General practitioner symptoms and conditions

i was told i was hypothyroid,but i felt fine! dr. put me on 88 mcg's of levoxyl and i all of a sudden came down with the worst case of acid reflux,which i did not have b4.also,heart palpitations.i choked down this med for 3 years,experiencing hours of burning after my daily pill.i could not take it any more! i put myself on a trial month without levoxyl ,and the burning and acid feelings are gone! i feel gr8! i dread being scolded by my doctor for going off it,but i could not take that burning anymore.ive been to 2 gastroenterologists,plus my general practitioner,all of whom said it was impossible for levoxyl to cause g.i distress.if that is so,why has the burning gone now that i stopped taking it?if u have experienced burning with levoxyl,could u kindly email me/i want to know-am i crazy,or is heartburn an issue for other levoxyl users also/plus,i never felt/looked ill in the first place,so even tho my thyroid functioning may not be optimal,did i really need medication yet?maybe someday i might,but i feel fine,i have long thick hair,decent fingernails,full of energy and not cold all the time-so why do i need meds at this point?(if i ever have overt hypo symptoms,i will have to take something,but why fix what is not broken?) ps-my b/p and cholesterol all very good too,altho apparently ive been hypo about 5 years.

I have been on Seroquel for about a month and a half.
When I first began to experience anxiety, I was given antidepressants starting with Celexa,(didn't work) Zoloft( made me feel worse), and Trazodone(same effects) , along with anti-anxiety medications.Nothing was working, and I ended up with Serotonin syndrome- HORRIBLE experience- did not sleep for a month, and it was as though my "fight or flight" response was on "hyperdrive".

Finally went to a Pdoc instead of a general practitioner,and he took me off what I was on . He put me on 50 mg. of Seroquel in the a.m., and 50 mg. in the p.m. before bedtime. I improved within several days, and have felt like myself for the most part ever since. I am thankful especially to be sleeping! Have gained some weight back, but since the serotonin syndrome caused me to lose 20 pounds in a month and a half, that is good. The first couple of weeks or so I had dry mouth, but that has gone away. There have been no sexual side effects like the ones caused by zoloft- that makes both my husband and myself happy.
Just hope if I continue to exercise and eat right that I won't experience the weight gain everyone is talking about.
My life is extremely stressful right now due to long-term circumstances beyond my control, and this medication is helping me to cope! Besides feeling some mild depression and grief due to those circumstances, I am just thankful to be functioning well again!

Ladies there are some things you should consider before raging out against your BC. First of all, and your doctor should tell you this, it can take up to four months for things to straighten out, but they will straighten out. Anything that means you should stop taking the pill now should be told to you by your doctor (in fact you have to sign off on it), so PAY ATTENTION. There are obviously other less serious side effects that aren't worth putting up with, like hair loss; call your Doc and say your going to stop because your hair is falling out. I had difficulty while on LoOvral driving: I would get body aches, become disoriented, and slowly pass out. When eating/drinking water didn't cure the problem, I immediately stopped the only change I had made - taking the BC. It isn't a listed side effect, just my bad luck with it. I hadn't had the problem before and do not have it with FEMCON. You need to use a little logic. If there is an unbearable side effect, stop and change pills, but please don't rage out (unless that's your side effect). If your worried about your OBGYN trying to give you an easy fix, ask your general practitioner.

I'm going to throw weight gain in right now. I haven't had any. Furthermore, I was told that I might by my Doc. It's temporary, may take several months but it will go away. Also, you body weight fluctuates up to five pounds a day, everyday. It depends on a lot of things ie. when you last went to the bathroom, when you last ate, how much water your retaining...

I suppose the first thing I should say is why I'm on FEMCON. I have alwasy had extremely regular periods (five week cycles - so cool), starting at age nine. In middle school I began to have very painful periods. In High School, the nurse would give me a heating pad and put me to bed for the rest of the day (other girls got 15 min). The pain was so bad I cried in my sleep. When I went to college my OBGYN started me on Yaz. I went about three months with no improvement what-so-ever, and a mild increase in my depression/anxiety. So I stopped, my cycle was now regulated to four weeks and never recovered. The monthly pain reduced to a lower constant over the next few months, but now had terrible spiking shooting pains, at one point I nearly fell down the stairs. Over the next two years a couple more pills were tried with no help and irritating side effects, none lasted long. I changed doctors. My new doctor, said he wanted to try me on a high dose pill tricycle to do a sort of hormonal reset. The jury is out but it seems to be on a good trend.

I have had several side effects with FEMCON. Or at least what could be side effects. I'm currently on a study abroad so any of them could be from an environmental cause, but I'm thinking not. The most irritating has been a pretty severe case of motion sickness, if it's moving and I'm in it, I get a severe migraine, which eventually makes me very nauseous (I don't throw up for anything, but this would have had anyone else I know talking to a toilet). That is steadily going away. The addition of a ginger tablet each day to keep my stomach calm didn't hurt any, either. Second most annoying was breakthrough bleeding and cramping. Starting in the middle of my first pack I got nasty brown breakthrough bleeding (varying degrees) and moderate cramping daily. Very aggravating when your cycle is three months and it lasted the whole time. This cycle I'm don't have either. I couldn't tell you if FEMCON is effecting my depression, but I did have a nasty spell the last time I saw my brother (then again he is my brother). I seem to be doing as well as I ever have since he left. I have some breast tenderness still, mostly in the nipples. During my first cycle it could be very painful, but now doesn't bother me much. Personally, I believed that I was rather insensitive (physically speaking) before, so this may now just be a normal level of sensitivity. I never really had a sex drive before but I've got a pint sized one now. Other short-lived side effects were: nausea, occasional dizziness (continuing, but I am more inclined to blame my diet of cafeteria food at this point), swollen fingers (water retention), heavy watery discharge (not an infection).

If your pill isn't right for you, you'll know pretty quickly. If you get side effects, read the reference packet. I don't recommend reading all of the piddly side effects (ie. headache, nervousness) before hand because you may cause yourself to get them. The mind has a lot of power over the body, if you worry about side effects your just might get them as a point of mind over matter. Do not ignore anything, side effects for most BC are the same, if you've read one packet you've read 90% of every other packet. If you think your having a side effect that's dangerous deal with it immediately, if it isn't listed in your packet - go to the ER or call your Doctor on the spot. If your having one of the generic temporary ones (or worsening of a previous condition), the packet is a good place to look to see if it's normal. If you aren't happy with your BC talk to your Doc. Be smart and give things a chance to normalize. I hope this note can be helpful to people.

I had mine removed today, my experience started in May 07; by the first week in June, I had reported to my general practitioner (GP) for first symptoms (headaches), by Dec 08, I had been to my GP, the neurologist and the rheumatologist FORTY SIX times. Prior to that, had been to her only 13 times in 10 years so I KNOW it's not b/c I'm a "sickly" person at age 38. My symptoms were awful, neurolgical mostly, made me think I had MS or Lou Gherig's disease. BUT after reading all the posts on this forum and the other Mirena forums and I'm convinced Mirena was the culprit (fingers crossed).

When the GYN took it out today, it had tissue on it so I'm SURE that it grows into your uterus. He had to manually dilate my cervix and go fishing for it -- very painful. Since then, I've been bleeding very heavily. Has anyone else had Mirena removed and saw tissue stuck to it? Heavy bleeding immediately upon removal?

I'm so glad I found this site. I have an IUD, but I have been talking Femcon FE for about 6 months because I had cysts on my ovaries which were making my life miserable. I have had countless yeast infections; I went to my general practitioner and she gave me antibiotics. They cleared up for about 2 weeks and then returned. When I don't have a yeast infection I still have discharge. I also have gained weight. It's only been about 5 lbs., but it's been all in my stomach. I exercise for 45 minutes every day and eat healthy, but I look like I'm in the early stages of pregnancy. I just finished my pack, and I'm never taking this again.

I was “poisoned” by Levaquin -- resulting in acute tendinitis in both Achilles tendons.

Background:
I am a healthy, athletic male in his mid-50s who has never had an Achilles tendon problem. In early July 2008, my doctor (general practitioner) prescribed Levaquin for an infection. I took the medication for 14 days, as prescribed.
Sudden onset of acute tendinitis in my Achilles tendons occurred near the end of the medication period. The tendinitis occurred in both Achilles tendons simultaneously. Nothing related to my lifestyle would have caused the tendinitis.

Symptoms:
Symptoms included the following at one time or another:
1. aching
2. sharp pain
3. feeling of heat/burning
4. tightness
5. pins and needles in small areas (micro tears?)
6. weakness at rear/base of each heal.
7. When I woke-up each morning my tendons and the back of my heal pads felt sore, weak and tight.
At the height of the problems, I had extreme difficultly walking and negotiating stairs, and I thought there was a risk that my tendons would detach from my heal bone.

Doctors’ Advice:

My general practitioner’s and my podiatrist’s advice was to: (a) not run, cycle, hike or otherwise exercise my legs in any manner other than easy walking and swimming, (b) gently stretch, (c) take ibuprofen, (d) ice regularly, and (e) use heal lift shoe inserts made by my podiatrist. Their advice was based on the view that the damage that was done is more like damage cause by an injury than damage caused by an insidious drug. My readings on the subject indicate that little is known about the mechanisms behind this fluoroquinolone-specific toxicity. It is believed that the tendon’s collagen fibers become disorganized and infiltrated with small blood vessels -- resulting in weakness. And there are no specific treatment plans for this problem.

After 2 months of living with these symptoms, I decided to change course.

My Approach to Healing:

Because I never believed my pain was the result of inflammation, I stopped icing and taking ibuprofen. Because stretching seemed to further weaken the tendon and set me back, I stopped stretching. Because I believe that the body heals itself best when used, I started cycling at an easy pace. I then worked-my-way-up to cycling more aggressively, and to walking in the neighborhood. That’s where I am today. Two days ago I had my first day without discomfort in 3 months. Yet, I have a long way to go. I am not yet hiking or running. It’s a slow healing process with occasional setbacks when I push my tendons a bit harder than I should, Given the progress I have made, I am hopeful for a full or nearly-full recovery in another few months.

Other things I have done in the past month:

1. Taken L-Lysine (1000mg daily), which is believed to aid collagen formation.

2. Taken Magnesium (250mg daily), which some believe may help leech the fluoroquinolone molecules from the tissues because of the affinity of these antibiotics for minerals.

3. Taken Fish oil pills (3000mg daily), which improves circulation

4. Used a heating pad, which improves circulation

5. Started regular Acupuncture (first time for me), which improves circulation

What you can do:

1, Be easy on your tendons until you get a handle on the problem. Don’t over-use tendons when they are in a weakened state.

2. “Listen” to your body and take steps you think best to help the healing process.

3. Tell your friends to beware of potential side effects from fluoroquinolones.

4. File a MedWatch report with the FDA at fda.gov.

5. Share your findings/advice on this forum.

Good Luck

I was on Aviane for almost 3 weeks, but had to go off of it a few days ago. I normally have anxiety and depression issues, but they went off the charts while I was on Aviane. My general practitioner said that bc pills don't aggravate mental illness, but I'm thinking "the hell they don't!". In addition to being really nauseas and having a near constant cramping in my uterus for the last few days I was on it, I was having severe mood swings, high anxiety, hysterical crying spells, and I just felt so hellish that I wanted to die. My boyfriend was having to calm me down at least once a day. I couldn't handle any stress at all. All it took was my dog peeing on the carpet to send me into a breakdown. Right now I haven't had a pill in two days and I'm finally starting to feel a little better. Hopefully this will continue and I can try another bc.

Welcome a board singulairsurvivor. I received back an email from the woman at the lung association,she was of course sorry for our experiancr,and went on to say the scientist that reviewed the data were some of the best,and the association has no ties to any product.then as i am watching the updates on the hurricanes,i am inendated with singulair commercials as once again it is allergy season,so what a windfall for Merck that this article came out this month and not next....Coincidense i think not shame shame shame on you.To all those unsuspecting people about to get their prescription .i am sorry

I am so thankful for this website. I have been on Loestrin for about 5 months now. Two months ago I started experiencing many of the symptoms the rest of you have been describing. I started having head aches, insomnia, hot flashes, and then terrible anxiety attacks. I've also been having horrible chest pain that extends out my left arm. At first I thought I was having heart problems, but, like many of you, EKG's and chest x-rays came back normal. The anxiety attacks have gotten so bad that I thought I was going to have to go to the emergency room the other night. When I talked to my doctor about it, we decided its stress and depression, and she prescribed me an anti-depressant. I was supposed to start it today, but I got a wild hair to do some research on Loestrin since its the only other med I take. And lo and behold... Thank goodness I found this before I started the anti-depressants. I plan on calling and getting my BC switched first thing Monday morning. You couldn't shove another Loestrin down my throat. I'm so frustrated, as I'm sure many of you are, that NO ONE told me about this. My doctor did not discuss these extra possible side effects because its a low dose pill. And my general practitioner completely overlooked the fact that it might be the BC pill causing all this. Not that I blame her. I overlooked it too, and it is true, we are our own best advocates. Thank you to all the women who posted on here. Just like many of you, I've been feeling like I'm absolutely crazy lately. With the mood swings and uncontrollable crying, no one understands. I think its ok to say this website might have just saved me several years of being on anti-depressants. Granted, I haven't had any bleeding problems like some women, and I love the three day periods. But I would take a 7 day period over how I feel right now any day. Does anyone have any suggestions of what BC to switch to? And can anyone tell me how long it took for them to get back to normal emotionally? Thank you so much...

I began using the NuvaRing in January with no problems. In April I started having severe sweating and severe chills - nonstop. I could not figure out what was wrong - I never associated it with the NuvaRing. I went to the Dr. and they tested me for all kinds of things and found nothing. Over the course of a month I was constantly at my gynecologist, my general practitioner, the emergency room, or urgent care. I missed a TON of work. Always the tests came back negative - and that I was fine. Finally they came back with that I had parvovirus B19 - which is a blood test and they had to send it to the hospital so I suppose it was true, but I kept saying that can't be ALL I have - there must be something else here - and they kept saying no, it's all the parvovirus. I went online and looked up symptoms for parvovirus B19 and chills and sweats was not a symptom. Parvovirus takes 4-6 weeks to go away. At the end of that time I will STILL having these chills and sweats and I found this website and BINGO - it finally all clicked. I removed the NuvaRing 4 days ago and I have not had any problems since. It's ridiculous. You just always have to diagnose yourself, and the Doctors say don't do that but what the heck? If I hadn't diagnosed myself I would still be miserable! I do not intend to use the NuvaRing anymore.

Hi, I'm a 25 year old male. I've had severe seasonal allergies for as long as I can remember. I'm to the point where the coming of spring usually means that I'm going to be visiting the emergency room inside of a few weeks. I've been involved with Zyrtec since the spring of 2003. During that season I experienced what could only be described as a near complete nervous break down. I had an issue involving administration at the college that I was attending losing some paperwork regarding a semester withdrawal ... as a result I ended up with 7 F's and owing the university around $4,000.

I ended up crashing. My family describes me as the guy "with a big heart" ... but I began getting into screaming matches with my parents that ended with me breaking down and weeping / sobbing almost hysterically while holding the door shut to my bedroom. I became incredibly "anxious" (that's how my families General Practitioner {GP} described it), but I'd describe my behavior like more along the lines of a parody of a guy that just smoked a ton of REALLY cheap pot and therefore began to think that everyone was out to get them and that no one had their best interests at heart. My GP decided that I must be on the verge of a nervous breakdown and put me on paxil in an effort to calm me down. In a way it helped keep me calm and drastically reduced the extreme emotional spells that I was having. I pulled myself off of Paxil (for another slew of side effects that I'll be posting on that tab) during the late summer and fall when I don't have as severe an issue with allergies and as my season approached I found a new doctor and when I brought up how I had eventually decided Zyrtec D was making me feel he told me that I was right on the money. He ran through the almost all of the side effects that are listed on this page and I was floored ... I couldn't believe that no one had told me about them. He put me on Astelin and since then I haven't had any issues. As a matter of fact, I'm totally psychologically sound now and I haven't experience a "heart flutter" since ... where as a few years ago I was on the verge of committing myself while on Zyrtec D.

As a little note: I'm currently taking Astelin along with the OTC Zyrtec on a once a day basis and the only side effects that I've seen show back up are: slight paranoia, a loss of energy and general virility, and a significant weight gain (about 20 pounds in the past 3 months that could be attributed to my near complete loss of energy) ... which is an ENORMOUS improvement coming from the prescription strength Zyrtec D.

I'd also like to mention that I don't have any disorders like bipolar disorder or severe depression ... but when I take Zyrtec I acquire a lot of the symptoms associated with those medical conditions ... the symptoms slowly subside when the season draws to a close and I stop taking the medication.

Hi ladies... I'm not surprised that you folks comprise most of the posting population considering the fact that this drug is prescribed to you. Well I'm quite interested in this drug and I do prescribe it to my patients however I am surprised at the magnitude of side effects listed here. I am based here in south-east Asia and I do prescribe Yasmin to my patients and I rarely here of these side effects. Perhaps this can be contributed to the fact that it (Yasmin) is available here under a different brand name however consists of the same chemical position. I am interested in the ones available in the U.S. Does anyone know how I may go about purchasing them. You can contact me personally on ****** thank you.

The Merck site doesn't direct link. Read the information for the General Practitioner.

http://www.singulair.com/montelukast_sodium/singulair/consumer/index.jsp

Merck's own website states that Singulair is not an anti-histamine. I cannot imagine any General Practitioner receiving a clear picture of how Singulair actually works from this site. Nor, are they being presented with the truth about the side effects. The whole site is a bunch of marketing FLUFF that never gets to the point. At the very least, the GP's should be on the rampage with us for being deceived.

I plan to rant about this later. What a dumbed-down presentation (Merck's site)? What an insult?

http://www.singulair.com/montelukast_sodium/singulair/hcp/allergies/efficacy/index.jsp

Thanks to all of you who have posted your experience with the Nuva Ring. I have been on it about a year, and have had side effects that I never attributed to the Ring.

I have been trying to lose weight and have been unsuccessful, despite my best efforts. I have gained about 15 lbs. in the past year, though I eat well and work out often. I CAN'T lose a pound! Plus, I am tired all the time, have limited sex drive, and often feel seriously depressed. I even went to a general practitioner to have thyroid test done, and nothing is wrong with me at all. I am not anemic and my thyroid is just fine. So? What's the problem here?

I happened to glance at an article in my newspaper yesterday about a woman around my age (I am 28) who was on Nuva Ring. She began coughing up blood, and it turns out she had a few clots in her lungs that they said had to be caused by the ring, as the woman had NO history of this in her family. I know that this a severe possible side effect and doesn't happen to many people...so then I decided to do my OWN research. I found this page and realized that perhaps my symptoms are NOT caused by anything my body is doing wrong, but just from this birth control. I just put my new ring in yesterday, but now I think I should take it out and go back to the diaphragm, because it seems to me that if these symptoms came on around the time I started the Ring, maybe they will just go away after I am off it for a while.

Geez, and it's crappy because aside from the possible harm it's doing to my body, I LOVE the convenience of the Ring. I sure wish I could stay on it, but I am getting too old to be irresponsible about my health. I used to be able to ignore the side effects on the package, because I figured it would never happen to me. But it seems that it's happening to so many people, I just don't want to take the risk anymore.

Again, thanks to those that have posted. I appreciate knowing I am not alone here!

I also have had many of these side effects, constant bleeding, bloated stomache, weight gain (or lack of weight loss), twitching in my abdomen, MAJOR swelling when I eat salty foods, depression . . . I feel so much better since I had my Mirena removed last week, after 4.5 months. I don't look pregnant anymore. I am back to my normal even keeled self. I ate something salty today and can still get my rings off. I haven't felt the "baby cicking feeling".

I wanted to add a thought. I definitely think Mirena should have been more forthcoming with these potential side effects, but it seems as though it is a pretty small number of us. My Dr. had only had 2 or 3 people that had bleeding for longer than 3 months. I know a lot of gals with this that have no side effects at all. So, maybe there are a group of us that just don't react well to medication. I know that the pill made me crazy. When I was induced my uterus went nuts and I had to have a STAT C-section. I know that my body is particularly sensitive so I really don't take any type of medication, under or over the counter. I guess my point is that for most women this seems to be an excellent option . . . just not for us. I do agree that we need to get the word out there because I am sure that there are plenty of other women having these side effects. I thought I was seroiusly ill and was ready to see my General Practitioner and start getting testing for everything.

This is a great forum and I am happy that it isn't just me. My Dr also told me there was no way the depression/mood swings could be from the Mirena but I just knew it was this litte device that was messing up my life . . . . .

I had the mirena fitted to cure my PMT's, I have had the mirena fitted 2 years now only side effect was a little weight gain until this last month i have had constant breast pain, I haven't seen this listed much as a side effect i am very worried has anyone else suffered with this side effect

heather

I was prescribed Sulfamethoxazole-TMP tablets for a severe UTI that I developed. I was given 10 tablets total--and instructed to take two per day. Within an hour of taking the first tablet, my UTI felt much better, however, the rest of me felt horrible! I got nausea, dizziness, extreme confusion and depression, and stiffness and pain in my neck and shoulders. I continued the medication anyway, b/c I never had sulfur or ANY medicinal allergies. I had difficulty sleeping the next few nights, I would wake up in the middle of the night for no reason. The soreness of my neck and shoulders then extended to my butt and thighs. I can't describe how uncomfortable this was. I was sitting at work literally writhing in pain from what I felt in my legs. (and I blamed it on my poor desk chair!!) This happened on day three of five. Also, while at work I had an "episode" if you will, where I became extremely confused and disoriented, and nearly had a panic attack. It felt like the world was crashing down on me!! It only lasted for 15 minutes or so, but I will not forget the way I felt. All the while, my UTI symptoms were getting better and better. I was completely unable to have a bowel movement...sorry for this information...but it will start to make you worry if you can't poo for 5 days!! Day four of five is what I like to call "The Enlightenment". I was getting in the shower, still dizzy as hell, and noticed that I was very itchy. I looked at my lower back and I was covered in red, itchy bumps. I was say they looked like small mosquito bites, all in a cluster of about 8 on either side of my lower back. I realized then and there that this medication really was ravaging my body like I had feared. I found this site and others online which confirmed that I wasn't crazy...just poisoned. Later that day I was resting on my couch and looked in the mirror and saw that my entire face was covered in a red rash. (and I got a horrific headache) The worst part is you don't really look outwardly sick or anything...you just feel terrible. Everyone I told was very nonchalant about it..."Oh just take some Benadryl". I've lost my faith in the FDA. I stopped this medication one pill shy of my last dose. I am terrified of the possible lasting effects and will never take this drug again!! PLEASE!! NEVER TAKE THIS MEDICATION!! YOU WILL REGRET IT!!

I am weaning off Zoloft. I began taking it in Nov. 2001 because I knew I would have post-partum depression since I had it with my first two. Zoloft changed my life so much for the better. That was almost 6 years ago. The past year I have decided that I can do w/o Zoloft. One, because I’ve learned how to choose to be happy. Two, because I don’t like being addicted to a pill. I know I’m addicted (or somewhat addicted to) because if I forgot to take the pill, several hours later, I would get weird feelings, like when I turn my head and move my eyes at the same time, a weird slightly dizzy feeling.
Here’s how I did it. In May and June, I took a whole pill (50 mg) every other day and every other day I took half a pill. That’s 2 months of that. Then, July and August, I took a half a pill EVERY day. Now that it’s Sept., I’m taking a half a pill every other day and NO pill every other day. I must say, this has been the hardest. It’s just 4 days into Sept. and I’m having those weird sensations a lot. My toes and fingers are tingly, too. I was planning on doing this for 2 months but I'm on the 4th day (2nd day of no pill) and I'm having too many tingles and weird dizzy sensations. So, I guess I'll continue taking a half pill every day and take NO pill ONE day a week for this month of Sept. Then, in October, I will take NO pill TWO days a week (but not 2 days in a row). Then, in November, I'll go to THREE days a week of no pill (but not 3 days in a row). And so on. I had hoped to be off by Christmas or Jan. 2008, but I see that it won't work unless I wean to a NO pill gradually. I knew all along that it would have to be gradual, and that's what I've been doing, but I had no idea that just missing a mere 25 mg. for 2 days (but not in a row, mind you) would make such a difference.
Now, if I get too many really sad days, I will consider going back on. But I’ve done really well so far. I know that God is helping me. He can lick it; I can’t. I have had just a handful of occasions where I was told something slightly disturbing or something happened to me that was slightly upsetting and it got me down, but only for the rest of that day. AND, I gave it to God and let Him deal with it. He wants to take care of my problems; He doesn’t want me worrying about it. I know that medicine like Zoloft may be the answer and if that is what I ultimately do, then I’ll just continue leave it to Him. I hope this helps someone.

Hi again. I think some readers may be misunderstanding what I am talking about when I posted my story and talked about natural progesterone. Natural progesterone is a bioidentical hormone derived from plants. It's only side effects are that it may make you sleepy, and it may calm you. It is NATURAL; I am not talking about synthetic hormones like in BC pills or HRT. You can buy natural progesterone cream in any health food store OTC. I happen to have mine compounded into a capsule in a compounding pharmacy. Natural progesterone and other bioidentical hormones are not manufactured by the pharmaceutical companies, and are therefore, not pushed by doctors. You will not hear about them from your general practitioner or your OBGYN. They are generally recommended & prescribed by holistic & wellness minded physicians. Dr. John Lee is a famous author who has written many books on the subject if you want to research him for more information. Or just google bioidentical hormones for more information. I just wanted to clarify what I was recommending. I think some of you just heard "hormone" and got scared. I totally understand. I think synthetic hormones are evil too. My friend and I have been suffering from anxiety as the result of Yasmin for a few years now, and we have tried several things together trying to recover ourselves. This is the only thing we found that works for us. I'm not saying it is the answer for everybody.

Andegags, Time is probably the only thing that is going to help. I take the Effexor to help with the shakes, but I should be off of it soon.
I am no longer on any BCPs. I cannot take artifical hormones after all that I have been through.
You are very young and I hope that you get better soon. Stay off the BCP's (especially Yasmin) and do not compromise your health or future fertility. Speak with your OB/Gyn and if you don't get the answers that you need on how to stop the shakes, speak with your internal medicine doc/general practitioner. You should not have to suffer like this, especially at your young age. Good luck in your last year of college. Enjoy your time with your friends, it flies by :-)

I am writing for my father. He takes Lisinopril, atenol, hydrochlorothiazide, and norvasc -- all for high blood pressure which he has had (genetic) since he was 65. Since he has added the lisinorpil, he has been having problems lifting his feet. He can stumble very easily and now must use a walking cane.
He is 87, active, and keeps up a 40 acre farm but is having trouble now because he is dizzy at times and has trouble lifting up his feet. His general practitioner and other BP specialist have told him it is not the lisinopril but when he doesn't take it the symptoms lessen considerably. He only takes blood pressure medication and nothing else. Has anyone else experienced having trouble lifitng their feet while taking lisinopril?

I TOOK LIPIITOR ABOUT 8 YEARS AGO. I HAD THE CLASSIC SIDE EFFECTS WHICH ARE NOW ACKNOWLEDGED. MUSCLE WEAKNESS, JOINT PAIN, TIREDNESS, TREMBLING AT ANY TIME I PICKED UP EVEN A CUP OF COFFEE. I WENT THROUGH EVERY NEUROLOGICAL TEST, ARTHRITIS TEST, ALLERGY TEST, EVEN TESTING FOR BONE TUMORS AND OTHER CANCERS. I ONLY TOOK THIS MEDICATION ABOUT ONE YEAR BEFORE THE GENERAL PRACTITIONER I WAS SEEING DECIDED MAYBE THE LIPITOR WAS TO BLAME. EVEN THOUGH I HAVE BEEN OFF THE MEDICATION 7 OR MORE YEARS, I STILL HAVE ALL THESESYMPTOMS. AT TIMES IT IS WORSE THAN OTHERS, BUT NEVER GOES AWAY. IS THERE ANY HELP FOR US WHO ARE VICTIMS OF THESE "RARE BUT SERIOUS" SIDE EFFECTS WHICH LIPITOR IS NOW INCLUDING IN THEIR ADVERTISEMENTS?