Medications symptoms and conditions

500mg 3 times a day for 10 days, vomited once, have had a horrible headache that started day b4 yesterday, still kinda have it, comes in waves, sux real bad lol

i have Sinusitis, Bronchitis, and a severe respiratory infection.

i see some guy on here mad cuz the doctor didn't tell him he would have bad headaches, like the doctor was going to know in advance he would. this anti-biotic affects different ppl different ways, its really not his responsibility to go over every single side-effect this very common anti-biotic is going to have, thats why the pharmacy gives you a huge pamphlet informing you on the medication, if you would had read it then you would see that headache, diarrhea, and constipation are all common side-effects

i didn't read it however, until i came here and read what i read, which is comforting really cuz at least i know why i have the headache so bad, and why i lost my lunch yesterday, was actually worried maybe i had an infection in my brain and thats why i had it, i know, sounds dumb, but what can i say, im paranoid lol

I am 40 years old and was prescribed lisinopril/HCTZ 20-25 a little over two weeks ago. I went in for a little congestion and low grade fever. I am a teacher and have many kids out with the flu, swine flu, etc. and felt that I needed to get checked. I came out with 5 medications, one of which was lisinopril. I have never had bp problems in my life. I am almost certain that the nurse practicioner wrote me down for something else and the dr came in and changed. I am usually a very calm person but in the last two days have experienced what I thought was a panic attack and anxiety, horrible anxiety. I haven't been able to face my students which isn't like me at all. During the first week I took my students on a field trip and had a really great day with them- much less stress than a normal day. I got home and my bp was around 138/98. I thought that was kind of odd. It has been under control since I started taking it. On this same day, I got blistered on my face and wasn't outside much at all. I have Rosea and thought that it had been aggravated. I believe now that it was the lisinopril. I know that it has a diuretic in it, but it doesn't make me go frequently. Instead I get a sudden urge and have had two "accidents" recently. I have a sometimes dry, other times full of mucous, cough to the point of nearly gagging. My neck muscles were already stressed out and tight, but have gotten worse. I feel a tightness in my chest constently. My lips are so dry that they peel all the time. I have no appetite and when I do eat I get nauseous and almost feel like vomitting. I have been lightheaded and dizzy. I am not sleeping and feel extremely tired all the time. But these last two days have been awful. I love being around people and right now can't stand the thought of it. I am guessing that lisinopril has caused much of these problems. I am about to go see the doctor today and think they will want to put me on some sort of nerve pill. I hate that!!!! I have a plan to achieve everything that these meds are supposed to. Exercise, change my diet, go see the chiropractor, do more relaxing things for myself and take better care of me! After reading these blogs I believe that I am going to take myself off of lisinopril and see what happens. My hubby is also on it and just last week developed an oozing sore and his left cheek - could be the lisinopril. I will pray for all of you bloggers and those who are unaware. This is definitely a poison to our bodies. I think I even read that it contains snake venom. Is this true????? I will update in a few days. Good luck and God bless!

I started on Ortho Tri Cyclen lo 4 1/2 years ago. About 3 months ago I went in to get my Ortho and was suddenly surprised by the low $7 charge since normally I pay $50(wonderful insurance). I was paying for the generic form(Tri-Sprintec) and for $7 I was all about it! Since taking it the only main side effect is HORRIBLE acne. I am 26 years old and have never experienced acne before.
My general doc told me to finish out the month and switch back to Ortho. He wrote a letter to my insurance company explaining his concerns for my acne and asked them to cover the cost of not only Ortho Tri Cyclen lo but Doxocycline and Defferin. Two medications that he prescribed in hopes to clear my face.
I have experienced larger ta-ta's too. Not that I'll complain about that one though. I've been an A my entire life....

I've been on Advair for 12 years.I'm 27 years old and fed up with all this medications that doctors prescribe.We are so brainwashed into thinking that we misbehave if we don't see a doctor.Let me tell you what: The majority of the doctors, only know to prescribe medication.They get bonuses from the pharma industries every time they prescribe their "new discovered"medicine.
Advair is supposed to be preventive, what you don't know it's for how long.Exactly!!!.....'cause it's not meant to cure Asthma, it's meant to keep you hooked for the rest of your life.
My worse symptom is a very fast heart beating.I'm a martial artist and every time i exert a fast burst of energy(while i'm sparring for example), my heart goes into pumped up mode.It beats very, very fast and i have to stop because it hurts.Sometimes i keep going no matter what and feel like i'm exercising for two people.When i stop, i breath very deeply for 5 minutes and all of a sudden it stops and beats regularly.
It's not fun, and one more thing: I'm from Argentina and my mom sends me the medicine from there cause it's way cheaper, sometimes i run out(i procrastinate sometimes), i'm left off with no medicine for a few days and boy.....I'm a wreck.The time you stop you go right back to where you started.I've been researching about an alternative to this "S***".I'm afraid 'cause i don't want to feel discomfort with my lungs anymore, but i strongly believe that there should be a natural alternative to all this laboratory drugs and i'm on a mission to find it.

I received prednisone intravenously at the hospital to prevent a severe reaction from receiving platelet transfusion. I have a bleeding disorder and IgA deficiency. Because of my bleeding disorder I have to receive platelet transfusion before any surgical procedures. When I receive the platelet transfusion 20 mins into receiving the platelets my face feels flush and a tightness and pain in my facial bones. I get a sudden headache with severe pressure pain in my head so severe that you feel as if your head is going to explode. My doctor recommended the use of prednisone to prevent me from having this reaction. 20 minutes after receiving the prednisone intravenously I felt my face turn flush with facial bone pain and a pressure around my face and top of my head. I felt the pressure in my head, but not the pain which I would get from the platelet transfusion. That night I had dizziness,severe headache,nausea,stomach pains,severe sweating,over heated,weakness and unable to concentrate. This went on for 2 days straight. Today is the 3rd day and I still can feel a slight pressure on the top of my head. I also felt eye pressure and I still have the headaches. I am schedule to see my doctor in 3 weeks and I will tell him that I will not take Prednisone ever again. I am sure there are other medications that can be given.

I have been on Campral for over a year now for OCD (nothing to do with alcohol). Apparently Campral has been shown to work for OCD, so after many other medications didn't help me, my doctor suggested it.

I take 666 mg a day. I've been up much higher than that, but higher didn't seem to make a difference, so I went back down. I am also on 250 mg of Lamictal a day.

Campral works very well for my OCD, better than anything else has.

The most amazing part is that for me anyway, unlike every other medication I've tried, Campral has had no side effects on me. It's like it's transparent -- very weird.

Who knows -- we're all different -- but I'd recommend it to people who have OCD and not found success with other medications.

Today is 10/28. I am Weezie1 and I posted on 10/26 about my severe drug reactions. They have gotten worse since I wrote my first post. The fever and chills are gone. But now I have been dealing with a rash/hives over all parts of my body. They are worse where close contact to sleeping clothing are - back, chest, neck. The one side of my face that I usually sleep on is purple every morning, along with that same side of my neck. I managed to get myself back to the doctor on 10/26 and am now on a 6 day dosage of steroids for the rash/hives. The steroids have stopped the hives from getting any worse. But it is taking awhile to go away. Any heat, anxiety, frustration brings them out again. I see I will be dealing with this for awhile. I go back to the doctor on 10/29 for a recheck. I lost 2 days from work because of this. My skin felt like it was on fire with hundreds of bee stings. Now I feel like I have a severe case of poison ivy. I have found some relief using Aveeno's oatmeal powder to do a bathtub soaking at night. Then I follow that with Aveeno's rich moisturizing lotion. The doctor may want me on steroids for longer than first prescribed.....not a med you want to be on for too long. All because of an UTI last week that could have been simply treated with a regular antibiotic if my doctor was not able to prescribe this sulfa drug to me on 10/19. Next time I will go with my initial gut feeling and refuse to take a medication when I see its extensive side effect list. I wish I had done so last week. I am suffering much more now than I was last week with my UTI. I filed an online complaint at the FDA's website. They mention it at their phone number that Weezie1 reported in my 10/26 posting here. I, unfortunately, expect to see additional patient complaints here every few days when I check back at this great medications site. And now I see that someone has internal bleeding. What next? A death? My blood pressure and heart rate were both increased for several days due to this drug. I could feel my heart pounding when I was sitting still and laying in bed. Thankfully, my BP is normally on the low side, but all the numbers went up by 10. We have to band together to get this crap off the market and out of the hands of doctors and unsuspecting innocent patients. Our voices will be heard if we speak in large numbers. Keep talking!Good luck to all.

I took aviane that is supposedly the generic version of Aleese.. which its NOT. Aleese was taken off the market and replaced with pill and they called it generic.
Well Aleese has don't wonders for some but when Aviane was introduced it was slightly different. Well, anyways..

I took it for a few days and don't say its not long enough. EVERYONE'S body reacts differently to ALL MEDICATIONS!
After my few days I was biting my fiance's head off and handing it back to him. Next day I was happy as a cucumber and days following I started to get a weird feeling. I felt itchy ALL OVER! And I felt short of breath a little bit and I HAD MASSIVE INCREASED ANXIETY!
I went to the doctor and they said I was having an allergic reaction to something. They couldn't figure out if it was the hormone in the pill or if it was the dye covering it.
NOW I have to go on the nuvaring to see if that does the something.

A few months ago I was diagnosed with a UTI and was prescribed Sulfamethoxazole (1 pill twice a day for 10 days). After a few days, my UTI was cured, but I continued to use the medication as I was instructed by my doctor and pharmacist. I had no side effects or allergic reaction for the entire period. However, on day 11 I noticed a small splotchy red rash on the right side of my body near my armpit. The next day the rash had spread to my legs, stomach and other side of my body. It was not raised and did not itch, so it didn't worry me. My boyfriends suggested that it might be a reaction to the medication, but the rash did not appear until at least 24 hours after taking my last pill. Five days ago, I became worried that I had contracted another UTI, so yesterday I visited the doctor again (a different one). She asked if I was allergic to any medications and I told her that I wasn't aware if I was. I did not think about the rash from a few months ago because I did not believe it was related to sulfamethoxazole. So she wrote me another prescription for the medication, but this time I was instructed to take 1 pill twice a day for 3 days. I took one pill around 4 PM yesterday and within 30 mins my entire body began to tingle and itch slightly. 2.5 hours later my face was bright red and severely hot and puffy. My eyes were as red and puffy as my face. Around 9 PM I began to chill and shake severely and I took Excedrin for a mild, dull headache. I took a warm shower, but I felt extremely fatigued and became nauseated simply from standing. So I got out with intentions of vomiting, but when I sat down in my bathroom floor I no longer felt nauseated. But my shaking became even more severe. I was cold, but also I was nervous and anxious because I felt mentally unstable. I have never battled depression, but I felt a slight bit of depression last night. I was very irritable and short tempered, which is very unlike me. My skin became so sensitive that I could not even stand feeling my boyfriend's breath on my shoulder. My body began to ache, specifically my ankle and knee joints, and it hurt to walk. I woke up around 2:30 AM with a fever of 100.4, so I took two Tylenol and the fever broke quickly, but I did not feel much better. This morning I feel a little better with no fever, but I still have slight chills and my whole body is red and itchy. Yesterday evening was a nightmare.

I have been reading all of your posts and I am surprised by what I am hearing. Especially the depression, loss of sex drive, and hair loss. I did check out their website (http://www.nuvaring.com/Consumer/aboutNuvaRing/possibleSideEffects/index.asp) and it seems they are actually pretty honest about the possible side effects. HOWEVER... although I checked the site before I started taking the ring 2 years ago, I kind of ignored the "possible" side effects as just that, "possible." Because I've never had any problems with medications or birth control before I didn't think they would happen to me.

Last week I 2 days late in putting in the ring and since then my breasts have been SO tender I can barely walk. Seriously, it's awful and I know it is the hormones from the ring. Until this point, I have had no problems with it, in fact I have really enjoyed its convenience and effectiveness. But after reading all of your posts I am wondering if I should rethink using it... I have been feeling really down, angry and anxious over the last few months and not really craving sex with my boyfriend like a 22 year old women should!! I don't want to over react and blame it on the NuvaRing if it could be other things in my life, but I also don't want to ignore it either because if taking the ring out would make me feel better, more healthy, less angry, etc...

What should I do?

i have a friend who went after her husband in a ctalsudden rage after starting the Lamital, she loss huge amounts of hair and it conytinues to fall out , was put out of her house,broke up her family and is a complete mess. She was on adderall, suboxone and the n the dr gave her this,i was trying to figure out what was going on with her and i looked up the newest of her drugs lamital and found out what was going on . Mt advice to all you bipolar people find GOD no one is ever happy all the time and we all go through really hard times . I am sober and take nothing for the last 20 yrs. When i first got sober doctor tried to tell me to take antidepressant, I said ," the difference between us is when all else fails i go to GOD and you go to meds"" YOU wont break. We live in a society run by drug companies that you are not allowed to have emotion, they flat line everyone.and when it doesn't work they give you more drugs till you are a blob of a person. Get off everything{ except if you need it for ceisures } It could take a yr to completely detox, be patient and go to na meetings

Just had to comment on these side effects I'm reading about Lipitor and other Statin drugs. I don't take anything and I never will after finding this site. Guess what, I have had high cholesterol since I was in my early 20's. When I say high... it ranged from 240 - 260...remember when 250 was OK? Well folks, it's 30 years later, my cholesterol is just about the same range, and Oh My GOD...I'm still here without any drugs.!!! They lowered the range so they could pass out the pills!!! Greed, greed, greed. Do you wonder why our Healthcare system is out of control? Well, when you keep feeding people medications that are presenting the side effects they do, making them sicker, they just keep testing and testing and testing for other things. Let's do blood work, MRI's, CAT Scans, Spect Scans, Pet Scans...Scan away...and guess what...all comes back OK...hmmmm why not look at the drugs you're prescribing. We need to see "all the side effects" listed. Not just some. They're misdiagnosing, Alzheimers, Fibromyalgia, MS, Lupus, Dementia, Arthritis, and on and on when it's been the drugs causing the diseases!
Ween off everything and anything you can...take your chances...when God wants you, he's going to come and get you no matter what you're doing...right or wrong!

I started taking 5 mg of abilify a few weeks ago. Before that I was taking 2 mg for 3 to 4 months. I also take 400 mg of lamictal and 20 mg of prozac. The prozac was very recently added.

Anyway, I have tried many different medications and apparently my depression is treatment resistant. Abilify has made me a cold, emotionless person. I have not cried in months. It is terrible when you feel so sad inside and you can't even cry. I have also developed a twitch in my eyebrow which is very hard to control. Most recently I have discovered, on my own and with the help of my mother, that I have akathisia. Although I mentioned a lot of symptoms to my doctor before, she claimed it was just anxiety.

But this is so much worse than anxiety. This is extreme anxiety, being unable to sit or stand still, getting anxiety with just the thought of having to sit still, getting urges to kick, feeling terribly restless inside unlike anything I've felt before, feeling like something terrible is about to happen...

I hate this. I don't know what to do. I'm seeing my doctor in a couple days and I'm just wondering what she will do. Will she take me off or will I get something even worse... will this go away..

My 16 yr old daughter had her series on Gardasil shots completed in March 09. I don't recall any major side effects right away. In the past three months, she has been throwing up after taking a few bites of food. She drinks a lot of Pepsi and has a lot of stress, so I thought she was developing an ulcer, so I told her to stop drinking pop for awhile to see if that helps. The symptoms have subsided, but now that I am reading this website, I am worried. Before the shots she had headaches or migraines, they run in our family, but I have noticed that she has them more often now. Another thing is her hair is everywhere. I thought she was damaging her hair with the straight iron, but geeze, now I don't know. All these problems might be tied to the Gardasil shot.

I have been on Methotrexate for about 1 year to treat RA. It has worked great for pain BUT I have noticed a lot of things going on that I've simply contributed to life. I have severe headaches, dizziness, extreme fatigue and major mood swings (depression and anxiety). I've seen some things posted on the internet about these being side effects. I am going to talk to my RA doctor and see if there is something we can do. I have been so bothered by these symptoms that I would just about prefer the pain to the constant feelings of irritability and depression. What are some other medications people are finding useful of RA with out the side effects????

I just got my Mirena removed today. I am SO excited. I have had it in for 1 year and it has been the worst year of my life. My symptoms were :MIGRAINES!- for which I was admitted to the hospital, they did all kinds of tests, and found nothing-( they even gave me an IV of morphine, and the migraine was so intense, i still felt it with the morphine.), arthritis- (or EXTREME ACHING in all of my joints, especially my hips, knees and lower back area., pain in my chest- like unable to breath, pain in my neck, I was sleeping 9 hrs a day and still exhausted and lately its been severe insomnia, cramping in my lower stomach and bloating really bad. I am 5"3, 21 yrs old, originally 107 pounds, and have two kids. After my daughter I was on Seasonique and although it made me have mood swings it was NOTHING in comparison to this. After my daughter I lost all the baby weight and then some. Even after I had my son in the 6 weeks before I got the Mirena, I lost all of the baby weight and was back down to 107 pounds. Now I weigh 130 pounds- and thats doing the same exercises and eating the same that I have always done. I have also never had ANY UTI's and I have had consistent UTI's since I have had it in, that have NOT gone away with various medications. I have had NO sex drive. Absolutely NONE, and I am 21years old! I felt very fatigued every day and it took all my strength and energy and mostly motivation that I HAVE TO provide for my family, to get up and go to work everyday. I read the brochure for Mirena when I got it inserted, and there were NONE of these side effects. I found some of these side effects on the Canadian website, and found people's horror stories of having Mirena in. I am SO happy to have finally gotten it out and am looking forward to being a normal healthy person again.

I had the Mirena placed in 2004 after the birth of my second child. I had weight gain, mood swings, hungry all the time (i would sleep eat), depressed, joint pain and was tired all the time. I eventually got it removed 3 years later and my symptoms got even worse. I was severely depressed, my sleep pattern was abnormal, my mind was fuzzy, couldn't concentrate, joint pain worsened and had absolutely no energy. I started itching and having tingling sensations and "bug biting" pain/sensation especially in my extrementies. It was weird. It stimulated a hormonal response that affected my central nervous system. I know it did. I will never be convinced otherwise. It was a shock to my system. There needs to be studies done in this. I finally drug myself to the my general practitioner 3 months later and I thought that I would get admitted in a psych ward. I was hardly functioning. No kidding. I had no reason to be depressed. My life was better than ever. I was not admitted, but I was put through the ringer for tests and my healthcare bills became outrageous. I had tons of blood work, sleep studies, saw a neurologist, had a myelogram, mri, and put on several medications which added to the weight gain. It has been almost 2 years now and I am just now starting to feel like myself. All of the tests were inconclusive. The neurologist dx was something neuromuscular. I am not on any medication now, but am not 100%. But I know that damage was done and I am older. So I'm afraid that I will never feel great again. I wish I had never had the Mirena. Never. I know I miscarried once and suspect that it happened twice. I didn't have a period for those 3 years but it was not worth it. This product should be recalled.

I have been taking Geodon for about 4 months now and it has relieved my bipolar symptoms remarkably well but in the last month and a half I have experienced a "Shocking" feeling to my heart that goes down my arms and legs. I was referred to a cardiologist and had a not so good EKG. I am scheduled for a ecocardiograma and to wear a heart monitor for a few days and then follow up with a nuclear stress test on Friday. The feeling is scary and recently I have not been sleeping. At first the medication was a miracle and I had for once in my life a normal sleep pattern. I guess I am worried about my heart. I take 180 mg every night along with a sleeping pill that was prescribed by my doctor. He was running out of medications that would help me. I have lost 27 pounds since being on the medication which is on the good side but is the cost going to be my heart? I will post what the doctor finds so that all of you can know what to look for or be on the watch out for. Many thanks for listening. B.

I got the Mirena 1 year ago, at age 46, when my youngest child was 13. My doctor did not do anything to dilate my cervix and the insertion hurt very badly. I almost told them to forget it! I have a high threshold for pain and had both my children without any medical intervention, so it is saying a lot to say the Mirena insertion hurt. I decided to get it because of my heavy periods. My periods are much lighter, but last just as long (6+ days). Since May I've had a weird rash on my legs and tailbone. The one on my tailbone looks like a bruise. My shins are mottled and itchy. I've been to numerous doctors and tried many different medications. They have gotten better, but have not cleared up. It seems that my legs are not getting adequate circulation. Also, my belly and area below my navel are bright pink and itchy. I, too, feel bloated and pregnant all the time. Ugh! I experience heart flutters and once ended up in the emergency room because the school nurse, where I work, thought I was having a heart attack. Does anyone else have a rash like I describe? This darn think was so expensive, I hate to have it removed but, if it is causing this rash, I'll have it removed right away!

Warning to Avelox users

As I am reading all these posts I am very alarmed. I just got out of the hospital because of an allergic reaction to Avelox. I developed a potentially fatal reaction called Stephan Johnson Syndrome. Please google this, as it might save your life. From what my doctors said, Avelox is a major offender of this syndrome. After reading the posts I see that a great many of you have the same symptoms I did. Even if the side effects don't seem that serious, stop taking the medication right away and consult your doctor. People who are most in danger are people with low immune systems and people who are allergic to other medications. PLEASE, I beg all of you to check this out, it can cause death in a matter of days. Fortunately for me we got to it early. Best of luck to all :)

I am 44 years old and have been taking singulair for about 4 years. 3 months ago I started experiencing crushing chest pain, tingling in my lower limbs, and felt very stressed out. I went to the ER last Thursday and was checked out for angina - the ER doctor told me I was suffering from chronic severe anxiety. I took Ativan for 4 days and felt better, but now the drigs are gone and I again having constant chest pain. In doing some research I found that anxiety can be caused by imbalance in adrenaline, and so started looking online to see if any of the allergy/asthma meds I am taking (adviar, singulair, allegra) can affect adrenaline. That';s when I found this website. Although i find the testimony compelling, I wish more folks would have poted about how their symptoms improved (or didn't) AFTER discontinuing singulair. Also I've noticed many of the stories are about children not adults; many people are taking more than one med for asthma, and most people's symptoms seem to come on right away whereas I have been taking sinulair for years and only recently have anxiety. I will stop singulair tonight and see what happens, but am wondering if anyone has come across further research that correlates singiulair with anxiety? My job life is really peaceful, I am otherwise happy, work can get hectic but that's true of any job, and I am out of ideas as to why suddenly at age 44, when I eat right and exercise - why get anxiety? Thanks for the posts, I'll try to remember to follow up after I am off Singulair for a few weeks.

hi, i've read through this several times, and it is now 3am and i find myself reading them again.

i was on both effexor and wellbutrin (generic versions of both) for quite some time, but didn't have full-on hair loss like I have now 'til about earlier this year when I was on wellbutrin only and was taking 150 mg twice a day. I got off of it because I have always had thin hair so I started to freak out when I noticed hair loss.

Unfortunately I became so depressed that I simply HAD to get back on it; and made the biggest mistake of my life by going up to the full 400mg dosage of the generic wellbutrin.

It killed me. I have very very very little hair especially on ONE side of my head, the left, and can no longer wear my bangs forward like I used to.

I went to the dermatologist (who I think was pretty bad, actually, because I went in for my HAIR and he didn't even do a strength test by pulling on it or anything!) and he said I had male pattern-ish baldness which is even more disconcerting because I can't hide the hair loss, I have a huge bald spot near the front of my head -- and I'm only a 21-year old female, people! This is beyond depressing, really. I'm beyond angry at my psychiatrist for always always downplaying the hair loss risk. I loathe him for it, in fact. But anyway.

I am going to start on biotin, and probably some prenatal vitamins, and maybe even tail Rx (******).

Thank you for posting your experiences, it has been a huge comfort to me (I wasn't lying when I said I read this thread many many times before and am reading it again now, at 3am!)

Hi all.

I just discovered this website, and reading all these comments makes me want to comment also. I, too, am on Lisinopril and am suffering many of the side effects mentioned here.

I'm a 54-year old male, and have had high blood pressure since around 1998-99. Nothing really controls it, although I've had episodic success from time to time. I lost a lot of my hearing last year due to a BP-related disorder called "hydrops" (my right ear particularly), and my eyesight has declined from 20/20 to "mediocre" in record time (although it's been largely stable now for 5 years).

Really, everything bad started when the medications began in 2002. For example, I now have Type II diabetes, almost certainly as a result of the diuretic I was prescribed from 2002-2007. I could also tell horror stories about clonidine, Toprol, Accupril, and others.

Latest event: I ended up in the hospital ER last Wednesday for what seemed like a minor stroke. I am now suspecting the Lisinopril because the symptoms so mimic much of what folks describe here. I've never had the bad cough, but the joint aches are awful. As for the stroke (actually, a TIA -- Transient Ischemic Attack) -- we'll know for sure after the MRI tomorrow, but my regular doc and the neurologist suspect it was NOT a TIA. Then I see descriptions here of tingling, neuralgia, and other symptoms identical to what happened to me!

Sadly, I don't have any simple answers to share. I've tried to cut all sodium from my diet, and I know that's helped. I am now trying a device called the Zona Plus (******), some $300 but possibly worth it. I used it for 90 days in 2007, then gave up and went to a no-salt diet ... and my BP dropped like a stone. I thought diet would do it all, but I was wrong. I should have continued using the Zona. So now I've started a new trial of it. We'll see what 60-90 days on it PLUS a low-sodium diet can do.

There's another device called the Resperate which is also kind of spendy. Anyone tried it and had success?

I'll be seeing my doctor this week or early next, and asking him to get me off the Lisinopril. But what to replace it with? Any ideas will be welcome.

In reference to my Sept. 20th posting, I have been asked to describe the
"warning signs" of oncoming seizures that I have. To review, I was struck by lightning while serving in the Marine Corp in 1977 and have had seizure disorder and myoclonic jerks and inner ear problems since that time. As I stated in the post on the 20th, I have been tried on "all" of the seizures control medications and they all make it difficult to function as an educational administrator. The best medical advice I ever received was to keep a diary of everything I could remember leading up to a seizure. This included any activities I had been doing, what I had eaten, what time of day it was, any stress or problems that I was having. We are all different and probable all have different triggers. In my case, I learned that as a seizure approached, I would become more light headed or dizzy (I have inner ear problems all of the time secondary to being struck by lightning, I just recognize when they are getting worse) The ringing in my ears increases, (I also have tinnitus all of the time also from the lightning, and over time you get use to it, but I can notice when it increases) When these signs start, I stop what I am doing regardless of what I am doing, If I am in a meeting, I take a break, if I am driving (I drive locally or with someone with me) I get off the road. (In 30 years, I have never had a seizure while driving and actually have never had a traffic ticket in that period, I try to be very carefully with what driving I do, knowing that one occurrence will cost me my licenses.) I try to rest and be quiet, if the dizziness and tinnitus continue, I take two ten Mg Valium tables and lay down. If I am by myself, I will call some and let them know where I am and how I am doing. The valium probable stops the seizures about half of the time and I believe that it always make them less sevier. I have warning signs once or twice per week, and have to take valium on the average of once per week, and will have a gran mal seizure once or twice per month. With Lamictal, I believe the seizures are less frequent and less sevier as long as I keep the dosage low enough to not block my warning signs. I believe everyone's seizure disorder is different and some may be like mine and be able to learn warning signs by keeping good records of what you can remember leading up to the seizure. Always do everything under the direction of a Dr. that you trust and have faith in. The more information you can give your Dr. the better your individual treatment can be developed. If you can develop warning signs, the seizures are much easier controlled and you can live a much better quality of live.

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!