Antibiotic symptoms and conditions

I was prescribed Cipro for 2 surgeries I had last week. When I picked it up from the pharmacy, the pharmacist told me to drink a lot of water as much as possible because it has a dehydrating effect and he told me it makes you more sensitive to the sun so if I have to be outdoors, to limit my time and apply sunscreen with a high spf as often as possible. I didn't go outdoors because of that, but Cipro made me very thirsty, but I expected it and drank plenty of fluids. Other than than, I did not have any problems. I never got constipated, it didn't bother my stomach but I always eat something when taking medications because I can't take them on an empty stomach. I didn't have any allergy problems, diarrhea, breathing problems or anything else. In fact, I liked this antibiotic much better than any other one I've ever been on.

I had 2 surgeries at once last week and was prescribed Meprozine 1-2 capsules every 4-6 hours. The first 4 days I took 2 at a time and within 20 minutes my pain was gone, I felt relaxed and a little drowsy and was able to nap, which I needed for at least the first two days after my surgery. Twice in 4 days, one of my legs twitched and once my arm twitched. After the first 4 days, I would take only 1 as needed, usually in the evening after I has been up all day and was in a little pain. I had slight dizziness when I first stood up the first day only when I would get up to go to the bathroom. Other than that, I had no nausea, and I have to eat something before I take any medication, no stomach pains, no allergic reactions (I am allergic to medications with codeine in it), no depression, no emotional swings (in fact, if I wasn't sleeping, I was so relaxed that I was able communicate normally, laugh, make my normal jokes, etc.), I did not hallucinate or see things. I was also on an antibiotic, which my pharmacist said would make me very thirsty so I attributed my dry mouth to that. Last year, I was prescribed several different strong pain medications for severe chronic headaches and they did nothing. I would recommend Meprozine for short term relief for pain management. I do know someone who got addicted to Meprozine after taking it everyday for several months because a doctor kept prescribing it to her, so it is definitely only to be used for short term use. If I ever have to have surgery again, dental work, or need something for pain management, I will be asking my doctor for a one time prescription for Meprozine.

To the best of my knowledge I never had any of the 'immediate' symptoms.
My problems are probably due to the fact that I was prescribed Cipro 3 possibly 4 times from Aug 06 - Dec 07 and then finished up Dec 07 with a round of Levaquin. My father is over 60 and was recently given Levaquin and had immediate and serious problems. He is seeing a doctor recommended by the CDC today. Yes, he is even working with the CDC on
this one. Due to all he is being told he is convinced that the medication is behind my medical decline as well. Since taking these medications (symptoms started slowly in 07), but after taking the Levaquin at Christmas time I never got up from the couch. My thyroid gland has quit working, my adrenals are shot, I have been diagnosed with fibromyalgia, chronic fatigue, blew out 3 disks in my back, vision is deteriorating rapidly, and really so many things I can't list them all. I had a complete physical
in Oct 05 and was given a perfect bill of health. Through Aug 06 I was riding my bicycle 33 miles per week. I'm still trying to figure out what hit me??
What my father has been told is that in some individuals Levaquin will attack the glands (like the thyroid) and will compromise the immune system. This damage appears to be permanent. All I know is that I went from being extremely healthy to terribly sick. If in a day's time I have enough energy to load and unload the dishwasher it is a banner day. I can
not work and seem to get worse instead of better as each day passes.

My husband also had pneumonia at Christmas and took Levaquin but does not seem to have had an problems. I suspect it was possibly the cumulative effect of having basically 4-5 rounds of the antibiotic in a years time. According to the people at the CDC that have spoken to my father the symptoms that I have can all be traced back to the medication. One never knows what effect a medication will have. Just please be careful when taking this medication, and limit how many times you take it.

I have been prescribed Levaquin multiple times for bronchial infections. The most recent being approx. a month ago. I have NEVER suffered a side effect from this medication. The types of side effects everyone is reporting here sound very bizarre. I know a number of people including my husband, friends, grown children, etc that have taken this medication multiple times as I personally have with no side effects whatsoever.

I knew it had to be that antibiotic!! My family doctor put me on Levaquin for a urinary tract infection a few days ago and the night before last I woke up in the early a.m. shaking all over and hurting in every joint in my body, and I have a foggy memory of it all too. It was very bad. I could not stand up without holding on to the wall because I was to weak and my legs felt like aching jello. I could barely move my neck and I thought I had meningitis it was that bad. I called 911 and the ambulance came for me. The doctor at the ER took blood work which was all normal and he told me I had a panic attack!, neck pain, and fatigue...I couldn't believe he told me I had a panic attack...I was asleep for goodness sakes. I have been hurting so bad that I was thinking I had something really serious. I hurt all over so bad that I can't even express it. I am so glad that all of you posted these side effects or I would not have known what was causing my problems. I will NEVER take that stupid drug EVER again and I hope they take it off the market. I hope someone will do something about this drug before it hurts more people like it has hurt all of us...I pray that you all will heal from the problems this medication has caused you.

I had bronchitis (being an asthma sufferer, during a bad cold this is expected). I went to my doctor, who handed me 5 days worth od samples of Avelox (400mg). Approximately 1 hour after my first dose I started shaking, feeling dizzy and nervous, had an upset stomach and abdominal pain and was itching on my knees, wrists, ankles, legs, elbows, arms and neck. I called my doctor who told me it was a mild side effect and to continue taking it. So, I did. Considering that I had been out of work with bronchitis and lacked the time to start a new antibiotic, I decided to listen to my doctor. The side effects intensified. I have now been off of Avelox (which I will NEVER take again) for 4 days and I am still not side effect free. They have definitely lessened, but not completely gone away.

This is a HORRIBLE antibiotic. I implore all who read this...do not take Avelox. Get amoxicillin, Ceclor,, Erythromycin... anything else will do just as good a job without side effects.

Hi All,

In addition to what I wrote earlier if you do have a history of hypokalemia (low K+ or potassium) that is very serious for that electrolyte controls cardiac and renal function. However, it is quite simple while you are on this antibiotic to increase K+ rich foods such as bananas, baked potato, OJ, whole milk, avocado (which has more K+ than 5 bananas) and do so judiciously during your therapy for infection.

It is also significant to alert anyone that infection (bacterial) causes some fairly significant physiologic issues from fever, to myalgia, vomiting and loss of fluids, and organ impairment. This antibiotic like Ciprofloxacin has a huge ability to permeate bone infection and non circulatory areas that most antibiotics never reach. It is important to understand that if you are feeling that ill to require that antibiotic you may not be getting around to feeling "normal" until you are past taking the medication, follow up with your provider and rid yourself of the infection.

When you end an antibiotic early or play games with such a drug you can rebound to a super infection that is not treatable by the same antibiotic or even anything more powerful and after this drug you are talking IV antibiotics in a hospital setting.

I would strongly suggest if you are handling secondary side effects then continue onward for the result of an infection out of control is anything but desirable.

I do run low on K+ either and find that Cipro is more K+ wasting then Levaquin. I also am on the smallest dosage (250 mg. QD) and having a positive result but yes, the lovely side effects. In another few days though when done those will be gone and I might feel 100% human again.

K. BS,RN,UM,QC,DON

I am a professional nurse with extreme allergies; however, please for you own benefit consult your physician but do not stop taking it unless he or she states adverse or of course, you have some reaction requiring emergency medical assistance (911).

Yes I am dizzy, weak, very nauseated (and with my emaciated body frame due to other health issues cannot afford to not eat), and the first 2 days of therapy got a whopper headache. However, I had a UTI that likely moved into the kidneys and also look to have stones and after 8 days am passing urine properly and not up every hour not passing urine; hence it is killing an infection that might kill me.

Early on with this drug we did prescribe higher dosages then perhaps necessary they have now cut back quantity and instead of doing BID dosing do QD dosing. You might require a lower dosage at my body weight they prescribed only 250 mg. a day and this has given me some side effects but is treating an infection that could be fatal...

K. BS,RN,UM,QC,DON

I used the NUVARING for about a year before I noticed excessive discharge. After performing a pelvic exam, my doctor said that I had vaginitis and prescribed an antibiotic. When I asked her if the Nuvaring could be causing the symptoms, she told me that it wasn't the cause. The following 5 months, I did not have a period at all and started having pelvic pain. I decided to quit using the Nuvaring to see if that would make a difference, despite repeatedly being told by my physician that it was not the cause. After I stopped, my period returned to normal and the pain subsided. I have always hated taking the pill but my health is way more important than convenience.

I am a healthy female with little to no history of adverse reactions to medications. I was prescribed a 10 day dose of Levequin (500 mg) for a minor but stubborn skin abscess. After the third day, I woke up with significant joint soreness in my fingers. Progressively the soreness spread daily to my wrists, elbows, ankles, knees, hips, etc. I did not suspect the antibiotic at first, but I know my body, and I know something was WRONG.
After my 8th dose I decided to look online...it is at least good to know that what I'm experiencing is definitely from Levequin. Thank you all for sharing your stories.

I especially found MERCEDESLANE posting on April 15th interesting. I guess this person works in the health care system. Considering this uncompassionate individual, who apparently wants everythone to know he has a Mercedes, can't spell (whine), and does not have basic grammar skills. Wow...my faith in the our health care system is stronger than ever. But what do I know, I'm just an "IDIOT" with shingles that needs to have a couple of glasses of whine while I pop my remaining Levequin.

i had the iud since sept 2006 and had it removed last week. i had felt it the entire time ive had it. id go thru hell with cramping and no bleeding. my weight would fluctuate from 135 to 150 in a matter of days, i haven't been able to get back down to my pregnancy weight of 117. i was so depressed that i tried to commit suicide. id cramp and bleed after sex, during i could feel it sometimes my husband could too. i had migraines that would last for days multiple times a week. my eyelashes, brows and hair has thinned out a lot. my skin is horrid with acne that would last for months with the same break out. i was bloated all the time. i was super moody, didn't have patients for anything or anyone. i am usually a pretty layed back person on mirena i was completely opposite, im surprised my husband hung in there! i was constantly constipated, frequent urges to pee, didn't want to out outside. when i was having it removed, my doctor couldn't find the strings, luckily she found them. my experience with mirena was horrible. i don't recommend it to anyone. after it was removed my stomach felt so much better. wasn't constipated, didn't feel a hard uterus, the pain that would shoot down to my feet stopped. my doctor did tell me i might have a mini period, which i am now. but im telling you i feel a lot better now that it is out of my body. if you knew me while i was using the IUD, you would think i am a different person now. i wish i had never gotten it in the first place...

I took tetracycline for 10 days (it had been prescribed for 30 days for emergency oral surgery...I had cracked a molar and it had to be extracted)

On the tenth day I was ready to die from the progressive side effects that were completetly intolerable.....I thought I was going to die and the fear was so unreal that I thought I was possessed by the devil or some evil force that was going to kill me and my family....it was horrific!!

Taking an anti-anxiety med Ativan helped but I also made the decision to stop taking the anti-biotic tetracycline...within 24 hours I felt fine....the racing thoughts, the heat, the chest pains and blinding fear were suddenly gone....I know now that this drug is not good for me and have asked the doctor for another antibiotic.....

If anyone experiences these symptoms stop taking this drug immediately....I took it for ten days and I wished I would have stopped sooner....

I especially don't recommend Tetracyline or any of its similarly-based antibiotics for anyone who suffers from depression or anxiety....

I hope my experience can help others understand the adverse side effects of this drug.

I have been taking doxycycline hyclate for acne for the past three weeks and find that I am now urinating a lot especially after intake of liquids and it seems as if I empty the same amount that I consume.This is really very annoying and inconvenient.

I started this antibiotic because of symptoms my ER physician thought paralleled those of lyme disease... At first I had mild to severe nausea... which was assisted with the intake of a meal or snack. Those symptoms I could deal with... that and a wonderful yeast infection that occurred around the fifth day. The side affects that became unruly, were those of confusion, panic, paranoia (I became extremely jealous/thought my partner wanted to leave me/ and felt un-trusting of just about anyone near - people mocking me, wanting to avoid me, unloved me), and had random bouts of crying - which affected my libido tremendously.... one moment I was in the mood.. the next I wanted to be held in a fetal position and cry. I finished the 14 day regiment about three days ago, however I still have some side effects remaining... I still have panicky thoughts.. almost flash backs of past anxieties... as though I am relieving them again... and paranoia... that people are talking about me, or scheming. I can understand these behaviors if they were pertinently normal.. and a justified part of my general existence... however, I am generally a stable, upbeat and cheerful individual with normal reactions to stress... being that the only time I act reasonably irrational is around my period, where I feel fat and uncomfortable. The panic and rage I felt on this medication was coupled with insane thoughts and neurosis.

I do not recommend this to sensitive individuals.... or any one who is prone to medication side effects.... truly an awful experience... glad there is a support group. Still waiting to return back to normal.

My 12 year old son has been on 60 mg of Prednisone for two weeks now. His side effects have not been bad at all up to this point. He's gained about 6 pounds. His brain is unusually active right after taking the drug, and this effects lasts a few hours. He's always been a wildly creative kid but prednisone seems to intensify is creativity and the productivity of his brain. He has Tourette Syndrome and his tics waned overnight after beginning the meds so that is a big bonus if prednisone is responsible for that. He has always been an insomniac since he was a baby but prednisone makes him sleepy, so sleepy he takes naps during the day and goes to bed early, sleeping soundly all night, so soundly he had an accident and wet his bed last night. His head sweats when he sleeps. He has infrequent periods of mild irritability. His appetite has increased but not unnaturally so. Seems like he finally has a sustained healthy appetite. He goes to 45 mg for two weeks tomorrow so I'm interested to see what new side effects this brings on. No stomach problems despite taking this along with very high doses of antibiotic. Maybe the prevacid he takes with Lactobacillus is helping with that and the fact that he takes his meds with small meals or lots of fluid.

I was prescribed LEVAQUIN 500mg/day for 30 days. In that duration this is the list of side effects: diarrhea, sleep disorders, insomnia or excessive, and I mean excessive fatique, washing the dishes made me want to nap. heart racing, trouble breathing, tingling sensation either on my left or right side of my body, headaches. I actually finished the script, and now I have a yet undiagnosed skin condition which looks similar to MRSA, but the culture came back negative. The skin sores are very painful, so my doctor put me on DOXYCYCLINE 400mg/day for 2 mos, it didnt help the skin condition and only worsened the effects of LEVAQUIN, now my doctor has me on BACTRIM, because he is convinced it is MRSA. I am also suffering from severe depression, i never contemplate suicide, yet i would drift in and out of daydreams of wanting to quit, dizziness, when I was on LEVAQUIN my equilibrium was completely off. This skin condition is very painful, and I am on my 3rd antibiotic since June. I think I need help too!

I took Doxy for about 2 weeks as a remedy for a bump on my eyelid. This first exposure to Doxy seemed only to cause a little skin sensitivity and burning in my fingers, no big deal.

When my eye problem didn't go away, my eye doctor prescribed Doxy for a second time a month later. This time my side effects were much different. Within a couple hours of taking my first pill I felt a bit off, I felt anxious and unsettled. I Continued on the medication for a total of five days. During this time my side effects progressively worsened. The first few days I had very abstract thoughts, and began feeling strangely claustrophobic. By day three I was beginning to feel paranoid and fearful over just simple everyday things. Day five is when it all hit the fan. I started having difficulty breathing and feeling extreme tightness in my chest. My feelings of claustrophobia had also worsened to the point where I began having panic attacks, like I was trapped inside my own body. It was at this point I made a desperate attempt to search the internet for a possible cause, in hopes it might be the Doxy medication I was on. I was somewhat relieved to find this website and read that others had similar symptoms, maybe I wasn't losing my mind. I immediately quit taking the medication, but unfortunately the symptoms didn't go away for several more days. That night I was unable to sleep, I had mild nausea, and would wake up in the middle of the night in a panic and would shake uncontrollably. Lovely huh. It gets worse. I began to feel extreme fear and paranoia like I was going to die, or lose my kids and family. I began to feel if this didn't go away, I would not be able to go on. Thank God it did, and by day eight the extreme thoughts began to subside. I continued to have the breathing difficulty and mild depression for several days after, but the worst was over. Within a month I was back to normal.

I write this as a warning to those who are taking this med and feel anything close to this... stop taking it! I am a healthy, normal, 40 year old male, that has no history of mental issues, other than a "blue" day from time to time, and within six days I was entertaining thoughts of suicide. The psychological side effects of this drug NEED to be addressed. This is very serious stuff!!!!!!! Though it may be a small percentage of people that are susceptible, for those who are, it is a deep dark hole.

Add me to the list. The funny thing is, I've taken Levaquin 4 or 5 times in the past without noticing any problems, but last week I was put on Biaxin for a sinus infection and had a terrible time with it, so the Dr. changed me to Levaquin, and now after 3 days I'm back in the same boat...heart racing, unable to sleep, elevated blood pressure, nauseous. It feels like my heart is on fire! I'm stopping this one today (only had 2 left.) This is awful, I know I was very sick and had to have some antibiotic, but after these two experiences I think I'd stick with the sinus infection!

I am 23 years old. I was prescribed Levaquin 750mg for a uti. I took my first pill at 3:00pm yesterday. That night, I wasn't able to sleep. I layed in bed, so tired, just wanting to fall asleep but couldn't. Then the cold sweats and trouble breathing started. By 2:00 a.m. I was having what I can only describe as a panic attack. It's 1:00pm the next day, and i've never felt this bad. THIS MEDICINE IS NOT GOOD.

I am currently taking levaquin for a sinus and double inner ear infection, i have also taken this antibiotic before,i am 35 years old. I think this drug works wonderfully and tell the doctor this drug works the best for me.i have noticed a harder time falling asleep if i take it too late in the evening and some mild stomach cramping if i do not eat at least 2 hours prior to taking it.i also take it with a full glass of water.some of the side affects listed in this blog that people are describing are normal if you read your insert that comes with the medication.And if you follow the directions and eat and drink with a full glass of water the side effects are not as severe.Unless you are allergic to the drug,i do not find it bothersome knowing i will not be taking it forever and it is just temporary that i will be having a hard time falling asleep.i do eventually fall asleep.My suggestion while taking this medication if you are in reasonably good health,is to read the directions about eating and drinking plenty of water and don't panic,that just makes things worse.

I was given Biaxin for a sinus infection that never cleared up. So the doctor gave me Bactrim. I took one before I went to bed. I woke up all jittery and full of anxiety. Sometimes this happens, because I do have agoraphobia with panic disorder. I took my second dose with breakfast. About 3 hours later my gums started to burn; like I ate too much salt. It was irritating, but did not realize it was from the antibiotic. Then my teeth started to hurt really bad everywhere, and it felt like electrical shocks going down my body. My skin turned all colors of blotchy purple and yellow. I started to shake so bad that it hurt. My Dad rushed me to the emergency room. I was given epi, steroids, and an anti-inflammatory. Then monitored for 2 hours. Which was hell, because I have agoraphobia.

I was sent home with prednisone and benadryl. It has been six days since this has happened, and I still have the chills. I feel like I have the flu. My teeth still hurt, and advil won't even help it. I have a constant headache. This medication should be banned. I only took 2 doses and became so ill. When do the side effects finally stop?

Let me start by giving you some history.

My sister is a 22 year old girl who worked full time and was never seriously ill until this summer.

During the last full week of June my sister started having headaches. She told me that these headaches were like none she had ever had before. Days later she started complaining that her legs and wrists hurt. She said that her legs were so tired and achy she could barely walk up the stairs. At that time I dismissed what she was saying. My sister constantly wears heels and I chalked up the complaint to a pair of shoes that were not yet broken in.

By July 4th, the headaches were so intense that she went to urgent care. The physician she saw in urgent care gave her an antibiotic and sent her on her way. By July 7th, she was having difficulty standing up and walking was almost impossible. My sister started complaining about severe joint pain. Her ankles began to swell and her stomach appeared distended.

On July 8th, my sister went to her primary care physician. I believe he sent her for an x-ray and said that she had a cyst on her sinus cavity which was causing her to have severe headaches. He then gave her another antibiotic and referred her to a rheumatologist never even thinking that these two symptoms may be related.

On July 10th, my sister saw the rheumatoid arthritis doctor her pcp referred her to. He dismissed her complaints saying that she probably has some form of arthritis, but that there are over 800 forms and it would takes months to pin point exactly which one she has. He then gave her a prescription for Celebrex and sent her on her way. She spent the entire week in bed because her joints were so swollen and achy that she could not move. She actually crawled to go to the bathroom.

By the middle of the following week, my sister's stomach began to burn. She contributed it to being a side effect of the Celebrex and stopped taking it on July 21st. We had no idea that the pain was so bad. My sister's last normal meal was on July 22. By the 23 she had no appetite and could not go to the bathroom. On July 24, the stomach pain was so bad that she could not work, or sit, or function. All she did was cry. She went back to her primary care physician who then prescribed her prevacid to help with the so called indigestion. He told her if the pain continues she could call him. On July 25th the pain became unbearable. My sister called her PCP as directed and he told her to go to the ER. Never once did he say he would meet her there! I brought my sister to the ER where they did an x-ray and cat scan of her stomach. They found nothing. At that time my sister had not gone to the bathroom or had anything to eat since the 22nd. The physician in the ER said that she was literally "full of shit" and needed to go home and take a liquid laxative. My sister is only 22 and my parents were away on vacation. We were stupid and didn't know any better and were so happy that they didn't find anything that we accepted his findings and got out of there.

My sister took the liquid laxative prescribed by the ER physician as soon as we got home. We waited anxiously for it to relieve her stomach pain. After many hours the laxative did not work and my sister ended up back in the ER. This time she was screaming in pain. One of the doctors there told her that if she couldn't calm down she needed to leave her ER. My sister did just that. At this point my parents (back from vacation) took my sister home and called Digestive Disease. A doctor there told my mom to give my sister 2 Enemas. He said that should relieve her pain. My mother followed the doctor's orders, but the pain did not stop. Sunday, July 27th my sister was right back in the ER - this time at another hospital. This time my sister was admitted to the hospital for severe stomach pain. After 5 days and numerous tests my sister was discharged. The doctors found nothing in her cat scans, x-rays or ultra sounds. The pain was more manageable (she was on morphine every 2 hours) and they said she was ok to go home.

August 1st my sister had a great day. She was sitting up in bed and seemed to be in good spirits. The following day she couldn't get out of bed. This time it was neck pain. My sister said the pain in the back of her neck was so severe that she could not lift her head up or move it side to side. By August 4th she was admitted to the hospital again. This time we brought her to University Hospital in Syracuse, NY. We were sure to get some answers there...or so we thought. As soon as my sister arrived in the ER they started treating her with antibiotics. They were certain she had an infection. They then told us they would have to do a lumbar puncture to check her spinal fluid for infection. We thought we would finally have an answer to what was wrong with my sister, so we agreed. The spinal fluid came back fine - no infection. At that time they admitted her to the hospital. While at University Hospital my sister was treated by a team of doctors. They tested my sister for lyme disease, west nile, lupus, leukemia etc. They performed a spinal tap, cat scans, x-rays, ultra sounds, blood smears, etc. All of these tests came back negative. The doctors could find nothing abnormal except for an elevated white blood count -22,000 (it was also very high during her last hospitalization), an elevated C reactor and a very high SED rate. After 4 days of numerous tests and pain killers (first morphine, then Dilaudid, then Dilaudid with a fentanol pain patch) they discharged my sister. The head doctor told her that he believed she had viral meningitis and that it would eventually work its way out of her system. By this point my mother and I were skeptical. We did the research and viral meningitis should only last approximately 10 days. Mig had been sick since the last week in June. No one was putting all these symptoms together. On the day of her discharge my sister started getting her stomach pain back. The pain was mostly on the left side of her lower stomach - under her belly button. Again she was told the pain was due to constipation and she should buy some Miralax when she got home.

My sister was home for a mere 2 days before she would be hospitalized again...for the 4th time. Her stomach pain was back and worse then before. My family could not believe this was happening. My sisters spirits were down and the excruciating pain was making her mentally unstable. This time the ER physician recommended a hematologist come in to see my sister. We just wanted answers so we agreed. This hematologist, Dr. R stated that she believed my sister had drug induced lupus. We were shocked as my sister was tested for lupus twice before and both times the test came back negative. Dr. R explained that she believed my sister got drug induced lupus from the Gardasil shot. My entire family was shocked. We had never heard of any severe side effects like this from the Gardasil shot. Dr. R asked my sister for her permission to test her again. My sister agreed and a week later my sister learned that she was positive for drug induced lupus. My entire family was so happy that my sister finally had a diagnosis and could begin treatment. We were told that after a 6 week steroid treatment (Prednisone) my sister would be back to her old self. We were ecstatic!

My sister was home from the hospital and on the steriod treatment for 10 days when things started to go wrong again. The doctors were very concerned with the dosage of Prednisone that my sister was taking (80mg. I'm not sure how many times a day). They cut the dosage down in half over the course of a few days to prevent kidney damage and other side effects. Once the Prednisone was decreased, my sister started getting sick immediately. Her forearms were very weak - she could not put any pressure on them. Her shoulders would tingle and she would get shooting pains down her right arm. One of her doctors believed she was developing fibromyalgia and prescribed her lyrica. Shortly after my sister began taking lyrica she started seeing stars. She had double vision and a migraine that would not go away. My mother called her doctor and told him about this. His answer was for my sister to stop taking the Lyrica. She did immediately.

On August 29th, my sister still had a migraine. This was day 3 without a break. She woke up early Saturday morning and began vomiting every 30 minutes. After a few hours of non stop vomiting my mother called her doctor. His nurse practitioner was on call and she told my mother to take my sister to the ER immediately. My mother went back into my sister's room to tell her they had to go back to the hospital and she found my sister having a seizure. My sister has no history of seizures. My mother called 911 and the ambulance came to bring my sister back to the ER...her 5th hospitalization.

Shortly after arriving at the ER, my sister had another seizure. Immediately after the seizure the ER doctor ordered my sister to have an MRI. My sister had one during her last hospitalization only 2 weeks before. That MRI was normal. This one was not. There are lesions all over my sister's brain. The neurologist told us that he cannot believe she does not have permanent damage. According to him there is no oxygen going to her brain.The neurologist also explained to us that her brain looks as though she has been poisoned. He said that her MRI is very similar to an MRI of a patient who has been poisoned with antifreeze. Later I learned that Gardasil has both aluminum and sodium borate (which is in both rat poison and cockroach killer). However, according to the doctor once your brain looks like my sister's all the poison is out of your body. My sister's team of doctors started debating as to whether this could all still be from the Gardasil shot...my sister's last shot was on 02/22/08. Some believe that the side effects started off as mild, but since they were left untreated for so long they've turned into a serious neurological problem. They told my family the only way to truly know what is going on is to do a brain biopsy.

Yesterday, my sister was transferred to Mass General in Boston. We were hoping for a bigger hospital, better technology, more seasoned doctors. So far my sister has been treated badly. When my mother told the doctors' about the Gardasil shot and the devastating effects it has had on my sister they dismissed it. When my mom asked the doctors to test my sister for heavy metal toxicity they completely ignored her. I fear that she will never get the proper care.

Was prescribed cephalexin (Kaiser) for a broken skin infection on my leg from a sporting accident. It was pussing and not healing well. Started taking cephalexin immediately after leaving the pharmacy. Within a couple days, my skin infection was not any better. Hives and bright red dots appeared on my chest, my arms, and my legs. Itching was intense - I couldn't sleep - would wake up in the middle of the night totally on fire - but I was told to stay on course by the nurse at the pharmacy and finish the bottle as I wouldn't want an antibiotic from losing its hold on the stronger existing bacteria. The hives, in the form of red patches, bumps, and streaks were visually traveling through my body and hives would break out. I resisted itching. Then one morning I woke up and my entire chest had a huge patch of hives taking up the entire space between both nipples and from the top of the rib cage to the collar bone. It was ridiculous. One week in, I called my doctor and went in for a check up. Instead of prescribing another class of antibiotics, my second doctor (and opinion) opted to stop taking the medicine all together. He determined the hives were an allergy to Cephalexin.

I started Levaquin 500 MG on Thursday Aug. 29, 2008. I did not have any problem the first night. But the second day at about 3:00 PM I was working on my computer when my finger joints started to get stiff and my hands and arms started to shake. I just thought I was tired and forgot about it. At 1:30 AM August 30, I was awakened by someone shouting in my ear , You are going to die. I woke up in a sweat and my heart pounding. My hand were stiff and my knee joints were very tight. I also was in a very bad panic attack.
I went to my desk and wrote my wife a letter telling her how much I loved her and my dog Abby. I then proceeded to give her funeral instructions as to which funeral home church and buriel plot.. This writing was 3 pages long. I called my doctor and they as much told me this could not happen. My blood pressure was 240 over 120 when I took it. I took a valium and this calmed me down in 10 minutes. They gave me a new antibiotic for my Bronchitis. So I thought the nightmares and pain was over. Not so quick last night at 2:20 AM I was awake by the screaming in my ears you are going to die. I tried to call my wife but I could not get the word out for help. I tried to move my hands and fingers they would not move. Finally I rolled off the bed and yelled my wifes name she did not hear me.
This drug has set back my recovery from my panic attacks. This drug should be badded by the FDA. But as usual the government does nothing to help the public only big business.

I found this site as I want to read on the side effect of this Kenalog which was injected to my face by the doctor to reduce the size of two liquid cists (apparently only one injections). After the injection, I had my period which is only 15 days after my last period, which never happened to me as my cycle is always longer than 30 days and is very regular. Per the doctor, I thought the "cist" would be gone in few days. It did not and instead, I experienced rashes on my entire body and after one week, my ankle and knee was swollen and it was rather painful and I can hardly walk around for two days. Together with the swollen on the leg, the injection on my face is also swollen up and my face looked really in bad shape. I went back to the doctor and I was given one week of antibiotics to drain away the "infection".
Since the cist is still on my face and it really bother me as it is red and very itchy, though my face is not that swollen / puffy anymore. I came back and see the doctor again to have him cheked up on my face. He just gave me one month of antibiotic. I have no idea that having that injection would cause me so much troubles.
It is now more than a month after the injection, my face has a hole as that was injected with kenalog and the other cis on the face is still there. The worse thing is that the cist is is getting very itchy and it was not so before the injection. I am still patiently taking the antibiotic and promised to comeback and see the doctor after one month.
I still having pain on my join and reading your comments, I realized the pain is definitely associated with Kenalog.
I'd love to hear more from you on how things turn out. Thank you.