Right arm symptoms and conditions

I took levaquin for 10 days and then cipro for 10 days after being misdiagnosed with bacterial pneumonia when I really had cocci mycidioidosus (valley fever) a creepy lung infection from a fungus that lives in the dirt here in Ca . Within a few days of stoping the antibiotics I experienced severe joint pain,dizziness,swollen neck ,hives,pain and tingling in my legs and feet,taste perversion,neck pain,hallucinations,nightmares,suicidal thoughts,dead skin,head ache,conjunctivitis. All of which I thought were valley fever related . A few weeks later I started noticing loss of vision and an inability to focus or concentrate on anything. I have ruptured 5 tendons and sometimes can't lift my right arm off the table.
I'ts been a year and 3 months and I still suffer from these side effects and about 3 months ago I started to notice some hearing loss and then ringing in my ears so load that it wakes me up!

This drug has ruined my life.I have lost 2 profitable businesses,a house a car .a commercial building, my credit score is 309 from 760 a year ago.All from a stupid antibiotic that should not be sold in the first place unless you are going to die if you don't take it.....personally I would rather be dead I think.

I think that we (the 1000's of people effected by this drug) should protest,march at ORTHO McNEIL's doorstep and perhaps the FDA....write a letter ,call or write to OPRA...do something ...It's not right that they get away with selling this crap.

Please email me ...I see 1000's of you on these sites...lets get busy!

******

Thanks for reading

I really wish I would have found this site before making the decision to have Mirena inserted. I had it put in yesterday, September 24,2009. It was the most painful things I have experienced. My Gyn had told me that I would have "period type camps" for a couple of hours after insertion. Well I spent my entire day on the couch with a heating pad on high and 800MG of Motrin. None of this touched the pain. I ended up having to take a sleeping aid so that I could go to sleep and hoped I would wake up the next morning feeling much better. Well I woke up this morning and the cramping was not as bad, but still more than "period type cramps". I also noticed that I was having very bad lower back pain. I was cleaning my house and every time I moved the pain would be stabbing. I have not spotted at all yet, but I know it has only been a day. Today I was working and noticed that my right arm went numb from the elbow to my finger tips and my eyes seem very tired.
I am a little upset because the Mirena booklet did not discuss any of these side effects. And also my Gyn had made it sound really promising because I cannot take regular birth control pills. I think I will be calling them on Monday and asking to have it removed. I really wish I would have done more research before having this done.

Last month, I went to see a dermatologist as a result of being bitten by bugs while staying in a motel. The doctor looked at the bites and one particular bite on my right arm, which he said was a tick bite. For that bite, the doctor prescribed to me a drug called Doxycycline HYC for Lyme Disease that I had to take for 30 days. Number one, I hate taking drugs and I have never taken any medication for that long a period of time, except for the Centrum multi vitamin I take on a daily basis.

I went back to the doctor's office earlier this month showing him more bites on my back and a rash on my right leg, the latter of which he said was an allergic reaction to the drug prescribed. He said Doxycycline HYC was the drug that is used to treat Lyme Disease and that I had to finish the course.

On Wednesday of last week, I had four pills left when I noticed a slight change in my vision. I took the pills Wednesday and Thursday and was done with them on Thursday to finish the course. By Saturday, my vision was very blurry and I only have one eye. I wear safety glasses to protect that eye with no prescription in the lenses.

On Saturday, I walked over to the pharmacy and the pharmacist printed out a report on that drug and there is an indication – along with many other side effects – citing blurry vision. On Sunday, I spoke with the doctor's colleague, who asked me whether I was also having headaches while taking that drug. I told the colleague I was having headaches but that I was taking Tylenol when the headaches occurred. The colleague not only told me I could have been prescribed another drug (which I was surprised to hear but would it have mattered anyhow because I only had four pills left) but he also said that my vision will get better but it will take time. I really wish I knew in what time frame my vision will come back because the colleague also mentioned that I may have to see a neurologist and I am wondering because of that statement if something happened in my brain during the times I was getting the headaches that could have affected my vision.

Then I was talking to a nurse friend yesterday concerning the blurry vision – which is still blurry since Saturday of last week – and she asked me if I have diabetes. I told her I do not have diabetes but she said blurry vision is associated with diabetes and that I could lose my sight.

I cannot believe all that has happened as a result of taking that Doxycycline HYC. I also went to have an eye exam and the eye doctor scheduled an appointment for October 8 to see me again to see if the vision clears up on its own. He said if it does not, I must now start to wear prescription lenses. But I am really skeptical about waiting that long because every day I wake up, my vision seems to be getting blurrier and blurrier. I am blown away about all of this -- all as a result of taking that drug. And I have to sit very close to the computer screen in order to see to type anything.

Because my nurse friend was talking about diabetes being associated with the blurry vision, I also went searching about that yesterday and found this statement:

"The use of antibiotics can affect blood glucose levels, at times contributing to elevations and in some cases a decrease in blood glucose levels, depending on the antibiotic used, as well as individual response. Antibiotics are also used for the treatment of infections, which often contribute to elevations in blood glucose, in and of themselves. In the case of Lyme disease the relapsing cyclic activity of the Borreila spirochete, may also contribute to times of elevations in blood glucose, due to the increased presence of infectious organisms during periods of such activity. It is important to discuss your blood glucose response to treatment with your Doctor, as improved blood glucose control during times of treatment
for any infectious state, helps the body put up a better fight."

I am stuck in my apartment scared to death and very, very, very depressed about this blurry vision. Moreover, I unable to drive to the locations I need to get to for my job because not only is it hazardous for me to drive on a consistent basis, but my bills are coming due and no way of paying them.

I am a Registered Nurse and feel foolish that I wasn't able to connect the dots sooner. Yasmin's effects for me were insidious thereby slipping under the radar as the culprit responsible for all of the side effects I was experiencing. On Yasmin for 3 years:

- feelings of shortness of breath
- heart palpitations
- horrible anxiety and feelings of panic (not good when you're a nurse in the
ICU)
- insomnia (never had trouble sleeping before)
- varicose veins on my stomach??!!
- strange weight gain around my abdomen I could not lose despite my best
efforts
- ear popping and a feeling of fullness in my head
- constant runny nose requiring new prescriptions for nasal sprays and
allergy pills that did not work
- new abdominal bloating (ultrasound was negative)
- UTI (never had one of those before)
- strange colored periods
- agoraphobia (previously outgoing)
- depressed--lost interest in things I previously enjoyed, moody & angry,
- horrible fatigue (unable to jog anymore without becoming drained for days
- sharp debilitating headaches (CT negative)
- breast pain
- cellulite I've never had before
- and last but not least, compromised circulation to my right arm causing it
to go numb and change in color (Doppler showed partial arterial
obstruction that has since improved since quitting Yasmin)

Quit Yasmin 2 1/2 months ago and everything is resolving itself slowly. A big price to pay for good skin.

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

I had my Mirena inserted in June 2009 and a few days ago and I started to feel numbness and tingling in my right arm,hand and fingers. Then it spread to my left arm, right side of my face and right leg and both feet. I called the OB/GYN to see if this was a side effect and they told me no. I am otherwise healthy and I even ended up going to the ER 2 days ago because the numbness was so bad. None of the docs said it was from the IUD. They ran all kinds of blood tests and an EKG which all came back normal. I went to the OB/GYN yesterday and had them remove the Mirena!! The OB/GYN thought I was nuts and said that my symptoms had NOTHING to do with the IUD...whatever!! I am so glad it's out and now I hope the numbness and tingling stops soon.

Headache, nasty huge clot filled period lasted for 6 weeks straite, heart problems with left ventricle - abnormal t wave - invertion - dizziness, shortness of breath, craving water, spilling b12 and vit d, inability to concentrate.... to an other wise health 37 fit female! Oh, and 3 months later, I have a spoon sized dimple on my right arm at the site of injection! I WAS NOT WARNED OF ANY OF THIS CRAP, NOR WAS I GIVEN THE PAMPHLET ABOUT POSSIBLE SIDE EFFECTS! I AM PISSED THAT SOMEONE SCREWED WITH MY HEALTH AND LIFE! I AM A SINGLE MOM WITH THREE SMALL KIDS!

I am a 40 year old female. I have had several sinus infections and had been placedo n Avelox before. The doc kept asking me if I had any plans on pregnancy and continued to stress the strength of the drug. However, I had NO idea what would become of this last time. I had been taking it for about 4 days and went to the ENT and was told to stop taking it because my sinuses looked good. That day I struggled to breath and had to literally gasps for air. I developed a bruise on my left arm that looked as if someone had pinched me. I didn't think much of it until I woke up the next morning with another bruise on the right arm. I continued to develop these bruises until there were 6 altogether. A few days later my body began involuntary jerking. I felt like I was having seizures. I became tearful and so afraid. This med needs to GO AWAY!!! I cannot imagine what would have happened if I continued to take it. BE CAREFUL if you're daring enough to continue it. Thank God I have a praying partner and family that would NOT let me go!

Just wondering if anyone else has similar side effects ... I have had Gall Bladder symptoms but all the tests say my gall bladder is working well. (Blood, sono and MRI with contrast) It all started a few weeks after the mirena was inserted. Extremely Severe pain in my right side that last for 8 to 12 hrs. Seems to feel slightly better with a few crackers (unlike gall bladder) and seems to move lower as it gets better (also unlike gall bladder). It does not move around to my back like gall bladder should or usually does. Gall bladder made sense since I have the risk factors ( women over 30, just had a baby etc)

Anyway, Anyone else having the right side pain? Thanks!

I was given Avelox by my Allergist three weeks ago because I had yet another sinus infection, she had me come in and pick up some samples she had with 5 days worth of 400 strength Avelox.
The night of the third dose I was awakened by numbing and tingling and pain in my right arm from the elbow down to my hand, I had never had this before. I called the nurse the next day and she said to stop taking the drug which I did. I figured now that I stopped taking the drug the symptoms would go away.
A few days later I was out shopping and within a few hours of walking around I began to have so much pain in my right foot/ankle/heel that I had to come home, I could not put my foot down.
Then within the next few days my knees began to hurt, behind the knee and in the side. It has been 3 weeks now and the foot pain is better but my hand,elbow and knees are bothering me so much I can't sleep. The other symptom feels like nerve pain in my legs, hands and fingers. I am really troubled by this, I am a very active healthy 62 year old Woman, I have not been able to exercise all of this time.
I went to see my Allergist who prescribed the Avelox and informed her of all of these symptoms. She said that this was a rare side effect and that I was particularly sensitive. I asked her if the symptoms would go away soon and she gently said that it would take time.
Then she said that she had prescribed Avelox to her husband a few months ago, she said he had the same reaction as me (how does this translate to a rare occurrence?) and that he was slowly improving. She thought I should go to a Physical Therapist or a Rheumatologist, I told her I can't afford that.
At this point I am scared I won't get back to how I was before. I have had knee surgery in the past but my knees were doing fine until this.
Have other people slowly recovered as my doc has suggested will happen?
I don;t know what I should be doing at this point. Help!
S.

Hi all I wanted to let you all know that I am done 6 lbs in the five days since it was taking without dieting!! I also wanted to add some symptoms that I had. Ringing in ears, tingling in my right arm and fingers, pain in right hip, trouble swallowing my food. I got something stuck at a restaurant before and had to go to the ER. Turns out it was all related to the horrible anxiety attacks I was having. Good luck to all of you wonderful woman on here!! Here's hoping we feel will all feel " normal" again.

Hi all! Well I got my mirena taken out on Wednesday. The Dr. was very sweet I told her my symptoms and she said lets take this out then! While she was down there she said " Hmm I'm going to look at a swab under the scope." She came back in and said that the mirena gave me a bad infection! I had to take some strong one time antibiotic that killed my stomach! I can't wait to start to feel better. I did notice I can see a lot better then I did, no more blurry eyes. The last 3 1/2 years have been utter hell for me. I've been in and out of different Dr. offices not finding anything. I was dizzy all the time, I started out small after I delivered my baby and gained 60 lbs since it was put in. I had a shooting pain on my right side, horrible anxiety attacks, blurred vision, fuzzy mind, head aches, ovarian cysts, lower back pain and bloated belly. I am so relieved I got this disgusting thing out of my body!!! I hope my life will go back to normal now.

I also had pins and needles in my right arm with sharp pain radiating from my wrist and elbow, although I am not sure if this was Yasmin or related to a car accident i was in. I stopped Yasmin about 5 days ago, so I guess time will tell.

Both my hands began to ache constantly to varying degrees- it felt muscular or nerve related - also the muscle in my upper right arm began to ache - this continued for months not knowing it was from Centrum Silver vitamins I was taking - Dr sent me for physical therapy - helped some but it came back. In preparing for a medical procedure I had to stop taking all meds & supplements for a few days before the procedure, and my hands STOPPED HURTING, & continue to improve, along with the soreness in my upper arm. I know it was the Centrum because I had tried over the past 6 or 8 months to stop taking other supplements/meds I was taking to see if that was causing the pain. The only thing I never stopped was the Centrum, because I had taken it for years with no problems, so I didn't think it was that, I thought it was something I had started taking more recently. Now I am sure it was the Centrum that caused it, because all those symptoms are totally improved. What a relief to have my hands and arm feeling BACK TO NORMAL again!! Thank you, thank you, thank you.

My doctor had me on a 10-day course of amoxicillin for a sinus infection. By the last day, I had contracted pneumonia and the sinus infection had rebounded until it was worse than ever. So, like many others who have posted here, my doctor prescribed Avelox. Fortunately I read the entire printout from the pharmacy, including all warnings of potential side-effects, both minor and serious. I grew concerned on day three when I had numbness and tingling all down my right arm, and following the warnings, called my doctor. Fortunately, my doc is a smart guy: he told me to stop the course of Avelox immediately, and if the nerve symptoms returned, I should go to the ER.

Some of the symptoms others here have mentioned -- many far, far more serious than mine -- seem neurological, as if the drug is also messing with brain function rather than just causing an allergic reaction (especially the seriously altered mental states).

A symptom that has occurred occasionally during the past weeks since I stopped the Avelox is an odd tremor in my eyes when I'm tired. My eyeballs shake quickly and sharply from side to side for about 10 seconds at a time. I had a similar reaction many years ago, when my doctor at the time prescribed a high dose of Paxil (anti-anxiety). The difference was that then the eye tremors stopped two days after I stopped the drug; the symptoms now started long after the Avelox was out of my system.

I linked to this webpage specifically because I was wondering how common adverse reactions to Avelox are. God knows we need some new antibiotics to fight the increasingly more resistant strains of bacteria. But if our bad experiences are as common as I fear, even though some people experience wonderful results, this is one drug that should be prescribed with extreme care. Not only that, but both the physician and the pharmacist should be especially diligent in explaining the more dangerous adverse effects so that patients (who don't always have a half hour to read through hundreds of single-spaced lines of instructions on drug sheets) are well-informed enough to participate in our own care. If that just means telling our doctors that the risks outweigh the benefits, please prescribe something else, so be it.

I started taking Aviane approximately 3 weeks ago because of my irregular menstrual cycle. I'm only 17, and since I was relatively healthy, my family doctor told me that there would be no serious side-effects. About 2 weeks into the pills, I started to experience shortness of breath and a constant pressure on my chest, near my thyroid gland. A few days ago, I had gone numb on one side of my body and lost some circulation to my right arm. Just last night, I was admitted into the emergency room because I had trouble breathing, nausea, tightness in my chest, dry throat/hard to swallow, tremors, near blackouts, fatigue, dizziness, weakness in my limbs, and heart palpations. They took tests and said all of them came back negative, but they still want me to check up with my family doctor soon. Apparently it was an allergic reaction to the chemicals in Aviane, but since estrogen and progesterone are natural hormones found in the body, I wasn't so sure. I had a fever last night, and my body could not stop shaking. We've contacted a few nurses, and they suggest I might be experiencing some of the side-effects of Aviane as well as a possibility of a viral infection. I don't think the benefits of Aviane are really worth it. I've been spotting ever since I started; my appetite increased along with my weight (I'm a bit underweight though so it's not that much of a problem); and obvious mood swings. I doubt many people will react to Aviane the same way as me, but it's very possible. So make sure you talk to your doctor about any possible side-effects and make sure you really want to start taking them. I haven't tried any other brands of the Pill, but I don't think I'm going to be starting any again anytime soon.

My story started about a year and a half ago. I got my first kenalog injection for ORAL LICHEN PLANUS and was told that it was safe enough to give to his own wife and kids and he convinced to take it. But little did i know that it was going to leave this huge dent in the top part of my right arm. The doctor said it would fill in but would take awhile. So in 4 months i went back for my second injection because it seemed to help my mouth but then strange things started to happen. I take blood pressure meds and have for 14 years and never had any problems until that second shot and my BP started to go up and down and i mean very low and very high. I went to my family doctor and he wanted to try other meds and i said no so he sent me to heart doctor and that was a waste of time and money. I just waited it out and in the mean time i stared to to drop a lot of weight and couldn't figure it out. Now it was time for third shot and by this time my weight started at 145lbs. is now 119lbs. The doctor said my problems are not from the shot. So my health started going down hill and my bp is now very high all the time and still losing weight. Guess what its time for fourth shot and i now weigh 109lbs. and i told myself no more shots because in the end every shot i took started to not help my mouth anymore. Well its been 5 months since my last shot and my bp is normal now and my weight is at 115lbs. I still have the dent in my arm. This is a very dangerous drug and i advise no one to try it. Someone needs to take it off the market. And before i forget- what it has did to me is i have very bad bone and joint aches but i hope in time it leaves and blurring vision and headaches everyday. I just want it out of my system.

I've been on Wafarin since September of 2008 because of a massive DVT stretching from my jugular vein to my right arm. Since the initial injection of Heparin and oral consumption of Wafarin I have experienced daily migraines. They seem almost like 'pressure-headaches' pushing on the sides of my head, temples, forehead and the bridge of my nose. My thrombosis doctors have sent me for Ophthalmology tests, MRIs, and plan to send me for Neurology tests as well to discover the cause of my headaches. They've put me on codeine, Tylenol 3's, Gabapentin, Naproxen, and Co Sumatriptan because of the fact that I'm so immune to painkillers in general (For the blood clot pains themselves, I was on Hydromorphone, Morphine and Codeine). Although the Co Sumatriptan along with the Tylenol 3's give me some relief, I can't help but wonder if the cause of my daily migraines are from the Warfarin itself.
My doctors are reluctant to agree with me, saying that they plan to take me of Warfarin within the next few months, but aren't certain of exactly when.

Abilify was recently added to my medication of Depakote 250 x3 (i have been on this for 10 yrs), Zoloft 40 mgs (8 years), and Buspar 40 mgs (8 years). I started taking Abilify last Tuesday the 17th of March. The first night I took it I had trouble sleeping..(but i also had some caffeine that night)...for the next few nights I still had trouble sleeping...I also noticed an increase in my pulse, rapid heartbeat...and my blood pressure! This past Saturday, my blood pressure was 141/91 which was my left arm, then my right arm was 138/90. My resting pulse was 90+ with my heart pounding. I went into work today (i work in a doctors office) and had a nurse take my BP and it was 153/95...now my BP is normally 120/60...the lowest its ever been is 90/70. So to have my BP this high is very strange. I called my doctor and she advised me to stop it ASAP and to call her if i have any more problems. I already have a scheduled appointment on 04/01/09.

I am a 46 yr. old woman diagnosed with breast cancer last April 2008. I had left mast. a month after and then had chemo on June till Sept. My last PET scan was inconclusive so my oncologist put me on femara. I have been taking it for 5 mos. now. I experienced slight pain in my right arm early December of 08 and told my onco that it might be the femara causing it. He dismissed that and said that I have arthritis. Now the pain is also in my other arm which extends to both shoulders. I have problems with my range of motion in both arms now and is thinking of just quitting Femara. I have also pain in my inner thigh muscles and have spasms cause by sudden movements. Occasional insomnia and frequent hot flashes are other side effects I have to suffer. I don't know if it is worth continuing with the little percentage of advantage in the long run and at present live with a diminished quality of life.

Hello,

I am a 55 year old Man and have been taking simvastatin for over two years now. Lately my back hurts from below the shoulder to my waist. Also my right arm and hand hurts. I feel numbness in my right hand a lot. My chest hurts on the left side as well.

I take 40mg of this drug every day and never rally thought about it much till lately. Seems like in the past two months things have gotten worse. I go to the VA Clinic where I live and have a regular Doctor there.

I was about to go see my Family Doctor today with all these pains I have been feeling, but then I googled Simvastatin, and started reading about all the side effects. I think I will just cut my pills into, and take a lesser amount to see if things get better.

last thing I need right now is more medications from another Doctor.. I can relate to all the pains for the most part, that all these individuals have posted. I know one thing for sure, I can't keep feeling this way and something has to change.

I had very high Cholesterol levels before taking this medicine, and it has dropped my levels extremely. Hopefully a lower dose will not only continue to keep my levels in an acceptable range,but cut down on these side affects.

Nobody should have to suffer all these bad effects..

I have been taking 1,000 mg for about 6 month to lower my LDL to 70 mg from 107 mg. I also take 81 mg aspirin about 30 min. before I take my 1,000 mg Niaspan. My HDL and triglycerides are fine. Lipitor did not lower my LDL and Vitorin caused the tingling in my right arm. After discontinuing Vitorin, I was put on Niaspan. The flushing is OK but the itching on my back was horrible not to mention insomnia. Itching comes and goes but what worries me that recently I have developed the pain in my toes, (excluding the big toe) and when I get out of my bed my feet do not want to support me for at least 5-6 steps. I have been always able to walk for miles! I realized that one of the side effects of Niaspan is elevated concentration of uric acid (gout) or glucose (diabetic condition).
Any similar side effects?

hi I got the shot in June "08. I was told there were no side effects. I now have a purplish red indention in my arm. It looks as if my arm is deformed. But waith there's more. Just a week ago I was diagnosed with degenerative bone disease in my right arm and shoulder. Possibly a side effect to the shot. When calling the doctor who admistered the shot she is always"to busy" to get me in for a shot. Now what do I do. I'm only 29 I should not have this wrong with me:(

I agree this is the pill from hell, I took one 500 mg. within 10 minutes,my heart was pounding and broke out in weps and a rash. Called pharmacist, was told to go to the er. or take benadryl. only took one pill. the next morning woke up shaky, went to work 2 hours later was itching was anxious, face and lips were numb. that night started having anxiety, hard to breathe, dizzy , back of head numb and tingling, thought i was going to pass out.. ended up in ambulance to hospital. er doctors said it was an anxiety attack. 3 days later, anxious, fearful, dizzy, and numbness in face and back of head. still have 2 sores on right arm, joints also hurt , words were slurred all this from 1 pill that was supposed to help me. i would advise everyone not to take this pill.

so, I was prescribed Avelox a week ago to clear up an infection caused by a ruptured ovarian cyst. I went on-line tonight because each night since I've started the medicine, I sleep less. I have turned into a total insomniac. I remembered the name AVELOX when my doctor prescribed it but I couldn't remember if I had any issues with it when I took it last, or when I even took it last. After reading your posts...it came back to me. About a year and half ago, I was prescribed Avelox for a kidney infection. Within a couple of days after taking the medicine, my right arm became completely inmobile and it was painful to even try to move it. I also had terrible abdominal pain. I went to the ER, only to have them ask me if my "home life was OK" or was I "depressed". They checked for the kidney infection but found no trace of one. I left the ER with no diagnosis...except they thought I was crazy. Gradually, after a week on Avelox, my arm pain went away but the abdominal and lower back pain became so bad that my doctor admitted me into the hospital. He feared the kidney infection (which the ER couldn't find) had gotten very bad. I was there for 3 days and they couldn't find anything wrong with me.They again couldn't even find any trace of a kidney infection. I was not eating, not sleeping, feeling constantly sick to my stomach and dizzy...and the abdominal and lower back pain was incredible. The doctors again were talking to me like I was a crazy person. They couldn't find one thing wrong besides a little dehydration.
I stopped the Avelox while in the hospital after no kidney infection was found. After a few days off the medicine I gradually felt better. Two days after leaving the hospital my doctor called and said that one of the tests they did said I could have possibly been exposed to Mono, so they chalked the who experience to being a possible case of Mono. That never made sense to me...but after reading your experiences, I'm sure it was the medicine. Now after remembering that I had taken this medicine before, I also remember sitting in the hospital drinking coffee! The prescription on the bottle I got last week reads "avoid caffeine". I know I drank coffee when I was on it before and I don't recall any warning about caffeine with Avelox last time. That said, I tried drinking a little coffee the 2nd day I was on it this time (I need my coffee, even though it said no caffeine). I was sooo jumpy, hands shaking, heart racing and lightheaded - like you feel if you drink many cups of coffee with no food - but I had only had a couple of sips. I haven't had any coffee for the rest of the days I had been on the medicine and I haven't felt that way again. I have also been drinking tons of water because the Avelox is making me so damn thirsty. My hands, lips and even my eyes are dry. The issue I am having with Avelox this round is flushes. One minute I'm fine, the next I'm flushed and my face is hot like I was running a marathon, but I was sitting still. Maybe with no caffeine and tons of water, you might feel better while you are waiting for this Avelox poison to get out of your system. Hope that helps. I'm going back to not sleeping...(It's 1:30 am ~aaarrrggghhh)