Regime symptoms and conditions

Extreme tiredness, ache behind my eyes. I have been on Lisinopril for about six months (10 mg). I wake at 7 a.m. and by 11 a.m. am so tired and feel so bad that I have to lie down and nap. Finally I decided to take it a night rather than in the morning since it was making me tired. That seems to be working. I started the new regime about a week ago and am functioning much better during the day. I didn't run across this comment in the testimonials so thought it might help someone. This is my own idea, not my doctor's.

I am 62, my bp 139/87 and just started lisinopril @10mg for the first week to increase to 20mg after that. I am 3 days into the regime and have no side effects.

I will post again after I increase the dosage.

Hi all, I first discovered this site back in May 2009 and posted on 25th June 2009.

I had my Mirena inserted in April 2007 after consultation with my Gyno and being told this is the best option available to me following constant bleeding and pain during menstrual cycles. Also had pollops removed during the same operation (which may have been causing the pain also). I was (like many) led to believe there were NO SIDE EFFECTS!!!! I can only assume we are part of some huge experiment??

I am 43 (soon to be 44 years old) with two adult children (18 and 21 years) and very happily married.

Like many others, my side effects are/WERE mood swings (recent panic attack - very scary!), headaches, abdominal pain, light bleeding for 2 - 3 weeks every month, fatigue and general feeling of unwellness, days of extreme sadness (would not classify it as depression), no interest in anything, almost complete loss of interest in sex, nausea, weight gain. Pre Mireena I had lost 35 kgs (approx 80lbs) with a lot of hard work. My gym regime and diet didnt change but I have still gained 15 kgs.

I use the "were" because I also made the decision to have the Mireena removed and like others was ready for a fight with my doctor.

No need to fight, my doctor listened to everything I said plus informed me she knows exactly what I am talking about because her two sisters had exactly the same problems and had the Mirena removed. Needless to say, THE MIRENA HAS NOW BEEN REMOVED. HOORAY!!!!

It has only been 8 hours so I don't really expect any miracles immediately although it would be nice to wake up and have lost the 15kgs I have gained.

To cut my very long story down, my doctor informed me of some interesting news about the Mirena. I was told at my age (43) to increase Progestron can send the body into Hormone overload, in fact we should be having more Oestrogen instead. The Mirena increases the amount of Progestron in the body, maybe that is part of the problem????

I am feeling so pleased to have the MIRENA OUT, will keep you posted on my progress. So far go good......no signs of bleeding yet.

I've been on a 7 day regime of Levaquin 500mg for an a infection that wasn't cured by other antibiotics and I can say it's worked. Yea I had a some muscle craps in the legs and some leg pain and a first day bout of nausea but overall, it's worked great for me.

I'd suggest that anyone on it do as my doctor said and either eat at least 1 cup of yogurt a day and/or take a Probiotics pill. The antibiotic/any antibiotic kills the "good germs" that help raise your bodies immune system and helps with digestion and the Yogurt/Probitic pills help grow the "good bacteria" back and ease the side effects while on it. Good luck to all

I have been on various cholesterol drugs (statins) including Lipitor with severe muscle weakness of the lower extremities. My doctor ordered Welchol and said since it contains no statins there would be no side effects. Within three days I experienced severe weakness and pain of the hands and wrists. It became worse as I continued taking this drug. I was unable to even hold a cup of coffee or golf. I discontinued it and it gradually subsided. I watch what I eat, go to aerobic classes six days a week and walk several miles four times a week. I am going to continue with this regime and Welchol is now my last experience with cholesterol drugs.

I have been taking Aciphex for about a month when suddenly I started have terrible stomach pains, severe diarrhea, and extreme exhaustion. The exhaustion was so extreme I was sleeping for 2-3 hours a day, not even planning a nap, just crashing on a couch.
I feel bloated and my mouth is dry and feels metallic..in short I felt plain awful!
I thought I was fighting off a stomach flu, but it did not feel "fluish"..I then had one of those light bulb moments..this was the only new medicine I have added to my regular regime.
I am stopping this drug immediately..will let you know if my instinct is on target.

I have taken Avelox before with only minimal side effects nausea and diarrhea were the only ones I got but they were enough. I have been suffering from chronic sinus and ear infections for going on two years now. My doctor gave me samples again of avelox on Monday. Last night I had to be rushed to the hospital. After throwing up all day I got a severe headache. I felt dizzy and out of sorts all day but when I couldn't take the headache anymore I tried laying down. With this medicine you can't take any pain relievers so I thought if I just went to lay down maybe it would ease up some. Well it didn't, and before I knew it I was shaking uncontrollably with tremors and could no longer put sentences together. My head hurt so bad I just wanted to stab myself to make the pain go away. At the er they gave me an IV with something to help with the headache.Anyway after taking a Ct scan and not seeing anything on there the er doc gave me the ok to go home and gave me a script for pain meds. I was having hallucinations, anxieties, and could not speak correctly. I am still having trouble making sentences, I am stuttering, which I have never done before. And I can't get words to go together to make a sentence. The Er doctor wants me to follow up with a neurologist. My tremors still haven't stopped and now I sound like the guy from rain man when I am trying to make a sentence. This is pure torture and I feel like I am in someone else's body.

I am a 65-year-old female. I was given Lipitor 10mg in Feb 07, which I appeared to tolerate, with the effect of reducing my high familial cholesterol. Because of a genetic enzyme problem, I am careful about my diet; having been a vegetarian for decades. I don’t smoke, and rarely have wine. By May that year my GP increased the dose to 20mg., but days later I was sent to A + E with cardiac concerns. The hospital adamant it had nothing to do with Lipitor.

By mid 2008 I told my GP of dizzy spells, and loss of balance, also swallowing difficulties, but after liver function tests I was reassured it couldn’t possibly be Lipitor.

Early October 08, saw me in hospital with a ‘stroke’, although the CAT scan and MRI were puzzling. I was sent home with no help or guidance after the Consultant insisted Lipitor was not a problem, and I should not reduce it, as it was already a very low dose. Unable to walk to the end of my street, my calf muscles feeling as though I’d run a marathon, and experiencing cardiac stress. Severe neck and shoulder pains, and confusion with words. Frequent muscle spasms in my feet, legs and hands, etc. etc. No energy for anything, and so difficult coping - living alone. End of Dec. a friend from out of town visited, and was alarmed, as she’d researched a web site for her brother, who was using a walking frame. I was astounded at the reports from users of Lipitor, so many suffering in the same way. Although my GP had arranged more laboratory tests for me, I was not prepared to wait.

On 6th January 2009, (almost 2 years later) I reduced my dosage to 10mg., and within days was experiencing improvement in many areas. By 17th January, I reduced to 5mg., (maybe a little hasty) and by 24th stopped it. By 28th my GP could see for himself, the considerable improvement generally, with a lower blood pressure reading.

By then, I could complete half, of what used to be my regular walking regime. To date, I am able to cover more than that, and hope I will eventually be able to cover the full distance. I’m hoping there will be no lasting damage, but am so thankful that my friend found this website. Its scary to think I had no quality of life, and doubt I would have survived more Lipitor. So I’m taking my chances with high cholesterol, and a near normal life.

M.

New Zealand

I have oesophageal ulcers and duodenitis, diagnosed by Gastroscopy exam. I have been prescribed 40mg daily for 8 weeks then follow-up Gastroscopy to check efficacy of drug regime. Seems reasonable to me to wait to see outcome. My reason for adding to this blog: Only been on these pills for a few days and am having headaches (though not severe); and have now become aware of duodenal pain;.

I was diagnosed with Diverticulitis and put on the usual regime of Levaquin (500mg a day) and Flagel. The case turned worse and was admitted to the hospital (they thought I had a blockage but turned out did not) and was put on IV of the same medication. Released from the hospital 4 days later and stayed on the Levaquin as prescribed. When I ran out, I called my regular doctor who sent in the renewal prescription. However the his aide made an error and the bottle read 500mg 4 times a day…nobody including the pharmacy caught it. So for 3 days I was taking 2000mg a day of Levaquin. When I started getting worse (truly thought I was dying), I got to the doctor and he said I had taken turn for the worse and could not figure out why. He asked if I was taking the meds and I said yes 4 times a day…his face when white. I had the bottle with me and he panicked. They apologized for the error and I was told to stay off my feet, no heels, they ran ekg’s that day and the following Monday, blood work to check the kidneys etc.

Subsequently, I have had extreme pain in my joints and muscles – everyday, all day. Some days I just cry it hurts so bad. If I bend down I can hardly get back up because of my right knee. I have talked with a doctor I happened to run into about this and she said that Levaquin dosage has saturated my body and gotten into the joint and muscles and takes a long time to work it out. I can hardly lift my arms above my shoulder without severe pain. Stabbing pains in my knees, shoulders, arms and hands.

I have not gone back to the doctor because when I mentioned the pain the when I was in that last time…he just wanted to give me more meds! I have been seeing a massage therapist who specializes in deep tissue restoration and repair. It helps some, but he as well says this is going to take a lot to time to work out.

I have depression to the point of feeling like I am a nothing and what good am I to anyone feeling like this. So like snoop45...that is exactly what i feel like!

dawn62

J.

I'm wondering if some of you could explain how the leg pain was. My 20 month old has been on Singulair for 2 months for ?asthma (he's has bronchiolitis once and pneumonia 2x since he was 6 months old and a chronic cough). His medication "regime" in working great-absolutely no cough in 2 months from a child who I started to think coughing was normal for this age. 3 weeks ago we were driving in the car and he started grabbing his right leg say "ooww, boo boo". and now in the last 2 weeks we have had 3 times where he holds his right leg crying in pain and will not walk, will not stand on his leg. One time lasted for about 2+ hours-he went to bed like that and woke up fine, jumping in his crib. 2nd and 3rd time it lasted about 1 hour and then he was fine completely back to himself. We had him seen but decline xrays and to just watch it for now. The MD said it could be a virus in his knee. I asked about side effects to med and she doubted it. But I started reading and now I'm suspicious. The weird thing is that it comes on strong and goes away just as easily. Wondering if anyone else could describe their leg pain in more detail. Thanks!

Im sad to find out all the problems people are having from levaquin. But now Im able to put 2 and 2 together because Im realizing whats been compromising my health. This is my second year with bronchitis and my second prescription of levaquin. I now believe its what has caused me horrible nightmares, suicidal thoughts, irritation, mental anguish, stress tendon/muscle pain in my arms and shoulders. I bent over to pick up my dog to help him into the car and I got a terrible pain in my chest. I thought I was dying. And I still have a rattle in my lungs after 2 weeks of levaquin so it has not helped at all. If anything it has caused me more problems that has opened the door for additional medications of unknown origin. I wish I could find a real witch doctor.

I went to my primary doctor last Wednesday. He gave me samples for a 5 day regime of Avelox to treat a head/chest cold. Well, the cold does seem a little better, but, I would have never traded that to the side effects I am experiencing now! I took my first daily dose of Avelox last Wednesday. On Friday I thought I had dry skin. By Sunday I was itching so bad that it was almost unbearable. My eyelids are itching, burning and swollen, my forehead looks sunburned from the itching and scratching, my chest, stomach, back and thighs feel tingly and are itching NONSTOP. I am taking an antihistamine, but it doesn't seem to be helping much. I hope this goes away. I cannot imagine what this drug does to people that have allergies and sensitivities to medications. I have never experienced an adverse reaction to medications before this. I would never recommend this drug to anyone.

I experienced the worst uncontrollable anxiety I have ever had in my life on a ten-day regime of tetracycline....I thought I was going to die and I was on my knees praying for help from God to extract the evil spirits that possessed my body...this drug is horrific for anyone with sensitity to medication or a history of anxiety...I have some anxiety and depression which is very controllable....Normally I am a stable happy-go-lucky stay-at home Mom in a happy marriage with a wonderful supportive family and inlaws....but this drug put me in a place I never want to go again...HELL on earth!

I cannot begin to list all the sideeffects this drug has given me...I was given a 30 day prescription for a molar extraction...oral surgery, which I ended on day 10 under the advice of my husband which was watching my deteriorating condition....wish I was never prescribed this drug.

I hope this posting helps others and I am glad it exists!!

Still experiencing some mild but tolerable side effects....

Recovering .....need a different anti-biotic

After having the third shot I noticed my hair began falling out (July 2007). It is now over a year later and after having numerous blood tests, visiting a dermatologist and doing tons of research, I have concluded that gardasil must be causing this. My hair continues to fall out, I have bald areas around the crown of my head and my mood is very depressed by this. I also experienced soreness in my legs and joints but these are not constant. My periods also are out of whack. They can be between 28-50 days apart. I would not recommend anyone getting this vaccine. I wish my OBGYN had not sold me on it. I was 31 when I got it but she said age didn't matter, she said one day insurance companies would cover this vaccine for all women no matter what age they are. I paid $190.00 a shot and now I have a thin head of hair that may one day soon be bald if it doesn’t stop falling out. I think they should take this vaccine off the market. If anyone else has had severe hair loss, has it stopped falling out after a certain point?

I have taken Flomax for three nights. Each night, I woke up after having a disturbing and rather intense dream. This kind of dream was something that might happen once per year. Three nights in a row is very unlikely to be an accident.

I WILL NEVER TAKE THIS CRAP AGAIN!

Of the last four medications I've taken, three caused unacceptable side effects!

Gosh... this is such a big surprise. I have recently read that pharmaceutical companies have been tampering with the results of drug studies. They also have a "buddy-buddy" relationship with the Food and Drug Administration and some members of congress.

I can't wait for November 2008 to vote against the regime that is in power and which allowed this kind of farce to occur in agencies that are supposed to help protect Americans from crappy "medicines".

I am a 50 year old women. I had bronchitis that turned into severe asthma.
Could not stop coughing. I have been on Singulair for over a year. Have had weight gain, Hand numbness,Stomach problems. Even had an colonoscopy but turned up nothing. Now I understand after reading all these posts. The weight gain alone was driving me crazy. Limiting myself to 1200-1400 calories, eating only lean meats and vegetables.Exercising and loosing MINIMAL weight over a 4 month period. I felt like I was doing something wrong. Ive thrown my Singulair away after reading your posts. Will figure out something else if my allergies and or asthma flairs. Just not worth it. Will repost after Ive been off a while.

The Nuva Ring was giving me a yeast infection. So I talked to my doctor about it. Now I am on a regime of taking a diflucan (perscription to get rid of yeast infections) the day before I insert a new ring. Between that and taking acidophilus daily, I have not had any signs of a yeast infection!

I started with 60 mg per day for polymyalgia rheumatica and now after two years have weaned myself down to 5 mg per day. I have a side effect that I have not read anyone else having. It has effected my taste buds. Many foods that I loved in the past, have a foreign taste to me. I am 66, male and have tried to drop down to 2 1/2 mg but the pain is too intense to remain at that level, so had to return to 5 mg. I have lots of pain in the feet and especially toes. I can tell that I am getting better and am very anxious to get off of Prednisone.

Pain in both shoulders following a regime of levaquin for bronchitis. Cannot lift arms, severe pain in shoulders going down to my elbow.

tendons in wrist and down outside of femars inside groin area sore , wrist swelled above thumb twice size painful. started occuring 2 days before end of 10 day regime of levaquin 750 mg. 2 x per day.

My husband has been diagnosed with Ulcerative Colitis. He is only 37 years old and has lived a very healthy life so far. Two weeks ago he started showing colitis symptoms and between Monday, Jan. 29 to Wed. Feb. 7 (9 days!) he lost 28 pounds! He was given a shot of Prednisone in the ER and prescribed a short regime for it with a gradual decline to ween him off of it as soon as possible. He seems to have the worst and oddest side effects. Has anyone ever experienced this with Prednisone...He slurrs his speech, drools almost constantly, has trouble swallowing, and his face from the upper lip down looks like his face is hanging there. (I had his doctor check for stroke and there was none.) That on top of the nausea, vomitting, dizziness, weakness, and being constantly sleepy. I know it all sounds real bad but he has actually improved since taking the prednisone. At least he's alive and getting better. Hope this helps.

i haven't slept one night since beginning prednisone and can't wait to finish my regime of it this coming saturday and hopefully sleep once again, what a horrid drug!

Hi, I was given prednisone for bursitis in my knee. It was administered 60mg for three days-40mg for three days and 20 mg for three days. On the eighth day of the regime I was given a shot of cordisone directly into the bursae. After the second dose of prednisone I began to expirence night sweats, insomnia, acid reflux, and premature ventricular contractions. the irregular heartbeat landed me in the hosptial for two days where they determined the drug had made me hyperkalemic (low potassium). I have had all the test and my heart is healthy. I have been off the drug for almost two weeks and still feeling the side effects especially the P.V.C.'s. Has anyone else had arrhythmias. Does anyone know the half life of this poison?

Thanks, Roger

I posted here in early Sept. about my problems with lisinopril. After reading other posts I started doing some google searches. Because a previous HBP medicine caused my thyroid function go down I was switched to Lisinopril. Two years later, my throid levels which had recovered are now going down again. Several posters mentioned suppelmenting with zinc to deal with the cough so many people develop. A "lisinopril zinc" search had several sites that all stated in practically the same words that no research showed a link to zinc and lisinopril but supplementation might be a good idea. (Don't dose yourself with zinc because that can cause things to go out of whack.) I also found an article by Dr. Ron Hoffman about "Drugs That Steal." He reported that ACE-inhibitors caused zinc to be depleted from the body.
Then, I googled "zinc TSH". TSH is the indicator of how your thyroid is working. There I found several articles about how low zinc levels may cause low thyroid symptoms. Ask low-thyroid sufferers how hard it is to get doctors to diagnose and deal with this wide range of symptoms that are often vague.
Now I'm stuck. Is it lisionpril or is it my thyroid? My doctor sees the HBP first and wants to add medications to deal with the first medication's side effects. But then suppose there are more side effects from the next medication. This is a real quality of life issue.