Review: could Miralax cause Myalgia (Muscle aches)?
Summary: Myalgia is found among people who take Miralax, especially for people who are female, 60+ old, have been taking the drug for 1 - 6 months, also take medication Xanax, and have Depression.
We study 9,027 people who have side effects while taking Miralax from FDA and social media. Among them, 196 have Myalgia. Find out below who they are, when they have Myalgia and more.
You are not alone: join a mobile support group for people who take Miralax and have Myalgia >>>
Miralax has active ingredients of polyethylene glycol 3350. It is often used in constipation. (latest outcomes from 9,275 Miralax users)
Myalgia (muscle pain) has been reported by people with high blood cholesterol, osteoporosis, high blood pressure, depression, multiple sclerosis. (latest reports from 73,469 Myalgia patients)
On Dec, 30, 2014: 9,021 people reported to have side effects when taking Miralax. Among them, 196 people (2.17%) have Myalgia.
Time on Miralax when people have Myalgia * :
|< 1 month||1 - 6 months||6 - 12 months||1 - 2 years||2 - 5 years||5 - 10 years||10+ years |
Gender of people who have Myalgia when taking Miralax * :
Age of people who have Myalgia when taking Miralax * :
Severity of Myalgia when taking Miralax ** :
|least||moderate||severe||most severe |
How people recovered from Myalgia ** :
Top conditions involved for these people * :
- Depression (41 people, 20.92%)
- Pain (36 people, 18.37%)
- Constipation (36 people, 18.37%)
- Osteoporosis (29 people, 14.80%)
- Muscle spasms (23 people, 11.73%)
Top co-used drugs for these people * :
- Xanax (77 people, 39.29%)
- Levaquin (50 people, 25.51%)
- Lasix (49 people, 25.00%)
- Neurontin (46 people, 23.47%)
- Percocet (45 people, 22.96%)
* 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 Myalgia while taking Miralax?
You are not alone! Join a mobile support group:
- support group for people who take Miralax and have Myalgia
- support group for people who take Miralax
- support group for people who have Myalgia
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.
- Can long-term methadone use cause or increase the risk of colon cancer?
I had a two-level spinal fusion at L4-S1 in 2000 after being injuried at work in Sept. 24, 1997. I lost everything after...the unjury, ability to do my job, my wife and family (couldn't take the strain) my home, my sense of self and purpose, direction and belonging...credit rating and ability to pay my bills.
After a long period of waiting to settle my workmens' comp. case, I returned home, from the Bat Area back to Arizona to take of my mother with a yet un dianosed case of moderate dementia.
Then, in 2011 I had a 2nd surgery to relieve spinal stenosis btwn. L2-L4, just above the fusion site.
I've been taking methadone since early 2004, a little over ten years, now. I've had high blood pressure since my injury.
Now, I waiting to be scheduled for a colonoscopy, with my father having had polyps and the way I've been feeling..drained, tired all the time, and stomach pains ( in addition to my chronic low back pain), I...
find myself wondering if there is any relationtionship between the methadone and other meds and cancer?
- What is better for motility. miralax or lactolose (1 answer)
what is easiest on guts had small bowel blockage recently and have diverticulitis
- 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
- Can i take ibuprofen when i'm on the medicine miralax to treat my massive head ache?
I was recently told by a doctor that I was constipated and that I should take Miralax. I personally don't think I'm constipated. My lower abdomen hurts and so does my head. Every single time I sneeze or cough it hurts really bad! I want to know if I can take some ibuprofen to treat the pain. But I don't want to get even more sick for using it when I'm not suppose to.
More questions for: Miralax, Myalgia
You may be interested at these reviews (Write a review):
- Severe tired taking miralax
I WAS CONSTPATED SO I STARTED USING MIRALAX UNDER A DOCTORS RECOMEDATION I HAVE BEEN FALLING ASLEEP BAD AN CAN HARDLY FUNCTION THIS STUFF IS NOTHING TO BE ON FULL TIME CANT DRIVE OR OPERATE MACHINERY DANGEROUS NO JOKE PEOPLE WARNING LABLE SHOULD BE PUT ON THIS PRODUCT AN WHY THE HELL NONE BEEN ALREADY!!!
- Hot flashes while taking miralax
After being on daily dose of Miralax for a year and then going off for a few months, after starting back in 2 weeks, experiencing hot flushes periodically all day long last around 30 seconds. I didn't realize when I first started the Miralax for the 1st year that my Hot Flushes may have been a side affect. I even had requested labs to test for menopause which show negative. Again, after I stopped the miralax the hot flushes ceased. As stated above they are back. These did not wait for me to be on the drug 2 or more years either it was within weeks of starting.
- 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???
- Mirroralax causes b.p. spike
Taking Mirroralax for three weeks. Noticed my B.P. Unusually. High 1 week ago, then last Sat. Right after taking the drug my B.P. Went to 186/101 - I am 65 yrs. old and never had this before. Called my Dr. Got bp medicene -stressed out trying to figure out what was the cause. Then yesterday
Took another dose and right after my bp again spiked up 186/99. Will never use this again.
- Hair loss with miralax
My hair started thinning out probably within a few weeks of starting Miralax on a daily basis. I continued taking it for approximately 6 months never thinking it was the Miralax. It being the only new drug I had been on, I looked on-line and immediately stopped taking it after seeing the side effects of hair loss approximately 3 days ago. So I have no long-term recovery to report as far as return of hair growth. I am keeping my fingers crossed and am already on vitamin supplements...B complex, multi vit, calcium and d. I did start on vit E in hopes that would help.
More reviews for: Miralax, Myalgia
Comments from related studies:
From this study (1 day ago):
I'm 27 wks pregnant, have always had constipation to extent, but this 2nd pregnancy beats all I've ever seen, I was so constipated I went to the er, they had me drink 24 oz 6(17grams) of miralax on Friday didn't hit til Saturday morning; now tonight sunday night I have severe burning uti and like symptoms. Before I took this much miralax I was peeing constantly no issues what so ever. Now I have double the issues! :(
From this study (3 days ago):
I also get joint pain
From this study (7 days ago):
Itching worse at night
Post a new comment OR Read more comments
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.