Dangerous medications symptoms and conditions

In 2007 I was diagnosed with HBP and enlarged prostate at the same time. I was working and had medical coverage with my PCP at Nova Southeastern University. The doctors there are very good. They put me on Terazosin for both. I quickly developed severe rash, hives, swollen face, neck, throat, etc and had to go to emergency. They took me off Terazosin and gave me Flomax for the prostate and Lisinopril for the BP. The Flomax works fine-noside effects that I can tell except decreased semen production. I am a 58 year old male. But I quickly developed a cough and the took me off Losinopril right away and put me on Diovan, which worked great with no discernible side effects. Then I lost my job and had to go to the VA for my medical in January of 2009. Because my medical history included my emergency visit for a severe anaphylactic reaction to Terazosin, they allowed me to stay on Flomax. But I had no such record for the cough caused by Lisinopril. So they insisted that Diovan was too expensive and I had to try Lisinopril. Despite my complaining about the previous experience they insisted. I was given a little pink pill which did cause me to develop a minor cough. But being a good soldier, I decided to live with it. Then in August I noticed that my refill no longer had a pink pill but a larger yellow pill. And that was when the problems started. I first felt like food particles were stuck in my throat and nothing could get them out. That feeling would eventually disappear on its own only to later return. I visited the emergency room several times with severe flu like symptoms, including a severe cough. I also discovered a yellow film covering the back of my throat. And my tongue had a thick yellow coating on it that went all the way to the back. In some places this had strands that extended above the back of my tongue for about a half inch. In addition there were bumps on the top of the back of my tongue. This stuff could not be scraped off. The emergency doctors would examine my mouth and throat, tell me nothing was wrong and refuse to take a throat culture. They scheduled an appointment with ear, nose and throat and then canceled it. Eventually they scheduled a CT scan, which showed nothing abnormal. Finally my PCP examined me and said I had a severe allergic reaction to Lisinopril. So a week ago she took me off Lisinopril and put me on Amlodipine. I'm actively researching the side effects of that and will get off if I see anything I don't like. But my goal now is to find natural substances to treat both the enlarged prostate and the HBP. The yellow coating on my throat is beginning to disappear. Still no difference with the yellow coating on my throat. I believe I have seen slight improvement in the cough, but not nearly enough for my liking. I worry whether I will ever be able to get rid of it. I do have more energy now. Any idea how long it will take to get rid of this cough?

October 22, 1998 I had resp. failure (with intubation). My new pulmonary doctor put me on Singulair 10 mg once a day, a few weeks after. Within time, I started to have numbing and tingling in my face, arms, and legs. March of 1999 the symptoms worsened and started causing pressure in my face, arms, and legs, and anxiety started to kick in. I was told I had neuropathy and to take mobic. Symptoms getting worse, and went to a rheumatologist in June 1999, and he was suspect of singulair. The doctor thought that what I was experiencing was due to the singulair. He (the rheumatologist) discussed this with the pulmonary doctor and the pulmonary doctor did not believe this to be the case. Not forgetting, in March of 1999, I had a ct of the sinus area, and low and behold 1/3 of the cavity was and probably still is full of polyps.

As time went on, symptoms getting worse, and not one bloody doctor could figure out why I was feeling this way. In addition, at times, I was put on steroids for my asthma (not including my inhalers).

Two years ago, my body went into shock, leaving my left side very different than my right side. Affecting: my head, my face, my eye, my ear, my esophogus, my lungs, my arm, my leg.

I have been depressed and anxious not knowing what the heck was going on with me.

Recently ruled out thyroid, and lupus, and possibly ms.

Last weekend, I reviewed the letter from the rheumatologist (dated 1999) and the ct report from March 1999 (regarding the sinus/ polyps) and made copies to present to a pulmonary doctor that I have recently been seeing.

This past Monday the 10th, I had my appt with him. He knew of my situation from the last few visits (in addition, I had met him this past March for a pulmonary rehab program, and thought he seemed to be knowledgeable and compassionate). While waiting for him to enter the exam room, he had read those reports before entering.

The doctor looked at my hands (red as a beet and swollen) and said "You have Churg-Strauss Syndrome, and get off the singulair."

I had done my homework from a few weeks ago, where I looked up untreated polyps.
Untreated polyps, can turn into vasculitis. There are many types of vasculitis, to include Churg-Strauss Syndrome.

I then cross ref CSS and singulair, and low and behold, BINGO!

I have been suffering for ten years, physically and emotionally because of this drug!

There is also recent updates from the fda (fda.gov) regarding singulair, of which most recently includes anxiety and depression.

I suggest before taking singulair, be aware of the side effects. As soon as a side effect comes up, contact your doctor. Also, be aware of existing conditions (like me, sinus problems and asthma) for this could lead to churg-strauss syndrome.

This info is indicated on the actual disclosure (the paper insert that indicates studies, side effects, etc...) not the handout that is given with the drug.

By the way, I am now working with a new rheumatologist in Los Angeles (Cedar-Sinai affiliated) and a new neurologist.

mdklezmer

I'm a physician. Usually Kenalog injections can be avoided and oral steroids used like prednisone. The local dimpling effect may occur if the injection is too shallow, actually there is a temporary "disolving" of the subcutaneous tissue, the muscle and joints are not damaged. It is usually viewed as a "cosmetic" adverse effect. The Kenalog injections was primarily designed for joint injection and the kenalog or similar depo form stays active in the joint for a few weeks. All steroid medications can cause irritability and this is usually temporary for a few days. Steroids can cause muscle weakness- this is usually associated with high doses for prolonged use like being on prednisone for 3 or 4 months. Steroids can have an adverse effect on menstruation, but this is usually associated with chronic use. The most serious problems with the steroids result in bone weakness(osteoporosis) and serious damage to joints like the back and hip. Steroids can also result in weight gain, diabetes, high blood pressure and cataract formation. I don't think Kenalog is any different than other steroids such as Medrol or Prednisone in terms of the side effect profile. These are dangerous medications that can also be very helpful in saving lives and diminishing pain.

I have been on Fosamax since 2003. In 2004 my left hip starting hurting so bad it would wake me up during the night. I had dislocated my left hip in 1994 so we put the pain down to complications from the accident. The x-rays were fine however so she sent me to a Rheumatologist to see if something else was going on. He told me I had Inflammatory Arthritis (even tho there were no markers in my blood) and put me on Plaquenil. After 6 months, the Plaquenil had done nothing but the Rheumy wanted me to stay on, and truthfully, I was afraid if I went off, the pain would become worse. Next came wrist pain so severe at times I couldn't lift a glass without wincing.To make a long story short, the joint pain has continued to migrate throughout my body. My thumb joints (where they join the palm) are so painful I can't undo jars or bottles, the small bones in my fingers ache all the time. I also get shooting pains in the long bones of my left leg and both arms. Back to the Rheumatologist last week. He said the Plaquenil was not working so he gave me an RX for Methotrexate 20 Mg once per week. This drug is one of the first-line chemo drugs for Cancer and it's effects on the body can be devastating. I have been crying since last Wednesday and had just decided yesterday to start taking this medication. I sat down at the computer to just test the drugs I am currently taking and one by one entered the drug name with "and joint pain". Plaquenil came up with only good things such as "less joint pain" etc. Mobicox also came up with good things. I entered Fosamax "and joint pain" and the top 15 hits were unbelievable. It was my problem in each and every article. I am dumbfounded. I have been seeking Dr.s help with my pain for 4 years, a GP, a Rheumatologist (2 actually) and an Orthopod, not one of these people ever mentioned a problem with Fosamax! What is going on. I am NOT going to be starting the Methotrexate and I feel I have been given dangerous medications over the past four years which I should not have been taking. I was a Personal Trainer and aerobics instructor for 12 years - now I can barely get through a yoga class without modifying the stretches because the pain is so severe.

Thank goodness for this site. I have made an appointment with my GP but I am stopping the Fosamax today (it was my day to take it). I pray I can regain some of the pain-free movement I used to have. In closing, I do have to say that I have regained some bone mass on Fosamax but...was it worth it? Was there another way I could have done this? Who knows. How long does it take for the pain to lessen after dropping Fosamax?