October 16th
2008
2:15 PM
I started taking flowmax due to low flow and dribble. im 37 and never had problems like this before. Flow was great after a day on the flowmax. after a week it seemed to stop working. My doctor insisted taking 2 .4mg pills instead of one. 3 days later flow wasn't any better and my lower back and groin started to hurt. I stopped the flowmax and now its one month later, flow is better but my pain in my lower back and groin isn't getting better. anyone else have this groin pain? ive had no ejaculation problems but my wife has commented that im always tired and my sex drive has all but disappeared.
-- By knodis | Reply | Private Message me
September 17th
2008
3:09 PM
I do not know if my symptoms are related to the Zometa treatment I received 11 mos. ago or not but am desperate to come up with some explanation for my symptoms. Over the past yr. I have had the occasional bend over wrong and experience upper back muscle pain, once about 7 mos. ago for no reason I had right groin muscle pain, couldn't lift my leg or cross it, eventually it went away. Then on 8/22 I had what the Dr. called acute tendinitis in my right hand, a week later my right groin, 2 days later my left groin,2 days later my left hand and now my right jaw. Each time the tendinitis pain is crippling but lasts usually only a few days and never more than one area at a time. So far my lab tests are coming up negative for most everything. Anyone else ever experience this transient tendinitis pain and so long after receiving the treatment?
-- By sunnyd49 | Reply | (1) replies | Private Message me
June 29th
2008
2:33 PM
Just wanted to add another little bit of fun side effects for everyone.
Last month, I woke up with a pain in my right groin. Since no gymnastics were involved, I treated with ice and ignored it. After a few days, pain was worse, so went to the ER (My home away from home) where a bone density scan was ordered. 4 weeks later I find out that I have a stress fracture of the lesser trochanter (part of the femour just below the femoral head - English translation hip fracture).
Turns out that long term therapy on warfarin (ie. over 1 year) also increases your risk of fractures.
And what does one do for this? Nothing. Orthopedic guy said just go as usual and no physio required. Easy for him to say since he does not have groin pain, and associated thigh/Knee/calf pain associated with accommodating my gait. Needless to say, seeing a new orthopedic guy.
I have started iron infusions monthly as my iron and ferritin levels are low (but hemoglobin is fine).
Still wondering which came first - the insanity or the warfarin!
Fiona
-- By fiona | Reply | Private Message me
February 3th
2008
5:16 PM
I have been on Warfarin since Sept 2004 when I had multiple blood clots in both lungs. Since then I have had two more PE's (one with a therapeutic INR) and a blood clot in my left arm (INR was also therapeutic). Genetic tests show nothing.
Since starting Warfarin I have had
- dizziness issues,
- eternal extreme fatigue
- hair loss
- short term memory and cognitive issues,
- joint pain and
- head aches all the time. I think the headaches are the worse since I can't take any NSAID's for them.
I have lost weight and push myself to exercise because it is supposed to make you feel better, right? Well not yet. I keep waiting.
I have not been able to return to work and worry about the long term implications of this.
Many times I have wondered about my sanity and if I was imagining all of this, so finding this forum at least lets me know that there is a possibility that it is not all in my mind.
I have been seeing a psychiatrist to help me work through the almost dying 3 times thing, but it is hard to accept since no one knows why I throw the clots. My INR is not stable in spite of close monitoring of Vit K and other drugs, and my INR must be taken twice a week.
-- By fiona | Reply | (6) replies | Private Message me
January 27th
2008
8:17 PM
Hey all. I suspect many of you would agree that one of the most infuriating aspects of this antibiotic nightmare is that seemingly, there aren't many {none that I've dealt with} doctors/nurses or pharmacists that will even acknowledge the potential {and VERY REAL} side effects of these drugs.
On 01/10/08 I was put on Cipro 500mg twice daily, two week supply, for epididymitis, which likely stemmed from a bacterial infection/urinary infection back in late Oct of 07. It's an infection that can require a lengthy dosage due to eliminate bacteria growth. I was also prescribed a painkiller along with it.
That night after dosing had horrible nausea/vomiting, and chalked it up to the painkiller ... which at that point it likely was. Within a few days the groin pain from the infection had subsided a great deal, and although felt a little 'odd' from the Cipro, nothing too noteworthy. At eight days into treatment, became nauseous around the clock with bizarre flu like symptoms. I called the doctor at the ER who had diagnosed me, and she switched me to Doxycilline {sp?}, which isn't a quinolone. After stopping the Cipro, nausea disappeared. However, within a week the pain of the infection returned, apparently due to the weaker antibiotic.
So I was re-checked on 01/24/08 and put on Levaquin, 250gm once daily. Within a day or so the pain subsided once again, but on the third day developed horrible diarrhea and pain in my left knee/leg. Stopped taking it immediately, and decided to research my dilemma online, where to my horror I've discovered all sorts of people from all walks of life experiencing debilitating side effects from this grouping of fluoroquinolone/quinolones antibiotics.
I'm now on Cephalexin, and the pharmacist I spoke with today assured me that it's not part of the quinolone grouping. He also suggested that I must be part of that small pool of the populace that has trouble with quinolone antibiotics ... one begins to wonder just how "small" this pool is given how the average person isn't likely to associate muscle/joint pain with the antibiotic they're ingesting.
How this POISON has lasted so long on the market without more exposure/media coverage speaks volumes about the state of corporate America, with nearly every social system compromised {usually at the expense of the corporation's victims} , with little or no help from the corporate owned mainline media, which serves as nothing but a megaphone platform for vested intertests to transmit "official" opinion to the unwary. So here I be with very painful knee, which I should add is already compromised due to a major tibial plateau fracture in 2001.
I'd love to know whose palms are being greased to keep this rat poison available ... hell, I even had to pay over our insurance co-pay fore the Levaquin, as it's apparently a "top shelf" drug.
Good luck everyone ... and it probably doesn't need to be said, but man, I know after this I will check and double check any and every antibiotic that may be perscribed to our daughter in the future!
-- By echo_in_light | Reply | (6) replies | Private Message me
Warfarin Sodium (2) Mirena (1) Zometa (1) Levaquin (1) Cryselle 28 (1) Flomax (1)
November 17th
2009
5:47 PM
I got my Mirena o June 18th, 2009. It is now November 17th and I have an appointment to have it removed this Friday. It started with unexplained hives and rashes constantly. The bottom of my feet, my palms, my knees, upper arms, throat and stomach. I was on constant high doses of Prednisone and anytime I started lowering my doses, the hives returned. I went to the ER three times for swelling and hives so bad I could barely see and could barely breathe. seemingly caused by NSAIDS, which I had never had a problem with before.Next was severe lower abdominal pain accompanied by groin pain so bad I could barely walk. Friends said it sounded like cysts, but, when I had an internal ultrasound done, nothing was found. After that I had severe breast pain and swelling. The final straw was the constant all over muscle aches and joint pain in my knees. I feel like I am 100 years old! I am tired all the time no matter how much sleep I get. I went to a dermatologist and I mentioned the Mirena, as I had to my OB, his response was "middle age". I thought I at first has Lupus, but, the rash did not fit that description. I changed detergents, blamed it on a foster dog, anything I could think of. Finally after reading so many posts and finally finding a connection with the rashes and hives, it can be nothing other than the Mirena. I even noticed that this device had the second most posts on this site. I can not wait to have the Mirena removed.
-- By jbugler | Reply | (3) replies | Private Message me