Tingling in fingers symptoms and conditions

#Was prescribed Simvastatin 40mg and Bendrofluizide for high cholesterol and blood pressure, have been taking statin for 4 months no headaches but limb problems, tingling in fingers on right hand, weight gain and severe stomach bloating look about 5 months pregnant most of time, which is no joke when your 61. The doctor said it was the statin causing bloating have stopped taking both medications for about 2 1/2 weeks now. Joints better, tingling nearly gone but bloating still there. Has anyone else had problem with bloating if so do you know how long it will take to go away
or what I can use to get rid of it, have tried indigestion remedies.

lood

Wow! I can't believe how many of us suffers from the pill from hell, Yasmin. I stopped taking it September 17 after 5 years and I'm worried as hell as to what's going to happen to my body now. But first things first. I seem to have gotten pretty much every side effect in the book.

About a month after starting it I got gastroparesis- paralyzed stomach- and I also became lactose-intolerant after 30 years of drinking a lot of milk. Go figure! I get a huge bloated belly as soon as I drink a little water even now. I have gained about 6 lbs that I can't shake no matter how much I work out and that has never been a problem before.

I had migraines from hell and headaches nearly every day the last few years.

I got panic attacks and was very nervous, had anxiety and it felt like an elephant was sitting on my chest. And that is SO NOT me or anybody in my family. And I know it was the pill cuz I had no reason to feel that way.

I had blurry vision at times. Fainted once in the mall for no apparent reason, I had never fainted before in my life.

I had no interest in my own life or in doing anything whether that was working, going to school, exercising, going out with friends, traveling, whatever it was I was not interested. Again, so not me. I could have died and I wouldn't have cared. I could have gotten a Ferrari and I wouldn't have cared.

I could sleep 10 hours a night, take 1-2 hour naps in the afternoon and go to sleep again at 10 pm, no problem. And the nightmares! Holy crap. Awful dreams about plane crashes, robberies and murderers EVERY night. Thankfully they seem to have disappeared now.

I have high cholesterol, through the roof actually! -no family history there either- and blood pressure is a little high but not too bad. My thyroid was a little elevated last time and the doctor thought it was due to Yasmin.

I snap at everybody and think that I don't love my husband when I actually do love him a lot. He has put up with me being so unbelievably bitchy for 5 year. Bless his soul!

Since I started Yasmin we have had sex about 1-3 times a year. I'm NOT kidding. I haven't wanted anything to do with sex.

I have heart palpitations at times. Shortness of breath just walking up the stairs in my house.

Dry skin no matter what cream I use. Major hair loss.

I went off Yasmin once before and didn't get my period back for over 6 months so I just started taking it again like an idiot cuz I wasn't planning to have kids then anyway.

I was never happy, never sad. Mostly mad or irritated, no problems there.

What else? How many hours do you girls have to read my post? ;-)

To sum it up. Yasmin has destroyed my life for the past 5 years but I was to blind and scared to get pregnant before that I just didn't care. And not caring about my own health was surely caused by that rotten pill too.

What can I expect now that I'm off the pill since 2 weeks? How long before the hormones are gone from my body? What can I expect and when does it get better? Can I go to the ob/gyn after 2-3 months if I don't get my period and have them give me something to start it? Or would that be bad? What about the weight, should it go up or down? Acne? Hair loss? What else? Have you had any medical problems that you needed medicines for due to Yasmin? How long has it taken you to get your period back? And most importantly; can this pill make me infertile???

If there is a class action lawsuit I want to be in it!

I'm 39 and have been on Coumadin for about a month. Was diagnosed with DVT in right calf after taking Yaz birth control for only about 4-5 months (no other pre-conditions - I'm a non-smoker, fairly active, not overweight, no recent airplane trips or long car rides.) I was on Yaz to treat severe problems with my period which has been the case since I was a teenager, but I was tired of having to call in sick to work every month, and had hoped Yaz would eliminate that problem. I had been on other BCPs when I was in my 20's, and never had any symptoms of clotting, so didn't think that it would be all that risky to try again, despite me being slightly older than the typical woman on BCP. Obviously, I am not taking Yaz anymore, and will not be able to take any other hormonal therapies for the rest of my life. But I guess that's minor compared to the risk of developing PE from an undiagnosed blood clot.

Anyway, I've been noticing I've been getting sudden, severe headaches since starting the Coumadin. I have a history of migraines but I usually only get one or two per year at most. Now I've had what feels a lot like a migraine twice in a matter of a couple weeks. My husband has also commented that I've been irritable and acting "spacy".

My INR has also been all over the place. They've been alternating me between 5 mg and 7.5 mg per day. For the first few weeks I was right where they wanted me - between 2 and 3, but then last Friday my results were 4.6!! Way too high. I go back this afternoon to see if anything's changed over the weekend, after skipping a dose and then doing 5 mg Sat. and Sun. I do hope they can find the right balance and don't have to keep tinkering with the dosage. I'm wondering if that's what's contributing to the headaches. Maybe if they can stabilize how much I'm taking from day to day, my body will adjust.

I wonder if anyone "official" is tracking the number of DVT/PE patients that can trace their onset of symptoms to Yaz. My sense is that this is a much more serious and prevalent side effect than their marketing dept. would like to admit.....

I was taking 500mg three times a day. After 1 week I developed severe joint pain and swelling in my fingers. I got an itchy rash on the bridge of my nose and over my eyes and inside my nose. The joint pain continued to my knees and toes. I have been off of the medication 3 weeks and I am just starting to feel a little normal. a different doctor put me on 800 mg of Ibupropen 3 times a day and after reading up on the side effects of Cephalexin I began taking Benadryl which has helped a lot.

I have severe numbness and tingling in fingers to the point of problems sleeping due to the discomfort. Also have pain and popping in both thumbs only. I heard from a friend that her brother had same symptoms with Pravachol, which is what I take. She said his doctor diagnosed osteoarthritis and thought it might be connected to Pravachol use. Anyone else know any connection or have similar symptom?

I was on Celexa for a year and a half and gained 40lbs!!! Has anyone else experienced this? It was a great anti-depressant but did make one somewhat lethargic. I also kept having small fits of depression here and there despite the meds. I just switched to Wellbuterin and its making me alternately spacey and moody, but i've only been on it four days. Does it get better?

I started taking Topamax Jan 07 while weaning off of Dilantin (for seizures) after brain tumor removal. Been having tingling in fingers and lips and I'm not yet up to full dosage (100 m.g. 2 x day). Memory Loss, about 20-30 minute attention span. After reaching and maintaining the maximum dosage I may report changes.

Hi,
Doc put me on Topamax for PTSD due to MVA. I am at 200 mg and having tingling in fingers and acrid taste in my mouth. Thinking I might stop taking it and just suffer the anxiety and stress. As others, I have lost some weight with the drug, in weighing the pros and cons guess I will check with my doc and see if he can reduce the dose. I was having trouble sleeping and getting flashbacks of the accident and the Topamax has helped but I really don't like the side effects. Best of Luck to all.

Positive side affects
mo more migraines
negative side affects
tingling in fingers and lips
eye twitching
discharge from my breasts..ya I'll say it.. doc said it was from the t-max.
confusion every once and awhile

Honestly though, I can go to work everyday and lead the normal life, with no migraines, and keep the shades open and let the sunshine in, so it's okay.