Review: could Pravastatin sodium cause Constipation?
Summary: Constipation is found among people who take Pravastatin sodium, especially for people who are female, 60+ old, have been taking the drug for 1 - 2 years, also take medication Aspirin, and have Hypertension.
We study 8,466 people who have side effects while taking Pravastatin sodium from FDA and social media. Among them, 134 have Constipation. Find out below who they are, when they have Constipation and more.
You are not alone: join a mobile support group for people who take Pravastatin sodium and have Constipation >>>
Pravastatin sodium has active ingredients of pravastatin sodium. It is often used in high blood cholesterol. (latest outcomes from Pravastatin sodium 9,285 users)
Constipation has been reported by people with osteoporosis, pain, high blood pressure, depression, high blood cholesterol.(latest reports from Constipation 80,049 patients)
On Nov, 27, 2014: 8,460 people reported to have side effects when taking Pravastatin sodium. Among them, 134 people (1.58%) have Constipation.
Time on Pravastatin sodium when people have Constipation * :
|< 1 month||1 - 6 months||6 - 12 months||1 - 2 years||2 - 5 years||5 - 10 years||10+ years |
Gender of people who have Constipation when taking Pravastatin sodium * :
Age of people who have Constipation when taking Pravastatin sodium * :
Severity of Constipation when taking Pravastatin sodium ** :
|least||moderate||severe||most severe |
How people recovered from Constipation ** :
|while on the drug||after off the drug||not yet |
Top conditions involved for these people * :
- Hypertension (13 people, 9.70%)
- Hyperlipidaemia (13 people, 9.70%)
- Neoplasm malignant (10 people, 7.46%)
- Metastases to spine (9 people, 6.72%)
- Lung neoplasm (9 people, 6.72%)
Top co-used drugs for these people * :
- Aspirin (47 people, 35.07%)
- Furosemide (26 people, 19.40%)
- Alprazolam (24 people, 17.91%)
- Atenolol (22 people, 16.42%)
- Zetia (21 people, 15.67%)
* 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 Constipation while taking Pravastatin Sodium?
You are not alone! Join a mobile support group:
- support group for people who take Pravastatin sodium and have Constipation
- support group for people who take Pravastatin sodium
- support group for people who have Constipation
Drugs in real world that are associated with:
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Can you answer these questions (Ask a question):
- 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
- Cymbalta r/t autonomic neuropathy
losartan 20 mg
tired all the time, dizziness, chronic constipation, stomach pains, pins and needles, diabetic type 2 hx alcoholism resolved, gerd, early satiety
- 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.
- Gastro with constipation in a 4 year old only cause pain at night?
In childrens hospital now have given the tag virus for stomach pain at night that is relieved by morphine
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The orthostatic BP started in mid April, I was only dizzy upon wakening then it would subside. I have never been a big breakfast eater so I started doing that. We were in Disney later in April and I was extremely fatigued, to the point of not wanting to walk, Disney would be the first time I passed out when getting dizzy. I of course said I had gotten too warm and was exhausted from work the previous week. The dizziness continued in the mornings & I passed out several more times. On May 1st, I passed out while putting my make-up on and hit my eye on the faucet and head on the tile floor, despite that I went to work thinking it would subside, it didn't. I went to the ER directly after work. They ran a B-met on me and my GFR was 11 and creatinine 3.95. They admitted me to a larger hospital for evaluation. While in there, they pumped me with fluids continuously, saying I had severe dehydration. My kidney function improved, my creatinine levels went back down to 1.34. After 5 days I was discharged and told to see a cardiologist and endo. The endo doc cancelled my appointment on the basis it was not his area. I had had a cortisol and ACTH testing which I guess was normal. I saw the cardiologist, who said it wasn't cardio. I had had an echocardiogram in the hospital and EKG monitoring. Cardio sent me to neurology, the PNRN did a basic neurological exam and drew blood for disease markers such as Lupus, sjorgens, hepatitis, ect. All disease markers came back negative, but my GFR was at 11 again and creatinine was 4.25, BUN 50 along with an elevated ACE level. They called me and said I sarcoidosis. I really don't have any of the primary S/S of this autoimmune disease. I don't know where to go from here, they are referring me to another neurologist at a bigger hospital. I can't live my normal life, can't walk on my feet due extreme pain and I pass out at least 2x a week, which is not good for my old body. My BP upon laying and sitting runs like 117/72, upon standing it drops to like 70/50-50/30. I am on 0.1 mg of florinef, I tried increasing it but then my legs swelled up for a gain of 23#. I talked to Mayo Clinic today and all there specialists are booked out thru December. I have to be able to work, I can't stay home any longer than September 8th! Please advise me!
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- 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.
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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.
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