Miracle drug symptoms and conditions

I think no one should post within the first 3 months of starting the pill... it's not a miracle drug or magic. Your body has to adjust to the hormones and you're not going to find a pill that doesn't cause side effects within the first 3 months. I am about to start my 4th pack and I am curious to know if anyone else has experienced heavy weight gain that they can NOT lose =/

I am friend and caretaker for TBI patient (Traumatic Brain Injury).(he has no short term memory and some cognitive problems. Seroquel is his miracle drug . He has been on it for about 5 years now and it has helped so much with inappropriateness and keeping him calm and functional. He had been in long term care facility for about 6 years and they over medicated with many potent drugs (just wanted to keep him inactive since he was young mobile male with TBI).He has been out and living with me for past 5+ years, it took a little while to change and modify the medication and is now taking daily low doses of meds: (20 mg paxcil, 750 depakote er, 50mg x 3 times a day (total 150mg) of seroquel (using 25mg pills), and 5 mg of lipitor and 100mg docqlace. He does have a weight problem which is a bit hard to control because he does want to eat a lot but having lots of fruits and vegetables around and asking him to wait 30 minutes after eating for his food to digest rather than getting 2nds has helped a lot too. Seroquel for him is in my opinion the most important one.

I was prescribed Lamictal around this time two years ago (July '07) for Borderline Personality Disorder. At first I thought it was great and I felt like it'd been a miracle drug -- the drive back home from the psychiatrist's office that day was such a feeling of relief because I was going to get my miracle drug, finally. Later the next month I moved away from home and began college in the lower half of the state and stopped taking the medication because I noticed that I feeling any difference, or experiencing any change in my moods. Infact, I felt exactly the same as I had before. I looked up the medicine derivative drug and found out that it has a "placebo-like effect with highly addictive qualities".... which made me think that once again, my problem is all in my head. I still feel like I need to be on some kind of medication, but I am not willing to part entirely with my authentic self just to make some other people's lives easier. If they think my mood swings and attempts at self-destruction effect them negatively, just wait until you are the one having them and you can't control them! I don't want to become a zombie, I don't want to lose my hair, and I don't want to gain 30 lbs, but I feel like there's nothing else I can do. But then again, there doesn't seem to be any drug that can help without the drastic side-effects.

Sheesh.

Wow!!! I can't believe it! I just found this site. I've actually been on Advair 500/50 for years now, about 7 years at least. Just as a bit of a background, I'm 24 years old, used to be extremely active, played water polo, was on the swim team, and was just overall very active in high school. I've had severe chronic asthma since I was 8 years old, so in order to help me stabilize my asthma, my critical care pulmonologist put me on Advair. It was a "miracle drug"! However, while my asthma was under control, I was experiencing all these other symptoms that everyone else has been talking about.
Anyway, to make things worse, I just talked to my (new) doctor and she told me that the Advair makes it so that some organ (I'm sorry, I don't remember the name) actually stops producing prednisone (or the same stuff that your body naturally produces itself to keep your lungs working correctly) if on it for long enough. It makes sense because for the first few years it was prescribed to me, I really only filled the prescription as I was getting sick as a backup, but other then that I was generally under control. For the last I'd say about a year, I've been consistent and used it regularly as the doctor actually prescribed, every day, twice a day, whether I was sick or not. Now, I can't go even a week without it, otherwise I'm in the hospital.
During the last year or so that I've been consistent with taking the medication, I've had major depression, gained 45 lbs, fatigue, anxiety, dizziness, nausea, heart palpitations, heartburn, leg pains, sore throat, sinus infections (we just finally decided I was just allergic to our animals and I've been on decongestants for pretty much the whole year, doing sinus flushes, etc and I'm still all stuffy!), unexplained bruising, crazy mood swings, muscle pains, headaches, heartburn, etc. I thought I was just completely crazy, I kept believing it was all in my head!!!
I'm going to my doctor today and asking her to prescribe me something else. The funny thing was, I was just on my way to the hospital b/c my doctor's been treating me for the last 3 weeks for vertigo accompanied by the heart palpitations and the nausea, she finally is giving up and is sending me to the emergency room. I figured before I went that route, I'd look into it myself. Go figure!

My husband has been on Singulair for ten years now. It was a miracle drug for us as his asthma and allergies were ruining his quality of life. Little did I know that the Singulair would have such drastic effects as well. He is a police officer who has been through some traumatic events in his career. I attributed his irritability, depression, anger, severe nightmares, heartburn, weight gain, and puffy swollen eyes to post traumatic stress disorder. He stopped taking the medication about two weeks ago after his prescription ran out and he saw the FDA report. He is once again the man I fell in love with. Now I know what has been causing all of the changes in him, and we have decided he will never take Singulair again.

I'm 15 years old and i've been taking prednisone for a few months, and from what i've read i'm on a really high dose. i was diagnosed with rheumatoid arthritis and another autoimmune disorder concerning my muscles at the same time. my doctor told me prednisone was my only choice; it was either that or i would lose the ability to walk. he told me there'd be side effects, but i had no idea it'd turn out like this or i would have fought harder for another course of action. i started out on 30mg twice a day, and since then was weaned down to 20mg twice a day and now i'm down to 30mg once a day. i've been looking up a bunch of information trying to figure out if there's a way to lessen the side effects or any hope at all that they will get better. apparently there isn't much. after reading a bunch of these stories i gotta say i'm not feeling great about this. i totally understand everything everyone is going through. i'm sure you can imagine what it's like being smack in the middle of high school with a huge puffy face, acne so bad on my face, chest, back, neck, and shoulders that wearing a bra could put me in tears, and mood swings so bad i've lost friends over it. everyone knows how brutal high school can be, where appearance and attitude are everything. and i try to tell my doctor about it and he literally looks at me like i'm a whiny teenager and says "you're just going to have to deal with it." and people like my mom and my closest friends don't get it either. nobody understands how beyond frustrating it is. i'll get into the worst moods and not have a reason for it, but i'll stay angry for hours or burst into tears over someone looking at me the wrong way. it'll get to the point where i have to isolate myself from other people because the abrubt mood changes get so bad. as bad as i hate to admit it, the pain from the arthritis is gone now and supposedly my muscles are doing better too. developing arthritis caused me to have to quit cheerleading, something i've loved doing for 6 years, because the pain got to the point where i couldn't get my arms above my head or bend my knees. however, i'd almost rather deal with the horrible joint pain than deal with the side effects of prednisone. if your doctor gives you and alternative method, take it. i've always been confident in the way i look and really outgoing and happy and now i sometimes catch myself thinking about suicide. that's shocking to me because i've got so much going for me, but this medicine makes me miserable. and when i complain about it, anyone i'm talking to just looks at me like i'm being a cry baby. my mom does too, she'll say things like "you just have to do this. i know it's not what you want but to be honest i'm sick of hearing you bitch about it."
i feel a little better knowing other people feel the same way - like nobody gets whats going on with them. the prednisone does give me days of really great euphoria and days when i feel like i could run a marathon, but waking up in the morning to the acne and huge face puts me to tears every day. i have to pee all the time, usually getting up at 2 or 3 am. i don't sleep well anymore and i do sweat all the time. which also sucks being a teenage girl. i'm always hungry, and when i eat i never feel full so i don't know when to stop. my neck and face have put on so much weight that when people see me in the halls or out and about they ask me what happened. mind you these are people i don't talk to, just ones i know from classes or whatever. and it's pretty bad when teenage boys i've never really talked to ask what happened to your face. kind of a blow to the ego, or whatever is left of it at this point.
i'd like to know if, as my dosage gets lowered, the side effects will diminish and when i'm off the prednisone completely if they will disappear altogether. any help there?
or if there is any way to help the acne or puffy face

my doctor just put me on something called methotrexate or something like that to help wean me off the prednisone, and does anyone know what those side effects will do? or if they'll affect the prednisone side effects?
i'm constantly obsessing over gaining weight and what my skin looks like and what i eat and how heavy my face feels and the occasional pressure in my eyes to the point where i just want to be put out of my misery.
and after reading other people's stories i really don't understand why this drug is still given out as freely as it is. but maybe all doctors are like mine, they just don't get it.
best of luck to anyone who's on prednisone, my heart goes out to you; i'm right there with you
sorry this became like a book it wasn't meant to be this long

I have been on Effexor for two years. It is a miracle drug for me with NO side effects. I was having panic attacks and severe anxiety that never ended. Once I started these pills I was saved from the despair and the hell of depression and anxiety. I have also learned through mind control, positive self talk, and breathing techniques to avert oncoming attacks. Life is great and I totally recommend this medicine.
I feel terrible for thos people who have had so many difficulties from it. I wish it could help everyone like it helped me.
I do however feel dizzy if i miss a pill. So I can imagine coming off this wont be fun.

I was prescribed generic Wellbutrin two weeks ago today. I took it for 10 days with no problems except mild headache, mostly pressure. I felt great even after only 10 days and had tons of energy. I know it usually takes 3-6 weeks for the full effects but I was already happy after only 10 days. I thought this was a miracle drug. On the 11th day I had a few hives on my inner thighs and on my chest but I didn't think too much of it. On the 12th morning I had tons on my thighs, entire torso from abdomen to chest, shoulders upper arms, neck and back. I even took pictures to show my doc of the ones of my back. I tried to get in touch with my doc which was this past Wednesday 5/27/09 but his office closed early that day. I then called my pharmacist. He told me to go to the ER immediately. He asked if I was having shortness of breath and I told him I couldn't tell if it was related to meds because I am prone it anxiety and I was a bit anxious about the hives all over. I went to the ER and they gave me a shot of Solu-Medrol (a steroid) in the hip and but me on a steroid (prednisone) pack for 6 days. I only took the prednisone that Wednesday night. Yesterday (Thursday the hives were visible but soo much better, and today (Friday) they are completely gone. I am so disappointed that I had this reaction because I loved taking buporion (generic wellbutrin). I wonder if it's just the generic that does it because I read someone else say that the name brand didn't give them hives but the generic did. I will have to check in to that. The ER doc told me to stop taking so my last does was Wednesday morning. (ohhh by the way I was on 150mg once in morning and once at night, so 300mg/day and I was on the wellbutrin SR kind)

I have been on Prednisone for 3 months for PMR (polymyalgia rheumatica)and so far the pros have far outweighed the cons. PMR is an extremely painful condition that affects the shoulders and hips especially at night and early morning, I spent all of December and January sitting upright in a chair trying to sleep, untill I was diagnosed and prescribed Prednisone and oxycodone. I started at 25 mg and I'm now down to 15mg. The side effects that I do have are weight gain (about 10 pounds), mild mood swings and insomnia.I am an avid bicycle rider (25-35 training miles per day on week days a lot more over the weekend),I am 60 years old and now back on the bike. The strange thing is after about one month back in training I am much stronger this year than last even with the added weight. Last year, a solo, 30 mile hard ride I would average about 17 mph this week I went out on my same training ride at 19.4 mph, over 2 mph faster. Everything I read about Prednisone says that it wastes muscles,but I have become stronger. Is it possible that it's the Prednisone?

I've received a few Kenalog shots over the past few years for pleurisy. I just got another shot today. For me it's a miracle drug. It relieves the pain within a few hours.

The only side effect I have ever had is a huge dent in my butt cheek where I got the shot. Having a dent in my butt is a small price to pay for relieving the excruciating pain of pleurisy.

Holy crap this website is depressing! Paxil is not all bad people! I've been on it for 1.5 years. I'm a 24 yr old female. I take it for social anxiety and panic attacks. It takes about 3-4 months for your body to adjust to taking it. You are likely to experience MINOR side effects. I had a lot of sweating, tiredness and HAPPINESS. Yes, I was really happy...its an anti-depressant after all. After that you might be a little more tired than you use to, but other than that it is fine. You can't quit cold turkey, you have to be weaned off of it...just like you will be gradually put on it. I take 30 mg a day, but started at 10 the first couple weeks. Don't get freaked out because of all the bad reviews on here. Everyone just wants a place to whine about their bad experiences and how horrible their life is. Paxil cured my panic attacks and my anxiety. I feel so much better. I think so much more clearly and I don't constantly worry about what everyone thinks of me. Would recommend paxil to a friend.

Ive been on meprozine or just plain demerol for 5 years now i do not take more then 1 pill in 24hr and then i try to put days in between doses i have OI a brittle bones and kidney stones and this is the only pain medication period that i can take with out having a bad reaction. as far as mood swings i don't have any if any thing it keeps me calm but it will only stop the pain if you take it on the first on set, if you wait and take it till the pain has gotten worse it simply wont work at all. there is one side effect it keeps me awake lol im the only person i know who can take this and stay a wake all night

My 13 year old son took Topamax for 5 months for migraine prevention. The day he started taking it, the migraines stopped. We thought it was a miracle drug. After 2 months he was experiencing nausea and stomach aches for a couple days at a time. These then increased to 5 or six days of nausea and a couple days of feeling fine. He was prescribed medication to help with the nausea but nothing worked. On the fifth month he was in bed for 22 days straight. The neurologist didn't think it was the Topamax, but I insisted he be weaned off. After 8 days of no Topamax, the nausea finally stopped, the migraines returned. The migraines are more manageable than the constant nausea. So no more Topamax!

I have been taking the advair diskus 100/50 for two years, and I also thought it was my miracle drug. I can breath great , and only take my inhaler a lot less. I also have hoarseness, due to the advair, but recently was told by my doctor I have a mild heart murmur. I'm not sure yet what I'm going to do, maybe talk with them on what else I could take instead of Advair. It's hard only because my breathing has been so good, but my heart is also very important. I have not had any leg problems, I have had some problems sleeping, not to bad.

I would like to say something about advair that is POSITIVE. I have taken this drug, with NO SIDE EFFECTS for 5 years now and it has made a huge difference in my life.
I have had no isues with thrush (i rinse and spit) or weight gain or hair loss or coughs-

please don't condem a drug just based on your experience. reading through these comments I see a lot of times this has been prescribed fr folks who were not ashthmatic or with COPD. This drug is not for folks who don't have hyper reactive airways-but for those of us who do, it has been a lifesaver.

BTW I changed careers 2 years ago and entered the health field as a Respiratory therapist and adair has helped many many people. But its not a miracle drug-it has a specific purpose and if hat is not your problem, its not likely to be a good solution.

My son is almost 4 but has been on Singulair since he turned 3. We saw an immediate improvement in his allergies and asthma and thought it was a miracle drug. That is until we started to see our sweet, outgoing little boy change into something we barely recognized. We thought maybe it was just a stage he was going through or something and didn't connect it to the Singulair until his doctor accidentally wrote his refill prescription for 5 mg. instead of 4 mg. After about 2 weeks on the 5 mg. his mood swings increased substantially. He cried for hours everyday at school. He had previous trouble with his emotions at school on the 4 mg. as well. He continued to cry and throw fits at his preschool so often that he was ending up in the principals office. At home, he became clingy and so emotional that he would cry about everything. After doing some research on Singulair, I immediately took him off the drug. Within 1 1/2 weeks off of the drug, my little boy was a different child. I thought maybe I was the only one who had noticed until his teacher came to the car and ask what happened. She said that he didn't even resemble the same child that started school. He is sweet, and calm. He can take discipline without crying and gets praise every day instead of going to the principals office. His trouble sitting still and listening to the teacher are gone and her push for us to have him tested for ADHD has ended. He is now a star student. The only difference is the removal of Singulair from his little body.

I have been taking a generic version of Wellbutrin SR 150mg for almost 2 months now. I also take Zoloft 50mg. Before I started the wellbutrin, I had been taking zoloft for over a year to help with depression. The zoloft was working very well for my depression, but it completely killed my libido and as a newlywed, I felt something had to be done as it was beginning to affect my relationship with my husband.
So my doctor prescribed the wellbutrin. For the first couple of weeks I experienced a lot of nervous energy, a shortness of breath, a bit of nausea, forgetfulness and confusion. I almost stopped taking it because I didn't feel it was helping my libido either. But I stuck with it and after 3 weeks, it felt like it was definitely having a positive effect on my sex life. My husband noticed it too. He mentioned how much more responsive I had become when we were intimate. After 2 months, I am absolutely convinced that it has changed our lives and our relationship.
It is not, by any means a miracle drug though. I have a few complaints about it, the main one being the CONFUSION that I experience for hours after I take it. I was taking it in the morning before I went to work and everyday I noticed that I was not as sharp and efficient as I usually am. I figured this was a temporary side effect so I kept taking it as usual, but it never went away! I kept forgetting everything, lost focus easily, had dull headaches, and generally felt as if I could not connect to what I was doing.
SO...about a week ago, I thought I would try to take it at night...when it's not as important to be sharp and focused (and more important to be turned on). And it has turned out great! I'm so glad I started to do it. It doesn't affect my sleep...in fact I think I sleep better. And when I wake up in the morning, my dull headache is gone and I feel less foggy. At work, I feel normal again. My short term memory has recovered and I don't get confused as easily.
If you suffer from a lot of memory loss and confusion from this medication, I definitely suggest taking it at night. It has really helped me! Thanks and good luck!

I just started on topamax and it has done wonders for me i suffer from cyclic vomiting syndrome and have suffered for many years making my teenage years absolutely horrible in and out of hospitals all the time, despite some minor side affects i have my life back i can go on vacations i can spend the week end at a friends house without being scare i might end up in the hospital its an amazing miracle drug and i thank my doctor for finding it and prescribing me it.

I have Autoimmune Hemolytic Anemia (AIHA), was diagnosed in Feb. 2008. Have been ill for several years and finally it came to a head in Feb. I had a blood transfusion and then in the hospital 6 days later with a hgb of 4.0. I was so toxic and my blood so screwed up I nearly died. I was given another transfusion then (total of 5 pints of packed red blood cells) and started on Prednisone. For 3 days given liquid Pred injections, starting at 1000mg, tapering down to 250mg., then on the pill form at 100mg. Sweat poured off of me dosing down. I was off work for 2 months. I am still tapering but am now at 1mg. DR. added another drug, Danazol, after getting to about 10mg because my blood started going crazy again. My side affects with Prednisone have been, Euphoria, no depression, LOTS of hyper brain activity, thoughts running a 100 miles an hour but body at slow speed.Visual problems and a feeling of being highly drugged. 2 to 3 hours of sleep each night, compulsive behaviors and a lot of pacing back and forth. Couldn't hold my concentration because my mind wandered so much. Extreme Tremors in my back, hands and head. Wanted to talk constantly, if no one was around I talked to my Chihuahua or the TV. My cheeks puffed up and became hard and had a fat pocket puffed up on left side of my neck. My dog thought I was crazy, she was tired of the lights being on at 3 or 4 in the morning. Legs looked skinny but didn't gain weight until I got to about 60mg. Gained 25 lbs total. Tapering caused bad spasms in my calves, feet and hands. Thigh muscles would get extremely weak each time I went down a dose. At 50mg I started getting sleepy and could hardly stay awake. Went back to work at 35mg and couldn't remember how to sign on to my computer. Some memory problems since I was in the hospital, couldn't remember how to spell words I knew as a young girl. Started having hip pain about 3 months into the Pred, that hasn't stopped. At 10mg feet, knees, shoulders hurt deep in the sockets, muscles below my neck knot up, may take a while to totally get off this. Read on a couple of blogs where people cut a 1mg tab into 4 pieces to taper off the Pred. because of side effects. Had thrush in the beginning and break outs of shingles. I hope to God I never have to get back on this drug again, it is so HARD on the body but it did do what it was given for, to repress my immune systems. My next step is Spleen surgery, hope this is a cure for me, am sick and tired of being sick and tired. Wouldn't advise anyone to take Pred unless it's a life or death situation. It's prescribed too liberally and people have multiple problems, worse than I have experienced. I've probably forgotten some things, but there's enough I've mentioned to give you an Idea it's not good, but if Pred is all you have then you do what you gotta do!! My puffy cheeks have went down though, now my hair has become curly but at least I have hair and my chihuahua stills loves me!!!

My 71 year old mother was put on Advair approximately two years ago after she was diagnosed with COPD. She has always been a tiny, petit woman her entire life, and after being placed on Advair she has nearly doubled in weight. This week she has broken out in shingles (herpes zoster) on her back and left breast. For a year she has had psoriasis on her right hand. Never before has she had so many rashes and skin issues since being on Advair. She has also experienced joint pain and numbness since being placed on Advair and began having panic/anxiety attacks as well - something she has never had in her life. Also, the hoarseness, or "lump in her throat" she is always trying to clear is nearly always present. Monday she is suggesting to her GP that she be weaned off of Advair altogether and we'll see what other options are available. Maybe this is the "miracle drug" for some; but for others it has been a nightmare.

I have to comment on some of the Lamictal "new comers". I've taken Lamictal for 1 1/2 years. For the first 6 months, this was the miracle drug. As months went by, I began all of the same symptoms: fogginess, weight gain, short-term memory loss, NO libido, headaches, and nausea, to name a few. As of this moment, I am weaning off of the Lamictal. HARD to do. This is not a drug that can be "stopped" immediately. On my fifth day of weaning off, I am dizzy, tired, weak, irritable, and have vomitted. Only about 3 days left. I am starting Topomax after. I'm anxious to see if there is any difference. Especially the weight gain part. I went from 120 to 135 in one year. (I run and eat healthy meals.) I will continue to take Effexor, which, in 2 years, has had little or no side effects. My advice to anyone just starting to take Lamictal is to GO SLOWLY. My doctor had my doses increase so rapidly that I didn't really see if the lower doses would have worked. (I take 200mg.) The bottom line is to do what feels right for YOUR body, rather than a specified dosage. Best wishes to you fellow BP-ers!

I have had trouble with eczema/psoriasis for several years and it has spread to most of my body. Hands, arms, elbows, back, chest and stomach, hips, back-side of my thighs, knees, bottoms of my feet, scalp, inside my ears, forehead, what haven't I mentioned? So far, Prednisone is the only medication I can take that clears it up. Trouble is, the doc won't let me take it long enough to completely clear the rash before I'm tapered off. After reading some of the other posts, I've got to say that I've never noticed any adverse reaction. My appetite is up a little, but my energy level is also up and I burn off any extra calories. I sleep better (no itching) and for longer periods, wake feeling better, have a better outlook for the day and am ready to go. I'm a salesman, so my mental attitude is important, and my wife and family all agree that I'm less moody and in a generally better frame of mind while taking Prednisone. I've noticed no stomach or bowel distress except for being a little less regular than normal. But no constipation and no diarrhea. I'm 61 so a few muscular aches and pains and joint stiffness are to be expected, but I've noticed no unusual incidents. While I don't advocate taking large doses (define large doses???) for long periods, I've read that taking Prednisone on an every-other-day basis can be effective while greatly reducing the risk of side-effects. I think Prednisone has been a real "miracle drug" for me and just wish there was something as effective without the side-effects.

I have asthma that was not controlled. I coughed and wheezed constantly. I had trouble eating, because even the food passing through the esophagus was enough to cause an attack. I was in and out of the emergency room for years, and the Ambulance folks knew to arrive with epinephrine when I'd call.

I started taking Singulair sometime around 1998. I haven't had any serious problems since then with asthma, and have had ZERO side effects.

Every drug has side effects for some people. For me, Claritin causes my heart to race. I can take that or that purple circurlar inhaler thing. I had a terrible reaction to that.

For ME, Singulair works. I am not sure it should be given to children if they are having severe problems. But it certainly should NOT be removed from the market...because people like me needed it to control their asthma.

My doctor prescribed lamictal after I reported hypomanic symptoms from prozac. The first couple of days on lamictal I thought it was the miracle drug; it really eliminated my mood swings. But as the days progressed, I began to have the following disturbing side effects:
- terrible insomnia (waking in the middle of the night and can't go back)
- horrifying violent dreams (of animals and people being hacked to death with machetes... interestingly, I reported this to my doctor and her response was, that just means your brain is adjusting to the chemicals...easy for her to say, she's not waking up with terrible memories of these disturbing dreams)
- weird pains and stiffness in my neck with swollen lymph nodes in the neck
- increase in anxiety and feelings of panic
- increase in feelings of anger and agitation
- feeling of detachment
- thoughts of suicide and the meaninglessness of life
- carbohydrate cravings and weight gain of nearly 4 pounds in 2 WEEKS!!
(weight had previously been stable for years)

These symptoms all appeared after taking the lamictal after only 2 weeks. Even though my doctor recommended actually INCREASING the dose of lamictal and/or adding prozac, I decided to wean off the lamictal (I was on the smallest dose of 25 mg) as an experiment to see if the symptoms would go away...
YES they did!! Every single one of them went away and were COMPLETELY gone after the second day of discontinuing the lamictal.

I know that this medication is being touted as the new miracle cure for bipolar II especially, but I think more clinical studies need to be done on lamictal. This experience was a very scary one and not unlike that reported by others on this site.

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.