Lipitor Side Effects - Constantly Tired
Apr 3, 2015
Since I got diagnosed with high cholesterol last year and was prescribed Lipitor it seems my health is getting worse and I am constantly tired. I sleep 8 to 10 hours and yet feel as though I have not slept. My doctor thinks it is my body adjusting to my new meds and told me to quit smoking and reduce caffeine. So I still feel so tired.
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My husband has been taking lipitor for about 10 years. About a year & a half ago he started showing signs of what I thought was dementia until I researched it online. I couldn't believe my eyes....he was a poster boy for the side effects of lipitor! I contacted our doctor about it but he wouldn't hear of him trying to quit taking it. I know we don't have to take the meds that doctors prescribe but they're supposed to be the experts & have our best interests at heart but I'm so worried that my husband will get worse.
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I know that it's known that lipitor has the side-effect of muscle tiredness and aches. Has anyone else have to deal with this? Man it's off the hook. I almost am paralyzed fro, lipitor. This horrible and I would like to talk to someone who's been through it. This is a very under-rated affliction IMO. I've been tested and it doesn't look like I have the Rabadolosis<sp? That spelling isn't even close. I was very scared before I realized what was causing this severe problem.. Now I know that lipitor has helped a lot of people, it brought my cholesterol down a bunch very quickly. Frankly i would rather have high cholesterol. I did have a stroke at the end of November, small, deep in the cerebellum. Hence the lipitor.
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I have recently been taking 40mg lipitor meds due to raised cholesterol. I have been on these for several months and recently have noticed that I an physically and mentally exhausted on a daily basis. I feel light headed and nauseas, sometimes I vomit. I have no appetite. I am struggling to complete my daily job and my social life as ended up non existent. I am always tired to the extent of I have a sleep in my car for half hour before going to pick my wife up from work. She finishes an hour later than me. Before I used to come home tidy up do some chores etc. Now there is no chance. Can lipitor side effects actually be this bad? Any feedback would be greatly appreciated. Thanks
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Just wondering if anyone else feels the same with this tiredness. Sometimes I will be fine then all of a sudden my eyes will want to close for around 5 mins then I will be fine. I'm always yawning and fall asleep a lot more if I simply lie down or watch TV. I haven't changed the times in which I go to bed recently so I'm not losing sleep, I've tried going to bed earlier but it makes no difference. It's making getting up for work really difficult.
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I had a heart attack in mid October due to a congenital enlarged artery. The stent was unsuccessful and I lost 10-15% of my heart. My EF is around 46/48 and the doctor has never mentioned heart failure, but I know I need to do all I can to try to prevent that from happening.
Anyway I am on metoprolol tartrate (beta) 12.5 twice a day, plavix, aspirin, lipitor, and in December the dr put me on a very low dose of lisinopril (Ace) 5 mg.
Lately my back has been aching as the day goes on and I feel like I can't take a deep breath. Let me clarify, when I sleep and when I first wake up I feel good and normal. But as the day goes on I start to get some muscle aches and my breathing seems weird. I don't feel like I'm about to suffocate and I can breath normally fine, but it's like I feel the need every few minutes to take a big deep breath and when I try I can't totally get a full really deep breath like I used to.
Could this be the lipitor or the lisinopril or maybe it's anxiety and it's all in my head because sometimes I don't even notice it. I take the lipitor and the lisinopril at bedtime and sleep well and wake up feeling well, this usually happens about mid-day or so.
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I am a 47 year old male (right weight for height) and reasonably fit running three times a week who has recently had to visit the doctor (first time in years) for severe neck pain caused by strenuous gardening work -so called leisure.
However my blood pressure was checked over the past few weeks and has found to be continuously very high ranging 190/115 to 150/90. My GP has decided to put me on ramipril starting with 2.5mg increasing to 5 mg and then 10mg over six weeks. On reading the comments about side effects I am really concerned which has now possibly increased my blood pressure further - really concerned on what to do, should I get a second opinion through my private medical before starting this treatment?
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I'm looking to start orlistat this week but after reading over everyone's experiences I'm a bit nervous to start. Are the side effects really that bad as I don't want to make a fool out of myself at work!
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I have just been put on nortriptyline for my pain has anyone else had this and did it work was there any side effects.
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I am about to use Viagra and I am a lot scared. I have never needed it but I guess I do now. So who knows about this drug, are there serious side effects. I do not want to trade one problem for another due to the drug itself.
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I used the tablets for 5 months and a bit, should be taking it for 6 months but i decide to give into not taking them due to really bad side effects.
When i started, i took 2 TWICE a day for 4 months but, rashes appeared on my cheeks, completely red and skin dried also on my nose. I couldn't bear the suffering, i applied creams like E45 (made things worse for me) then i switched to sudocrem, applying it to my face where the rashes were. this seemed to help stop the rash from getting any worse. I went to see the doctor who said i should cut down on the tabs to 1 Twice a day so i finally started to heal from the rashes. I carried on using the tabs this way until the rashes appeared on my nose again, it was really bad.
To those who suffer from Eczema, be warned as this course may effect it, making it really bad. This is the reason why i have to quit from this 6 month course (am finishing on 5 and a bit months) As for acne, it helped clear it up nicely even old scars until a point where my skin could heal no further ( i stayed the same after the 3rd month) so hopefully, changes are permanent and my side effects will go away from stopping this course.
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I have been having joint pain, general body pain, fatigue, depression and anxiety for years. I was dx with fibro about 3 years ago. It was first suspected almost 20 years ago. My mouth and eyes are painfully dry. My lips constantly crack. I recently had a PAP done and the GYN remarked how dry my vagina was (I'm not sexually active so I never noticed).
I recently saw a rheumatologist here in the State (I had previously seen one in Korea). She did a bunch of blood work. My Vit D was 28 (reference range was 30-70). RF, ANA were negative. CRP not done, but has been elevated in the past (multiple draws over a two year period, but none in the last year). ESR was 58 and has been elevated for 20 years (I went through a lot of blood work in high school and nothing was ever found, but it was with ID, not Rheum).
Rheum was next to useless. She said the sed rate wasn't relevant and that there was no need to worry about the Vit D (which was lower in the past) even though I was taking 2000 IU a day.
After talking to my GP, he had me increase the D supplement to 4000 IU/day. He also wrote me a new referral to a different rheum. This one specializes in seronegative arthritis.
I try to be an informed consumer. Current rheum just wants to throw more pills at the issue without getting to the root of it. It seems like if I go in with a fibro dx, everything must be fibro. How do I approach this new appointment (in September!!) to finally figure things out? This new doctor will be in the UH system as are all my other docs. I think she'll have access to previous lab results, if not I can pull them up in my EMR.
I could use words of wisdom, advice, a kick in the butt (if necessary), etc.
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Put on this drug for HBP 2.5mg then 5 mgs had various problematic side effects went to doctor to advise him of my problems with this drug. He then increased the dosage to 10 mgs which I have taken now for 2 months and the problems have multiplied to a point when I have become so ill with all the problems highlighted in these messages that I stopped taking the drug and started to feel better within 3 days. I wonder now what the reaction will be from my GP when I tell him that I want to try an alternative drug. Having high blood pressure I could do without worrying about his comments which other people have endured when they have asked to have an alternative drug.
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I have found reading the posts about PA very helpful, i was diagnosed early last year with PA and have injections every 3 months they have helped enormously with my symptoms, please could any one tell me about the side effects of the B12 injection, i have had various syptoms which i have just put down to the whole PA thing, but would like to know....
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I'm on week 7 of 10 mg, and am pleased to say that my pounding heart, dry mouth and nausea have disappeared, I've only had a couple of headaches, my jaw clenching and tensing up have almost gone. I'm still struggling sleeping but I've never been good at that anyway, so I'll just see how that goes. I don't feel like skipping through life every day, but I certainly don't feel really low any more, I just feel 'steady'. Stick with it everyone, and thank you for your support.
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I'm on my 12th week. I've been diagnosed before with GERD. Now due to the pregnancy, it seemed to worsen as I experience painful heartburns. My doctor recommends I take omeprazole along with antacids. I've been taking antacids because I know they don't bare side effects on pregnancy. I am not sure though with omeprazole. I'm scared. I am afraid it might harm the baby. Anyone here experienced the same?
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I've been on Amitriptyline for 6 months for pain management - lowest dose 10 mg in evening and I am getting on fine after the side effects at the start!
This week I've been started on fluoxetine 20 mg per day for other issues. GP said it might interact with the Amitriptyline but might not so give it a go.
Has anyone else taken these two medicines at the same time? How did you feel?
I've taken fluoxetine before so I'm ready for the crazy initial side effects (off work for 4 weeks so I can get through it!)
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Has anyone had luck with Zoloft ? Any bad side effects ?
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Just in case that side effect sets in - does anyone know the effect of taking sildenafil citrate (viagra) when on ramipril??
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Don't do it. The operation went as expected. The side effects were not explained at all. First it does change sex. The tingling feeling that occurs when achieving orgasm will never happen again. Not what was stated by the nurses who obviously were fed a lie, how would a female know? The second thing was urinating problems. Don't be in a hurry because gravity is the master now. The day I went home I found out that pushing only made the flow stop. That was only part of the problem since I now could not hold as much as could previously. It will be that way forever. So now how to I get it reversed at the cost of the insurance? I have been to a urologist but cannot get them to admit that those are serious problem. The year I got my vasectomy I was told I have Multiple Sclerosis.
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Anyone out there use metformin if so what side effects r u feeling currently taking metformin 1000 mg once a day
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