Bad case symptoms and conditions

i ave a friend who has just had a bad case of the flu which has turned into pneumonia. her doctor out her on levaquin! i almost had a heart attack, called her and begged her to stop it. i sent her a bunch of info about it. why not put her on augment, something with less chance of adverse effects.
now i find she had a stroke over the weekend and is in the hospital! has anyone heard of anything like this on levaquin?

I just got my second shot a week ago and have felt like absolute shit ever since! I have horrible migraines, a lot of head pressure, am extremely dizzy, really tired and weak.. basically feel like I have a bad case of the flu that just won't go away. Not to mention the arm I got the shot in this time is still extremely sore. Seeing all of these side effects is scaring me to death! Do they ever go away?? I seriously don't know how much longer I'll be able to function like this, in fact every day I seem to feel worse. I really can't afford to be sick right now.. I have a 6 month old to take care of, work full time, and am trying to get through high school. What a nightmare. My heart goes out to all of you that have experienced life threatening side effects from this shot. I will definitely NOT be going back for the third one!

I am 17 years old, about to be 18, my fiance is my first and only sexual partner, and I am beginning to HATE loestrin. I have been on the pills for approximately a month and a week. When I first started them I would get extremely hungry and the more I ate, the hungrier I got. It was like a bad case of the munchies, not that I've ever smoked pot. But I was seriously eating anything and everything, even foods I didn't like. My stomach felt a little weird for the first couple days, but nothing too bad. Then I started taking the brown pills, and all hell broke loose. There were the cramps. Horrible, HORRIBLE, cramps, which I am still having 3 days after going back on the active pills. Cramps all through my lower abdomen and stomach, and the feeling that at any given moment my right ovary might drop out (which might actually provide some relief) I actually doubled over crying with the pain in the shower yesterday, and would have fallen and surely hurt myself if my fiance had not been in the shower with me and caught me before I hit the ground. Intense hunger. Followed by bought of nausea, that make me want to puke, but I can't. I am very, very, sensitive to smells. Perfumes, food, cologne, things that I formally found the smell appealing, now disgust me. My lower back, is KILLING me! I get dizzy spells, and lightheadedness frequently, and feel like I may black out. Most of the time I can get myself to a spot where I can sit down and let my body sort things out before I actually black out, but I'm waiting for the day I can't. I have been getting terrible, awful headaches that stay with me through most of the day. Sleeplessness. I had my "period" 3-4 days early, if you can call it a period. It was nothing more than a day and a half of light pink spotting and brown discharge that only showed up when I wiped, I didn't even need a pad. Now, we did start having unprotected sex (with the exception of the bc) at 5 or 6 days instead of 7, and I forgot to take my pills until 9-12 hours after I was supposed to a couple of times. Couple that with the lack of a normal period and all the side effects that could also be the side effects of early pregnancy, and I'm pretty worried. I would love to be a parent, as would my fiance, but I would have liked to have graduated high school first. If these symptoms turn out to be just the pill *** with my body, I would rather just take my chances either with a condom or no protection at all. Sometime in the next week or two I will probably be taking a pregnancy test as I am afraid to wait for my next period and continue the pills because if I am pregnant I know that it can cause damage to the fetus. If anyone has wound up pregnant while on loestrin fe please email me and let me know how you found out, and how things turned out. My email address is ****** Thank you so much for any help you can give a scared teen.

Hey people, I'm glad that I found this posting myself! I've battled depression/anxiety for the past couple of years but thought I had gotten. Then I was Rx'd doxy 100mg twice a day for my cornea in my eye not working based on a clogged gland. Since I've been taking it I have been sick to my stomach (OK I new that was coming) and have had hot flashes and sensitivity to light (didn't see that but OK), and yesterday I felt totally detached from rational thinking. I felt nervous all day, was a bit light headed, and battled a bad case of depressive thinking. Today has been a bit better but I worry about this feeling returning. I need to continue taking the meds for I need to be able to see clearly. Has anyone else felt 'nervous w/hot flashes' while on doxy? I'm also taking fish oil omega-3 but it hasn't ever affected me like that.

I've had numerous side effects from Synthroid, but the ones that finally scared me off the drug were the thoughts of death, dying and suicide.

These thoughts came as casually as thoughts of what I'll wear tomorrow, which was more frightening. They also came unbidden. First, I was thinking about death generally. About a month later, I began thinking about dying, and the whole process of dying. Then, when I started thinking about just walking in front of a train, I got on the Internet and did some research.

Synthroid was the only medication I take daily, so I stopped taking it at once. And about a week later, the thoughts of death, dying and suicide stopped. My doctor refuses to prescribe natural thyroid, so I'm out of luck until I find a doctor who will help me.

I have been taking Quasense for 2 months now, and i feel horrible! I was on reclipsen before for extremely long and heavy periods, and it worked great, but then i switched to quasense and I have gained 8 pounds (doesn't sound like much? I'm four foot eleven!!) I have horrible mood swings and frequent headaches. I am having many digestive issues too, lately every time I eat I've been getting absolutely terrifying stomach cramps, and also just one bite of something fills me up completely! I've also been kind of gassy.... eek! No spotting, which is nice, BUT NOT WORTH IT! also, i have been super sensitive to smells, random things make me gag and i have to run out of the room. THIS PILL IS HORRIBLE!!!!

I have been booked into hospital for the marina fitted on the 20th. As i was only told it would in most cases stop periods i thought great. However as that is all i was told about this product i thought i would complete some research for myself prior to my appointment! (Hence i ended up here through google!) And i am Freaked out by your stories. I was told of No such things, given no information on the product either, Just that this would be a solution for my every day spotting. There is no way i will take a chance with this now, One bad case story is enough, when it is serious pain, hair loss etc!
Great Site this, thanks so much for the stories... Take care x

This is the second time i'm writing on here. I posted my Mirena side effects a few months ago and thought i'd update my side effects....

before i had the mirena put in i was doing GREAT losing weight right after my 4th baby. i actually lost 15 lbs and weighed less then when i got preggo. within a 3 week period of getting the Mirena put in, i gained 11 lbs! and my dieting and exercise wasn't doing much good. my doc recommended that i watch was a eat a little more carefully and exercise MORE.... how much more do i have to watch was i eat and exercise?? anyhow, its been almost 6 1/2 months since i had it up it and im just experiencing more and more side effects. now i had what looks like a really bad case of eczema all over my body. especially on my knees, elbows and my knuckles. my scalp is really itchy, i've GAINED 30 lbs, my hair is falling out like crazy, by bones are killing me especially my lower back, ankles and shins, my mood swings are horrible i feel like im PMSing all the time and when i get my period which is still messed up and lasts for 2 weeks i get even moodier! i am always really tired, i feel like my chest is about to explode, whenever i eat i get really nauseous, i feel depressed all the time and have bouts of crying spells.... i've always had migraines but the mirena seemed to make them EVEN WORSE now. IDK, i've just about had it with the IUD. the only good thing about it is...im not pregnant!! and i don't understand why doctors keep brushing all these symptoms off as if we are all crazy when we say we are experiencing something that we know wasn't there before the IUD...

I took Avelox five years ago to clear up an sinus infection that kept coming back every 2-3 weeks. I was prescribed regular antibiotics each time, it would go away, and then come right back. To get rid of it for good, my doctor prescribed me 400mg of Avelox, one per day for five days. It totally wiped out the infection and it never came back. Awesome, right?

Unfortunately it also destroyed most of the bacteria in my stomach leading to a bad case of c.diff for 2 weeks and permanent lactose intolerance.

It did exactly what I needed, but the price was very high indeed. Though my health has been better since then, I still get sick 2-3 times a year. The duration lasts longer than for most people, but I don't care. I do not take antibiotics anymore. If I ever do, it will need to be a life threatening condition.

You sound just like me! My joint pain was so bad i thought I had a really bad case of arthritis. Some nights i felt like my legs and wrists were broken! ... and this makes it hard to look after 2 kids under the age of 3. My husband and i have been in marriage counseling for months now, and I have been for solo counseling for depression, anxiety and an over-eating disorder... all of which has been pretty much cured since the removal of my Mirena on Feb. 14th! I was forewarned by the women on this site that, after removal, I would have some bad spells during PMS and ovulation time.. which I have had. And during those times i started to doubt my diagnosis. Looking back now, the puzzle fits so perfectly, I don't see how I could have doubted it. I just never understood PMS until this Mirena came along. I never had it before. Get that evil thing out and look forward to getting better. No birth control method is worth this kind of sacrifice. I'm so lucky my husband stuck it through. A lot of men would have given up on me long ago...

i can't believe all these posts, i come on here everyday now, i'm so glad i found it. i had my mirena fitted in oct 08, and have completely changed since. before i was a happy, energetic, optimistic, fit, healthyish, now i'm in counseling for anxiety and depression, in the doctors evrery other week (not kidding) i'm so glad hes nice and understanding! here are my symptoms in 5 months

aching joints, (been referred to a rheumatologist),
depression and anxiety (been referred to a councilor),
head aches,
tired,
smelly discharge,
excessive bleeding, (8 weeks),
painful periods,
pain underneath ribs (not sure if its related),
dizzy,
don't feel like me any more,
forgetful,

I am scared to death after reading what everyone is going through. I was put on Levaquin for 10 days and got to day 9. My joints ached so bad I thought I had arthritis, and even had my Dr. do blood tests for it (I had no idea it was the Levaquin). I am only 35 years old and never worried about arthritis before this. Also, within 5 days I started developing hives all over. Again, I was stupid and didn't realize until day 9 that the hives were because of this med. I told my Dr. and he told me to stop taking it which of course I did. I assumed the hives would go away after the med was out of my system. But a week later the hives were unbearable. I was put on prednisone (another issue altogether) and that helped the itching, but now every time I try to go off or back off the prednisone the hives come back- and they are terrible! Now my Dr. thinks the hives were from something else because there is no way that the Levaquin is still in my body. But after reading what other people are going through on this med, I am convinced this stuff is as everyone says- POISON!! I am so worried about the joint and hip pain that was so bad I couldn't stand for long without excruciating pain in my right hip. It felt like I had a one hundred pound weight just sitting on it. And my hands were the worst. I have a newborn and could barely pick him up without worry that I'd drop him. I don't know what to do.. Is there anything to do?? I'm still on the prednisone, and have been for a month. I need to get off of it but every time I do I itch so bad with the hives that I cannot function. Also because of the prednisone I noticed last night that I am getting "moon face" my face is swelling up and there are a million side effects from that drug too. How long does this last? Has anyone else fought the hives that come with this? Please help me, I am so scared!

I take the Lisonopril and HCTZ and within a few days, I started experiencing dizziness (bad case of Vertigo), fatigue. My doctor took me off. It has been a week now, and I am still suffering from the side effects. Crappy I tell ya! I won't take that stuff anymore. God will just have to take me, because I am done. A co-worker told me her doctor prescribed it, but her grandmother said take Ordorless Garlic tablets. That was a year ago. No more High BP. I am trying that. Won't hurt.

I was giving prednisone for only 5 days (not sure about dose, but it tapered to one pill on the last day) for a bronchitis induced severe asthma attack. I have only had asthma twice in my 50 years, both times associated with a bad case of bronchitis. The "doc in the box" reduced his original dosage due to the 3 corisone injections I recently had in my spine. After reading these posts I feel grateful I wasn't on a higher, longer term dose. I have some of the same side effects listed here including uncontrollable appetite, fat gain around the middle, water weight gain, constantly having to urinate, superhuman energy, heart palpitations, and approximately two weeks after finishing, I began to get a mustache (hairs that were previously white became brown over a two week period). I have read on the internet and been told by my pharmacist that this is temporary. I have also read and been told that the 2mg estradiol I take every day since my hysterectomy causes the body to retain and not rid itself of the steroids as it normally would (estrogen is actually listed as drug interaction with prednisone). The doctor in the box apparently just ignored this interaction and prescribed it anyway. However the main reason I am posting is a very strange possible side effect that occurred approximately 1 week after my final dose. I was awakened in the middle of the night with SEVERE pain (felt like bone pain, not muscle) in my right knee that lasted until morning. By mid morning it was gone. The next night I had the same experience but in both knees. It lasted about 5 more days, gradually tapering in intensity, and then just went away. I do have severe arthritis in my lumbar and cervical spine, having had surgeries to repair injuries from a snowmobiling accident. I have normal arthritis elsewhere for a 50 year old, but have NEVER had issues with my knees. Has anyone had this strange symptom? None of my doctors (internist, rheumatologist, physiatrist - who gave me the injections and prescribed physical therapy for my spine) had any explanation. The only explanation I have is the prednisone because I had taken the Z-pac (antibiotic) with no side effects several times in the past. Weird!

Incidentally, I am off the prednisone for about 5 weeks, am still hungry all the time, still fat, still bloated. Unfortunately the extra energy is gone. Best of luck to everyone on this strange drug. My heart sincerely goes out to all of you on long term therapy. God bless.

Very high tolerance for medications incl 60mg morphine, 20mg oxycontin 4x day, however, I just cannot seem to tolerate Fentanyl. Have tried it two times in past, both the 25mcg and 50mcg. The first week or so is great, after that the side effects are more than I can tolerate. All of these side effects were extreme and unbearable not just mild. They affected my ability to function and sent me to bed on more than one occasion. Extreme fatigue, nausea, sweating, anxiety and weakness. I felt as though I had a very bad case of the stomach flu. Both occasions I stuck it out for 2-4 weeks till I finally had to quit using it. Any suggestions as to why would appreciated. Some of my side effects aren't even listed in brochure.

I was on prednisone while getting over pneumonia to help with my breathing. I was only on it for 7 days and the doctor didn't have me go off of it gradually. I missed the last dose on the 7th day and by bedtime, my muscles were sore enough it almost hurt to lay down. I took the last pill that night before I went to bed and had no muscle soreness in the morning. After that, the muscle soreness came back, along with dizziness. My pulse was also higher than normal. Two days later at night, I was still having muscle soreness and dizziness, although not nearly as but, but I was having a lot of trouble breathing and my pulse would refuse to go below 100 no matter what I did and the problems continued thought the night. The next morning I went to the clinic that prescribed me the predisone because the information they gave me said to see a doctor if these problems persisted. I told them I thought I might be having a predisone withdrawal because my mother, a nurse, said it was the most likely problem from experience. They completely ignored that saying it had been several days since I've stopped the steroid and kept asking me about my asthma (inhalers weren't working and it was definitely not an asthma attack -- I've had plenty of those, to all different degrees) and ended up giving me medicine for anxiety, which helped the closing of my throat, but none of my other symptoms. Three days later, my resting pulse is down to 80, but my breathing is so much worse than it would be with just my normal asthma and taking my inhalers as much as is allowed. I had no noticeable symptoms when I was on the prednisone except being less able to sleep. If it keeps up, I intend to go to a different doctor to see what is really happening, but I don't think it's 'normal' to have the withdrawal symptoms for this long after only having it for 7 days. I know I took it when I was younger (I'm 22), but I don't remember ever having issues going off of it before.

I was injected with Kenalog in Mid July 2008 to reduce the swelling in my tonsils (I had a bad case of tonsillitis). I was asked if I have allergic reactions to steroid injections, and to my knowledge, I don't. So I was given a shot in my upper right buttock on Thursday (mid July). On the following Friday I was no better (still mid July). I was still not able to swallow my own spit, let alone eat or drink, so I went back Friday morning. I got another shot in the same location of Kelanog. I was not told of side effects; I was told the swelling would go down in my tonsils/throat. Again, no results.

That Friday afternoon I was admitted into the hospital for care. A weekend of fluids and other drugs got the infection out. I stayed infection free for two weeks. It hurt for a week afterwards on my right buttock, but no bruising. I healed up, had my tonsillectomy (sp), and healed fine after that.

I noticed nothing wrong with my upper right buttock until about two weeks ago. I am in the process of getting a large rib/hip tattoo piece finished, and about two weeks ago I noticed a spot that looked like a small bruise a few inches from my tattoo in the spot where I was administered the Kenalog shots. I didn't put it together then. Two weeks later (This past Thursday, September 25, 2008), my tattoo artist was about to work on me and said, "You have a dent in your butt, what happened?" I had no idea it was even a dent. The "bruise" like mark now looked like a burn scar, red, and smooth and deep--dented.

The red mark is still dented and the same color. It's about the size of an inch from one side to the other. However, each day since it has been dented, the dented area has expanded fairly rapidly. The dent is now not only in that red area (the injection site), but also along my hip/upper thigh. It's getting deeper and traveling outside the red area, and the red area is the same color. This discoloration just started. I heard this is called Tissue Atrophy due to a misadministered Kenalog injection.

Does this dent go away or stop "spreading" by itself? How will I know if it will stop spreading; is it different for everyone? How can it be properly diagnosed as well? Can a biopsy be done to prove that this it what it is? Does anyone have any insight?

Also, it's been 2 1/2 months before I saw any of these effects...why does it seem like my effects came later than others? Is that possible?

Thanks.

I was prescribed the 4mg methylprednisolone pack along with 50 mg tramadol for acute tendinitis in my wrist. I took the first 3 days of the prednisone and only 2 doses of the tramadol over the three days. For a total of 60 mg of prednisone.

The first day I had hot flashes and insomnia but attributed it to the tramadol because I had never taken it before and had taken the prednisone several years ago for poison ivy with no adverse reactions. I didn't take the tramadol the second night and then took it again last night along with my daily dose of prednisone. I had extreme difficulty falling asleep, heart burn, hot flashes; and tossed and turned all night trying to fall asleep. At around 2am, I began to have difficulty breathing, tightening in my chest, confusion, and racing thoughts. It felt as though my throat was closing up on me. My anxiety progressed to the point that I was pacing back and forth. I woke my husband up and told him to prepare to take me to the ER. After calling my insurance's 24 hour help line, it was recommended that I go to the ER. I had an x-ray, blood work, urine drug screen, and echocardiogram. Luckily, everything was negative. The ER doctor told me that I likely had a reaction to the prednisone and commented that some people will experience these symptoms when taking it. He stated that he had a similar reaction when he took it and it felt like he was climbing the walls, which is an accurate description of my experience that night. He recommended that I either stop taking it altogether or call my primary care provider and cut it down. He prescribed me xanax and administered some to me at the ER which greatly helped. The next day I stopped taking the pred but am still having dizziness, chest tightness, hot flashes, and mental dullness. I have decided to never take this medication again. Fortunately, I don't have any of the physical sx that some have experienced, and my heart goes out to you. I think the mental symptoms were traumatic enough for me and can't imagine having both as I would be a basket case. I have mood swings, some melancholia, and am very fatigued.

I think it is imperative to research any medication that is prescribed to you before you take it. Many providers will say that side effects are rare, but my experience is that side effects are more common than rare. My prayers go out to those of you who are going through what I am going through. I hope that it clears our systems quickly because this is no way to live. I'd rather put up with the pain of tendinitis or carpel tunnel than to have these symptoms.

At 50mg a day, Topamax, taken at night, makes me feel very heavy, tired and numb all day. I have been on it for 3 months so far. I also have other side effects mentioned in previous posts. I hate feeling tingly in hands and legs (from the knee down) and sometimes in my face. It is supposed to go away - soon? I get a bad case of my legs falling asleep in almost any position I sit in other than total upright (which is not comfortable). My lifr-long instiable appetite is hardly affected. I'd say maybe a little bit. I do notice taste difference in drinks and food, sometimes more than other times. I need this medicine for Migraines, it has help relieve my symptoms, but I think I need to continue to increase the dose because I still get Migraines and feel pressure in my head a lot.

Hello Everyone,

I am 33, male, I have been doing sport actively for at least 10 years (swimming and running) and I have been leading a health-conscious diet. I have a hereditary high-cholesterol condition, a type which appears in adulthood (so they say). Since 2004 my blood tests have showed roughly the following results: HDL 1.1, CHL 6.2, LDL 4.1, TRI 4.38 (mmol/L).
I have been taking Zocor 40mg for about less than a month and recently I have been experiencing cramps in my left lower arm, fatigue, itching (this morning for example I was woken by the cramp in my left arm, not nice). I have just read all your posts and have decided to abort my Zocor treatment at once. I have bought Q10 capsules and vitamins and started to drink 4 liters (herb tea) a day. I hope the pain will soon abate because now I have a totally dysfunctional left arm (I can't grasp because of the pain).

I am going to write in a week's time about the de-Zocoring of my body. In the meantime, I wish a speedy recovery to everyone.

Peter

Was on Vytorin for 2 years & experienced no noticeable side effects during that time. It lowered my cholesterol to 179. Had a hysterectomy (complete) in Dec., 2007. In May, 2008, I began a sudden on-set of severe numbness in both hands (especially when lying down)--classic carpal tunnel symptoms and intense pain in all joints. When I move from a sitting position to stand up, I can hardly do it. This is what I thought I would feel like at maybe 80 years old--not 46 yrs. I thought maybe it was because I'm not taking hormone replacements, but my doctor said it could be the Vytorin & he took me off of it. I've been off for 2 months, but the symptoms are not improving. The carpal tunnel seems to have lightened up a bit, but the joint pain (especially hips) has not gotten any better. I wonder if it ever will????? Also experience fatigue, foot pain, & weak fingers.

I went through a horrible withdrawal from ativan two and half years ago. It sent my CNS into overdrive. But I eventually got better. I have been extremely well and able to teach full time this past year. Then I got a very bad case of poison oak and was put on prednisone for 9 days, starting at 40mg. and then coming off at 10mg. I am so very sick again. It took me a year and half to recover from the benzos. How long does this horrible diarrhea, nauseousness, inner vibrating last???

Hello,
I have just found out about this and have been on cipro and levaquin and guess what. 2 weeks ago i was jumping in a pool and the tendon in my arch let loose. I went to the orthopedic doctor and he sent me for MRI then put me in a boot cast. It felt like i stood on a golf ball and it still hurts like hell. I have problems walking on it still. My doctor stated that i will most likely be flat foooted now in the foot that the tendon let loose. then i seen this on the news. Damn i have never had problems in my foot. He called planter facititus.

HI guys I was given pred at 60mg then over the next several weeks I tapered off. it is now about 3/4weeks since I took the last tablet. Whilst i was on them I developed quite bad hand tremors/shakes and since taper off to a low dose I have started with muscle twitches all over. Has anyone had experiences like these? And how long did they last?

I had a really bad case of strep throat because I thought it was a cold or flu and didn't go to the doctor for 12 days...but then I finally went because my throat hurt so bad and my glands were so swollen. I don't have insurance and maybe that's why the doctor gave me ten free samples of avelox right off the bat instead of just prescribing penicillin. I took the first dose and I would say my sore throat and swelling were 80% gone within the FIRST THIRTY MINUTES. So, definitely this is a very strong antibiotic compared to the Z-pak (zithromax) I've taken for bronchitis before. It's now day 4 and I have to say I am reluctant to take it for 10 days!! I haven't had any severe reactions, just bloating, diarrhea, dizziness, and some tiredness. And pretty strong nausea for the first hour, so I have been pushing the dose time from 9am to gradually later at night where I am not so sensitive. I am 33yrs old, healthy and eat well usually so I think my strong constitution has kept me from some of the more severe reactions I see above. HOWEVER, I do feel that it's a bit too strong! Surely there must be some way to lower the dosage of this antibiotic? I feel that it's worked well, but it just is too much like a SLEDGEHAMMER!