Duration symptoms and conditions

I'm 23 and more than halfway through my first month on Loestrin. It's been absolutely horrible. I have terrible insomnia, nausea, acne, food tastes different, and as a result I have no desire to eat. I have been extremely moody, depressed, and dizzy. My sex drive has actually decreased, and I am NOT happy about that. My period lasted 10 DAYS (as opposed to the usual 5), and I had worse cramping this time around than when I was not on the pill. I also bled very heavily for the duration. I took Ortho a couple years back and had no side effects other than mild headaches the first month. I do not even want to wait to see if Loestrin levels out. I'm terrified to stay on it.

Last December I was also prescribed Doxycycline Hyclate 100mg for mild acne. I am 17. After a few weeks of taking it my acne appeared to have been getting better and I felt quite relieved. However, after about a month and a half of taking it, I woke up one morning with what felt like extreme heartburn. My stomach felt like there was a lump in it and in the middle of my chest where the esophagus and stomach connected, there was extreme pain whenever I swallowed anything. At first I thought this was just due to excessive acid in my stomach, but as it turned out it was the medicines reaction to a virus/cold I was getting -- the symptoms were nearly like an ulcer (which is what we initially thought). After stopping the medicine for about a month, I was fine and I started taking it again. Now it's been about the same duration of me taking it, and once again I feel as though I'm developing another case of what feels like extreme heartburn/an ulcer. Has anyone else had this problem?

Sorry to post again, but NO ONE REPLIED TO MY POST!

I am 5 days post removal and need reassurance. Unlike everyone else, I have NOT felt better right away. I am just as tired (if not more), more irritable, and JUST GOT ACNE on my face and arms 2 days AFTER removal! I'm still dizzy and the brain fog is just as bad. Have not bled a drop at all.

I know everyone is different, but my removal experience has been completely different... don't feel better, no bleeding/clots, no immediate improvement. IS SOMETHING WRONG WITH ME??? Was it not the Mirena after all???

Hi...I've been on Topamax since October of last year. I take 50mg. in the morning and again at night. I haven't noticed any real significant decrease in the migraine frequency, just in the duration. Whereas sometimes I'd be in bed for an entire day, sometimes 2, now they only last until the early afternoon. A big plus. However, there are some side effects that I just can't live with. The dry mouth is a pain in the butt but that I can deal with. What I can't deal with is the almost complete loss of my short term memory. It's so bad that I will ask a person the same question numerous times in a 5 minute time period and have absolutely NO recollection of having asked the question previously. I have found myself walking down the street and not known where I am. I dial the telephone and not remember who is going to pick up on the other end. And I'm dazed and confused on a good day. On a bad day it's worse. I can't live like this. So...I was wondering if others had the same awful symptom that I'm experiencing. I have others that bother me but that one is the worst. Also, how do I wean myself off of this medication? Thanks for listening.....D.

Well I have looked at a lot of web site for information about birth controls and this one by far seems to be the best. I'm 22 years old and have been on and off birth control since I was 15. So far every one I have tried has caused either nausea or Sever Break through bleeding. Last November I decide to give the depo shot one more try, for the first month I had no break through bleeding. But in December it started and never stopped, here it is April 30 and I experienced maybe 5 days during my duration of the depo shot no bleeding. So I went to the doctor today because I have come to realize that my body may need a higher dosing of hormones so she prescribed Femcon. Now in the past I have had the same problems that have been posted on here but when I was not on birth control! Birth control, controlled my symptoms a little but never stopped them. So im hopping that Femcon control that awful breakthrough bleeding I experience with many other contraceptives. At the end of my pack im going to update! Todays day 1

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

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

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

NO SIDE EFFECTS: POSSIBLE HELP WITH SUPPLEMENTS had very serious sinus infection. two weeks of anit-biotics with no result, symptoms got worse, before taking levaquin for an additional two weeks. within three days was back on my feet. i previously have taken the supplement MSM for continual joint pain in past years, and was pleased to find a wide array of other health benefits from taking it. Having two kids, building a home and busy work schedule led to neglect of my heath supplements. (not smart) Resulting in immune dysfunction, chronic sinus infections over the last two years. After realizing that my health was was in ruins, i decided to start taking my supplements again around the time of my course of levaquin. started taking my multi's again and more importantly my MSM ( similar to chondroitin or glucosamine) Note: I recently read that MSM has been proven to help the body fight infection, as it is required to be present for the body to fight infection. MSM is simply (organic sulfer) found in everyday food we eat. with processed foods and preservatives this element is removed. To make a long story short, after first taking levaquin, I did have some minor joint and back pain (among other things) started taking MSM and effects were diminished, and then gone. After reading what others went through, i made the correlation between the two, and with my previous history of joint pain i would think that i would be a prime candidate for these symptoms. It worked for me, it may work for you, and the worst case scenario is that is doesn't work but you become stronger and healthier from taking it. Brief History. I use to love to play basketball. after joint pain and swelling could only play once a week, and couldn't even walk up stairs the next day. after taking MSM continually for a couple of weeks i was able to play daily, for as long as I wanted. a true miracle. The good news: its at the health food store, it's really cheap, and its a completely natural supplement. take 1000 mg daily with meals or without. its worth a shot for no symptoms.

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 was prescribed this Levaquin antibiotic for 7 days duration. Day one I started feeling nausea, fagtige, my brain just thinking weird stuff. I thought it was my sickness. Day two my condition was took a deeper turn: I couldn't sleep, I was so hot (inside my body) took off my cloth ran around the house like a crazy person, even thought it was cold in the winter. I started thinking of suicidal, depression. my heart beat was pumping so fast, I tried to calm my self down by listen classical music, that didn't help either....I went to emergency room, doctor prescribed me a different antibiotic...that medication still affect me today...I still keep the bottle to remind myself of that medication...long story short..

My wife has sinus infection. Her doctor prescribed Levaquin. She took one last night (08/12/08), she couldn't sleep, headache, nausea...etc. I warned her many times before about this medication, but I didn't realized she taken the medication or bought this medication...

THIS IS A SERIOUS. LEVAQUIN IS A BAD MEDICATION. STOP USING THIS LEVAQUIN NOW. we need to organize a group for FDA to prohibit this medication for good. Even class action sUit to stop the company from manufacturing this medication. If anyone knows how and where to go about these, please let me know. This is for real, our health is more important. Thank you !!

i was giving the "free sample" packet of Femcon Fe by my ob-gyn to help with the irregularities of my periods due to PCOS.from day one its been a major pain!a headache and insane nausea!it was awful...and this trend continued non stop through the entire 3 1/2 weeks of use.headache nausea fatigue moody tender breast heartburn...heck...i began to think i was flipping pregnant and took a test to reassure myself i wasn't and that this birth control pill was just really working me over. i know one must allow their bodies to get used to the b/c...but this was ridiculous! i finally threw in the towel last night and stopped taking them.in my third week and already i'm spotting with incredibly bad cramps nonstop.makes me think something is seriously wrong...wait i know..its this freaking pill! i think there is a hidden agenda to these pharmacal companies handing out free samples of b/c....using you as little test subjects without being up front about how bad the effects are on the body.heck...i was foolish enough to be convinced....a minty chewable birth control pill.AWESOME!...cha! they should include on the packaging"This product has the tendency to totally annihilate your sense of comfort during the entire duration of consumption".screw this pill...i'd rather deal with the side effects of my last pill which is like cake and ice cream compared to this one here!

My 7 year old son was put on singulair 7 months ago and the behavior changes that have since occurred are incredible. While he has always been temperamental it was never to this degree. The most minor situation can cause an outburst that will continue for 30 minutes or more. Some days the rage and tears are endless. My older son was on singulair for years because of his asthma with no problems. I am so grateful to have found this site and information. I took my son off the singulair 3 days ago and I am hopeful that things will start to improve.

My profile: I'm 31. Asian. Never had BC before this. Have 1 5yr old son. The type of person that would 4get to take the pill if need to do so everyday. Been on Nuvaring for 6 months now.

I read thru the post here and was intimidated, but I have to say it's working out better than I thought. I didn't notice any serious side effects like blood clot, dizziness or weight gain. Though, I noticed now I have shorter and shorter period duration as the month passes. Now, it's just 1.5-2d where it used to last me 6d: 3 heavy, 3 light.

Another side effect is a decrease in sex drive and being dry... but since my husband is aware of that he help me be stimulated and give more fore-play time. Also, we make sure to stock up on lubricant.

Overall, I can compromise with the side effects that we observed so far, therefore it's not a big deal. The relief of having to worry about unexpected pregnancy is certainly outweight the little inconvenient side-effect that Nuvaring has on me.

I've been on Lyrica 75mg 2x/day for Fibromyalgia for 1 1/2 wks. I was on Neurontin for 4 years before trying this new med. The side effect that I'm hoping goes away soon, is around 3-4AM every night that I take Lyrica I wake up to pee and when I lay back down when I close my eyes the room spins like crazy. It's exactly like a night drinking in college but I haven't touch any alcohol in months. The 1st few days that sensation did not go away until the afternoon, but now it's usually gone by the time I wake up to go to work around 7AM. Hopefully it'll just keeping shorter in duration. Other than that side-effect it does quite a good job controlling FM pain.

Here is some perspective for you all. I take Singulair and do well on it and in ACTUAL studies it has one of the safest safety records. Understand that post marketing reporting does not mean there is a correlation between the event and the product. Throughout the life of a drug the companies must disclose any report of side effects reported to them REGARDLESS of causality. A popular antihistamine that is OVER THE COUNTER also has suicidal thinking/behavior listed in its post marketing section. However, just because patients who had reported having these thoughts while taking the product doesn't mean it was a result of the product! Maybe they had a depressive personality and were also on multiple other medicines to treat that. You must look at the "Adverse Reactions, Warnings and Precautions" sections of package inserts to see the side effects that were actually seen in studies. You can die from ulcers derived from over use of aspirin or ibuprofen. Decongestants can throw off your blood pressure and these events are documented in actual studies! Listen to your bodies when taking any med. If you feel differently report it to your doctor.

These are all drugs people, there are potential side effects. There are also side effects to those "natural" over the counter remedies that are not nearly as regulated by the FDA or studies by the drug companies.

To anyone out there who has experienced side effects to singulair timed to when you started it, talk to your doctor, stop taking it and see if it goes away. Same advice for any product prescription or over the counter medicine. Side effects can be a combination of many factors (what other meds are you taking?) But understand for many people this product is the safest and most effective treatment for them. The FDA and Merck are reviewing all information to see if there is any correlation to the reporting. But singulair been around for about 10 years and prescibed to billions of people and is known to be one of the safer medicines out there overall.

In between the legitimate posts on this site I get the sense there is a lot of ambulance chasing going on. People looking to cash in on this big drug companies. We want drugs, we want them cheap and with no side effects which is not a reality. Keep stepping up the regulation and make the companies hire more lawers to protect themselves and jump through even more hoops and see what happens to the price and access to new meds. Even better, see how regulation has impacted the development of new medicines around the world (here's a tip, it will dramatically decrease). Drug companies certainly aren't perfect but which industry is?

Please, when taking any medicine over the counter, prescription or herbal supplement listen to your bodies to see if the potential benefits of the product outway the risks or side effects. Report any changes to your doctor.

WOW! I guess I will consider myself one of the lucky ones after reading all of these side effects posted here. Let me first say that I have tried many inhalers -- serevent, flovent, ventolin etc etc -- and the asthma kept getting worse. Then my doctor suggested Advair. I've been taking it for several years now. I knew that all medications have side effects and I read through the list carefully. The medicine was a Godsend! It helped me so much that I would have recommended it to most anyone. Recently, however, I've started having the occasional heart palpitations and recurring sinus infections. I'm beginning to wonder if it is time to move on to another drug. I'm in my early 30s and have been trying to conceive for a few years to no avail. I recently read that Advair can cause irregular cycles and now wonder if it is playing a part in my fertility struggles. Only other symptoms I have are tooth sensitivity and occasional leg cramps -- however, these existed prior to starting Advair; they might have become more prevalent but I don't believe Advair caused them.
I'd like to hear from anyone who is currently trying Asmanex...that might be my next drug.

I was given Cipro 500mg twice daily for a UTI. After 4 days on the medication I developed severe joint and tendon pain. Every joint in my body was in pain! I have called the doctor and they had me stop taking the medication. I continue to have pain in my joints. By the end of the day, my knees are killing me! Will this ever go away. I am seeing the doctor tomorrow, I am so upset over this, I am in my mid-30's and am feeling like I am 80! I am a grade 1 teacher and have 3 young kids at home, I hope things will get better!

I am 56 year old New Zealander, had stent inserted 1 year ago.
Was first put on Lipex, after 6 months on that would have welcomed departure. Came off it voluntarily and problems went away.
NZ is too mean to provide Lipitor with out a fight, so after much cajoling my doctor finally got permission to provide me with it.

At first it was fine, but slowly the same symptoms as with Lipex returned.
I have every single symptom I have read about here.
Joint pain, short term memory loss, nausea, swollen ankles and by association I am getting pretty depressed.

I had to come off beta blockers for similar reasons.

Finally this week I have developed kidney pain and have decided that that is it.
Lipids are out for the duration, I am told that half an onion a day will reduce your cholesterol naturally, so that is where I am going.

Thank you all for providing me with proof that these drugs do not work for all of us.

I also experienced stabbing localized headaches for a few weeks after my Tegretol dose was increased from 100mg 2x daily to 200mg 2x daily. The pain was so severe that I would have to stop what was doing for the (albeit brief) duration. The pains usually radiated from just over one eye, but could occur from any point. They stopped completely after approximately three (miserable) weeks.

Tegretol was prescribed to help mood swings and agitation and I must say it has worked beautifully in conjunction with an anti-depressant to aid sleep and CBT. I wish I'd found this combination 15 years ago!

I suffer from chronic gastritis, not diarrhea, just inflammation, have taken this for sinus and upper respiritary infection. 250mg four times a day. It has helped me with alleviating the constant constipation I suffer from, but it has really made my gastritis worse, to the extent that I am having throat irritation through acid reflux now! Also felt shaky and weak about an hour after each dose, and so very tired, overwhelmingly tired and weak. Have completed the course, but would not wish to take again. I can't have Penicillin drugs because of allergy. VERY IMPORTANT, I was on a statin pill (Lipitor) and was told my the pharmacist to watch for muscle problems, after first day on EM my leg muscles seized up and were cramping badly, I stopped the statin for the duration of the antibiotic. If you are on statins, beware.

I have mixed feelings about Advair. Quick history-at 30 I was dx with Asthma, at 32-COPD. I went on Advair after the COPD dx. Primarily-it certainly helped my breathing-gloriously. I have since gone on and off Advair periodically. Before last year (Pneumonia)-I had not been on the Advair for more than four months. BUT the Pneumonia combined with the COPD reduced my lung capacity by 25%. I allowed my Dr. to prescribe it indefinitely. However within a year I had gained thirty pounds. I started reading more, and found out that the AMA recommends only a six month duration of Advair therapy. My asthma symptoms had worsened over the last three months of that therapy. My untrained hypothesis is that if you exceed the recommended six month treatment-you will suffer the above outlined side affects. I simply quit it. Granted, my asthma symptoms increased for about three weeks-so I kept my handy little inhaler nearby, and gave myself one month to see if the asthma symptoms would decrease. They did. The long term-I have now been off of the Advair for nine months, and I rarely use my inhaler (knock on wood). The long term benefits of the extended Advair use has been a decreased problem with SOB- yes upon exertion(that is one of the symptoms of COPD), it is still present, but I can usually ride that out with patience, and rest. In conclusion-I would not hesitate to go back on the Advair upon my next COPD exacerbation, but I will absolutely stay within the six month suggested period. And, this time I will eat a lot of lo cal foods. Smile. It is always nice when people with chronic illness can smile over their disease. This has been my experience over the last five years that I have been introduced to Advair. One more suggestion-see if you can get your doctor to try you on the 250/50 before jumping right on the 500. The 500 is noted to have the side affect of increased SOB, and Asthma attacks-more often than the 250. One more note-although your doctor might forget to mention this-Advair is a steroid- and, steroids are known to cause weight gain. What can be done to reduce this affect-I do not know-Prednisone will do it too,now a combination of the two-which I have, of course, utilized a half dozen times or so in the last five years of my dx- is almost a guaranteed weight gain. If you manage to find out how to avoid that particular side affect-please let me know, and suggesting a vigorous work out to a patient with COPD in a bit insensitive, but if you have any other plausible ideas-I am anxious to hear them.

Today i was proscribed with 50 mh prednisone ,5 tablets .4 times a day so that is 1000mg of prednisone a day has anyone had same thing .i was dyagnosed with optic nuritiritis.i am really scared to take this medicine and so many mg a day. please help!

I have been taking los dose (50mg) Trazodone as a sleep aide for about 3 months. Since the first week I have had horrible headaches, worse than any migraine I've ever had. These headaches are always one sided and cause hearing problems for the duration of the headache. Nothing,and i do mean NOTHING will stop these headaches except percocet. My Dr is having me do an MRI just to be sure theres nothing wrong in my head, but I honestly think its the Trazodone.

Biaxin Side affects were mild for the first four weeks. I've recently experience fast heart rate, headache, pins and needles in feet and hands, tremors in hands and the medicine isn't working on the infection. I will consult my doctor about stopping the use. The first four weeks were actually pleasant. No real side affects. I would take this drug again but only for a short duration.

I have been on mirena now for 10 months. I was on the depo for 10 years prior. I loved my depo adn only went off of it after Kaiser said I could not do it any longer. I was told that mirena was a god send and a lot like my depo. I can say that the combination of depo and mirena I have not had any period at all. but that is where the happiness ends. I have experienced moths of breast pain. it hurt to touch them let alone put anything on them. after about 6 months and numerous trips to the vet it disappeared. then I got a small rash on my neck and by my arms. went to dermatology and since then I have been there, or to my primary or an allergist every week since then. the rough severley itchy skin is constant. remarkably every 29 - 32 days it fades for 2 days or so and just when I am sure it is going away wham back it comes and each time it is getting worse and worse. having never had any skin problems before I believed the doctors tha tit was folliculitus, then they said dermatitus, then they said uticaria and then hives or the last straw i was causing it that it was in my head. i just got a new allergist and while she doesn't knwo if it is my mirena she can tell me I have histamine levels that are off the chart. my husband is allergic to a lot so we already use free & clear everything and my housse is spotless but I am still being told it is soemthing I am doing to myself. I have also been reevaluating my things and I relaize I have been experiencing a lot of numbness and joint pain. so much so that my primary sent me to a rhuematlogist and he ran every test for lupus, and many other diseaeses adn even cancer. I was going crazy. Iwas beginning to think maybe I was mental. I have since been researching mirena and I am finding it so much more than what the pamphlet says. I finally got the nerve to call my ob, adn she ahs since been researching things with me and we know for sure that no matter what next week I get my mirena removed. I am just feeling so alone and depressed. I am 33 years old and instead of enjoying my new marriage I am contemplating a divorce becasue I do not want him to be stuck with soemone who might be crazy. seeking support and anyone else who feels this way.