Migraine headaches symptoms and conditions

I just happened to do some research about lisinopril, and happened to stumble into this website. I am 43 years old, newly diagnosed with type 2 diabetics, i also have a history of hypertension and migraine which is under control. my physician just switch my medication from Norvasc to lisinopril, Im already on my 3rd week of taking it, 20mg a day, however, i noticed that i have more frequent headaches, more of a migraine headache that pulsate in one side of my head, i tried taking some over the counter medicine, but with no relief, i went back to see my doctor, and i was given some sumatriptan for the migraine, but at the back of my mind, i already suspected that the lisinopril might have triggered my migraine headaches, i have a relief when i take the sumatriptan, however the migraines keeps coming back. and its been seven days already, i was not able to work one day, because the migraine made me nauseated and vomit. i was doing well with my other medication, and never had migraine like this that last for 7 days up to now.after reading the comments. i have second thought of taking this medication.it seem like it might be the one that triggers my migraine headache. what do you think?

I suffer form migraine headaches as well. The Doctor diagnosed me with a condition called "Cluster Headaches". Meaning they come in clusters. They come for a while a leave for a while. No cure, just try relieve the headache. In the past I took extra strength Goody's (w/Caffeine) or Excedrin Migraine, both with Coca~Cola. Both worked, the Goody's a little better but it is not available in California for some reason. It generally took about 45 or longer to start working, sometimes I was doubling up hoping it would be faster. After waking in the middle of the night for over a week with a throbbing head pain directly behind my eye socket I went to the doctor and was prescribed EPIDRIN 325-65-100 MG. The Doctor said to take it the moment I felt the headache starting. That night when it started I RAN to the bottle and took 2 with water. Within 15 minutes I actually felt the pain stopping. At first the throbbing would "skip a beat", then it would just stop as I laid still. Next thing I knew I was sleep. I have not experienced any side effects and I am on day 3. So I will say Epidrin works, don't be afraid to take it when the pain starts, there is no need to take them beforehand, "In the event" you think you will get the headache.

L. G.
Ontario, CA

Just wondering if anyone has experienced sinus congestion (not relieved by antihistamines like Claritin, Allegra, Zyrtec) and not having a cold?

I've been slowing working my dose up on Wellbutrin from 75 mg. a day to 100 mg. to avoid side effects. However, I'm experiencing a sharp rise in migraine headaches and this weird nasal congestion. I can't find where anyone has noticed 'nasal congestion' as a side effect.

Dr. today suggested I stop the medication for 1 week and see if these two possible side effects disappear; which I plan to do. I am small and sensitive to all antidepressants and have to go low and slow. 16 years ago there was ONLY Brand name Wellbutrin which is what I took.....75 mg. twice daily and I didn't have any problems. Don't know if I'm reacting to the fillers, dyes and substances in these Generic Wellbutrin by Teva.

Anyone out there that has nasal congestion or Migraines from Wellbutrin??

Thanks. L.

This is a sad yet enlightening day for me. I can't believe the things Nuvaring has caused for me. I am so glad that I questioned it earlier and found this site as a result. I originally tried NR in February 06 and continued for about six months. I don't really remember side effects from that time. We had a newborn and I was finishing my last semester in college, so I wasn't exactly sleeping a lot. I will say that my libido fell off the face of the earth. It has taken a while to get it back even a little bit. Ever since then I have asked my doctor what could be done and she just would tell me it's normal to lose my sex drive after having a baby. So in May my doctor put me back on NR to help shrink an ovarian cyst that she is worried about. She had me stay on the NR for 6 weeks straight through. I just took it out last Saturday and I will be done with it forever.

Here is what I experienced during my six weeks:
- Libido- zip. zilch. non. nuf said.
- 2 migraine headaches
- Severe neck pain to where I was about a day away from calling a chiropractor
- Couldn't wear my contacts for the past month- my eyes got really dry and itchy
- EXTREME burning during and especially after sex- and if I had to pee, my husband would have to give me a wet towel to ease the burning pain.
- Lack of appetite
- Really bad mood swings/ depression- I am a really optimistic happy person and for the last month I feel so negative and down about everything. I want to cry a lot and the anger has been awful. My boss and I got into multiple arguments and I wanted to walk out of my job. My son has been on my last nerve for no reason, and don't get me started on my poor husband.
- Waking up multiple times in the night and having trouble falling back to sleep.

Once I removed the ring, I have felt lighter and happier. I even sent my husband a racy text message because I was thinking about sex! And my neck pain has disappeared. Unfortunately, for the last week I have woken every night at 3am and stayed up til around 4:30am. My cramps have been awful. Usually they were really bad the first two days of my period. This time, they have lasted for 4 days so far and don't seem to be stopping. I have gotten extremely constipated and this is something that doesn't happen- I usually go the other way. So my stomach has been a wreck of gas pains and cramping. I have been exhausted.

I just wanted to share my experiences. My husband and I were talking the other night trying to figure out what was going on with me, so I feel a bit more reassured that I am not a psycho after reading so many others' problems. I took my computer in to him and read some symptoms to him and he was as shocked as I that this may all be from the NR.

I had 3 cervical shots the last 5/28/90.I started side effects. Puffy face, night sweats, increased appetite, weight gain, before the 3rd shot but didn't realize it's connections to the shots until after the 3rd shot. Additional effects: indigestion, hormonal changes (my period stopped since the 1st shot and is spotty), and the worst...horrible migraine headaches daily. It has been significantly hurting my life-mostly the headaches. No one has an answer or any help. The doctor who administered the shots has no insight since these headaches are so long lasting. Any one experience these type of effects and can tell me if they have worn off. It has been 6 weeks since the last shot!

I have taken Lurpron Depot 3.75mg June 11, 09. I am due another injection July 09,09. I had to get a prescription of prometrium 100mg from the OB/GYN because of the night sweats and hot flashes.Since the injection, I have had and currently experiencing migraine headaches in the frontal lobe and temporal lobe areas. I have slight pain in the temples. I am going to see a neurologist because I was told the lupron may cause brain bleed with people whom have pituitary cancer. I would like to know if the CoQ10 and red yeast rice interacts with Lupron.

Hello,
I have been on Yaz for a little over a year. I have experience a few side a affects, which has me on the path to changing my birth control. Since I was 18 I was on Othro Novum, last year I decided to try Yaz to help me with my mood swings during my period. I have notice I have gained about 8 pounds this year. I have been working out for the last month and my weight has not moved. I went on that website for yas and weight gain. Thinking okay limit my calorie in take and workout. That has not work. Recently, I have been having BAD migraine headaches. I had a migraine headaches the entire week before my period and during the week of my period. I went to a neurologist earlier this week and he prescribed me migraine medicine and told me to get off the YAZ. Oh yea and decrease sex drive. Sex is thing from my mind. So, now the question is what do I go on now. I am 26 and I didn't have this many problems on my previous birth control. I thought about Yasmin but I hear you can have a decrease in sex drive with that too. So what do you go on then?????? lol

I have read the posts below and thank goodness I found this site! I got an injection on Wednesday, 6/17, in my right knee and for the first 24 hours it hurt like heck - more stiff and painful than prior to the injection. On Friday I woke up shaky and started to feel anxious. My face and chest flushed a bright red which lasted all day. Saturday was worse; shaky, heart racing or palpitating, head/neck pressure with headache, hot flashes, nausea and stomach cramping/pain. I even actually had a panic attack (already a predisposition for me). I became uncontrollably weepy and depressed! Today, Sunday, I STILL have major anxiety and headache/pressure. I'm convinced the injection brought all of this on because before this, all I had was knee pain. So, WHEN will these icky symptoms start to subside? I was told the cortisone was good for 4-6 months. I can't live feeling like this everyday for that long!!! Any suggestions or encouragement?

I have been taking Ambien CR on and off for two years. I began to get migraine headaches two years ago which my gynecologist told me was as symptom of menopause. I then began to note everything I ate and all medications I took when I got these debilitating headache. The only thing in common was I had taken ambien cr the night before. I had massive headaches that even prescription medication would not cure. They would start near my temple and radiate up the side of my head. I would always get them on the right side. I began to notice that when I did not take any ambien for a while, no headaches. As soon as I had one dose of ambien cr, the next day I would wake up with a horrible headache. I have since discontinued taking it and I would rather be awake than live with that kind of pain again.

I have had the Mirena for about 2 1/2 years. I had it inserted about 3 months after I had my daughter. Initially I thought it was great, but in the past 12-18 months I have noticed so many negative side effects that I believe must be related to the hormones in the Mirena. My PCP ignored my complaints but I have experienced the following since having the Mirena inserted:
sore/tender breasts, pretty serious weight gain(I diet and exercise a lot and don't lose a pound), severe acne on the chin and jaw line, coarse/dark facial hairs on the jaw line, migraines in the right side of my head, lower back pain in the left side(almost like a sciatica) fatigue. low sex drive, some mood swings, and the expected spotting. Although my PCP dismisses my concerns I have made an appt. with a new gynecologist to discuss my concerns and possible removal of the Mirena. Although the prevention of pregnancy is great the side effects are becoming unbearable and seem to increase over time. I would think twice about opting for this method of birth control.

Hi everyone,

I decided to go online to look for Mirena side effects because I have been having a lot of problems every since I got mine. I felt so relieved when I found this website because I realized I wasn't alone. I've had my Mirena for 3 and half years, and I have experienced almost every single side effect that the other girls on here have. I didn't have any of these symptoms before getting Mirena. After my first child I didn't have any side effects but after my second child I got mirena and this is what happened.

My hair up front on top has gotten very thin and I have always had very thick hair. I have always been a very laid back, friendly, happy person but since I've had the Mirena I've been moody, irritable, depressed, and I have had anxiety attacks. It also seems like I have a harder time feeling satisfied or happy about anything. I've had migraine headaches and joint pain which I never had before.

I'm 5'11 and I had always been extremely thin. I didn't have any problems losing weight after my first child, but since I have gotten Mirena I have gained a lot of weight in my stomach area but nowhere else. It's almost like a swelling or inflammation that won't go down. I've also had the strange feelings in my abdomen of movement that the others had, but I know I'm not pregnant. I've had these feelings for almost 2 years now.

It hurts really bad sometimes when my husband and I have sex, especially if he hits the spot where the Mirena is. My sex drive is completely gone, which seems like a common problem among the others here. I also noticed that fishy smell that the others have talked about that won't go away no matter what products you use or how much you wash. I also have gotten acne on my body which I had never had before in my life. I have some on my arms, face, chest, and back. It's terrible. I also have had the lack of energy so many of you said you had.

Even though there are all these terrible side effects, I think the worst one is that I don't feel like myself anymore. My husband says I don't seem to get excited about anything, and I seem more withdrawn. I have much more social anxiety than I did before, and sometimes I feel like my heart is racing and I can't get it to stop. I would have it taken out right now if i had the money to get my tubes tied. Unfortunately I don't have health insurance so I'm trapped for now.

I originally started YAZ about two years ago primarily to help with irregular or extended periods. I went off for about 8 months and had very light if any periods until about two months ago when my symptoms started back up. I went on YAZ for a month and my first week on the white or placebo pills the bleeding was extremely heavy. I'm sorry if this is graphic but I went to sleep for 5 hours with a tampon in and woke up soaked in blood. I freaked out and went to the ER and was told this is a normal side effect of this pill. Just prior to this I experienced:

terrible migraine headaches
brain fog
loss of focus
inability to think and communicate clearly
increased sensitivity to sound
terrible anxiety around people
mood swings- I didn't realize this until reading everyone else's posts

From my hospital visit I also learned my blood pressure was extremely high which could be a result of this pill.

I am so thankful to everyone on here that were so brave and kind to share their stories. I hope my post will be just as helpful.

thanks,

S

I have an appt tomorrow to have this thing removed. I am so looking forward to it. It only took a month to get the appt (feel my sarcasm?) but I don't care because I know I now have my life and health to look forward to. At least, now I can see results as I work out (compared to nothing b/f), no more migraine headaches (NEVER had any headaches b/f the Mirena), no more mood swings, and all the other crazy stuff that came with this thing.

This is a follow up for my previous post about my symptoms...I will post again once it's removed and once I start getting my life back. Please take the Mirena out if you have the slightest incing that it's the cause of your symptoms - you know your body better than anyone.

I have been on NR for 3 weeks now. I'm 23 and haven't taken any form of BC in a few years but now that I am in a serious relationship I wanted to protect myself. I was so excited about NR because I didn't have to remember to take a pill everyday and my GYN told me that there are virtually no side effects. YEAH RIGHT!!!!! I thought I was crazy for the way I have been feeling lately but after reading all of these posts I am soooo relieved to learn that i'm not!

The first side effect I noticed that came on immediately and has not stopped since I started NR is a cramping feeling in my lower abdomen. It feels like period cramps only not quite as bad. It doesn't really hurt it's just annoying. The second side effect I noticed which started about a week after I began NR was that I lost my sex drive almost entirely! My boyfriend and I just spent a week on a cruise together alone and we didn't even have sex once!! The other side effect I have is migraine headaches. I got my first one the 2nd week after starting NR and they are horrible!!! I'm also constantly hungry! I have gained 10 lbs in the last 3 weeks! And every time after I eat I get really nauseous for about an hour or two. The last thing is that I have been super moody lately. Things that normally don't bother me I am getting really irritated and annoyed about. I'm already on medication for anxiety and mild depression which I started way before the NR so I know that the NR is what is causing it.

I was recently tested for a hormone imbalance which came back negative a few months ago so all of these problems HAVE to be coming from the NR. They all started within the last 3 weeks which is when I started using the NR.

For any woman out there who is considering taking NR PLEASE PLEASE PLEASE seriously think about. I have heard more bad than good about this product!!!

I was recently put on Yasmin, I've just finished up my first pack. Some of my friends told me to read the blogs on it cause it's not all that it's cracked up to be. I was originally put on it due to PMDD. I get hellacious PMS and i was told that this pill can help. I also take antidepressants to treat mild depression, so the low/single dose hormone is essential for me. Throughout the past month I've had two migraine headaches which is unusual. I do get headaches but not like these. I can't even open my eyes, eat, or have any noise or light around. It's really awful. I do have the dizzy spells and some gnarly pain in my lower abdomen and in between my shoulder blades. It feels like cramps but I'm not having a period yet. I'm hoping these side effects will go away as my body adjusts but frankly, from these blogs I'm really leery to keep taking this pill. Any recommendations for a girl who needs a monophasic pill and need extra help staying sane during PMS? Any news helps. Thanks and best of luck to us all.

03/11/09 went in to have a blood test the MD had ordered. I met with the Md-- told him that the metoprolol 100mg twice a day had not agreed with me. I asked to change my prescription to what i had been taking before -- Norvasc 5mg twice a day along with a diuretic. A week later I went for my lab results. The AST(SGOT) 232 and ALTSGPT) 516, being dangerously high. Md asked if I had ever had hepatitis B. My answer was no. I asked him to check my blood test results of 11/08. The results were AST(SGOT) 24 and ALT(SGPT) 37. I told him I thought it could be the Metoprolol. The Md told me he wanted for me to have CAT scan and to refer me to a GI doctor. Went home praying to the GOOD LORD and received peace about this whole situation. I searched on the internet and found on ****** Metoprolol-induced hepatitis: is the rate of oxidation related to drug-induced hepatotoxicity?L. MS.
University Department of Pharmacology and Therapeutics, Royal Hallamshire Hospital, Sheffield, United Kingdom. Hepatology. 1989 Jan;9(1):163-4. Also found Hepatic toxicity is reported in at least one case report. ******
" 56-year-old female with a history of migraine headaches developed seronegative hepatitis associated with metoprolol. Her signs and symptoms resolved within 48 hours after discontinuing metoprolol, and were reproducible on rechallenge."
My results for hepatits were negative.On 3/31/09 I had lab tests and 4/01/09 the Md faxed my results AST(SGOT) 29 and ALT(SGPT) 43. I have not gone back to the doctor. I am taking milk thistle daily. I have learned a valuable lesson and am passing it on to others.

I started Yaz in December 2008 to combat what seemed to be PMDD and perimenopausal symptoms. The cure is worse than the ailment. I've been plagued by feelings of extreme apathy and disinterest in everyone and everything in my life. There's the old joke, "Sex or a sandwich?" I can't even be bothered for either one. I've been short tempered, extremely fatigued - even after sleeping 10-12 hours at a time. I fought with my BF on Saturday and hurt him beyond anything I've ever done or said to him. And he is the kindest man I know. I've had piercing back pain, intermittent chest pain, difficulty breathing, migraine headaches, nausea and intermittent heartburn & GI upset, dizziness, blurred vision, vaginal dryness. The depression is what was the corker for me. I have such a high tolerance for physical pain and it takes extreme circumstances for me to see the doctor. Now that I think about it, I didn't even get to see my doctor...I called in November to make an appointment, explained my peri symptoms to the nurse, then received a prescription for the Yaz....Well, enough is enough. I simply can't live like this. I called them yesterday and was directed to stop IMMEDIATELY. I've since made an appointment with an acupuncture doctor and will discuss finding a GYN who focused on midlife women and uses natural remedies. To all you beautiful women who posted here, you saved my life yesterday. I am forever grateful for your honesty, because I thought I was going crazy and the solution was kick everyone and everything in my life to the curb.

Hello-
I am here to share my story about topamax in hopes that others may read this and not have to go through what I did. I went on topamax for the prevention of migraine headaches. It worked great to prevent my headaches but gradually I could not talk, I stuttered severely, and I have memory and other cognition problems. At my doctors recommendation I stayed on the medicine for about 6 months because he assured me that the stuttering would go away. I was in such awful pain that I agreed with him. Needless to say that 6 months was not me. I couldn't talk and I couldn't think. Now when I think back on it, I wish I had just endured the pain. When I went off of the medication I still stuttered. It was not quite as severe but it was bad. It effected my work, my personal life, and daily menial tasks. I could no longer communicate. I was devastated. My doctor was puzzled and said that he had never heard of this before. So to make a long story short I went to a speech clinic, bought casa futura techs small talk device, and tried some anti-stutter meds. My speech now, 2 years later, is much improved thanks to the smalltalk but guess what,? I still stutter. Manageable and not very noticeable to others at times but my speech has not returned to pre-topamax status. I looked into sueing the drug company to bring awareness about this issue but did not get much positive feedback from attorneys. IF YOU ARE ON TOPAMAX AND ARE STUTTERING, STOP TAKING IT. IT MAY NOT GO AWAY WHEN YOU DISCONTINUE THE MEDICINE. It is not worth it. You cannot put a price on speech. I don't care what the physicians desk reference says, what your doctor says, what the corrupt drug companies say. I know my experience and it has been a catastropohic effect from topamax. Find a different med if you have speech problems! Please, for your own sake. Thanks for letting me share my story.

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

I got my Mirena IUD inserted at the end October 2008. I had a tubal ligation with the birth of my fourth child so my IUD was supposed to combat my battle with endometriosis. Needless to say, I am not pleased. After insertion I spotted for about a month. Finally that ended and I was blood free for about one month and as of January 1st, I am bleeding again. Happy New Year!!!! At first, I didn't know where to attribute my horrible depression, severe acne, and migraine headaches but now I have an idea since discovering this website. I am 31 and have NEVER suffered from acne not even during those adolescent years. The spotting is the worst. It is this horrible dark brown color with a horrific smell!!! I was starting to wonder whether or not it was actually blood. I contacted my doctor's office and was told that this was normal. I was given an antibiotic because they assumed the smell was from some type of infection. Well that didn't work. My doctor didn't want to remove it thinking that eventually my periods and bleeding will stop permanently. That day has not come yet, and I don't know how long I can endure. I really just want it out. I am tempted to contact my family practitioner and have him to remove it. I just know, I want it out!!!!!! I am just grateful for finding this site and finally realizing that it is not just me. I am looking into some herbal treatments to try to ease my discomforts with my endometriosis. I don't think I want to risk dealing with any more IUDs, birth control pills, or shots anymore. It just seems like to much to loose at this point.

After reading some of these side effects, I'm posting in regard to my 24 year old married daughter. I'm not sure of the time line, but she started Gardasil last year, and I believe she has had 2 doses so far. She had had migraine headaches before, but in the last 6 weeks they have become more frequent and severe. Right now, she has been immobilized with a severe migraine for nearly a week, and none of the usual medications help at all. Her internal medicine specialist is sending her in for a CT scan Monday morning to rule out a brain tumor, or the recurrence of a benign cyst in her sinus cavity like one she had 8 years ago.
She has also had dizziness, nausea, vomiting, among other symptoms. I am very worried about her.

I have been on Yasmin for a little over a year. I also have suffered from migraine headaches for a few years. My doctor kept putting me on different meds to help with my headaches but nothing has worked. These headaches I've been getting lately aren't at all like my normal migraines. I get sharp pains in only one side of my head and it feels like there is so much pressure that my head is going to explode. It hurts to breathe through my nose, and if I sit up or stand it gets worse. I have been depressed and irritable so he put me on anti depressants. Then I find out all of these things that I have noticed happening like my legs feeling weird and my pains in my chest are happening to other people on the same pill. I have an appointment next week and I'm definitely bringing all of this up.

I have been on Advair 2X a day for 2 weeks with a history of migraines. The last 3 days I have had 3 separate migraines with preceding scotomas- the third migraine headache on the third day- was the worst ever and didn't respond to migraine medicine. My husband figured out it was the Advair and I stopped the medication. For those with a history of migraines- don't take Advair as run the risk of severe migraine headaches.

I'm writing in behalf of my 15 year old daughter who is trying loestrin24fe to get some relief from her back pain and migraine headaches (which she inherited from me). She had a full period after just 10 days and has had a non-stop headache since starting this pill that won't stop even with her migraine medicine. I know it takes time for bodies to adjust, each is different and the doctor says give it 3 months- but she is considering just stopping because her headaches are so bad. I'm just not sure she can hold out for 2 and a half more months to give it a good try. Her acne is a lot worse too. Moody- yes, this was another thing we were hoping the pill would help with but hasn't. I'm sure this site is biased for people having problems since if it's working okay- why look up information on it? In any case, 30 years ago the lowest dose pill made me depressed, I barely made the 3 month mark before I stopped and I thought it would be different now. I have spent years before and after having kids using an IUD, and for me, that has always been the greatest birth control!

I recently started taking topamax for migraines. After increasing my dose to 75 mg twice a day, I am almost migraine free. However, my hair is extremely oily and having to wash it with a clarifying shampoo twice a day. Nothing else has changed other than my this medication so I am assuming it is a side effect of the Topamax. Has anybody else experienced this?