Catch 22 symptoms and conditions

I was prescribed Cipro for a UTI infection 2x3days the first day I felt really bad! I was tired and had stomach pain along with nausea. The second day I also had stomach pain with headache and tiredness, my mind was foggy as well as my vision was blurred. I took it even though our clinic is against all medication for this exact reason bad reactions and death. I did some research this morning and have STOPPED the Cipro. I will start a 21 day detox to get this out of my system. I will help fight to get this product off the market! My niece is turning 10 years old and she has also been prescribed this medicine she has had many medical problems. It feels great knowing I may finally be able to help her. I know god has forced the infection upon me to help others. Please!! do the research before you take any medicine only you can make the decision. WE ONLY HAVE ONE BODY TAKE CARE OF IT!!! NO ONE ELSE CAN DO IT FOR US!!!

ive been taking prednisone for 2 doses..(2 days0 my legs were so sore when i woke up the first day i could barely stand i did do a little running around i am 28. but nothing that would have caused this.its painful to sit because it causes them to get stiff. it hurts to walk because it causes them to have to straighten out. its a catch 22. i cant call my doctor until Monday. so i don't know what else to do. no matter what i cant stop taking them im told.so i have no idea what to do. im in so much pain i cant barley do anything.

I am a 40 year old female. I found out 3 years ago that I have factor V. I've been hospitalized for 17 PE's. I was being treated with coumadin, plavix, lovenox. My INR will not stabilize. The doctor has now put me on 30mg. of warfarin a day. and my INR still sets at 1.2. My side effects are awful. I feel tired, week, cold, weight gain, but most of all the terrible headaches. The doctor says it has nothing to do with the warfarin. I stay depressed and now losing hair. I've taken my doctors advice and I'm going back to the cancer center where they are more experienced. I feel like I'm dying everyday and its not in my head. I do believe its side effects. And if its not moving my INR than to me it seems useless to take such a high dosage. Its a catch 22.

I started feeling much better very quickly after being off Lipitor now 7 months. However, the symptoms I had using the RX has cause significant problems. I fell so many times with my weak joints and muscles, that I had severe problems. I now need to have knee replacement surgery after falling so many times injuring my knees and weakened muscles to support myself. I am getting cortisone shots in that knee, as well as physical therapy. My MRI shows a torn meniscus, stretch PCL very thin, cartlidge loss and debris, still swollen with csyt after all these months. With no meds, and lack of being able to exercise, I now have hig-chol back. On and on it goes.... a real catch 22. Take care of yourself, watch out for symptoms. I ignored sx's thinking it was stress but after reading adverse reactions, it fit me to the T.
My original posting re: Lipitor is Forestseaski on Jan. 2, 2009

C.

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 went on this website and read all of these helpful comments before starting loestrin24fe. After reading them i have to admit i was nervous because of all of the negatives i read about. I am starting my 3rd pack of loestrin24fe and i have to say i have not experienced many side effects. Some minor nausea the first week, minimal spotting for 3-4 days week 3 of the 2nd pack and larger breasts. However,.....my worst symptom which is affecting my relationship is my loss of sex drive!!!! Since starting this pill, i have no desire to have sex and sexual intercourse is just painful and not pleasurable at all!! is anyone else feeling this way

I was a 2:42 marathoner. I used a synthetic varnish containing isocyanates, pentanedione, organic solvents, in one 7-hour session; the company-recommended respirator did not in fact prevent transmission: Severe chemically- induced asthma, plus neuropathy, plus, plus.

I've used Advair 500/50 for six years. There have been many diverse effects from the chemical exposure; I'd not questioned any being Advair side effects. But the raised blood pressure was not initial, and certainly not a priori. Diminished hearing, diminished eyesight, anxiety. Again, not to lump in, but these questions are new for me. But the point I'd like to bring before this group is this: In August I was diagnosed with ehlichiosis , and was prescribed 28 days on doxycycline. They recommend eliminating many possible antagonists to the doxycycline. My respiratory capacity had been continually diminishing. My ongoing physician said this was to be expected and recommended only the next more powerful steroid. Not a good solution. Before all this I was strong; repaired myself. In the absence of constructive answers, wondering if the Advair was weakening me, making me dependent, I quit the Advair as well on beginning the doxycycline. Today is eleven days post-doxycycline. Eight days ago there began with increasing severity, a terrible wracking deep cough producing dark yellow mucus. Painful. No fever. Grevious throat from the wracking, but I question whether this is a cold or infection. It's just in my lungs. Maybe it's as though I've thrown off an epithelial coating. These past two days the quantity of deep yellow mucus is not as ready, but the wracking and coughing is more severe. And my lung capacity, my respiratory capacity, is frighteningly diminished. Until these past two days I'd considered this an infection, especially post-doxy. But it doesn't feel like an infection. And I'm scared. Is this because I quit the Advair abruptly after long regular use? Have any of you had a similar experience. Can you discuss the effects of abruptly discontinuing Advair. Have you stayed off it. What's happened to your respiratory capacity. Have you any professional studies, trials or experience to recommend. Thanks.

I was put on a 5-day dose of Levaquin, and am on my 4th day. After the first dose, I started to get severe itching and pain in my vaginal area. I know it's a yeast infection because I had it once before. I have also had really bad insomnia for the past two days. Called my doc; she told me to continue the medicine and perscribed Diflucan and monistat 3-day. She also said to take Benadryl for itching, but I am feeling really tired already, and I think the Benadryl would just make it worse. I am very tempted to stop taking this med right now, but not sure if it's ok to do that. Has anyone else gotten a yeast infection from this? Thanks, and I hope everyone starts to feel better soon.

I have been on Toprol-XL 25mg for 3 months. Shortly after I started this medication I developed hip/upper thigh pain which feels better when I walk. It seems the muscles are very sore in my legs. Never had this prior to taking this medication. It just gives you a sick feeling. I am going to start weaning myself off of this med by cutting it down to 1/2 a tab. I will say one thing it has regulated the PAC's but perhaps the flutter in my chest that will not hurt me, is better than the side effects of this drug. Of course the doctors deny that this drug has these side effects.

Just resumed my 25mg of toporol XL after a miserable 5 day trial on lisinopril. My main symptoms are PVC's, chest tightness (chronic), lightheadedness. These seem to be somewhat helped by the medication, and I wonder about upping it to 50mg (MD fine with that), but I really don't want to be on it. Originally put on for high BP (150/90), and persistent PVCs. I need to lose about 40 pounds to get the BP back to normal, but if this toporol puts the weight on that is truelly a catch 22. Anyone find any supplements that could be helpful? Please feel free to email me. Thanks Liam

I've been taking 50 mg. daily (and conscientiously) for several years. I've been taking thyroid supplements (synthroid and similar) for 35+ years. For 15 years, I've been struggling with the gradual weight gain commonly associated with menopause and stopping smoking cigarettes (after 30 years of 1+ packs daily). HOWEVER, It was about six years ago that the problem became a 50 lb. overweight and BMI in the waist-over-35" serious problem. I was always strong, quick to build muscle, and enjoyed being active. Swam .5 mi daily or walked 3 miles (or both) frequently until about menopause time. But then: about four years ago, I started having some pretty serious trouble breathing associated with exertion. Body aches and pains that I've described as arthritic, may also be involved here! Hence decreasing exercise and real worry about engaging in exercise. I've also been taking Lipitor and Avandia.
Frankly, I'm feeling that all my meds except Synthroid can cause me to gain weight - the catch 22 being that my elevated blood pressure and early type-2 diabetes are also negatively affected by overweight!! Now what???? Dr. appt, very soon, folks!

I have been taking Topamaz spinkles (30mg a day) for 3 months. I can't tolerate higher doasages. Migranes have lessened in intensity, although I still have a least 2 a week. I have toruble with my memory and hair loss. I have had a slight wt loss. I have no sex drive. Food does not interest me.
I started taking topamax because migranes were interferring with school. Catch 22 - I failed last semister due poor recall. I am taking myself off topamax. I may have migranes, but at least I will enjoy sex.

I have been taking lisinopril for about 2 years. I work out at the gym and follow a low fat diet and have lost 40 pounds. The medicine doesn't make you gain weight, what you EAT makes you gain weight.!! No coughing, no nausea, or feeling like I can't breathe---just normal BP's. If I forget to take it and check my BP, it is elevated. So I go right back on it. It works for me. Keep a close record of what goes in your mouth, and you'll probably be surprised. Remember, the BLT's count too---that is, the Bites, Licks and Tastes.!!

I take Ambien before I go to bed, but I keep waking up at 6AM and cant get back to sleep. I get a horrible headache from sleep deprivation. IT helped me alot for about 2 weeks. Now it is hurting me and if I stop taking it I cant get to sleep!!! What a catch-22.

I posted on this forum last December...(see Mon, 20 Dec 2004 01:46:35 -0600 by Guest, #8483). This is a follow-up to that post. I have continued to take Singulair daily since then, despite reading the postings. I still feel the heaviness in my chest, especially at night, and a weird sort of buzzing/vibrating when I exhale that started when I first began the drug. I can't tell if it is coming from my chest or my nose. Also, my joints are very achy. I started to think I was getting arthritis in my fingers, but then remembered the side effects others were having on Singulair. In addition to the pain, I am lethargic, especially after I take the pill each night. There has been a marked change in my personality. I am angry, impatient and depressed. I used to be one of the most tolerant and patient people around. I have gained approx. 13 lbs. since December. I have also experienced multiple sinus and upper respiratory infections since being on the drug. In general, I just don't feel great. I feel much weaker, overall. I don't know what to do since the Singulair has had a huge positive effect in combating my allergies and asthma. It's a catch 22.

I'm 27, and have never taken BCP's before.
I've been on Yasmin nearly 4 weeks with few side effects (one unacceptable).

Bad: After 2 weeks on Yasmin, I developed unbelievable scalp itchiness (never before) to the point of wanting to scratch holes in my head. Often. Random spots of amazing itchiness (arms, ears, chest, legs, back, hands) arrived a few days later that rival contact dermatitis in severity. There is nothing else I can attribute this to besides Yasmin (I hope it is not allergy based, as I basically have no allergies).
I've tolerated the itching for nearly 2 weeks, and will give it another 6 to see how it goes. It's not an acceptable side-effect.
Otherwise, I've just gotten slight spotting (skipping placebo pills) and a decrease in sex-drive. Not impressed. I had no sex-drive for 2 years because of a prolactin secreting pituitary tumour. Once that was treated, my sex-drive was amazing. Everyone should be able to feel like that! I'm attuned to that now, and it is diminished. Will give Yasmin a trial though. Sadly a catch-22, since I'm taking it because I've found someone special.

Good (?) side-effect: Oh my god, I've lost my chocolate-drive. I enjoy one chocolate, not most of a packet like I used to. Could not believe this. Hormones are amazing.

Sorry to hear all the serious side-effects posted here. I hope you all find what is right for you. Without quality of life, what is left? Best wishes.

Not been here for a couple of months and very interested to see all the new postings, some quite alarming. Still on 5 mg. a day. Re: Rosemary's post. Yes, I too have a high reading at the doctors - we usually have a joke about it now (but not to the level of yours Rosemary). My decent quality monitor at home, best reading last week 124/72. About the worst 140/85. Have had to take another Zantac (ranitidine) tablet today - due to excess acid - cannot source this down to any particular food I've eaten over the past 12 hours or so. Hair loss? Still out on this one as I tend to have thicker growth in Summer and thinner in Winter (in UK). The annoying thing is that I've been on Lisinopril now for 18 months as a purely preventative measure. But this is a Catch 22 situation now. If I stop taking it, in my innermost thoughts I would think: "am I shortening my life, or my good health? Should I carry on with these tablets for the sake of my wife and kids?"