several months though, I've begun to have severe symptoms. Actually, looking back, I realize I've had some of these symptoms for awhile but they were so easily attributable to other causes that I didn't pay close enough attention. I am weak to the point of not being able to walk a city block without being tired; my breathing is so labored sometimes just moving around my apartment is a problem. My knees and lower legs are painful, especially after walking. I get frequent, painful spasms in my lower arms and wrists. My speech has become slurred (I sound drunk) and my voice very hoarse - both so much so that people have trouble understanding me. I have trouble concentrating, am forgetful and am often dizzy and light-headed. I take medication for GERD, hypothyroidism, depression and asthma. But in case you think these symptoms could be from one of those (as I did!), I can assure you that I have had multiple tests which determined my thyroid levels are good, my BP is excellent, I have no signs of cardiac disease or diabetes, no sign of any type of stroke, no signs of any type of cancer or blood disease, no sign of pulmonary problems (other than asthma). I stopped taking Lipitor four days ago after consulting my doc. But I got to tell you, I am scared to death that I've been on this drug so long these symptoms won't go away. Any advice or suggestions would be most welcome.

Well just started yesterday on the 500mg levaquin tablets. Ended up with the flu and waited 6 days before going to see the doctor. I have known for a long time that any antibiotic is bad for you due to the fact they kill all benificial bacteria also. I had severe food allergies for ten years due to them. Only by accident did i find out that what had happened was candidiasis which is also a bacteria that we all have in our system was allowed to grow out of control due to all the good bacteria being wiped out. With this information at hand I was able to treat my what you would call long term side effects. By reintroducing good bacteria back into my system I was finally able to beat all the symptoms. Now I know that with levaquin I will have to reintroduce all over again. The important thing to remember is you have to reintroduce right away. Its the candida that in most cases that causes the problems most people experience. Anytime you kill something in your body you will create toxins that must be eliminated. Anyone not educated about candidiasis should read up on it in whole. Most doctors do not recognize this condition or even believe. I have posted on curezone.com in the candida forum under ( crapshot ). I firmly believe that when probiotics are (good benificial bacteria) reintroduced ASAP the recovery time from the side effects of levaquin or any antibiotic will be diminished greatly. I do not believe that any one probiotic works better than the other but when used rotate brands to allow a better assimilation into your system. Tho dairy products due have good bacteria added for our benefit when candida has grown out of control at this point your better off with a product like Three Lac or Primal Defence or the likes.

Kim123 - you poor thing, I will have you in my thoughts.

My main side effect has been SEVERE panic attacks and anxiety that of course comes with insomnia, nausea & chest pains.

I am trying very hard to recover without further medication and I'm trying to do it on my own. Sarah, another lovely lady on this site, has been very helpful in regards to this and has suggested some helpful tips.

Have you tried perhaps going to a homeopathic doctor? I tried that and he gave me some teas to help with my nerves, I just started yesterday and I think I need to give them about a week to find out if they work.

I also have an overwhelming feeling of sadness, for no reason at all. I'm just hoping it passes soon. I have been off this pill for three months, and I also took it for three months - so cheer up your recovery time may be less than mine.

All the best kim, and my advice is to distract yourself, keep busy doing things like washing dishes. I know sometimes you feel there's nothing that will help at which point all I did was cry hysterically and cry and cry, after that believe it or not I did feel a bit better.

If anyone has completely recovered, please let us know how many months you have been off yasmin.

Good luck ladies.

Claudia.

I received a shot of kenalog at the top of my left buttox after going to the emergency room because my throat was nearly swollen shut when I had mono. It was about 2 months after I had the shot that I noticed a weird dent where the shot had been given, the dent continued to grow in diameter and get deeper over the next couple of weeks. I went to the medical facility my college had on campus and after 2 NP's and 2 doctors came to look at it, 1 person asked if I'd had a kenalog shot at any time. He explained it to be a tissue atrophy caused by the shot and then told me that before a doctor administers that shot, they are suppose to explain the possible side effect to the patient and have a waiver signed. I went back to the hospital that I'd had the shot at and explained the situation to them and asked why I wasn't instructed about side effects and why I did not have any type of waiver presented either. They took a few days to get back to me, but the facility had aggreed to do reconstructive surgery on it at no charge. The only problem was that between my school/work schedule and the time it would take to have the surgeries/recovery time I was not able to have it done. However I would strongly suggest anybody else who's had this problem make this point to the facility they received their shot at. I was 19 at the time of the shot, and am 24 now. A minimal amount of tissue has regenerated on its own, however there is a scar-like marking about 2 inches long and about 3/4 of an inch high in that spot along with a small dent that still remains. The spot is very tender still and by this point, I'm assuming it will always be with me. Hopefully this helps anybody that's had a similar problem. Laws on the shot/procedures could vary by state so I would check with someone who is 100% familiar with medical laws in your state/area.

I too have been experiencing alot of the side effects listed in the many testimonials here. I didn't relate what was happening, but just noticed that there was an inconcistency in the way I felt while taking Advair. Since the pollen season has started, I began taking l/2 doses of Advair a day... I exercise intensely about 4/5 times a week, and noticed that instead of having more "lung" endurance I felt like I almost had the onset of a chest cold or bronchitis. I would get very out of breath the harder I exercised....with muscle fatigue, hipe pain, long recovery time, raspy throat w/phlegm. The wierd thing too was that I had hunger pains in the morning that would continue even after I had eaten... almost like a burning feeling. I just stopped taking Advair, and use my inhaler when needed. I still feel very fatigued, which is very frustrating to someone who exercises as much as I do. It's been about two days, and I am waiting to feel better, hopefully.

HI,
My doc prescribed Yasmin to me because I have heavy heavy periods that come every three weeks due to fibroids. As a result, I have anemia, am up 2-3 nights during period time because of heavy bleeding - then have up to a week recovery time where I'm exhausted because of all the bleeding I went through. I was on Alesse for 12 days last year because I was going crazy! I had extreme moodiness and anxiety. I have the pack of Yasmin in my cabinet and last month I found this site, read everything and decided against taking it. Here it is only 20 days later - got my period and don't know what to do. I'm happy to see that there are some who have had positive results, but since I had such a bad time on Alesse - I don't want to go through what all of you have endured - it's terrible - but I'm sick of the frequent periods and heavy bleeding. If you have any suggestions, please post or email me at Andelmar@aol.com. Thanks and I hope all of you with negative side effects are feeling better - it's certainly no way to live!