Ibuprofin symptoms and conditions

I have to say I am SHOCKED over this site but had to read every bit of it. I am a TRUE believer in the Mirena and until I came across this site while searching for sites to send a friend to encourage the Mirena I never knew how many horrible things could happen for someone on the Mirena. HOWEVER, I guess this is proof when with any type of birth control including Mirena it is said it's not for everyone. I happen to LOVE mine. I'm actually on my 2nd insertion. My first one went very well, after a crampy insertion and 2 days of horrible cramps controlled by ibuprofin I was left to enjoy 5 years of birth control w/out problems. I can't take the pill as no matter the dose I spend the 1st to weeks nauseated and vomiting in the morning, I tried the Depo Shot (personally that is the EVIL OF ALL EVIL birth control methods, gained 68 pounds in 11mnts never going over 105 pounds except for pregnancy in my life, have battled to control my weight since therefore I believe it destroyed my metabolism forever, major depression to the point of medication and medical leave from work & the world). And after an accident pregnancy no way was condoms going to be enough for me. My Dr. recommended Mirena and I gave it a try. I was not lucky enough to go period free my first insertion I did have a max of 3 days of period with little or no cramping. My second not as good, I now have about 5 days of spotting only if sex promotes it and occasionally after using the bathroom a little blood on the toilet paper, never needing to actually use any feminine products. I use to get ovarian cysts all the time, small enough surgery was only needed once but I knew when one was there and I knew one they "popped" as my doctor would call it. I haven't had that problem since I started with Mirena, I'm told its due to the small amount of hormones (hence the reason my Dr suggested Mirena versus a non hormone IUD). My sex drive has not been affected one bit...in fact like one of the positive posts I just read...my husband and I have discussed more then once prior to coming across this site how much more of a sex drive I do have, although we contributed it to not being pulled down in the dark world of depression from the Depo shot...and the freedom of placed once & forget for 5 years type birth control. I have 8 friends and coworkers that have the Mirena...One person had a problem, hers "fell out" in the toilet and she had been cramping and in abdominal pain for a few days prior not connecting it to her Mirena...but after 2 months of other methods she had another one placed and has had no problem since...that was 2 years ago. It stinks to hear how horrible this "wonder bc method" is for others...(are you seeing how terrible the other methods were for me first for me to feel this is the wonder of all wonders) and of course I'm concerned with the fact that most of you that had a problem had SEVERE problems..not just a small one here or there. But I'm going to bet that on the flip side the methods that caused me hell might work for one of you. I have 2 more years left on this 2nd cycle...I pray I never have the problems you do if I chose a 3rd insertion...however, with science today we can only hope your complaints are taken seriously and the makers of Mirena continue to improve so that less and less people run into these side effects. I'm not sure I would have another option...SCARY!

I just got a root canal because my tooth is "dying" and it was causing severe pain throughout the whole right side of my face, head, and ear. I asked the Ortho not to give me Percocet or Vicodin because I get nauseous / puke profusely. I took an Ultracet and luckily I only felt a twinge of nausea... just on the brink of nauseous but I could live with it. It also made me feel really dopey and high. I liked the feeling because I had been days of severe pain and finally it was gone after the numbing from the dentist and the Ultracet... However, when I took one just before bed (4 hrs after 1st dose) I did get nauseous. I also felt twitchy and restless. My mom takes Ultram religiously for her headaches, and takes two at a time... I don't know how she does it. She is dependent on them. I went to work today and took one because my face started pulsing again. It was interesting because I didn't get nauseous and I felt more productive. I did get dopey for about 45 minutes but it went away and the pain stayed gone well after that. So in my short experience with this drug, I've noticed the side effects aren't as bad during the day (maybe because I'm moving around more and not concentrating on them). I've also noticed that if taken during the day I got a little bit of an energy burst after the 45 minute dopey phase passed. Now it's night time again and my face hurts again, so instead of taking a full pill, I broke it in half (Verified with pharmacist that it's okay), and took an 800mg ibuprofen. Hopefully, I won't get sick and I'll sleep through the night without a pounding face alarm clock.

How interesting -- I'm a 56 old female. Went to my Dr. because couldn't shake a chest cold, feeling like lungs not a full capacity. She listened and agreed there was too much wheezing. She gave me an Advair 250 inhaler, although when I asked, said that it would, my lungs would eventually clear themselves up. Instructed me to take twice a day for 5 days, then once a day until I felt I didn't need it anymore. The third night I was up all night with deep ache in my wisdom teeth, some bleeding in the gums, used ice packs and ibuprofin (sp?) to get through the night. After another day and night like that I could only think it was the Advair so stopped it. Saw my dentist 2 or three days later -- pain was decreasing, but wanted to be sure there was no infection. Showed denstist the inhaler but she said it couldn't be that and there were no signs of infection. So -- tried Advair again but again by the 2nd night I was up again with the ice packs, pain killers and bleeding gums. No more Advair for me, and I'm relieved to read that others had the same reactions I did as it means I'm not completely nuts.

Hi, I had the Murena inserted 2-7-08 at 2 PM. I am 43 years old.I nearly passed out at the doctor's office due to the pain. I felt like like my body was trying to expel the dog-gone thing. The literature said I would experience some discomfort during the insertion. That was an understatement!! I went home and by 4:30 I was cramping very bad. I called the doctor and he said to take some more Ibuprofin and to go to bed.Said to keep an eye on it I was bleeding very badly. I had to change tampons every 2 hours and wear a pad. It was gross with large clots. I took some strong I buprofin the rest of the weekend and called the doctor again. I know he had to think I was whining. I ran a fever and felt like crap. I went in to see him and he checked to see if I was expelling it. He said no. I continued to have a period-heavy- until my 6 week follow-up visit. He said "Let your body adjust, and if you continue to have problems, we can discuss taking it out." I had a period for 3 months.With wearing tampons for so long, I was concerned about Toxic Shock Syndrome. I still have brown slimy stuff every 2 weeks ago. I just never know when it will be, no set day. I used start my period every 4th Tuesday on the dot that lasted for about 2 1/2 days. since then i have gained 18 pounds. I can't check to see if the thing is there because I have a very long vagina and can't reach it with my fingers..and it's gross. I don't really have an appetite. I have been depressed. I don't have a lot of energy. I don't want to go anywhere. I don't desire sex (no wonder you don't get pregnant!) I have started to get acne. (I haven't had acne since high school). I am thinking about getting it taken out but don't want to risk pregnancy. I was on the pill for 15 yrs off and on and have some concerns about it at my age. I thought this would last me until I hit menopause and then wouldn't need birth control. Anyway, at least I am not crazy..there are others with these issues.

I am so glad this site is here. I started to think I was crazy. I got my Mirena put in on June 30th. Since then I've experienced excessive bleeding, stomach cramps and recently began to experience nausea as if I were pregnant. My bleeding has been so excessive that prior to having a baby I never really had long periods nor did I bleed heavily enough to go through a pack of pads. Now, I got through a pack of pads in two weeks. The nurse at by GYN says to take 800 mg of Ibuprofin inorder to stop the cramping and excessive bleeding. Ive found that taking 800 mg in the AM and at night stops the bleeding and cramps but, does this mean I will be taking Ibuprofin throughout my time with this birth control??

I was so sure I was pregnant I went out and got a pregnancy test to check. Thank god it was negative. I just had my first child May 8th and I'm not ready for another child right now. I've recently relocated to a new area and I'm still enjoying being on an extended maternity leave. Not to mention... I scared the heck out of my husband!! I feel so unsure about Mirena but I'm willing to try it out a little longer but, in addition to Mirena I'll certainly be using another birth control method for back up like a spermicide or something.

I thought I was going to die for the first couple of days after I had Mirena inserted. The pain was unbearable! I had to take Vicodin and laid in bed in the fetal position crying and fighting the pain and nausea. I thought, "What have I done!?" But, eventually the immense pain went away. But not for long. I have horrendous cramping before, during and after every period. I go through Aleve and Ibuprofin like crazy. Then, I ended up with ovarian cysts, I thought I was dying, it hurt. Now, after reading these postings, I realize that I have even more side effects to blame on this device of torture! I'm bloated, gained a crap load of weight, am bitchy ALL the time, I always feel exhausted, and wish I could disappear. I friggin' hate this thing. I have been thinking about having it removed for a while. I have now made my decision.
Good luck to everyone else out there dealing with the effects of Mirena!

Hi I'm 26 years old and I got the Mirena in November 07. I have been bleeding since then, Also I have some sharp pains in my stomach it gets worse when my husband and I have intercourse. I have been to the doctor a few times now and they give me these pills to take for 14 days and i have done this two times now and its not working. I have another appt Aug 5 to try a different kind of pill. But I'm not even sure I really won"t this in me anymore. If anyone have experienced this please let me know and what did you do? Also I'm scared to get it out because it hurt so bad putting it in. Does it hurt taking it out??

THANKS SO MUCH
Amanda

My 8 year old daughter had to take the liquid form of this medication for a UTI..2 tsp/twice a day for 10 days. On the 5th day she had a high fever, so I gave her liquid ibuprofin. Then she started throwing the antibiotic up and she was getting fevers up 105. The ibuprofin would only get her down to 100/101 range. She then started to complain about her neck hurting, so I was thinking meningitis! She was thirsty all the time and said it felt weird to swallow. After 4 days, I finally found 3 websites regarding side affects, including this one. I'm definitely not giving her any more of this antibiotic. Her UTI however seemed to be gone in 3 days.

Day 21 on Welbutrin XL 150 mg. - prescribed to help stop (light) smoking habit & for depression. I loved it - smoking urges not nearly as strong, more energy, very few emotional outbursts & general sense of calm, happiness & well-being. I haven't felt this good for 4 years. Have tried other meds in past but quit due to weight gain & sexual side-effects. Yesterday I developed HIVES. Damn. Saw nurse practitioner today. She wants me to switch to Lexapro. Told me to start w/ 1/2 a tab @ bedtime tonight. AAaaarrrgh! Anyone have any experience w/ Lexapro?

I started taking Prilosec a few months ago and didn't notice any acute symptoms, but a week or so ago my pharmacy used a generic form of this
( Omeprazole) and I have been having debilitating headaches every day all day. I thought t was from my arthritis but it continues. Yesterday stopped taking Omeprazole to see if it will make a difference.I woke up today with a MAJOR headache. What I have been trying if 2 2mg Valium and some ibuprofen to see if this helps. At least it eases the pain. I have been taking Relpax (migraine pills) but after a while the headaches come back. This is so bad, guess I will have to go back to the doctor if this doesn't work. Anyone else having bad headaches too? Thanks for letting me let off steam.

I have had Mirena inserted about three weeks ago. Putting the IUD was not painful,but was not prepared for the major cramping that came right away. since then I have had cramping ( like the first day of menstrual cycle) which seeed tone triggeresd by my urination, and bleeding pretty much everyday. I had to take 2 ibuprofin (800 mg) to deal with the pain. My hair started to fall out and I thought it was a result of having the baby. My skin was itchy (didn't know why).
My doctor has checked me 2 times. The last time was this thursday (10/18) and my mission was to remove it. She checked my urine (fine), did a pelvic and ultrasound ( fine). Dr.gave me a prescription for antibiotics for week to see if my symptoms will improve.
However, after reading all these blogs, I just cannot deal with the pain, unpredictability of when the bleeding will start, having little or no sex life (husband is not happy about that), I am going to have it removed ASAP.

I have been taking 10 mg for about 1 1/2 months now. My blood pressure went down, but about 2 weeks ago I developed an irritating "tickle in the throat" cough. It has become worse every day since to where I am not able to sleep soundly at night. I am in school full-time and have to excuse myself from class because I cannot stop coughing.

I did go to the doctor on Friday and she suggested I take cough medicine every 4 hours and ibuprofin to reduce the irritation. Additionally, she suggested carrying a damp cloth with me and breathing through it when a cough spell comes on and when I am at home take "steamy" showers. These were suggestions to relieve the symptoms and after trying all of these ideas (which is a pain in the ?!@#) I still have no relief. If fact, the cough is getting worse daily and I actually threw up on Saturday because I was coughing so violently.

Even though my bp is down, I cannot live with this cough. I am going to stop taking it and look for alternative ways to lower my bp - because the doctor does not seem to realize how severe this side effect is. If anyone has any good alternate bp treatments - please email me! Thank you.
annebranson@comcast.net

About 2 months ago, I was prescribed Sulfameth/Trimethoprim 800/160 tabs for an inflamed, swollen nose which extended to puffiness and an apparent fluid sac under my left eye -- the actual cause for this infection has not been determined.

The doctor prescribed a 14-day supply (1 tablet, twice daily), and said I could stop taking it after 10 days if I wanted, or finish out the supply if I so desired. After about 5 days, the swelling had pretty much subsided, particularly under the eye, but I continued taking the medication through the 13th day. During the first 12 days, I did not notice any adverse reactions.

However, on the 13th day, just after getting out of the shower, I noticed red welts on my chest and back, purple splotches on the underside of my upper arms, and generalized redness across the rest of my body and limbs. I did not immediately associate these symptoms with the antibiotic, because the first 12 days had not caused me any problems.

However, a friend theorized that it might be an allergic reaction to the antibiotic, and suggested I stop taking it to see if the symptoms subsided. Since I had only two tablets left, I decided to heed the suggestion, and the redness did go away after about 2 days. I resolved to tell the doctor about this reaction on my next visit, but have not been back there yet.

Earlier this week, I experienced the beginnings of similar tenderness and swelling on the left side of my nose, and still do not know what might be the cause for this. I decided on Wednesday morning to take one of the remaining two tablets of Sulfameth/Trimethoprim, and within an hour or two began to itch a lot -- primarily on the back but also on the arms. I thought that taking a shower might relieve the symptoms, and it did somewhat.

Around dinner time, I took the second (my last one) remaining tablet, and about an hour later went out to join some friends. I had a slight headache and took an Ibuprofin tablet just before going out. Within the second hour, I began to feel chills (even though I was wearing ample layers of clothing), and the headache had not diminished -- so I took another Ibuprofin. The symptoms seemed indicative of a low-grade fever.

After excusing myself and going home, I laid down to watch TV, and the chills got so bad that I was obliged to curl up under a blanket, even after turning up the central heat. The headache got so intense, I had to hold an icepack against my temples and forehead for some relief. Later, when I took my temperature, the fever had progressed to 102 degrees; still later, it had climbed to 104. This worried me, since I have read that brain damage can occur at 105 degrees.

During this time, I decided to switch (from Ibuprofin) to taking three aspirins, to see if that might be more effective in reducing the fever, but it persisted at 104 degrees for all of the night and into the next morning. I made a point of drinking lots of fluids (water & juice) and tried sleeping, but woke up about every two hours.

On Thursday, about mid-day, the fever finally began to subside -- though I noticed a fatigue and soreness in my calf muscles, most pronounced if I stood in one position for more than a minute or so. The only relief was to move about, or to sit down.

By evening, my temperature was back to normal and I felt well enough to visit with some friends again. However, several hours after returning home, I felt dehydrated and had another headache; my temperature was back at 102 degrees. I drank more fluids, took aspirins, and had another night of fitful sleep.

By Friday afternoon, my temperature had reduced to about 100 degrees, and my calf muscles still displayed the same symptoms of soreness, as though I had over-exercised them. It's a very uncomfortable feeling.

Lesson learned: I will be asking my doctor to note in my file that I am allergic to sulfa-based meds, and hope that normalcy returns over the next few days. I have also gained a deeper appreciation for the manner in which the human body fights off foreign substances! ;-)

NEGATIVE:
Lisinopril is my "only" medication, other than a random ibuprofin. at age 58, I began on 20 mg for elevated BP control...that was almost five years ago.

I went through some light headedness at first (mostly my imagination, I suppose) as, "anything" new psychologically messes with me. My BP "did" drop to acceptable quickly, and just a year ago required a jump up to 30 mg (as I either became system-tolerant of its effects, or, my current level of inactivity has impacted my BP).

REVIEW:
Although I had the normal "minor arthritis" and a few gout toe attacks beforehand; After 8 months or so of Lisinopril application, I began to "really" have chronic joint pains (thumb, elbow, knee, big toe). As an active type, this began to slow me down-so I returned to the doctor for a comprehensive set of X rays-which supposedly revealed Impact Osteo-arthritis at the afflicted joints,... at that point, I also mentioned two other observations;
One, I just feel sort of weak, like possibly tired and unrested muscle-wise, Two, My random gouty big toe attack appeared like it was trying to manifest ...but, never did (fully) on six or so occaisions.

After almost two years into my Lisinopril, I began having cramps (actually, severe soreness and tightening)in my foot bottom and calf muscles... I assumed it was from lifting, and standing a lot. My muscle fatigue seemed worsened, and, I noticed a "visual" loss in my muscle size and tone...I "was" now much weaker than last year in my lifting, tugging, and shouldering abilities.
This accompanied with the constant joint stiffness had begun to physically modify my daily abilities and routines.

After two years on the Lisinopril, Unexpectedly (and in a physically quiet week) I had an episode of right knee pain and excruciating (very severe) 24 hour-a-day ankle/calf/thigh muscle cramping that went unabated for three horrible days...exhausted from no sleep, the inability to relax at all, after trying ice, heat, hydr-therapy and popping so many Ibuprofins, it was off to the hospital.

Some knee cap injections of steroids-a calcinated meniscus diagnosis-and a dismissal of "why the muscle cramps ?" and I was healed, Sorta'

With my continuing decline in joint movement, and sore, weak muscles, my overall activity level dropped, my inabilities to now lift, or bend fluidly caused me to appear much older (physically) and hobbled than my years.

A year ago (just before the increase in dosage), I took some time off. And really self-reviewed my present physical condition with that of 4 years earlier. The "only" change was adding Lisinopril...and of course, normal aging.

My annual lab tests are still enviable.
My genetics and family history refute what is happening.
My sexual and physical prowess has diminished greatly.
My energy level and stamina is very poor.
My whole life-style has been modified (destroyed actually),
to accomodate this new dynamic of muscle/joint problems.
My musculature appearances have diminished from inactivity.
I feel, move, look and hurt "old".
My insistance that this problem is muscle/tendon rather than joint related ALWAYS goes to deaf ears.

Before these complaints could even be filed with my doctor (for my fourth-year annual physical), I began the left knee, then the "both" knee flare ups again; the Doctor visit (and 10 mg increase in dosage of Lisinopril) advised me I was just getting old.

In the 6 months or so since my last doctor visit, I have experienced a worsening of strength, and a now "constant" knee pain (every step). My sixty day abstinence from alcohol had zero impact on my overall, the one year salt ban has shown me nothing, and I just recently went back to square one and a full rethink of my dilemma.... I came away suspecting my Lisinopril.

I am going to seek another Doctor for a review and perhaps a change from Lisinopril.

Michellep~

I just read your post and I am soo sorry you have been treated this way! I am in medical school right now and I am very concerned for you! The symptoms you are describing are very consistent with a blood clot in your leg. One of the most dreadful side effects of birth control pills is what they call DVTs (blood clots in the deep veins in your leg). The part we worry about is that the clot can break off little pieces and send them to your lungs, heart and brain. The vision changes could unfortunately be a sign of that already happening. I know that going to the ER sucks and can many times be a financial burden, but as a tax-payer (more than willing to have my tax dollars go to your hospital bill) and a medical student...please go to the ER!! If you start having pain in your chest or blackouts of any kind, dial 911. The ER has to treat you and you don't have to sign their forms saying you will pay. You have to give consent, but they can always write what you don't pay off. Your life is worth it!
(ps, you might want to get a different regular MD)

As for the leg, take a couple aspirin. Not tylenol or ibuprofin (advil, motrin, etc.), not aleve either. Get some good old-fashioned aspirin (bayer, etc.) It will help take the swelling down, cut the pain a bit and it will help your blood clot less if you indeed do have a blood clot.

Please let me know how things turn out!

kelly

this stuff has some wild side effects !!!

went to a doctor and got some info...people saying they felt like their teeth were rotating around in their sockets !

Also he had one lady who kept reaching down to floor to pick something up...when he asked her what she was doing she said her left arm kept falling off !

Suggest all of you try some other drug...this is my opinion for what it's worth.

WOW, has this site been a life saver!! I was put on Yasmin 3 months ago, because I had a 4 inch cyst on my ovary. I also was told I was peri-menopausal because of the hot flashes. I thought all of these symtoms I was having was from the menopause....until reading all of these testimonials. I immediately went off of Yasmin one week ago. I to had horrible side effects:

- Frequent spotting
- Extreme mood swings
- Irritability
- Low self-esteem
- Headaches/Migraines
- Heart palpitations
- Lightheadedness
- Difficulty concentrating
- Insomnia
- Fatigue
- Severe bloating and weight gain (even with diet and exercise!!)
- On edge all the time
- Breast pain
- Toe pain (as if I had broken them)
- NO libido
- Rash/itchy armpit

I had been suffering severe hot flashes, night sweats, insomnia, severely dry skin and uneven tone AND pigmentation
- Terrible mood swings and PMS, much worse than before yasmin, and depression
- dry skin over ALL of my body
- restless sleep
- forgetfulness
- cellulite looks worse
- enlarging of pores on face

My periods used to be 2 or 3 days and very light... with Yasmin they are were very clotty with severe cramping that would wake me from my sleep. I used to have headaches the first 2 days of my periods before....now they are worse and lasting a week!! They have prescribed me Flexeril and 800 mg of Ibuprofin, which doesn't do much for the headaches either.

And to think I was blaming this all on Menopause!!! I will do an update after I am off of Yasmin for a few weeks.

Has anyone else had soooo many symtoms??

Thank you to ALL of you for sharing your experiences!!

Been on Singulair since 98. I am 53. I too get heart palpitations and difficulty breathing for a short period a few minutes after taking it but only once in a while. It helps my asthma but if I go off of it for a while my breathing is quite impaired for 4 or 5 days then improves but not to the level achieved with the Singulair. I dream more and have some nasty nightmares especially if I take ibuprofin at bed time. The reason I go off of the drug periodically and take Ibuprofin is that I am much more succeptible to muscle cramping, spasms, hip pain and tendonitis while on this drug. I used to be a runner/racer but had to quit race training because my back and neck would cramp up. I get tendonitis easily in my forarms from activities that never bothered me before. I have had back spasms for 2 months that did not improve with ice, heat, Ibuprofin, chiropractic or physical therapy until I remembered the Singulair connection two days ago and stopped taking it. Today I am noticing improvement for the first time. Once my back heals up I think I will try reducing the dosage to 5 mg and see if it is enough to help my breathing without the muscle problems.

No new side effects, just want to reiterate what Levaquin did to me. What I resent is that no doctor involved ever mentioned problematic and painful side effects of the drug, yet when I had to be admitted to the emergency room for severe muscle and joint pains, the first thing the ER doctor said was "Levaquin causes painful, swollen joints and severe muscle and tendon pain, including rupture of the Achilles tendon."

Amazing that an unknown ER doctor, who had seen my case for less than 5 minutes, immediately caught and explained the cause of my problems. Thank God I hadn't forced myself to exercise, which I had considered doing, as I have now read on this website that exercise exacerbates the problem and could have caused ruptured tendons.

My main symptoms, which gradually grew worse as I continued the drug for 10 days, were metallic taste in my mouth, feeling of tiredness and heaviness in my body, increasing muscle and joint pain, especially in my knees, eventually spreading down the back of my legs toward my ankles. When I finally gave up and went to the Emergency Room, I could barely walk in; had to hold on to walls, chairs, etc. just to stay upright.

The ER doctor stopped the Levaquin and started me on Ibuprofin to combat the inflammation of the joints. (yet another drug??) So far it has been 24 hours since I stopped the Levaquin and I feel a little better - can almost walk again. I hope and pray the side effects will go away quickly, but I'm concerned since reading other people's lingering problems.

Thank you for this forum; I wish I had discovered it sooner!

I took Levaquin for 10 days and then 15 days for prostatitis. (was prescribed 21 days worth) I started getting muscle and tendon pain after 13 days of 2nd course of tx. I was also taking ibuprofin, which disguised some of the symptoms. Weekend before last, I did a lot of walking (5-6 miles a day)
since then my ankles have been very sore and swollen. Almost as they are badly sprained. The rest of my muscles are still somewhat sore and weak feeling. I have always been very active physically, but for the last few weeks have been very dibilatated. My prostatitis seems to have alleviated,
I am 59 years old.

I just finished taking 10 days of Levaquin for a sinus infection. I have had the sinus infection for about 4 months, and it finally knocked it out. I had only minor side effects (joint pain). I finished the Levaquin 2 days ago and I am feeling much better. The one thing that I want to say is to not take ibuprofin or drink caffeine while taking Levaquin. If you have to drink caffeine, do so at least 6 hours after taking it. Caffeine enhances the effects on the nervous system. I hope you all get to feeling better.