Nose bleeds symptoms and conditions

i was put on prednisone 3 days ago due to asthmatic bronchitis. i was put on 60 milligrams a day. which to my understanding is a really high dosage.
long story short my cat would not stop meowning and it made me so darn angry that i wanted to throw him around the room and kept chasing him around screaming at him to shut the bleep up and tearing him out of the window every time he tried to get up in the window. i love my cat dearly and he is like my child. i have never EVER treated him badly. he gets more love and affection than most people give their children. he was crying and scared to the point of defecating all over my room. this had no affect on me. it just made me more angry. normally when an animal is scared or hurt i am incredibly empathetic.
on top of it i have had severe nose bleeds, and severe heart palpitations. this is after only being on it for three days.
i know this product is good for its purpose but as far as the side effects go, i think i would just rather live with my asthma symptoms. i was scared that i was going to lose control and injure myself or my cat or anyone who got in my way. i do not recommend this drug by any means.

I have been on Femcon FE since May 8th, 2009. I know not long, but I have a side effect that I have not seen listed here. Anyone having issues with nosebleeds?

I haven't had any for over 5 years then suddenly I have 2 massive ones. I have had some of the sick to my stomach feeling like others have mentioned here. But that is all to this point.

I was put on this med since I was showing a thick uterine wall, painful periods, heavy periods, and bleeding between periods.

Its just the start of the med so I will give it the time to work, but I am sure keeping records of how I feel each day, when I have periods how it goes and what happens between periods.

Anyhow just wanted to ask about the nose bleeds.

TYTY

Thank you so much for this site... I thought I was alone and loosing my mind. I started on Coumadin in Dec 2008... after 3 months I am falling apart... I can't seem to get anyone to listen... I am tired and cranky, gaining weight faster than I can keep up... I have dizzy spells and headaches, nose bleeds and just an overall feeling of not being me... like said above me... I miss me. The symptoms are so similar to being depressed its hard to pull yourself out... its hard to explain to other people how you are feeling because your doctor continues to tell you it is all in your head... I am a mess.

I've only been on topamax for about a month and a half and already I'm feeling some interesting side effects. In the first week of taking the medication I had such pressure behind my left eye I thought it was going to pop. It eventually went away and has not come back (thank the Lord). I also experienced some pretty nasty numbness, tingling, and uncomfortable pins and needles in my fingertips and toes/sole of my foot. The tingling in my hands usually lasted a few hours and the tingling in my feet only lasted for a couple of minutes. This tingling is never predictable.

Eventually the tingles went away and I was tingle free for a while. But in the past few days they came back. It actually coincided with my PMS. The tingles came back and with intensity about three days before my period started. I was wondering if it was common to have a side effect return or increase in intensity around your menstrual cycle? My hormones are pretty nutty and the reason I'm on topamax is to stop severe migraine auras and slight seizures that are tied to my menstrual cycle.

The feet tingles are the worst. It feels like I'm being jabbed with needles and I hate when it happens while I'm sleeping because it wakes me up and I can't fall back asleep again until they go away... they are that irritating. The hands I can deal with because I'm used to my left arm going numb when I was having the auras.

My sleep patterns have been disturbed because of topamax... I'm not too peeved about that. I still manage to get enough sleep. However there are times when I'm out with friends or having conversations and I'll know the word I want to say and I'll just bust out the wrong one. Like for example saying symphony instead of sympathy. My friends have gotten used to it and know what I'm trying to say. It cracks them up when my word salad produces sexual innuendos on accident when I really mean something else. BUT it's really messing up job interviews at the moment. I'm a bright and articulate person who is getting her BA in Anthroplogy and Archaeology, minor in History and am trying to get research assistant jobs at museums and universities. It's really hard to get a job when you are sitting there sounding like an uneducated moron high on crack.

I haven't had problems with memory, thank the Lord. Even though I've got the word salad going on (and it's strange... the word jumbles are only when I'm speaking... I'm super coherent when typing) I'm not forgetful. I was able to make it through finals week perfect, while juggling a full work load. I hope I don't start losing my memory.

I haven't lost any weight (AW SHUCKS!!!!!). I was looking forward to that one. How soon should I expect to lose weight by, if I do in fact lose weight? I'm a difficult duck when it comes to weight loss. I've been at a stable weight since I was 13. I'm an athlete so my body is my temple sort of thing. But in the past two years I've put on a little bit of unwanted weight in certain areas when I stopped hitting the weight machines :( My question is, if I haven't lost it yet... will I lose any?

I'm also classified as type II bipolar, obsessive compulsive, and anxiety disordered. I've noticed my mood has stabilized. I'm not as all over the place as I used to be. My highs could get pretty high and when they would get up there my obsessive compulsive would almost go on a little joy ride. And when I was low, I was super low and my anxiety would take the depression out for a spin. But now I feel a calmness and a zen that I never felt previously. It's not an apathy I can certainly tell you that. I feel like I am in control of my life. I thank topamax for that.

Reading all of these posts I just worry that the honeymoon period of my medication maybe over. I worry about other side effects cropping up. I think that I can deal with my tingling extremities and that I can manage my word salads. I don't want the pressure in my eye to come back. I also don't want to start exhibiting the other side effects. What is the possibility that I will start exhibiting more side effects or are you generally stuck with what initially presents in the first month or so? My doctor also does NOT intend on increase my dosage. He thinks 50mg once a day will do me just fine. Oh and one last question, anyone else experiencing the side effect increase coinciding with PMS?

Sorry for the super long post! All replies are welcome!

hello, im 25 and was diagnosed with lupus nephritis 4 years ago, among other meds i was taking 60mg of pred for about 8 months with chemo for my damaged kidneys. in three years my dose went up and down between 60mg and 15mg. the side effects i had were at first extreme water retention, my skin was like play doe, swollen vulva, swollen leaky breasts, hamster cheeks, extra chin, i had extreme hunger cravings , wanted to eat every thing in sight but my husband helped me to maintain a proper diet and i did not gain any weight except for my face and breasts and water retention for around 5 months after diagnosis. i also had all the other effects like racing heart, chest pain , breathlessness, tiredness, excitement, bad mood swings. now after 5 years i have CAREFULLY weaned MYSELF down to 5mgs a days the moon face has gone down but i have the fatty deposit at the top of my back at my neck that happens with long term use, but only i can really notice it, i get nose bleeds cause skin is thin up my nose, i use glycolic moisturiser and have glycolic peels on my face to help with skin renewal keeping ageing at bay and also have factor 50 sunscreen on prescription, take zinc for my hair loss (prescription 220mgs) has helped a lot with hair loss, use pure glycerin on my body to keep the skin soft and less delicate( glycerin can be quite gloopy and stickes on the skin for a good hour before soaking in but does wonders and is in most mosturising creams, use mouth wash for gum desies to keep the bleeding at bay and keep the teeth strong, i buy probiotic yogurt dring and pills for digestive system to get rid of the gas bloating and constipation/diarrhea, take meds to prevent bone problems, drink a pint of full fat milk with some nesquick mixed in every day, i get bad headaches after eating sweet things sometimes that can last all day, i just live with them. don't take pain killers, they just go after ive slept
im constantly finding new ways to cope with the preds, and am now 3 and half months pregnant with my first baby, doc told me 4 days ago that he wants to start putting up my steroids to protect baby and me, so im panicking a bit about the moon man coming back, and hair loss has started again big time also cause of pregnancy. once ive had the baby im going to start back on my routine. perdnisolone is a nasty drug but also a life line for many people who cant get off it and need if for the foreseeable future until something can take its place, so im jus trying to stay 1 step ahead of the drug, the only thing i struggle with is exercise , starting to loose my memory more often, and eye sight is playing up, keep going cross eyed!!! gonna try that mangasteen stuff, worth a shot...
thanks for reading, sorry bout spelling.
love l.

I am so thankful to have found this information!!!!! We have an appt tomorrow afternoon because of my 3 1/2 yr old daughters chronic leg pain. It hasn't fit the growing pains symptoms and I have to give her Tylenol or ibuprofen every day - she is inconsolable with pain at times. (She has been on Singulair for 2 years!!!) After reading these situations, I checked singulair's side effects which include 2 other symptoms that my daughter has all the time without explanation - nose bleeds and stomach pain!!! I am taking all this to the doctor appt tomorrow. We missed a nightly dose of Singulair once before and she had to start breathing treatments the next day, every 2 hrs for a few days until we got her breathing under control again. I am anxious as to what our alternatives are and what they're side effects may be....
Thank y'all for sharing your experiences !!!!

In June 07 I rushed into having the coil fitted, having had a double rollover with two beautiful babies successively, only 13 months apart. No 2 baby had his first birthday end-Mar 08 and as I was no longer breastfeeding I suppose I began to stop making "new baby" excuses for my moods, brain fog, lower back pain, extreme fatigue, irritability if not getting a nap in the day even though had good 8 hrs sleep on night and weight gain (dress size).

Over the last few months I have gone on to experience severe PMS symptoms (which I didn't have prior to coil), clearly a build up within the body for not being able to bleed regularly. These included crying spells (for no reason), feeling very flat/exhausted almost like "out of body" old woman (I'm 33) and feeling bloated/pregnant - they would last roughly two weeks and then I would get a day's bleed which explained the cause. I even took a pregnancy test although it was negative. For me the final straw has been the onset of migraines (a year on) lasting several days and just being constant.

Having two energetic toddlers and little family support, I simply didn't have the luxury of continuing with these symptoms and could no longer tolerate the thing inside me. Luckily, my hubbie agreed and so had coil removed on Friday (total of 14 months) . Already, 2 days on, the bloating and brain fog have eased off. The migraines are still present but am assuming it will take a while for body to sort itself out. I'm so looking forward to feeling like "me" again with and getting fruity with the hubbie.

Additionally, have had nose bleeds over last few months and a yeast infection - not sure if these are linked in!

My 17 yr old daughter received her first Gardasil on April 17,08 with only pain at the injection site on June 16th 08 she received the 2nd within days she started complaining of severe headaches and eye pain so I scheduled a routine eye exam thinking that her glasses may need to be updated. After her exam her optomatrist called me intot he room telling me that she had severe swelling of her optic nerve and scheduled her for an MRI before we could get that done she went to the ER for severe pain in the eye and headaches there they did the MRI and it was normal no tumors or anything that would cause such headaches. On July 3 she called me from work asking to be picked up because the pain was so bad she could not function at all she was weak, dizzy and overall just not feeling good. I took her to the ER again where they performed a spinal tap and tons of bloodwork and admitted her for pain control on July 5th she had a 2nd spinal tap and every day more bloodwork was performed so far ALL tests ran have come back normal. She was in the hospital 5 days. She seen her ophthalmologist a week after being released and we talked to her about the Gardasil and she felt there was enough "coincidence" to have my daughters pediatrician file a adverse reaction form. That has been done and my daughter has learned to live with the pain since nothing seems to help it anymore. Also the last 6 weeks she has had bad insomnia and nose bleeds.

I am writing for my 14 year old daughter who was put on YAZ, not for birth control as she is not sexually active but for her mood disorder, which I believe is just being a teenager in general...but her therapist told her that it would help her moods, acne and that it even would help her loose weight! cant stand doctors at this point, have no faith in the system at all. I should have had her read this site because..... since day 2, severe stomach pains, throws up every day. shortness for breath ~ pains in her back and shoulder and down her arm like a heart attack. nose bleeds, headaches and OMG moods ~ cant even express the mood that she has been in for 3 weeks. so last week I take her to the doctor ~ of course a nurse practitioner sees her instead of the doctor that is not in. and asks my 14 year old if she would like prilosec or pepsid or zantac? asks a 14 year old and then offers her naperson and tells her that she should try these along with the YAZ. when I questioned the rational of keeping her on this drug she became defensive and said we should try it out for a couple of months. I allowed her to try this way for 2 days and then said nope no more pills. Just came home from the doctors office where they immediately took blood and is sending her for a sonogram to see if she has any cysts in her ovaries. I am just disgusted with the medical doctors who push pills and pharmaceuticals who don't give a damn but to make money. Will keep my eyes out for the lawsuits now. For camp refund for all the days she has missed for taking this horrible drug. hopefully she will not have any long term problems. will always think of this pill if she does.

Hello everyone. Im twenty years old and this is my second attempt of using Nuvaring. The first time I was on it I thought I was ok, but when I think about it today..(two years from the first time) things weren't ok. I had thoughts of suicide and lacked self worth. However, I decided to get off because of financial reasons. This being my second attempt, Nuvaring is has already provided me with about 4 migraines a day. At first I thought they could be managed until they were accompanied by nose bleeds. Ive lost my job, fiance, and social life due to the mood swings and irritability that I now have. This will be the final time that I will ever use this CRAP!!

Hello everyone. Im twenty years old and this is my second attempt of using Nuvaring. The first time I was on it I thought I was ok, but when I think about it today..(two years from the first time) things weren't ok. I had thoughts of suicide and lacked self worth. However, I decided to get off because of financial reasons. This being my second attempt, Nuvaring is has already provided me with about 4 migraines a day. At first I thought they could be managed until they were accompanied by nose bleeds. Ive lost my job, fiance, and social life due to the mood swings and irritability that I now have. This will be the final time that I will ever use this CRAP!!

I was diagnosed with graves disease last year, I had a really acute case that turned me into a total nut job.
In October after going through several thyroid storms and the doctors not being able to keep me stable with medications, I had a full thyroidectomy in October.
I started on .100 mcg of levothyroxine and then the dosage was gradually decreased, I started having a lot of random body aches, mood swings, lots of muscular pains and no energy.
They ended up raising my dosage and detected that I had a large vitamin D deficiency, after several treatments of taking 50,000 units of vitamin D, and also adding my levothyroxine dosage I started feeling better. I still have mood swings here and there, and feel sad periodically, but the last month or so I've been feeling more fine than I have in a long time. They have me on .170 mcg of levothyroxine for two months now. Last week I started getting headaches more frequently, and one of the times I got this nose bleed.
This past weekend I got a headache, and then later that night I had another nose bleed.
I don't usually get nose bleeds or this many headaches so I'm a little concerned.
Also the last time I was getting headaches and constant nosebleeds was when I was really hyperthyroid.
As far as the doctors go, I'm in between insurances and quite honestly I've been frustrated with both my pcp and endocrinologist...

with taking tcp, after a few days of usage, i started to develop nose bleeds where i hadn't ever had a nose bleed before that. im not sure if it was caused by the drug but to go 16 years with out ever having a nose bleed to having 3 in two days is quite bad. and another thing never drink for the entire day and night after taking one of those pills as it causes extreme headaches and eye irritation (sorry for the bad spelling im dyslexic)

nose bleeds ( bad ) and memory loss

My daughter 19 has only had two gardasil shots but started having nose bleeds. She would wake up in the middle of the night and her nose would be bleeding. She has never had a nose bleed before, now she gets them a few time a month. I am not having her get the final shot.

In September of 2007 my then 13 year old daughter was put on Singular for mild asthma. At the time she was a straight A student, vice president of our school and a popular girl who's guidance counselor described as "the glue of her grade" because she was so well liked. In November she told me that she was struggling with advanced Latin and Science. She asked to drop down to on grade Latin so we did. In December her science teacher notified us that she had a C average. She told me that she thought she had ADD/ADHD and she couldn't keep up. At the same time she was having a lot of problems with friends at school and we just attributed it to being 14. 3 weeks ago we discovered that she is significantly behind in English and it was then that she told me that she is been having horrific night mares. She said that they usually involve someone killing her or her killing herself. She said that they were so graphic that she couldn't repeat it out loud. She also said that she would feel waves of anxiety that would come over her at school and she would act "witchy" to the kids in her class for no real reason. She said that sometimes when she is trying to do her homework she will read the same passage for 2 hours and still have no idea what it's about. She also said that the suicidal thoughts from her sleep happened during they day and that she had thoughts of her harming herself. Fortunately her pulminologist told us that this may be caused by singular and we immediately took her off of it which was 2 weeks ago. She has only had 1 "bad dream" not even a nightmare since. She had one anxiety attack 3 days after she was off it and she describes her moods as the "cloud lifting....slowly". Now, we have to pick up the pieces. Her grades have suffered, her friendships have suffered and most of all her self esteem is very low. I'm grateful that we found out the cause but I feel as if my daughter lost a year of her life and I worry that because Merck won't admit there are side effects we can't find out how long it remains in their system. Is anyone else concerned about the long term affect and has anyone pursued a class action suit to try to get this drug tested properly?

Boy i thought i was the only one and my family thought i was just making this stuff up. I have asthma and have had it since i was 10 now age 23. Recently i went to the doctor because i was using my albuterol inhaler to much i was using one a week. The doctor told me i had bronchitis now even worse so he put my advair 250/50 ive been on it for about 2 months. One week after taking it i notice my voice changed and my troat was bothering me, i was having nose bleeds. This week i started having really bad headaches my hands fall asleep at night without my even sleeping on them, also bad back pains my legs get bad cramps at night. One bad thing i really hate is i know i have gained a good mount of weight about 30lbs in so little time. My husband notice my mood swings ive been having towards him getting mad at him for no reason. Thank goodness im not going crazy seeing that im not alone. IM GONNA STOP TAKING THIS MEDICINCE AND CALLING MY DOC MONDAY MORNING!!!!1

I have two children on singular as of September 07. When my 6 year old was an infant he was always congested, we changed his formula a couple of times until the doctor decided to do a blood test to check for allergies and the results came back as an allergy to milk. He then started to have sinus infections and had to have his tonsils and adenoids removed. The surgeon said the coughing and the snoring would stop after surgery but it didn't. I was having problems with seasonal allergies myself and was put on Allegra and Veramist so I decided to take him to the allergist as well. He was tested and was also found to have seasonal allergies. Within a day or two after taking the Singulair 4mg chewable tablets he started sleeping through the night with no coughing or sneezing in the middle of the night. My friend just recently had a similar problem with her daughter who is around ten years old. She was found to have asthma but the inhalers that she was put on didn't completely work, so the doctor put her on singulair and her mother said the Singulair is the best. My 14 year old son also has food and seasonal allergies and takes Singulair but not on a daily basis only as needed and he doesn't have any problems.

I'm totally shock..about this....my 10 year old daughter is been on singular for the past 2 years, and she struggles in the school with concentration issues, sinus infections ,cramps in her legs, nose bleeds..and after reading this I can not believe that I 'm intoxicating my child because the pediatrician never told me about those side effects.....I can't believe this medication is in the market with safe issues....So what is the real meaning of safety for the doctors in our days.....scary!!!

I am always tired and kinda shaky I cant figure out if its the Lamictal or Seroquel which ever I am stopping it when I find out what it is I cant handle the side effects I am very sensitive to the side effects of any meds.

I have read a lot of these blogs and I am seeing that many other people have the same side effects. I was diagnosed with hypothyroidism when I was in 6th or 7th grade I think and I am now a high school senior so about 5 years taking Synthroid. the doctors said that my antibodies had completely destroyed my thyroid gland so I wasn't getting any of the hormones I needed which became very noticeable when I started gaining weight and loosing energy in 5th grade. I haven't really seen any weight gain in a while but I still look like I am overweight. I am 5'6 and 130 lbs so I am about average. Side effects that are also occurring are rapid mood changes, one minute I am happy and something sad happens or I think about something and ill be tearing up. I feel depressed a lot. I am currently on 150 mcg. also during 9th and 10th grade I was put on this drug to stop my puberty so that I could grow more while on the Synthroid I guess it helped a little with height but I still look like a freshman. I don't know if I should stop taking it or keep taking it because I stopped for about a month once and started getting really sick, I would get really bad nose bleeds at random, had constant migraines and felt sick to my stomach. I started taking the Synthroid again and felt fine. I really don't know what to do.

the truth.

word of advice...dont take "prescription drugs" unless its for life-threatening issue, but for anything else dont take it, prescription drugs are'nt always good and ALWAYS come in with numerous side-effects.

i use natural ways to cure my syptoms for now on, for example, good nutrition, exercise, sleep, herbal tea drinking, talk therapy, you see, there is a alternative. the doc just want me to take meds and get money from the insurance for doing so.

they say its "hospital policy"..i think now i see the corollation between money and meds

i took geodon at 20mg for 6 months because the docs "said" it "prevents" any chance of pyschotic behavior, i was like, oh no doc, i dont have those behaviors, i try to convince them, but they hold me against my will and i had to take it in order for them docs to release me from the hospital..because its "hospital policy".if i dont take it..i dont leave.

in the first place...i went to the hospital to talk so i can feel better from my arguments with my family, not to be treated with medication, i did'nt expect that, they prescibe it to me without my knowledge and consent, but they got consented it from someone else,and its none other than my parents who were my enemies at the time, and my parents use the oppurtunity to use that so they can further punish me. and now im pissed...and am going to press charges for couple million dollars because the damages is too great, my body is like heating up even if its dead in winter, having feel like im going to get nose bleeds, which rarely occurs but did on several occasion..if it did..it last up to two minitues continuasly, so i stop taking it in protest, i feel a little relieved, but the damages is too great, i even lost my job because i was so exausted, i could'nt even perform my hard work duties anymore , and iam feeling that my metabolic rate is severely high, which produce excess body heat in the process. and beggining of this year, i feel that iam developing a sensitivity to extreme heat due to the meds. i dont know the extent of the sensitivity, and iam also developing a fatal disease called neuroliptic malignent syndrome. i want to avoid that at all cost. im not for sure, but i need a physical test done...the whole nine yards.

neoroliptic malignent syndrome(NMS) is life threating neorological disorder most often caused by an adverse reaction to neoroleptic or antipyschotic drugs.
in two weeks after the initial drug being taken or whenevr takened,
the first syptom to develope is muscular rigidity, followed by high fever and changes in cognitive fuctions and other symtom may vary. but includes blood pressure, confusion, coma, dilirium, muscle tremors, when symtoms do appear, they can peak intensity within three days. these symtoms can last 48 hours to 40 days. seek medical help when occured for over a week.

a raised creatine phosphokinase(CPK) plasma concentration will be reported due to increased muscular activity, the person may be hypertensive and suffering from a metabolic acidosis, which means the blood ph level is low than 7.35 due to the increased production of hydrogen by the body, or the body inability to form bicarbonate in the kidney, this can result in diarrhea, coma, or even death. together with respitory acidosis, its the two main acidosis.

unfortunately, the symtoms may be reported as symtoms of "mental illness" by the doctors which delays treatment.

but thats is all i can say...

i dont know now..but this damages doned to me might last years, i hope its not permanent.

just remember people....ask questions about your medications you're taking, if you feel the docs is covering the truth and just says the "good things" about meds, find other sources, i studied for two years to come with a report that corresponds to my symtoms, i just want to be accurate so i can have proof so i can take them to court!!!!

and of course, as with personal opinion for evryday life, "certain things and objects, rules and regulations is not for everyone but applies to some, evryone has different preferences, like certain meds, favorite colors of their cars, radio stations, etc...remember..

nose bleeds -tylenol acts like aspirin and thin the blood

I am a 34-year old women who started 50 mg of Toprol-XL 4 days ago for a rash of panic attacks I experienced earlier this week, after having high blood pressure and occasional panic attacks in the last 3 months. Since then, I've had migranes for the past 2 days, bad allergies, stomach pain, loose bowel movements, slight difficulty breathing, frequent urination, and tiredness/lethargy during the day with trouble sleeping at night. I was already feeling strange my 2nd day on it and called my internal medicine doctor, who, of course, told me to stick with it. At this point, I'm ready for safer, natural alternatives. I'm will call the doctor tomorrow to tell him that my mind is made up and ask for instructions on how to wean off of it safely.

I have been on 40mg for about 4 months now. My feet ache a lot after work now and I have started having nose bleeds. Could these be symptoms caused by this drug?