Prevention symptoms and conditions

Until yesterday, I took 14 days of a 4 week prescription of 100 mg twice a day doxycycline for a tick bite rash. I rarely take any medication. The first week I just had mild side affects. Late in the second week I started to notice that I was becoming increasing anxious for no apparent reason. Even after hard exercise the anxiety seemed to be persistent as if an impending panic attack. Yet, I had no external reason to explain the anxiety.

After two additional days the anxiety seemed to keep ramping up and I began to get very dizzy when I moved suddenly or bent down to pick up items from the floor. The pressure behind my eyes also feel like it was increasing. I was afraid my blood pressure was spiking but in actuality it was probably either cranial pressure or simply an fight or flight anxiety response. I also experience some pretty vivid dreams.

I finally searched online and found no official symptom of anxiety for doxycycline but found people complaining about it unofficially. I spoke with my pharmacist who also said she had no listing of anxiety as a known symptom for the drug. She suggested I stop taking it and see if my symptom subside.

It has been 24 hours since my last dose and the anxiety has reduced substantially but not completely. I feel like I have a hang over today but otherwise I do feel an immediate improvement. I am still a little dizzy but not like yesterday.

Like all drugs, you should be very cognizant of how the drug affects your body - even if a physician tells you otherwise because only you can really tell and everyone has different bio-chemistry which reacts in different ways to different drug compounds.

I'm taking 2.5 mg twice a day for migraine prevention and chronic daily headahces, and it works great. I would much rather deal with the mild sedation it causes than the pain I was going through. I can get out and do stuff more often now. Before klonopin I was laying in bed crying from the pain most of the time. Anyone who says they would rather deal with the headaches than the drugs has not been in as much pain as I have.

Hello to All
I'm 33 yr old female who began taking Topamax 2 years ago, after diagnose with Pseudotumor Cerebri,(elevated intracranial pressure),doctors still don't know why i have PTC, it is common overweight women, certain medications, secondary to disease, which all did not connect with me as I was not overweight, have never taken any medication, other than OTC allergy or pain relievers, and all secondary diseases I was tested, and nothing, with a history of migraines headaches, that suddenly became unstable, with vision disturbance I was put on diamax, it lowers elevated intracranial pressure, finally help for this horrible headaches, , I had a side effect it elevated my glucose levels to dangerous levels, due to elevated intracranial pressure I was hospitalize, undergoing several lumbar punctures and eye surgery for decompression of my optic nerve, doctors still unsure of my diagnosis, but telling me I must have surgery for a spinal fluid shunt, I was terrified, I decided to try and consulted with another neuro ophthalmology who had a totally different opinion, I switch doctors and this is when I was prescribe TOPAMAX 25MG to start, now I'm taking 250mg daily, at first the fact that I was going to be OK, that I can continue my life without shunt, no more lumbar punctures, the fact I was not loosing my eye sight, I can go running, rock climbing, after been told I couldn't, I was convinced TOPAMAX was a miracle. The 1st side effects constipation; decreased sweating, drowsiness, dry mouth, loss of appetite I lost about 20 pounds, family friends were really concern, after a while I gain it back, numbness, tingling, I was ok with it, because I no longer had debilitating headaches, had perfect vision, surgery was out the question. and I was stable, but then I suddenly experience seizure, 3 different occasion, no explanation, severe joint leg pain, trouble with speech, bruising, light sensitivity, severe acne, irregular menstrual cycle, vaginal issues, anxiety, heart palpitations, and the worst one yet, the reason I began to search on line mood swings, I'm in the medical field and the people that I work with tells me I'm just getting older, depression, 1st sings of menopause, I'm very active healthy women, with normal daily stress 2 children and 16 years marriage, I have seen my family doctor, had blood work done, and all normal. I have told my neuro about my experiences, and he says is not topamax, my ob says take birth controls it might help, im just lost any one suggestions?

Do cholesterol lowering drugs do any good? Thats a good question considering the debilitating side effects everyone here is complaining about.
Advertisements in the USA claim "30% reduction" in heart attack and strokes, but does that mean that everyone that takes the drug reduces their individual risk by 30%. Not exactly. The advertisements boast what is called relative risk reduction. The absolute risk reduction is what counts and is less than 1% on most statins. So how did lipitor do on prevention of events? Here is the bottom line: If you are a middle aged male, 100 MEN will have to take lipitor for 3.3 years to prevent one MAN from a heart attack or stroke. WOW! You have to treat 100 guys for over 3 years in order for one guy to benefit.

I had been taking Wellbutrin XL 300mg for a number of years with great results I told all of my friends how great it was. Then when the generic Budeprion XL came out my insurance company automatically filled my Rx with it. The nest time I saw my Dr. and was to get a new refill he didn't even know about the generic. I guess I have been taking the Budeprion XL for almost 2 years, since it first became available. I started noticing brain fog and as time went on more depression and anxiety, no zest, frumpy, and just not feeling like I used to. Last June when I saw my Dr. I asked him if a patient could become tolerant of a drug after taking it a while since I was experiencing more depression. We talked of HRT as a thing to try since I was experiencing perimenopausal symptoms as well. However I was faced with a cancer scare a week after that appointment and all thought s of HRT went out the window for me. I received the Prevention newsletter this am which contained the article on Wellbutrin XL vs the generic. I am upset that this can be happening, but also happy to know that there may be a solution to my problem as simple as a change of my Rx.

I was prescribed Topamax for prevention of migraines, since they are getting worse, and my usual meds didn't seem to be doing the trick.

I only took it for 9 days at 25mg dose (1X per day) and at day 8 I awoke with the most HORRIFIC back/side pain, I could hardly stand. It worked for my headaches, but now I still have back pain, and I have to call the doctor, as I am showing serious signs of KIDNEY DISTRESS.

To the best of my knowledge, I did NOT have any issues with my kidneys before taking this med, but I may now. I was told about many of the side effects, but NOT this one. I sure hope this drug hasn't pushed me into some kind of renal failure. I would rather deal with the migraines any day. Thanks, Topamax!

Hello-
I am here to share my story about topamax in hopes that others may read this and not have to go through what I did. I went on topamax for the prevention of migraine headaches. It worked great to prevent my headaches but gradually I could not talk, I stuttered severely, and I have memory and other cognition problems. At my doctors recommendation I stayed on the medicine for about 6 months because he assured me that the stuttering would go away. I was in such awful pain that I agreed with him. Needless to say that 6 months was not me. I couldn't talk and I couldn't think. Now when I think back on it, I wish I had just endured the pain. When I went off of the medication I still stuttered. It was not quite as severe but it was bad. It effected my work, my personal life, and daily menial tasks. I could no longer communicate. I was devastated. My doctor was puzzled and said that he had never heard of this before. So to make a long story short I went to a speech clinic, bought casa futura techs small talk device, and tried some anti-stutter meds. My speech now, 2 years later, is much improved thanks to the smalltalk but guess what,? I still stutter. Manageable and not very noticeable to others at times but my speech has not returned to pre-topamax status. I looked into sueing the drug company to bring awareness about this issue but did not get much positive feedback from attorneys. IF YOU ARE ON TOPAMAX AND ARE STUTTERING, STOP TAKING IT. IT MAY NOT GO AWAY WHEN YOU DISCONTINUE THE MEDICINE. It is not worth it. You cannot put a price on speech. I don't care what the physicians desk reference says, what your doctor says, what the corrupt drug companies say. I know my experience and it has been a catastropohic effect from topamax. Find a different med if you have speech problems! Please, for your own sake. Thanks for letting me share my story.

Hello,
I'm a 38 yr old female who was prescribed Topamax about 8 weeks ago for Migraine prevention.
So far, the drug is working fabulously for it's purpose.
Here are the pros and cons that I have experienced:

PROS: No migraines. Yippee!, A small amount of weight loss. This did not happen until just in the last week or so. My mood has stabilized.

CONS: Flat tasting soda, Dry skin, Dry eyes, dry mouth, (drink LOTS of water to combat this). Blurred vision, bouts of memory loss and slurred speech, loss for words. Some of these improve as your body adjusts. Worst for me is that if I miss a dose or don't take it at the same time every day (50mg in the morning, 50 at night), I'll have middle of the night anxiety attacks or even amnesia.. short-lived attacks, but very terrifying.. I always think someone is out to kill me. But again, for me, it's short lived and it only happens when I'm not taking the meds on a schedule.

Overall, I am happy with the drug. I am not experiencing hair loss or tingling. I drink a TON of water because I hear kidney stones are common with this medication.
I will endure all of the above to prevent the wretched migraine....

I hope this helps someone...

Take care and remember, God can help in your healing.. ask Him for it.. :)

God Bless..

My 13 year old son took Topamax for 5 months for migraine prevention. The day he started taking it, the migraines stopped. We thought it was a miracle drug. After 2 months he was experiencing nausea and stomach aches for a couple days at a time. These then increased to 5 or six days of nausea and a couple days of feeling fine. He was prescribed medication to help with the nausea but nothing worked. On the fifth month he was in bed for 22 days straight. The neurologist didn't think it was the Topamax, but I insisted he be weaned off. After 8 days of no Topamax, the nausea finally stopped, the migraines returned. The migraines are more manageable than the constant nausea. So no more Topamax!

My doctor prescribed 25 mg Topamax every evening for headache prevention. I had headache and nausea for several days before starting the Topamax, then after starting the Topamax, the headache pain got worse and I also had pain in my back and ears. I did not get the tingling in extremities but noticed some decreased sense of feeling in my face for a few hours after taking the medicine. The pain got progressively worse then I became depressed and suicidal. I was convinced my life was so bad that I wanted to die. I take 100 mg Zoloft daily for depression and still feel a little depressed and was hoping Topamax would help with this, too. I took Topamax to help with headaches and depression and it made both much worse to the point where I was seriously suicidal. I stopped the Topamax after only 5 days and the pains and nausea have gradually decreased to the point where today I have been virtually pain free most of the day for the first time in 2 weeks. I read on the internet that there is an increased risk of suicide while taking anticonvulsants, but it's rare. I am convinced I am one of the very unlucky people who becomes suicidal on this medication. I have 2 beautiful children, a great job, excellent health other than headaches and depression, and plenty to live for. I still can't believe that less than a week ago I just wanted to die and didn't care about seeing my children and family ever again or ever getting back to my job that I love. It's so hard to believe a drug can cause that kind of thinking. I'm pretty sure my doctor doesn't think the Topamax caused me to be suicidal and has no intentions of reporting my case to anyone. I suspect it's not as rare as they say to become suicidal on this med, it's just not reported enough. I wouldn't be typing this if I were still taking Topamax because I would be lying in bed suffering in pain, sleeping, thinking about how good it would be if I would just die. I went for a CT scan of my brain soon after getting off this med and I remember thinking that I hoped I had a tumor or anurism so I could die. I found out today I don't have a life threatening illness and I am happy about that now and can't believe I was thinking such bad things only a few days ago. I hope doctors take more care in prescribing this medication to people who have a history of major depression because I'm afraid people are going to feel like I felt and kill themselves on this med. I think this drug is great for some people and should be available, but people need to be warned that they may become suicidal and given instructions on what to do if that happens. I had no idea if I should go to the ER or call someone or what, so I just got people to watch my kids and called in sick to work and stayed in bed for a few days. I don't miss work often and am very committed to my job and my children are first in my life, so not being able to care for my kids or go to work made me feel so much more depressed. My doctor referred me to a neurologist and I hope to find some way to get relief from the head, neck, and back pain and the nausea. A few days ago I thought I would kill myself if my doctor couldn't find what was wrong with me and I felt terrible for no reason. Now I have hope. It's just not right that a drug can take away the ability to have hope.

i just started yasmin yesterday, and from reading what you guys wrote yay bigger boobs!! and prevention from pregancy!! thats more along the lines all im really looking for? will this happen for me and maybe even a bit of weight loss??! not too much tho

I just wanted to comment to all of you asthma sufferers. I grew up with bronchitis and my brother with asthma. We were always getting sick while young, about every 6 weeks. My nephew inherited asthma from my brother, and he had it very bad, was always getting sick, needing oxygen, etc. While in his teens, someone told him to start playing an instrument like the trumpet or trombone which really exercises your lungs. He started taking lessons in school and it didn't take very long at all to notice a remarkable difference. His other siblings would even get sick and he wouldn't! The exercise, being natural, is a far better and healthy prevention, and makes your lungs stronger. I can't believe doctors don't spread this amazingly helpful advice around. I'm VERY sure they must have heard this before. Wouldn't news like that spread like wildfire through the medical community? But they would probably lose some business!!! So I wanted to help pass it around. I hope it helps some of you!

I am 23 and just completed my series of Gardasil. The first shot hurt right away but the pain subsided a few hours later and I had no other reaction. I had the same occurrence with the second shot. I just had the third shot 3 days ago. The day after I had it done I experienced significant pain in my arm, collarbone and shoulder, chest pain,chills, headache, fatigue, stomach cramps, and swelling in my arm. I could barely lift my arm to do anything. I had the same symptoms the 2nd day and today I am experiencing a low grade fever, muscle pain all over, extreme fatigue after plenty of sleep, headache, chest pain and heart burn, swollen glands and throat pain. I am pretty sure this is an effect of this vaccine. If I would have known sooner I would have not finished the series. I would advise anyone out there looking into this vaccine to NOT go through with it. I have an appt with my doctor tomorrow to discuss this.

I have been on Cymbalta for about 6 months now and I have had to learn to live with at least 7 days a month of yeast infection symptoms. I know this is a side effect of Cymbalta, as I advocate against using medication whenever possible. I have only had this condition since starting this med, and over the counter creams and suppositories don't affect it or help at all.

Has anyone else had this? My doctor does not believe there is a link but I know this to be my truth.

I got Mirena put in on July 5, 07...never had a child but Dr. said since I was 36 and not planning on having children, Mirena was a good alternative to the pill which I had been on since I was 19. On the pill I had very light 2-3 day periods and with diet and exercise, could lose weight. Now, almost a year on Mirena...the only good think that has gone away from when I was on the pill is the migrane headaches that I was starting to get on a monthly basis...but, in their place...I have gained weight, tired, have acne, cramps erratically throughout month, never know when my period will show up...some months it does not, some months it lasts 4 days (like last month), and I always feel bloated - esp. in the abdomen. I've even wondered on occasion...am I pregnant?? why do I feel so bloated?? One other weird thing, since I started running this year, I get this weird sensation that I have to go empty my bladder...this also occurs while doing intense stomach crunches...but it is not incontenance..nope never have bladder problems...it is just this funky feeling - sometimes almost a burning feeling around my uterous. Have not seen anyone post this - but it did not happen before Mirena when I ran or did sit ups...now it does - doubt this is coincidence.

Some of these symptoms truely could just be simply the result of ovulating again - that is what my Dr. told me...that on the pill I never released an egg...so now my body was getting used to ovulating again. Well...if that is the case, I just can not stand it anymore...I get it removed June 26th - next week so hopefully I'll be able to post back that these symptoms are gone or have removed. Going to go on the pill again...which has its own side effects...but I sure did not have as many when I was on it. Husband has offered to go under the knife to take care of him...but I'll see how the pill does again. Hoping to reclaim my life and actually lose weight as I've been dieting and exercising while on Mirena to no avail!

HI I AM 37 YEARS OLD AND 1 WEEK AGO I WENT TO THE DR FOR HEADACHES EVERY DAY, AND MY DR TOLD ME IT HAD TO BE DUE TO STRESS, BECAUSE MY BLOOD TEST AND PAP SMERE CAME BACK NORMAL AND I WAS PERFECTLY HEALTHY. SHE PRESCRIBED CELEXA AND SAID THIS SHOULD HELP. ALL OF A SUDDEN I HAVE NO SEX DRIVE, HEADACHES, NAUSEA, DIZZY, LOSS OF APPETITE, SHORT OF BREATH, MOUTH IS DRY, VERY EMOTIONAL, MY WHOLE BODY ACHES. IM GOING TO THE DR. AND HAVING HER TAKE ME OFF I WOULD RATHER JUST HAVE THE HEADACHES. DOES ANY ONE ELS HAVE THESE SYMPTOMS?????

i'm 17. I have extremely bad asthma. and i've had it all my life. i remember being 3 taking nebulizers. i don't know it had gotten better, worse or stayed the same over the years. but i started taking asthma preventers medications because it was really out control. i have horrible allergies all together (which really is all asthma is) but little, tiny things will set asthma attack off instantly, like a short breath from under my bed or even steam from the dishwasher o_O. so i needed to go on preventers. i went from prevention inhalers, pills then finally advair.(and no doubt it works the Best) i was still kinda a kid at the time so it was 100/50, im to young to remember any side effects. but 100/50 wasn't cutting it, so i went to 250/50 , im still on it today. its hard to notice rashes, sinus, mental etc, problems because i have soooo many other allergies. plus im taking medications from them to.
i'd say im pretty healthy though, despite asthma i still play sports and i don't have to use my inhaler THAT much when i take advair it does work good, and i don't really notice all the symptoms/ side effects mentioned in the other comments, its a very good possibility some people are just allergic to advair, i was allergic to some meds i was on, plus, advair is a drug. Every drug Will have some kind of side effects unless its all natural. i question albuterol, i'll find myself reaching for puff when i don't even need it. O_O ! even with the new cfc free inhalers they have out.

Hi all. I'm posting again after being off Advair for about a week. I've noticed a dramatic change in my emotional health. The anxiety that I've been suffering from for the last three months while on Advair has now entirely vanished. I feel like my old self again, and friends and family have also noted the difference. I won't ever take this medication again-- I'd rather deal with my asthma in a preventive way.

I was prescribed Lamictal strictly for migraine prevention. I'm up to 200mg/day and have been for 3 or 4 months now. I honestly don't think I see enough of a reduction in headaches to justify the breakouts. It's not severe but irritating to always have a couple of pimples when my skin is normally clear. Additionally, my skin is remarkably DRY, despite the acne.

I began Topamax in August after 6 months of ongoing severe migraines. They stopped immediately. My DR had warned me of weight loss but I thought who cares? I weighed 130 at the time. I have had a fatigue problem for years so I really can't attribute that to Topamax. I did become very sick (exhaustion-couldn't get out of bed) after Christmas and had my DR take my ANA which was 1280 (high). I have also experienced hair loss but I did not find that on the "side effects". I called the hot line to see if there were other reports of affected the ANA count and they had no data on this. Has anyone else had this experience? Meanwhile, it is 8 months later, I am down to 96 lbs and worried, have lost all fat & muscle - no migraines!

Thank you so much for all the information! My son was prescribed Singulair pills this fall. He has been taking them for seasonal allergies and we had no problems. These were the sample chewable kind. Then came the pills... Unfortunately I did not see the news or read the article about the side affects of Singulair. Within 4 days my happy well adjusted 10 year old had serious sleeping problems along with stomach aches. He will wake up screaming and crying and cannot tell me what is wrong. He said he had a nightmare but doesn't remember what it was about.

My husband was away on a business trip when I started him on the medicine. He came back to a very unhappy and sleepy child. I asked my son what he was scared of and he asked me to tell daddy that he does not feel safe while he is out of town. He can't sleep unless he is by one of us. He's not safe. His bedroom is 15' from our bedroom! He loves his doctor and begged that I call Dr. Becky so he can talk to her.

I could not take this anymore and started thinking about what was wrong. I went through all his activities, friends he's played with, school problems, anything! Then it hit me, effects of Singulair!

Wow, what an eye opener. Fortunately my husband did not have him take it this morning. He will not be going back to this medication. Ever!

Thank you for the information once again. I hope everyone's child gets better. Everyone wants a happy well child. No child should have to go through this. They have enough pressure as it is without the meds making things worse.

Maeri

I have been on Topamax for a year. I am on a low dose of 25mgs morning and night for Migraine prevention (instead of the Verapamil I had been taking for years). I am pleased with the results. No migraines. I do not drink soda any more due to the after taste but thats fine. I think I am a little more "hazy" in my thought process but not to an extent of it interfering with my life. I will see how I continue.

First time user of Niaspan ER. First night I woke up red-faced and puffy; later same night fiercely itchy. Took four baby Niaspan (81 mg) the next night 30 minutes prior to Niaspan...no further problems. I'm planning on trying to cut down on Niaspan to 81 mg, which my doctor wants me to take anyway. Trying to balance HDL & LDL levels.

I'm on Topamax, Atenolol, and Citalopram...all for migraine prevention. We added the Topamax to the regimen (100/day) about 6 months ago. The first 6 weeks were the worst for side effects, especially the metallic taste, tingling hands, 'stupid' feeling, and fatigue. However, I did eventually adjust, and the migraines did decrease in frequency and intensity. They were not completely eliminated, but when I still get them, I find that I can abort them with the 'rescue' drugs easier, and they don't last as long.

If you like soda's and are upset by the 'flat' and metallic taste caused by Topamax, there are some sodas that don't taste quite as bad. Coke Zero and Diet Pepsi Max seem to be a little more carbonated and have a 'zingier' taste. After about 3 months, some of the carbonation 'feel' came back and I could drink things like beer again, without it tasting like I was sucking on a rusty nail.

I use to get the 'stupid' feeling to for about the first 2 hours after I took my morning dose. I couldn't remember words, and would forget what I was talking about in the middle of my sentence. I started taking my meds at 4 am, so that I had a chance to sleep the 'stupid' off by the time I got up at 6 and left for work by 7am. Then I'd take my evening dose after dinner, because my kids don't care if I'm an idiot...just as long as I'm not cranky :-)

When I have a migraine, I usually want to drive a pick-axe into my head, so all-in-all, these side effects aren't too bad in comparison, and make me a much more pleasant person to live with.

My 16 year old son took Levaquin 6 months ago and had a bad reaction to it. His symptoms were severe muscle weakness (he would get exhausted walking from the parking lot to a store and back, severe joint pain (in thumbs, wrists, elbows, knees, and ankles), dizziness (he felt like the room was moving away from him and would lose balance), and headaches (a severe pressure in the back of his head that was constant and then shooting pains in his his head that would come and go for no reason). I should say he was in top shape before this and wrestling in the 125 pound category. He took Levaquin to prevent an infection after sinus surgery.

Now 6 months later, his joint pain is completely gone except for his knees. They still hurt when he does squats and they are not good enough for him to go back to wrestling, but he can walk around pain free. His dizziness is also gone as well as his muscle weakness. His headaches are still there and still constant, but not as bad as they once were; however, he has had them 24 hours a day, 7 days a week for 6 months. He is on Lyrica which has helped make the headaches subside.

I have taken him to more than 16 medical doctors of all specialties, had multiple MRIs, CT Scans, blood tests, spinal tap, and an MRA. All come back negative. Thankfully, despite all of this, he still remains happy and positive that he will once again be 100% healthy; it will take lots of time, but he will get better. I know the first three symptoms (joint pain, dizziness, weakness) are clearly Levaquin related, but I haven't heard much about the headaches from people. Anyone else out there that has suffered from a constant headache after Levaquin? I REALLY want to hear about headaches from others!!!!

By the way, we have filed a medwatch already. I also know that Levaquin is not approved for anyone under 18 years old and he never needed such a powerful drug to prevent an infection, but there is nothing I can do about that now except to warn others. One of his UCLA doctors wants to write a case study on him to make this more known to others and I am helping him with that.

If anyone has questions, please feel free to ask. If you have had a headache from Levaquin, please let me know where in the head the pain was, if it is constant, what it feels like (pressure, shooting, throbbing), how long you have had it, and what, if anything, helped. THANKS.