Care physician symptoms and conditions

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.

WoW! I am SOOOOOOOOOOOO glad I found this website!

I had been taking Lisinopril HCTZ 10-12.5 once daily since April of this year. I was on Labetalol 200mg/2x's daily as I developed Hypertension during my pregnancy. Once I delivered my baby I was then switched to Lisinopril HCTZ by my primary care physician.

The Lisinopril did wonders for my blood pressure but by mid-June I started having side effects. I went to my doctor numerous times and then to the ER since I thought I was having a heart attack. The ER doctor suggested that I was having panic attacks or just symptoms from the cold I had. So, I went to my primary doctor and she immediately jumped and gave me Prozac. Never once did either doctor ever link the symptoms to the Lisinopril.

My symptoms included:

*Light Headed
*Dizziness
*COUGH COUGH COUGH!!!!!!!!
*EXTREME DIARRHEA - Everything I ate or drank came out like water almost immediately!
*Chest Pain and pain down into my left arm and fingers
*Chills
*Blurred Vision
*Rapid Heartbeat
*Cold/Sweaty Feet
*Sweating
*Bloated Feeling
*Tight/Itchy Skin
*Rash on chest 2x's
*Nausea
*****Panic attacks and feeling like I was going crazy!!!!!******

Upon finding this website Friday, August, 22nd, I went to my doctor and told her NO MORE was I taking this medication! It's POISON! I am now taking Ziac 5/6.25 once daily. Ziac like Labetalol is a Beta Blocker rather than an ACE Inhibitor and may not be as effective but I sure would rather this than Lisinopril.

I am still experiencing some of the side effects of the Lisinopril but I am hoping that they will deminish soon. PLEASE!!

I, like a lot of others have mentioned on this website felt like I was loosing my mind. I felt like I couldn't explain all the things I was feeling because some of the feelings just didn't come out right and did make me sound crazy. At one point my doctor told me it was "all between my ears!" Okay?!?!?

I hope this has helped others and I plan on making a complaint on the FDA website, this medication needs to be removed from the pharmacies! It's poison!

If anyone knows how long the side effects last after stopping this medication I would surely appreciate the info!

Three days into the ultram 200mg, once a day, I experienced a "tonic clonic seizure" what is formally known as a grand mal seizure.

From what my husband tells me it was so severe that he had to call the paramedics. I don't remember the entire seizure at all. I faintly remember seeing 4 heads coming to me down the hallway, and that was all I remember. John, my husband told me that was the paramedics and the fire department. Since they did not see the seizure taking place I was not taken to the emergency room or hospital.

I do remember laying on the bed for 4 days after the seizure unable to move, eat or drink. I was completely exhausted. I've a follow up appointment with my primary care physician on Tuesday, as in required by law to be seen and I believe I may have to sign a paper requiring me not to drive for the next 6 months.

I'm worried to say the least. I'd never had a seizure before in my life and I'm 47 years old now. I'm still experiencing nausea, inability to eat...even though its been just 2 weeks since the seizure.

I have been going through depression and extreme exhaustion and not wanting to be alone in a room since the seizure. The abdominal pains feel almost like when a menstrual period will start, severe enough to make one bend over double and an aching inside as well. Having had a hysterectomy over 7 years ago, I know that is not the issue.

My husband was having gastrointestinal problems for about a week. The PA at his primary care physician's office prescribed Levaquin for 7 days. Blood taken ½ hr after Levaquin started showed liver levels to be a little high. By the 3rd or 4th day my husband was jaundiced. Blood taken on the 6th day revealed liver levels dramatically higher. He is still jaundiced and liver levels are still at the higher level. Had ERCP procedure, CT scan of abdomen and MRCP, but no conclusions other than stricture of bile duct and possibly pancreatic cancer, although a mass has not been seen on any film. Has this happened to anyone else on Levaquin? Doctors want to try ERCP again and if that does not work then the Whipple Procedure which is major surgery to remove a possible pancreatic cancer that they have not seen.

Have been taking Lisinopril for approximately 6 months. Was previously taking Benicar, but insurance company strongly recommended the generic form.

Have experienced depression, eye problems, extreme leg pain, mood swings, sinus problems tightness in my chest, and severe rash and sores over my entire body.

Went to a dermatologist for the rash and sores. She took a biopsy and the report stated I was allergic to something. Had to use 4 anti-itch medications and 4 pills to be taken internally. Rash never did completely clear.

After having a nuclear stress test, my primary care physician referred me to a cardiologist. My left circumflex artery was 90% blocked, so a stent was inserted.

So I should be feeling alot better with all this being done. NO!! Have had more problems since the stent.

Am going today to the dermatologist again for the rash and sores and am taking the Lisinopril so when the biopsy is done, the lab can check to see if this is the culprit.

Also, am going to my PCP today for the leg and back pain. Am going to let him know I will not be taking Lisinopril anymore. An alternative blood pressure medicine will have to be prescribed.

Thanks for all the information. I will update my situation as soon as I know what is going on.

I have been on Levoxyl for about 9 years and have felt awful. I have had weight loss, dry hair, thinning hair,dry skin, muscle aches, migraines and the list goes on. I just got out of the hospital Monday after 4 days of testing of my heart and lungs. I was admitted for racing heart. The doctor's conclusion was anxiety! They said that Levoxyl has nothing to do with my rapid heart rate. The endocrinologist prescribed taking levoxyl .050 on day and .075 the next also a beta blocker, Xanax and Zoloft. I can not take any of these meds b/c they make it almost worse. I KNOW it is not Anxiety and it from the Levoxyl but what do I do?? I am a mess right now can not be in this condition with four young kids and a husband. None of the doctors would say it was the Levoxyl and instead prescribed more and told me to check up with blood work in 6 weeks. I took the .050 yesterday around noon and by 7:30pm my heart rate picked up again and continued until 4:30 this morning. I can not sleep more then 2 hours at a time and wakeup feeling like I am crawling out of my skin. PLEASE let me know of any solutions.

I am 20 years old and have been on Yaz for a year now. Before the Yaz I was on OrthoTriCylcen Lo for 3 years and tried a few others that didn't do well for me at other times. My Gyno prescribed me Yaz because I had heavy bleeding and intense pain every time my period comes, and I have been known to be very moody. I have a past medical history of heart problems and GI problems. My Gyno said Yaz could also help the anxiety from those issues. The first month into the Yaz I noticed horrible nausea, I couldn't eat anything, major stomach pain, headaches, very lethargic, back pain, leg pain, and increased anxiety. I went back to my Gyno about a week later because my pain was so bad and my bleeding was heavier and MORE painful. She said to give it a few months so my body can adapt and everything will be better. She then said that my other side effects (like nausea and back pain and anxiety) were unrelated and I needed to see my primary care physician. My mom told me to stop using the Yaz, but I decided I wanted to keep trying it. So no I see my primary physician once a month because I am so "sick." I am on like 10,000 meds to try and help everything. Even he doesn't think it could be the Yaz. There are days where my pain levels are so high that I cannot sleep or get out of bed. I have had blood work, MRIs, Sonograms, Colonoscopys, Ultrasounds, etc.. I am so tired of this. At this point I feel like the doctors think i'm a hypochondriac. I have an apt to see my gyno again (for the 5th time), i'm printing out this page and showing her i'm not crazy!

I was given a free 10 day coupon for Avelox by a physician to treat an awful cold that wouldn't go away. He also wrote a prescription for, and I got it filled at a pharmacy, an inhaler. Avelox is the WORST medicine I have ever encountered in my 69 years!! I took it for 4 days and QUIT (today) the *^%(% thing. Who wants to be dizzy, crabby, anxious, short with people, impatient, thirsty all the time, constantly gasping for breath, and NO energy at all?
Bayer should be prosecuted, condemned for creating this poison pill. I can't believe this med it is still allowed for public consumption!??

I'm 29, have been on birth control pills for 10 years, and switched to Yasmin about 2 years ago. I a small varicose vein in my right within 2 months of switching, but didn't think a relationship between my vasculature and the pill existed. I can now trace the entire vein from my right hip to my ankle. In the 2 years since starting Yasmin, my ankles and lower legs swelled heavily...but at very random times. It often began at the start of the 7-day sugar pill regime and finished by the time I started a new pack. I assumed that the estrogen withdrawal going into the sugar pills was too much for my body to handle and that the diuretic effects of Yasmin were obviously absent during that time. I also noticed leg cramping, heart palpitations, and I started waking up in the occasional hot sweat in a drenched bed.

So, after making sure that my heart and kidneys were healthy, my gynecologist prescribed continuous hormone Yasmin and claimed it as the "ultimate solution". For 4 months, I have skipped the sugar pills for each pack and started new packages immediately. I have not had a period since, and the edema has continued (still at random) and has become exponentially worse. In the last few weeks alone, the vein in my right leg has become massive, my legs are so distended by the end of the days on which they swellI that I can't fit into pants which are otherwise loose, I am noticing other large veins "surfacing", little veins are breaking everywhere, and I can now see most of the blood vessels beneath the skin in both legs. My primary care physician told me I have chronic venous insufficiency...a diagnosis I'm not okay with. I'm very worried...the changes and ensuing damage have happened way too quickly to be venous insufficiency. I am going to ween myself off of the pill, but don't know what the next step should be. Endocrinologist? Another OB/GYN? Anyone have ideas or similar experiences to share....

My husband has been taking TriCor 145 for app. 1 year. He is a marathon runner with no history of heart or other health problems. When his doctor first prescribed TriCor, my husband was asymptomatic. His doctor prescribed TriCor to help raise his good cholesterol levels after a brief attempt to correct HDL levels through diet and exercise. Recently, he was hospitalized for three days due to high blood pressure (136/100--no previous problems with blood pressure) and slow heart rate of 37 BPM. His primary care physician has failed to return numerous calls to discuss titrating him off TriCor so he will discontinue use on his own.

Here's my story, and if anyone has any thoughts of which pill to try next, I'd love to hear them.
A while ago, I had been on Orthocyclen for several years, which worked great for me, but stopped taking the pill back in late 2005 when my long-term relationship ended. I just wanted to give my body a break, you know? I went back on a different pill, Loestrin 24-FE, the middle of 2006, because my doctor wanted me to try something low-dosage, and as a result I had lots of problems with spotting and readjusting to a new pill. Loestrin continued to piss me off with the spotting, which was the only real side effect, but my doctor wanted me to keep with it to see if it lessened. It never did. So in August of 2007, per my doctor's suggestion, I changed to Femcon (great name for a lady vitamin - it sounds like the name of a Transformer), and around this time started to notice some mild dizziness.
I'm in great shape and very healthy and active. Last summer I even ran a half marathon, and about a week later the dizziness started. At this point I didn't even consider that the dizziness could be related to the new pill.
The dizziness was steady, and I was starting to have some problems focusing on my computer monitor at work, so I finally saw my primary care physician, who referred me to a neurologist. He did some minor tests with me, and based on the results, told me he thought I was getting migraines. I've never had migraines before in my life, so this was all new to me. And it was interesting because I didn't really get headaches, just dizziness and lightheadedness and some blurred or jumpy vision. It definitely starting freaking me out, and even impacted my running because I didn't know if I'd lose my balance (I never did, but still) when out for a run. I'm 31 years old, by the way. The neurologist finally suggested the link between the dizziness and the pill, and suggested I try something even lower dosage. So I switched to Yaz.
I'm in my second month of it, and trying to power through to finish the pill pack just so I don't mess up my period too much, and I am a disaster. I should also mention I've had some major life changes as of late, moving to a new city, new job, and newly living with my boyfriend, so I'm sure this plays a part. But I have been an absolute train wreck since I started Yaz. The dizziness has gotten far worse, making me feel like I'm in a fog, sort of detached, hard to focus. Been awful to my boyfriend, when only weeks ago we were SO EXCITED to finally be living together and having this crazy adventure together. He asks me now why we can't just be happy. I get annoyed so easily, have had massive mood swings, and several panic attacks. Everything you all are describing - heart palpitations, headaches, nausea, insomnia. All the things I used to love to do, especially going out and exploring and being social (I just moved to NYC for god's sake!!!) are daunting and almost terrifying, and all I want to do is lay on the couch at home and hope the dizziness subsides. I was seriously contemplating psychological therapy, and my boyfriend was trying to get me to try yoga, but how could I possibly even do the poses when I can barely balance myself?? The only time I feel remotely normal is when I force myself to go for a run and just try to power through the light headedness.
I am finishing up the pack on Friday even though I should take it through the middle of next week, and I'm going to give myself a couple months off and go back to sucky condoms just to try and clear my head. Then I'm going to see if my doc will put me back on Orthocyclen.
Has anyone else experienced dizziness or light headedness on these pills? Have you found a pill that works for you?
Any suggestions on which birth control pill (or method) I should try next? I'm so tired of putting hormones in my body, but I'm not ready for kids yet and really hate condoms. I was looking into the ring but I hear that's just as bad. Sigh. If only they could do temporary vasectomies.

I've been taking Metoprolol for moderate high blood pressure since July2007.
I've been dealing with weight gain....nightmares....sleep disturbances and more within weeks since I began.
I wasn't sure what was going on with me.
I'm 55 and attributed all this to some sort of midlife crisis or something psychological.
I've contacted my primary care physician and will hopefully have an appointment within the next several days.
In the mean time I was told to STOP taking the medication and that he will assess my BP and alternative meds when we meet for my appointment.

Hi ..this is a follow up on my first posting of Jan 31 (see kookoo). I have been off Lipitor (20mg/day) for about 6 weeks now and I feel better than before but nowhere near normal yet. Hands are stronger but weakness in arms still persists. I have not had a bad tremor incident in about 2 or more weeks. But I have a lot of involuntary twitching and light burning in my arm muscles. I constantly feel like I have a stiff sore neck and the fatigue is unbearable some days. My neurologist (my hero since he is the only one who believes this is statin related) has sent me for additional tests like EMG, MRI and thoracic vascular scan to eliminate other causes. So far all my tests have come back within normal ranges. I still cannot exercise much because when I try it seems to trigger the burning and pain in my arms. Night time is very scary to me for all my symptoms seem to heighten and I think this brings on some added anxiety which leads to sleeplessness. Well I fired my primary care physician and am scheduled to see someone new next week. Hopefully she will listen to me more intently and have some beneficial suggestions. Hang in everyone, I have to believe we are on the right track and soon someone with some sense will finally listen and do something about these terrible statin drugs. KOOKOO

My primary care physician gave me a scrip today for Lisinopril for my sorta-high-at-times BP. I am a Hepper and I have significantly reduced my viral load from 1.1 million in 2001 down to 39,000 as of last summer through a strict regimen of vitamins, supplements, prayer, stress avoidance, and basic all around clean living. With what I have to face every day with this Hep C...If my dr. thinks I'm gonna take this stuff, he's as crazy as a peach-orchard boar!

The scrip is sitting here on my desk. I go back to my doctor in six weeks. I guarantee my BP AND my weight will be down to acceptable limits....And when he says, "I see it worked", I'm gonna hand him the scrip and say..."Ya reckon?????"....hehehehehe....

fingerpik

I was prescribed Levaquin 1000 mg. for 5 days for pneumonia the last week of December 2006. I was also prescribed Prednisone. Everything I ate tasted like metal. A couple of days after I started taking the Levaquin I started experiencing muscle cramps in my rib cage which are so severe it makes me double over in pain. After more than a year I still have the muscle cramps which now include not only my rib cage, but the arch of my feet and sometimes legs. I have a torn tendon in my left arm which didn't happen until about a month ago, but I am sure it is caused from muscle damage from the Levaquin. I am also on Advair Discus 250 which I didn't take before using the Levaquin. I didn't require inhalers or other medication before the pneumonia. My doctor now says I have COPD caused from asthma and chronic bronchitis. I used an Albuterol inhaler when I first got sick because the pneumonia was so bad. I thought after taking the Levaquin I would get back to normal. But even after the infection was cleared up I would get out of breath, so I returned to my doctor. She did an x-ray and said I had COPD and prescribed the inhalant. What I don't understand is that I didn't have breathing problems before the Pneumonia. I didn't have joint pain and muscle cramps either. I have had to quit working this past year because of it. I cannot go without the Advair, I can no longer walk long distances without pain. I have constant muscle pain just trying to do normal housework. How long do the effects last? Must be a lifetime.

So...
The Geodon seemed to make me too drowsy and I felt it was causing my sleep issue. I couldn't wake up in the morning. It was like I was still in REM while trying to wake. I could sleep until 12 noon and then realize I was late for work. Adderall barely seemed to help anymore.
After swearing off medications forever, I finally hit rock bottom realizing that my BiPolar had gotten the best of me. A DUI, WAY BAD CREDIT...I dug my self a hole of DEBT! My compulsive EVERYTHING had dug me a hole that thank God my Mother is still willing, after 22 years, is willing to help pull me out.
On my own, no psychiatrist involved, with my samples of Geodon and a prescription of Adderall provided by my primary care physician...I decided to go back on medication and so far...a week into it, I have noticed a significant difference...and so has others. Yes, I still might not want to wake up in the morning, but I am able to effectively work and actually somewhat enjoy doing it. I feel like I want to do things where as before...I just wanted to sleep or lay on the couch watching TV. I want to have a future and I want to better myself, where as before I wanted nothing but another drink and some pills. I feel that my quality of life has already improved and I hope with seeing my new psychiatrist on Tuesday, he might better my therapy.

Here is my current problem before asking my doctor.... hadn't taken any adderall for days. I took the Geodon at night, 60mg one day and 80mg the next thinking it might help with my sleep but it didn't do a thing. I Then the next day I took adderall around 7AM and 80mg of Geodon about 9PM and I couldn't keep my eyes open about 1-2 hours after taking the Geodon and I over-slept that morning and didn't wake up until after 10:30am when I am suppose to be at work at 9:00am.

Is it common for the extreme drowsiness to occur with the combination of Adderall in the morning and Geodon at night? I know before when I took both never missing either one, I was always extremely drowsy and that's one of the reasons I stopped taking meds. But after experiencing Geodon without adderall, I am wondering if the TWO don't mix well.

PLEASE HELP.

I was given samples of Levaquin 750 mg by an urgent care physician for a UTI. Fortunately, he only gave me 3 pills because I did not sleep a wink for 72 hours. My heart raced and I was concerned that I could not rest. The first day that I did not take a pill I was able to return to my normal sleep habits, thankfully. I should also note, although I did not sleep, I operated with an excessive amount of energy and no other side effects.

I had two Kenalog injections (not sure of the dose) several years ago to help curb the effects of dyshidrotic eczema on my hands ... and wound up not ovulating for about three months. This had not even been brought up as a potential side effect when my dermatologist recommended the injections, and she acted as though it was a very small thing when I called about it later on. I was not given a drug information sheet (nor, I have to confess, did I ask for one).

In my personal experience, though, the relief from the pain, blisters, cracking and bleeding on my hands was worth not having a period for several months, but if you're trying to get pregnant or already have female problems (i.e., PCOS, etc.), I would make a point to discuss these things with your dermatologist and/or your regular care physician before progressing with the injections.

I took this medication seven years ago. After a couple of days I broke out into hives. When the initial Hives went away I kept itching. Then, the itching began to spread all over my body. I have been turned away by many doctors who wished me luck and said they were sorry but they couldn't help me. Since then, I have become a science project for doctors. I have taken a number of medicines to calm me down and an assortment of creams and lotions. One spray that takes the itchy hives away for awhile is CLOBEX. It's very expensive. It costs me $250 a month (out of pocket). The only medicine that relieves the condition for about a week is prednisolone (another drug that's not so great for you). I now take that once a month for one week’s relief. Each night, I have to scold myself in the shower to relieve the itching for a few hours so I can go to sleep. I'm currently at a new Dermatology Clinic. Guess what they prescribed for me? CEPHALEXIN, the drug that caused the poor quality of my life I now have. Doesn't anyone listen to the patient? The only best medical friend I have is my Primary Care Physician who has greatly supported me all these years. I pray that someone may read this and I have an answer me.
If you have not yet taken CEPHALEXIN, think about it long and hard. It's not for everyone and MAY not be for ANYONE. If you've read this far in my note, I consider you a new friend.

Someone please help!!
Still Itching in New Jersey.

I'm glad I found this site. From the moment the Mirena was inserted, something was different about my body. It was inserted in October 2006 - 12 weeks after the birth of my twins. I thought it was a good idea until the side effects started. In November 2006, during a staff meeting, I felt an INCREDIBLE pain on the left side of my lower abdomen. I thought it was a one time occurrence, until I felt it again every month before my period was due. Then, during a routine check up with my primary care physician, he noticed that my blood pressure was extremely high (150/100). After monthly check-ups and blood pressure medication, it still hasn't resumed a normal range. I would have been able to manage these two side effects, but things got worse. In July 2007, I started to experience shortness of breath. To be honest, I have allergy asthma, but it didn't feel like a regular attack. So, I went to my pulmonologist for a check-up. He conducted the following test: breather-lizer (to check my breathing pattern), blood oxygen level (stationary & running up stairs), EKG, x-ray of my lungs, blood test and a CT scan of my lungs to see if I had blood clots. All the test came back negative!!!!! He answer - it's your birth control. Went back to my PCP to get my blood pressure checked, and it was still high. So, recommended that I get an Eco-cardiogram of my heart. Of course, it came back negative! Actually, my PCP said that I'm extremely healthy. However, the hormones in my birth control could be causing an adverse reaction to my system. Keep in mind ladies, I've gone to my OB to get the Mirena removed and her only concern is that I can't get pregnany any time soone because my twins are 12 months old and I had a c-section. So, my uterus won't completely healed until Januar 2008 (18 months post-partum). To finish briefly, I also have been having extruciating headaches; teenage acne; neck, shoulder & back pain; fatigue; and to top off the list - I have gained 25 pounds since the birth of the twins. In summary, I would not recommend this product to anyone - not even my worst enemy!!!! I'm going to call my OB again tomorrow to schedule an appointment to get it removed. If she refuses, my PCP said to call him and he'll strongly suggest that she take it out. If she refuses him, then he's going to send me to another physician at his affliate hospital that will handle this situation.

On June 4, 2007 my husband had achilles tendon surgery on his left leg. He will be in a cast until July 19th at which point it will be determined if he has to be cast again. He took Levaquin 750 mg for 10 days beginning April 10 - 19th. On the early morning of April 21st he was CONVINCED that someone was trying to break into our home, he called 911 TWICE and the police came to our home to find nothing. I forgot to mention that he was also taking 500mg of Lortab for the extreme pain in his legs. Just after the police left for the 2nd time he took 2 steps and fell, rupturing the left achilles and tearing the right. I took him to the emergenceny room and he was so dehydrated that his kidney function had pretty much subsided. After 2 more visits to the emergency room he was hospitalized with Kidney failure. After a different round of antibiotics and fluids he was released after 4 days in the hospital. During his stay the swelling is his legs was terrible and the pain with the ruputures and tears of tendons was unbearable. After a vist to a rheumatologist she immediately diagnosed his injuries as a result of taking Levaquin. So currently he has a cast on his left leg and a boot on his right in hopes the right will heal without surgery. His primary care physician apologized because he didn't know about this drug. Surely there is something that can be done.

My main problem with Lisinopril is the coughing. Coughing, coughing. coughing. I will be fine for 2 to 3 hours and then start with this awful cough. People will actually turn away from me if I am out shopping and a cough begins. I presume they believe it is contagious. Sometimes I end up vomiting and I cannot catch my breath. Coughing at night is really a problem because of lack of sleep. Doctors believe my cough is due to allergies because I have post nasal drip. However, none of the medications they have given me stop the coughing. I never had this problem until I began taking Lisinopril. Lisinopril is my first Blood Pressure medication.

My 8 yearold daughter after about 2 months of being on singulair started having muscle spasms on her right side of neck and face. Later the spasms started getting worse. She said like she felt someone was jerking her head. She also started having uncontrollable kicking spasms. We had an MRI of her brain and spine done. Nothing, she was fine. We had a biospy of a small lesion from a prior cut; nothing again. Finally, we took her off the singulair, the only drug she was taking. She is now fine. Her primary care physician, said mmmmm, possibility. It just seems too coincidental that the spasms started after she began taking singulair then stopped after we took her off. Anyone else, have similar experience??

Bruce, don't take the shot anymore, go to a E.N.T. allergy Dr. & start the shots for allergies. I think these weekkly shots last for a period of at least 4-5 years every week. Check with your primary care physician for a referral. I'm gonna do just that!! No more Kenalog shots, there's to many side effects that hurt you in the long run!!!!!!!

My problem is itching. I have been on Zocor for 3-1/2 years and it did its job by lowering my cholesterol. I started itching about three months ago (all over). I have been to Primary Care physician, dermatologist and allergist. The itching seems better but still have it after being off the Zocor for almost four weeks. I take other medications so I don't know for sure about the Zocor but had to start somewhere. How long after stopping the medication should the side effects disappear?
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