Regimen symptoms and conditions

I am 50, pretty healthy, but have had a new condition of inflamed and severely painful joints and muscles limiting activity. Doc put me on 60 mg prednisone for 3 days, then 40 mg 3 days and 20 mg 3 days. First day was ok. Since then I have been a raving lunatic! I read the post about the person chasing their cat around and had to laugh and relate. I flipped off the neighbors workers because they were backing up a truck and it was noisy! It is all I can do to keep myself in check. I have canceled/rescheduled all unnecessary appointments until next week when I am finished. I "sleep" about 3 hours a night. Last night I peed the bed. I eat constantly. I have to work and concentrate (teach college) and that is so hard. I imagine my students must think I am on meth. I can't take it any more. I have 1 day left and I am not going to take the last one. I hope that this regimen will have calmed down the inflammation and if it recurs I will seek alternatives. AM NEVER going back to prednisone unless it is life or death situation.
Good luck to all those out there who have to take it long-term. Bless your hearts.

I was prescribed a 10-day regimen of 500 mg capsules, 3 times/day for a tooth infection. First dose at 9:00 pm last night (Friday). Woke up seven hours later with intense itching back of the neck and inner part of both elbows. No other symptoms. Spreading across shoulders and stomach. I'm taking generic antihistamine and applying calamine lotion. No really relieving the symptoms but I'm hoping they will subside my 9:00 am this morning. I'm glad I don't have to try to work in this condition. No plans to take a second dose.

I just began doing research on Yaz because I just got married and my sex drive is completely, totally, unequivocally GONE. I'm 25, and I've been on it for about six months. How depressing! My body will not lubricate at ALL or respond to ANY kind of touch. My husband has developed a complex, thinking it's him. :(
After a while I began to think it was the Yaz. I've developed urinary tract infections out of nowhere; I never used to get them.
I'm getting off this pill ASAP because what's the point of birth control if you don't have sex anyway??
I feel really terrible for all of you women with mental side effects, because I know exactly how you feel. However, I've had an opposite experience. Positively, it increased my breast size and cleared up my skin. However, I was already suffering from mental illness previous to starting Yaz. I have Bipolar disorder with added anxiety issues. I was on a regimen of daily Lamictal with occasional use of Xanax for anxiety. My attacks had gotten so bad that I had to go to the emergency room. After a time, I leveled out and decided to stop taking medication because it made me feel flat. I began feeling anxious again, and it was around that time that I started taking Yaz. For me, someone who was ALREADY suffering, Yaz completely turned me around. I have never felt happier, more secure, and more normal mentally in my entire life. My moods are fantastic, I have a huge amount of energy, and I feel like nothing can stop me. It's not mania, though, as I have none of the pathological side effects. I'm just really really happy. I will miss the mental benefits of not taking Yaz, but to me, losing the intimacy with my new husband has just not been worth it.

This can be a great benefit to someone who is perhaps bipolar, but I think if you're healthy mentally to begin with, it can have the opposite effect.

I have only been taking Yaz for a week, but noticed the negative side-effects almost immediately. I am on a steady regimen of anti-depressants and couldn’t understand the sudden on set of mood-swings (extreme anger, irritability, sadness, lack of interest, flat-mood, etc.). Also, I have been very fatigued (wanting to sleep 14-16 hours a day).

I am contacting my physician in the morning, but doubt I will continue taking this medication.

I do not recommend Yaz to any woman currently taking prescription anti-depressants.

I have been taking Sulfameth/Trimeth for a presumed UTI/kidney infection. I was given a 2 per day regimen for 30 days. I am almost half way through and cannot take it anymore. I have experienced nausea, hot flashes (and I am man!), sleeplessness, photosensitivity and now my whole chest cavity and stomach feel raw and inflamed. I do not the diarrhea that others complain about, but I am taking a potent probiotic. The nausea and raw stomach subside when I eat, but that only lasts for a couple of hours max.

My 18 year old daughter had a terrible allergic reaction to omnicef 2 weeks ago after a 10 day regimen. Sadly, it happened 2 weeks after my nephew had an allergic reaction to the same medicine. His situation did not end so well. He was taking the medicine for strep. The allergic reaction started with hives and got worse. After some aggressive research on my brother and sister-in-law's part, my nephew was diagnosed with an allergic reaction to omnicef followed by rheumatic fever. I should have refused the omnicef for my daughter, but who knew.
My daughter is 2 weeks into annoying hives that continue to pop up in different places. Her feet are swollen and we are very concerned. She has taken steroids, Kenelog cream, benadryl, as well as prescription strength antihistamines. Tomorrow she is going to see another doctor to find out what is going on. Cefdinir/omnicef is no longer welcome in our extended family.

I am taking 100mg 2x a day of Minocycline to treat my acne. About 2 weeks after the start of this medication, I gained 10 pounds virtually overnight. I know it was that fast because I see a weight loss doctor weekly and I'm on a very precise diet and exercise plan and it I was fine until about day 14. I went to bed the night before and woke up the next morning with an additional 10 lbs. Right now, I've been taking it for about 6 weeks and have managed to keep the weight gain to a minimum average a week by adding additional workouts to my regimen for a total gain of 14 lbs. Although it's treating the acne very well, the money I've spent to lose 53 lbs over the course of a year just to turn around and gain 14 in a matter of weeks is extremely frustrating. I did not have this side effect with Doxcy, but sun exposure was causing severe burns so we switched meds.
When I return to the doctor in a couple of weeks, I will see if there is an alternative solution.

I have been taking 20 mg. for two weeks and I have developed a dry cough, pain in the middle of my shoulder blades and my left arm. I tried to cut my grass and felt like I was going to die. I am 48 year old male with BP of 140/90. Lisinopril has lowered my BP as low as 90/60 so I cut the dosage in half. Now I feel like my throat has been ripped out and I'm hurting all over. I will never take Lisinopril again. I was on Benicar, but it was expensive and didn't really work. I am going to start exercising more and try the health food stores.

I have burning sensation on hands, weak legs and watery eyes. I take 50mcg on alternate days. My latest TSH is 37.8. My medic has asked me to take 25mcg on Sun, Tue, Thu, and Saturdays and 50mcg on the remaining days of the week. I have yet to start this regimen

I was involved in a MVA about 4 years ago. I was prescribed oral prednisone for my back and neck pain. I took the recommended pack but about 3 days into the regimen I began having EXTREME pain in my joints- especially knees, hips, and ankles. I was not even able to walk by myself. My doctor never even suggested that it could be a side effect of the prednisone and told me that I had to finish the rx or it would be possible for me to have major reactions such as heart failure, etc. I was so scared that I finished the rx. My side effects included weight gain, mood swings, increased appetite, etc. but the worst was the joint pain. I survived the treatment and swore that I would never take the drug again. Well, never say never. My back pain continued and I went to a pain management doctor who recommended spinal injections. He said that the prednisone injections should not have the same side effects as the oral med so I received the injections. He said that he used a reduced amount of the prednisone during the procedure. I had great results with a reduction in my back pain for several months. I just this week had another injection and now I am in experiencing the same horrible pain in my joints as I had the first time with my oral rx. Is this normal? I have contacted my dr for pain med but I know that I am just covering up the side effects. Any one else have similar situation? What do you do when the treatment is worse than the ailment?

Hi! I am 29 years old and have had asthma since i was young. As i entered high school i had very rare exacerbations but around 4 years back attacks became more frequent. I visited my doctor and he advised me 40mg of Prednisone a day for 5 days (20mg in the morning and 20mg at night). He mentioned that this was safe and no tapering was needed for this short burst. So every time i start having exacerbations i just follow this regimen. I have had no tapering or withdrawal symptoms and i can breath very well even after the Prednisone is off.

Recently, i had an exacerbation as the New Year started. So i started my regimen again on Jan1. But after 5 days, my symptoms were not relieved yet. It seemed like my asthma, triggered by an acute bout of Bronchitis, was worse than before. So i continued this regimen until 12 days. I was taught before that as taking Prednisone approached 2 weeks, it would be wise to taper. So on day 13 - 15, i took 30mg of Prednisone per day (15mg in AM, 15mg in PM). On day 16 - 18, 20 mg per day (10mg in AM, 10mg in PM). On day 19 - 21, 10mg per day (5mg in AM and 5mg in PM). On the 22nd day, i had 5mg once a day only. The next day, i woke up very drowsy, with muscle and joint pains, dizzy and light headed. But i just fought it and went on my day feeling sooo out of it. And at night, i just felt chest tightness. I again had difficulty of breathing unrelieved by around 3 puffs of my inhaler (which was a combination of a long acting bronchodilator and an inhaled corticosteroid) which was also good for acute events of asthma. This provided no relief until i took a total of 15mg of Prednisone again. The next morning, on day24, i felt better. I tool 10mg thinking i could maintain myself on 20mg a day. But as the day progressed, as still had these joint pains and wheezes and difficulty of breathing. So a night i took 20mg again. I started reading on Prednisone and tapering and noted that these symptoms might have been an adrenal crisis, I haven't consulted my physician yet. But am trying to taper myself off decreasing my dose 5mg every 3 days. I hope i can get back when i learn more.

I hope this helped people in some way. Stay healthy everyone!

I have been taking 12.5 mg Metoprolol for my palpitation and occasional racing heart. Few days ago I got a rapid heart rate again and I increased the dose to 25 my as original prescribed. Now I have chills, cold hand and feet, insomnia, shortness of breath, chest pain, etc. I have cut back to 12.5 mg. The problem is that even with 25 mg my heart races once in a while but I can't tolerate increasing this drug. I want to wean off of it. What is the best way to stop this drug?

I can agree with so many of you who've shared your experiences - for about a year I felt more like 'the old me' on Wellbutrin, but in the last six months I've become progressively more fuzzy-minded. It scares me that there are times that I worry that I won't be able to finish a coherent sentence... like I'm speaking in slow motion waiting for individual words to filter through the fog of my brain so that they can be spoken. OK, it's certainly not always like this - and so far only my husband seems to have noticed, but I dread muttering the wrong thing in a business setting. Perhaps worse than this, in the vanity that is our present reality, I've seen significant hair loss from the top of my head - my squeaking clean pate is SHINY in the mirror and I hate it!!! It's winter now, but I can't wear hats all the time, and I just don't happen to work in a 'fashion forward' industry where I might hope to make hats a trend for all to follow. I will be weaning myself off of Wellbutrin and looking into oral and topical arnica b/c I'm nervous about trying Rogaine and begging stuck with that regimen for the rest of my life. The women in my family all have lovely hair; I'm 40, not 80!!

My son who is just 17 has been on the drug for just a week and the very first day he was on it he experienced severe back pain. He was not able to stand up. It got worse, he felt as though he had to eat continuously or he would vomit, the more he ate the more nauseous he became. This is not somatic, because he had no idea that I had added a new medication to his regimen. He has ADD and a mild mood disorder. I have stopped the medication and will notify the doctor tomorrow. He was only on the medication for 4 days. I am a nurse practitioner and this medication is not worth the multitude of severe side effects for the diagnosis of mood stabilization.

I started Femcon FE about 7 months ago because I needed to start a birth control regimen because I was getting married. I started this pill 3 months before my wedding so my body would have a chance to adjust.

I have ALWAYS had normal and regular periods like clockwork. I've never had any issues with my periods in my entire life, until I started Femcon. The first month I was on the pill was fine...I got my period like normal. The second month my period was horrific....I bled for 13 days straight and had horrible cramps, unlike any I ever had before.

The 3rd and 4th month I skipped my period because of my wedding. I was one of the unfortunate that would have had my period on my wedding day, which is the ONLY reason that I skipped.

I am now in month 7 since I started the pill and it's been 3 months since my wedding. I've yet to have a period at all since the wedding even though I am taking the pills like normal...it's been a full 3 months with no period. I've had light spotting the last 2 months, but absolutely no period. I am getting concerned. What's the deal???? Has anyone else had this problem?

Hi, I am a 45 year old male with high cholesterol. prescribed 20mg. of Lipitor to control it. Am having a strange twitching muscle in my right calf since I started the meds. Forearms hurt, trouble sleeping, twitching in my sleep, apparently, tiredness. I'm worried about going off it. My dad died of a heart attack. Would it hurt to try going off it for about 3 months?

I was admitted through the ER in sept. i had previously taken Bactrim for a bug bite on my foot three months prior. I had been severely bruising and had some lab work done. I got a call from my Dr. around midnight to go to ER immediately. My platelet count was at 11,000 a normal being 100,000-400,000. I went to ER and was admitted for 5 days. After running test after test there was no conclusion to what had caused this low platelet count but I was diagnosed with ITP. From here they put me on 50 mg/day of Prednisone for 1 month. I have now started to taper 40/ 2 weeks. 30/2 weeks. But then the side- effects started to come so fast. At first it was just sweating, minor anxiety, mood swings, and slight increase of appetite. Now that I had tapered my adrenal gland is suppressed much more and I am going through withdrawal. I am 21 years old I am 5'7" and I weighed 118 two weeks ago, since I have gained 12lbs of water weight. I am working out daily and eating healthy, although it is more than I used to eat. I have some family friends that work at Stanford University and they are ITP specialists. They told me their regimen for Prednisone is a 5mg/wk taper instead of 10/ 2 weeks. So the past two weeks I have been going down by 5. Today was my second day at 20 mg. I have gone through all of the mentioned side- effects except the back hump. I am hoping and praying that these symptoms will clear asap. And to everyone else out there your not alone.

I had been taking 160/25 for the last couple of yrs. Was doing ok, on it until june of this yr. I started having circulation problems. Hands and feet numb and cold when I would wake in the night. Then finger joint problems started. It came on so fast. I had read that arthritis could be a side effect on another blog. So I started to reduce the meds. slowly to see if that would have any change in the conditions I was feeling. It did! I continued to lower the meds. and got myself off the Diovan HCT. I have been working on the natural method of lowering the Blood pressure. Kelation, exercise and diet. I won't go back to the Diavon.

For Medications.com October 18th
Earlier this past summer I took this drug for ninety two days after I was prescribed this medication when I visited the doctor for a bladder infection and I was told I also had high blood pressure. No tests were done except for a urine test at that time and no follow up tests were done later. This drug not only gave me a slew of other side effects but pushed my simple bladder infection to where I no longer urinated in a normal manner regardless of the amount of fluid I added. Only after discontinuing this drug did normal urination return after a few days.
Allergic reactions were as follows. Severe debilitating stomach cramping resulting in swelling of the abdomen, and all digestive organs. Angioedema. (no pre history of this) Urine flow continued to lessen even with increased fluid intake, resulting in bladder pain and a sensation of bladder being pushed from the body. Lack of energy, flu like symptoms, insomnia, leg cramps, many bouts of rapid heart beat, some lasting for awhile, even after stopping the drug. Lack of appetite and a change in taste buds. I had several bouts of angioedema but thought it was 'something I ate, stress etc', as within a month of my diagnosis, my daughter had an extreme reaction to Ciprofloxin (see floxintoxin under that medication) and anything that was going on with me was put aside. She was debilitated by her drug reaction and was unable to walk etc, so I thought I wasn't handling stress too well as I was getting older. Each bout increased in severity leaving me lying debilitated on the couch for four days, eventually for a full week until luckily by that time my daughter was able to take care of herself and began thoroughly investigating this drug only to discover that Lisinopril was the true cause. The warnings with this drug are not very explanatory and leave so much out that should be for patients to read and digest to make their own health decisions and it takes a lot to dig deeper on the Internet to find the true adverse reactions.
We thought by stopping the drug I would get back to normal quickly and I did with the help of a herb called marshmallow which reduced the swelling after a couple of days. However after I thought I was cured I stopped marshmallow and within a couple of days had another angiodema reaction and I thought it was because there must be traces of this drug left in my system. I then took marshmallow for over two weeks and feeling fine I stopped again. Then another episode hit me with not only the stomach problems but a severe bout of coughing that lasted a couple of hours and trickled into a few days. It was then I began digging on the Internet to find the words I wanted to hear, that this drug caused long term problems. I found it by adding UK after other words and found this and much more.
ACE-INHIBITORS
A particular group of heart pills called ACE-inhibitors (the chemical names end in -pril, e.g. enalapril, lisinopril, ramipril) can occasionally cause urticaria, although they more commonly cause angioedema; about one person in 100 who takes an ACE inhibitor is likely to get this problem.  
The reaction is not caused by true allergy, allergy skin and blood tests do not show it, so why does it happen?  Reactions are thought to occur because an unwanted pharmacological effect of the drug causes the release of compounds similar to those released in an allergic reaction.  The only way of showing that a regular medication is the true cause is by stopping or changing the treatment.
To complicate matters, the angioedema attacks may not start until the individual has been taking the ACE inhibitor for months or even years making it difficult to spot the relationship. Also, attacks may continue for several weeks after the drug has been stopped.
I could not find anyone doing following to patients with adverse reactions and I think that is a very bad problem. We are on our own. I do hope this helps others and if you want copies of all my research let me know.
Now I am hoping there won't be any more bouts but I'm still taking marshmallow and when I think I have the courage I will wean myself off it slowly and watch for signs. Believe me angiodema isn't fun and you can't see it on the outside of the body which makes it difficult to understand.

So far I haven't seen anything in regards to my symptoms with Yasmin.

After going the past two years and having only two periods, I was diagnosed with PCOS. My Gyno told me that the only way I would be able to have a period, and delay the harmful side effects of this disorder would be to go on Yasmin. I agree that my mood swings the 1st month were terrible. I almost punched my own mother in the face because I didn't like one of her jokes. That's not me. But that is something common with BC. They are hormones your body takes in to regulate your cycle. And because my body doesn't' regularly produce the hormones needed for menses, I expected mood swings. The catastrophic depression and PMS were the main reasons I stopped taking the pill years ago.

My problem is a bit different. I haven't gained weight. As a matter of fact, I think I've lost a bit. My problem is my skin. Before the pill, I had flawless skin. It was always really sensitive, but because I was cognizant of this fact, I took every preventative measure to ensure its healthy appearance. But now my skin in a mess. I have a rash spreading all over my body. My eyelids have a hard crushed rash of skin folding over, and my under-eyes are the same way. All across my face, I now have raised red patches of skin that burn, and the only change I've made to my daily care regimen is popping that little pill every night. The rash is now spreading to my shoulders and a bit on my legs.

Has anyone else developed skin problems, or could this all just be coincidental in my case?

I

I am taking 20 mg in combination with 12.5 HCZ. It has kept my BP in the normal range of 110/75. In the first day of my lisinopril regimen, I experienced a strange tickle at the back of my throat. My doctor said it was probably nothing. That gradually, over 6 months developed into fits of coughing that hit 2-3 times an hour and continued throughout the night. It was the coughing that made me finally decide to stop the drug. I also had constant mucus drainage down the back of my throat that I'm convinced is connected with the Lisinopril as well, although my doctor disagreed and said I had a low-grade, long term infection. Well, after 3 courses of 3 different antibiotics, it was still there. In the last week, I developed increased coughing fits, and was having an allergic reaction causing rashes under my arms, and itching in all the tender places. Doctor said the rashes and itching was a reaction to the Hydroclorothyazide. I'm now on Norvasc 10 mg. Hopefully this will be a better experience and still give me good control of the numbers.

I want to add something to my original post. I only took this med for 10 days (5mg) and was miserable. After 3 weeks I was beginning to feel better (having 1 bad day, then 2 good) when suddenly I experienced pain in my left side, numbness and tingling. My doctor sent me for a kidney scan. Five days after this new pain began, I developed another rash. I realized that I had shingles. So PLEASE be careful if you have any symptoms. This puts a terrible stress on your immune system. Apparently my immune system couldn't handle the stress and the result is shingles. So, I'm miserable again and probably have another 3 weeks to go before I begin to come out from this episode.

Also, for those of you who are switching to another blood pressure medicine that is an ace inhibitor (as lisinopril is), you will not tolerate those either. They are all made from the same ingredient, snake venom.

My doctor added Lantus to my medicine regimen including Byetta 10, Metformin 1500 twice a day. On the Byetta I lost 35-40 lbs very easily. The moment I added the Lantus I was bloated and over a 2 months I had gained back all the weight I had just lost. When I asked my Doctor about the bloating and weight gain she said she didn't think it had anything to do with the Lantus. But I was losing weight until she added the Lantus! I don't think that's just a coincidence. What should I do? Should I go to a doctor who specializes in diabetes instead of my family doctor who I love dearly?

I too have been on a regimen of 750mg of Levaquin for an infection on my leg. On day 2 I could not figure out why my upper keft arm was hurting me so much. I as so many others, wrote it off to hanging drapes and cleaning out my pantry. Four days later the pain started in my right arm and again, I was trying to figure out what in the world was going on. It's an intense pain like I've never had before. I have Crohn's disease so I wrote some of it off to that as well. I saw my Doctor today and didn't even think about telling her about the Levaquin (different Doctor prescribed it). As I lay in bed this evening unable to sleep I decided to do some research on Levaquin as it was the only thing I could think of that was causing problems. Boy, did I discover something. Thank you all for posting your issues on this website. I will be seeing the prescribing doctor tomorrow and will let her know the outcome of the drug and will make sure that I will never be taking Levaquin again. Too bad we can't get this word out to everyone being prescribed this drug. It's dangerous and hardly worth it. There has to be something else out there that we can take. .

I started Doxycycline Hyclate several days ago (100 mg 2x daily) as part of 3 week regimen to treat Lyme Disease. I have had some stomach upset, a generally reduced appetite, and cottonmouth... but by far and large the biggest effect has been this overwhelming exhaustion.

Went to bad at 9:30 last night and woke up at 9:00 am this morning but could not drag myself outta bed until almost noon. Its now the middle of the afternoon and I feel like a complete zombie. Spacy and unmotivated, my head might as well be made of wood and can't pull it together to even take a shower yet.

I am a real outdoors guy and keep up a busy routine of work and exercise. Another 2 and a half weeks of this is gonna drive me nuts. I guess it is better than having Lyme, but does it get any easier?