Medwatch symptoms and conditions

Oh my! I've been having severe anxiety since i've started singulair. The anxiety leads to shortness of breath which is extremely scary r someone with my medical condition. I had to have valve replacement surgery 4 years ago so I am very sensitive to any abnormal feelings I have. I took claritin d or about 8 years and I wanted to get off this drug because of the pseudoephedrine. I am off this drug starting tomorrow and will take regular claritin without the pseudoephedrine. The anxiety I had was so great I might actually consider legal action.

I am 61 years old. I started taking Lisinopril 10mg, once a day about 6-7 months ago. Because of cough, I switched to Diovan 80mg, once a day (samples from my physician friend). After running out of Diovan samples, I started taking Lisinopril 5 mg, once a day again about three months ago. For better BP control, I ended up again taking Lisinopril 10 mg, once a day about 5-6 weeks ago. I started to simultaneously suffer from having persistent, extensive and progressively worsening joint and muscle pains in my both sides of neck, both shoulders, both upper arms, left elbow, left lower arm, both wrists, both hands, all fingers, both knees and left calf muscles. I had difficulties walking, moving my arms, shoulders, doing anything with my hands at the peak of the pains about 7-8 days ago. In the night, my fingers were very stiff and uncomfortable that I hardly could make a fist and I had difficulties getting up to go to bath room because of pains. I felt like I were a 90 years old man. Even Cataflam and Advil did not work well to relieve the pain. As a retired physician, I started to suspect it was Lisinopril-induced side effects. I searched on Google and found this web site. Now, I realize that I am not alone. I got my Lisinopril from CVS Pharmacy. I immediately stopped taking Lisinopril about one week ago. All my joint and muscle pains have been dramatically subsiding (although not completely disappeared) without taking any NSAID pain killer. Even "cough problem" became much worse during the same time. I am convinced that Lisinopril I got from CVS caused my serious, extensive, multiple joint and muscle pains. Perhaps, FDA should look into this side effect: whether it is common ACE inhibitor related side effect or it is possible manufacturer, country origin of the product related problem (made in a non-USA country and imported by CVS?). I would never take Lisinopril again. Posted by myh810.

I continue to read and sit here crying. I wish I could reply to each and everyone of you...this drug needs to be stopped. The company needs to be held responsible for their actions. Avelox needs to be off the market!

I was given 6 tablets to cure a sore throat. After the first 2 tablets, I suffered severe abdominal pain and was told to take Imodium to relieve the pain. When the pain went off, I continued taking the third and fourth pill but stopped taking it when I felt unwell. Then the chills and the crying started. I couldn't sleep and thought I was going crazy. I didn't make the connection until I read this website. It has been almost a month since I stopped taking the medication and like most of those who had suffered similar symptoms, I have never had any emotional or mental problems and this is scary. Someone should tell the drug company to post a serious warning on this awful side effect which can really destroy lives. Can someone who have found a solution tell me how long will this last and if there is any way to expedite relief of symptoms because I cannot even concentrate on work, sleep and carry on effectively with daily activities. Thank you.

I am pissed that this drug is given out, my son is in a hospital because of this Biaxin, he has temmors, sweats on hands and feet , blood pressure elevated , cannot talk, nightmares, intense stomach pain, headace, rubbing hands , rubbing face , rubbing head , itching, chest hurts, feet sweats, cannot focus, fear of death, cannot sleep, we do not know if he is going to come out of this, we discontinued the Biaxin 9-22-09 he in lock down and being watched 24hrs. He was on this Biaxin for 6 days. Please do not take this product. The Doctors will defend this product since they get money from the drug companies to push there product. I will be looking for a lawyer!

I took levaquin (750) for a bronchial infection about 9 months ago. My doctor gave me individual samples with no info. on any side effects. Like most people, I trusted my doctor and took the pills without question. The aftermath has been a complete nightmare as I have suffered severe joint pain, depression and an atypical anxiety that at times that feels like a drug induced brain fog. I've seen numerous specialist searching for an underlying process causing the symptoms but nothing is ever found. Since the beginning I've contended that the Levaquin was at the root of my problem, but no doctor has ever given that thought any consideration. Prior to the Levaquin I was perfectly fine with no history of any joint pains or mood disorders. Does anyone have any ideas on how to reverse or heal the process?

Ladies,

My Mirena was removed Monday morning and my blood pressure was 165/101. Yesterday I was feeling considerably better but still had numbness in my arm last night. This morning, 2 days after removal, my blood pressure was 138/92 - still high, especially for someone not overweight, but an improvement over Monday's pre-Mirena.

Thank you to my friend Jackie who has located the FDA website (below) to file complaints. We must ALL file!!!! Although this website has absolutely been a Godsend to me and others, it isn't enough that we air our complaints to one another then let the matter rest. We must take this off the market! Strength in numbers, Ladies!

http://www.fda.gov/downloads/Safety/MedWatch/HowToReport/DownloadForms/UCM082725.pdf

Seriously, does anyone know anything about how to get a class action suit initiated?

L.

I had Mirena inserted in February 2009. Since that time I've had mild weight gain and acne. These were fairly tolerable, however, in the past 2 months I have had hair loss (I pull out 10 or more strands every time I run my fingers through my hair). I've scheduled an appt. to have it removed.

Please be sure to report the side effects of this drug at:
1-800-FDA-1088 or www.fda.gov/medwatch

You are encouraged to report negative side effects of prescription drugs to the FDA. Visit www.fda.gov/medwatch, or call 1-800-FDA-1088.

I URGE YOU TO PLEASE SUBMIT ANY ADVERSE EVENTS OF THIS TERRIBLE KENALOG DRUG TO THE FDA--JUST CLICK THIS LINK AND COMPLETE THE FORM: http://www.fda.gov/medwatch/. The FDA is responsible for assuring safety of medications. Therefore, it is imperative that the FDA recognize the adverse effects to provide any credibility to a class action suit. Please consider forwarding your case to the FDA to force them into action and begin addressing these atrocities. Here's my case: I am also a victim of having the Kenalog injection administered over a year ago to alleviate poison ivy itching symptoms. Prior to having the injection, I was not informed of any side effects. Not only did the injection not alleviate the symptoms, but has resulted in a discolored and uncomfortable indentation in my left buttock area and psychological anguish because of disfigurement of my body. It is over a year later and the indent remains and continues to cause discomfort. The dermatologist who administered the injection stated that there was nothing I could do to reverse such effects. I reported my case to the FDA (Food and Drug Administration) Med Watch and strongly urge others to report their adverse event to the FDA (see link above).

I had a 103 fever Thursday went to my doctor Friday she prescribed this to me and I started taking it same day - that day - hardly any side effects until later that night...took a shower and I looked like I had spider webs all over me - then the real fun started...I started to swell up, I have not slept since that first night and needless to say, I have stopped taking the Avelox now. My fingers are so swollen they are like coctail weenies and it is hard to type - my legs are so swollen it hurts to wear shoes and I have bright red dots all over from my knees down. Is this permanent???? I'd rather not have this look for summer. : ( I feel like I am all "craked out" for lack of a better term but I am exhausted form the no sleep, etc. Oh yeah and the best part of this whole thing, I am so itchy I want to peel my skin OFF. Who the h*** lets this remain on the market?? Better yet - why do doctors keep prescribing it knowing all this - oh yeah I forgot MONEY...
I really hope all of this goes away? I am terrified cause most of the posts I have read thus far say most people deal with this for weeks +!!!!

Here's my horrible experience w/ Doxycycline Hyclate (100mg prescribed 2x day)
I only took 3 doses of this and vomited one of those.(there appeared to be blood in vomit) I was taking this for pelvic infection. I had severe nausea that came in waves. I also had severe drowsiness to the point that I could not lift my head up. I felt a sense of being "out of body" and extreme dizziness that almost made me feel like I was falling. I had confusion, disorientation, forgetfulness, and an inability to concentrate. I felt bone chilling cold, that alternated with sweating and hot flashes. My face, hands, and arms became puffy. I was very drowsy but could only sleep a couple hours due to insomnia. When I did sleep I had very weird and vivid dreams. I also felt a general sense of panic the day after I stopped taking it. This stuff was nasty and I will never take it again.

It is wonderful to have a forum like this to share stories and complaints but NOTHING WILL ACTUALLY BE DONE UNTIL REPORTED TO FDA. It takes many people reporting symptoms for Fda to even care or take notice. PLEASE PLEASE PLEASE HELP YOURSELF AND OTHERS BY REPORTING TO FDA. Go to www.fda.gov/medwatch. It is really simple to do and this is the first time I have ever reported anything. (and first time I had any major drug reaction). It is also confidential.

My experience on this drug after only 3 doses was very scary. I hope I will feel better soon. It is 1 1/2 days now after last dose. I will try to report back on here when I am feeling better. The half life for the med is about 18 hours, which means by tomorrow I will still have 25% left in my system. I am hoping after 2 more days I will feel back to normal. I have had as much water as I can tolerate and took dandelion root to help cleanse my liver. Take care everyone and remember to report any symptoms you had to the FDA at www.fda.gov/medwatch

Update from A., Well it's been since Monday that I was finished with a 10 day course. I'm still having terrible knee pain, and bad burning in my left shoulder! I'm drinking a bunch of water.....When I try to get up from a seated position it's like my legs have a hard time straightening out!

I DID report it to the fda.gov/medwatch.

When I see my Dr. next week, I'm gonna let her know just how bad this messed me up.....as I've got Fibromyalgia and I'm already pretty MESSED up to begin with!

I 'm in the process of filing for disability.....that's how messed up I am! I'm also going to have my dr. run the Creatine Kinase blood test....any others I should ask for???? If you know PLEASE reply to me, Thanks in advance!

Previous link did not work. Try this again.
http://www.fda.gov/medwatch/safety/2006/Nov_PIs/DiovanHCT_PI.pdf

P.S. I have ALL of these symptoms
headache, dizziness, nausea, gastroparesis, depression, acid reflux, join pain, fatigue, anemia, hair loss, thyroid disorder (low)

I have been on Diovan HCT for about 9 years!!!! I have felt like crap for about 5 of those years! I recently was searching the internet to find out a possible diagnosis for my feet swelling! I showed this to an ENT dr. at a recent appt. and she thought it could be Cellulitis, however the antibiotics did not help the redness and swelling in my feet. Now, after extensive research, I do believe I have GOUT. After trying to figure out why I would have GOUT at age 39, I have read that the "thiazide" can caused elevated levels of uric acid, which forms crystals in the joints. I also have "anemia" which doesnt get better with medication and the reason I felt I was constantly tired over the last few years. I have also had severe joint pain...foot pain, back pain and hip pain. And an overall feeling of listlessness. After reading an article listed on the FDA's site on this drug, I fully believe this drug is the cause of 90% of my problems. I am going off this tomorrow, and calling my Endocrinologist. Did I mention I have diabetes too? Which has severely exacerbated in the last few years. Try this site for viewing adverse reactions (hopefully this will work)

www.fda.gov/medwatch/safety/2006/Nov_PIs/DiovanHCT_PI.pdf

Please feel free to report this drug to the FDA http://www.fda.gov/medwatch/

First I'd like to say that we can all file a report with the FDA. We don't have to hope our doctor does. http://www.fda.gov/medwatch/report/consumer/consumer.htm . If the link doesn't work, go to fda.gov and look for Report a Problem. All this complaining does nothing if it's not reported to the FDA. Okay, now it's my turn to complain!

I plan on calling my doctor to have the Mirena taken out ASAP. Insertion wasn't pleasant, but not horrible. I never had many cramps, spotted only a week or so, had one period in 3 months. My breasts got sore before my period so I took a pregnancy test. First time in 20 years or more that my breasts hurt other than when I was pregnant. Nope, not pregnant. My complaint??? I spend 10 hours or more in bed at night and I'm still exhausted. It definitely started within the first 30 days of having it placed. I almost mentioned it to my doctor during the follow up visit, but thought maybe it was just a coincidence. Three and 1/3 months later, I drop and fall asleep from exhaustion by 8 PM (usually before). Sometimes I wake up in the morning feeling drugged, like my body is dead weight. It's terrible.

October 22, 1998 I had resp. failure (with intubation). My new pulmonary doctor put me on Singulair 10 mg once a day, a few weeks after. Within time, I started to have numbing and tingling in my face, arms, and legs. March of 1999 the symptoms worsened and started causing pressure in my face, arms, and legs, and anxiety started to kick in. I was told I had neuropathy and to take mobic. Symptoms getting worse, and went to a rheumatologist in June 1999, and he was suspect of singulair. The doctor thought that what I was experiencing was due to the singulair. He (the rheumatologist) discussed this with the pulmonary doctor and the pulmonary doctor did not believe this to be the case. Not forgetting, in March of 1999, I had a ct of the sinus area, and low and behold 1/3 of the cavity was and probably still is full of polyps.

As time went on, symptoms getting worse, and not one bloody doctor could figure out why I was feeling this way. In addition, at times, I was put on steroids for my asthma (not including my inhalers).

Two years ago, my body went into shock, leaving my left side very different than my right side. Affecting: my head, my face, my eye, my ear, my esophogus, my lungs, my arm, my leg.

I have been depressed and anxious not knowing what the heck was going on with me.

Recently ruled out thyroid, and lupus, and possibly ms.

Last weekend, I reviewed the letter from the rheumatologist (dated 1999) and the ct report from March 1999 (regarding the sinus/ polyps) and made copies to present to a pulmonary doctor that I have recently been seeing.

This past Monday the 10th, I had my appt with him. He knew of my situation from the last few visits (in addition, I had met him this past March for a pulmonary rehab program, and thought he seemed to be knowledgeable and compassionate). While waiting for him to enter the exam room, he had read those reports before entering.

The doctor looked at my hands (red as a beet and swollen) and said "You have Churg-Strauss Syndrome, and get off the singulair."

I had done my homework from a few weeks ago, where I looked up untreated polyps.
Untreated polyps, can turn into vasculitis. There are many types of vasculitis, to include Churg-Strauss Syndrome.

I then cross ref CSS and singulair, and low and behold, BINGO!

I have been suffering for ten years, physically and emotionally because of this drug!

There is also recent updates from the fda (fda.gov) regarding singulair, of which most recently includes anxiety and depression.

I suggest before taking singulair, be aware of the side effects. As soon as a side effect comes up, contact your doctor. Also, be aware of existing conditions (like me, sinus problems and asthma) for this could lead to churg-strauss syndrome.

This info is indicated on the actual disclosure (the paper insert that indicates studies, side effects, etc...) not the handout that is given with the drug.

By the way, I am now working with a new rheumatologist in Los Angeles (Cedar-Sinai affiliated) and a new neurologist.

mdklezmer

I URGE YOU TO PLEASE SUBMIT ANY ADVERSE EVENTS OF THIS TERRIBLE KENALOG DRUG TO THE FDA--JUST CLICK THIS LINK AND COMPLETE THE FORM: http://www.fda.gov/medwatch/. The FDA is responsible for assuring safety of medications. Therefore, it is imperative that the FDA recognize the adverse effects to provide any credibility to a class action suit. Please consider forwarding your case to the FDA to force them into action and begin addressing these atrocities.

Here's my case: I am also a victim of having the Kenalog injection administered over a year ago to alleviate poison ivy itching symptoms. Prior to having the injection, I was not informed of any side effects. Not only did the injection not alleviate the symptoms, but has resulted in a discolored and uncomfortable indentation in my left buttock area and psychological anguish because of disfigurement of my body. It is over a year later and the indent remains and continues to cause discomfort. The dermatologist who administered the injection stated that there was nothing I could do to reverse such effects. I reported my case to the FDA (Food and Drug Administration) Med Watch and strongly urge others to report their adverse event to the FDA (see link above).

I have been making inquires as to how and if the fda will conduct investigations in to permanent damage left from this drug.Although on taking my son off this drug i saw a 90% improvement,i am still missing the final piece,is it that he lost 3 years to this drug or did it do damage that cannot be fixed,we as parents need to know.The FDA responded to my letter,they said if they see a trend in reports from medwatch,it may prompt an investigation .I am asking all who still have missing pieces to file a report.What has happened is a tragedy,we need to explore ever option for continued success for our childrens future.Good Luck to all,Keep Fighting

I was prescribed singulair for asthma 7 years ago in my late 30's. I experieinced mild side-effects first including vivid dreams/nightmares, insomnia mixd wiht bouts of over-sleeping for work, runny nose, etc.

Then I developed a series of kidney infections, increased irritability, lack of concentration and heart palpitations.

Depression set in, along with the obsession of shotting myself in the head, running away to far away places, and risk-taking behavior.

I became difficult to work with and left a good paying job/career and suffered increasing irrational teenage rebellious behavior that i chalked up to a mid life crisis, until the suicidal idealization and late night insomnia and cutting hateful things into my skin with razor blades set in.

Then I left another job and had no health care. In months my outlook improved and problem-solving reason returned. A year later, with new medical insurance, I renewed my prescription, only to find the bad thoughts and gloom returning.

Within weeks my doctor and pharmacist warned me about the suicidal side-effects of the drug.

Now that my life is a train wreck, who do I sue?

I cant imagine subjecting a child to this medication.

Please seek alternatives and protect your children.

You are encouraged to report negative side effects of prescription drugs to the FDA.
Visit www.fda.gov/medwatch, or call 1-800-FDA-1088.

I'm glad I decided to research this thing before I decided to get it put in!! I'm in the last month of my pregnancy and I really don't need something that has a slight chance of making me feel like what all of you have described. I still have a few months to decide on what I want to do or go with.
Have any of you lady's reported any of these bad experiences with the FDA?? If not, I think that you should so if they get enough responses, they'll take it off the market.
Here's the info and link again www.fda.gov/medwatch, or call 1-800-FDA-1088.

I have an appointment to get the Mirena put in next Wednesday, but reading all these side effects that some of you have had, I don't think I'm going to get it. I am proned to yeast infections and uti's especially. Anyway, I went to the Mirena website and I found this at the bottom. Maybe you all could write or call this number to tell them about the negative side effects that you're having.

IMPORTANT INFORMATION ABOUT MIRENA®:
Only you and your healthcare professional can decide if Mirena is right for you. Mirena does not protect against HIV or sexually transmitted diseases (STDs). Candidates for Mirena have had a child. Mirena is not appropriate for women who are or may be pregnant; or who may have a distorted uterine cavity; acute genital infections including pelvic inflammatory disease; cancer of the cervix, uterus, or breasts; unexplained vaginal bleeding; or acute liver disease or tumors (benign or malignant). In rare cases, perforation or embedment may occur. Mirena may become completely or partially dislodged. In the rare event you think you're pregnant, contact your healthcare professional without delay to be evaluated for ectopic pregnancy. Ovarian cysts may occur and typically disappear. Persistent cysts should be evaluated. Missing periods or irregular bleeding is common in the first few months, followed by shorter, lighter periods.

You are encouraged to report negative side effects of prescription drugs to the FDA.
Visit www.fda.gov/medwatch, or call 1-800-FDA-1088.

Being a scientist, I am reluctant to say my symptoms are completely due to the statin (Crestor) that I've been on for 2.5 yrs. Started with a bulging/herniated disk in my lumbar region 4 months ago. Then increasing leg pain and major leg/foot cramping at night. Had my blood checked for electrolytes and CPK. Electrolytes were ok but elevated CPK (muscle breakdown enzyme). Doc took me off Crestor and now a month later, no cramping and much reduced leg pain. Am going in for a cholesterol check next week to see what the levels are. I wonder how much the Crestor played in my herniated disk. Certainly it has played a role in the leg pain and cramping as I no longer have it to the same degree. The FDA and surgeon general talk about putting everyone on statins. BIG MISTAKE!!!! Maybe CoQ helps, but I am done with statins.

Wow am I glad I found this page. I thought I had a brain tumor or something.

I had taken an albuterol inhaler years ago with good results. I saw a doctor recently and mentioned I had been using an OTC epinephrine inhaler to control my asthma. He recommended I go to something... gentler? So he gave me prescriptions for Singulair and Ventolin HFA.

Two days later, I got the worst headache of my life. I thought I was going through withdrawal from caffeine or sugar (which I began as a result of seeing the doctor). FIVE DAYS LATER I was still fighting it. Not withdrawal, not for that long. Since I'd taken Albuterol before, I suspected the Singulair.

I was fine for a couple weeks, until the headaches inexplicably came back. They were focused around the sinuses, so I was popping decongestants, antihistamines, snorting Afrin, using a Neti-Pot, you name it. I got periodic relief but nothing lasting.

Finally I decided to go off the Albuterol, thinking that because I was older, I had maybe developed a new sensitivity. Within 24 hours my headache cleared, and it hasn't come back. Only then did I start searching the internet for side effects, and I can only conclude that I am sensitive to the new propellant.

Thanks for posting your experiences. You can also tell the FDA about this problem by going to ******