Verizon symptoms and conditions

I am just in shock. I have been on Avelox for 7 days now, and I can tell you that the side effects are not worth it. I still feel sick and have the bad cough. Now, I also have Thrush. But the weirdest and most upsetting part of this was that I didn't notice any of the other symptoms. So I went all week, talking a mile a minute, sweating, dry mouth, hallucinations, etc. Then on Saturday, a few of my friends staged an intervention. They actually believed that I was taking Crystal Meth - ICE. I was heartbroken, confused, and mad. I knew I had not done any illegal drugs, but several of my friends were convinced.

I went to the doctor today and found out that it was the Avelox. However, I had already taken today's dose. I even told the doctor about the situation with my friends and asked if this drug could be related. He said no, it must be the steroids and sent me on my way. As luck would have it, the pharmacist saw me in the store and approached. I asked him if Avelox could make me feel the way I was feeling. He told me that I should have never been prescribed Avelox and Effexor as they had drug interaction issues. He also told me that my symptoms were disclosed on the pamplet. The problem was that I got the Avelox as samples after the Augmenton didn't work.

So, I came home took the meds for the Thrush and watched tv. I haven't slept since Thursday, nor have I eaten since Saturday. I am hearing and seeing things. Now I am scared to go to sleep because I may not wake up. My heart is beating fast, I can't stop talking, dizzy, blurred vision, disoriented but extremely happy given the circumstances, paranoid, jittery, extremely thirsty even though unable to pee.

This is just horrible. I am not a drug adict and do not do Meth/Ice or any drug like that, but now my best friends are doubting me. They don't understand or believe that an antibiotic could do this and how am I supposed to prove it to them? It looks like, just because I got sick, I may lose some of my closest friends... Remember, most drug adicts and alcoholics DENY it first. Great, huh. Now everyone is going to be watching me to see if I am on drugs. I feel violated because evidently I got all high on this antibiotic, didn't enjoy it, and now am suffering the consequences.

What makes it worse is that people I love now don't trust me, and I didn't even know what was going on

I had a little case of pneumonia and the doctor prescribed avelox to me. since the first day i took it i experienced numbness in my legs and i was feeling very weak, i thought those symptoms were from pneumonia so i continued to take avelox. after taking avelox for 6 days i saw my doctor and i told him about everything i was feeling, numbness in my legs and arms, tingling in my whole body(even my lips), and i felt very weak. my doctor gave me some tests and everything seemed to be fine. but i kept feeling really bad, i started to get chest pain. i went to the ER and they ran some tests, they told me i was fine. they told me to go to a neurologist. later that day i read on the back of the prescription and i saw that everything i was feeling i saw as side effects on the prescription. By the time i saw that i have already taken all of the medication. now i'm waiting to see when the side effects will go away. i wonder why any of the doctors i went to didn't know these were side effects from the medication, i will never take this medication again.

I had my Mirena removed a month and a half ago and I feel GREAT. I am a MOM again. My kids aren't afraid of me anymore which was the worst part of the side effects. I am starting a new job this week as a nurse (I got my license 2 weeks ago) and am GLAD that the Mirena will not affect my attitude at work.

I have noticed a huge difference at home. The sex drive is still non existent but it wasn't there very much even before Mirena. I am more willing to do more and be there more often. Things are so good, that I don't plop my kids in front of the TV so I can go off to my room or the table to be online. Tomorrow, I am calling Verizon so that they can shut off our TV, Internet, and Phone services. We have cell phones, the library has computers with internet access, and we have a DVD player attached to the TV.

I am so EXCITED!!!!!!!!!!

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 +!!!!

I am a 36 year old woman living in hell for 3 months now.

In early October of last year I was admitted to the Hospital with diagnosed bronchitis a possible pneumonia. I was given Avelox which is a member of the Fluoroquinolone drug family. At the time I was in sever distress, could not breath, and was extremely weak from the infection. I stayed in the hospital for 6 days while they gave me Avelox along with various other meds to treat my symptoms and was released after finally getting a clear chest x-ray. The drug had done its job. But it was a week later that hell started. I was re-admitted to the same hospital with sever abdominal pain. They told me that I had hepatitis due to a reaction from the Avelox. My Dr. Also suspected I could have Wilsons Disease so he prescribed a liver biopsy, to say the very least this was a painful procedure. The biopsy came back negative and the liver function began to return to normal just as the pain everywhere else began.

joint and muscle pain
headaches
insomnia
uncontrollable twitching
arm and leg numbness
neck pain/spasms
a mass on my left breast (further diagnosed after mammogram, CT and Biopsy as a side effect to the Avelox)

My internist, Rheumatologist and the liver specialist all suspect “Post infection pain syndrom”.

However, after hearing now 3 separate times from 3 seperate Dr's about the possible side effect of Avelox I did a little research and every single one of my “symptoms” are on the lists of dangerous side effects for this drug. Now none of my Dr.s can tell me if I will ever get rid of the pain I am in. None of them seem to be able to do ANYTHING but treat my symptoms. By treating the symptoms all they can do is pain management which means pain killers. I simply can not function day to day with most pain killers so I am forced to live with the pain.

More drugs than I have ever taken, Dr.s visits, time off work, stress and a standard of living that simply put is not living, not to mention the tremendous outlay of cash...to say the least I am frustrated.

I have been on Lisinopril about 2 years, 40mg a day. Ive developed a cough, and i have knee pain now, which i never had before. Upon looking up side effects of this drug, joint pain was one. This stuff sounds like poison, and im going to cut back to 20mg a day and check my pressure. Eventually i may go off it all together and take my chances with high blood pressure. Contact me if you want, it would be nice to discuss this with any one, i also get nausea at times.

Update on my experience with Lisinopril.
After 3 ER visits & 2 hospital stays the palpitations quit when the HCTZ (diuretic) was removed. Adjustment of dosage got the B/P readings down to acceptable levels but some side effects remain after 2 weeks. Dry-eye syndrome and over-the-counter drops do not help. I'm up most of the night-time.
However in the daytime after I exercise I feel sleepy and can sleep for a couple hours time.
Wondering if this side effect will go away or what. Anyone with the experience ?

Well here goes, I paranoid, cant go to the bathroom a lot of times, sweaty t times, sick at stomach here and there, get cold limbs sometimes. Cant remember short term at all, I honestly forget 1 minute ago , but not all the time, there is long term memory loss, which i really hate, NERVOUSNESS is horrible, stress and anxiety can be very high , unless my life is in an ideal status which is nearly never, I do get flu effects on and off, I must change patches every two days 10 percent of patients must do this, or you get withdrawals, and that is an experience in its own, you get body tremors really bad back aches, all over. nausea, tremors. If you get really hot a sweat because of the enviroment my patch runs out qucker and then you feel like you are about to collpase from to much drugs, its sort of like you get so weak and thirsty you feel like you will drop dead any moment. so avoid hig heated areas for lenghty time. I double cover my patch with clothing if outdoors without a choice.Im aggressive at times and then im often very depressed, a lot of times. Crying spells , stupid stuff i cant control, and Im no wimp so its hard to deal with. Im an ex jarhed so the weakness is character is hard to swallow. However if I didn't wear this patch i couldnt make it through a day without so much pain, that it would be unbearable. I was in the hospital weekly before this patch. I have severe back issues, things that cant be fixed, well thats it in a nutshell, there is more but you can ask me if you want, i have been on the patch for 3.5 years.

Back again Oh my am so confused on what to do.. I was taken off this med(LISINOPRIL) at my extreme constant complaint- and put on another--well either I have atypical reactions to all these drugs or am still having side effects from the Lisinopril-- I am taking diavon now-- I feel even worse-- rash is back head hurts so bad I could cry and I am weak all the time.. I could pull every hair that is left on the top of my head right out! I now have that rash around my neck and upper legs- was told before it could be the shingles hey I never had them before,, never.. my nerves are shattered I cry a lot and am hesitant to change again-so I stopped this is day 2 and my headache has subsided
What are we to do I am at wits end.. I know I need something but what today I am at 140/90 going back up,, any suggestions? I started taking Zinc yesterday was told that I am experiencing LOW ZINC LEVELS DUE TO THE LISINOPRIL(HAS ANYONE ELSE BEEN TOLD THIS?)

Muscle weakness, pain, tingling

After taking levaquin, I still suffer from muscle weakness, pain, and tingling several years later. My doctor who is one of the top specialists in New York has seen what this drug has done to me and is doing research for an article in a medical journal to put the word out of the horrible side effects of this drug as well as increasing the knowledge to hopefully figure out how to counteract this.

If you are/have suffered similar results, please contact me at ****** and we can discuss how you can send your case information to my doctor for the study and medical journal article. We need more scientific studies and literature out there about this drug and the side effects.

Please let me know if a class-action lawsuit is ever filed against this Pharm Co because I will file a suit to get this dangerous drug off the market. Yasmin/Yaz almost took my life in January 08. My OB/GYN put me on Yaz in Oct 07 for bad periods and cysts on my overies. Within a month my entire personality changed and I started losing my hair. I experienced a complete loss of sex drive, became depressed and was either constanting crying or raging at someone. However, my adult acne did clear up. On 1/27/08 I experienced extreme pain in my calf that moved up to my thigh within 48 hrs. I went to the ER and was told that no only did I a condition called DVT (Deep Vein Thrombisis-blood clot) in my leg but that the clot had broken off and moved into both of my lungs and I had bi-lateral pulmonary embolism. I can't even describe how incredibly painful this was. I was admitted into the hospital for 1 week and was put on powerful blood thinners, which I will be on for about a year. It's now been nearly 6 months since I was diagnosed and the DVT and it is still in my uppper thigh. But am grateful to be alive. If you would like to contact me I would be glad to answer any questions regarding this situation and my email addy is ****** PLEASE DO NOT TAKE YAZ OR YASMIN OR LET ANYONE IN YOUR FAMILY TAKE THIS MED, IT COULD KILL YOU.

Hello, Ladies.. I am 33 yrs old.. I have suffered a stroke from taking these birth control pills yasmin.. I was only taken these pills for about 4 months.. I woke up one day with a serve headache.. I had taken all the amount of tyelnol I could take in a 8 hr day. And the headache did not go away.. I just thought it was the weather or something.. It lasted for 2 days.I am a single parent of a 9 yr old daughter.. I woke up on monday morning still not feeling good. I got up and was going to start the day like I normally would.. Well I got in the shower and then got out and felt very dizzy. Then the next thing i remember was that my arm was shaking uncontollably and would not stop shaking.. I had to get my daughter up and she got dressed and got me dressed and called my dad.. Then she called 911. I was having a seizure.. Then by the time the ems got here my left side was completly numb.. Could not feel anything.. So then they did a ct scan.. I had a blood clot in the main vessel of my brain and it was bleeding.. Then they told me and my family that I may need brain surgery.. Then had to be transported to riverside methodist hospital.. Then I went into a full blown seizure.. I don't remember that at all. I remember curling into a ball and shaking and that is all that I remember.. Then I was at the hospital for 2 weeks.. Then when I came home about 4 days after that I went back.. My right side was going numb.. That was due to I was having more seizures.. I would love to get together with all of u and form a class action suit against this drug company. I am not like this but this is my life and the lives of other people.And not only that I have a daughter to raise and think about.. So if any of u would like to contact me..Please feel free to do so.. My email address is mcottrill2@verizon.net..

Well all i can say is it is about time they investigate this stuff! My daughter was put on this 2 yrs. ago and was on it for 1 year off and on. It was a complete nightmare. She experienced nightmares, leg pains, crying all the time, getting into trouble at school, teacher would call every week about something, several urinary tract infections,which lead to many test of why. Really bad mood swings, and aggression. I used to hate it when she got of the school bus. Because i knew it was going to be on the minute she walked in the door. She would cry to me and say she" hates her self" and "mama i do not know why I am so mean." I kept taking her back to her ped. and she would ask are you still giving her the singulair and one day i said no. The doctor got mad at me because i told her i did not like that stuff. She said it was fine to give it to her. I told everyone i knew not to give it to their child because finally i realized it was making my child depressed and feel worse. I am so mad about this. It makes me sick. I want to sue the makers of this drug.

I have been on synthroid for about 3 yrs. I am considered subclinical (can't find hypothyroidism with blood test- normal range).
Grant it, the medicine took away the almost angina pain and loss of breath. However, my body seems to have deteriated structurally. I have tremendous lower back pain, that worsened. I have been in pain every day since. I starve, (veggies - then dinner). It's been very, very difficult. Always looking for help.I'm hoping that a natural hormone will change this, I know my husband will be glad; he won't have to hear me cry anymore.

I started taking Yasmin Feb 2005. By October I had 55% of my right lung full of blood clots and 75% of my left lung full also. Yasmin made me come way to close to death. I was on blood thinners for over a year and now I'm unable to ever take any hormones ever again, including ever having any children. I'm definitely in search of a class action lawsuit!!!!!!!!

I keep getting dizzy, quick blackout and fainting spells since taking this medication. I also get sweats/chills. I also urinate more and am always tired. I am thinking it may be from the medication but my doctor says no and I am not sure I believe him unfortunately. Did anyone else have these spells when taking lisinopril?

I am SOOOO glad I found this site. My daughter is 6 years old and has been on Zyrtec on and off since she was 18 months old. About two years ago we added in Singulair. Two weeks ago she was diagnosed with ADHD and Oppositional Defiant Disorder and they want to start her on meds for that. I got to thinking about when all her behavior and academic problems started and it was shortly after we started the Singulair. Before the Singulair she was a brilliant, outgoing, well-behaved happy little girl. Now she has trouble remembering short and long term, trouble concentrating, extremely fidgety, impulsive, can't complete anything she starts, extreme persistent stomach pains, diarrhea, occasional vomiting, and extreme frustration. I stopped both the Zyrtec and Singulair 4 days ago and am now reconsidering any meds for ADHD. I am going to wait and see how she does without Zyrtec and Singulair in her system. I am excited to see if there is an improvement! I had no idea these two drugs were so dangerous!

I am a 32 yo Mother to 4 children. My ONLY purpose for taking Yasmin was to control the severity of my periods. After the fourth child my periods became so heavy, crampy and unbearable that I had to do something. I have been on Yasmin for a little over a year now and all I can say is had I known then what I know now...I wouldn've said to hell with that!!!

Mood Swings, I mean my god ladies, they are awful, my husband of 10 years never once called me a Bitch and now I hear it all the time it seems, the weight gain was off and on. My metabolisim slowed to a stop basicaly, my hair started to fall out of my head and found itself on my face. The sobbing for no reason (at a dog commercial ladies..a dog commercial) constantly being tired, then not being able to sleep when i knew I was exhausted.

My libido was non exsistant which caused termoil in my marriage for a period of time. There was nothing I could do. I felt so helpless. Out of control, sad, sick, and in general just BLAH!

Secondly the medication was supposed to help reduce the severity of my periods and make them shorter..HA HA HA HA HA!! That's the biggest joke. They are still the same now as they ever were. 8-9 days, filling a super pad within and hour and a half, having to wear both tampons and pads just to go out in public. I have had no pills for a week. I quit cold turkey so to speak and I have had spotting lots of spotting, headaches, and bloating associated with nausea. I am glad that I am off of the Yasmin pill and I'll never go on Yasmin again!

I would love to know of a lawsuit pending against them, so that I could be returned all the money I spent in copays, to feel worse than I did before I started taking it.

I started using Yasmin right before I was married May 2006. We wanted to have children but, wanted to wait a little bit. I bled the whole month and experienced major weight gain. I had cramps and felt awful on it. I didn't feel like myself. My husband and I started to try for children in Sept of 2006. We stopped taking it. I continued to bleed when I stopped taking it.

A few weeks later we got a positive sign on a pregnancy test. We were so excited!! A few days later I started to bleed. I went to the doctor and after blood tests and ultrasounds they found something on my right ovary. At first they thought it might be cancerous. After more tests we found out it wasn't cancerous but there was a cyst.

I had had previous doctor visits with nothing showing. A clean bill of health. Now all of a sudden I take these pills and I have a cyst on my ovary. We continued to watch it and they came to the conclusion that I would need to have it removed. In November I had my right ovary removed.

Our chances have lessened since the removal, I stopped taking the pill at the end of January. We have yet to get pregnant, and have been trying most of the year. I continue to have my period monthly but, we are not pregnant yet. I find it difficult to lose weight too, although I'm still trying. I don't know if we are ever going to get this stuff cleared out of my system. No one ever warned me of possible cysts, of the dangers of using vitamin C, and we were told that we should have no problem, as soon as we stopped taking it we should have no problem getting pregnant!!
LIES, LIES, LIES.

I'd be interested in participating in a class action lawsuit. We may never have kids because of this.

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 just returned from seeing a hematologist for bruising and bleeding under and through the skin of my forearms. Luckily, it is not a bleeding problem, but a dermatological condition known as "cutaneous atrophy". I read on this website that is a side effect of the kenalog injections.

I've been getting the injections in both my knees for the past year (shots every four months). The injections help the pain in my knees, but I think I will just take darvocet for the pain and tell my rheumotologist that I do not want any more of these injections. I've also experienced the excessive sweating around my neck and upper back, not knowing why. Scary side effects.

I was prescribed cephalexin for infection in my head and after the third day of using it I broke down into hives and started itching throughout my whole body.

I received a kenalog shot in my hip, I have atrophy. I am in alot of pain and the doctor just blows it off like it is nothing, just a normal side affect. But it is my hip, I have a dent in. I am not sure what to do, if anything.

My son has been on and off for almost 2 years now and we started on it when he was in 1st grade and now he's in 3rd we don't put him on it for the summer just for school purposes, but we tried other meds and they didn't work like Adderall XR 10mg a day. We were on 20mg way to much he wasn't active at all almost zombie like and very quiet, so we wanted him to still be a kid and be who he is, without taking that away. So, the dose that he is on now is working so far but you can definately tell when it is wearing off, he seems like someone else said very emotional and crying and agitated, I fell bad having him on this but if we don't his grades drop. He really has low self esteem too. He isn't hungry but he's able to focus and concentrate. The dr. says he has ADHA but I don't see the Hyperactivity? I see ADD. I recieved an article from a friend on bad things in children and adults who are on AdderallXR who have died. I am now concerned this is why I am writing this messge. If anyone wants the article I will be happy to email it to you, just email me ******

I have just went for my 7th Remicade infusion. I didn't even get a third of the way done with it. They had to stop it becuause I started to itch real bad and broke out in hives. I always get severe muscles aches about 2 weeks before my treatment to the point where I can't walk or move. My doctor always puts me on a two week treatment of Prednisone to make the pain go away. I'm hoping that this is the last of the Remicade for me. It worked wonders at the begininng but now my body just doesn't want it anymore. Anyone experiencing anything like this??Please email me! ******