Pravastatin sodium and Lipodystrophy acquired - from FDA reports
Lipodystrophy acquired is reported only by a few people who take Pravastatin Sodium. We study 11,739 people who have side effects while taking Pravastatin sodium from FDA. Among them, 2 have Lipodystrophy acquired. Find out below who they are, when they have Lipodystrophy acquired and more.
11,739 people reported to have side effects when taking Pravastatin sodium.
Among them, 2 people (0.02%) have Lipodystrophy acquired
Number of reports submitted per year:
Gender of people who have Lipodystrophy acquired when taking Pravastatin sodium *:
- female: 0.0 %
- male: 100 %
Age of people who have Lipodystrophy acquired when taking Pravastatin sodium *:
- 0-1: 0.0 %
- 2-9: 0.0 %
- 10-19: 0.0 %
- 20-29: 0.0 %
- 30-39: 0.0 %
- 40-49: 0.0 %
- 50-59: 100 %
- 60+: 0.0 %
Top conditions involved for these people *:
- Hiv Infection: 1 person, 50.00%
Top co-used drugs for these people *:
- Norvir: 2 people, 100.00%
- Isentress: 2 people, 100.00%
- Truvada: 1 person, 50.00%
- Reyataz: 1 person, 50.00%
- Prezista: 1 person, 50.00%
Top other side effects for these people *:
- Weakness: 1 person, 50.00%
- Sleep Disorder: 1 person, 50.00%
- Sinusitis (inflammation of sinus): 1 person, 50.00%
- Rhabdomyolysis (a condition in which damaged skeletal muscle tissue breaks down): 1 person, 50.00%
- Rashes (redness): 1 person, 50.00%
* Approximation only. Some reports may have incomplete information.
- Subscribe to monitor Lipodystrophy acquired in Pravastatin sodium
- Subscribe to monitor Pravastatin sodium
Do you take Pravastatin sodium and have Lipodystrophy acquired?
- Check whether a drug or a condition causes Lipodystrophy acquired
- Predict new side effects and undetected conditions
- Connect with people like you, or share your experience to help people like you
- Print a copy of the study and bring it to your health teams to ensure drug risks and benefits are fully discussed and understood.
- Want to find out more about the FDA reports used in the study? You can request them from FDA.
Pravastatin sodium has active ingredients of pravastatin sodium. It is often used in high blood cholesterol. (latest outcomes from Pravastatin sodium 13,741 users)
Lipodystrophy acquired (a regional loss of subcutaneous adipose tissue which usually starts in the face, extends downward acquired) has been reported by people with hiv infection, multiple sclerosis, acquired immunodeficiency syndrome, diabetes, gestational diabetes (latest reports from 2,424 Lipodystrophy acquired patients).
Drugs that are associated with Lipodystrophy acquiredLipodystrophy acquired (360 drugs)
Could your condition cause Lipodystrophy acquiredLipodystrophy acquired (183 conditions)
Pravastatin sodium side effects
- Pravastatin sodium side effects (11,745 reports)
Browse all side effects of Pravastatin sodiuma b c d e f g h i j k l m n o p q r s t u v w x y z
What would happen?
You are not alone. Join our personalized support groups:
- Support group for people who take Pravastatin Sodium and have Lipodystrophy Acquired
- Support group for people who have Lipodystrophy Acquired
- Support group for people who take Pravastatin Sodium
You may be interested in these posts
- Hi, My name is Mary and I've been using pravastàtin for appx. 3 years and recently started trying to understand why I have such heavy pain in my chest and so hard to catch my breath.
- Tamoxifen restarted UTIs, was reduced by bladder control medication and didn't like possibility of clots. Started A 2 weeks ago. Bone density was tested a few years ago and was good. I eat and drink most of the calcium producers. No side effects so far.
- I'm just starting the drug Pravastatin and I have been on a magnesium drip for almost 2 years for fibromyalgia... I'm not very good with drugs... my doctor feels that it is genetic as I don't eat fats... I don't eat meat...my mom and dad both had cholesterol I have a sisters and two brothers...
- I've taken citralopram for over 7 years and I'm the last year I've had significant fat loss causing dark caving of my flesh
- Well I was put on pravastatin before and I was have to stop it but I can't remember why 3 days ago my dr put me back on and also put me on Mobic which also I was on 15 years ago and I have to stop that one also then, and also he put on amlodipine besylate so I'm not sure which one have that...
- Will you have Pleural Calcification with Depression?
- Will you have Nerve Root Lesion with Gabapentin?
- Will you have Breathing Difficulty with Valsartan?
- Will you have Facial Pain with Keppra?
- Will you have Asthma with Frova?
Active Support Groups
- Support group for people who have Depression and Pleural Calcification?
- Support group for people who take Gabapentin and have Nerve Root Lesion?
- Support group for people who take Valsartan and have Breathing Difficulty?
- Support group for people who take Keppra and have Facial Pain?
- Support group for people who take Frova and have Asthma?
- What to expect when you have Depression and Pleural Calcification?
- What to expect when you take Gabapentin and have Nerve Root Lesion?
- What to expect when you take Valsartan and have Breathing Difficulty?
- What to expect when you take Keppra and have Facial Pain?
- What to expect when you take Frova and have Asthma?
- A study for a 15 year old boy who takes Zantac
- A study for a 49 year old woman who takes Gleevec
- Drug comparison of Lexapro, Celexa, Wellbutrin, Zoloft for a 71 year old woman
- A study for a 62 year old man who takes Brilinta
- A study for a 35 year old woman who takes Methotrexate
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.