Multiple sclerosis and Vitamin k deficiency - from FDA reports
Vitamin k deficiency is reported only by a few people with Multiple sclerosis. We study 4 people who have Vitamin k deficiency and Multiple sclerosis from FDA . Find out below who they are, other conditions they have and drugs they take.
What to expect?
You are not alone!
Personalized health information
On eHealthMe you can find out what patients like me (same gender, age) reported their drugs and conditions on FDA since 1977. Our tools are simple to use, anonymous and free. Start now >>>
On Oct, 10, 2017
4 people who have Multiple Sclerosis and Vitamin K Deficiency are studied.
Number of reports submitted per year:
Gender of people who have Multiple Sclerosis and experience Vitamin K Deficiency *:
- female: 100 %
- male: 0.0 %
Age of people who have Multiple Sclerosis and experience Vitamin K Deficiency *:
- 0-1: 0.0 %
- 2-9: 0.0 %
- 10-19: 0.0 %
- 20-29: 0.0 %
- 30-39: 75 %
- 40-49: 0.0 %
- 50-59: 25 %
- 60+: 0.0 %
Most common drugs for these people *:
- Depo-Provera (3 people, 75.00%)
- Avonex (3 people, 75.00%)
- Paxil (2 people, 50.00%)
- Celebrex (2 people, 50.00%)
- Aubagio (1 person, 25.00%)
Top symptoms for these people *:
- Injection Site Pain (3 people, 75.00%)
- Injection Site Haemorrhage (3 people, 75.00%)
- Hepatic Steatosis (3 people, 75.00%)
- Diabetes (3 people, 75.00%)
- Memory Loss (1 person, 25.00%)
* 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.
Subscribe to the study: get notified of updates to the study.
Do you have Vitamin k deficiency and Multiple sclerosis?
- Check symptoms - is your vitamin k deficiency caused by a drug or a condition?
- Get alerts to symptoms - forecast your symptoms and get alerts
- Join related support groups - you are not alone, join a support group on ehealth.me
- Report the side effect - help people in need and in real time
- Ask a question - ask a question related to the study
- write a review - share your experience related to the study
- More tools...
Expand the study to include reports from both FDA and eHealthMeVitamin k deficiency and Multiple sclerosis from FDA and eHealthMe reports
Multiple sclerosis (a nervous system disease that affects your brain and spinal cord. it damages the myelin sheath) can be treated by Copaxone, Tysabri, Avonex, Rebif, Baclofen (latest reports from 463,870 Multiple sclerosis patients)
Vitamin K Deficiency
Vitamin k deficiency has been reported by people with high blood pressure, atrial fibrillation/flutter, epilepsy, preventive health care, pneumonia aspiration (latest reports from 520 Vitamin k deficiency patients).
Browse all symptoms of Multiple sclerosisa 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
Could your drugs cause Vitamin k deficiencyVitamin k deficiency
Other conditions that could case Vitamin k deficiencyVitamin k deficiency
What would happen?
Can you answer these questions?
I was diagnosed with MS in 2002, and began taking Avonex to treat it. I was on it for about 10 years after which my neurologist determined it was no longer effective in slowing disease progression. For the last year or two I have had a great deal of difficulty standing up straight. My balance ...
I have relapse/remitting MS and Polycystic ovaries (Pos). I also have hypothyroidism, IBS, restless leg, obstructive sleep apnea and I am bipolar. I have been seeing a psychiatrist and/or a psychologist since my 30's for depression. I have tried to commit suicide twice. Can't figure how to add ...
You may be interested in these reviews
I am a 65 year old female and I was diagnosed with MS eighteen years ago, though I suspect I have had MS since my late twenties. I always took good care of my teeth and they were quite nice. In the last few years I started having trouble with them and about eighteen months ago they started ...
I was officially diagnosed with MS back in April and unofficially diagnosed back in February. I would assume that I have had PCOS since I was a teenager but I have for sure had it since 2009 after an exploratory lap. I am pretty freaked out with the MS diagnosis more than anything else.
Trying to get off baclofen has anyone had bad withdrawal symptoms doing this we are tapering it daily...I was on 3 months and side effects hit me worse than disease and researching withdrawal symptoms just scares me thank you
I've had MS for 34 years and been SPMS for about 15. My dad broke his pelvis a year ago. I am the closest sibling to him, My wife is a kind caring person and has been and continues to be a great help with me helping through my dad's situation. The increased stress dealing with this ...