Urgent care center symptoms and conditions

I had a Kenalog injection in May. I was on vacation in Vegas and had bad allergies and ear pain due to my allergies. I went to an urgent care center and they injected the shot in my right butt cheek. I noticed an indention in that spot today and never would have linked it to the injection. I did online searches and put it together. I called the urgent care center and spoke with a nurse who told me that muscle atrophy at the injection site is a side affect and yes it can take several months to show up. In my case exactly 5 months to the day. The doctor called me back. I asked why he did not tell me about the side effects. His response was that only 1% of people get this kind of side effect. I highly doubt that this is accurate considering I can google it and find many people with the same reaction. I asked if it will go away and he said it may never go away. I am 27 and in shape. I am interested in pursuing this legally if it does not go away. It is pretty upsetting.

About 2 and 1/2 months ago I went to an urgent care facility since I felt like I was suffocating. I am a long time smoker (30 years) and have not had any problems with breathing accept for the occasional morning cough. Long story short, the doctor after hearing my breathing and taking 2 xrays said "you have a pocket of infection in your lung and COPD". I didn't realize it was that quick and easy to diagnose COPD and thought there were more extensive tests to prove that, but I went along with the doctor. The doctor prescribed Advair, an antibiotic, ProAir HFA (albuterol pump rescue inhaler), a decongestant and prednisone. I thought that was an extreme amount of medication but the doctor said she was being proactive. After a couple albuterol breathing treatments and a shot of steroids at the urgent care center I was on my way.

I finished the treatments of antibiotics and steroids as prescribed, but I never took the decongestant (did not want to over-medicate myself). Immediately after starting Advair my joints ached and I felt over all like I had the flu. With my 1 weeks checkup with the doc I mentioned this and she just smiled. About a week after that the achy joints starting easing up, but I started cramping in different muscles. For instance one week I would have a dull cramping in my leg that was persistent during the day and worsened at night. Then the leg stopped cramping, then the lower part of my back started in to a point it was hard to get out of bed, walk or bend over. Then when that stopped something else started up. Then during the last two weeks that I was on Advair I was having periodic chest pains, tightness in my chest, (once again) difficulty breathing, and my vision started to go (blurring)...that with the lower back pain. I am almost 50 years old and have been in excellent health my whole life, and honestly I have never felt as bad as I did while on Advair.

I stopped taking Advair 6 days ago. No, I did not call and ask the doctor's advice because I knew what the doc would say. The first day after quitting Advair I had restricted breathing so I used the rescue inhaler once. The breathing issue became better during the remainder of the day. Slowly the cramping in my body and chest eased up. Today (6 days later) my vision is back to what it was, no chest pains, occasional restricted breathing and will use the rescue inhaler during those times.

I think it's too early to know the long lasting affects of Advair, but at this stage in my life (unless I am worse off with my breathing than I am right now) I don't care to use the medication.

I HAVE TAKEN AVELOX BEFORE FOR A URI/BRONICAL ASTHMA AND I DIDN'T HAVE ANY PROBLEMS . THE SECOND TIME I WAS PRESCRIBED THE AVELOX WITH IN 20 MINS I STARTED TO BREAK OUT FROM HEAD TO TOE IN A VERY BRIGHT RED RASH AND FELT LIKE I WAS ON FIRE . I FELT LIKE I COULDN'T CATCH MY BREATH AND STARTED TO GET VERY ANIXOUS .I WENT TO AN URGENT CARE CENTER AND HAD TO GET A SHOT OF BENADRYL TO STOP THE REACTION . I WILL NEVER TAKE THAT STUFF AGAIN . IT IS VERY NASTY STUFF AND WOULDN'T RECOMMEND THAT ANYONE TAKE IT. STAY AWAY FROM IT FOR YOUR OWN SAFETY ...IT SHOULDN'T BE ON THE MARKET !!!!!! ITS BAD NEWS

Wow....sounds like Kenalog is not a drug to be administered without careful consideration of the pros out- weighing the cons. I had a Kenalog injection in my elbow at an urgent care center while on vacation about 8 mos ago (painful elbow was impacting vacation activities). It took my pain away 100%. Never gave it another thought even until just recently when it began hurting again. Did, however, notice the atrophy at injection site...and a grayish tone to skin. Indentation has not grown, but certainly has remained. My elbow is also super sensitive. Feels like the nerve is right there under a thin layer of skin.....so sensitive. I also have leg shakiness, hip weakness, anxiety, nausea, and increased heart rate....I assume these are related as I did not have these issues prior. These issues bother me way more that the indentation on my elbow. Dont like not feeling well. I guess the learning is that all medications are foreign to your body and thus have potential side effects. One needs to ask questions and or do own research on their own prior to consenting to take a mediation to be sure the benefits are worth it.

Sadly, I am just another case among many it seems. I am a 26 year old female who was prescribed ciprofloxacin for a UTI at my urgent care center. I have health problems to begin with and did not want any more. You know, I’ve had to take all kinds of meds over the years, including harsh ones, but it was never so bad as to prompt me to write comments on the internet about it. What does that say about Cipro? When I got home from the doctor I read the paper before swallowing the pill, which included the description of side effects. Unfortunately, it did not include the truth about what could happen to you while even taking this drug for a short time. If there had been some kind of warning about the strength and potential risk of taking this drug, I most likely would have steered clear from it since I am sensitive to medications and already suffering. The paper led me to believe false information, listing some common antibiotic side effects, and I ended up starting treatment. Some of the negative effects I experienced while on this medication for only 2 days were: severe muscle/overall body weakness, difficulty breathing, fatigue, mental confusion, difficulty concentrating, anxiety/nervousness, restlessness, mild carpal tunnel pain, slight vision change, stiffness, pain, an overall feeling of terrible heaviness, including of the chest, and possible heart palpitations. It felt like the medication was damaging my body; like it was eating away at my muscles or something. I've never had chemotherapy before, but some how that's how I would imagine it. It felt like it was doing damage to every cell in my body. The worst part is the weakness and altered thinking right now. I hope these symptoms go away completely. I felt better after quitting the drug, but not completely. I am just thankful for my hope in Jesus Christ. Even if things don't improve, I am comforted that He cares for me. I am going to be praying for this terrible situation where doctors are just handing this out for common problems without giving proper warning. May fewer and fewer people have to suffer because of Cipro and this class of drugs. I am also going to report this to the FDA and hopefully to my doctor’s office. I would like to see clear and extensive warnings on this drug, if not for it to be taken off the market. My personal advice to any one who is currently on this medicine and experiencing side effects would be to: drink milk or eat other dairy products to lessen the symptoms. It seemed to temporarily help me.

I have been taking Lamictal since October of 2007. I experienced some of the symptoms (muscle pain in the head and neck) before I started the medication. I have experienced panic attacks since July of 2005. I have had mild heart palpations since I was in my mid 20's (I'm 36 now). I have had what I would consider a below normal energy level since my mid 20's also. Ok so like everyone else I am thinking I'm a hypochondriac! However, I was diagnosed August 28th 2007 with having Lyme’s Disease and also Hyper-Thyroid (same time, same lab-work). Two weeks later I was diagnosed with Bi-Polar Disorder (this is one thing I knew I was battling but didn't know how to handle it). My physiatrist started me on Lamictal and I did the standard ramp up to 200mg. I also was started on a 90 day treatment of Dyoxicycline for the Lyme’s and Methimazole for the Hyper-Thyroid. I was very very weak and was only able to stay awake for short periods of time (4 to 5 hours max). Just an fyi, I am not overweight, lazy or unmotivated. I have the physical appearance of perfect health. This, I think works against me as the Dr's seem to think I'm just whining. Mater of fact; my Primary Care Physician never tested me for Lyme’s. I went to an Urgent Care Center which tested me for Lyme’s disease and I came back positive (they also tested my Thyroid levels and found the problem with my THS levels) I told my Dr the results and he insisted I have same test done again. Guess what, new tests, same results.
My symptoms today are very similar to what I have seen posted many times. Muscle pain (entire body, some areas worse than others), heart arrhythmia, racing heartbeat, intense palpitations, nausea, foggy “un-plugged” mind, fatigue, weak muscles, muscle cramping (especially after repetitive motion, such as strumming a guitar), panic attacks (much more severe) and the latest addition to the group, Insomnia. Muscles pain in my head, fore-head, jaw, temple, neck (front and back), shoulders, is terrible to say the least. The pressure in my fore-head (right under my brow) makes me feel like I need to close my eyes or rest (resting does not relieve anything). The front of my neck is so tight at times it feels like my jaw is being pried down. I could go on and on.
On my quest to find out what else is going on with my body I have had 2 Echocardiogram’s on my heart and abdomen, 2Nuclear Stress Tests, blood work out the wa-zoo, MRI of my brain, 2 CT’s of my Head and Neck, Chest X-rays, Endoscopy, Colonoscopy, and all revealing nothing.
Most doctor’s I have encountered seem to want to treat the symptoms, not the problem/disease. I believe I know why; we (the ones who are there for solutions) tell them what the symptoms are (how we feel). We of course are thinking “this will help with a diagnosis of the problem/disease”, when in fact (I feel); the doctor’s thought process stops there. They don't know what’s wrong with you but they do know what your symptoms are so....bingo, let's treat the symptoms. Don’t misunderstand what I am saying. I’m not saying, “Most doctor’s don’t know what they are doing” or “don’t take your meds”. I am saying you and I are one of the 20 to 30 patients most doctor’s see daily (100+ weekly). They may be caring and good people but they are just as human and fallible as you and I. My advice is this; (and I am taking my own advice) don’t always “pop” into your body what the doctor suggests/prescribes, without doing your own research. Heck most of us won’t buy a car or more importantly, send our kids off to a college with out doing your own research (we just don’t trust those shinny brochures). Your body and your health are worth you doing your own research. Just keep in mind, Pharmaceutical Reps are always at your Dr.’s office (sit in the waiting room for 10 minutes and I’m sure you will see one). Reps are paid to do one thing; encourage (push) the Dr.’s to promote use of the Pharmaceutical Companies drugs.
My wife and I have been doing our own research on Lamictal (after a year of taking this stuff) and the side effects associated with this drug. We have searched through many (many,many) web sites for information and we have talked with pharmacists and Dr’s for opinions. Although I’m am not thoroughly convinced that Lamictal is the cause of all of my symptoms, my wife and I have decided to lower my Lamictal slowly from 200mg to 100mg. I am now taking 150mg daily (three days now) and plan on staying at this level for a total of two weeks before lowering to 100mg. I do fear dropping the dosage to quickly (potential side effects) or lapsing into a mania. To help avoid a manic episode my wife and my immediate family are all “up-to-date” with my course of action. They are on “Red Alert” and have promised to keep a close eye on my behavior patterns and moods. (I don't want to put them through another hyper-mania episode, its much too devastating). I do want so badly to feel healthy and alive again and at this point I am rather frustrated with the Dr.'s ability to help me achieve this goal. Remember it is called “Practicing” Medicine. So now I’m going to practice a little, very carefully and cautiously.
As a foot note; I have recently (past two weeks) been re-tested for Lyme's with a negative response. I am keeping in mind Lyme's test are very inaccurate (still hoping this one is accurate). My thyroid is under control and normal, so.... let's see if dropping below 150mg of Lamictal will eliminate some of these other symptoms. I will keep you posted.
Erik

90% BLOCKAGE OF MY SUPERIOR SAGITTAL VEIN IN MY BRAIN..... HUGE BLOOD CLOT IN MY BRAIN DUE TO LOESTRIN 24FE...AND 4 OTHER SINUS VEINS WERE TOTALLY BLOCKED THE CLOT HAD BEGAN TO TRAVEL DOWN INTO MY RIGHT JUGULAR!!!!!!!!!!!!!! ALL DUE TO LOESTRIN 24FE .... I ONLY TOOK IT FOR 6 WEEKS.... I THANK GOD EVERY SINGLE DAY THAT I AM ALIVE!!!!!! LADIES AND ANYONE THAT HAS A LOVED ONE THAT IS TAKING THIS OR ANY OTHER HORMONE BASED BIRTH CONTROL PILL:::::::::::::::::::::::::::::::::::::::::::::::::::::::::::::::::::::::::::::::::: PLEASE READ BELOW!!!!!!!!!!!!!!IF YOU HAVE ANY QUESTIONS OR HAVE HAD SIMILAR THINGS HAPPEN TO YOU PLEASE PLEASE PLEASE FEEL FREE TO CONTACT ME…… GOD SPARED MY LIFE FOR A REASON SO EMAIL ME @ ****** please ****** if I can help I am here I am only an email away…. May u be blessed…. Also there was a woman they told me that got married went out on the floor for her first dance with her husband and collapsed she too had a blood clot in her brain but wasn’t as lucky as some of us may and have been so if u have a headache and are taking these pills, please it is better to be safe rather than sorry…. We all have too many people that love us and will miss us and be so hurt if we were to pass away…. Please listen to your body, if it is rejecting these pills then stop taking them….. I don’t even know u but this world doesn’t deserve to loose you!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!

****** ....................... I was placed on Loestrin 24fe Feb. of 2007, after taking it for a month and a half I got a sudden and terrible headache on a Tuesday at lunch and no matter how much Advil or Tylenol I took it wouldn't go away, well finally I went to the 24hr urgent care center at about 1a.m.Thursday morning. after 3 shots of morphine that didn't work, a Dr. (MALE) trying to tell me that it was just a migraine (from birth control and I should switch to the Depro shot) and I didn't treat it fast enough, so I had to stick it out, mind you they had given me three shots of morphine by this time and my head still felt like it was going to explode. needless to say he discharged me and the nurse that was caring for me said against her better judgment she was letting me go home but grabbed my hands looked me square in the eyes and made me promise ( swear to GOD ) if I didn't feel any better or my headache got worse by the morning I would go to the nearest E.R and demand that they scan my head because at this point she said you don't have to tell me that the medication isn't relieving the pain I can look at you and tell you it isn't working... long story short.. I kept my promise to her and ended up back at the E.R less then 12hrs later ( AND THAT IS WHAT SAVED MY LIFE, HER MAKING ME PROMISE TO SEEK MORE CARE) they to put me in minor care and said it was just a migraine headache, gave me morphine again (Which didn't work this time either) until I gave the run down of being at the urgent care center just a few hours earlier and the nurse making me promise to make them scan my head because her concern was what was causing the headaches that wasn't responding to the morphine?? Finally the Dr. (Male) listened to me and ordered a cat scan, said something looked abnormal the Dr. moved me to the real E.R. and then ordered an MRI then B4 they could wheel me back to my room in the regular hooked back up to my i.v. the wheeled me back and did MRV's with and with out contrast. A neurologist came and gave me my diagnosis and told me i was lucky to be alive that I was at extreme risk 4 seizures and strokes and that i needed to notify someone at home of what was going on. I was admitted from the e.r directly to ICU. My diagnosis was Superior sagittal venous thrombosis. I had a 90% (blood clot) blockage of the main vein that runs down the center of your brain (Dr. say its from the Birth control) feel free to write me with any questions, just be careful, with any birth control choice that involves hormones. theres more to this story I am not some crazy lady I am very lucky to be alive and would never want anyone else to go through the hell I have been going through since April of this year.my email address is ****** Thank you again Nurse ***, Fl for saving my life..... You are truly one of God's angels walking among us. Check this out below... I cut this from a posting on the internet about cerebral venous thrombosis which they also refer to the blood clots of the veins in ones brain. take care, hope to hear from you soon. Headache is the most frequent symptom in patients with cerebral venous thrombosis. However, patients presenting with headache due to cerebral venous thrombosis are uncommon. The association between oral contraceptives and cerebral venous thrombosis is well known. We report the case of a young woman who was admitted to our department for sudden onset of headache. She had been taking oral contraceptives for 6 months. Early pharmacological approach with analgesics failed to alleviate symptoms. Magnetic resonance imaging (MRI) showed thrombosis of the posterior and middle thirds of the superior sagittal sinus (SSS). Because the patient was oligosymptomatic, medical treatment with high-dose heparin was started. A clinical follow-up showed headache regression after 2 weeks of therapy. Subsequent MRI showed partial re canalization of the SSS. The patient continued oral anticoagulants for 3 months. Eighteen months after discharge, the patient was symptom-free. We conclude that new, persistent or atypical headaches in patients taking oral contraceptives should be carefully evaluated for cerebral venous thrombosis.

I'm so glad I found this site. I, too, thought I was going crazy! The first two months were ok on Yaz. Lost some water weight and my periods were light and short. As the months went on things got worse. Depression, anxiety heart palpitations that sent me to the Urgent Care Center, extreme fatigue, irritability, irrational mood swings, absolutely NO sex drive, neck and back pain and an increase in my acne. This has been 3 months and I can't stand it any more. It just amazes me that doctors still don't even consider that extra hormones in our bodies would not cause some of the horrible side affects we are experiencing. Good Luck to all.

I have a sinus infection, and my doc gave me biaxin. My first dose didn't affect me, I went to bed as soon as I got home from the urgent care center, I slept well into the afternoon. When it came time to rest, I went to bed at midnight, laid there restlessly, with a very sore throat even more sore than I began with. I grabbed a throat lozenge, fell asleep for 30-45 min, weird dream but I can't remember it well. I woke up with a sore dry throat again, not even tired, frustrated, I decided to take my meds again, not having checked this website first!!! D: now my heart is racing, I'm wide awake, its 4:45 in the morning. I am crying on and off. The pain in my throat has subsided, its still scratchy, and my lymph nodes are very swollen. I can't breathe through my nose and it feels like there is still drainage in the back of my throat. I have no appetite either, I force my self to eat b/c I get stomach pains. I am wondering if I should hold off the biaxin for a couple of days and see if I improve.. because I feel like I'm simply getting worse.

90% BLOCKAGE OF MY SUPERIOR SAGITTAL VEIN IN MY BRAIN..... HUGE BLOOD CLOT IN MY BRAIN DUE TO LOESTRIN 24FE........... THANK GOD I AM ALIVE!!!!!! PLEASE READ BELOW ....................... I was placed on Loestrin 24fe Feb. of this year, after taking it for a month and a half I got a terrible headache on a Tuesday and no matter how much Advil or Tylenol I took it wouldn't go away, well finally I went to the 24hr urgent care center at about 1a.m.Thursday morning. after 3 shots of morphine that didn't work, a Dr. (MALE) trying to tell me that it was just a migraine (from birth control and I should switch to the Depro shot) and I didn't treat it fast enough, so I had to stick it out, mind you they had given me three shots of morphine by this time and my head still felt like it was going to explode. needless to say he discharged me and the nurse that was caring for me said against her better judgment she was letting me go home but grabbed my hands looked me square in the eyes and made me promise if I didn't feel any better or my headache got worse by the morning I would go to the nearest E.R and make them scan my head because at this point she said you don't have to tell me that the medication isn't relieving the pain I can look at you and tell you it isn't working... long story short.. I kept my promise to her and ended up back at the E.R less then 12hrs later, they to put me in minor care and said it was just a migraine headache, gave me morphine again (Which didn't work this time either) until I gave the run down of being at the urgent care center just a few hours earlier and the nurse making me promise to make them scan my head because her concern was what was causing the headaches that wasn't responding to the morphine?? Finally the Dr. (Male) listened to me and ordered a cat scan, said something looked abnormal the Dr. moved me to the real E.R. and then ordered an MRI then B4 they could wheel me back to my room in the regular hooked back up to my i.v. the wheeled me back and did MRV's with and with out contrast. A neurologist came and gave me my diagnosis and told me i was lucky to be alive that I was at extreme risk 4 seizures and strokes and that i needed to notify someone at home of what was going on. I was admitted from the e.r directly to ICU. My diagnosis was Superior sagittal venous thrombosis. I had a 90% (blood clot) blockage of the main vein that runs down the center of your brain (Dr. say its from the Birth control) feel free to write me with any questions, just be careful, with any birth control choice that involves hormones. theres more to this story I am not some crazy lady I am very lucky to be alive and would never want anyone else to go through the hell I have been going through since April of this year.my email address is ****** Thank you again Nurse ***, Fl for saving my life..... You are truly one of God's angels walking among us.

Check this out below... I cut this from a posting on the internet about cerebral venous thrombosis which they also refer to the blood clots of the veins in ones brain. take care, hope to hear from you soon. Headache is the most frequent symptom in patients with cerebral venous thrombosis. However, patients presenting with headache due to cerebral venous thrombosis are uncommon. The association between oral contraceptives and cerebral venous thrombosis is well known. We report the case of a young woman who was admitted to our department for sudden onset of headache. She had been taking oral contraceptives for 6 months. Early pharmacological approach with analgesics failed to alleviate symptoms. Magnetic resonance imaging (MRI) showed thrombosis of the posterior and middle thirds of the superior sagittal sinus (SSS). Because the patient was oligosymptomatic, medical treatment with high-dose heparin was started. A clinical follow-up showed headache regression after 2 weeks of therapy. Subsequent MRI showed partial re canalization of the SSS. The patient continued oral anticoagulants for 3 months. Eighteen months after discharge, the patient was symptom-free. We conclude that new, persistent or atypical headaches in patients taking oral contraceptives should be carefully evaluated for cerebral venous thrombosis.

I've had asthma since I was a teenager, and about 9 years ago I went to an allergy and asthma specialist and had the whole gamet of tests run to find out why my allergies and asthma were worsening. I was prescribed Advair, Albuterol, Prednisone, & Servient. At the time, these were the only medications I was taking and never experienced any severe side effects. My asthma was much better and by my one year check up, I had almost completely stopped using the Albuterol for sudden attacks. Due to my graduation from college, I was no longer covered under my parents insurance and due to the cost of the medications, discontinued my treatments. I felt fine, hadn't had any attacks or breathing episodes, so I felt I could do this without any problems.

Fast forward to this summer. My asthma symptoms had returned and my PCP put me back on the Albuterol. It helped the sudden attacks, but I was blowing through an inhaler in a month. Last week I found myself in my local urgent care center, barely able to breathe, gasping for breath. I'm 31 years old with an almost one year old. They gave my 3 breathing treatments and prescribed Prednisone (only 5 days worth), Albuterol, and the Advair. After a week on the Advair, I feel so strange. I haven't had to use my fast acting inhaler since last week, but I feel like my heart is going to jump right out of my chest. I have a constant headache, a weird ache in my right arm, can't sleep even though I am exhausted, and my mind is constantly racing. It's like I can't slow down. After reading all these crazy side effects and comparing them with my own, I'm stopping the Advair. I have an apt. with my asthma specialist in 2 weeks and I will be sure that he doesn't put me back on this med. It's awful...can't imagine taking any drug with a side effect of death.

I was placed on loestrin 24fe Feb. of this year, after taking it for a month and a half I got a terrible headache on a Tuesday and no matter how much advil or tylenol i took it wouldnt go away, well finally i went to the 24hr urgent care center at about 1a.m.thursday morning. after 3 shots of morphine that didnt work, a Dr trying to tell me that it was just a migraine (from birth control and i should switch to the depro shot) and i didnt treat it fast enough, so i had to stick it out, mind you they had given me three shots of morphine by this time and my head still felt like it was going to explode. needless to say he discharged me and the nurse that was caring for me said against her better judgment she was letting me go home but grabbed my hands looked me square in the eyes and made me promise if i didnt feel any better or my headache got worse by the morning i would go to the nearest E.R and make them scan my head because at this point she said you dont have to tell me that the medication isnt relieving the pain i can look at you and tell you it isnt working... long story short.. i kept my promise to her and ended up back at the E.R less then 12hrs later, they to put me in minor care and said it was just a migraine headache, gave me morphine again (Which didnt work this time either) until i gave the run down of being at the urgent care center just a few hours earlier and the nurse making me promise to make them scan my head because her concern was what was causing the headaches that wasnt responding to the morphine?? Finally the Dr. (Male) listened to me and ordered a catscan, said something looked abnormal the Dr. moved me to the real E.R. and then ordered an MRI then B4 they could wheel me back to my room in the regular hooked back up to my i.v. the wheeled me back and did MRV's with and with out contrast. A neurologist came and gave me my diagnosis and told me i was lucky to be alive that i was at extreem risk 4 seizures and strokes and that i needed to notify someone at home of what was going on. I was admitted from the e.r directly to ICU. My diagnosis was Superior sagittal venous thrombosis. I had a 90% (blood clot) blockage of the main vein that runs down the center of your brain (Dr. say its from the Birth control) feel free to write me with any questions, just be careful, with any birth control choice that involves hormones. theres more to this story I am not some crazy lady i am very lucky to be alive and would never want anyone else to go through the hell i have been going through since April of this year.my email address is ***** check this out below... i cut this from a posting on the internet about cerebral venous thrombosis which they also refer to the blood clots of the veins in ones brain. take care, hope to hear from you soon.

Headache is the most frequent symptom in patients with cerebral venous thrombosis. However, patients presenting with headache due to cerebral venous thrombosis are uncommon. The association between oral contraceptives and cerebral venous thrombosis is well known. We report the case of a young woman who was admitted to our department for sudden onset of headache. She had been taking oral contraceptives for 6 months. Early pharmacological approach with analgesics failed to alleviate symptoms. Magnetic resonance imaging (MRI) showed thrombosis of the posterior and middle thirds of the superior sagittal sinus (SSS). Because the patient was oligosymptomatic, medical treatment with high-dose heparin was started. A clinical follow-up showed headache regression after 2 weeks of therapy. Subsequent MRI showed partial recanalization of the SSS. The patient continued oral anticoagulants for 3 months. Eighteen months after discharge, the patient was symptom-free. We conclude that new, persistent or atypical headaches in patients taking oral contraceptives should be carefully evaluated for cerebral venous thrombosis.

Prescribed Levaquin from Nextcare doctor after severe bronchitis with cough and wheezing for 3 weeks was not helped by Azithromycin or Albuterol. 4 days into the 500mg daily dose, I could not walk on rt leg. Knee pain and snapping so severe. Next day lt knee began to go out and snap. I had to scream each time I tried to straighten or bend my rt knee. Concurrently, left index finger swelled 2x normal size with pressure and pain as if it would pop. Rt wrist so sore that if it is touched, feels like all the nerves are exposed and being stabbed. Next my back began to hurt. This all happened before I realized it was toxicity from the antibiotic. I called the pharmacist explaining symptoms and she said mostly women get them and just take the last pill.
I did not, and went back to Nextcare dragging my right leg. The doctor then said he was 80% sure it is a reaction to Levaquin as my chest xray and blood tests came out negative for pneumonia or Valley Fever. So he said just rest a week. My symptoms are getting worse, I am trying to get into an orthopedist and have discontinued all my daily activities for the 9th day now as my rt knee is so horribly painful. It is snapping at least a hundred times a day with movement. I WAS an avid tennis player and have canceled everything due to pain and immobility. I have no support from any doctor so far as the urgent care center just does not care for individuals with a problem that they cannot dx as a cold or some simple thing.
I am in fear for my life after reading www.fqvctims.com site.
Help us all that we are allowed to be given poisons like this.
Ortho-McnNeil knows, so do the doctors, but enough of us have not died yet I guess. I can only hope I will not be one of them.