Pins and needles symptoms and conditions

11 days ago I had indigestion and following that I had continuous heartburn. Doctor said it was gastritis and prescribed me gaviscon and omeprazole. I took one omeprazole pill in the morning after breakfast everyday for 5 days when I started to have the following symptoms: bad cramps/aches on left shoulder blades/neck, cramps/pins and needles in left arm, numbing of hands at times, nausea, tightening of the chest, sweaty cold hands and feet and lastly the most painful of all, numbing of my throat! The doctor checked my throat many times and said that it is not swollen yet I am positive there is something wrong with it. It is actually not sore when I swallow, just feels numb and cloudy? Sometimes I can't yawn fully because my throat closes up when I do and I cannot speak too much as I get breathless. I see that people here have started getting these symptoms via a long term use of this medication and not mere 5 days. Either way, I stopped taking it since today however symptoms are still present and stronger than ever tonight. I cannot sleep as I am too afraid to, as I have also been getting very vivid nightmares. I have started taking Ranitidine (twice a day)from today and I am a bit nervous about whether it is going to bring me nasty side effects too or not. I really just want the omeprazole's side effects to go away first but it seems as though it may actually take some time.... anyone had this numb throat which has caused difficulties in breathing? I also couldn't go to sleep before because when I would lie down my chest and throat felt like they were closing up even more and if I tried to sleep I would feel as though I couldn't breathe. Does Randitine cause nightmares!?

Hi
I am in the UK - where any knowledge of side effects related to Yasmin appear to be non-existent. I was prescribed this to treat my endo after having problems with another pill (constant bleeding and mood swings).
Initially it was like a magic pill - immediately improving the mood swings and stopping the constant bleeding. Then after about 4 days I felt so nauseous I wanted to go home from work - this lasted a few days.
A week and half into my first pack, I suffered continuous asthma attacks - with no obvious cause, this developed in hours to spontaneous vomiting along with a hacking cough.nI was prescribed antibiotics for "infections". The symptoms continued until it was unbearable and I was put on anti-vomiting tablets. and changed onto a different antibiotic.
A week later back at the doctors surgery I had a series of tests - awaiting results as I type, as I have very dark urine, stools that are not "normal" (clay or yellow), pain in my stomach, pins and needles, continue to vomit if don't take the anti vomiting tablets. Have now stopped taking Yasmin and await results...
HOw long does everyone appear to improve after stopping taking Yasmin? Also does this sound like I may have a case of hyperkalemia? (I am awaiting results).
Many thank

Like many of you in this forum, I'm experiencing the pins and needles feelings all over my body, especially on my arms and face. I have weird lapses in memory. I attributed the joint pain I've been feeling this past year to being a 45-year old runner. However, upon reading so many comments regarding joint pain, I can only ascertain this isn't just something caused by age and running. Is anyone of you men experiencing erectile problems? Since starting Lisinopril a year ago I've noticed performance difficulties. My doctor said that can be expected with high blood pressure and prescribed me Cialis. Good Lord is that drug awful! I'm going to flush my bottle of Lisinopril right now and call my doctor tomorrow and discuss a safer alternative to this medicine.

Was prescribed HCTZ and started taking it off and on in early August. Pain in the butt cutting the pills in half. Started to feel weird feeling in my left ear and cheek and then numbness spreading up my face, forehead and scalp.(I did have a few beers the weekend before this happened) Took myself to ER. MRI, CT, full blood work, thyroid check, EKG, heart and lung xray. ALL PERFECTLY NORMAL. Of course I was diagnosed with possible MS, Belle's Palsy, and was told I might just be wired weird.

Went to primary the following day for follow up and was told that my blood pressure may have been the cause of the episode. Prescribed Lisinopril and started taking it immediately 10/12.5. Started feeling good pretty quick, but noticed a few crazy dreams and almost like I was falling.

Missed a few doses and and had a few beers over the labor day weekend. Started meds on Monday but started feeling pins and needles coming back in different parts of my body. Continued to take meds and then went camping. Had a few beers around the fire. Woke up next morning with slight case of Vertigo. Continued with meds through the weekend and have felt dizzy, dumb, tired, my eyes don't move correctly, my left arm has felt numb and swollen, my left cheek tingles and I feel so swollen in my gland area under my ears. Knee pain too.

I didn't take a dose today, and I feel 100% better. Still tingly and numb in spots, but better. A little anxious and my heart feels like it's beating really deep and fast. BP is 154/82 after going down quite a bit on the drug.

Anyone else had trouble with the alcohol? Any similar symptoms? This site has calmed me down as I've always been a worrier/hypocondriac type. any response or idea would be really appreciated. Thanks everyone...good luck!

I began getting debilitating headaches 3 years ago. They were everyday and not the classic headache (no visual, nausea etc). It felt like a jackhammer to the back of my head every single day. My neurologist told me they were migraines. I was skeptical as every other migraine med had not worked. I began on Topamax at 25 mg twice daily. I started at this dose for a month. The body really needs to adjust SLOWLY to this med. My side effects were pins and needles in the hands and feet, strange taste in foods, flat tasting sodas, drastic cut in appetite. My doctor assured me these would go away. Headaches did not start to improve until the second month when I went up to 50mg twice daily. By the third month I was up to 100mg twice daily and I feel like I have my life back. I still will have occasional migraine breakthroughs, but nothing like the misery I had before. Within 5 months or so, food began to taste normal again and the pins and needles stopped. I dropped 30 pounds total on Topamax. It has been a life saver for me!! My advice for anyone thinking about this drug is to ease your way up slowly until your body adjusts. One week on a dose is not enough time.

My husband stumbled across this website and first I would like to thank everyone who have posted their experiences on the NuvaRing. Because of you guys I now know I'm not losing my mind.

I started the NuvaRing March of 2008 and I started getting dizzy spells May 2009. I actually got my first dizzy spell when I was driving. Everything started to spin very fast!! My husband had to grab the wheel and tell me how to slow down and how fast to do it. That was the scariest thing ever!! My head felt a numbing sensation in my head. I had a pain above my left eye and it would shoot up my head and down my neck. The dizzy spells would come whenever, once every 8 days to twice in one day. I have had an MRI and an MRA done and nothing. The docs have had me on so many migraine meds to try to get a handle on this and nothing has helped. My longest migraine lasted for 14 days, that was in May. This month (July) I got a migraine on the 13th, took the ring out on the 21st, and had a dizzy spell this morning but this afternoon and especially this evening I feel amazing.

Since getting on the NuvaRing, like so many of you, my sex drive does not exist. It has caused so many fights between my husband and I. Its hard to tell him that he is still attractive but I can't explain why I'm not excited. So thank you for writing your experiences. He got to read that I'm not the only one and I wasn't making it up.

These last three months have been hell for my family and I. I have been like Dr. Jekyll and Mr. Hyde. So much tension has caused everyone to walk on pins and needles when they are around me.

So lets sum it up here, after being on the NuvaRing for 14 months I started getting dizzy spells, migraines, nausea, neck pain, twice I've puked because of the room spinning so damn fast, and very very VERY low sex drive.

I'M NOT CRAZY!!!! :)

I took this garbage for four days until I had to go to the ER for shortness of breath, chest pain, stomach pain, pins and needles sensation in limbs, hot flashes (felt like I had a fever) and blurry vision. The worst was the complete and utter mental breakdown, I became suicidal and had just horrible images coming through my brain.

It's been a week now and while the depression/suicidal thoughts have subsided, the anxiety, exhaustion, shortness of breath, and stomach pain remain. I'm curious how I can still have these horrible effects taking into consideration the half life of this drug. It should be out of my system now.

Any idea of how much longer this is going to last?

Started on Doxy 200mg every 12 hours for Lyme Disease about 7 days ago and have had painful pins and needles sensation in my hands - on and off since about day 4. The top of the hands seem most affected and any exposure to water (and the resulting evaporative cooling) causes elevated sensation for about 1-2 hours. Any exposure to sun causes a painful sunburn-like sensation. I will be staying out of the sun and hope the pins and needles will go away soon.

I was prescribed 750 mg Levaquin for 7 days for a bacterial skin infection that I got under my breasts from inverse psoriasis. I took one pill and it hit me like a ton of bricks. I was up all night long with feelings of dread and like I was on a bad acid trip. The next day, I was so exhausted, I could barely even lift my head off the pillow and literally slept all day. The day after that I was going through withdrawal-like symptoms and my husband finally took me to the ER. The nurse practitioner there told me she NEVER prescribes Levaquin because she sees so many patients coming into the ER who are experiencing horrible side effects. I quit taking it obviously but am still feeling shaky and weak. Also, today, both of my feet started feeling like they were asleep with the pins and needles feeling. Also, I have TMJ and my jaw is aching as well. All of this for a little skin infection that the doctor didn't even examine. He just got the results of the cultures back but didn't actually see the infection to determine if it actually needed something so strong. I am taking Keflex now which isn't near as bad and is helping just fine. The difference is the cost. I'm sure the doc got a huge kickback for prescribing the higher-cost Levaquin. I will not be seeing him again. All doctors are interested in is prescribing drugs. They don't ever try a natural means of healing which I do not understand. I am so frustrated...I hope this crap gets out of my system soon!!!

I will be honest with you I was having these symptoms before I was put on Doxycycline for Lymes Disease. The pins and needles in the hands, lightheadedness, major fatigue, shortness of breath. That was the reason I went to the doctor. I knew something was wrong and I also had been bitten by a tick. The blood test came back positive and I started on Doxycycline immediately. I actually get up about 6 and take the 1st dose and then go back to bed and the morning nausea stopped. The only new side effect is the very foggy feeling. What ever the side effect is can not be as bad as the symptoms of Lyme's Disease, before you stop taking the meds please read the symptoms, they are definitely are worst than the cure.

I want to know if anyone has experienced severe joint pain while on Doxy. I was prescribed this med on a Monday. I (like an idiot) doubled up on my first dose Monday evening because I know you can do that with other antibiotics to jump start the process. What can I say? I don't like being sick. Well....Tuesday morning, I took my 2nd dose and went to work. Very soon after taking the second dose, I broke out into a very itchy rash all over my back that soon spread to other parts of my body. I called my doctor and was immediately taken off the Doxy and prescribed Augmentin. Later that night, I began aching all over. I woke up in severe pain throughout all of my joints, and was in a terrible mood.....obviously. As the day progressed, the pain continued, but seemed to be moving randomly about my joints. My ankles would hurt for a while, then my arms, the my shoulders, etc. That night, I took a Benadryl (still itching from the rash a little), some ibuprofen, and went to bed. I woke up feeling a lot better. A lot less pain in most of my joints. It was a good day. However, today, Friday, I am still in some pretty bad pain in my hands. Anyone else have a similar experience??????

I've been on Topamax (100 mg 2x per day) for 5 years as mono therapy for epilepsy. I switched over from Depakote which was a *nightmare* and it has been great, no seizures. I've had the pins and needles, diminished vocabulary and memory, and intermittent eye twitching but this week my right eye (why is it always the right eye?) has started twitching almost constantly. It is frightening and embarrassing and I am not sure what I should do.. I guess it's back to the neurological drawing for me because I am not sure why it's happening now. Has anyone else had the eye twitching occur after long term use?

I have been taking 40mg lipitor for over 9 years now.

I have had back issues since an injury to one disc (L4?), and had microdiscectomy in 2001? Took about two years to actually get close to normal.

The last few years, I have had multiple issues with shoulder pain, wrist pain, elbow pain, lower back pain, Upper rump muscle pain , and now both hips are killing me (the shoulder, upper rump muscles and hips are by far the worst). And I am now so weak in my lower back muscles, that it feels like I will (and do) pull out my back.

I have seen NO many doctors I can't even name them all. I have had operations, multiple injections (cortisone) taken pain meds, etc. Nothing has helped and in the last year and a half, I have gotten steadily worse. To the point where I can't really do much of any activity. Sleeping at night is painful. Can't lie on left shoulder, and can't lie on either hip for more than a few minutes. If I fall asleep on my side, the pain wakes me up. When I try to walk, 80% of the time, I end up with a pain in my upper right rump (sacroiliac area), that I MUST sit down to get the intense pain to go away, which it does. But comes right back when I walk again.

I have had x-rays, MRIs etc, and never reveals all that much. Disc issues, yes. NOt much else.

Recently, I have begun to get a nasty clicking (catching) on my left jaw (joint?). Not really painful, but something definitely wrong. My dentist sent me to his Chiro. I went and liked him right away. I had gone to another chiro for years and I believe in them. But this one is the best I have seen.

Anyway, one of the FIRST things he suggested, was that it was POSSIBLE that the Lipitor is causing all of my problems. Put me on COQ10, and doing multiple adjustments and treatments. I will be seeing my regular doctor 5/26, and my chiro wants me to see if he will take me off lipitor and put me on Niaspan instead.

I guess my question is: Can Lipitor be fine with me for so long, and then in such a short period of time, turn me into a compete wreck from the pain and wasting away of my body/muscles? I've told doctors for over a year now that there is SOME connection as to all these issues and pain. One Doctor, of course, gave me the "you are getting old" bull. Yes, I am 56 yrs old. But I understand the process of getting old, vs the complete failing of ones body.

Also, IF it is the Lipitor, can it possible all go away? Or should I expect some damage forever?

One more thing, the last ortho I went to the other day for a second opinion, wants me to do a EMG, to see if there is muscle damage. I was not planning on doing it, but wonder now, should I? He was not doing it because of lipitor, as he never even talked about that to me. I had shoulder operation and have not had the results I feel I should have had.

I am 72 years old and in 1995 I had an artery blockage and had angioplasty.Upon my release from the hospital I was put on several prescriptions, beta blockers, cholesterol, Aspirin, Vitamins, etc. which I had been taking regularly for 13 years without any problems. In 2008 after having chest pain and going to the hospital my heart doctor advised me I had Atrial Defibrillation and put me on Warfarin and also told me to stop taking all the vitamins I was using along with my daily aspirin dose and one of my prescriptions. Since then I have had constant shoulder and muscle pain in my arm and leg. I have had several treatments by a chiropractor and several physical therapy treatments and the pain has not subsided. My memory has gotten worse also however I thought that was due to my age until I read some of the above side effects of Warfarin. I definitely have a lack of energy and also changed my diet due to the Warfarin. I have informed my heart doctor about the problems and he advised it is not due to the Warfarin. I don't agree with him after reading all the posts, but I am not a doctor. I will continue my prescribed dosage and Pt/Inr tests as schedule for a while, but if my pain etc doesn't get better I will probably do like the lady's posting and stop the warfarin on my own.

I have been on Topamax for 2 1/2 months. My dosages have been varied due to side effects that scared the daylights out of me. Never more than 100 mg a day, at which point I was a vegetable. After such terrible side effects - pressure in the eye, blurriness, loss of speech, coordination, complete exhaustion, inability to work, stopping mid sentence with inability to complete sentence - I finally had it. I talked to the doctors all along that I was terrified what was happening to my mind and body but they just said it was too soon to tell if the meds were working or not.
Out of pure frustration and concern for my own well being, I decided to try to taper off Topamax and then stop completely. I lost feeling in feet and hands, pins and needles, weakness in feet and hands as well as spasms- lovely. Frightened me so much I wound up in emergency thinking something else must really be wrong with me. MRI said all was fine as regards to MS or stroke, etc. Whew!
Continuing to withdrawal and mad as @#*! that the Dr.s don't know what they are prescribing to poor patients, Topamax is a dangerous crap shoot. Funny to me how something as horrible as this drug can be prescribed in our government, yet medical cannabis prescribed properly with little to no side effects is a crime in most states.
What have I learned from this experience?...be your own advocate. Don't let anyone ever push you into saying something is black when you clearly see it is white. Get angry, state your feelings if you feel you are being harmed and brushed off and not helped. You still have the brain cells in you to make good decisions though Topamax and pressure from others about "not taking your meds" may knock you confidence for a loop.
I'm thankful I live in CA where I can make legal choices that are not available to others in the USA. Shame on the drug companies, shame on the Dr.s that need to do their homework, shame on our FDA for letting this horrible drug on the market whilst holding back natural herbal relief that grows right out of the ground for all to use legally. Shame on me for not doing my homework earlier and doubting myself and letting other decide for me for so long now.
Good luck, hope you all find some comfort and fire in this message. We are our own best advocates. No one knows us better than ourselves. Freedom of choice is a wonderful thing - so thank you makers of Topamax, for helping me to find the strength inside to tell you....JUST SAY NO! to drugs - your drug in particular. May you be recalled and not harm any others, and may your profits plummet as you have make you $ on the suffering of so many others.

I have been on Lipitor for five weeks. I can't believe how awful I feel. I ache all over. I my arms and elbows are sore; I have had pins and needles in my hands; charley horse like spasms in my calves (mostly at night); sharp knife like pains in my upper thighs; even my teeth hurt. I am a 46 year old female – I can’t believe this. I have made an appointment with my doctor as I have to get off this drug. I have experienced some blurred vision and hearing impairment too. If I hadn’t of found this website – I truly would have thought I was a bit crazy….
I have never had any symptoms like this before and never thought of myself as an old lady - but that is what I feel like. It is unbelievable.
.

I have had pins and needles feeling in my fingers and toes, pretty strong too, I've been on Topamax before so I knew what to expect, I've had the loss of appetite and the soda tasting flat, as well. Some confusion with words, not being able to put together a complete sentence, like you know what you are trying to say but it's not coming out correctly. There may be times where you are somewhat staring off into space. My neurologist explained all of the side effects to me before prescribing me drug but also gave it to me as sor of like a ladder, to where I could build up to it so the side effects are not as bad, I went from 25 mg 4 night to 50mg at night for 4 night, then 75mg for 4 nights now I'm on 100 mg at night, so I've gotten used to it again, I still get the pins and needles and the confusion but if someone is considering taking Topamax, ask your doctor about trying to build up to it first by doing 25, 50,75 then 100.

I was prescribed Niaspan ER, and the first night I took the 81 mg aspirin an hour before. So this was 11 pm. I tried to get to sleep, as I do usually have a hard time getting and staying asleep anyway.. BUT, four hours later, I had this severe face flush, I had burning in my ears, my face, my neck and as I was told I might have this, I tried to remain calm.. then the ITCHING started up, I wanted to rip off my skin, I itched so badly! I scratched my wrists, then my upper legs, my stomach area.. even ripped open a little sore there... this itching almost drove me crazy! I admit I got panicky.. and my heart started racing and I felt like my throat was closing up.. this is something I experience with my allergy to contrast dyes... I swore I'd never take another Niaspan! Scared the heck out of me. I don't know what else I will be able to take to lower my triglycerides and total cholesterol. I am 56 and just found out with an EKG that I have had a heart attack already. So this is all scary to me, but the burning and itching and rapid heartbeat don't seem worth it to me! Anyone else have this kind of experience? What did you do? thanks

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.

I started to take Atenolol after my kidney disease caused my bp to be extremely high. I'm on Avapro 150 mgs a day but at my last doctor's visit my doctor decided to put me on Atenolol for a rapid heartbeat. After about a week I began to feel extreme fatigue consulted doctor and he said it's not the Atenolol so I continued taking until my I started to feel pins and needles in my hands and feet. One morning I got out of bed and my left foot was swollen and curled up into a ball, the pain was excruciating. I was rushed to the emergency room where they said I pulled a muscle, I didn't. I asked the emergency room doctor could this be the Atenolol since I only started taking the drug for a few weeks when these symptoms began. He stated no that's not one of the side affects. After looking online I found that it is one of the side affects. So I stopped the Atenolol and after a few days was able to regain feeling back into my toes and slowly my foot. I still have pain and have trouble walking but hopefully I will recover. DO NOT TAKE THIS AWFUL DRUG. Either the Doctors know the side affects and are allowing us to be used as quinny pigs or their receiving some type of kickback from the pharmaceutical companies for prescribing this drug. If you know anyone taking this drug who is experiencing the above side affects stop the drug immediately before it's too late. If I had continued the drug I would have become paralyzed or worse stopped breathing. Another thing they are telling people that they have MS Multiple Sclerosis so they can treat you for yet another disease you don't have.

IF YOU FEEL/EXPERIENCE ANYTHING ABNORMAL FOR YOU OR DO NOT FEEL QUITE YOURSELF SEE YOUR G.P./NURSE AND SERIOUSLY CONSIDER GETTING THE MIRENA COIL REMOVED
This medication may be suitable for some people but if you experience any of the following, I urge you please, please please, 'demand' that you want the Mirena removed. My symptoms were noticeably worse around my time of ovulation. I've also found out that people previously treated for/suffering from depression should not be prescribed this medication. (I've been on Prozac in the past). I had it fitted in Aug 2007 to combat very heavy periods and severe PMT at the recommendation of my G.P.and had it removed Sept 2008. Symptoms I experienced :-

Dry/furry mouth
Headaches (over time these became migraines)
No concentration
Poor memory
Lethargy (constantly tired and drained)
Smelly discharge (still noticeable straight after washing)
Very heavy legs
Numbness in my legs
Joint pain and clicking (mainly in my shoulders and knees)
Developed facial hair (mainly under chin and jawline)
Hair loss
Weight gain around my stomach (without increasing my food intake)
Feeling constantly bloated.
Spotting randomly for duration of Mirena being fitted. (Brown spotting)

Panic Attacks ( awoken in the middle of the night with them) escalating to the following:-
Palpitations (for no apparent reason)
Clammy/sweating palms and feet
Aggitation ( during an episode if someone was talking to me I wanted to really yell at them 'Just shut the **** up! You're doing my head in!)
Feelings of madness (actually wanted to run away from my own mind)
Pins and needles/Tingling in my hands and feet
Electric shock like surges going through my body (my nerve endings were obviously suffering)
Muscle tremours/shaking (mainly arms and legs)
Eyes became extremely light sensitive
Heightened awareness of sound

Insomnia
Terrible nightmares
Depression
Feelings of detachment from the real world.
Visual disturbances
Episodes of blurred vision

These symptoms did not appear straight away but appeared gradually and with more veangance the longer I had the coil. The more concerning episodes I experienced happened after about 3 months and very erratically. I could not predict when or what time of day I was going to have an episode or pinpoint any reason for bringing on an attack. I had no control over the effects, was absolutely petrified when I experienced a panic attack and just had to ride it out.
All my G.P. did was prescribe me anti-depressants to which I reacted badly. Blood tests also failed to show anything abnormal.
I even tried herbal medicines as an alternative and experienced similar reactions to the prescription drugs. I've now become very pill-phobic and would rather ride out and get over symptoms myself. Paracetamol & Ibuprofen being the only medicine I trust to take now. I had a horrendous year and everyone suffered. Not only my family, but I was signed off of work for 3 months. It was a very worrying time for my husband and my children, who all had to keep an eye on me and witness the effects of my symptoms. On looking back now, I don't know how I managed to function at all and even do my job. Most of the time my energies were spent concentrating on trying to appear normal and held-together to the outside world.
Although I feel 100% better in myself, I noticeably experience more migraines and headaches than I ever did in the past, along with palpitations, usually during my week before. Two days before it I often really feeI like I'm losing the plot! I also really bloat up now a week before my period, feel sick and have a feeling of being ' very full', so am hungry but don't really want to eat. One of my big toe-nails has gone black over the past few months and not through injury. This has just been sent away for analysis. The one on the other foot is raised/ridged/thick/yellow, but normal growth has resumed half-way up now, which I feel co-incides with the state of my health on having Mirena removed. The nurse I saw recently explained that it is true that nails and hair show the history of our health so, for me, this would seem true.
I wish I'd been made fully aware of all possible side-effects of this medication and am now actually concerned that the effects I've suffered may have left some permanent damage.
In spite of all this, it's so good to be me.

LOL- EVERYONE! I'M SITTING HERE SEARCHING FOR SIDE EFFECTS FOR MIRENA AFTER REMOVAL. I HAD MIRENA FOR 1 1/2 YEARS, AND I REMOVED IT ABOUT 2 MONTHS AGO. I HAVE EXTREMELY HEAVY BLEEDING SO I FIGURED I WOULD SEARCH IF IT HAD SOMETHING TO DO WITH THE REMOVAL. WHEN I HAD MIRENA INSERTED, I HAD ABSOLUTELY NO PROBLEMS! THE ONLY SIDE EFFECT I HAD THE ENTIRE TIME WAS EXTREMELY LIGHT PERIODS FOR 2 DAYS, BUT I GOT THE PERIODS EVERY OTHER WEEK! WHEN IT WAS REMOVED, I FELT ABSOLUTELY NOTHING! NO PROBLEMS! I WAS IN SHOCK BECAUSE I THOUGHT IT WAS GOING TO HURT. THE ONLY REASON I DECIDED TO HAVE THE MIRENA REMOVED IS BECAUSE MY HUSBAND AND I PLANNED A TROPICAL VACATION, AND I DIDN'T WANT TO BE BLEEDING ALL THE TIME, SO I FIGURED-GET IT REMOVED AND GET THE DEPO ( I HAD DEPO FOR 9 YEARS AND HAD NO PROBLEMS, AND NEVER GOT MY PERIOD). WELL, HERE'S A FUNNY STORY!! THE REASON THIS VACATION IS IMPORTANT IS BECAUSE I AM CONSTANTLY DEPRESSED, ALWAYS CRYING, EASILY AGGRAVATED, LOST ALL MOTIVATION, LAZY-I STOPPED CLEANING/ COOKING, I DON'T GO OUTSIDE WITH MY LITTLE ONES- MY HUSBAND DOES, ALONG WITH EVERYTHING ELSE. NO SEX!! MY HAIR IS FALLING OUT , EXTREMELY BAD ACNE (RESULTING IN MANY TRIPS TO THE DERM. AND SHORT HAIR CUT), I SOMETIMES FEELS PINS AND NEEDLES ON THE RIGHT SIDE OF MY BODY FOR DAYS! I WENT TO THE DR. AND SHE SAID I WAS EXTREMELY OVERWHELMED, STRESSED AND DEPRESSED! I ALSO HAD A THYROID TEST. MY THYROID IS FINE, AND AS FOR THE MEDS THAT WAS PRESCRIBED FOR DEPRESSION- I NEVER TOOK THEM ( I'M NOT A PILL TAKER-CAN'T REMEMBER!) SO AFTER ALL A TROPICAL VACATION IS JUST WHAT I PROBABLY NEED TO SNAP ME OUT OF WHATEVER MY PROBLEM IS! WELL, AFTER READING THIS , ALL I COULD DO IS LAUGH!! YOU SEE, LOOKING BACK----IN THE PAST 2 MONTHS- I HAVEN'T CRIED, I AM FILLED WITH TREMENDOUS JOY WITH LOTS OF ENERGY. I TOOK MY KIDS TO THE PARK AND FOR LONG WALKS NUMEROUS TIMES. I CLEANED THE ENTIRE HOUSE AND IT'S STILL SPOTLESS, COOKED ALMOST EVERY NIGHT, I HAVEN'T HAD A SISSY FIT, OR FELT SOME TYPE OF ANNOYANCE YET, MY FACE IS CLEARER, MY HAIR HASN'T FALLEN OUT AND GREW LONGER. AND MOST IMPORTANT I LOST 34 POUNDS! ( 174-140). RIGHT NOW AT THIS CURRENT MOMENT I FEEL BETTER THAN EVER! MIRENA BEING THE CULPRIT NEVER ONCE CROSSED MY MIND. I SUMMED UP MY PROBLEMS TO BEING STRESSED FROM MARRIAGE, 3 HIGHLY ACTIVE CHILDREN AND RUNNING A BUSINESS. SO I SIT HERE IN MY GLORY AND CHUCKLE TO MY SELF THINKING ABOUT ALL MY POINTLESS NAGGING & CRYING & BLAH BLAH BLAH. AND I THANK YOU WOMEN FOR OPENING UP AND BEING HONEST BECAUSE I NOW KNOW WHAT WAS WRONG! THANK YOU.

My son has had asthma and allergies since he was a newborn, thanks to and undiagnosed RSV infection that led to him being in an oxygen tent for 5 days. Since that time we have had him on several different medications to control it. Mostly, just albuteral through a nebulizer. Controlloing it this way worked for a while but eventually we put him on singulair. My son who was always the smallest boy in class went to being the heaviest. He also had terrible nightmares about his teacher and really bad cramps and pins and needles in his legs and feet upon waking EVERY DAY. He even began walking funny because of it. He had stomach cramps and diarrhea. His grades were awful all of a sudden and nothing could keep his attention. He went from being an easygoing easy to please child to being aggravated by the slightest thing. He was always getting in fights with other kids. He thought noone liked him and he began not liking himself. I took hm to a hypnotherapist to try to ontrol his anger but that did not help. NEVER in a million years did I ever think it was Singulair until I heard about someone else having the same experiences. Needless to say I have stopped giving him his singulair and in only three days have already seen my easygoing son coming back. Hopefully his side effects will completely go away.

I have to admit I am dumbfounded. I "stumbled" upon this information tonight.
I am a very healthy and active 40 year old female with no health issues other than seasonal allergies and asthma. I went to the dr. 4 weeks ago for a sinus infection. I was prescribed 5 days of Levaquin (called a “Lev-pak”??). The sinus infection seemed better but the symptoms of that came back after 10 days and I went back to the dr. only to be prescribed a 2nd round of the same medication. Again the sinus infection seemed to get better and now a month later I went to the same dr. again today because the sinus problem came back but worse. Today I was prescribed a different antibiotic called Avalox. Since I had not heard of this drug I decided to look it up before taking it.
I now look back over the last month and am horrified that I have had these bizarre symptoms and here they are experienced by 100's of other people. And this is just one website, with people that took time to speak up. Just one. All of sudden I already feel better because I can explain so much. Not once was I warned about this drug either by the doctor or my pharmacist.
Everything I am about to describe I have either blamed on still being sick (and getting sicker from the presumed infection) or have blamed on other meds taken in addition for congestion, headache, stomach problems, wheezing, etc.

I have had ridiculous sleep patterns. I was either SO awake some nights that I felt like I could run 10 miles or SO exhausted by bedtime that I could barely walk up the stairs to get to bed. I have had extreme nightmares and dreams. In addition I have had at times practically NO peripheral vision combined with a blinding headache. I also had ringing in one or both ears that was very random. I seriously thought several times that I might have a brain tumor. I have had all these weird stomach issues. I have felt bloated and my abdomen area has been painful at times. I also have gone from either having bad diarrhea to being very constipated. My heart has raced at times both while doing physical activity OR sitting still. For about 3 days after the first round I had sharp pains in my left side (abdomen and arm). I have experienced bizarre hot flashes combined with being freezing cold minutes later with no fever at all. And last my right leg, particularly my knee and foot have just hurt at odd times (just waking up, walking up and down stairs, after sitting for a few minutes). All of these things separated seem so random so I never suspected Levaquin. Having read page after page…they are ALL explained.

I can’t tell you how much better I feel right this moment. I feel sane again. I will never, ever take Levaquin again and am so thankful I was smart enough to get information before taking Avalox, which would have been round three of this poisonous family of antibiotics. I don't know how long it will take for the Levaquin symptoms to go away but at least I'll know why these things are happening. Thank you.

hey. its great to see that i am not the only person going mad with the side effects of the pill!

I started taking Yasmin in august 2008 and stopped in January 2009. after 2 months i found i had slight leg cramps and very itchy calfs and underarms that turned my skin into tiny red dots after i scratched them. i also got extremely red and blotchy inner thighs. the constant itchiness and the fact that i felt disgusting, made me go see my doctor who put me on yasminelle. ive been on yasminelle for about 2 weeks now. the itchiness has gone but i have major leg, foot and arm cramps. its hard to point my toes and sometimes difficult to stand or walk. extreme sore pins and needles in my hands and feet are also an issue.

i know side effects are different for everyone, but why are doctors still prescribing something that will give so much pain to people.

im finishing this pack of yasminelle and then stopping for good. i'm only 18 and my life's just beginning. im way too scared to take the risk of staying on the pill! if this is what its like after half a year, what is it going to be like after one year. or even more.