Broken blood vessels symptoms and conditions

Reading over some of these posts and wanted to share my experience w/Lamictal. Been on it over 2 year, 400mg/day. Sever bipolar with mixed & rapid cycling episodes. Oh YEA...I have side effects too: blurred vision that comes and goes, super klutziness, confusion, hard to complete sentences sometimes (just can't find the words sometimes for the simplest sentence!), dizziness, prone to broken blood vessels under the skin when bump into something or carry loaded grocery bag over my arm, jittery, short term memory loss, feeling really stupid like my brain isn't working sometimes. BUT...I will stay on this med because it rally works for me and the above effects are and bad, just frustrating. It took me a good 5-6 months for the meds to work as they should. Be aware that it won't make things perfect, mood swings and even moderate episodes can be expected. I am pretty much in a constant state of mild/moderate mania (2 hr sleep/night, hi energy, talk to fast, mind racing,etc), which is fine for me, as it really curbed the depression (maybe only 1 day every 2 months now and its NOT a BAD downer) I have found the drug is a good "stabilizer" keeping me mostly in a normal to moderate swing...never any severe swing. If the side effects are not unbearable, stick with the med, just be patient. It sure works for me. Learn to laugh at the klutziness and stupid moments and understand its the med and you. GOOD LUCK TO YOU ALL!

I have been using restasis. I recently developed extreme redness--broken blood vessels in one eye. It also looks like a area of darkened blood at the top eyelid. It looks terrible. It does not hurt.

I am 43 (female) and have been on Singulair for a couple of months now and the benefits have been AMAZING! I have chronic generalized eczema and pronounced facial flushing which led to swelling and Rosacea. Since starting Singulair (with a Zantac and Reactine) my skin is almost always cool (it's been YEARS). The benefits for me have been as great as what the steroids do for my skin. I can tolerate more triggers and the freedom and self-esteem boost is unquestionably life changing.

But recently I started to bruise, over every-little-thing -- even a blood pressure cup created a ring of broken blood vessels. Then about 3 - 4 weeks ago I started getting deep lower leg pain, and cramping in my calves and arches. This grew more regular, and my hips joined in and I am now rarely without the pain and deep aches. Then the weakness started, it was most pronounced in my dominant hand, I can hardly write or hold a pen now. Typing is difficult now as my hands and forearms are so weak. Yesterday I couldn't pinch my fingers to pick up a potatoe chip! My arches are curled with aches, I am weak all over and getting really uncoordinated. Going up the stairs is a chore, going down is just wacky -- it's harder than going up I am so wobbly and my knees want to give out. It's getting so pronounced that I realized that this must due to something I'm taking and the only thing I'm taking new is Singulair so I decided to Google "Singulair Side Effects" and the first link I clicked was Carrie's post, which I replied too. Then I realized there was more and have been reading all the other posts.

I am grateful that it is just side effects and nothing more sinister. This weekend the accumulated symptoms had me a bit frightened. I was washing my hands and it felt like I sprained my fingers doing it. The ligaments just sort of let go and things began bending the wrong way. It happened when I bent over to put something in the dishwasher, it was like the rib cage lost it's shape for a moment (I don't know how else to describe it). THAT felt bizarre and got my attention. Not being able to pinch my fingers to pick up a chip was the final clue that something is going wrong here. I will stop taking the Singulair now. It's a shame this happened, it was really doing it's job for me. The price of the side effects is too high though.

I am 40-years-old and took Singulair for about two months. I first took it for about two weeks and got horrible symptoms and then stopped for a week and then tried it again for about a month. Never again will I put Singulair into my body. My symptoms were chronic and severe muscle cramps and twitching, restless legs, body aches, numbness, tingling, hair loss, weight gain, and skin changes (urticaria and angioedema). I also used to suffer from menorrhagia to where now I barely get a cycle. I cannot blame Singulair for the headaches/migraines because I have been a headache/migraine suffering for many years.

When I first stopped taking Singulair the symptoms calm down. But since then they have come back with a vengence. I have been to several specialty doctors (family doctor first, endocrinologist, neurologist, allergist and rheumatologist). Now please let me defend myself by saying I see my family doctor and gynecologist yearly for a physical and also when I am sick and I have always been basically a very healthy, and slender woman with thick hair. I was on no other medications other than ibuprofen and acetaminophen for the headaches/migraines. What they have found so far is that I have secondary autoimmune hypothyroidism (only my TPO antibody and thryoglobulin are extremely elevated, but my TSH, T3 and T4 are completely normal), and allergies to everything outside (no food or pet allergies) and idiopathic lupus (because my skin has developed urticaria and angioedema).

I am going for an EMG and MRI of the brain in one week because they are trying to rule out MS. They have been saying that my symptoms look like MS or lupus. They have ruled out lupus because my blood tests do not show lupus only my skin is acting like lupus. My allergist put me on doxepin for my skin and twitching symptoms. This medication has helped my skin and slowed down the twitching.

I am not trying to blame Singulair, but it is very strange that I was a basically healthy person with some outdoor allergies and mild asthma. I would get pneumonia once a year also (always around the holidays). Now, I feel like crap since taking Singulair. My legs are the worst of all the symptoms along with the constant twitch under my right eye. This can drive a person insane, especially when you are trying to relax and your body cannot.

Thanks for listening,
Carrie

Was on Prednisone 2 years ago for respiratory problems 30mg. Gained 25 pounds, fat face, felt tired, etc.

However 2 years later, after weaning off Prednisone my muscles ache, joints are most always stiff, esp. hands plus my feet feel numb and my short term memory has not returned to normal----does any one else out there have similar problems. What can be done?

My son is 7 years old. He has been taking Singulair for about 4 months. His pediatrician switched him to Singulair after I complained that he was having severe mood swings, depression and anxiety. I suspected that the Pulmacort he was taking for asthma could be to blame. He still has some of these problems, but I think they have improved, however, he has suddenly developed a petichiea rash (I don't know if I spelled that correctly! It's a rash that looks like broken blood vessles all over his body). He looks AWFUL. I took him to 3 pediatricians and a dermatologist. The blood and urine tests they did on him all came back normal. The dermatologist found a picture and description in his book of this condition. It is called Chronic Pigmented Purpura, which basically means 'broken blood vessels'. He said the cause was unknown and it would "go into remission in 1 or 2 YEARS!" Anyway, I called my pharmacist and asked if this condition could be a possible side effect of Singulair. He said from the Singulair literature that a 'vascularitic rash (whatever that is) developed in 1.6% of Singular patients, which was .4% higher than the ones not taking it'. Has anyone out there been experiencing a rash like this??? I don't want to keep my son on a drug that would do this to him, but his asthma is much better since he started the Singulair. I don't know what to do.