Mono symptoms and conditions

My daughter is now 20 years old. she received her 1st gardasil shot in 3/08 and the second in 8/08. She didn't get the last one and will not be getting it. From the day she got the first shot we should have known something. She nearly fainted immediately after both shots and complained of weakness and flu like symptoms. Started feeling poorly in the days and weeks to come. It was the end of her senior year the doctor tested her for mono. and it was negative but she had an extremely heavy schedule at high school. He chalked it up to the stress of that. Between the two shots she started having numbness and pains in her hands,elbows and arms. She continued to feel poorly and terribly irritable in the upcoming months. We saw a orthopedic doctor for her pains in her arms. He referred us to a neurologist. She was beginning her first year of pharmacy school and we put off the neurologist because she didn't have much time until spring break. During her 1st year of school after her 2nd shot. Her personality changed completely. Became insecure, moody, very anxious , constantly complaining of flu symptoms, bladder infections and had a hard time urinating. When my daughter returned home from her first year away at college I knew immediately that she had changed. She had been a very bright, intelligent, independent daughter and came home the daughter from hell. I couldn't believe what I was seeing. She was miserable, disliked pretty much everything. I had been talking with the doctor and friends over the course of the year and they all said that she was in a very stressful field (pharmacy) and college life takes some time to adjust. Then just a few weeks home from college she was complaining of dizziness, light headedness, headaches and saying she was having an episode. I thought maybe low blood sugars.....until I witnessed one. She was having Myoclonic seizures. She could feel them coming on but couldn't move or react. By the time I witness one of them she hadn't slept in 3 days. She was diagnosed within a week seeing a neurologist and having 50 to 60 a day. It took 4-5 weeks to get them under control in and out of the hospital . She has been on many seizure medicines it seemed like if it worked to stop the seizures she had crazy side effects. She was diagnosed with Juvenile myoclonic epilepsy. No one in our family has ever had seizures. I asked about the shot right away everyone said no and it was dropped. Since last July 08 we have been trying to help our daughter get her life back and it has been the worst year of our lives. She was unable to return to pharmacy school. The first fall 08 she was completely disabled. It looked as if she had had a stroke. They were saying it was the meds or maybe she had a breakdown of some kind. I am learning that it was side effects of this horrible shot. This is why I am posting this lengthy message because I wanted to let other people know that you and your daughter are not crazy!! We just started 2 weeks ago investigating the possibility of the gardisil shot being the reason for this madness. We have learned many things and are very sure that it was the shot that change our daughter.. I was contacted by a friend of a friend about a similar girl having the same pains in her arms and the focal seizures. I am learning more and more everyday about similar situations.. If this information can help one person it was well worth the time to jot it down. I will be praying for all of your families out there dealing with side effects from this vaccination.. I will let you know what we hear when we visit the neurologist at the end of the month. Any comments or information that may help us help our daughter can be sent to ******

My 19 year old daughter received the first shot in March 2008. She immediately had a severe back pain. She had her first seizure in April. She got the second shot in May and had more seizures, fatigue, headaches, severe stabbing stomach pains, body aches and pains, tremor, hair loss, vision problems, 2 UTI's, mono like symptoms - swollen glands, bruising and bleeding gums are the most recent symptom. She had daily seizures throughout the summer and they are now about every 5-6 weeks. She is fighting to recover from this horrible nightmare called Gardasil. Thank goodness we figured this out and she did not get the third shot. If you want to sign the petition to get this vaccine in front of Congress go to: http://www.thepetitionsite.com/14/investigate-gardasil-vaccine-risks-now

I was given Levaquin after a post surgical Staph infection was confirmed. I too had the side effects described by so many others. Extreme muscle aches, joint pain even in my fingers, insomnia, nausea, vomiting, dizziness. My Dr. said to try to fight through it because the Staph infection needed thia particular antibiotic to cure it. I am 5 days into my 10 day dose and I can't keep taking the pills. I am scared and don't want to end up in the hospital again. He tried to give me a prescription for Bactrim but I said no because i can't take it. I have worse side effects with it than I have the Levaquin. I can't stay wake for more then 1 hour and I dose off but wake up with 15 minutes feeling drained. I can't walk very far without my legs feeling like jello. My WHOLE BODY HURTS!!

I have been on Yasmin 31/2 months and Had no side effects it was great So we got home from our honeymoon and the moodiness and crying at absolutely nothing started, getting married there is a lot of change new house last name church etc. so i just thought it was that I have become SUPER EXHAUSTED and don't feel myself i went to the doctor because i thought my mono had come back i just turned 20 I don't know whats wrong, until i come on here and other web sites. it could be the Yasmin but im not sure, my husband has been so amazing I just want to feel myself again. if any of you have suggestions please tell me!! please. I have an appt with my gyno Monday to maybe switch but im not sure. let me know thank you!

My girlfriend completed her first two shots earlier this year with minor side effects (nausea, fatigue, nothing major.) Upon completing her third shot last month, she has been vomiting frequently and unexpectedly. She had major issues with insomnia, and she has been experiencing severe nosebleeds almost daily, in addition to constant nausea. Her last period came over two weeks later than expected. She has been extremely tired and had been diagnosed with mono, but after reading these side effects, it's exceedingly clear that these are all effects of the gardasil shot!
Gardasil is clearly an extremely dangerous treatment. There is minimal evidence that it works, and thousands of people have fallen severely ill to this "miracle drug". You do the math.
Don't force it upon yourself or your daughter, as gardasil is HARMFUL.

Update.... well my 6yr old son came off Singulair on 3-29. His sinuses drained finally (only waiting past year for that to happen) 9 days after coming off. His sinus problems have been gradually going away. He is now only taking claritin and sudafed when absolutely needed. BUT he started with sore throats. He never had a problem with tonsils only adenoids which they took out in Feb. Now since stopping the Singulair his tonsils have become constantly infected and twice the size so he will be having them removed in July. Some of the antibiotic don't seem to be working as he has been on them so much over past year. Im wondering if the Singulair was hiding the fact there was a problem with the tonsils as well.

I too am in shock as well as relived about the news on singulair. Last night my 15 year old son called me (he's at the beach on spring break w/ friends), first he said Mom don't be mad but I haven't been taking my singulair and I feel better he then proceeded to tell me what he saw on the news about singulair and he was not ever taking it again. My son has been on singulair for the past year and as I write this I want to cry thinking of how I have treated him the past year because he went from a loving happy child to a tired, moody, grades falling, bouts of anger where he would tell me to just leave him alone he didn't care anymore about school or anything. He would stay awake at night and I couldn't get him up in the morning. Over the past 8 months I've had him at the Dr.s office trying to tell them something was wrong with. He shouldn't be so tired, angry, falling asleep in class. He was tested 3 times for mono with neg. results and I was told it was his age. Last month at my wits end I took him to the Dr. and demanded a complete blood work up because either something was very wrong with him or maybe he did developer teen add or emotional problems. The doctors diagnosis: depression and fluctuating hormones of a teenager. I'm furious at myself for all those nights trying to understand why he could pay attention in class, wouldn't remember his homework, getting angry when I would tell him theres no way you can be that tired all the time, telling me he hated fighting with me over school,and just wished he could quit school altogether. He even lost interest in his favorite sport and would get so frustrated at how he felt he would cry at night say he was sorry he didn't know why he felt so mad inside and I would try to understand but not know what to do.
I asked his Dr.s on several occasions if singulair could cause him to feel like this and every time they told me no and blamed on his age and being depressed about school. He will not be taking singulair again!.

Daughter was sick for 6 weeks with what started as a virus . Dr.'s said virus needed to run it's course and allergies were also bad so they put her on Singulair. When she wasn't improving they said she had mono. No improvement, still mono. Still not improving, more specific test, not mono. Dr's chalked it up as she had a virus and was now just depressed from being down for so long. Well when you have mono u r told not do anything and only rest. After weeks of doing this she was depressed and weak. Then we were told that the diagnosis was wrong and we were had been trying to nurse the wrong sickness. Dr's said to send her back to school. By that time our daughter was so far gone it wasn't possible. Every time we left the house she would scream and panic. Experiencing exhaustion and not her self (She loves school & was always a very happy child) I knew there had to be something wrong with her. They sent her to the hospital lab twice and found nothing. Still trying to say she is only depressed but now being rude about by saying that we were just giving her, her way. My husband & I decided that the Dr.'s were not doing there part and trying to get to the bottom of her illness. So we began looking at what had been different in her life over this period of time (5 weeks).The only thing that had changed in her life other than her catching a virus was that she was put on Singulair. We had enough common sense to know that some people may have a reaction to some medicines that others won't. And just because not every Dr. has experienced this doesn't mean it can't happen.We read the pamphlet and all of the side effects. Even the rare ones she was experiencing. Shaking that looked like seizures, body aches, numbness in fingers and toes, extreme fatigue, loss of appetite, weight loss, irrational behavior, anxiety, paranoia, coughing, depressed, swelling of the lips, hallucinations, blurred vision,screaming every time she left the house, and complaining of constant pain. We felt like that had to be what it was. So we researched it and found on medications.com story after story of children who had gone through the same thing that she was experiencing. Dr was very rude and said she had never heard of that before and just send her back to school. So my husband ad I made the decision to take her off the med. The day before we rushed her to the hospital was her last day on the Singulair. That turning point was the seizure like shaking,hallucinations, saying that she couldn't hardly see us.That night in the ER they ran a CT Scan and found nothing. They admitted her in the pediatrics unit and we began a week that felt much like a month. They started her on an IV. They called in different Dr's...resident Dr's, pediatricians, etc. Everyone said our theory on the Singulair was possible but since they had never personally experienced a case of that they just weren't sure.When no one could figure out what was wrong they then called in a neurologist. He was very concerned and immediately started assessing her and ordering blood work and tests. She had an MRI and an EEG. All came back normal. He listened to our theory and said it was possible but to be sure he wanted to test for for everything else to make sure nothing was being missed. She had lost 5 lbs before her hospital stay and not sure how much more after that but while in the hospital when I bathed her, it was so sad to see her stomach all shrunken in. They put her on 5 different medicines while in the hospital that we were so upset and torn because then we felt like she was being drugged. They had her on an IV the whole week she was there and hooked up to monitors.She had a couple of really bad episodes while she was there where she felt like she couldn't breath, couldn't stop shaking and then she lost her speech which scared us to death. They ended up sedating her to calm her down. That one episode was on a Wednesday and then Thursday they gave her another medicine and it looked like she was having a bad reaction to it....her eyes were open but she couldn't move her body. We were freaking out thinking something was wrong. I ended up crashing and had to be carried away. All the result of everything going on of course.Everyone on the staff was very frustrated at not being able to help her. We felt like we were loosing our baby.We continued slowly getting through the end of the week and weekend dealing with all the symptoms still. Dr came to the conclusion that he felt she had got a bad virus. Although, he never dismissed the fact that it could be the Singulair but said unfortunately there was no test to look for that. He said parents usually know their kids better than anyone though.Dr. said when she was released she would have to go to inpatient rehab because of the anxiety issues and because she had not walked for so long (4-5 weeks).Dr came in Monday morning and said if she did not start drinking more she was about 2 days away from a feeding tube. During the day she started drinking more and when he came back in that night he said she had drank enough and he took her off the IV and said she could go home and we could do outpatient rehab. We were so happy to take her home even though we knew it would be hard. So the next day, Tuesday, was very hard and we had very serious episodes with not talking, loss of hearing, shaking, still not walking and passing out. We called the Dr. at the hospital and they said it was all due to the anxiety. We were praying over her so hard. Well Wednesday she woke up and said she had no more pain, she was hungry, and she started walking again. We got our baby back! And there is no doubt in our mind that it was that Singulair. We know that it was. From the time we took her off of Singular to the time she was totally restored was 9 days. It happened just like the all the other parents had described. As soon as it was out of her system she all of a sudden came back to us. We decided to not take her back to those pediatricians. I recently took her for a follow up with her Allergist,who was not aware of what had happened and after hearing the story said that he had experienced two of his patients being allergic to Singulair and they had hallucinations. They were pulled off the medicine immediately so their cases were not as extreme as hers. Please be cautious! This was a devastating experience! Please feel free to email us. I have documented our whole story if you would like it emailed to you.

I don't know if this a side effect of this drug or long term effects from the Prednisone and having mono, but ...lack of sex drive, can't perform sexually, depression. Anyone have these?

I had a sore throat. The first doctor said mono. The 2nd doc. said no mono or strep --must be viral. Third doc says viral and puts me on predinsone, levaquin and darvocet because my uvula was swelling from infection. White count was elevated and had low grade fever. That was Friday..............................The Monday after that I had severe pains in my left side. After teaching went to ER they said gas after 2 minutes. Next day level 8 pain same side went back to ER. They said skeletal prescribed me 4 more drugs and told me it was viral too. Went to internist on Wednesday had to miss teaching he scheduled CT on Thursday morn. Level10 pain almost passed out on Thursday eve missed school/teaching. Friday admitted to ER at different hospital beyond any level of pain I have ever had, blood pressure through the roof, heart palp, they gave me morphine and phenagrin and muscle relaxer for spasms.

Here I am a perfect state of health get a sore throat and the next week I am in the hospital because of the 2nd ct saying that I am full of poo. 4 weeks later I am still in pain, missed 12 days of teaching and now they say i have ibs. I miss my active life before. I believe the combination of these drugs caused this. I am young no children and very healthy. Ultrasound,s blood works, 2 ct scans with dye, colonscopy, xrays show no probs. Which is great but still in pain. Anyone PLEASE HELP the doctors are taking their sweet time while I have lost weight and stay in bed which helps the pain. Bending over, lifting, eating, pooing, sneezing, coughing, hiccuping can make it worse. It is intense SHARP pain. I have cut out everything med wise except for Miralax and now I have diarrhea and joint pain.

They want me to take Dicyclomine and IMIPRAMINE, MIRALAX and Levisin sublingual and Diflucan.

I am a physician and have prescribed levaquin to many people. I have had some of them complain of what they thought were serious and variable side effects but mostly I attributed their problems to anxiety and hypochondiasis. I now know differently. I took levaquin, and for over a year I have had serious CNS anxiety, insomnia, joint and tendon pain, and widespread peripheral neuropathy. It has been an awful time and since realizing that the effects are often long term I have been able to identify many other patients who have developed serious long term problems with anxiety, depression, arthropathy and tendonopathy, neuropathy and possibly endocrine effects like gonadal failure and worsening of diabetes. There are no long term studies done post marketing to identify these effects and to unify all of these problems into one syndrom of fluoroquinolone toxicity. This is a big problem and I believe thousands of patients have been adversely affected by the use and misuse of levaquin and probably the other fluoroquinolone antibiotics. I have other colleagues who are beginning to recognize the long term consequences of levaquin and the fluoroquinolones. More research and study needs to be done. In the mean time I am sure that Johnson and Johnson, Ortho- Mcneil, will continue to refute that the incidence of serious adverse reactions is much higher than they report.

I had taken yasmin for a month and noticed severe side affects- nausea, panic attacks, dizzyness, fainting and i went to the ER to get tests done. they all came back normal. Even after I stopped taking the pill I still felt sick for a long time. The pill brought down my immune system causing me to now have Infectious Mononucleosis (Mono). I've had that for two weeks already and because of my low immune system I have also gotten Pneumonia. I was perfectly fine before I started the pill but ever since then my health has gone down hill. I am going to try another different pill again in December but I don't think I'm going with any similar ingredents...

MY LITTLE GIRL HAS BEEN ON SINGULAR FOR A WEEK AND EACH DAY SHE HAS GOTTEN A LITTLE BIT CRABER AND DIDN'T WANT TO GO TO KG.WHICH SHE LOVES OR DANCE CLASS .TWO DAYS AGO SHE WOKE UP IN THE MIDDLE OF THE NIGHT AND SAID HER EAR HURT, SO I GAVE HER SOME TYLENOL AND AFTER 1HR AND HALF SHE WENT BACK TO SLEEP.FRI. NIGHT SHE WAS ON THE FLOOR NEXT TO HER BED SCREAMING AND CRYING LIKE SHE WAS HAVING A NIGHT TERROR (SHE HAD THOSE ALL THE TIME WHEN SHE WAS LITTLE BUT HAS OUT GROWN THEM) SHE KEPT SAYING SHE WANTED TO GO HOME AND HER ARM HURT ,I GOT HER TO GO BACK TO SLEEP AND HOUR LATER SHE WAS UP SCREAMING AGAIN.TODAY SHE GOT UP AT 8 AND WAS LAYING ON COUCH BY 9:30 SLEEPING WHEN SHE WOKE UP SHE HAD 102.3 FEVER AND I KNOW NOW THAT IT IS THE MED. BECAUSE WHEN OUR THEN 2YR OLD (NOW 3) WAS PUT ON THIS MED. HE GOT A FEVER AND HUGE SORES ON HIS TOUNGE AND WAS COMPLETLY MISARABLE THE DOC.KEPT SAYING THAT HE HAD MONO AT 2 NOT. I TOOK HIM OF THE MED. AFTER I FIGURED OUT THAT WAS WHAT IT WAS AND HE HAS BEEN FINE SINCE .I SHOULD OF NEVER LET THEM PUT MY 6 YR. OLD LITTLE GIRL ON IT .

No Need to Experience the Flushing of Niaspan !!!!
NOT an allergic reaction OR a "cardiac" reaction,.. it IS temporary & it is PROSTAGLANDIN !! Try this,...
Not a big deal. ~90% of ALL patients can tolerate Niaspan / ER-niacin
1-2 gms/day,.. IF,.. the prescriber knows a few tricks. Dr. Wm. Castelli, he uses plain ole crystalline niacin AND Niaspan. 40 years ago, ALL they had was IR-Immediate Release aka plain ole crystalline niacin,.. 3-4 gms a day MONO therapy. The patients FORGET THE ASPIRIN which prevents the flush. If you forget to take an aspirin AT LEAST 30 min before dosing,.. FLUSH! Taking with the dose is too late. SOLUTION 40 YEARS AGO?
Alka-Seltzer ; that`s a 325 mg of AQUEOUS aspirin, no need to take sooner,.. wash down the niacin with that. AFTER,.. you eat 3 TBS applesausce whil waiting for the ALKA-SELTZER tablet to dissolve. Use just enough water to swallow pill, so you get all of the 325 mg aspipirin in the ALKA-SELTZER. 90% of patients get through the 'rough' 1st 2-4 weeks & stick with it after. IT IS THE ONLY DRUG WITH AN FDA INDICATION TO HAVE BEEN PROVEN TO REVERSE CAD, REGRESSION.
Remember; hot drinks, alcohol, spicy food less than 2-3 hrs prior to Niaspan is a NO-NO !!
Take care,.. ...be well... Steve the Lipid Guy

Hi, my 14 year old daughter was prescribed Topamax about 6 months ago due to migrains that started when she had Mono. The mono lasted a good five months and the nuerologist to whom we were referred prescribed Tomamax after nothing else worked.

This morning as she was leaving for school, she said " I will take Aleve twice a day for the rest of my life, the Tomamax has made me stupid and I can't take it anymore!" With that my beautiful, brilliant daughter was out the door.
I am sick that I didn't look into this drug sooner. I found this site and am floored at all the side effects that sound exactly like hers. She has always been an A+ sudent who works hard, she lately has been saying she feels dumb, can't remember things, her knees hurt, her hair is falling out, she can't think, she is depressed etc. I have been downplaying her symtoms and blaming it on the mono. I am outraged at the craziness this drug has obviously caused and my failure to recognize the cause.

My questions now are, can she quit the Topamax immediatly and when, if ever can she expect her cognitive ability to return?

Please tell me the effects are not life long and what my next step should be to help relieve her of these symptoms.

Peace, Becky

The flushing is tolreable. The itching is intolerable. I'd rather have heart surgery than suffer with that infernal itching. My cardiologist believes the severe itching is unrelated to the Niaspan because the reaction has only occured twice since I started taking the medication 6 months ago. I disagree. It seems to me the itching is caused by the Niaspan, together with some other unknown factor. There may be something to the "spicy food" suggestion posted by others. Last night, I ate a bunch of hot peppers an hour or so before taking the Niaspan. I woke at 3 am, with a mild hot flash, followed by the dreaded itching. Pure torment! My chest, back and legs were bright red. A cold shower helped a little. On the first occasion, two months ago, Benedril help some, but relief did not begin for over an hour after taking it. (Take at least two tablets!) But last night, I didn't mess around with Benedril. Instead, I took two codine tablets I had left over from surgery. Relief! If you are suffering from this terrible side-effect, may God be with you!

Lauren- May 2005 through August 3, 2007: The following is my daughter’s story which I put on paper so that she could bring it with her to the gynecologist in case I couldn’t be with her. I didn’t want her to forget anything. Someone suggested that I post it to a website:
The most recent issue seems to have started when she first went away to college in the fall of 2005. She came home one weekend with a stomach virus (vomiting, nausea), but it seemed to never completely go away. She was taken to the ER a few times, just to be treated for dehydration and sent home because there was 'nothing wrong with her'...Over the next few months she seemed to constantly feel sick, nauseous, fatigued, and get a lot of headaches. We took her to her primary care doctor, who did blood work and treated her for heartburn, acid reflux, etc.. During this time, she actually had appendicitis and had her appendix removed. After that she continued to feel sick. So we moved on to the gastroenterologist who ran many tests: cat scan endoscopies, more blood work, and were told that they couldn't find anything wrong. Then we started with a nutritionist to help her eat healthier and hopefully reduce the nausea which subsided occasionally but never let up. Nothing there helped. Then it was back to another gastroenterologist with no results. Over this time, anxiety was hitting her big time. She was finishing up finals in her first year of college and was constantly skipping classes because she was too nauseous to get out of bed for her 8:00 classes. Home for the summer - no relief. She decides she couldn't go back to her college for her 2nd year so she enrolled in community college - not exactly the plan, but at least she was on course with her classes and doing well. Still stressed and nauseous, we started with the neurologist who prescribed many medicines and ordered an MRI, which showed nothing (no problems, not no brain!). Back to the primary care doctor who finally diagnosed her with Irritable Bowel Syndrome, which fit the current symptoms of nausea, severe diarrhea while vomiting and the finale: passing out. So, back to the state college for 2nd semester of sophomore year. But the medication for IBS was making her too sleepy to get through the day, so she discontinued it. The symptoms had subsided a bit but towards the end of the school year got worse again - just in time for finals, again. During that semester at school, she sought counseling at school which seemed to help her stress level, but she still had daily ‘melt-downs’, so the therapist sent her to a psychiatrist for meds. The doctor started her on the lowest dose (25mg) of Zoloft. As she started to feel a bit better, they increased the Zoloft over the next few months until she was at 100 mg. Home for the summer, the symptoms came and went, but about 2 weeks after she started the 100 mg, she confided in me that she was feeling depressed and actually had thought of 'not caring if she died'. We immediately took her to the psychiatrist upstate who had treated her at school and whom she had seen once since she left school. (She had also continued with the cognitive therapy at the college.) The doctor told her to start weaning off the Zoloft, but start Seraquel (another seratonin-based drug). She also said she was going on vacation and Lauren needed to be seen often as she switched medications, so she advised us to find another psychiatrist closer to home to monitor her progress. So the new doctor put her on Wellbutrin, continued to wean her off Zoloft, and continued her on the Seraquel. He also ordered blood work and a fasting glucose-tolerance test (all of which came back normal/negative). The symptoms got severely worse over the next 2 weeks: constant nausea, vomiting, dizziness, weakness, fainting. On Monday, she spoke with the psychiatrist and he told her to stop all meds. We continued to believe that the recent symptoms were caused by either the psychotic meds themselves, still in her system or the withdrawal of the meds. By Tuesday night, she had been vomiting for almost 24 hours and I had to take her to the ER, not because I thought they could figure out what was wrong, but to re-hydrate her because she was becoming dehydrated. After 7 hours, and more blood work, x-ray, EKG, she was released and proceeded to get nauseous on the way home at 4AM. BUT, a very nice nurse came in while Lauren had fallen asleep and asked me why my daughter was on so many meds. I basically told her the above story and she asked me when Lauren started on birth control pills. I told her that I took her to my gyn. in May of 2005, before she was going off to college and we told him about the terrible menstrual cycle (heavy bleeding and 1 day a month home with cramps all through high school) and he put her on Ortho-tricycline low. At her 3 month check, she told him she was losing large amounts of hair. He changed her contraceptive to 'Ov-con 35'. In November, she complained of nausea and he switched her to Yasmin. She has been on it ever since. The nurse asked me if I was aware that every symptom that Lauren has had since October of 2005 could be a side effect of oral contraceptives!! She told me about a book to buy, written by Dr. John Lee about hormones and imbalances. She told me not to stop the b.c. pills abruptly, because since they are synthetic hormones, and with what her body was going through, it might put her into an hormonal chaos, similar to a full-blown menopause! So we are now reading the book, waiting to do saliva- testing and trying to see a gyn. to help us. Her own gyn. has a personal family emergency and is on a temporary leave of absence (as we found out when his office canceled her yearly check-up twice in the last 10 days). We are trying to get her in with one of the other doctors. She cannot start a 3rd year of college still feeling ill!
Added to the above is the fact that my husband’s sister called to see what was going on with Lauren after she got a phone call from her mother. It turns out that my niece, Heather (age 23), has been making the rounds with the doctors and having testing done (MRI, blood work, etc.,) because she has been nauseous and passing out. Guess what medicine she is taking…..Yasmin!

This is the list of most of the medicines (besides the 3 oral contraceptives) that she has been on during the last 27 months because of the side effects of Yasmin, and no doctor suggests she stop her oral contraceptive pills for a few months!
Prochloroperaz (5mg), Topamax (25mg), Prevacid (30mg), Zofran (4mg), Omeprazole (20mg), Amitriptyline (25mg), Amitriptyline (50mg), Inderal (60mg), Propranolol (10mg), Amitriptyline (10mg), Sertraline (Zoloft) (25mg), Sertraline (Zoloft) (50mg), Metoclopramide (5mg), Sertraline (Zoloft) (100mg), Seroquel (25mg), Wellbutrin (150mg), Dicyclomine (10mg), Compazine (severe reaction: Extrapyramidal), and other anti-nausea meds in 4 trips to the ER (one due to the reaction to Compazine!)

My 13 yr old daughter was given yasmin because irregular periods. Bleeding all the time. she got regulated but after reading this site i realize why she has had the awful side effects that she has had. She started taking y around october of last year. She plays competetive soccer and she was not able to keep up ..Shortness of breath tiredness looked as though she was out of shape. We never thought it could be those y pills. never crossed our mind. march she was diagnosed with mono so we just decided to take her off because she had mono. she has not had y since march and she is still tired all the time. back hurts hot flashed heat intolerant. will this y leave her system soon?

i've been taking the generic reglan for a month for gastroparesis. i become depressed fast, have been having increased migraines, severe exhaustion as if i had mono, and just recently began lactating. I've stopped taking the medication to try my own trail if the side effects are even worth it. I'ld rather deal with stomach pains and not eat then the spells of depression and other side effects.

I really don't think anyone too young should take this product. I have only taken it for about 3 days (I know I probably sound like a hypocondriact because I haven't waited long enough to see if the side effects subside) but even in the first couple of days I felt really weird. I felt like I was sick with mono or something. I felt really tired for the first half of the day and then at night I was awake. My change in mood has made me feel a little out of it. Also my acne got much worse just in 2 days. Instead of it just being a bad it was like every new pimple was beneath the surface of my skin. I also take doxocyclin with yasmin but it doesn't seem to do much. I also feel really lathargic and odd. Very tired and my head just seems to be floting.

I know I have only been on this for 3 days but, I have work to do and I can't let this pill bring me down in that. I have to be alert and know whats going on in order for me to do my job. I don't want to be someone who still has side effects long after just starting to take this pill.

I can't say much else but I that I don't want to risk my sanity for this. I really don't think I need it now. I am only 15 and I just want other young people to be aware of the side effects. Although I was not perscribed Yasmin for pregnancy reasons, just know that taking this so early may cause problems. Anyway, good luck to all and I hope whatever BC you choose it is right for you and your body!

I have been on Nuvaring for 2.5 months... thank god i read this. I'm not someone who usually gets side effects to drugs but Nuva Ring is a whole different story. I'm tired all the time! I used to be able to stay up all night but since I started the ring I need to sleep all the time. I'm in college my roommate convinced me to get tested for mono beacuse I was always sleeping and couldn't even stay up to study for finals! I also have been getting horrible mood swings. I have always been the nicest most easy going person until I started the ring. I have also been having back and stomach pain (like acid stomach) as well as numbness in my hand, I'm not sure if this has anything to do with the ring but it started right when I started the ring.. has anyone else had these sideeffects.. Thanks!!!

After taking Niacin for several years, I have the itching problem and my legs started to weep. Has this happened to anyone else? Eating beef seems to maximize the itching. JT

OMG! Tonight is my second night on Niaspan. I took the aspirin beforehand etc.. I am experiencing severe itching. I'm about to cut off my fingernails, I'm itching so badly. As I type, one foot is rubbing the other - I ITCH EVERYWHERE AND CAN'T KEEP FROM SCRATCHING!!! And it won't stop! I tried taking 2 benadryl about a half hour ago, and thus far no relief. If it continues to worsen I'll call the "ask a nurse" line to see if I should go in to poison control or the hospital. This is crazy!

About six months after my daughter started taking yasmine. her moods changed, her personality changed, she was is a state of depression and was having panic attacks regularly.she lost an excessive amount of weight and was thinking about suicide. I asked her doctor and a gyn if the yasmine could possibly be causing these side effects. They both said no. So she started getting treatments for depression and anxiety and was put on medication. Paxil. This medication seemed to be helping at first but then she started having the same effects as before and she was still taking the yasmine. in the last 3 months she has been taking the birth control shot and has not taken yasmine or paxil and is now doing great. I'm really disappointed in her doctor's because a lot of her misery could have been avoided if we had been told this earlier. My daughter was on Yasmine for 2 years before I finally decide to check the side effects from the internet myself. Now she says she feels so much better and is back doing things with her friends again is having a fun teenage life. Never again will I let her use Yasmine!!!!