Review: could Clonidine cause Rash (Rashes)?
Summary: Rash is found among people who take Clonidine, especially for people who are female, 60+ old, have been taking the drug for 1 - 6 months, also take medication Aspirin, and have High blood pressure.
We study 9,229 people who have side effects while taking Clonidine from FDA and social media. Among them, 454 have Rash. Find out below who they are, when they have Rash and more.
You are not alone: join a mobile support group for people who take Clonidine and have Rash >>>
Clonidine has active ingredients of clonidine. It is often used in high blood pressure. (latest outcomes from 9,672 Clonidine users)
Rash (redness) has been reported by people with rheumatoid arthritis, high blood pressure, high blood cholesterol, osteoporosis, depression. (latest reports from 150,999 Rash patients)
On Jan, 3, 2015: 9,217 people reported to have side effects when taking Clonidine. Among them, 454 people (4.93%) have Rash.
Time on Clonidine when people have Rash * :
|< 1 month||1 - 6 months||6 - 12 months||1 - 2 years||2 - 5 years||5 - 10 years||10+ years |
Age of people who have Rash when taking Clonidine * :
Severity of Rash when taking Clonidine ** :
|least||moderate||severe||most severe |
How people recovered from Rash ** :
|while on the drug||after off the drug||not yet |
Top conditions involved for these people * :
- Hypertension (81 people, 17.84%)
- Angiogram (58 people, 12.78%)
- Nuclear magnetic resonance imaging brain (54 people, 11.89%)
- Pain (40 people, 8.81%)
- Anxiety (37 people, 8.15%)
Top co-used drugs for these people * :
- Aspirin (169 people, 37.22%)
- Lisinopril (127 people, 27.97%)
- Epogen (113 people, 24.89%)
- Magnevist (109 people, 24.01%)
- Norvasc (107 people, 23.57%)
* Approximation only. Some reports may have incomplete information.
** Reports from social media are used.
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 Rash while taking Clonidine?
You are not alone! Join a mobile support group:
- support group for people who take Clonidine and have Rash
- support group for people who take Clonidine
- support group for people who have Rash
Drugs in real world that are associated with:
Could your condition cause:
Can you answer these questions (Ask a question):
- What drug helped most to get rid of rash?
Antihistamines did not help my itchy rash from this drug. What else can I use or get from my doctor?
- I have been told by my gastroenterologist that i have gastroparesis, what are my treatment options, if any?
I've had a CT scan and a Gastric Emptying study completed. My stomach is only 35% emptied after 4 hours, it should be at least 90% empty at that point. I have a colonoscopy and esophagealendoscopy scheduled for the first week of the year. What are my treatment options at this point?
- What type of seizure do people have using clonidine
My son has been having drop seizures & i believe the Clonidine may be causing them.
- Alprazolam & amoxicillin
Have Diverticulitis from having Diverticulosis. Have had high blood pressure for
about 4 years and it is controlled with the Norvasc & Clonidine. Enlarged prostate is controlled with Flomax & Avodart. Meclizine is for vertigo, take 2 25mg per day, 1 Am & 1 PM. Take 1 Norvasc AM & 1 Flomax PM.
- How long does redness last after picato?
After 3 and a half weeks, I still have a huge red splotch on my face where I applied picato gel according to directions from my dermatologist. I'm very worried that it will be permanent. I had a huge water filled blister the morning after my first application of the gel. I used it two more times as directed. After a week, some of the redness was going away but I've seen no more improvement in the past two weeks. I'm still scaley, rough and red.
Has anyone else experience this? I went by the doctors office the first morning and was told it was as expected. I've called back and been told not to worry. I see the dr in two more weeks, but for now, I'm quite upset that permanent damage has been done. I was not warned at all that this could happen. The photos in the medication packaging led me to believe that in 3 weeks, all redness would be gone. Info needed for sure. Please let me know. Thanks
More questions for: Clonidine, Rash
You may be interested at these reviews (Write a review):
- Respiridone causes hyper activity
My 7yr old is taking intuniv in the AM and respiridone @ pm but it makes run around crazy like a boost of energy
- Lamotrigine severe rash
I started taking 100mg of Teva-Lamotrigine Nov 22 once daily. I got a refill on Dec 5 that was Mylan-Lamotrigine. Two days later I woke up with an odd hot feeling rash all over my body and severe fatigue. I went back to bed 1/2 hour later after taking my regular Wellbutrin and the Lamotrigine. I woke up late morning. It got progressively worse during the day and I had a headache,fever and chills. I took the anti-histimine Aerius later that day which didn't help. The next day I went to a walk in clinic and they said it wasn't the Lamotrigine and thought it was a virus and did a throat swab. The fever and chills went away after a few days but I still have the rash. Finally after a week I saw a doctor that agreed it was the drug and I am now on the second week of Prednisone steroid treatment and prescription Reactin which is helping slowly. I have reported it to the Mylan drug company.
- Rash from eating kale
I ate kale for the first time on Monday. I only had a small bowl of fresh mixed green salad, so it wasn't entirely Kale. By Tuesday, I had a small rash on my left hip. I ignored it at first. Thursday evening, I decided to eat a large kale salad with other veggies and salmon, all of which I have eaten regularly aside from kale. Friday morning, my entire body was covered in the same rash that appeared Tuesday. I went to the ER. The doc said it was some type of allergic reaction. The ONLY thing I did/consumed different was the kale. I can't find much about it's reactions, though.
- Had nms in 2005, will trileptal increase chance of recurrence?
In 2005 I had NMS, which was not detected by my drs for 4 months. I'd been on Lexapro & Seroquel for 2 yrs, but was weaned from Lexapro & placed on Lamictal 3/05. Began getting low-grade fevers, which I was told were not caused by the Lamictal. I quit taking it anyway, fevers (along with uncontrollable shivering) continued & got higher. By 5/05 my temps were reaching 105 deg F. Husband said I became combative, refused to go to hospital. Early June/05 he came home to find me wrapped in blankets, with a temp over 105 F. He tried to place me in a tub of cold water, said I was rigid & screamed when he tried to move me. I was in the tub, speaking "in tongues" (his description, I have no memory of this). He called 911, took me to hospital. I woke, no idea where I was or why. After a lumbar puncture & 2 days in ICU I went home. The fevers continued...2 weeks later he came home to find me wrapped in sheets, towels, blankets, with the heat on full (it was in the 90's outside) he called ambulance again. I awoke to find myself under an ice blanket with nurses pushing large vials of dantrolene into both arms, several liters. Another LP, a stint in ICU...this time they told me it was NMS. The dr who dxd me said he was surprised I was alive, & not a vegetable, as my temp had peaked at 109 deg F. I suffered brain damage; short-term memory loss, brain can't control my body temp, my blood pressure went up. An arteriogram showed completely healthy heart & arteries, no plaque at all. I lost all body fat as well as some muscle mass. The fevers continued even after stopping the Seroquel. I visited my PCP for a checkup in 9/05, temp was normal. I started shuddering, my temp went up a full degree every 5 minutes. PCP admitted me to ER, my heart rate was over 272 B/M; they stopped my heart 3 times to "reset" it, which didn't work. I spent 3 days in hospital. Several months later my P doc tried me on Lamictal alone; I got Stevens-Johnson syndrome. I stopped the drug as soon as the signs appeared. I've been untreated, except for Neurontin & Primidone, until my manic episodes became unlivable. 3 weeks ago I went 8 days with no sleep, became psychotic. My P doc gave me Trileptal, which has evened my moods, but I've been getting low-grade fevers (highest was 103.6). Would having had NMS in the past make me more prone to falling to it again with the Trileptal? It's the only new med I've taken in over a year.
- Losartan cause deep vein thrombosis
have had two knee surgeries ,a lumbar decompression, after this three surgeries start taken Losartan potassium and two months later have had a lumbar fusion after this I suffered a Deep Vein Thrombosis, continues taken Losartan for more of year and half, I notice is a bad combination when my older physician increase high dose of Warfarin I was losing mi Vision and stopped Losartan by my self and my vision is great now. my new physician told me that is OK that I had stopped taken Losartan. and I strongly believe that this cause me the DVT.
More reviews for: Clonidine, Rash
Comments from related studies:
From this study (10 months ago):
After taking these meds, most for ten years, I began to have a rash. Started around my ankle and has spread all over my body, except my face and neck...three biopsies have noted that I do have an allergy but no other information. Started after I had my knee replaced. Has anyone had rashes from any of these meds?
NOTE: The study is based on active ingredients and brand name. Other drugs that have the same active ingredients (e.g. generic drugs) are NOT considered.
WARNING: Please DO NOT STOP MEDICATIONS without first consulting a physician since doing so could be hazardous to your health.
DISCLAIMER: All material available on eHealthMe.com is for informational purposes only, and is not a substitute for medical advice, diagnosis, or treatment provided by a qualified healthcare provider. All information is observation-only, and has not been supported by scientific studies or clinical trials unless otherwise stated. Different individuals may respond to medication in different ways. Every effort has been made to ensure that all information is accurate, up-to-date, and complete, but no guarantee is made to that effect. The use of the eHealthMe site and its content is at your own risk.
You may report adverse side effects to the FDA at http://www.fda.gov/medwatch/ or 1-800-FDA-1088 (1-800-332-1088).
If you use this eHealthMe study on publication, please acknowledge it with a citation: study title, URL, accessed date.