September 8th
2008
9:04 PM
I have been io Lisinopril for several months, and the only side effect I can say is a VERY ANNOYING rash on the inside of my upper thighs. It comes and goes and gets worse with warmth, like a heat rash. I also have now developed a rash on my butt that is looks to me like shingles. Very itchy, to the point of bleeding from scratching. I treated with diaper rash ointment and triple antibiotic ointment to not much improvement. Reently tried a jock itch ointment which seems to be working. Also took myself off Lisinopril 2 days ago, and things are getting better, but very slowly........
-- By fibaguy | Reply | (2) replies | Private Message me
September 5th
2008
11:24 AM
The anti-depressant Doxepin elliminates many of the negative side effects of Geodon, shaking, restlessness, salavation,,,,
Doxepin is a anti-histimine and most anti-histimines would most likely do the same thing but Doxepin lasts all day and is a good anti-depressant also. All of the negative side effects of Doxepin are only temporary also.
May 17th
2008
1:46 AM
Hi,
I just found this site, as I am looking for an explanation for the extreme joint pain that I am having, along with swollen ankles/feet. I have been dealing with some type of chronic contact dermatitis that no one has been able to solve, since last July. I have been on numerous steroids, then on Cyclosporine, for several months, which can play havoc with your kidneys. I also started taking Singulair for the itching, which is one of the few things that has really helped. Since November, I was taking Singulair on and off. But, as I recall, I began taking it daily since around late January. Around late February, I began having joint pain, which still continues, and lately, is becoming excruciating! When it first began, I blamed it on the Cyclosporine and kidney breakdown. But, since I have been off that, the pain has continued to worsen. Then I thought it may have something to do with the Doxepin, which I also take at night for the itching. I stopped taking that two nights ago, but the pain continues to worsen.
Now, from what I am reading, these blogs make me believe it could be the Singulair. Can anyone tell me how long it takes for the pain to go away once you stop taking the Singulair????? I will gladly stop taking it if this pain will go away. In fact I will be thrilled, because I was suppose to begin testing next weak for possible Lupus, because it doesn't seem that the Physicians who prescribe Singulair, are well aware of these issues.
I would appreciate anyone who can give information as to how long it takes for the side effects to subside. Thank you!!!
(In pain in Boca Raton, FL)
September 4th
2007
10:46 AM
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
November 19th
2006
10:13 AM
Took Lamictal for about a month and a half for depression, starting June 206. Did help flatten out & stabilze mood. Started with small 25mg dosages and ramped up. By the time I got to 175mg, for some unknown reason, I started to get bad "pins/needles/elctric shock-type" pains in hands & feet, then progressed to arms, legs & trunk areas, with some body twitches and deep, inner aches. Symptoms started in mid August 2006 and still remaining today, mid November 2006. Fearing these symptoms will never cease has me under alot of anxiety. Hard to get to sleep at night. Has made life very difficult to manage. Has anyone else experienced these side effects? Was not taking any other med at the time.
-- By anthonyochoa | Reply | (1) replies | Private Message me
September 4th
2006
7:06 PM
I orignally started taking 25 mg for chronic hives after a roller coaster w/any thing containing blue dye, prednizone, allegra, claritan. Finally I stopped taking all colored meds only white or pale. I have a lot of wgt gain since this ordeal started in Nov. I did not know Doxepin could cause wgt gain. I am now taking 50 mg at night for insomnia and it does have an antihystamine in it. I think I am going to cut back to 25 mg again and get off this. One Dr. told me anything with antihystames are a wgt gainer. I also take Zoloft in the a.m. which helps okay and Doxepin can also be used for that but mainly helps me sleep and gain wgt :-)
-- By laura703 | Reply | Private Message me
February 26th
2005
10:01 PM
I have been a diabetic for 42 yrs. I had been experiencing severe pain in my toes, feet, and legs where the nerve endings twitched and ached so bad, I would be up all night soaking and massaging my feet and legs. I was diagnosed with Neuropathy and was prescribed Doxepin at bedtime. It has helped tremendously.
-- By terybhr | Reply | Private Message me
February 10th
2004
2:42 PM
I have a blister like rash that just appears. The doctor gave me Doxepin for this. I can't relate this rash to using an antidepressant for the cure. Is there any realation? The only side effect I have from using this is, being very lethargic for awhile when I first wake up.
-- By bgooden | Reply | Private Message me
February 5th
2004
8:22 PM
i was diagnosed w/eczema &psoriasis on both my feet on the bottom.i was prescribed doxepin to help with the relentless itch i was experiencing.i take 2 pills each nite before bed. i did feel groggy the next day but i found if i got a good nite sleep the grogginess wasnt so bad.i do want to ask people if anyone who has ever used this drug if they or anyone they know has ever had a weight gain because of it.....
-- By michelle242113 | Reply | Private Message me
October 21th
2003
5:58 PM
I just went on Sinequan/Doxepin a week ago. I have been very lethargic since. I find myself falling asleep all day even though it helps me sleep. I am taking this medication for stomach nausea and I see that its used for bed wetting, depression, and obsessive-compulsive disorders... anyone else taking this for other reasons???
-- By renny | Reply | Private Message me
Doxepin Hydrochloride (7) Singulair (2) Lisinopril (2) Ultram ER (1) Sinequan (1) Geodon (1) Lamictal (1)
September 11th
2008
4:25 PM
I was on Lisiniprol for 91 days as an ACE inhibitor for diabetes and kidney protection. All was find except for a constant feeling of burning blood all the time. It was tolerable though.
But on day 91 I developed hives. 14 days after that I was broken out from scalp to sole of my feet -- feeling miserable and no relief in site.
Dr. told me that I was allergic to something and to take benadryl. 3 doctors later I was told that I had hives and had to learn to live with it. He increased my benadryl.
I took myself off all my meds except insulin -- not knowing what was going on. I researched and discovered the this drug should NOT have been given to me because I also have SJOGRENS (an autoimmune disease akin to Lupus).
The hives got worse, my benadryl was increased by the drs. Finally I passed out due to benadryl toxicisity (overdosed) and they put me on prednisone.
To this day -- 6 months later -- I still have hive outbreaks that are miserable. I have missed a day from work every 7-10 days. The prednisone helps, but as a diabetic it sends y blood sugars through the roof. My rheumo has put me on doxepin (an antidepressant) because it has an antihystamine property that seems to be helping.
It is also useful for the rheumotoid arthritis that comes from Sjogrens and such. I am sleepy a lot -- but that could be from the doxepin.
I will never take Lisiniprol or any other ACE inhibitor. I am suffering and the worse part of it: the doctors and medical profession don't care and simply tell me to learn to live with it.
-- By hwylder | Reply | Private Message me