Sudden onset symptoms and conditions

I had a sudden onset of tinnitus in my left ear about 2 weeks after starting to take singulair nearly a year ago.. I had not made the connection until I read about ototoxic medications on Wikipedia. I will try stopping Singulair and see if my tinnitus improves. I'll report back.

Warning: I do not know if this is related at all (or if there is anyway to know for sure). I accidentally saw a connection looking up conspiracy theories, and I can't seem to find any "real" information about it at all.

My daughter at 14 years of age had this shot. She didn't feel good after, but I thought "normal" vaccination reaction and haven't thought about it since. Feeling a bit faint, a fever, and such.

However, last September (a few months later) she was diagnosed with autoimmune hemolytic anemia. It started with her heart racing, she looked pale (and sometimes even yellowish), tired all the time, her urine turned a dark color, and fainting. Not knowing anything about this I assumed that she was dehydrated, and had her drink lots of water. Until she started fainting, at which time I took her straight to our family doctor. (Another reason that I wasn't to worried is she actually had been to many doctors who didn't seem to think this was abnormal.)

She started on high doses of prednisone to keep her immune system depressed, and has now moved on to mercaptopurine (as the steroids made her suicidal.)

I plan on bringing this "possible" connection up to her hematologist and I will report back (she has an appointment on the 11th.). However, I think it is better to do a little scare here, and possibly help someone rather than take for granted that I am not sure... (So take this information with a grain of salt.)

Also note that this was sudden onset, they can find no cause, and we have no family history nor any of the other typical reasons (sometimes can be "medicine" induced.) 10 months later she is still testing positive on her combs test though.

Hi,

I'm fit, tough and extremely healthy. Tried Mirena. Ok for one year then within six months I experienced increasing upper abdominal pain and ultimately the sensation of something bursting central chest and the first of three Emergency Hospital admissions. Bloods clear. Xrays clear. ECG's clear. Endoscope clear (had experienced severe and sudden onset gastroenteritus/IBS acid reflux, extreme food intolerance.) Also had a large cyst needed draining (and multiple smaller) appeared in left breast. Lymph glands in neck up. High histamine, raised albumin, white blood cells relating to allergy/parasite. Allergic reaction/systemic rejection of coil?
No uterus pain at all.(Not had period for over a year)
So very ill after sixteen weeks being consistently told it wouldn't be the coil I took it out. Hard to describe but an extreme sense of relief, reduction in pain from entire GI tract swelling/sensitivity.
QUESTION.
One week on huge improvement but I still have continual upper body/chest pain (diaphragm?), and additional pain sharp pain through left ribs to shoulder blade, worse with sudden movement. Anyone had residual/slow to improve nerve damage? Need to be fit for my job.

Thank you for reading.

PS. Its not a 'coil'. Its a nasty sharp edged piece of plastic.

Took Limbrel in the morning. Developed the sudden onset of violent chills at night with fever, body aches and nausea. Symptoms subsided over the next 24 hours or so. Assumed it was a regular flu-like viral illness. Took Limbrel again after a few days and the same thing happened. I thought it might be the Limbrel and the other comments posted convince me it was.

Update: I took Levaquin 2 months ago, stopping after 7 daily doses of 500mg for an upper and lower RI. I did not have the extreme reaction to it that others here suffered. I had general fatigue, brain fog, loss of appetite, dizziness and tight joints. I had always exercised regularly prior to Levaquin. I also had a sudden onset of bloating and inability to digest food. Doc said Levaquin wouldn't cause those symptoms. It's hard to tell if it was the Levaquin, but...

Now 2 months after my last Levaquin dose, my joints seem OK, I can exercise, although I don't push it too hard since that can aggravate any joint damage done by L, the brain fog is better, and the digestion is still a problem sometimes.

Levaquin symptoms can appear months after the last dose, so I am being vigilant.

God bless everyone here who has had horrible experiences with Levaquin and I hope that your bodies will heal as the months go by. I will be posting updates in the future.

I've been taking levaquin for a sinus infection and had a sudden onset of joint pain - especially in my hands and hips. Also had bad upper back pain. And I never had any of these problems, except mild arthritis in my hands that only hurts once every couple of month. It's horrible - feel like I'm 100 years old - and I'm 54 and very active. So glad I found this web site to see that the medicine may be the cause of my problem -hadn't considered that until I read your comments here.

I am a 52 year young female with sudden onset of high blood pressure. Was seen by a Cardiologist and given the usual tests such as EKG, treadmill, and so on. My tests were fine and he put me on Lisinopril HCTZ 20-25mg. After taking this medication for one week my blood pressure was within normal limits however my pulse races at times and I must sit down until it passes. I have been experiencing pain in upper back when taking a deep breath and mild chest discomfort. Further tests are underway to determine if I am having lung problems such as pulmonary hypertension. Has anyone had similar symptoms? Thank you

I have been on nuvaring for about 14 days and have been spotting ever since my period ended. Today at work I got a sudden onset of really debilitating lower back pain and cant figure out what could have happened to cause it. My only relief comes from lying down or sitting. When I came home i started researching side effects for the ring and lower back pain didn't come up. However this site did and has helped me shed light on what i think is the problem. I'm left to wonder if this pain will subside after a complete 3 month cycle of taking it? Part of me just wants to take the darn thing out to prove the hypothesis correct. But I really have a hard time taking the pill. Very thankful that I found this site because it will probably save me time and money of going to the doctors and trying to figure out what the hecks wrong.

Hi everyone, I just came upon all this yesterday and can't believe it! I have been thinking I am going crazy and have been going down a shame spiral! I have had the Mirena for about a year after the birth of my twins. When I first got the Mirena I really didn't seem to like it...I had weird bleeding, cramping, headaches but my doctor told me there were really no side effects except for the on and off again bleeding so I didn't think much of it. Soon, I started having heart palpitations and weird panicky feelings when I would be out places which I have never had before. I wrote it all off due to the rough twin pregnancy and moved on. Soon, I really started worrying something was wrong with me because of all these weird things, the headaches and heart palpitations and panicky feelings, also I started feeling foggy like I was walking around feeling out of it and sometimes a little dizzy or something just having weird head feelings. We always had in the back of our minds that it could be the Mirena but never really took action. Just for the past couple of months things have gotten much worse. Those panicky feelings really got worse and combined with anxiety and sad and crazy depression thoughts and feelings. I also have been feeling this weird nervousness.....even in my quietest moments of my day. This is so out of my normal character and I feel like I can't even remember what I used to feel like. I have been to my PCP who gave me medication for anxiety and have had a hard time adjusting because I just can't believe all of this craziness and I just keep thinking is the problem really my IUD? Then my mom came upon this because she just felt that me feeling this way is just to weird and I feel like I relate to all of your stories! I have truly been feeling like I am going crazy...and I have never felt this way before...ever. I called my doctor yesterday to talk with her and I am going to have this removed...although I am a little nervous about the after effects. I just keep thinking a year ago I was fine.. and now look at me...I am on anti-depressants...how did this happen?? I know that I have stress but there is no reason for me to be feeling this way. I would love to hear about anyone else who felt this way and got the IUD removed and how that went. I know that I probably won't feel better right away...but I am hoping with time I can forget all of this and move on.

See my earlier post (from concerned mother on 8/5/08 at 8:29pm) regarding my daughter's severe reaction to the Gardasil vaccine during October - December 2007. As stated, she continues to experience menstrual problems (nausea, vomiting, diarrhea, severe cramping) which incapacitate her. In October 2008, her annual pap test showed precancerous cells. She is going for a re-check in February (I will post the outcome once it's known). The doctor wanted to wait 6 months for re-check but we are not comfortable with that. Just wanted to remind everyone to get their annual pap exams!!!

I was diagnosed with asthma as a child. In late teens it seemed to not be problem, however after 50, I started developing symptoms of asthma again as evidenced from COPD tests. I am currently using Advair 250/50 since 55 yo.

One symptom, that I have not seen addressed here is that of "slow healing" after injuries. I injured my back awhile ago, and it seemed like 2 years before most of my symptoms were gone. To this day I still feel lingering effects. Then I scraped my shinbone. It seemed like it took forever to heal, and now there is an ugly red/purple scar where the minor scrape was.

I had never taken so long to heal before, and read that this was a problem with taking Advair. I never figured my asthma was that serious in the first place, so I simply cut back on the Advair to once/day or less as it seems still to keep my breathing OK. Sometimes, after a few days of not taking Advair, I feel some minor difficulty with breathing.

Now that I am 63, and so concerned about "slow healing", which I attribute to Advair, I have asked my Dr. to perhaps take me off Advair and simply take Albuterol when needed. Then I read that Asthma patients should only use Albuterol if that is sufficient to control symptoms and to advance to Advair to control more severe symptoms. Another article says that Albuterol does not heal Asthma, only assists with sudden onset of breathing difficulties and that I may still damage my lungs if I do not take Advair.

I remain at a loss as to what is best: Taking Albuterol when needed (perhaps a few to several times/week) or as I was doing before, contrary to recommended dosage, of 1-2 times/day. Fortunately my Dr. goes along with my changes, but tells me if symptoms get worse, she will put me on Advair 2X's/Day (which I probably will ignore dosage because of healing side effects, and use once/day or less).

I will report back later after trying Albuterol for time without the use of Advair at all.

I have had numerous side effects with tramadol (nausea, heart skipping beats, restless legs at night) but I was too desperate and needed something so I just started taking 2 half pills a day (total of 50 mg). Well, now I've quit after about 2 years because I have sudden onset swelling and tendinitis in both of my achilles tendons. There was absolutely no trauma involved and tramadol was my only medication. After doing research online, I found that this is a rare side effect to some other medications but it hasn't been mentioned for tramadol. I truly believe this is a side effect that just hasn't been reported yet. Also, it can lead to both tendons rupturing. I just hope I stopped the medication in time so that it doesn't lead to that. It's only been a few days and I have a lot of pain and difficulty with stairs. I think this will take a while to get over -- like all orthopedic related problems.

I have been diagnosed with a pericardial cyst and thought that the problems I have been having were related to this.....until I found this site! I have been taking omerprazole for over a year now and have had several disturbing symptoms. Heart palputations, racing heart, night sweats and hot flashes, sudden onset of nausea that lasts for about 5 to 10 minutes then goes away and horrible chest, back and rib cramping, which is the same feeling as having a severe gall bladder attack. Recently the worst has happened. In the past I have had the sweats thinking it was only menopause and chest pain thinking it was the acid refllux. We shall see....as of today I am stopping the drug to see what happens. In the past week the most severe problems have occured. I started with bronchitis and the antibiotics and prednisone the doctor put me on seemed to be having side effects which I have never had before with them. The only other medication...omerprazole. (haven't had bronchitis since BEFORE I started taking the omerprazole) After the first day I began having severe chest, back and rib cramping which seemed to worsen by the day, more so that ever before. Then came the swelling in the hands and feet until they looked like I had elephantitis. There is aching somewhat in my arms with a strange weakness. And...the heartburn became so bad that I feel like it's coming out of my mouth. So..the doctor increased the omerprazole to 40mg or up to 80mg if needed. I have been taking 40mg and it didn't seem to really cure the reflux! So I was going to increase it. Not now! I believe after reading all the posted side effects everyone has been having, most of my problems are being caused by one thing....omerprazole! I was truely believing I was having a heart attack, but since I just had ALL the tests done and was given a clean bill of health and better with the exception of the pericardial cyst, I couldn't believe this to be the problem, so back to the doctor I went. She has put me on motrin for the pain and skelaxin for the cramping which seems to be helping. But, and this is the big but, I am going to come off the omerprazole and see if this will begin to eleviate the symptoms completely. Will update this in a couple of weeks when the drug is totally out of my system. Thank-you for this site and keep posting.

I was “poisoned” by Levaquin -- resulting in acute tendinitis in both Achilles tendons.

Background:
I am a healthy, athletic male in his mid-50s who has never had an Achilles tendon problem. In early July 2008, my doctor (general practitioner) prescribed Levaquin for an infection. I took the medication for 14 days, as prescribed.
Sudden onset of acute tendinitis in my Achilles tendons occurred near the end of the medication period. The tendinitis occurred in both Achilles tendons simultaneously. Nothing related to my lifestyle would have caused the tendinitis.

Symptoms:
Symptoms included the following at one time or another:
1. aching
2. sharp pain
3. feeling of heat/burning
4. tightness
5. pins and needles in small areas (micro tears?)
6. weakness at rear/base of each heal.
7. When I woke-up each morning my tendons and the back of my heal pads felt sore, weak and tight.
At the height of the problems, I had extreme difficultly walking and negotiating stairs, and I thought there was a risk that my tendons would detach from my heal bone.

Doctors’ Advice:

My general practitioner’s and my podiatrist’s advice was to: (a) not run, cycle, hike or otherwise exercise my legs in any manner other than easy walking and swimming, (b) gently stretch, (c) take ibuprofen, (d) ice regularly, and (e) use heal lift shoe inserts made by my podiatrist. Their advice was based on the view that the damage that was done is more like damage cause by an injury than damage caused by an insidious drug. My readings on the subject indicate that little is known about the mechanisms behind this fluoroquinolone-specific toxicity. It is believed that the tendon’s collagen fibers become disorganized and infiltrated with small blood vessels -- resulting in weakness. And there are no specific treatment plans for this problem.

After 2 months of living with these symptoms, I decided to change course.

My Approach to Healing:

Because I never believed my pain was the result of inflammation, I stopped icing and taking ibuprofen. Because stretching seemed to further weaken the tendon and set me back, I stopped stretching. Because I believe that the body heals itself best when used, I started cycling at an easy pace. I then worked-my-way-up to cycling more aggressively, and to walking in the neighborhood. That’s where I am today. Two days ago I had my first day without discomfort in 3 months. Yet, I have a long way to go. I am not yet hiking or running. It’s a slow healing process with occasional setbacks when I push my tendons a bit harder than I should, Given the progress I have made, I am hopeful for a full or nearly-full recovery in another few months.

Other things I have done in the past month:

1. Taken L-Lysine (1000mg daily), which is believed to aid collagen formation.

2. Taken Magnesium (250mg daily), which some believe may help leech the fluoroquinolone molecules from the tissues because of the affinity of these antibiotics for minerals.

3. Taken Fish oil pills (3000mg daily), which improves circulation

4. Used a heating pad, which improves circulation

5. Started regular Acupuncture (first time for me), which improves circulation

What you can do:

1, Be easy on your tendons until you get a handle on the problem. Don’t over-use tendons when they are in a weakened state.

2. “Listen” to your body and take steps you think best to help the healing process.

3. Tell your friends to beware of potential side effects from fluoroquinolones.

4. File a MedWatch report with the FDA at fda.gov.

5. Share your findings/advice on this forum.

Good Luck

THIS IS A HORRIBLE DANGEROUS DRUG!!!!!
Doctors prescribed this to my mother for 5 years!!!! Because of it's devastating side effects it is FDA approved for short term 4-12 weeks and only as a last resort. And NEVER for Parkinson's patients. It is unclear if Reglan caused the Parkinson's like symptoms or if she had it prior. Either way the doctor was so wrong to prescribe this medication to her. She is completely disabled can't walk or even get out of a chair had a auto accident and falls one time a metal frame fell on her head causing a hospital visit another time she fell into cactus! I was horrified to learn that no one caught this error. Not one doctor or the drug store told my parents REGLAN could cause her to end up using a walker and unable to function even the simplest daily tasks and that these symptoms could be permanent.

I don't know if it was the two kenalog injections but I began to menstruate-three years post-menopause. I immediately was seen by my endocrinologist, trans-vaginal sonogram and endometrial biopsy done. i just received a call tonight informing me that a polyp was found and I will need to have a D & C. It sounds like endometrial hyperplasia and this is a very sudden onset - I had the same sonogram in February and all was fine.
I have now found out that steroids can "wreak havoc" with our hormones. I was schedule to have epidural injections of steroids for back and neck injuries. I will not have them now or ever- they are not as benign and helpful as many doctors would have you believe.

Have been taking Januvia since March, developed ankle pain and swelling, diagnosed with Achilles tendon rupture and tendinitis needing surgical repair. Now with severe sudden onset of left shoulder pain without any precipitating event, unable to elevate left arm secondary to pain.

Have been taking Januvia since March, developed ankle pain and swelling, diagnosed with Achilles tendon rupture and tendinitis needing surgical repair. Now with severe sudden onset of left shoulder pain without any precipitating event, unable to elevate left arm secondary to pain.

I think Fosamax KILLED MY MOTHER. My mon was previously healthy with no known medical problems. No hypertension, no high cholesterol, no diabetes...nothing. She was taking Fosamax for osteoporosis prevention. She developed an acute liver failure. There was no viral, bacterial, or cancer linked to this sudden onset of liver failure. She received a liver biopsy and within one week was dead from bleeding from the biopsy site. I have recently found some journal articles linking Fosamax to acute liver failure. MY HEART IS BROKEN. Do not take this drug without doing in depth research on its side effects and discontinue it immediately if any side effects occur. God Bless.

I have been on Paxil off and on now for about 5 years.... the current length of treatment for the past 1 1/2 years. I need to be on it ( or something for that matter ) for my panic disorder. I am a 36 year old nurse/ manager and some days was almost debilitated by panic attacks. Depression was part of it, but not nearly as much as panic. I must say, that I have been experiencing memory loss now for about a year.... I thought maybe it was due to overwork/ stress...which I do understand it COULD be. However, I find it interesting that I am seeing so many more people with memory loss than I imagined. Is it due to stress in this type of people's lives, or is it in fact, the drug Paxil?
Keep in mind this is an SSRI ( Serotonin Reuptake Inhibitor ) ~~ even though there is no solid evidence (YET!) this is a side effect of the drug, I would bet my license on the fact that that it is!
I have tried time and time again to wean myself off of Paxil.. ( with and without my Dr's advice )--- I did succeed for a few years to be without the medicine, however being on a slew of other meds in the interim did not help as much for the panic as does the Paxil. Paxil, honestly, scares the hell out of me!
Besides the "numb emotions", memory loss, sexual appetite decrease, yawning, lack of sleep, etc... the side effects of coming off of it are worse! As I read earlier, it IS addictive, indeed! The brain gets used to the drug being there ( as with any addiction ), and the "surges" of dizziness, sweats, and out-of-body-like experiences I experience coming off of the drug are excruciatingly harder to bare than the depression itself. Those above symptoms of withdrawal are just that....withdrawal!
Once your body is "allowed" to reuptake serotonin (as it is supposed to), this is when those symptoms raise their head...sometimes for weeks or months until they subside.
I would welcome anyone with help on this matter---is there another Drug out there that can help with anxiety/depression symptoms, and not cause the plethora of side effects we have all discussed here?
Diane

Started on Metoprolol about two months ago for a sudden onset of heart irregularity, mostly skipped beats. I'm already experiencing some of same problems described on this site. Because of that, I was looking for information and ended up on this site. My symptoms include daily headaches, inertia and lack of motivation, feel like sleeping all day long, wt gain, foggy headed, bloating and stomach discomfort. These symptoms have either started or intensified since I started on this medication. I plan to wean off this as soon as possible, with or without the doctor's cooperation. I've had a cardiac workup since I started the medication and no problems were detected.

Have been on Januvia for 3 weeks, Very bad left shoulder started about one week into treatment. I initially thought that I had slept on my shoulder "wrong". Left leg pain started last week. Lower leg feels tolerable sitting however when I stand & walk, get shin splint type pains. Shoulder is improving & leg pain intensifying. I called doctor's office this morning and relayed symptoms to the nurse. I told him that I was discontinuing Januvia until I heard otherwise. He took my number but physician did not return call today. I find it odd that there is no mention of this type complication in the patient information handouts. I have taken Motrin, Aleve & Extra Strength Tylenol without relief.

I had bacterial pneumonia a few weeks ago they gave me Levaquin as well, After the hospital I notice some pain in my left arm. A week later I was unable to straighten my arm now the pain has moved up to my neck and back and is slowly reaching my right shoulder. It seems that though you ask doctors question you never get answers and yes its true about this pain I have been in agony for almost a month now and can not find any type of relief. I was treated with a 7 day regimen of medication and I don't know what is worst the pneumonia or the pain. If there is any where to find relief as a natural source please post it

Thank you

Hey all. I suspect many of you would agree that one of the most infuriating aspects of this antibiotic nightmare is that seemingly, there aren't many {none that I've dealt with} doctors/nurses or pharmacists that will even acknowledge the potential {and VERY REAL} side effects of these drugs.

On 01/10/08 I was put on Cipro 500mg twice daily, two week supply, for epididymitis, which likely stemmed from a bacterial infection/urinary infection back in late Oct of 07. It's an infection that can require a lengthy dosage due to eliminate bacteria growth. I was also prescribed a painkiller along with it.

That night after dosing had horrible nausea/vomiting, and chalked it up to the painkiller ... which at that point it likely was. Within a few days the groin pain from the infection had subsided a great deal, and although felt a little 'odd' from the Cipro, nothing too noteworthy. At eight days into treatment, became nauseous around the clock with bizarre flu like symptoms. I called the doctor at the ER who had diagnosed me, and she switched me to Doxycilline {sp?}, which isn't a quinolone. After stopping the Cipro, nausea disappeared. However, within a week the pain of the infection returned, apparently due to the weaker antibiotic.

So I was re-checked on 01/24/08 and put on Levaquin, 250gm once daily. Within a day or so the pain subsided once again, but on the third day developed horrible diarrhea and pain in my left knee/leg. Stopped taking it immediately, and decided to research my dilemma online, where to my horror I've discovered all sorts of people from all walks of life experiencing debilitating side effects from this grouping of fluoroquinolone/quinolones antibiotics.

I'm now on Cephalexin, and the pharmacist I spoke with today assured me that it's not part of the quinolone grouping. He also suggested that I must be part of that small pool of the populace that has trouble with quinolone antibiotics ... one begins to wonder just how "small" this pool is given how the average person isn't likely to associate muscle/joint pain with the antibiotic they're ingesting.

How this POISON has lasted so long on the market without more exposure/media coverage speaks volumes about the state of corporate America, with nearly every social system compromised {usually at the expense of the corporation's victims} , with little or no help from the corporate owned mainline media, which serves as nothing but a megaphone platform for vested intertests to transmit "official" opinion to the unwary. So here I be with very painful knee, which I should add is already compromised due to a major tibial plateau fracture in 2001.

I'd love to know whose palms are being greased to keep this rat poison available ... hell, I even had to pay over our insurance co-pay fore the Levaquin, as it's apparently a "top shelf" drug.

Good luck everyone ... and it probably doesn't need to be said, but man, I know after this I will check and double check any and every antibiotic that may be perscribed to our daughter in the future!

I am going on day 4 of stopping my Effexor cold turkey. I was on 300 mg and taking 20 mg of Pexeva. I am stopping cold turkey after being on this medication for three years. The withdrawals are terrible, I don't know why any doctor in their right mind would ever prescribe this medication for anyone. I have those wonderful brain zaps every ten seconds, the only thing that momentarily makes me sane is food, as if the 30 pounds this medication has gained me aren't enough, stopping it is going to pack on another 30. I am a bundle of anger and rage directed at anyone within distance. I am at the toilet every night waiting and praying that I can just throw up. When I finally can fall asleep I am jolted awake in a puddle of sweat having just had yet another nightmare. And when I say nightmare, I mean the kind that have me screaming out loud in terror waking my husband. Minor daily tasks are ignored due to the fact that putting one foot in front of the other is too much to handle. I can't stand this feeling and only pray for the day that it will stop.