Blood flow symptoms and conditions

I am a 48 year old female who had just recovered from pneumonia and was prescribed avelox for a lingering sinus infection. Within hours after taking just 1 400 mg pill, I began experiencing a severe reaction. First there was a rash all over my body, with swelling and flushing all over. Then I became nauseated to the point of dry heaves and my temp went to 104 digress. My body then had neurological shakes, I could not control them -- just like Parkinson. I had no energy to move. My husband rushed me to the ER where I was treated with steroids, liquid benadryl, nausea medicine and IV fluids. After a few hours, I was released. Two days later, after another trip to the ER because of tingling, rash and no blood flow to extremities the same treatment was given. It has now been two weeks and I am just now feeling like I am coming out of this and getting back to normal. I have just spent over 10 days in bed, untold amount of money at ER and lost two weeks of my life.. BTW, the ER Doc said he would never prescribe Avelox to anyone due to the numerous reactions he has seen. If there is a class action suit, count me in.. Never let anyone take this drug..

I started taking lisinopril 20mg Nov. 12, 2008. I've never smoked poison ivy before, but that's how I describe the constant side effect. Sinus and upper gums, upper chest. A dull allergic feeling. Some days I am preoccupied with it, gets depressing. Does keep the BP down. I am weaning the dose down to stop. I know you're not supposed to stop taking them, but I am sick of feeling sick. I've told the doctor twice, I think he thinks I am imagining it. I don't have insurance, it cost me $300.00 out of pocket to see him for ten minutes. I hate felling trapped like this.

43 yo Male 5'9, I weighed 259 lbs 2 years ago. I am now 221 lbs. I want to be 200 lbs. Work out 3 times a week gym. Take vitamins. Diet is better than what it was.
Can't say I am not trying. But if all BP meds are like this, I will no longer take them, and just take my chances.

I have been on Toprol-XL (BRAND) for 3 months. I took the generic for 2 months with no change in BP so I requested the brand name. I found your website by surfing the web looking for answers to my complaints. I have weight gain, vivid violent dreams, extreme fatigue, my breathing is slow and I am just dragging around in a fog. I felt better when my BP was high and I didn't take all this medication. Currently, I am taking first, Lisinopril, then added Toprol XL AND then added Clonidine. My BP is still not properly controlled. I am going to the doctor today to have my medication changed. Thank you for sharing your comments.

I needed my copper coil changing and at my appointment I was recommended the Mirena due to increased blood flow. I did not have an opinion either way and took the advise of the family planning doctor. I had not until now read any reviews on this product. I was going to make an appointment to see my doctor due to my increasing depression. I am now going to have my Mirena removed this week.
These are my symptoms to date, (5 months).
No Periods (cool)
Very heavy and larger breasts, all new bras and have to wear sports bra to bed due to very painful breasts. I cannot run at the gym and have to walk on the treadmill.
I have put on weight and this is more of a problem I cannot lose any of it. 1-2lbs a month. I go to the gym, play squash and tennis.
People have noticed my weight gain.
I feel bloated and puffy.
Feel very tired and have to go to bed in the day at weekends.
I have been feeling very depressed and have got rather worried about it.
My partner says I have changed as a person.
I did have a very healthy sex life, mostly me leading and I am now not only not bothered either way, I actually do not want any sex at all.
I feel sick and have actually been sick.
I always have a bruise and I don't know how I got it.
I am moody and have become quite lonely.
I think that is plenty to be going on with.
I have read out what all you lot have said to my partner and he just said get that thing out and he is calling the doctor tomorrow to get the snip, something we have just left till now.
I am going to have mine taken out this week so hopefully I will get back to the 'normal' me very soon.

I feel it lowers the rapid blood flow to the lower section which makes for a not so happy camper. Things are too soft, like wilted. Has anyone else had that experience?

I have been using the NR for about 2 years now. I absolutely loved it and haven't had any issues with it. No serious side effects. BUT I saw the ad on TV about the lawsuit and it made me put two and two together. And also to research it which has explained some depression and sexual side effects that I have realize I have been having. Most serious is I have been having unexplained heart issues as of the past 3 months and my doctor cannot seem to find a reason. It feels almost as though there is something blocking the blood flow to my heart about 2-3 hours out of the day at random times during diff activities to include just sitting at my desk at work.. It is very concerning and my doctor is even less concerned. I know my body and I know when something is wrong, and something is wrong with my heart/arteries/blood flow. I am 27 yrs old, I do not smoke and i am in good health. No reason for my heart to feel the way it feels and it is SCARY. I finally decided to research the NR to see IF it has anything to do with it and I was shocked to find some of my symptoms associated with the lawsuit being filed. I have put in an inquiry to see what can be done and hopefully get some answers and get my health back to normal.

I started taking Femcon fe in late December of 08. It's been about a year since I've taken any birth control so I was having problems remembering to take them. I did what the pills instructed when you forget and I took 2 pills on the same day. I forgot again to take them and repeated the same thing for 7 days only. I just decided to stop taking them and start fresh when I get my next period. Little did I know I was going to have a blood flow. I thought I was getting my period, but it wasn't red it was a burgundy color. I've been bleeding for 3 days know and it's getting heavier. Another side effect is lack of sleep. I haven't been able to sleep at night. It's been 2 nights and I can't sleep. Also, I have been urinating much more than usual and having bowel movements much more than usual. Anyone experiencing the same things? Cramps, bad headaches and mood swings. After 7 days all this!!! I will not take these pills anymore!

I took Levaquin 750 for 10 days for a sinus infection. I took first 5 doses, went to see my doctor again 6 days later because I was still sick. She prescribed again 5 does of Levanquin 750. I am still coughing and I feel very tired. It did not help at all. I am still sick and I have muscle pains in my two calves and stress Achille tendon. I am a runner and I have sometimes problems with my calf: I have been not running too much recently and I was wondering how come suddenly I had those muscle pains in both my calves. I am not sure if it is related to Levaquin, but when I read all those comments, I am worried. Why I have been prescribed this antibiotics if it is obviously dangerous?

I am so thankful for this site. I thought maybe it was just me. For one, I am allergic to Sulfa. My doctor knows this, as does my pharmacy. Still, they give me Lisinopril with Hydrochlorothiazide which you should NOT take if you have a sulfa allergy. From day one, I started with anxiety, agitation, nausea and what felt like a racing heart - though my pulse was normal. Day three I called the doctor and they said this was normal as my body "adjusted" to the medication. It has been over two weeks and the same thing keeps happening. I tried taking the meds at night to hopefully sleep through the side effects but no - it just kept me awake. I put another call in today and have yet to receive a return call from my doctor. I hope the doctor calls me and NOT the front desk girl because I have a lot of questions and concerns. Other symptoms I have been experiencing since I started Lisinopril are sever muscle cramping last for over 24 hours, dizziness, heavy chest/racing heart beat, restlessness and less frequent urination. For a 37 yo female who has to "potty" constantly, even throughout the night, going once in an 8+ hour period is not normal! The worst side effect though is definitely the anger and agitation. I feel like I am going to burst out of my skin or die banging my head against the wall. Last night I tossed and turned for 2 hours in agitation. I thought I would surely have a heart attack from the stress. Oh yeah my BP has NOT dropped at all (tho it fluctuates on or off the meds) on the 20 mg dose. Go figure.

I just recently had the mirena iud inserted. Oct 30 2008. 3 months after having my first child under a normal vaginal delivery. When I have asked my doctor regarding any side affects he stated that women may have heavy bleeding the first 6 months/ and that after those 6 months that your periods will actually disappear.

The first week that I had the mirena in, I began bleeding almost instantly. Blood clots the size of my closed fist came out of my body from the uterine wall I suppose. I went through a super tampon/ and a pad in an hour and a half. ( I am one of those women who normally use a super tampon maybe once in a while/ normally a reg. size does the job) This bleeding has not stopped since the mirena was inserted.

Looking at a computer screen is part of my daily routine at work. It seems as though my eyes feel blurry through out the day as I am working. Towards the end of the day I can barely stand to look at it. This has never happened to me before. It is almost like I want to turn all lights off and sit in the dark, with no noise(headaches).

Of course sex drive is at the all time low. Who is in the mood to go for it when you are bleeding with a terrible headache?

The first few nights I had a horrible time falling asleep and staying asleep.

Well... at this point I have had headaches... all day for a week now. My head hurts like someone is pounding it against a wall. I have not had a headache in years. My stomach has been upset/ feeling as though I may have to throw up.

I am afraid that I may start seeing the other symptoms that ladies have talked about.
When you had the symptoms did they all happen at once or one at a time over different time periods?

I've been on Loestrin for almost 5 months now, but I'm still not so sure how I feel about it. Before I took the pill, I had 7 day long, heavy periods, headaches, cramps, vomiting- the whole nine yards. The first month I took the pill, I got my period as usual, but for about 5 days ( the 5 days I happened to be on vacation, fun). The next month, my period lasted about 4 days, the next month three days, and this past month I didn't get it at all. I have to admit, I was quite relieved when I read some of other comments with women also having missed periods, or no periods altogether, as I'm not ready for a mini-me quite yet. The only major problems I've had with this pill so far are severe mood swings, which my boyfriend doesn't appreciate very much, and the last few days I've had severe pain in my lower abdomen, which, if it persists, will force me to visit my gyno. Overall, I do like this pill, it's really toned down my migraines, which I've had for years, and seems to be quite effective at lessening my heavy blood flow and severe cramps.

I have been on Lisinopril for approx 5 years, during a routine year end blood work-up, I have developed a problems with my creatine levels 1.48 and Glom Filt Rate, Est 37. My physician had me do a 24 hr urine for further testing but insisted that I no longer take the Lisinopril. Several of the tests have come in and he advised me that I have only 50% blood flow to my kidneys. It appears to me that the Lisinopril has caused some kidney damage. I also have a great deal of muscle pain, but do to my age (55 years) I thought it was jus a part of the aging process. What do you think?

I got my Mirena on 6-12-08 and still currently have it. I am 22 years old and have two little girls. Before the Mirena I used pills and the patch and never had any problems at all. This thing is a nightmare! I have been twitching-especially my eyes and lips, I cant get my fingers to stop shaking. I have been experiencing the 'drunk eyes' that bulgebegone mentioned. The cramps have not stopped for the month I've had it, even though I was told it would be a week at the most. Also, like so many other women, I was told that I may spot very lightly for 6-9 months and then stop getting my period-after it was inserted. For the last month I have been hemoraging almost exactly the same as those few days in the hospital after giving birth-when they give you the big diapers to wear! My husband hates it too, when we have been able to have sex, he says most of the time it's ok, but then the strings will poke him and it's a very sharp pain. Last Friday I spoke with my doctor about this to see what options we had and I asked her to shorten the strings and she said no, without an explanation at all! I also just read the article below in an email I received. I am now making an appointment to have this removed!!!!!
> I am sure most of you have a daughter, a granddaughter, a niece, a friend
> or
> a friend's daughter... this might be worth checking out.
> PASS THIS ON EVEN IF YOU DON'T USE IT!!
>
>
> Recently, this past week, my cousin Nicole D. (age 31... a newly
> graduated student with a doctoral degree about to start her new career as a
> Doctor...) was flown into a nearby hospital, because she passed out. They
> found a blood clot in her neck, and immediately took her by helicopter to
> the ER to operate. By the time they removed the right half of her skull to
> relieve the pressure on her brain the clot had spread to her brain causing
> severe damage. Since last Wednesday night, she was fighting for her life.
> They induced her into a coma to stop the blood flow and then operated on 3
> times. Finally, they said there was nothing left that they could do.
> Multiple c lots in the left side of her brain were found, the swelling
> wouldn't stop and she was on the life support. She died at 4:30 that day.
> She leaves behind her husband, a 2-year old, Brandon and a 4-year old,
> Justin. The CAUSE of DEATH they found was a birth control she was taking
> that allows you to only have your period 3 X's a year. Doctors said it
> interrupts life's menstrual cycle, and although it is FDA approved... it
> shouldn't be. So to the women in my address book, I ask you to boycott this
> product and deal with your periods once a month, so you can live the rest
> of
> the months that life has in store for you.
> Please send this to every woman you know - you may save someone's life.
> Remember you have a cycle for a reason.
>
> FYI: T he name of this new birth control is Lybrel. If you go to
> ******
> you will find a least 26 pages of information regarding this drug. The
> second birth control is Seasonique. If you go to ****** you will
> find at least 43 pages of information regarding this drug. The warning and
> side effects regarding both pills are horrible.

I'm 46, female.. developed blood clots on my lungs for apparently no reason, found them when going to ER and complaining of bad headache, nausea and left shoulder and back pain. I haven't had a recent surgery, nor was on birth control.

I'm dealing with anxiety, depression, unusual headache, horrible back and upper shoulder pain, itching of head, hair falling out during shampooing, , tightness in chest, trouble swallowing, really bad pain in hips, legs and feel like feet swell. I don't sleep well, even on Ambien.. doesn't keep me asleep. I awake in the mornings around 4:30 with diarrhea, nausea, headache and feel awful. Never get a good nights sleep. My hips hurt as well as dealing with parathesias down right arm and into hand.. feels like needles sticking in my hand. Most days I feel wiped out in the afternoon.. as I try and drag myself out of bed to get some excersise.

Does anyone deal with parathesia's down their arms or hands.. what feels like nerve pain?

Has anyone ever tried Aggrenox, also known as Dipyridamole instead?

Or actually tried the real Coumadin, instead of the generic Warfarin?

Has any other woman out there been told not to use a tampon when on her cycle, as this will cause more menstrual bleeding?

I'm so tired of Dr.'s not having personal experience of their own with this drug.. and telling the patient that they are crazy and need to be on anxiety meds or anti-depressants. I just found out that Warfarin is the main ingredient in RAT POISON..

Has anyone EVER gone the totally nutrition route, juiced and gone radical, telling their Dr.'s that they were getting off of all meds?

Does anyone suffer from feeling like their ears are full, or hearing loss?

I'm so tired of feeling afraid.. and tossed around by Dr.'s who really don't want to do the research, nor listen to their patients.

I'd love to hear from anyone who has some insight..on any or all of the questions..

It kept me bleeding day in day out it's ridiculous!!!!! I was depressed like crazy, I recently stopped the shot and the blood flow of my period is much better, my hair is growing , and I'm living life to the fullest, no depression. I wish the doctor would have been truthful about the damn side effects

Had my coil fitted in Nov 2005 and have only now just realised my many symptoms started around that time.
My lack of sex drive, I am now on anti depressants, I sweat so much my face and down my back. I have put on weight and my mood swings come and go I often end up in tears at the slightest thing. I constantly have a watery discharge which means having to wear panty liners. My memory is terrible I find I have to write everything down at work as soon as it is said or I forget.
But the worst thing is the sweating my underarms stay dry its my face & it runs down my back it is really getting me down I am always looking flushed and hot I did think it was the menopause as I am 45 this year but I have tried various herbal remedies with no effect any one have any suggestions.
My GP is not keen on me having the coil removed as my periods were so heavy I often could not leave the house for fear of the blood flow showing through the pads.
Karen

I've been taking Wellbutrin on and off for several years now. It works for me and my depression and doesn't cause weight gain. Unfortunately, a lot of my hair was gone before I researched it and found that this seems common with many users. I stopped taking it for several months and my hair loss pretty much stopped. Some grew back in around my hairline and my head felt better, but not a significant regrowth on my crown. It definitely stopped coming out like it was. The improvement took about 3 months. I started taking it again and within 2 months I noticed that I was again loosing hair. I use Nioxin shampoo which slows it some, but will stop taking it again. In my research I found that some vitamins, scalp massage or yoga where your head is down and you increase blood flow helps. Hair color also helps for several reasons. I found, however, that while on Wellbutrin my scalp was very sensitive and sometimes had a burning sensation. My dose if very low at 75-150 mg per day. What a shame this side effect it is because this is a very effective medication! However, I have no doubt whatsoever that it's causing my hair loss.

I had a viral infection and was put on Levaquin 750 mg. After being on it for 5 days my joints began to hurt. I didn't think the medicine caused it and I continued to take it. Until the 7th day I began to research and found this web site. I quit taking it. I was unable to stoop down and it hurt really bad to walk up or down stairs. Regular walking was some painful. I also had some pain in my wrist. I've been off the medicine for 6 or 7 weeks and I'm still having bad joint pain in my knees. I'm unable to perform normal activities. I'm not saying Levaquin caused it; but it's just that when this started was while on it. If anyone knows how long this might last or if it causes permanent damage, please let me know! I will be going to a specialist in 1 week to get this checked.

Our son started taking Singulair when he was 2 for severe allergic rhinitis and cough variant asthma (in addition to Zyrtec, which didn’t control all of his symptoms). He is 5 now. For the last three years, he has been an increasingly violent, difficult, defiant, argumentative, volatile child who has intense mood swings--one minute he’s laughing uncontrollably, the next he’s weeping over nothing. His doctor and therapist recommended that we see a psychiatrist to have him evaluated for bipolar disorder, which used to be unknown in children. Because he has such chronic sleep problems, the doctor also suggested we take him off Singulair (and increase his Zyrtec dose) to see if it improved his sleep issues. Within a week, he was sleeping much better and was a calmer, happier, gentler boy. He suddenly could take “no” for an answer without flipping out and trying to hurt me. We thought that we were just in an unusual, calm window that would shift either to mania or intense sadness or both, any minute. We also thought that his behavior change might be due to sleeping better. We were enjoying the rare reprieve. Over the last weekend, his springtime allergies really flared up. We gave him Singulair on Monday and by noon, he was completely out of control. I had to strap him into his car seat at one point to keep him from hurting either me or himself. It finally occurred to me that Singulair might be causing his “bipolar” disorder. Of course, we stopped the Singulair. After two days he was a new boy. Yesterday, I Googled “Singulair bipolar children” and got a few hits. I am stunned to read how similar other families’ experiences have been to ours and I feel sick that we gave this drug to our child for three years.

Weight gain,muscle pain/tiredness especially in the lower legs. Fatigue/lack of energy, moodiness. Also intestinal bloating/gas.

Getting adequate exercise is problematic given I can't get my heart rate into my target area, and the almost constant pain and dead feeling in my lower legs. It gets to the point that I have to stop walking and wait for the blood flow to reach my lower extremities. I am assuming this is a large contribting factor to my weight gain.

I am 34 and started taking loestrin 24 at the advice of my doctor cause I have really heavy periods and a lot of breakthrough bleeding mostly due to fibroids which has made me quite anemic. I was hoping this would help. I started Loestrin 24 about 16 days ago. On the ninth day I started breakthrough bleeding and it hasn't stopped! I feel like it's become a full fledged period! I just hope the bleeding stops soon. I have pretty bad cramps and backaches. I've been popping many advil. Also, my breasts are tender and they're definitely bigger (I liked my boobs the way they were!). As far as mood, the first week was fine, but I was pretty lethargic and depressed the second week. Starting the third week yesterday, my mood has been much better. It sounds like people have had success after the 3 month waiting. Me, I'm willing to duke it out for another month for the almost-nothing periods. But 2 more months of this I don't think I can handle. I'll let you know what happens

I receveid this email today.

Date: Wed, 12 Mar 2008 11:24:01 -0400 (EDT)

I received this information and thought that it was very important so pass
it on to friends and family.

MENSTRUAL CYCLE-PLEASE READ!
PASS THIS ON EVEN IF YOU DO NOT USE IT

Recently this past week, my cousin Nicole Dishuk (age 31...newly grad
student with a doctoral degree about to start her new career as a
Doctor...) was flown into a nearby hospital, because she passed out.
They found a blot clot in her neck, and immediately took her by
helicopter to the ER to operate. by the time they removed the right half
of her skull to relieve the pressure on her brain, the clot had spread
to her brain causing severe damage.

Since last Wednesday night, she was battling. They induced her into a
Coma to stop the blood flow, They operated 3 times.. Finally, they said
there was nothing left that they could do. They found multiple clots in
the left side of her brain.. The swelling wouldn't stop, and she was on
life support.. She died at 4:30 yesterday. She leaves behind a husband,
and a 2yr old Brandon and a 4yr old Justin.. The CAUSE of DEATH - they
found
was a birth control she was taking that allows you to only have your
period 3 X's a year... They said it interrupts life's menstrual cycle, and
although it is FDA approved... shouldn't be -

So to the women in my address book - I ask you to boycott this product &
deal with your period once a month - so you can live the rest of the
months that your life has
in store for you.
*Please send this to every woman you know - you may save someone's
life...Remember, you have a CYCLE for a reason!

Fyi.
The name of this new birth control pill is Lybrel. If you go to
Lybrel.com> <<
http://lybrel.com>> , you will find at least 26 pages of information
regarding this drug. The second birth control pill is, Seasonique. If
you go to the website of, Seasonique.com <
http://Seasonique.com
http://seasonique.com>> <> , you
will find 43 pages of information regarding this drug. The warnings and
side effects regarding both pills are horrible.

Please, please forward this information to as many daughters AND sons,
co-workers, friends and relatives. Several lives have already been
changed.

Stay away from Prednisone

My prayers to all of you who take these destructive "medications". here's my short story.

I had been diagnosed with Sarcoidosis back in 2003. My doctor gave me 60MG per day (three 20 MG tabs) for over six months, with the weening off period lasting another six. To make a long story shorter. I went through many of the same problems like, bloating in the face and body, rashes, a bump that looks like a wart--that still won't go away, and a continuing state of memory loss. I get baffled easy now. I also continue to go through mood swings.

But here's the kicker, I haven't taken Prednisone for over 3 years and I was trying to begin lifting weights. I thought I popped something in my arm, but the doctor says that I have "aseptic necrosis", that has developed in my left shoulder and soon to start in both sides of my hips. For those who don't want to "google" the term, basically parts of my shoulder and hip bones are not getting blood flow and are dying (necrosis).

With my memory loss, I am having difficulties performing at work and doing routine tasks at home. I did not think this "medication" would have affected me this much.

Prednisone needs to be on the banned list of medicines.

I have asthmatic bronchitis. In June 2006 I came down with an infection in my lungs, which also set off my asthma. Between the two I was hospitalized and put on 240 mg of intravenous Prednisone and the antibiotic Levaquin. I was cured of the infection and was able breathe normally again but it took a great toll on my body It took me 3 months to taper off of the Prednisone and almost a whole year to feel myself. I was a strong, physically active person before this happened to me and I have not gotten my energy level and endurance back to what I was before I was sick. When I was released from the hospital I went from 160 mg of intravenous Prednisone to 80 mg of pill Prednisone. That step down was too severe and I went through intense joint and muscle pain in my body that it woke me from a sound sleep in the middle of the night. I luckily had an old Vicodin that I took which only made the pain bearable. I should have upped the Prednisone to make it go away but I wanted off. This pain lasted one week with each day getting less. The side effects I experienced from then on were so plentiful that I almost can't remember them all. The physical problems were, thin skin that bruised or ripped and bled profusely with the slightest bump, blurred vision, sensitivity to light, muscle cramps in my legs and hands, sleeplessness, dry mouth and frequent urination. My stomach bloated and got stretch marks. I didn't have any before that. The muscles in my thighs and upper arms atrophied so bad that I could not walk up stairs w/o using my arms to help. My arms were also very weak and I got hemorrhoids; another muscle that was affected. I had a bad case of the drops. I couldn't hold on to anything and broke many glasses. I got moon face that took a couple of weeks to go away after I was off the Prednisone. Because I was on such high doses, my hair died and stopped growing. About 40% of it fell out in one month. It took 6 months to grow back and it all grew back curly. On January 30, 2008 my bronchial tubes closed again due to a sinus infection. Again I was hospitalized with 240 mg of intravenous Prednisone and Levaquin. This time I responded much better, because I jumped on the infection/asthma instead of waiting. I stepped down from 240 to 180 to 90 to 60 and decrease 5 mg a day until I was off. This time I did no lose my hair land did not get hemorrhoids. The other physical effects were pretty much the same but much less severe. However, this time the emotional effects of Prednisone were much worse than last time. I was not a nice person. I was short tempered and argumentative and even had to stop myself from resorting to violence a couple of times. That is definitely not who I am. Prednisone stops your adrenal glands from working and adrenaline is you chemical way of coping with stress. I have been off of the Prednisone for one week and still find it hard to cope with the slightest controversy. My brain is still in a fog and I get confused easily. I cannot handle too many questions at once and forget things. My face is still round. Both times, I have found it the hardest dealing with the Prednisone at the very end and even after I finished taking it. I think it builds up and even though the chemical is suppose to be out of your body in 24 hours, it's effects stay a lot longer. I thought I knew what to expect but the second time was different again. It is a horrible drug but my trade off was breathing. Sometimes I think, that if I have to go through this a few more times, the side effects will kill me before the asthma. I wish all you Prednisone users loads of luck and stay positive.