Review: could Coq10 cause Muscle pain (Muscle aches)?
Summary: Muscle pain is found among people who take Coq10, especially for people who are male, 60+ old, have been taking the drug for 2 - 5 years, also take medication Aspirin, and have High blood cholesterol.
We study 1,517 people who have side effects while taking Coq10 from FDA and social media. Among them, 60 have Muscle pain. Find out below who they are, when they have Muscle pain and more.
You are not alone: join a mobile support group for people who take Coq10 and have Muscle pain >>>
Coq10 has active ingredients of coenzyme q - 10. It is often used in health. (latest outcomes from 1,757 Coq10 users)
Muscle pain (muscle pain) has been reported by people with high blood cholesterol, osteoporosis, high blood pressure, depression, multiple sclerosis. (latest reports from 73,475 Muscle pain patients)
On Feb, 11, 2015: 1,517 people reported to have side effects when taking Coq10. Among them, 60 people (3.96%) have Muscle Pain.
Time on Coq10 when people have Muscle pain * :
|< 1 month||1 - 6 months||6 - 12 months||1 - 2 years||2 - 5 years||5 - 10 years||10+ years |
|Muscle pain||12.50%||25.00%||12.50%||0.00%||37.50%||0.00%||12.50% |
Gender of people who have Muscle pain when taking Coq10 * :
|Muscle pain||49.15%||50.85% |
Age of people who have Muscle pain when taking Coq10 * :
|Muscle pain||0.00%||0.00%||0.00%||0.00%||0.00%||0.00%||30.43%||69.57% |
Severity of Muscle pain when taking Coq10 ** :
|least||moderate||severe||most severe |
|Muscle pain||20.00%||30.00%||40.00%||10.00% |
How people recovered from Muscle pain ** :
|while on the drug||after off the drug||not yet |
|Muscle pain||0.00%||0.00%||100.00% |
Top conditions involved for these people * :
- Blood cholesterol increased (9 people, 15.00%)
- Osteoporosis (7 people, 11.67%)
- High density lipoprotein decreased (6 people, 10.00%)
- Blood pressure increased (4 people, 6.67%)
- Arthritis (4 people, 6.67%)
Top co-used drugs for these people * :
- Aspirin (26 people, 43.33%)
- Fish oil (22 people, 36.67%)
- Vitamin d (20 people, 33.33%)
- Niaspan (16 people, 26.67%)
- Plavix (9 people, 15.00%)
* 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.
Get connected: join our support group of coq10 and muscle pain on
Do you have Muscle Pain while taking Coq10?
You are not alone! Join a mobile support group:
- support group for people who take Coq10 and have Muscle Pain
- support group for people who take Coq10
- support group for people who have Muscle Pain
Drugs in real world that are associated with:
Could your condition cause:
Can you answer these questions (Ask a question):
- Can clobetasol propionate topical cream cause muscle pain
Applied Clobetasol Propionate topically to my rash for 1 1/2 weeks and have experienced muscle pain and some numbness ever since.
- Am taking symbicort for copd, woke up with sinus discomfort, can i use fluticasone nasal spray (1 answer)
Developing sinus infection. Can I use fluticasone nasal spray
- Does anyone else have trouble getting to sleep since beginning to take brilinta? (1 answer)
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.
- What causes ideopathic polyneurothopy if not diabetic? (3 answers)
Numbness in ball of foot. Started on one right side and progressed to both. EMG indicated Ideopathic Polyneurothopy. Pre diabetic with A1C of 5.8 - only one reading ever exceeded diabetic criteria at 6.6. Started 6 months ago with slow progression. No pain, minor tingling. Not constant but progresses during day if working and wearing dress shoes(weekends much better). Eases quickly in evening with no shoes and only stocking feet but does no go away. Feeling is not so much numbness as it feels like sand under balls of feet, swelling (no real swelling) or bunched up sock. Again, no pain but very annoying. Dr (Neurologist or Family Dr) do not seem concerned.
- Has anyone had tingling in hands, arms, feet, legs from lisinopril that did not go away when they quit taking it? if you got rid of the tingles, how did you do it? (2 answers)
After 9 months on Atenolol I started getting tingling in my left hand. Also had a pulmonary embolism. A doc switched me to Lisinopril and the tingling moved to my legs, feet, both hands and arms. My calf muscles are very tight and my legs ache. Plus dizziness and other things. After 3 years of going round and round with doctors and no one finding anything wrong with me, I found posts about Lisinopril and tingling and I quit taking it. But the tingling and aches have not gone away. Has anyone else had this problem and does anyone know how to fix it??? I get nowhere going to doctors, they find nothing wrong with me. Thanks
More questions for: Coq10, Muscle pain
You may be interested at these reviews (Write a review):
- Ampyra vs kidney stones
Started taking Ampyra Sept 1, 2014.
Had a severe kidney stone in mid-September.
Another two weeks ago.
No family history or them. I also have no history of them.
Drink fresh squeezed lemon daily and lots of water.
Take Ibuprofen when it starts up.
Ampyra is helping with leg strength a tiny bit.
My MS is 40 years old so it is acting like it is old!
- Faslodex driven hell
I have metastatic breast cancer...which has spread to my bones. Needless to say...I'm not a happy camper. Faslodex was my oncologist’s drug of choice for me. I've been on it since July 28, 2014....My first month was loading dosage...and each month that has followed I receive two injections in my tush...250mg each...for a total of 500mg monthly. Tomorrow, Monday November 17, 2014, will be my third round...not including the month of loading. As per my PET scan one month ago...the Faslodex has not started working. From everything I have been told...and read...it takes four to even six rounds to start working...if in fact it works at all.....@%^&*@#...says it all...if ya know what I mean.
What has kicked in from Faslodex...are some horrific side effects......About a month ago...I started having a strange little cough...dry...most of the time.....At times the cough becomes uncontrollable for aprox 15 / 20 minutes...then calms. NOTHING works at relieving it...although I suck down water like it is my last drink on earth...and use a wonderful...soothing throat drop, Halls Breezers...Cool Berry...which eases me...even if it is only psychologically, it is magical. The cough has gotten considerably worse over time...and for those that don't know me...I am sure they think I smoke ten packs a day. My voice is also affected at times due to the cough. My breathing is horrific...and I can no longer walk for any length of time...or for more than a short distance.....Nor can I walk and talk without coughing...and or losing my breath. Stamina...this I have none of!!! And this past week...the shit hit the fan.....Joining the cough...are bone and joint pains...as well as muscle pain. When I called my doctor...@ Sloan Kettering...I spoke with the nurse...and she had not a damn clue as to what might help. As a matter of fact...she told me that she has never heard of any of the side effects that I am now having. WHAT'S WRONG WITH THIS PICTURE???? EVERYTHING!!! However...when I check reputable sites...I find not a few...but hundreds of other people with the same side effects.
From what I have read on all the sites...the only way "WE" are going to get help with issues like these...is by sharing with one another. Not one of the individuals that I speak of has had any positive help with their side effects from their doctors. Am I pissed off??? You bet I am. As for depression...that only comes in small doses for me.....like yesterday...when my body hurt me so badly...my cough was out of control...I had difficulty breathing...and I could not stand on my own two feet without holding on. That moment in time has passed...but for how long??? What will I be hit with next??? When???
- Latuda stoped hypoglcymia (1 response)
I have hypoglycemia and have had to be carefull of my sugar intake. Started taking Latuda and now i can eat sugar like most people do
- Zopiclone causing sweating and memory loss
Been on 10mg Zopivane for probably 5 - 10 years. In 2013 migrated to 15mg Zopiclone. Previously experienced hot flashes 3 times a week and in 2013 has increased to 3 to 5 times a night. Usually I have 3 hours sleep, then after midnight the flashed start. In the morning there are sopping wet clothes all around my bed. Doctor has prescribed a beta blocker to alleviate the sweats, but there is no change. Short term memory is poor - could the Z pill be causing this?
More reviews for: Coq10, Muscle pain
Comments from related studies:
From this study (1 year ago):
My doctor is working by process of elimination to determine what causes my muscle pain. It occurs on the top of my shoulders, up my neck, my upper and lower back, and down both arms to my wrists. The most severe area is the top of my shoulders and my neck. I also suffer from a radiating headache up the back of my head, probably because of the pain in my neck and shoulders.
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.