Would you have White blood cell count increased when you have Psoriasis?
Summary: White blood cell count increased is found among people with Psoriasis, especially people who are male, 30-39 old, also have Hypertension, and take medication Raptiva.
We study 298 people who have White blood cell count increased and Psoriasis from FDA and social media. Find out below who they are, other conditions they have and drugs they take.
You are not alone: join a mobile support group for people who have Psoriasis and White blood cell count increased >>>
Psoriasis (immune-mediated disease that affects the skin) can be treated by Humira, Enbrel, Methotrexate Sodium, Stelara, Clobetasol Propionate, Methotrexate. (latest reports from Psoriasis 68,495 patients)
White blood cell count increased
White blood cell count increased has been reported by people with schizophrenia, high blood pressure, multiple sclerosis, depression, rheumatoid arthritis.(latest reports from White blood cell count increased 23,523 patients)
On Nov, 25, 2014: 298 people who have psoriasis and White Blood Cell Count Increased are studied.
Gender of people who have psoriasis and experienced White blood cell count increased * :
|White blood cell count increased||44.86%||55.14% |
Age of people who have psoriasis and experienced White blood cell count increased * :
|White blood cell count increased||0.00%||0.00%||0.81%||6.85%||13.71%||23.39%||23.79%||31.45% |
Top co-existing conditions for these people * :
- Hypertension (37 people, 12.42%)
- Psoriatic arthropathy (24 people, 8.05%)
- Depression (21 people, 7.05%)
- Diabetes mellitus (15 people, 5.03%)
- Cardiac disorder (14 people, 4.70%)
- Hypothyroidism (12 people, 4.03%)
- Pain (11 people, 3.69%)
- Pruritus (11 people, 3.69%)
- Asthma (11 people, 3.69%)
- Dry eye (10 people, 3.36%)
Most common drugs used by these people * :
- Raptiva (99 people, 33.22%)
- Humira (85 people, 28.52%)
- Enbrel (71 people, 23.83%)
- Aspirin (21 people, 7.05%)
- Amevive (17 people, 5.70%)
- Prozac (16 people, 5.37%)
- Methotrexate (15 people, 5.03%)
- Lipitor (15 people, 5.03%)
- Prednisone (14 people, 4.70%)
- Cyclosporine (13 people, 4.36%)
* Approximation only. Some reports may have incomplete information.
How to use the study: print a copy of the study and bring it to your health teams to ensure drug risks and benefits are fully discussed and understood.
Do you have Psoriasis and White Blood Cell Count Increased?
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- support group for people who have White Blood Cell Count Increased
Could your drug cause:
Other conditions that could cause:
Can you answer these questions (Ask a question):
- How long did the hives/itching eyes last?
had back to back allergic reactions to iv abx - after clinda (april 2014) developed sjs - still having hives around my eyes, watering, and severe itching. have been on 4x dose zyrtec, prn benadryl. when will this go away?
- What drug can be substitute for metoprolol with psoriasis
My psoriasis got worse after being started on metoprolol in 2005. What drug can be substituted for metoprolol. My other medications for hypertension are losartan, chlorthalisone, nifedipine.
- Does having factor v leiden affect my ability to use the injection or pill for of psoriasis medication?
I was diagnosed with Factor V Leiden after my miscarriage. During my second pregnancy, I had to take Lovenox(sp?) injections daily. After my pregnancy I developed Psoriasis. I have tried topical solutions with no luck. I am wanting to explorer stronger medication but when I asked my dermatologist, he said he didn't know how the meds would interact with my Factor v, so he would not prescribe them. Do you know if I am able to use the stronger meds if I have Factor V?
- If i take garcinia cambogia will it interfere with my other meds?
I take 40 mg of Lisinopril, 20mg of Pravastatin, 5mg Amlodipine Besylate, once per day.
I take 100 mg of Sertraline Hcl Tabs. (one and one half per day)
I use Clobex as needed for Psoriasis on my legs.
I am on oxygen 24 hours a day @3 liters.
I do take nebs twice a day every 12 hours of Performist and Budesonide Inhalation Suspension
My age is 66 and I am obese. I weigh 315 pounds and I want to lose 150 pounds.
I do not have heart disease, but I am sure that I am headed in that direction. My blood pressure is right around 137 to 145 over 70 generally. My pulse is from 60 to 75.
I believe that my psoriasis is stress related.
I always have problems with yeast in moist areas. I have not had a yeast infection vaginally for many years.
- Can i take meloxicam and (1 answer)
have taken meloxicam for ten years now and i,m looking for a substitute for it so as not to wreck my stomach
woulld the glucocimine sulphate do the trick
More questions for: Psoriasis, White blood cell count increased
You may be interested at these reviews (Write a review):
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It has been one week since I stopped taking it and today my leg psoriasis is starting to fade away. Has not itched all day today. TYJ!
The patch on my scalp is doing the same. The scalp thickness has improved tremendously. I just hope I don't start having trouble with my BPH again, so for so good.
- Etanercept and irritability
I have been on Etanercept for 8 years for Psoriasis. Previous to this I was on
Methotrexate, Cyclosporine, Retinodes and ACTH injections.Since being on 25mg twice a week I have been 98% clear.The only side effect to date is "Irritability" which lasts about 24hrs.
This Drug has been my saving grace.
- How an integrative wellness approach cured me of insomnia, ibs, and more (1 response)
For 10+ years, I suffered with insomnia and a host of other problems including intestinal distress, headaches, psoriasis, anxiety, cognitive issues, hypothyroid, chronic itching, restless leg, etc. Traditional medicine, aka taking drugs, was not working to heal me. Since childhood, I’ve had IBS, headaches, and upper respiratory problems. Then, in my early twenties, after childbirth, I begin to suffer with panic attacks. I managed to get the panic attacks under control, but the insomnia never went away. I took both Ambien and Clonazepam at different times in my life. When I expressed my concern over taking these meds, my doctor reassured me and told me that some people just have to take sleeping meds for their entire life. I read literature on insomnia and tried most everything – no late night eating, no TV or electronics before bed, sleep in a cool room with complete darkness, meditate, sleep labs, etc. etc. etc. Even with the sleeping meds, I never got restful sleep. Most days, I felt like it was all I could do just to get by. For at least the first half of each day, I felt that I was in dazed stupor until the meds in me would start to wear off. I was first on Clonazepam and then switched to Ambien. When I made the switch, I suffered through withdrawal for about a week. It was horrible -- no sleep, hallucinations, etc. For years, I had silently suffered – my family, friends, and colleagues having no idea to what extent. I felt that mentally, cognitively, and physically I was slowly slipping away. My love for my child and my desire to nurture and provide for him is what kept me going. Without this purpose in my life, I fear that I might have given up somewhere along the way.
Finally, a few years ago, I went to see an integrative medicine doctor. After years of being in the darkness, I am finally living again. My IM doctor put me on natural supplements, a natural thyroid replacement, and, most importantly, tested me for food allergies/sensitivities. My test results yielded that I could not tolerate wheat, gluten, yeast, and dairy. I took these results seriously and I completely eliminated these things from my diet. After two weeks of adhering to my new diet, I already felt better. In fact, I felt so much better, that, one evening, I decided not to take my Ambien. I have not taken it or any sleep or anxiety medicine since. My doctor was as surprised as I was and did not really anticipate that the diet alone would cure my insomnia. In fact, he had told me that, since I had been taking sleeping meds for so long, eliminating them completely would be a long process that we would have to work through together. Nearly all of the symptoms I listed have disappeared. I continue to take my natural thyroid replacement and the supplements my doctor suggested. I have the occasional migraine and a few patches of psoriasis -- but nothing like the severity I had before. I am 47 now and I am on a journey of healthy transformation. I eat healthy foods, exercise regularly, and truly feel healthy, younger, and physically stronger than I have in 15 and maybe 20 years. Jokingly, my husband used to refer to me as "fragile." Well, not anymore. In fact, he has told me that my body seems like a completely different one. He has had a front-row seat to my transformation and he is as much "in awe" of the changes in me as I am in myself.
Ten years ago, I was not optimist about my future. Today, I am full of hope, wonder, energy, and excitement. I believe we have the ability to heal ourselves, but we must be diligent in our pursuit of knowledge, persistent and strong in our will to make lifestyle changes, and patient that results will come as long as we are doing all the right things. By the way, giving up foods I had eaten my entire life was not difficult at all once I did it long enough to realize the tremendous benefits of not eating them.
- Psoratic arthritis and trigeminal neuralgia
hi i suffer from psorisis and psoratic athritis i was just diagnosed with trigeminal neuralgia i was looking for the connection between the two and i see that there is one from your study
the thing is all 13 people in the study said to have psoriatic arthropathy yet only one said to have psoratic arthritis yet to the best of my knowledge it is the same condition just a diffrent name which means all those studied have psoratic arthritis like me
also i have not been taking those medicines in the study yet i have the same condition so if you take me into account could be the oly conecction between all of us is the psorisis and psoratic arthritis and not the medicine
More reviews for: Psoriasis, White blood cell count increased
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