Concoction symptoms and conditions

My acne has been HORRIBLE! I never had it as a teenager, and now at 22, it is horrendous. I finally figured out that the acne had its onset about the same time I began Wellbutrin. I am also on Prozac, which I love, but the mix has been really great for my mood and ability to function. Any suggestions for a similar med to Wellbutrin that will eliminate the acne problem? It is comforting to see that I am not the only one with this issue!!!

I'm on here researching a different med, but couldn't help notice this thread on Wellbutrin. It's been about 7 years now since I was on Wellbutrin, but I am still enduring the consequences. Back then, there was not a word on the label about Wellbutrin (given to me to help deal with ADHD) and high blood pressure. Later they added that warning, but most people (and doctors!) miss it. I ended up in the ER on Wellbutrin with hypokalemia (low potassium), which can be fatal. It's a terrifying condition. The ER doc fixed the immediate problem with a potassium concoction, but ever since then my BP has been sky-high no matter what meds I take. Only exercise seems to help at all, and this despite having since then lost 25 pounds. I would consider my case an isolated event if not for the fact that since then two people -- one a person friend, another a client -- reported the exact same thing. They were on Wellbutrin for one reason or another, and ended up in the ER (one admitted for overnight observation). Do me a favor, folks: if this has happened to you, please email me using the "privately message this poster" link. Thanks!

The medical professional is particularly unhelpful in this matter. Talking with medical personnel about fluoroquinolone poisoning is a go-nowhere exercise. In an era when Monsanto genetically-modifies our seed stock you might think medical caregivers would advise us in advance that their prescription antibiotics mess around with their patients' DNA. (IT's that deregulation thing, yes?)

I experienced painful calves and a strange dream, possibly a nightmare, immediately, e.g., on the very same night, after having injested one Levaquin dosage for a prostate condition and maybe a year after separately having taken cipro for a week to combat traveler's diarrhea. The post-Levaquin early evening dream was strange insofar as I rarely drempt, and I never recall having been roused to wakefulness by a dream shortly after having gone to bed. Early on I did NOT associate Levaquin with the really terrible symptoms that I experienced within 60 days of having injested Levaquin.

My wheels fell off when I entered a period of insomnia. I thought my sleeplessness was stress-related because my health history includes a major depressive episode 11 years ago. I presented myself for help to a psychiatrist who prescribed a small dose of an atypical antipsychotic as a sleeping aid. My drug-induced sleep felt like a coma that lasted each night for a couple of hours. There were heart palpitations, agitation, panic attacks, racing heart, racing thoughts, insomnia, depression, paranoia, poor cognition, body shuddering, muscle twitching, night sweats, and pain in both Achilles heals. The symptoms filled a note book page. I felt like Jean D'Arc who was being burned chemically at the stake from the inside out. I would rise in the morning and then minutes later fall back into bed. I could stare off into space and completely lose track of time. I could not even find the right words in mid-sentence. I could not fill-in the registration papers when I presented myself for a second opinion at Mayo Clinic. I became a full babbling idiot. My wife said that I had retreated or devolved into some kind of primate or ape who communicated solely his emotional states by means of eye contact only.

I asked my doctors if the sum of levaquin and cipro had pushed me over my peak quinolone tolerance level. Or was it the medicine that the psychiatrist had prescribed to make me sleep? . I was no stranger to depression and I knew my symptoms were not merely emotional or psychological in nature. Why did I always feel as if I had been poisoned? The psychiatrist decided my paranoia warranted higher med levels. I declined the advice and stopped taking the meds altogether. My anxiety today is lower, my sleep is improved but fitfull. My neck aches. My head feels as if it were in a vise. It's not a headache and it's not painful, but there is a tingling, crawling, scorching sensation at my forehead and behind my eyes as if someone had beat me with a pillow and then filled my head with novocaine.

I'm not sure there's a moral to the story. It might sound a tad over-the-top, but I think we're faced by a pharmaceutical plague. There's really no excuse for the absence of informed consent. There is nowhere above ground, e.g., nowhere on main street, and no-one with whom you can speak in order to take the full measure of fluoroquinolone poisoning. If you are at this URL merely to find out about the FDA's recent black box warning re: Levaquin's link to ruptured tendons, you are in for peep into hell. Read the other thousands of postings on this site, and decide for yourself who bears the ring of truth.

Thank you so much for this information. After a year of endless blood tests, specialists and other diagnostics with no answers I have been diagnosed with chronic fatigue to label a concoction of symptoms that include dizziness, extreme fatigue (I have been a runner daily for 8 years but can no longer run), regular 'infections' akin to my vagina being on fire, irregular pap smear, difficulty orgasming (previously never a concern) and so many of the other symptoms listed above that it feels like a checklist reading this amazing site. As I work in a hospital I have undertaken extensive review of medical journals to see if any clinical studies have identified concerns with the mirena - I couldn't find any and so have dismissed my symptoms as unrelated but have always had a gut feeling about it. From being extremely active and passionate about my work, I have had to scale back and back until I now work only three days and rest for the remainder. I can't thank you enough for validating my suspicion that the mirena might be the culprit - it's the only variable my husband and I can think of since the symptoms emerged. I'm going to get this stupid thing out of me as soon as possible.

I started taking Lamictal about six weeks ago for epilepsy. Now keep in mind, I was on Dilantin which worked great for 17 years and then suddenly stopped working. I have been in medication hell since then. First Topamax made me dumb as a rock. I would space out all the time. Worst drug ever. Then Keppra which was better in that my memory/ability to speak came back but I had these intense ups and down. I had rages constantly. Now I'm on Lamictal. So far, it's better than the Topamax and the Keppra, however the dreams are very intense as are the night sweats. I'm also experiencing much hair loss. Fortunately I have a full head of hair but I'm afraid I will eventually lose it all.

I was on Celexa for about 5 weeks for panic attacks and anxiety but wasn't getting much better. My doctor switched me to Zoloft, I was on it about 10 days but I decided to discontinue it yesterday because it was causing extreme drowsiness, horrific headaches, weird crying spouts, and more anxiousness. Today, the first day being off Zoloft is harsh, I was in bed half the day and I feel like I'm in a dream and the headache is still there. Although , its about 630pm now and I feel a little better than earlier but not much. Hopefully tomorrow will be better? I'm also on Ativan.

Who would ever give this horrible concoction of chemicals to someone for 30 days? Someone is lying to the drs. please stop taking the poison.

It's been a year since I discontinued taking Yasmin. To recap, my problems with Yasmin were heavy, extended periods (longer than 7 days); moodiness/irritability; hemmorhaging; extensive bleeding (2 1/2 months); hair loss. I discontinued the Yasmin during the 2 1/2 month bleeding cycle. It took another month and a shot of Depo-Provera to stop the bleeding. Even then, my next period lasted 2 1/2 weeks. Before Yasmin, I had regular but heavy periods. At least I knew what to expect!

Since then, my periods are somewhat better. They last only 5 - 7 days now, but they are still somewhat irregular. Sometimes they'll come every 4 - 5 weeks, sometimes after 3 weeks or as long as 6 weeks. The cramps are the worst tho! I had a relatively "normal" period in July that started on the 14th and stopped on the 20th. It's now Aug 6th and I'm on day 2 of another period, only 2 1/2 weeks later. I'm not cramping per se, but I have a feeling of pressure in my lower abdomen and shooting pains down my right leg. Oh joy! My hair has started to grow back in, but it's all coming in silver-grey. Ah well, that's what Ms. Clairol is for.

I'd like to thank the makers of Yasmin as well as the medical "professionals" who push this "hell in a pill" on the unsuspecting public in order to get kickbacks as well as "perks". Thank you for screwing up my reproductive system. Thank you for causing me even more pain than I was already in. Thank you for ignoring my calls for help when I consistently and constantly told you that something didn't feel right when I was on this concoction. Thank you for continuing to lie to the general public when you say there are very few side effects with this pill. Will it take someone dying from this pill for you to acknowledge that it bad medicine? Lord knows I came close to it!