Postings symptoms and conditions

OMG!!!!....This Is Totally Happening To Me Too. I had my Mirena put in in 2007 and ohh for the past year or so I have started having Excruciating Pain in My Left Leg, Lower Back, upper thigh all the way to my foot...Also I have had to go to the ER quite a few times with Migraine pain so bad it was incapacitating. I have just called my Doctor and am going to insist this thing be removed..Thank you for the Info...I hope this puts an end to this PAIN!!!

I was prescribed 7 days of Avelox 400 mg for bronchitis. On my fourth day of taking this medication, I began to suffer from severe abdominal pain, cramps and debilitating diarrhea. These symptoms were so bad that I missed a whole week of work. I was taking each pill with dinner in the evening and then I was up all night back and forth to the bathroom. I took 6 of the 7 pills and then refused to take the last one when it became obvious that Avelox was the cause of these symptoms (the only side effect listed on the bottle was dizziness, which I did not experience). I have now been off Avelox for 2 days and I am still suffering from severe abdominal pain and diarrhea. I am afraid to eat anything because it goes right through me and it is very painful.

I am taking probiotics now to regain the good bacteria in my digestive tract, but I am still in a lot of pain. My sister, who is a physician assistant, told me that it should take from 48 hours to a week for this to flush out of my system. She said that Avelox is an extremely strong antibiotic that she only prescribes for confirmed pneumonia.

I am otherwise a very healthy 42 year-old woman with no allergic reactions to any medications which is why it took me so long to make the connection. I would not recommend this medication to anyone and have told my sister that she should not prescribe it either.

These postings have really helped me. I feel lucky that I did not suffer more severe symptoms.

Well hi all. I see we have some new ladies on here since I was here last. I had my Mirena removed on Feb 14, 2009 after it nearly ruined my life and my marriage over a nearly 3 year period. Feel free to read my old postings. My Mirena symptoms have been gone for months now. My chronic pain has been diagnosed as Enthesopathy. It may or may not be related to the Mirena, but I'm getting treatment from an internist, not a moment too soon! I was at the point where I couldn't go on another day. The interesting thing is, Enthesopathy is a disease of the ligaments and tendons. I couldn't figure out why I had little to no pain whatsoever when I was on my period, and my pain and mood and depression got progressively worse as my period approached. I wouldn't be surprised if the Mirena is involved in this. Anyways, I recently did some research and discovered that during our period, we release a hormone called relaxing, which relaxes our ligaments and tendons (among other things). So it's nice to finally put things together and make some sense of it all.
Since the removal of the Mirena I have energy again, I used to be so sluggish I would cry, sex drive is back, I'm not crying all day and am very happy, not angry at my hubby, no more insomnia, and my hair is still growing back. I didn't realize how much I had lost until it started growing back and see all this 1-6" -long hair.

I am really glad that there are these other postings on here so that I know that I am not alone. I am 49 years old and had my mirena inserted day after labor day. I was told that it would help with my medical conditions but so far I believe that they have only made them worse. I have yet to stop flowing and to be honest would prefer how it was before hand with just one week for severe heavy flow instead of 2 months so far of heavy. I have started with acne something that I never had as a teenager and I feel like someone has inflated me into a balloon. I find myself walking around in a haze all the time and I also find myself very depressed and with no or very little energy which is all so uncommon for me. I have an appointment in 3 days with my family doctor and this thing is coming out one way or another even if I have to pull it out.

I just had a mirena put in on Thursday, after the recommendation of the obgyn (she said she had one).
When I was asking my questions I was concerned about the acne, since I never really had it in my life and the possible headaches. BUT reading the above postings is not very encouraging: low libido, weight gain, mood swings. I will surely be back to post the results after a month.
Note: I have not had children, but since I was prone to severe pain/length of periods that is how mirena was suggested.
INSERTION was excruciating! "3 small cramps" was in fact pain that left me quivering and in shock. Doctor's need to be more transparent about the insertion process (especially if you have not had kids).
I will be back after my 4 week check up with the latest report. (and if need be, I will be assertive in the removal demand.)
Thank you so much, ladies.

After you read a representative sampling of this website's testimonials, you certainly ask yourself inter alia: Can this be true? Did thousands of people inject an antibiotic from the fluoroquinolone family, which crippled them for longer or for shorter? Most of us, I suspect, never really get beyond the initial litmus test: Did this medicine poison me or save me? (The answer depends, of course, upon the age, gender, medical condition, and most importantly, the DNA make-up of the individual patient. For hundreds of thousands of patients this antibiotic is a boon. For thousands of other misfortunes this antibiotic is a disaster.) But there is another important question here.

Who gains from self-revelation? To be sure individual sufferers gain certain emotional catharsis from posting their adverse drug reactions (ADRs) to levaquin. E-postings are one-way anonymous tracks that form ruts on a well-traveled trail of tears. Unless these postings are hoaxes written by mischievious gnomes, then they consitute prima facie evidence for a causal link between levaquin injection and sundry crippling ADRs.

Curiously, this e-forum cannot be used as a tool for organizing thousands of potential litigants who might coalesce under a class action lawsuit. Yes, we can analyze each other's anonymous revelations to see if they muster our respective sense of the "ring-of-truth" re: levaquin toxicity, and we may contact each other one-on-one, but no-one can harness this intoxicating communication's technology to reach simultaneously all respondents en masse as a bloc.

So, who wins? The emotionally unburdened e-poster who learns belatedly that s/he is not alone and that prescription medicine likely caused more pain than the underlying malady for which s/he is being treated? Or big pharma that continues to manufacture and market a medication that poses downside risk to many consumers who unwittingly incur more damage than therapeutic value?

Indeed, who wins in a forum where consumers anonymously reveal their symptoms and unconfirmed suspicions? The answer is big pharma wins. Pharmaceutical companies data-mine our postings to estimate the frequency and bredth of ADRs about which consumers complain. House statisticians estimate the ratio of active complainants : silent complainants, i.e., the ratio of complaints who show up on this website to the far heftier percentage of complainants who never post on this website because either they are technology-challenged or they are incurious. House actuarians proceed to estimate how much operating profits their employers must set aside to cover losses in out-of-court settlements or in awards made to plaintiffs in class action lawsuits.

I think this is how the game is played in a behavioral sink where billions are made in a deregulated marketplace that allows predators and prey to interact anonymously. Sorry to be such a downer, but I fathom only the desperate plight of tens of thousands of levaquin consumers for whom no monetary award ever will compensate them adequately for their suffering, and the hundreds of millions of dollars at stake in court awards if consumers ever brought to bear their aggregate numbers and draw a bead on their big pharma tormenters.

I think it a true horror and shame that pharmaceutical companies have not devised a test which determines in advance which patient safely may consume levaquin and which patient's DNA places him or her at risk. I suspect the genome technology is available, but would dig too deeply into big pharm's bottom line. The economics of "parachutes-for-everyone" is infeasible. We are all guinea pigs in a B-grade movie featuring Russian roulette, billion-dollar pay-offs, and an FDA that pretends not to know.

I have been on Lantus & Humalog for about 3 years. I am a 75 yr old male T2 and the only other meds I currently take are Toprol XL and aspirin. After reading all these Lantus postings, I decided it was time to quit Lantus just to see what happened. Like one other person said, "all of a sudden the fog lifted"! I am a different person. I can now sing in church (after 3 days off of Lantus). Before this, I did not have enough breath to sing. When I was on Lantus I had many sleepless nights, suffering from RLS and leg pain. Now I am sleeping the entire night through. These benefits are the tip of the iceberg, I just feel better all over. Needless to say, I am injecting more Humalog now to make up for the absent Lantus but that will not be a problem. Please understand I am not advocating this for anyone else, I am simply reporting what happened to me. I see my doctor in a couple of weeks and can't wait to share the news with her.

So glad I found this site.
My doctor is trying to convince me to having the Mirena fitted as I'm having very heavy periods every 2 weeks that last approx 8 days. I initially said "no", but was still given information regarding Mirena to take home & read. I was beginning to reconsider but after reading through these postings I will be sticking to my guns & will NOT have it fitted.
Thank you for taking time to share your experiences as it has helped me to make a more informed choice.

I'm so glad I found this website - thanks to all of you who have shared. I had a Kenalog injection in May 09 and about a couple of months ago noticed an indentation in the side of my leg. I had it given in my leg instead of buttocks due to other health issues currently going on. It is sore sometimes and hurts sometimes when I bend down or exercise. I also had abnormal periods for several months and didn't realize that it was related to the injection. I had a sinus infection/ear infection and had to get on a plane to go out of the country the next day, otherwise I would have never done this. No one mentioned (or I think knew) anything about the possible muscle/skin side effects. Does anyone know about a class action suit regarding this? I've already made a report with the FDA. I am working with a dr that is doing soft tissue work on it weekly, this does seem to be helping, the indentation decreases quite a bit, but it the indentation increases if I don't have the soft tissue work. I'm hoping I won't have to have plastic surgery to fix this, but looks like I will looking at all the other postings. Does anyone know of a class action law suit regarding this? I tried the person listed in Delaware's e-mail listed on the posting, but it wouldn't go thru.

Hi been off Yasmin for 2 days now, I had 7 days left in my pack but I thought there was no time like the present..... boobs not as tender, I have talked about coming off the pill to my husband, showed him other postings all had the same symptoms as me....he understands the low sex drive thing and hopefully knows i was not making excuses that there really has been a problem....he is glad as he wants his old wife back! Feeling confident that if being off the pill works out I can come off the antidepressants and I really really really hope my sex drive comes back!!! Will keep you informed. Still have the sore stiff neck and the tiredness not sure if it is a symptom that Yasmin has created. I will let you know if this improves. DO NOT TAKE YASMIN - THIS IS MY ADVICE.

Well, about a year ago I was put on Lamictal and didn't experience any side effects, but was also on Lexapro, Trazodone, and Klonopin. I stopped all of the medication besides the Klonopin as I was doing well. However I recently was put back on a low dosage of Lamictal as a mood stabilizer. It's been a week. The only side effect I'm having is headaches! I have a headache all day long. Tylenol doesn't help, it doesn't go away. Once my dosage increases in a week I will only be on 50 mg of Lamictal. I just want the headaches to go away. Did anybody experience headaches while first taking the drug? I'm scared of all of the postings of memory loss and hair loss. I sleep fine, I'm not anxious, I had my first vivid dream last night since I started taking the drug. I don't want to go back on an anti-depressant. Any opinions?

I too have been experiencing the same side effects listed by most of you. I have also been seeing a gastroenterologist for about 9 months now because of stomach issues. All symptoms point to gallbladder disease but the tests come back normal. I called my gyne today and they seem unconcerned with what I have told them and advised me to continue to take my pills until my annual visit in October. I'm done with this pack on Saturday and am thinking of going sans pills for the next month until my appt. Any advice on what pill I should switch to when I do see my dr.?

I have been on Yaz for 3 years. I am now 39- I took it to help with Pre menstrual tension and moodiness, and mild acne. I have done nothing but shed like a DOG since I have been on it, I have no sex drive, I have gained 5 pounds, which is a lot since I am only 5ft.4 in. I just found out the real kicker... I have signs of kidney disease now, high creatinine levels, and can only link it to the use of YAZ. There is a class action law suit forming against Bayer Co., and anyone using this should check it out. They are talking about the possible RECALL of this medicine, and I would hate to think of any young girls out there ending up with kidney damage like me. Please be informed before you continue to take it.

I had my first Mirena five years ago. I loved that I had no periods... it was wonderful! I just had my second one placed two weeks ago and I have been getting flushed, have panic attacks, and a weird "shock-like" feeling in my vagina. The panic attacks are driving me crazy and I wasn't sure if it could be related. After reading several postings, I realize it could very well be the Mirena. But why don't I remember this with the first one? I did get the "shock-like" sensation before.

I had Mirena implanted about almost a year ago and I have had ZERO negative side effects. There was little pain during insertion and I have not had any cramps, headaches, mood swings, nausea, depression, NOTHING. This has been great for me.
While I was on the pill, I experienced mood swings, headaches, acne, cramping and all the other "normal" things that come along with having hormones.
If you are considering Mirena, please rest assured that it does the trick for some of us out there. Had I read these postings prior to insertion, I would have been scared to death. It has been great for me and it can be good for you, too if you are considering it.

Hi All,

I am so glad that I found this group of postings. For the past 5 days I have been experiencing muscle pain which began on the inside of my left knee day 1. On the second day I had significant pain in both calf muscles as if I had begun a new calf workout routine(I haven't) as well as pain in the large back muscle that runs down either side of the spine. Day 3 I noticed serious pain in my forearms and wrists. The forearm pain is causing hand cramping and my thumbs don't seem to function properly. I tried to sign a credit card receipt today and could barely grip the pen. I now have pain in my neck muscles as well.

I know I have taken Levaquin in the past 6 months, I am just not exactly sure when it was. I am definitely going to research that. I went to the Dr. yesterday to discuss my muscle pain. He took 2 viles of blood. He said he is going to check for Lyme's disease and other infection. I am hopeful it is not something serious. I must say thought, many of the posts above sound a lot like what I am experiencing. I am going to be beyond angry if I have a permanent condition from taking Levaquin. Some pain I believe I can deal with. It is the current poor function of my hands I am most concerned with.

I wish all of you the best in recovering. If my condition turns out to be something else I will repost.

Thank god I found this site! My body has been going crazy ever since I started taking Yasmin two years ago and I didn't put two and two together until reading all of these postings and realizing the Yasmin might be the culprit.

I'm a healthy 31 y.o. who exercises regularly, doesn't smoke and has been on various oral contraceptives for the last decade without too many side effects beyond slight moodiness and minor weight gain. About two years ago I switched over to Yasmin. About two months ago I came across this site as I was researching hypertension which I had developed. I was confused and didn’t know what was causing it as I am healthy, unstressed and have a history of low blood pressure. But as soon as I found this site it all started coming together and I realized Yasmin had done much more than raise my blood pressure. I immediately went off the pill and almost right away many of my side effects went away. Here's what I've experienced since being on the pill:

-Weight Gain: Almost right away I gained ten pounds. I’ve effortlessly lost five of those pounds since going off the pill.
-Seborrheic Dermatitis: After a few months of being on Yasmin I developed a painful scalp condition called Seborrheic Dermatitis. Side effects of this are inflamed scalp, redness and most importantly, hair loss. The doctor said it is generally brought on by stress but on further research I saw that it is also caused by hormones, so it wasn’t a stretch for me to realize Yasmin might be the culprit once I saw this site. Over the last couple years I’ve been using all sorts of prescription shampoos to make the problem go away and nothing helped. But as soon as I went off the pill my scalp condition cleared in only a month without the use of shampoos.
-High Blood Pressure: Before I went on the pill my BP was about 100/70. During the time I took Yasmin my BP slowly climbed to above 140/90. Within two weeks of going off the pill my BP was back down to pre-Yasmin levels.
-Irregular Heart Beat: After about a year and a half of being on the pill I started to suffer from seriously irregular heart beat which went away immediately after I got off Yasmin.
-Hyperpigmentation: I know any birth control can cause this but none of them ever have until I went on Yasmin at which point it sprung up all over my face. I’m hoping the dermatologist can clear it up now that I’m off the pill.
-Tightness in Chest: Happened around same time as irregular heartbeat and is now gone.
-Anxiety: I’m not sure I can blame Yasmin for this one since going off Yasmin has not caused it to go away. But enough posters on this site mentioned it as a side effect and it wasn’t a problem for me pre-Yasmin, so I wanted to mention it.
-Irritability: I’m generally easy going and don’t let the little things bother me, but as soon as I went on Yasmin everything started to bug me. Now that I’m off Yasmin I’ve been in a much better mood.

If anyone is on this pill or thinking about going on it, I implore you not to. Too many risks especially since there are so many other pills out there that don’t have many side effects. I mean, there are close to 5,000 postings on this site, mostly against this pill while if you search the web there are almost no other pills that generate this kind of attention. That alone tells me something. I hope the makers of the pill pull it from the market immediately or doctors stop recommending it.

I just read many postings here regarding lisinopril/hctz and the sexual problems it had caused you. I'm a 26 year old male, just married, and am having major problems with my sex drive and erections as well. I've been to several andrologists and they all concluded that 'everything is fine' and that i shouldn't be having the problems i'm having (based on many blood tests of course). I actually used to have a very high sex drive and no problems at all with erections, but i started losing my sex drive slowly but surely a year ago when i started taking lisinopril/hctz. Few months later, my erection started getting weaker and weaker as well. Now, i almost have no sex life. I quit lisinopril/hctz just 3 weeks ago, and i THINK i'm experiencing better morning erections, but still my sex drive is abnormally low. Sometimes my wife gets offended. I may get an erection during foreplay, but the erection is usually short lived, since i have no sex drive in the first place. Could anyone please share with me their experience with quitting this poison, and please let me know if you recovered your sex drive/life. Many thanks,

I just read many postings here regarding lisinopril/hctz and the sexual problems it had caused you. I'm a 26 year old male, just married, and am having major problems with my sex drive and erections as well. I've been to several andrologists and they all concluded that 'everything is fine' and that i shouldn't be having the problems i'm having (based on many blood tests of course). I actually used to have a very high sex drive and no problems at all with erections, but i started losing my sex drive slowly but surely a year ago when i started taking lisinopril/hctz. Few months later, my erection started getting weaker and weaker as well. Now, i almost have no sex life.

I quit lisinopril/hctz just 3 weeks ago, and i THIINK i'm experiencing better morning erections, but still my sex drive is abnormally low. Sometimes my wife gets offended. I may get an erection during foreplay, but the erection is usually short lived, since i have no sex drive in the first place.

Could anyone please share with me their experience with quitting this poison, and please let me know if you recovered your sex drive/life.

Many thanks,

i had my mirena inserted 2 1/2 years ago after i had my 4th child. I just had surgery to have it removed it had moved and went through my uterus. Very painful, this is after having very horrible eczema and hives all over my hands and feet. I can't use my unless i have gloves on because of the blisters and they are permanently scarred from the eczema which we think was caused from the mirena because i didn't have it until about 2 months ago when i started other symptoms. Then i found out that it had went through my uterus which required laparoscopic surgery to remove and to top it off no health insurance so what i thought was going to be a less expensive birth control just cost me about 30,000.00 including doctor bills!!!!

Hello Ladies, I have read all your postings I am now convinced Mirena is the cause of my problems. I just hung up with my husband, I told him I am getting it removed. My right arm is numb must of the day, I have heavy discharges it's somewhat like when your pregnant and you loose your mucus plug.sorry tmi. Very moody, neck pains, left hip and leg pains at night. Every night it's worst. I've had it since 2/2008. Forget about wanting to have sex. I'm tired all the time. I am getting removed ASAP. Just wanted to share my side effects.

Hi All, Hope everyone is holding up well. I've been on warfarin for year and a half now and like most of you i find it has changed my life a lot. I'm only 22 and i hate taken warfarin. I have gained weight and feel depressed. The thing that scares me the most is that i was sick at the weekend and i found there was blood in my sick!!! Has this ever happened to anyone before as it scared me a little.

48 year old male - Hello all, I started with 10mg zocor (Simvastatin) off and on for about 2 months. No real symptoms other than it made me very nauseous. My cholesterol sky rocked and my doctor informed me that I needed to take it regularly and also increased my dosage to 40mg. I have been taking it religiously for about 3-4 months now and my cholesterol has improved very much, but about 2 weeks ago I started feeling pain in both my inner elbows, at the joints and along the sides. Its hard for me to lift things at times. Sometimes it’s a burning sensation and sometimes its sharp pain. My Doctor informed that it was the simvastacin and now wants me to change my meds to Lovaza (900mg omega-3 ethyl esters). I am going to stop using the zocor, but what do you guys think? Is there something better for me too use?

chronic diarrhea x2 weeks-began 4 days after initial dose of lisinopril.....
diarrhea x 12+daily.....
also, experienced headaches, nervousness, waking at night, sweats, acid-like taste in mouth. I discontinued usage, went to dr-she gave me an RX for procardia via nurse without even seeing me on the sole complaint of chronic diarrhea X2weeks......I surely hope this is the solution, and from the postings here, it does appear that Lisinopril is poisonous.
Good luck everyone. My prayers are with all experiencing similar ill effects.