Expecially symptoms and conditions

I am 18 years old and this is my first experience with BC. Loestrin FE 24 has ruined my entire view of BC. I have suffered many side effects of this pill, I am currently on my third pack of Loestrin. The side effect I have experienced are:
1. Moodiness/ Depression: I experienced this side effect during the first pack of Loestrin. Extreme depression was prominent at the beginning, I would randomly cry and I constantly down. Let alone my mood swings. My boyfriend would agree that I could be up and down within min.
2. Headaches: I have had horrible headaches daily with Loestrin. I started with my third pack of the pills. The headaches are terrible, it seems like I can only numb them with ibprofen but I can never fully get rid of it.
3. Spotting: How annoying is spotting? This side effect also started with my third pack of pills. I shouldn't even see any sort of menstruation for at least another 5-6 days. But yet here I am.
4. Massive acne before menstruation: I have always had really clear skin. Let it be before, during or after my period. But with Loestrin I am constantly breaking out. ESPECIALLY before my period.
5. Bloating/Constipation: I constantly feel bloated and feel like I am always constipated. I don't know what to do besides switch pills. I can't take it any longer.
P.S. This pill makes you feel that you are always pregnant. I see the signs but they are identical to the symptoms of the pill. So beware. I highly recommend NOT taking Loestrin FE 24

I was on 100mgs of Topamax a few years ago for migraines and lost about 15 pounds. It worked okay for the migraines, but I backed off on the dosage because of the side effects. But recently, the headaches returned so I increased back to my full dosage.

So now I feel exhausted all the time. I run a lot and have trouble getting energy to exercise. This morning at a meeting it took me about 30 seconds to remember my secretary's name. I feel like I have to push through this mental wall to concentrate, and on my job I need to concentrate. My mouth feels dry all the time. Some days good food just tastes like crap.

Now I'm remembering why I quit taking this drug in the first place. I don't have seizures, which is why they made it. I have migraines. There are other medications to fight headaches, and this drug just isn't worth the side effects.

I HAVE BEEN ON PREDNISONE FOR 10 YRS. I AM ON 5 MG FOR 4 YRS. I AM HAVING SEVERE PAIN IN RIGHT HIP. I CAN'T LAY ON RIGHT SIDE AT ALL. WHEN I WALK OR BEND ITS FINE. BUT TO LAY ON BACK OR SIT OR RIGHT SIDE I HAVE SEVERE PAIN. I SAW THE DR TODAY HE SAID THE TOP OF THE FEMUR IS SOMETIMES EFFECTED BY PREDNISONE. LIKE BLEEDING OR OSTEOARTHRITIS. HE GAVE ME NAPORSIN. DOESN'T WORK STILL HAVE SEVERE PAIN. I HAVE POLYMYOSITIS. THE PAIN IS SO BAD IT HAS BEEN GETTING WORSE OVER 6 MONTHS. GOING FOR XRAYS. I AM A NURSE AND CAN'T FIGURE OUT WHAT HE IS TALKING ABOUT.

I have been on Yasmin for about 5 years. I have never had an issue. I am worried that everyone on this site is making Yasmin look bad. You all need to remember that not everything will work for every person, everyones hormones are different to begin with so when you add the pill to these different levels of hormones you will get different side effects. To the people with low sex drive, did you perhaps think that this could be due to depression or the aging process? Many women suffer from low sex drive, those on and off the pill. Your sex drive will not be consistent throughout life, mine dropped in my early 20s and now is rising again, it may drop again, it can also be due to stress. All that said if you're suffering side effects that you think are attributed to Yasmin, or any other pill, stop taking it! Not everyone's body will handle it.

I am 20 weeks pregnant & was prescribed Labetalol 200 mg 2 times a day and about 15 minutes after taking it I began experiencing some of the worst breast/nipple pain imaginable. It felt like someone was ripping my nipples off. I am so glad to see other people have had this side effect too, because it was not listed on my side effects sheet.

My 16 year old son took Levaquin 6 months ago and had a bad reaction to it. His symptoms were severe muscle weakness (he would get exhausted walking from the parking lot to a store and back, severe joint pain (in thumbs, wrists, elbows, knees, and ankles), dizziness (he felt like the room was moving away from him and would lose balance), and headaches (a severe pressure in the back of his head that was constant and then shooting pains in his his head that would come and go for no reason). I should say he was in top shape before this and wrestling in the 125 pound category. He took Levaquin to prevent an infection after sinus surgery.

Now 6 months later, his joint pain is completely gone except for his knees. They still hurt when he does squats and they are not good enough for him to go back to wrestling, but he can walk around pain free. His dizziness is also gone as well as his muscle weakness. His headaches are still there and still constant, but not as bad as they once were; however, he has had them 24 hours a day, 7 days a week for 6 months. He is on Lyrica which has helped make the headaches subside.

I have taken him to more than 16 medical doctors of all specialties, had multiple MRIs, CT Scans, blood tests, spinal tap, and an MRA. All come back negative. Thankfully, despite all of this, he still remains happy and positive that he will once again be 100% healthy; it will take lots of time, but he will get better. I know the first three symptoms (joint pain, dizziness, weakness) are clearly Levaquin related, but I haven't heard much about the headaches from people. Anyone else out there that has suffered from a constant headache after Levaquin? I REALLY want to hear about headaches from others!!!!

By the way, we have filed a medwatch already. I also know that Levaquin is not approved for anyone under 18 years old and he never needed such a powerful drug to prevent an infection, but there is nothing I can do about that now except to warn others. One of his UCLA doctors wants to write a case study on him to make this more known to others and I am helping him with that.

If anyone has questions, please feel free to ask. If you have had a headache from Levaquin, please let me know where in the head the pain was, if it is constant, what it feels like (pressure, shooting, throbbing), how long you have had it, and what, if anything, helped. THANKS.

I had Mirena since March 2007, 2 months after my daughter was born.it hurt terribly going in, but I felt at the time it was ther most convient birth control. Since then I have noticed I have awful mood swings expecially before my period. I thought I maybe had PMDD. But I also have some other symptoms eveyone else is listing, like weight gain. I have gained maybe 10-15 lbs since March. I am loosing alot of hair. I feel very tired ALL the time. I have been getting cramping in my upper legs. Sometime my arms will just get weak even if Im brushing my teeth and I will have to stop for a minute or they will give way, weird I know...
but mow I feel better its not just me.

I have recently been hospitalized for diverticulitis and was on Leqquin 500 Mg and Metronidazole 500 mg. From the 2nd day of medication I began to have a lot of aching expecially in shoulders and hips. I just thought that my arthritis was acting up as I was in active. Symptoms became worse each day and finally on the 7th day they were intolerable and I looked up info on the computer and was horrified at what I found. I stopped the Rx and after a week was able to see my doctor. She assured me that the Rx was not the problem and it was indeed my arthritis but as time goes by my symptoms have decreased by have not gone away. This goes on my list of Rx not to ever take again. I believe it is very dangerous to some people and I am one of them.

Hi,My biggest side effects are the hair loss,limb swelling,insomnia,halucinations(unless my dead dog really is a ghost),memory loss,numbness in legs and arms,tingling in arms and hands expecially when I cough or sneeze,sinus stuffiness and infections and cronic bronchitis.Allthough I have these side effects I personally think that I am better off taking the singulair for my asthma(does not help my allergy symptoms at all) than when I was on all the allergy meds and streoids.I used to have a bag load of those and I was allways having attacks,was depressed and thought of suicide but then I did the study for singulair about 15 years ago and thought it was a miracle cure so I waited for it to come out on the market.I know it is not a miracle cure but I don't have to take those other meds anymore and I only use my fast acting inhailer mabee once a month now.I am now 6 months pregnant and will be looking for an alternative treatment from a hollistic/natural Dr. after I have the baby.There has got to be a better way to control this disease,I hope,naturally through diet and other remadies with less or no side effects to treat my allergies and asthma.If anyone knows of such tratments,please post it.Thanks.LR

All you ladies, and expecially femalepara:

You shouldn't tell ANYTHING about this pill, as long as you haven't been taking it AT LEAST over a few months!!

Reading such a post like "I just started taking it TWO WEEKS ago and this is so much better than..." feel like a slap in a face of someone who had suffered and is still suffering because of this nightmare pill!!

Surely everyone reacts different on medicine, but you always should be careful and very sensitive about ANY symptoms you experience while taking Yasmin!!

In my case the worst symptoms started after 2 YEARS on it!!! Then another 2 very bad years (always tired and dizzy) without noticing, what this chemical was already doing to my body and then the total breakdown after 4 years on this stuff!! The first 2 years I thought it was the best pill I ever had taken and then in 2004 my life nearly was about to end because of that sh....!!!!

So please ladies, don't tell anything about a medicine as long as you weren't on it at least for one year!! Believe me, before that point you don't know ANYTHING about it!!!

I wish you best of luck, that everything stays that good as it does at "2 weeks" on it. In my case the diuretic effect changed into the opposite!! After about 3 years on it I got such bad water retention I've never had before in my life and cellulitis all over my body (not only legs or so!!), even at my arms!!! After about 4 years on it I looked as if I was pumped up with tons of water, my face looked like a big balloon (I ALWAYS was a very fit and slim person BEFORE!!! I swear!!), my belly wobbled with every move I made.... It was terrible!!! And still, even after one year WITHOUT Yasmin all the water I had retained is not gone completely. I'm just so thankful that it gets less every month; already I lost about 10 pounds during the last 4 months and my body and face finally starts looking like my old self!!

So again: Please be careful with that medicine and don't praise it to the skies since this is a bit hasty at such a short time on it!

All the best to everyone out there, who's still suffering or recovering of their personal "Yasmin nightmare"!! God bless you!!

Silke

I have been on dilantin for 20 years for seizure disorder called cortical dysplasia. Didn't even know I had it until 2004 when I had a grand mal seizure that lasted too long and different tests were run by my neurologist. It was suggested at that time that I switch from dilantin to something else due to taking it "too" long but all I knew is that it kept me seizure free and I was unwilling at that time to change. Well now here I am in 2006 with the side effects of the dilantin taking the chance of switching meds. Have been put on topamax, have been taking it for about a month. Very difficult transition for me, expecially when the dilantin was stopped all together. A lot of it was "in my head" I believe as I knew the dilantin did work and was not so sure about the other but I have struggled with feeling "hung over" in the mornings, confused, off balance, slow in answering questions, and anxious regarding these symptoms. My Dr. assures me I will adjust as my dosage is increased. Just when I get used to one I have to go up so it is very stressful times for me at the present but at this point I'm willing to ride it out. I have a MRI and a 24 hr. ambulatory EEG scheduled within the next 2 weeks so we shall see the results from that, but in response to side effects.......yep.....at least for me...but some are mind created

I am totally suprised at the various things Neurontin is prescribe for. Neurontin is an anti-seziour medication. I am taking Neurontin, Lamictal for Bipolor as they say...which I truely do not believe in diagnoses at all. I just attended an all day conference put on by Dr. Glasser, intitaled, also his book, "Danger, Psychiatry can be dangerous to your mental health."
The pharmicutical companies are making lots of money off of us since we are ginipigs. I have expereinced on anti-psychotic, Prolixin, shouldn't be on in the first place, only 2nights..spent two hrs in ER. As for Paxil gained 100lbs on (Jan97-Aug.02), & when tapered of had withdrawal symptoms (week after I started withdrawal, I saw a story about it on 20/20) even though withdrawal symptoms left it took me a yr to recover, whats positive of getting off the med, I have lost the 100lbs, + 5 more. Depakote, also caused some weight gain and some hair loss (taken off this before yr before paxil) One thing dr. never tell you is the long term effects or if there is any withdrawals.
I think the best way is to learn the ends and outs of all your medications you are taking. You know your body better then they do. Even if prescribe medication, learn all u can about it before taking it. Expecially the medications that effects your brain. I also feel that some of this medications can cause harm to a brain. You do have choices and its your life. (There is much more to this story about me, for example, pinch nerve in neck for 13yrs). If u would like to know more about me or have any questions I will be more then happy to reply back. ******

Since starting Lotrel in May, 2002 I have in the past 6 months developed severe muscle and joint pain expecially in my legs and ankles. I used to run 3 to 4 miles 5 times a week. I can
hardly do two miles walking now. Could this be Lotrel 5/20?

What an awful day! I went to ER thinking I was having a heart attack because of the severe pain in my chest, neck and expecially right arm. After all the testing they sent me home saying it "might" be a reaction to the Levaquin I have been taking for five days (for a colon infection). I was convinced it was the levaquin since I am a very healthy 50 year old woman, hiker, runner ,ect and I have not taken an anitbiotic for over five years (for a tooth problem). Now all of a sudden I have this horrible aching and pain in my upper body. Needless to say, I am getting off the drug and will pursue this with my doctor on Monday. After reading all of this, I am hoping that the symptoms will leave and not cause permanent damage. I willalso contact the FDC and drug company. Thank all of you for writing this or I would have not known what happened to me.