Review: could Pravastatin sodium cause Rashes?
Summary: Rashes is found among people who take Pravastatin sodium, especially for people who are female, 60+ old, have been taking the drug for < 1 month, also take medication Aspirin, and have High blood pressure.
We study 8,478 people who have side effects while taking Pravastatin sodium from FDA and social media. Among them, 226 have Rashes. Find out below who they are, when they have Rashes and more.
You are not alone: join a mobile support group for people who take Pravastatin sodium and have Rashes >>>
Pravastatin sodium has active ingredients of pravastatin sodium. It is often used in high blood cholesterol. (latest outcomes from 9,302 Pravastatin sodium users)
Rashes (redness) has been reported by people with rheumatoid arthritis, high blood pressure, high blood cholesterol, osteoporosis, depression. (latest reports from 146,455 Rashes patients)
On Feb, 1, 2015: 8,478 people reported to have side effects when taking Pravastatin sodium. Among them, 223 people (2.63%) have Rashes.
Time on Pravastatin sodium when people have Rashes * :
|< 1 month||1 - 6 months||6 - 12 months||1 - 2 years||2 - 5 years||5 - 10 years||10+ years |
Gender of people who have Rashes when taking Pravastatin sodium * :
Age of people who have Rashes when taking Pravastatin sodium * :
Severity of Rashes when taking Pravastatin sodium ** :
|least||moderate||severe||most severe |
How people recovered from Rashes ** :
|while on the drug||after off the drug||not yet |
Top conditions involved for these people * :
- Hypertension (62 people, 27.80%)
- Diabetes mellitus (39 people, 17.49%)
- Hyperlipidaemia (26 people, 11.66%)
- Dyslipidaemia (24 people, 10.76%)
- Hypothyroidism (21 people, 9.42%)
Top co-used drugs for these people * :
- Aspirin (64 people, 28.70%)
- Lisinopril (31 people, 13.90%)
- Enalapril maleate (29 people, 13.00%)
- Synthroid (28 people, 12.56%)
- Furosemide (25 people, 11.21%)
* 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 Rashes while taking Pravastatin Sodium?
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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?
- Is pravastatin na is also used for lower mcholesterol?
need to know ,as i read a study that patients 60+ years old with Pravastatin sodiun, Impotence is Found
- 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
- Has anyone had side affects and/or drug interactions from xarelto and prevastatin?
I currently take xarelto after a bout of multiple blood clots in both lungs...I have just been diagnosed with high cholesterol and dr wants me to take prevastatin and I'm concerned about side affects and/or drug interactions
- Does anyone else have trouble getting to sleep since beginning to take brilinta?
Am trying to figure out just why, since stent insertion, I have developed insomnia which keeps me from getting to sleep at night. Brilinta is the only new drug I am taking.I am very sleepy, falling asleep in my chair while watching TV, but wide awake when I go to bed and staying awake until two or three in the morning. I do not nap during the day and am pretty active with cardio rehab and walking the dogs three times a day.
More questions for: Pravastatin sodium, Rashes
You may be interested at these reviews (Write a review):
- 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.
- Terrible excessive sweating from hydrochlorothiazide
I guess I fit the profile of who gets excessive sweating from HCTZ. I am a 65 year old female and suffered from excessive sweating for two years. With just very little exertion, I would pour sweat from the top of my head. It would run into my face and all over my hair. My hair would be ringing wet. I had heavy perspiration in the groin area and down my back also. I had to change clothing 2-3 times a day and wash up or shower that many times also. The doctor tried changing my Cymbalta and put me on Wellbutrin instead. It did absolutely no good. I went off the wellbutrin and back onto the Cymbalta. I did some research and saw that HCTZ could cause excessive sweating. Both my doctor and my pharmacist said that they had never heard of that. I went off the HCTZ, and my sweating stopped almost immediately. My doctor and my pharmacist were very surprised. I'm one of those people who frequently have different reactions to drugs than are typical. If you're having excessive perspiration and are on HCTZ, try going off of it. It just may be the culprit!
- 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.
- Bone infections involving my teeth crohns and prednisone over the past 12 years
Dentist  tell me the abscesses are in the bones and I've had several root canals, bridges, bone surgeries that last 3 years, teeth became so mobile after the bone economy I had them pulled and now a partial one month ago. Bone loss etc. I don't have the ridges in my mouth that most Crohn patients have. Appears to affect the upper teeth.
Crohns diagnosed at the age of 39. Moderate to severe.
Dentists state the problem is the use of prednisone and having Crohn.
- Ideopathic hypersomnia from mantle cell lymphoma
I have an unusual idiopathic hypersomnia surrounded by the circumstance of also having Mantle Cell Lymphoma. I awake each day at around 7:00 am without an alarm after 7-8 hrs sleep. By 8:00 am after a cup of coffee and breakfast, I feel fully awake and 100% normal.
Around Noon and 12:30, I begin to feel sleepiness coming on. This is nothing like the mid-afternoon low many people experience. A cup of coffee or a little fresh air do nothing.
By 1:00 pm - 1:30 pm, I feel deeply drugged (like I've taken Ambien) and need to sleep. I sleep 3-4 hours of fairly deep sleep (I don't hear the phone or someone at the door). I have vivid dreams near the end of the nap and about half the time I have auditory hallucinations at the beginning or the end of the nap (I generally don't have these at night).
When I awake, I feel like it's morning again and need a cup of coffee to get me going again. For the rest of the evening, I feel about 80% of morning alertness and energy levels.
I go to bed at about 10:30 every night. It takes me about 15 - 20 minutes or so to fall asleep. I get up once a night to urinate, due to slight incontinence from prostate brachytherapy. I generally fall right back to sleep. Even when I sleep more or less than average, or go to bed significantly later than normal, I still feel the 1pm sleepiness at the same time and in the same duration.
I have tried Nuvigil and it works well enough for me to stay awake during the afternoon if absolutely necessary. I'm feel about 70% of normal, but don't sleep well that night and don't feel fully rested or awake the next day. If I force myself to stay awake, the intense sleepiness goes away around 4:00pm - I feel sluggish but do not need to sleep until my normal bedtime.
Diagnosed with Mantle Cell Lymphoma in June of 2013. I noticed worsening early afternoon sleepiness up to six months before diagnosis. After diagnosis, I gradually became more sleepy and began needing naps of 1/2 hour to 1 hour. By the time I began treatment for MCL (Oct 2012, I was sleeping in excess of 4 hours every day despite getting a good night's sleep. This and the increasing size of my spleen were the determining factors for beginning treatment. During 6 months of chemotherapy (Rituxan/Bendamustine every 4 weeks) I continued to have these naps. After achieving full remission, I received high dose chemo followed by an autologous stem cell transplant in May of 2013. About a month after the transplant, when I gained a little strength back, I needed only a light nap of 30-45 minutes, but gradually the heavy naps returned to the current 3 hr/day level, despite my strength and endurance returning to nearly normal levels. My nighttime sleep pattern has not changed significantly all this time.
I had an Overnight sleep study that showed no significant apnea, but because I didn't sleep normally at the center, the test was inconclusive. It was followed by an MSLT which showed that I did not have narcolepsy (no early REM). I was then prescribed an auto-PAP machine for three weeks to check my sleep hygeine at home. Minimal apnea was noticed, and most of the episodes were from my changing position triggering a boost in the PAP pressure. I slept significantly worse because of this.
Because of the clockwork nature of the daytime sleepiness and the correspondence with my lymphoma, I would like to investigate an endocrinological source for my idiopathic hypersomnia but the sleep centers here in Wilmington are not equipped to handle this investigation.
More reviews for: Pravastatin sodium, Rashes
Comments from related studies:
From this study (2 years ago):
I have developed a rash on several parts of the body.. Small bumps and red all over.
From this study (2 years ago):
i have a rash with raised red areas that are shiny on my legs and arms mostly. it itches severly
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