Deaths symptoms and conditions

I am 18 years old and ive been on the nuvaring for about 2 months.. Ive been depressed, angry for no reason, snappy at my boyfriend and on top of that- my once amazing sex drive has dropped off the face of the planet. Ive been on edge and anxious, ive had constant headaches all day, plus calf/foot cramping. Ive woken up in the middle of the night almost every night since i put the ring in.

I just took it out this morning after researching and looking on multiple websites, and im so so SO happy i found this website.. Already im noticing a difference in myself this afternoon and its awesome.

I find it sickening that when i brought this up to my gyno she had no idea about the symptoms i had been having and i type in "nuvaring" in google and it brings up thousands of pages of symptoms, side effects and even deaths.. Its scary.

Ladies, do your research, no more nuvaring for me.

My 9 year old daughter got her first shot in Dec. 2008 and her second in Feb. and the last in June. We have have been to the doctor a lot of times due to headaches with the doctor's opinion being that it's "allergies". She is now on allergy shots with still no relief from the headaches. I listened to her pediatrician and got her the shots. I feel so bad now after reading all the problems others are having with this vaccine. She also has had a change in her attitude aggression,moodiness,cries often, and she says she's depressed. If anybody has any suggestions for us please let me know. I love my little girl and know I'm worried.

I am 20 year old female and have a bad family history of high cholesterol, iv been taking 40mg/day of lipitor for nearly 2 months.

Hi...Am 33 years and had been on prednisone for 4 months till about a month ago. It was in June last year that I was down with Viral hepatitis along with pyelonephritis. I was eventually diagnosed with Autoimmune hepatitis and therefore administered this drug with an high of 40mg for two and gradually tapered subsequently.
Two months of medicines and I had this pain in my thighs especially when I had to get up after lying sedentary. After 1.5 months subsequently the pain worsened to now include all my joints including the leg muscles. Things have really become more painful now. The gastroentorologist who put me on this drug has advised me to see a rheumatologist. Now I am torn between trying to understand whether this is a part of my treatment or my ailment (rheumatoid arthritis is also an auto immune disorder) and only praying that it is a part of the treatment.
The Doctor's have not been clear on how long this pain will persist. Regular walking, getting up, getting out of the car, turning the cap of a bottle is painful and getting worse with my ankles and knees swelling.
The moon face, the hump, the acne are all ebbing. However this pain is killing. Anybody has any idea how long the pain will last?
Thank you and best wishes to you.

My 16 old daughter took the Gardasil shots. Since then she has complained about being tired all the time. Stomach pains , loss of consciousness. She states she feel like an old woman. Has missed several days of school because it. Please help me warn others go to the
******and let people know this is the Bogalusa, La. Newspaper. I had the article wrote.

I don't have any side effects from Gardasil- I've been reading postings because I read about a young lady in our local newspaper that is sick from a round of vaccinations. Immediately Gardasil came to mind. There have been almost 10,000 emergency room trips from this drug and many deaths,
My heart goes out to all of the young women on this board. We have been so deceived by big drug companies. My advice to combat this is to cleanse and detox the body thoroughly-remove the poisons and then rise up and speak out against what is being done to millions of young women. You can have a great impact because you have been through it.

Hi, I am a 47 year old female and have been on Coumadin since Nov 1997 after developing several DVT's after surgery for a broken kneecap. Coumadin makes me feel like crap and the only time i have felt good in the last 11 years is when i have come off the medication for dental work or surgery. Some of my side effects are cold chills and cannot warm up, upset stomach, retaining fluid, heavy periods, added weight and my fat looks flabby even though i work out 4 times a week, lethargy, a very heavy neck on occasions and the list goes on and on. My coumadin has become very sensitive to what i put in my mouth. With "nutrients" added to so many foods i find i am now reading labels more than ever. The worst "nutrient" is Omega-3. This can cause bruising and bleeding without any help from Coumadin. Several deaths have been reported in the Australian media. I believe there is research being conducted in Norway using Kiwifruit as an alternative to Warfarin. I hope this is so and they are successful soon.

As a follow-up to my post earlier today about my daughter's severe reactions to Avelox.... I wanted to add that we weren't given a prescription -- the doctor actually put a weeks worth of samples into a bag, individually wrapped pills. So even IF there was a warning on the box or a pamphlet included with this toxic drug -- we wouldn't have gotten them. Doctors get these samples from the drug companies and hand them out like candy with no regard for their patients and obviously no knowledge of what they are giving them. This is very wrong in my book. If anyone knows of anything that can be done to stop this drug from being given out - please post here.

Individuals thought to be injured by the human papillomavirus (HPV) vaccine may be eligible for compensation from the National Vaccine Injury Compensation Program (VICP) as of February 1, 2007. This coverage permits individuals to file a claim for compensation beginning on February 1, 2007.

To be eligible for compensation, claims must be filed within one of the following periods:

within 3 years after the first symptom of the vaccine injury; or
within 2 years of the vaccine-related death and 4 years after the start of the first symptom of the vaccine-related injury from which the death occurred; or
2 years from the date the vaccine is covered for injuries or deaths that occurred up to 8 years before the date the vaccine is covered. The HPV vaccine is covered by the VICP as of February 1, 2007 and claims have to be filed by February 2, 2009 for injuries or deaths that occurred on or after February 1, 1999 that do not qualify under the other filing periods. Although two years from the date of February 1, 2007, would be February 1, 2009, under the current Rules of the United States Court of Federal Claims, the deadline under section 2116(b) of the PHS Act would be February 2, 2009, because February 1, 2009, falls on a Sunday.
This answer reflects the current thinking of the United States Department of Health and Human Services on the topics addressed. This answer does not create or confer any rights for or on any person and does not operate to bind the Department or the public. The ultimate decision about the scope of the statutes authorizing the VICP is within the authority of the United States Court of Federal Claims, which is responsible for resolving claims for compensation under the VICP.

http://www.hrsa.gov/vaccinecompensation/

30 seconds after i received my injection i felt like i was going to pass out. I also felt like i was going to throw up. I advised the front desk they ran and got my doctor.she came and got my baby and carried him to the back for me and i laid down for a few min. I feel fine now but I have always been great with shots so I figured might as well have it insurance pays for it. I thought it was very strange, she said thats a common reaction???? I asked if there were side effects before the shot and she sad no.

Just started today with 40 mg dose of Sortis (Swiss-branded Lipitor).
60-90 minutes later, I am very dizzy, sweating, funny taste in mouth.

I am done... no more. My cholesterol is normal, but recommended as complementary treatment with Glucophage, as I am very slightly diabetic.

I am still spaced out as I write this note. Called the MD to tell him that I the one dose is all that will enter my body.

One of my best friend ended up in the hospital about 4days ago when they were giving the vaccine at school everyone was getting sick from it including me u had a high fever n was throwing up two of my other friend felt dizzy and fainted right after receiving the shot. The girl who ended up in the hospital fine bow but she couldn't feel her legs or arms they were bum as she told me at one pibt she stopped breathing and feel to the floor u do not trust the gardasil vaccine after hearing and seeing the damage it could cause, I've decided that I am not going to take the second shot and neither are my friends, I say it's unface and before sending this vaccine out to schools they should be 100 percent sure about them, only in the year 2006 there were 21 deaths from it and over 1000 side effects. They should just be more careful!

First off, your OBGYN is a moron if they told you it only takes a month to adjust to the pill. It is more common for the body to regulate to the pill at a minimum of 2 months and 3 months is not uncommon. So it can easily take 3 months for your body to adjust to your pill. And sometimes longer if you were on another pill and switched to another OC.

Amenorrhea(no Period) can happen on Loestrin 24. Notice the first for letters of amenorrea are AMEN. Is that a bad thing? To put this in the most basic lay terms....Birth Control tricks your body into thinking its pregnant. Thats it!!! Do pregnant women have periods? ..Of course not.

Regarding your lack of sex drive comment...that is ridiculous. The progestin in Loestrin 24 is norethindrone acetate. That is androgenic...it is one of the few pills that increases your sex drive.

I suggest if you want a pill that lowers your sex drive try yaz or Yasmin. It is anti-androgenic and lowers sex drive. It also is the ONLY pill that has extra warnings by the FDA for hyperkalimia. ...basically extra dangers if you take it my Advil, Tylenol or ANY NSAID. REMEMBER THIS PILL HAS only been around for 10 years and has been tied to several deaths in Europe. Google search yaz or Yasmin +death.

Loestrin has been around for 45 years. tried and true.

ALSO if anyone is a smoker and takes birth control you are guaranteed to have Bleeding and spotting.

Boy, after reading all the negative testimonials on Lipitor, I will throw mine in the garbage. That is what they are meant for. I have severe headache, and muscle pain, and foggy head, and I have only been on the crap for 2 months. I believe a lot of people's health is being ruined, and a lot of deaths are happening as well because of Lipitor and other statins. Mark my word, one day this drug will be withdrawn from the market, and the poor Pharmacutial companies will be in huge trouble.. They have the world convinced that we all need statins to bring cholesterol down.. The era when my parents lived , and lived long lives, and on farms, with butter, bacon, lots of fats, and never heard the word STATIN. I think every one that is writing to this forum and complaining about LIPITOR, should make a phone call to PYzier and tell them your side effects, that is the only way anything positive will come from this forum.. thank you for listening... I have called Pyzier and told them as well.

Let me start by giving you some history.

My sister is a 22 year old girl who worked full time and was never seriously ill until this summer.

During the last full week of June my sister started having headaches. She told me that these headaches were like none she had ever had before. Days later she started complaining that her legs and wrists hurt. She said that her legs were so tired and achy she could barely walk up the stairs. At that time I dismissed what she was saying. My sister constantly wears heels and I chalked up the complaint to a pair of shoes that were not yet broken in.

By July 4th, the headaches were so intense that she went to urgent care. The physician she saw in urgent care gave her an antibiotic and sent her on her way. By July 7th, she was having difficulty standing up and walking was almost impossible. My sister started complaining about severe joint pain. Her ankles began to swell and her stomach appeared distended.

On July 8th, my sister went to her primary care physician. I believe he sent her for an x-ray and said that she had a cyst on her sinus cavity which was causing her to have severe headaches. He then gave her another antibiotic and referred her to a rheumatologist never even thinking that these two symptoms may be related.

On July 10th, my sister saw the rheumatoid arthritis doctor her pcp referred her to. He dismissed her complaints saying that she probably has some form of arthritis, but that there are over 800 forms and it would takes months to pin point exactly which one she has. He then gave her a prescription for Celebrex and sent her on her way. She spent the entire week in bed because her joints were so swollen and achy that she could not move. She actually crawled to go to the bathroom.

By the middle of the following week, my sister's stomach began to burn. She contributed it to being a side effect of the Celebrex and stopped taking it on July 21st. We had no idea that the pain was so bad. My sister's last normal meal was on July 22. By the 23 she had no appetite and could not go to the bathroom. On July 24, the stomach pain was so bad that she could not work, or sit, or function. All she did was cry. She went back to her primary care physician who then prescribed her prevacid to help with the so called indigestion. He told her if the pain continues she could call him. On July 25th the pain became unbearable. My sister called her PCP as directed and he told her to go to the ER. Never once did he say he would meet her there! I brought my sister to the ER where they did an x-ray and cat scan of her stomach. They found nothing. At that time my sister had not gone to the bathroom or had anything to eat since the 22nd. The physician in the ER said that she was literally "full of shit" and needed to go home and take a liquid laxative. My sister is only 22 and my parents were away on vacation. We were stupid and didn't know any better and were so happy that they didn't find anything that we accepted his findings and got out of there.

My sister took the liquid laxative prescribed by the ER physician as soon as we got home. We waited anxiously for it to relieve her stomach pain. After many hours the laxative did not work and my sister ended up back in the ER. This time she was screaming in pain. One of the doctors there told her that if she couldn't calm down she needed to leave her ER. My sister did just that. At this point my parents (back from vacation) took my sister home and called Digestive Disease. A doctor there told my mom to give my sister 2 Enemas. He said that should relieve her pain. My mother followed the doctor's orders, but the pain did not stop. Sunday, July 27th my sister was right back in the ER - this time at another hospital. This time my sister was admitted to the hospital for severe stomach pain. After 5 days and numerous tests my sister was discharged. The doctors found nothing in her cat scans, x-rays or ultra sounds. The pain was more manageable (she was on morphine every 2 hours) and they said she was ok to go home.

August 1st my sister had a great day. She was sitting up in bed and seemed to be in good spirits. The following day she couldn't get out of bed. This time it was neck pain. My sister said the pain in the back of her neck was so severe that she could not lift her head up or move it side to side. By August 4th she was admitted to the hospital again. This time we brought her to University Hospital in Syracuse, NY. We were sure to get some answers there...or so we thought. As soon as my sister arrived in the ER they started treating her with antibiotics. They were certain she had an infection. They then told us they would have to do a lumbar puncture to check her spinal fluid for infection. We thought we would finally have an answer to what was wrong with my sister, so we agreed. The spinal fluid came back fine - no infection. At that time they admitted her to the hospital. While at University Hospital my sister was treated by a team of doctors. They tested my sister for lyme disease, west nile, lupus, leukemia etc. They performed a spinal tap, cat scans, x-rays, ultra sounds, blood smears, etc. All of these tests came back negative. The doctors could find nothing abnormal except for an elevated white blood count -22,000 (it was also very high during her last hospitalization), an elevated C reactor and a very high SED rate. After 4 days of numerous tests and pain killers (first morphine, then Dilaudid, then Dilaudid with a fentanol pain patch) they discharged my sister. The head doctor told her that he believed she had viral meningitis and that it would eventually work its way out of her system. By this point my mother and I were skeptical. We did the research and viral meningitis should only last approximately 10 days. Mig had been sick since the last week in June. No one was putting all these symptoms together. On the day of her discharge my sister started getting her stomach pain back. The pain was mostly on the left side of her lower stomach - under her belly button. Again she was told the pain was due to constipation and she should buy some Miralax when she got home.

My sister was home for a mere 2 days before she would be hospitalized again...for the 4th time. Her stomach pain was back and worse then before. My family could not believe this was happening. My sisters spirits were down and the excruciating pain was making her mentally unstable. This time the ER physician recommended a hematologist come in to see my sister. We just wanted answers so we agreed. This hematologist, Dr. R stated that she believed my sister had drug induced lupus. We were shocked as my sister was tested for lupus twice before and both times the test came back negative. Dr. R explained that she believed my sister got drug induced lupus from the Gardasil shot. My entire family was shocked. We had never heard of any severe side effects like this from the Gardasil shot. Dr. R asked my sister for her permission to test her again. My sister agreed and a week later my sister learned that she was positive for drug induced lupus. My entire family was so happy that my sister finally had a diagnosis and could begin treatment. We were told that after a 6 week steroid treatment (Prednisone) my sister would be back to her old self. We were ecstatic!

My sister was home from the hospital and on the steriod treatment for 10 days when things started to go wrong again. The doctors were very concerned with the dosage of Prednisone that my sister was taking (80mg. I'm not sure how many times a day). They cut the dosage down in half over the course of a few days to prevent kidney damage and other side effects. Once the Prednisone was decreased, my sister started getting sick immediately. Her forearms were very weak - she could not put any pressure on them. Her shoulders would tingle and she would get shooting pains down her right arm. One of her doctors believed she was developing fibromyalgia and prescribed her lyrica. Shortly after my sister began taking lyrica she started seeing stars. She had double vision and a migraine that would not go away. My mother called her doctor and told him about this. His answer was for my sister to stop taking the Lyrica. She did immediately.

On August 29th, my sister still had a migraine. This was day 3 without a break. She woke up early Saturday morning and began vomiting every 30 minutes. After a few hours of non stop vomiting my mother called her doctor. His nurse practitioner was on call and she told my mother to take my sister to the ER immediately. My mother went back into my sister's room to tell her they had to go back to the hospital and she found my sister having a seizure. My sister has no history of seizures. My mother called 911 and the ambulance came to bring my sister back to the ER...her 5th hospitalization.

Shortly after arriving at the ER, my sister had another seizure. Immediately after the seizure the ER doctor ordered my sister to have an MRI. My sister had one during her last hospitalization only 2 weeks before. That MRI was normal. This one was not. There are lesions all over my sister's brain. The neurologist told us that he cannot believe she does not have permanent damage. According to him there is no oxygen going to her brain.The neurologist also explained to us that her brain looks as though she has been poisoned. He said that her MRI is very similar to an MRI of a patient who has been poisoned with antifreeze. Later I learned that Gardasil has both aluminum and sodium borate (which is in both rat poison and cockroach killer). However, according to the doctor once your brain looks like my sister's all the poison is out of your body. My sister's team of doctors started debating as to whether this could all still be from the Gardasil shot...my sister's last shot was on 02/22/08. Some believe that the side effects started off as mild, but since they were left untreated for so long they've turned into a serious neurological problem. They told my family the only way to truly know what is going on is to do a brain biopsy.

Yesterday, my sister was transferred to Mass General in Boston. We were hoping for a bigger hospital, better technology, more seasoned doctors. So far my sister has been treated badly. When my mother told the doctors' about the Gardasil shot and the devastating effects it has had on my sister they dismissed it. When my mom asked the doctors to test my sister for heavy metal toxicity they completely ignored her. I fear that she will never get the proper care.

this might help anyone who is looking for more information. This site is trying to get the FDA to investigate more into this drug:
******
Under the "documents uncovered" area, it lists SEVERAL woman who have been hospitalized from this shot from Jan. 2008. Very scary stuff.

also, a post the one of my friends sent me from a news story:

10 deaths have been linked to Gardasil since September 2007, and there have been 140 reports so far this year of serious side effects such as miscarriage and Guillain-Barré syndrome.

Well. We’ve already lost 18 girls, some as young as 12, in the effort to spare them from the mere possibility of cervical cancer later in life. Others have developed debilitating and potentially life-threatening ailments within weeks of being vaccinated, and others still have had spontaneous abortions or given birth to babies with birth defects.

Also consider this: Cervical cancer usually develops in your late 20s to mid 30s. The protection period of Gardasil is estimated to be 5 years. That means, if you receive your first set of shots when you’re 10 years old, you’d need at least 2 to 4 additional booster shots to make it through your 30s. And THAT means you’ll have to expose yourself to the potential side effects of Gardasil over and over and over again.

But now to the real clincher, and I want you to read the following section as many times as you need to let this truly sink in…

U.S. statistics show there are 30 to 40 cervical cancer cases per year per one million women between the ages of 9 and 26, which is the age bracket that Gardasil targets (and was tested on).

According to Merck, Gardasil was shown to reduce pre-cancers by 12.2% to 16.5% in the general population. So, instead of ending up with 30 to 40 cases of cancer per million, per year, in that age bracket, the HPV vaccine can potentially bring it down to 26 to 35 cases of cervical cancer.

What that means is that you would have to vaccinate one million girls to prevent cervical cancer in 4 to 5 girls.

Further, about 37 percent of women who develop cervical cancer actually die from the disease, so vaccinating ONE MILLION girls would prevent 1 to 2 DEATHS per year, at the bargain-basement price of $360 million per year, plus potentially lifelong suffering for an untold number of women, which has no price tag.

Is this REASONABLE?

******

After having the third shot I noticed my hair began falling out (July 2007). It is now over a year later and after having numerous blood tests, visiting a dermatologist and doing tons of research, I have concluded that gardasil must be causing this. My hair continues to fall out, I have bald areas around the crown of my head and my mood is very depressed by this. I also experienced soreness in my legs and joints but these are not constant. My periods also are out of whack. They can be between 28-50 days apart. I would not recommend anyone getting this vaccine. I wish my OBGYN had not sold me on it. I was 31 when I got it but she said age didn't matter, she said one day insurance companies would cover this vaccine for all women no matter what age they are. I paid $190.00 a shot and now I have a thin head of hair that may one day soon be bald if it doesn’t stop falling out. I think they should take this vaccine off the market. If anyone else has had severe hair loss, has it stopped falling out after a certain point?

The following article in the WSJ may explain the reason for the significant number of Adverse Reactions to statin drugs.

Why You Can't Tell Where
Your Medication Was Made
April 8, 2008; Page D1- Wall Street Journal
Bananas come with those little stickers listing their country of origin. Why not pharmaceuticals?
That's what some consumers -- and even some physicians -- are asking since the Food and Drug Administration linked the deaths of 19 people to contaminated batches of the blood thinner heparin from China.
*******

I encourage every patient with a bad experience taking statins to contact the FDA (see, July 1, 2008 posting for FDA contact info).

The following article in the WSJ may explain the reason for the significant number of Adverse Reactions to statin drugs.

Why You Can't Tell Where
Your Medication Was Made
April 8, 2008; Page D1- Wall Street Journal
Bananas come with those little stickers listing their country of origin. Why not pharmaceuticals?
That's what some consumers -- and even some physicians -- are asking since the Food and Drug Administration linked the deaths of 19 people to contaminated batches of the blood thinner heparin from China.
******

I encourage every patient with a bad experience taking statins to contact the FDA (see, June 29, 2008 posting for FDA contact info).

The nausea is tolerable, generally short-lived as long as I eat prior to taking the Chantix and drink plenty of water.

I have a sense of...fogginess....detachment, while at the same time, seem to sense clear hidden messages in the way people look at me, in what they're saying to each other, and to me. Yep, it's probably paranoia.

The nightmares are horrible. I dream specifics about deaths of loved ones, in horrible detail. I also awaken at least once a night gasping in terror, unable to get a breath.

The thoughts of suicide are strangely comforting and don't seem wrong at all. I'm depressed, but comforted knowing that I can end it if I really want to. Bizarre and I know it on some level at least.

I'm bruising easily this time. I mean REALLY easily. A small bump results in a hard, raised, dark bruise.

I developed a rash on my stomach that's been there for 3 days but seems to be clearing today.

This is my 2nd time taking Chantix and I'm 3 weeks in. I had the same symptoms last time and expected them this time. I'm smoke free but plan to continue with the Chantix as long as possible. The urge to give in and have one cigarette is too strong post Chantix. I tell myself everyday that the thoughts are NOT me, and that I can let them come and not act on them because it's the drug, not me.

I went on the ring a couple of years ago.I never had a problem with feeling it inside me or falling out. My boyfriend cant detect it either. It is convenient and easy to use. Around the same time of starting the Ring, I felt like I was starting to lose myself and sense of personality. I have experiences almost all of the above symptoms: major depression, acute anxiety, sleeplessness, weight gain, acne, fatigue, loss of sex drive, and now I'm learning that NuvaRing is linked to 12 deaths. Blood clots. Scary stuff. I am getting off this thing strait away and hopefully I can rediscover myself and my health. I guess I'm lucky my boyfriend stuck with me thru this. It can only get better from here....

I have already posted on Friday about my granddaughter. But I want to say that with all of the stories about Singulair being so similar and so heartbreaking that organization is the key. Merck and the FDA are so closely allied that the truth may never come out in scientific terms.I an only hope that with the deaths that have occurred and forced this out into the open that parents and children who have been so scammed and victimized will have a voice. Nothing is worse than harming a child and these companies knew about these side effects(by their own admission) but marketed them to the doctors and the public anyway. How is it that a few doctors knew the dangers and others didn't? That's bizarre, unless most doctors get rewards from the drug reps for prescribing this drug. Did the reps tell them , "Oh it works great on allergies but turns your 9 year-old into a sad, depressed, suicidal and bipolar child?" Even if they didn't there's enough knowledge out there given to doctors at conferences, journals, etc to inform them. That's their job. I am writing to the governor, my congressman, my Senator every day until they hold hearings on what us parents and our poor children have been through with this drug. Please do the same.It may fall on deaf ears but it's a small price to pay for the damage this drug has done.

weight gain started almost immediately i gained 20 kgs during both pregnancies on zoloft. Although my anxiety/panic and outbursts of uncontrollable anger, and irrational thought patterns all stabilized remarkably on zoloft I have NO interest in sex, and uncontrollable urge to drink alcohol and I cannot stop until i pass out. Also, void of emotion ...haven't cried in years despite traumatic events that have included the deaths of grandparents, a divorce in the family and a miscarriage. Each time I try to go off this stuff I end up experiencing amplified symptoms of my original problems as well as severe depression and paranoia so I get scared and go back on it.

Recently took a twenty day run of 500 mg Levaquin for a cellulitis infection that popped up after a knee surgery. It seems that unlike most people I tolerate the drug pretty well. The only side effect I have noticed is a little muscle stiffness when I wake up which is quickly remedied through light stretching and a warm shower. After being put on this medication I looked up it's side effects and was frightened by how many people have had terrible and debilitating side effects. Next time I'll trust my doctor and not look them up. I think any lost sleep and nervousness can be attributed to worrying about side effects that never came up.