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Extreme pressure symptoms and conditions

Here are side effects posted by other members, that mention extreme pressure.
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50 Side Effects posted for extreme pressure

October 1th
2009
6:19 PM

Vertigo, weakness, fatigue, exhaustion, aching numbness in arms, numbness in face arms and legs, extreme pressure in head and neck, burning feeling radiating from the base of my neck through shoulder blades to arms, foggy brain, waking up feeling (for no reason) like I have a major hang over, chills, aching feet, weight gain, feeling very fearful of my symptoms because they feel like nothing I have ever experienced.
THESE LAST 4 WEEKS HAVE BEEN HELL!
I had my Mirena inserted on June 30 2008. I experienced mild discomfort for the first 4-6 weeks. The spotting was the worst of it and that was no more than an inconvenience. I was happy with my choice of birth control.
Then this hell began about three months after insertion.
During the last week of September the symptoms listed above started. They were mild at first but by within a week and a half I felt HORRIBLE. I suspected that it may be the Mirena, but at the same time I thought I was dying.
October 1 or 2nd (it is all a blur) I was home by myself when I started feeling the numbness and head pressure coming on again (my symptoms were coming and going, not constant) so I laid down on the couch to get off my feet. All of a sudden I felt like I was losing consciousness. I grabbed the phone and called my husband to get me to the ER. I thought I was dying. A blood clot or something. Once there, they did blood test after blood test, an EKG, urine tests, and basically I was told that there were no major system problems. I know this sounds a like classic anxiety, but I know it is not. I have to say they were very good there and encouraged me to see my family physician (whom I had already been to earlier that week) again.
I called to make an appointment to have the Mirena removed the very next day. My GYN kind of shrugged off what I was going through saying that it was anxiety and asked if I still wanted the thing removed!!! of course I did. Having that thing removed was very empowering. I was feeling so helpless and it was the one thing that I could do to possibly help my situation. The feeling of relief was amazing.
I did see my family physician again who agrees that what I am going though is related to the Mirena. She did ordered a CAT scan (came back negative) just in case.
Post removal (It has been 17 days) I have been slowly getting better. My "episodes" are getting more and more diminished and further apart. I have noticed that I am flooded with exhaustion after each of these "episodes". I also never know when there going to strike making it hard to make plans. My husband has been very supportive through out and was convinced before I was that it was the IUD. He has volunteered to get a vasectomy.
GOOD LUCK TO ALL YOU LADIES.
If you have stumbled across this because you are desperately searching for answers, all I can tell you is that I believe that the Mirena IUD has had devastating effects on many, many women, but hang in there you are not alone and you are not insane. What you are experiencing is very real. Have it removed ASAP!!!!!!!!!!

-- By calybo | Reply | Private Message me

June 20th
2009
10:10 AM

Sorry to post again, but NO ONE REPLIED TO MY POST!

I am 5 days post removal and need reassurance. Unlike everyone else, I have NOT felt better right away. I am just as tired (if not more), more irritable, and JUST GOT ACNE on my face and arms 2 days AFTER removal! I'm still dizzy and the brain fog is just as bad. Have not bled a drop at all.

I know everyone is different, but my removal experience has been completely different... don't feel better, no bleeding/clots, no immediate improvement. IS SOMETHING WRONG WITH ME??? Was it not the Mirena after all???

-- By ameigh | Reply | (8) replies | Private Message me

March 19th
2009
2:15 AM

My time on Biaxin was one of the most TERRIFYING experiences of my life! (And I’m a cancer survivor, haha).
It all started when a doctor put me on Biaxin (500mg) for having Pneumonia. I was to take one pill at night and one pill in the morning for a week. The 1st day on the Biaxin was fine. Then the second night, I started to experience changes in my behavior. I began to cry and become extremely emotional to minor things.
The 3rd day I woke up and took my pill and started to feel extreme pressure pushing on my brain. I also got very agitated, grumpy, hyper, and over stimulated. That night I took my Biaxin pill and got 0 hrs of sleep. I was up all night paranoid, scared, hallucinating, crying, shaking, nervous energy, pacing back and forth, thinking in my head “what is happening to me!” The next morning, I took my Biaxin pill and then experienced the same horrific side effects. I was calling my family and telling them that something is going wrong in my head and I need help. It was as if I was having a panic attack. My stomach cramped up, my head hurt, and my heart was beating 10x its normal pace. I also felt hopelessness, couldn’t concentrate, shortness of breath, and worst of all the feeling of paranoia and the thought that my mind is being possessed.
Finally, I got on the internet and looked up “side effects of Biaxin”. Thank god I found this website and was able to see I wasn’t alone. I called my family and told them it’s the Biaxin making me crazy. That day I went and saw my doctor and he said, “Yes, Biaxin can cause emotional distress and all of those other horrible things you are going through." He says it is rare to get that many crazy side effects, but it is possible. He said to stop taking it, and go home and rest. I needed to allow my body to recover from what has happened the last 4 days.
I will never take Biaxin again for as long as I live. I literally thought I was going insane. The feelings and thoughts I was having was absolute torture and an emotional rollercoaster. I thank this website and all of you for your posts. This website truly helped me discover that Biaxin is a dangerous drug that is not intended for everybody. Especially not me!!!!!

-- By cameronaz | Reply | (1) replies | Private Message me

March 9th
2009
9:40 PM

Like most of you all I am on Topamax 100mg. I am a 27 year old female that has suffered from severe migraines for over 20 years that would last up to 2-3 days and completely debilitated me. I would bleed from my tear ducts from the extreme pressure and I would need to be in a quiet, cold, closed off room to be left alone until the migraine was gone to continue on with my life. It was ruining my life and taking over my day to day routine. I could never really commit to anything without the constant worry in the back of my mind about a possible migraine until I found Topamax. Now on Topamax I went from 4-5 migraines weekly to 1-2 monthly, it is truly amazing, however there is a catch. Although the medication is wonderful and I will never get off of it at the rate of success that I am at, I do have side effects. I have extreme tingling in my extremities, (hands, feet) along with my face. It feels like they are constantly asleep. I also have noticed the poor tasting carbonating drinks along with my taste buds changing with certain foods that I use to be so fond of. I also have a very smokey haze where it almost feels euphoric if I wake up in the middle of the night. I have horrible nightmares of people that I have not seen in or thought of in years, memory loss and spelling issues-all goes away after 3-4 months of uses. I had shortness of breath, however that subsides as well with the use of the medications along with several other side effects. I have lost over 30lbs that is along with diet, so I can't say it is all Topamax. I have noticed little nodules that have been showing up on my hands since I stared taking the medication that I am in ? about I have a call in to my neurologist to see if he has heard of any such thing. Other than that I love the medication, because if not having migraines is one of the side effects-lol I can handle the side effects. I hope that this will help anyone that might have anything similar to what I am going through. If you can shed some light on my nodule situation please let me know. Thanks

-- By marfam23 | Reply | (2) replies | Private Message me

October 20th
2008
10:53 PM

Vertigo, weakness, fatigue, exhaustion, aching numbness in arms, numbness in face arms and legs, extreme pressure in head and neck, burning feeling radiating from the base of my neck through shoulder blades to arms, foggy brain, waking up feeling (for no reason) like I have a major hang over, chills, aching feet, weight gain, feeling very fearful of my symptoms because they feel like nothing I have ever experienced.
THESE LAST 4 WEEKS HAVE BEEN HELL!
I had my Mirena inserted on June 30 2008. I experienced mild discomfort for the first 4-6 weeks. The spotting was the worst of it and that was no more than an inconvenience. I was happy with my choice of birth control.
Then this hell began about three months after insertion.
During the last week of September the symptoms listed above started. They were mild at first but by within a week and a half I felt HORRIBLE. I suspected that it may be the Mirena, but at the same time I thought I was dying.
October 1 or 2nd (it is all a blur) I was home by myself when I started feeling the numbness and head pressure coming on again (my symptoms were coming and going, not constant) so I laid down on the couch to get off my feet. All of a sudden I felt like I was losing consciousness. I grabbed the phone and called my husband to get me to the ER. I thought I was dying. A blood clot or something. Once there, they did blood test after blood test, an EKG, urine tests, and basically I was told that there were no major system problems. I know this sounds a like classic anxiety, but I know it is not. I have to say they were very good there and encouraged me to see my family physician (whom I had already been to earlier that week) again.
I called to make an appointment to have the Mirena removed the very next day. My GYN kind of shrugged off what I was going through saying that it was anxiety and asked if I still wanted the thing removed!!! of course I did. Having that thing removed was very empowering. I was feeling so helpless and it was the one thing that I could do to possibly help my situation. The feeling of relief was amazing.
I did see my family physician again who agrees that what I am going though is related to the Mirena. She did ordered a CAT scan (came back negative) just in case.
Post removal (It has been 17 days) I have been slowly getting better. My "episodes" are getting more and more diminished and further apart. I have noticed that I am flooded with exhaustion after each of these "episodes". I also never know when there going to strike making it hard to make plans. My husband has been very supportive through out and was convinced before I was that it was the IUD. He has volunteered to get a vasectomy.
GOOD LUCK TO ALL YOU LADIES.
If you have stumbled across this because you are desperately searching for answers, all I can tell you is that I believe that the Mirena IUD has had devastating effects on many, many women, but hang in there you are not alone and you are not insane. What you are experiencing is very real. Have it removed ASAP!!!!!!!!!!

-- By calybo | Reply | (4) replies | Private Message me

May 29th
2008
10:27 PM

My wife started on 6.25 dosage for her inability to sleep properly. It helped her sleep. However, the 6.25 stopped being responsive and her MD prescribed her a higher dosage. Once she started taking the higher dosage, her thought process was impaired and had extreme pressure headaches along the head, face and neck. Her mind was so screwed up that she started to have suicidal thoughts and intense feelings of fear that she would start to have panic attacks. I do not know how these drugs get FDA approved. Went to a naturopath who did a hormone test and found that her hormones were unbalanced. Went on bio-identical hormone replacement therapy and she is herself again. She is also able to sleep properly.

-- By marcosoul | Reply | Private Message me

September 30th
2007
7:34 AM

I am a 24 yr old male that got diagnosed with HBP on my 20th birthday. I frequently felt jittered, on edge, flused easily, extreme pressure in my head, headaches, not being able to concentrate, felt run down, among a lot of other symptoms, decreased libido. My BP still ran in the 130 range. I decided to do a trial of not taking it and monitoring my BP closely. I have found my BP to be the same if not lower so far and it has been 5 days. It may be too soon to tell, but i'm going to keep monitoring. I feel great so far. I can concentrate, got my drive back, I feel good.

-- By tram602 | Reply | Private Message me

September 17th
2007
7:36 AM

Zyprexa has ruined my life!!!!! I went in hospital in 2001 with what I would call mild delusions now compared to after being given zyprexa. As soon as this med was started I began to have extreme pressure on my back constricting my breathing, could barely get dressed look after myself walk from one end of a hall to another, began vomiting day in and day out and diagnosed with severe acid reflux, waking up night after night gasping for breath and finally diagnosed with sleep apnea - this is before I gained the 85lbs from this and other atypical drugs. Experienced sleep paralysis where I would wake and feel like I couldn't move my body, vivid nightmares, and symptoms of td with constant twitching of my body during sleep. These side effects continued for 5 long years. I still suffer from acid reflux, sleep apnea and osteoarthritis in my knees. This is a very dangerous drug. I wasn't on the drug very long but other's were tried with no avail to the side effects until I was switched to zoloft and risperdal. Now I am having high blood sugar results with at home testing. I am searching for people in Canada who have experienced any of these side effects as I am added to the Class Action Lawsuit that has been initiated here and hoping there are others who can add their names to the suit who have experienced similar side effects. If you or a loved one has experienced any of the above and are from Canada please contact me at ******

-- By lisa20cb | Reply | (1) replies | Private Message me

January 2th
2007
11:05 AM

I have been on Lisinopril for 5 months with HCTZ. Stopped the HCTZ and went to straight Lisinopril 10 mg and I couldn't urinate and felt extreme pressure in my bladder. Urine smell was very strange. Stopped taking it and everything was fine.

-- By eboger | Reply | Private Message me

September 14th
2006
9:53 AM

Extreme headache, back pain, extreme pressure and pain in sinus, fatigue but unable to sleep, dizzy spells. Took medication for three and a half days for an infection but will discontinue today

-- By teresa642 | Reply | Private Message me

December 26th
2002
11:51 AM

Classic Migraine, sensitivity to light, nausea, extreme pressure and blurred vision. Tried everything else, finally Imitrex. First 30 min. I felt a cold sensation, especially in my facial area. Felt as if my bloodstream was flowing again. Then, suddenly realized I felt like myself again. My concern, women in my family have a very strong history of high bp & strokes around age 50 (I'm 34)... have I found my miracle drug or am I putting myself at a higher risk for more serious dangers?

-- By guest204 | Reply | Private Message me


 

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