Better with time symptoms and conditions

I have been on this pill for 1 and a half months now. Shortly after I started taking the pill, I started my period! I'm not talking spotting, I'm talking full-blown period--severe cramping, cravings, mood swings, and all. The whole month (last month) I was on my period. Again, I WAS ON MY PERIOD FOR A WHOLE MONTH! I just got off of my period after I stopped taking the first month's placebo pills. Normally, when I'm not taking any birth control at all, I have VERY regular periods. The extreme side effects of the first month were incredibly shocking to me. I'm still having crazy mood swings; I really hope this gets better with time.

I to was put on Lipitor 20mg. took it about 1 month and had such pain in my leg muscles I couldn't hardly walk . I went to my doctor he said go off it and I should start Zocor in . A month the pain was worse I couldn't even walk around the mall . I couldn't sleep at night the pain was terrible. Once again I told the doctor he said stop it and we will wait 6 weeks and start Crestor. In six weeks the pain should be gone. It didn't go away I could hardly walk at my job teaching at a Pre School. The pain unreal.I have type 2 diabetes under control for years. Still is.I was told I had arthritis. But now they tell me I have spinal stenosis. I'm on paxil for the depression they said I had and. I feel as bad now as I did 4 years ago when I was on statins. I can hardly walk, my life is pain in my muscles that never leaves and now my back. I was active and watched my weight and walked 3 miles a day. Since taking these meds. I can no longer work, go shopping or go anyplace I have to walk . I have gained a lot of weight . I have something wrong with my knee .I have tried to explain this to 3 doctors and no one listens to me. My health turned for the worse when I started taking Lipitor in 2005. I don't think I'll ever get my life back I am only 58 years old and can't work to support myself.I can't even hold my 1 month old grandson and walk or lift him from his bed. Reading all your messages . I know my health going down like this is from the statin drugs I took . When I sit , I can't walk when I stand Then .I gotta sit in 5 to 10 minutes.And the pain in my knee has progressed. No doctor wants to hear my story and believe me. Thank God I found this web site and read this for my self now I know I'm not crazy. How can I get myself better ? Will I live the rest of my life in pain, and not able to function.Every time I see a doctor they give me another pill to take. I want to just throw them all away .There must to be an answer to this.

I was given the drug Levaquin 2 times in Nov 26, 2008 and 3 times in one day on Nov. 30, 2008. Now I have Tendinitis and Left Frozen Shoulder. I have to get Surgery in 1 week and numerous Physical therapy. I also have it in my knees, I complaint about these things while I was in the hospital and they never wrote it down. I have Severe Knees pain, left shoulder pain, severe migraines, blurred vision, right wrist paint.

I am been taking Lunesta for many months now. Yes, the taste is horrible but it does get better with time . I am a severe insomniac and would never let just that side effect keep me from my sleep. I love it and it works wonder for me.

I started using Yasmin 2 weeks ago & am having serious problems like heaviness in my chest, short breath, nausea, headache, acidity. At one point I felt as if I got an heart attack! My physician sent me for an ECG yesterday & I am worried about the results! I hope to recover from all these side effects soon because my work is getting affected due to discomfort.

I had Mirena put in about 5 weeks ago to control heavy periods. After about 2 weeks I started experiencing a foggy head feeling and bouts of dizziness. I didn't relate this to anything and thought it might be from lack of sleep. Last week I stated having spells of rapid heartbeat and nervousness that lasted anywhere from 10 minutes to 10 hours. Exercising is out of the question since it makes me now feel lightheaded. I feel like I can't think or concentrate. At first I didn't think the symptoms were related to Mirena, but since I am otherwise very healthy and don't take any other medications, I started doing a search online and came to this website. I called the doctor and told the nurse my symptoms and she called me back to say that they never heard of anything like that and I must have some other medical problem...They insisted it was not Mirena causing the symptoms. I mentioned that my symptoms are actually ones listed by the manufacturer as "possible" side effects. They disagreed with that. Now I'm thinking of going to another doctor to remove it, if they'll do it. Can anyone tell me if they had these symptoms and if they got "better" with time? Or do they just get "worse"..??? If I knew that they would improve I would hold on a little longer. Has anyone had improvement after the first few months?

Hi a little over a year ago i received a kenalog injection for allergies and have been having a lot of the same side effects you all have been having. I have a very large indentation on my butt. I have an appointment with a plastic surgeon to see about have the indentation fixed just out of worry that it will keep getting bigger because it has over the last 12 months. I have also had problems with my period. I have went from having extreme bleeding to 2 periods a month to now bleeding for 3 weeks at a time. I have also lost a ton of weight and am down to 115 pounds even though I eat all day long. A drug of this kind should not be on the market!!!! ON THE PACKAGE INSERT FOR THIS DRUG NONE OF THESE SIDE EFFECTS ARE LISTED. Somebody should be held liable. If any of you have any information on a class action lawsuit please let me know. Surgery to fix this is very expense not to mention just looking at it in the mirror and knowing that it could have been prevented if someone would have informed me that it could have possible happened.

1. Blood Pressure 180/120 resulting in an emergency room trip
2. Weight gain of 25 POUNDS! Most/all of which was water and came off within the first week of being off from Yasmin.
3. Bloating and extreme water retention. See # 2.
4. Severe leg muscle cramping and foot pain
5. A mental feeling of not caring and general fogginess
6. Complete loss of libido
7. Acid reflux (probably from the diuretic in Yasmin)
8. General weakness in my muscles (there were times that I could barely open a revolving door).

I was on Yasmin for a year. I have been off for one month. I am still on blood pressure meds, but they don't think the Yasmin is out of my system. Has anyone else gotten hypertension from Yasmin and if so, how long did you have to be on blood pressure meds?

Some of my symptoms are getting better after a month, and some are not. If anyone is reading this to decide whether or not to take Yasmin, please don't. You may not have any symptoms right away and you may think you feel great, but that is the scariest part. When symptoms come on gradually, you hardly notice them until you are in the hospital emergency room.

I have had my IUC for 10 days and I want it out already. After only 10 days I am so bloated and my breasts are huge. I have a metallic taste in my mouth, dizziness, and anxiety. I only have it so I can use estrogen for menopause. Forget it! Is there anyone out there that can tell me these things get better with time? Why do the doctors push Mirena? Why?

I have posted my symptoms for about a week, I am HAPPY to say that I have only been off of YAZ 12 days and have already experienced some improvements. Im am sleeping again, and eating normally, the emotions have calmed down a little, I am still experiencing the cloudiness in the head, and a lil anxiety, and my stomach is still messed up occasionally. however I am able to get through the day without feeling like I am a completely Crazy person. I was only on it for a month, and I have never felt this way in my life, I heard that it will take about two months to completely leave your system, so everyone experiencing the effects of this EVIL drug, hang in there it will get better with time, you all are in my prayers. God Bless

I am a male of 67 years old. I took Lipitor for a year, and after a few months of taking it, I felt muscle pains in my arms and shoulders, as well as my back. I felt weak and could hardly put my socks on by myself. I told my family doctor that I thought the problem was caused by LIpitor. He said it couldn't be possible, but he couldn't figure out what was wrong, so he sent me to a rheumatologist, who gave me an initial diagnosis of polymyalgia rheumatica. I went back for a checkup, and although the sed rate was normal, the C-reactive protein was elevated. He felt his diagnosis was an accurate one. He prescribed prednisone for me. I had some doubts about it, since I am diabetic, and was concerned about the elevated blood sugar it might cause. Well, it did elevate my blood sugar, and I weaned myself off it within three months. My blood sugar went back to normal, and while the prednisone helped the symptoms of muscle pain and aches, after I stopped it, the pain returned with a vengeance.

About a year passed after discontinuing the prednisone, and I felt worse and worse. Any time I engaged in physical activity, such as yard work, I was almost incapacitated for two or three days. I felt weaker and weaker, and by now, my activity is about ten per cent of what it was three or four years ago. I am unable to do anything physical without paying a heavy price.

I would tell the doctor that I felt the problem was caused by the Lipitor. He would dismiss my comments, saying that the pain should have gone away after discontinuing Lipitor. He sent me back to the rheumatologist with results of recent blood tests. Both the sed rate and C-reactive protein were normal. The rheumatologist touched my back and other areas, which caused me to jump. He said it might be fibromyalgia. I told him again that I thought it was caused by the Lipitor. He said the same thing my GP had said: if it had been the Lipitor, the pain would have gone away when I stopped taking it. I know the Lipitor caused the pain, because I tried red yeast rice for a couple months. The pain increased to almost unbearable, so I discontinued the red yeast rice. If I were not susceptible to the pain from the Lipitor, would the red yeast rice have increased the pain?

So here I am with a fuzzy diagnosis from the rheumatologist, and no clue from my family doctor (that he will verbalize, at any rate). My life has gone steadily downhill. I used to be a strong, active person, but now I can do very little, and my strength is a shadow of what it formerly was. What can I do?

I would like to let people who are new to the Lamictal "experience" that it was VERY uncomfortable for me during the first few months also. In fact even at the very low introductory doses, I did not think that I could ever function in society.

The extreme confusion, the memory problems, the spaceyness, the feeling of detachment from everything that surrounded me... at the time I felt that I would never be able to function as a worker, a friend, or as a social being.

As time went on though, things did clear up for me. It took a few months, but I'm guessing that my brain function/chemistry finally somehow regulated itself, and my side effects did clear up. I am at a dosage of 600mg per day now, and yes, I do sometimes feel detached, but I certainly can function. My memory has also improved. It sometimes takes me a second or two to find the "right word" during my conversations, but a simple, light hearted mention of the problem resolves the issue for the person that I am speaking to.

If you are just getting on Lamictal, try to be patient. I have found that in time, it has helped me much more than the side effects hurt me. It did take a few months to get used to, and I did have to explain to others at work that I may be acting strangely for a couple weeks because of it... but the overall effect is quite nice now.

Lamictal now helps control my seizure problems almost completely, and has the added benefit of making me feel much more confident, and balanced.

When i was 13 i was put on paxil for major depression. I stayed on it till i was about 17 after a downward spiral of depression that lead to a suicide attempt. After that the doctors decided that Paxil wasn't benefiting me anymore and decided to take me off of it, cold turkey. At that time i was on 40mg.
I started getting zapping headaches, muscle spasms, i was sensitive to light, my body ached, i had hot flashes, pretty much anything over stimulated me... i was irritated with just hearing anyone talk, i was completely out of touch with anything around me and i didn't feel like i was real.. I basically shut myself in my room for over a month getting over paxil. My family was afraid i was planning suicide.
After that, it's made me afraid to take any of my prescribed antidepressants, but i just cannot go through that again. At the time they put me on it, there was nothing that said that it was addictive, i was even told that there was no proof that it was addictive.
Also, I still experience the headache zaps to this day, and im 22 now, and i never had those type of headaches before paxil. I really think my mental illness is a lot worse from paxil. I have depersonalization disorder now, my short-term memory's crap, im more uncoordinated, im a lot more depressed and social phobic.. i know part of it could be from not taking any meds at all.. but i know that paxils really screwed me up, and i would have been a lot better not taking it at all. I just wish they would have warned me before putting me on it, or warning me before taking me off.

1st MONTH...HORRIBLE!
2nd MONTH...NOT TOO BAD..BUT NOT GREAT!
3rd MONTH...GETTING MUCH BETTER!

i am halfway through my 3rd month and i feel like there is hope! i skip the sugar pills and just go ahead and start my new pack..don't know if that helps or hurts the side effects..i figured if i'm spotting/bleeding for a week plus i really don't want to add another 5 days..

the 1st month i had every side effect possible...extremely emotional..nauseous..bleeding for weeks..dizziness..headaches.. depression..exhaustion..i had to eat tums every night..leg cramps..facial breakouts..etc.

the 2nd month i still had all of the above but just not as intense..

currently things are so much better..i still have spotting for 4-5 days..have only had to eat tums a couple of times..a few leg cramps..

the first month i hated the pill and was ready to quit but decided to give it 3 months to get used to it..so far i'm gonna stick with it..

if you're just starting the pill don't get discouraged yet..i know it's not fun but it does get better with time!

HI, i too have to say i am kind of relieved after reading this website that i am not alone with my experiences of the kenalog injection. I was given kenalog injections to treat hayfever, although i wasn't told the name of the injection. They did help and i probably would of continued this year if it wasn't for the side effects.
I was told that to have one a yr was safe, then just before xmas i noticed a dent on my hip, this started getting larger and looked almost like scare tissue, I too was worried i had some sort of flesh eating disorder. The dent is still there and i will never have that injection again. I also have been experience problems with my hips and pain around my coxis,i am not sure if this too is related to the injection. I was told by my doctor who is very good that the kenalog had eaten my fat tissue causing a dent and that it will get better in time.

I HAVE BEEN ON YAZ FOR 3 MONTHS NOW, AT FIRST IT WAS OK LITTLE SIDE EFFECTS LACK OF CONCENTRATION, MOOD SWINGS ALWAYS MAD EVERYTHING SEEMED TO BOTHER ME BUT SINCE 3 WEEKS AGO I'VE EXPERIENCED A SEVERE CHANGE I STARTED FEELING SHORT OF BREATH, CHEST PAIN, HEAVY CHEST AND PROBLEMS BREATHING, FAST HEART PALPITATIONS, NUMBNESS IN MY FACE CHEEKS HANDS AND THE BOTTOM OF MY FEET. SOMETIMES I FEEL LIKE IF I WANT TO PASS OUT, SO I WENT TO MY PRIMARY PHYSICIAN I HAD A CHEST X-RAY, EKG, LUNG SCAN(PERFURIN AND VENTILATION SCAN) AND A VENOUR DOPPLER ON MY LEGS AND LAST BUT NOT LEAST BLOOD TEST, EVERYTHING CAME BACK PERFECTLY NO CLOTS OR EMBOLISM, MY PRIMARY PHYSICIAN SAID I AM IN PERFECT CONDITION SHE ADVISE ME THAT WHEN I FEEL THIS WAY TO GO TO THE EMERGENCY ROOM IT HAS PAST 3 WEEKS AND I STILL HAVE THE SHORTNESS OF BREATH, NUMBNESS, HEAVY CHEST, AND ALL MY DOCTOR SAYS IS GO TO THE EMERGENCY ROOM BUT IF SHE DID NOT FOUND ANYTHING WHY DOES SHE WANT ME TO GO TO THE EMERGENCY ROOM ANY WAYS I DON'T THINK THEY'LL FIND ANYTHING WRONG (WELL SHE DID NOT FOUND ANYTHING) BUT THE THING IS THAT SHE TOLD ME I COULD STILL KEEP ON TAKING THE YAZ PILLS. AFTER READING ALL THIS COMMENTS NOW I KNOW IT MIGHT BE THE YAZ BUT THERE IS ANOTHER ISSUE I HAVE HAD SEVERE DIZZINESS FOR 3 ALMOST 4 YEARS NOW I HAVE BEEN TAKING MECLIZINE 25MG FOR THE SEVERE DIZZINESS AND SINCE I STARTED YAZ THE SEVERE DIZZINESS DISAPPEARED I AM NOW SEVERE DIZZINESS FREE. SO I REALLY DON'T KNOW WHAT TO DO I AM WONDERING IF THE SHORT OF BREATH AND NUMBNESS IS GOING TO GO AWAY IS IT JUST THAT I HAVE TO ADJUST OR WHAT? AS I SAID I HAVE HAD FOR ALMOST 4 YEARS NOW SEVERE DIZZINESS( I GET REALLY REALLY BAD THAT I DO NOT KNOW WHATS WORST FOR ME NOW THE DIZZINESS OR THE SHORT OF BREATH AND NUMBNESS). I AM GOING TO MAKE A APPOINTMENT WITH MY OB TO SEE WHAT SHE THINKS. HAVE ANYONE OUT THERE HAD THE SAME PROBLEMS I HAVE? WILL THE SHORTNESS OF BREATH AND NUMBNESS GO WITHIN A COUPLE OF DAYS? DO I HAVE TO GET ADJUST TO YAZ? PLEASE SOMEONE OUT THERE IF YOU HAVE HAD THE SAME PROBLEM PLEASE TELL ME WHAT YOU DID TO FEEL BETTER? SHOULD I JUST STOP THE YAZ PILL? THANKS AND SOMEONE PLEASE ADVISE ME

Just wanted to let you know that I took Paxil 6 years ago for about a month and had to come off because of the side effects. The medicine worked great for me as far as made me feel "normal". I was able to be happy and sad when most people do. My very first side effect was 2 to 3 days after I started I had my first hot flash in the K-mart. I thought it was weird then it became something that happened the whole month I took it. I couldn't sleep at night and would lay awake with my eyes wide open but was tired all day long. I also had stomach pains and would vomit often. I had a constant headache. So I came off and tried Zoloft. It didn't have as much side effects but it didn't help the anxiety/depression. My doctor did say if I could put up with the side effects they would get better with time, but I couldn't stand it.

I took Lipitor for about 2 years- 5 mg.
Leg cramps-soreness throughout my muscles- very sore buttocks-
my legs are shaky- if I use them too much; (as in walking 3 miles)
I am (was ) an avid body builder that could squat with 100 lbs- and now ( I am a health conscious -non drinking- NO other medication 104 lb slim female) have quivering legs if I stand for too long. I even had a muscle biopsy- and it cam back negative- I have not had a statin for 6 months- but I still have cramps- and abnormal liver values- and I have NO other conditions-I have been scanned from head to toe - open MRI- closed MRI -but the muscle stiffness- soreness- especially legs- continues-
does anyone know how long it lasts? I have also been tested for liver cancer- thank God-negative.
I really feel that Lipitor did this- has anyone else gone from fit as a fiddle to a quivering -achy person- I have gone through 5 doctors- internal - gastrointestinal - neurologist- hematologist and all is negative- just high liver values and muscle pain. Thank you so much.Maxine

Ok, here is my Mirena experience. I have gained weight, my hair and skin are just awful. I have a bloated feeling all the time. I have had consistent constipation issues and I am so tired of having this thing. I am calling today to have it removed ASAP. I had this inserted nearly 3 months ago and none of these symptoms have gotten better with time.
:( I would not recommend Mirena to anyone.

I wish I would have found this site earlier. I just had Mirena put in last Wednesday Feb. 13, 2008. I have had terrible lower abdomen cramps, a headache, blurred vision, loss of energy and I am very nauseous. I am hoping this gets better with time. I didn't have any complications when I had the procedure done, it didn't hurt very bad and I only spotted very lightly. But the next day was much worse. The cramps were so bad I was folded over. Can anyone please tell me if these symptoms will go away or will I feel like crap til I get it out? I have only had this for 1 week and I am already scared that this was the wrong decision. Help me please.

I to have a huge dent in my right butt cheek. I would be interested in a class action suit. This is ridiculous! It has been about three months since I received the shot. Has anyone noticed their dents getting better with time?

I took Levaquin 500 mg. because of recurring Cellulitis. I will NEVER take this antibiotic again! I fell into a sense of hopeless and felt like I was hit by a mack-truck. I have been experiencing joint pain like never before. THe doctors have said it is okay to return to exercising, but i will not likely be able to do that because of the ongoing joint pain. My knees, feet, ankles, wrists and fingers continue to be painful, even 2 weeks after being off this medication. I continue to struggle with ongoing low-grade nausea and occasional dizziness, which is scary when driving! This is the worst medication in the world and should be taken off the market. I am PRAYING that these side effects go away.

I started getting panic, palpitations, anxiety, bouts of crying, no sex drive, odd taste in my mouth. I only had the taste and lack of libido since early on but felt fine and than whammo the crying and palpitations and anxiety hit. I asked the doctor if it could be the Yasmin even tho id been on it for a while, i got the royal fob off and some lame comment about 'us girls doing funny things sometimes' whatever that means!!!!! It got worst, i couldnt stand to be in the college where id gotten the palpitations to start with so dropped out and i couldnt understand why, but i was cool to still work nearby the college, I had some odd behaviour tho, like i suddenly couldnt park on the ground level for fear of the levels collapsing, i was scared of dying, of freak events, of flying and i LOVED flying, the syptoms waxed and waned and then a few months lather while still having intermittent anxiety a stressful period popped up and that was it i was gone, worst time of my life, allergies, nauseus, paranoia, depression, nightmares, horrific mental images and distressing thoughts, suicidal thoughts. Crux of it was it sucked big time!!!! That was 3 years ago and im still trying to put myself back together! The original syptoms did get better with time but ive never been quite the same.

I am 48 yrs old, and was prescribed lisinopril in early 2007. It immediately lowered my BP. Due to the stress of my job it took me awhile to notice that the headaches, dry eyes, hollows under my eyes, lack of color to my face, were in fact not from my job but from the medication. It took someone I work with to say to me, "You know, you can go on high blood pressure meds, but if you make the lifestyle changes you need to make, you can also go off the high blood pressure meds." Since I stopped taking the lisinopril, the headaches (like a sinus headache, but deeper), the hollows under my eyes, have greatly improved, my face has color again, and the only symptom I'm still experiencing is dry eyes--hoping that will get better with time, also.

I'm going to start a serious search for a homeopathic alternative. Would appreciate any info anyone out there has re: that. I've also quit my job, gone back to graduate school, and will spend the time now to pay attention to what my body is telling me rather than run to the doctor and get some drugs.

Chantix causes nausea, constipation, sleep disturbances, strange dreams. The first two can be treated with diet, i.e., taking only on a full stomache with lots of water, and the second by increasing fiber. Sleep and dream issues seem to get a little better with time. OTOH, I was a 30-year smoker, and I haven't smoked since Mother's Day!