I would like to know if anyone has had any of the following problems
relating to Montelukast medication. I was prescribed 5mg daily by my GP,
sometime last year. 5mg is the child dose, I am 49 years old but my GP
thougth it best to try me on the low dose due to my having unexpected side
effects with other prescription drugs that I have had.
DAY ONE - no problem
DAY TWO -no problem
DAY THREE - peak fpw rate started going up
DAY FOUR - peak flow rate as good as with inhaled steroids. But unable to
have erection.
DAY FOR, FIVE AND SIX - head feels fuzy, mild flu like sypmtoms, anxiety and
short burst of very dark morbid depression.
DAY SEVEN - problems persist but now have heartburn as well. Also, Wake up
every morning exactly at 7am and immediately roll out of bed as if I have
only just laid down (I mean all my muscles and joints have the flexiblity
and strengh that I would have if I were half way though jogging around the
park). Also feel that something really wrong is happening but can't work
out what it is.
DAY EIGHT - stopped medication and went back to steroids. Montelukast side
effccts gone within 36 hours.
After two weeks I tried again.
DAY ON - no problem.
DAY TWO - feel like previous problems are coming back.
DAY THREE " " "
DAY FOUR - feel weird, when out on street are avoiding people and keeping to
the shadows. If sometone appears on the pavement in front of me I sometimes
deliberately walk in front of them to have a collision. My head feels like
its trapped in a horrid black maze. Anxiety, depression and paranoia.
DAY FIVE- my girlfriend appears after a two week holiday. She thinks I seem
odd. She says I am taller that I was when she lst saw me, I look at myself
in the mirror and eventually realise that she is right. Appears that my
posture has changed, I ma standing exceedingly straight and my shuolders are
pushed back, I look like I have been working out in a job for several
months.
DAY SIX - very bad flu like feeling, nasal cavities feel swollen, head
feels like its about to explode. All the other described sypmtoms are
presnt and worse. If I eat fish or bacon or any other strong smelling
meat then after an hour or two I am so convinced that some body is cooking
these same foods (due to my being able to smell them) that I go down to the
kitchen and then the garden to look into next doors kitchen, shortly after
the imagined smell I vomit everything out. Moderate headache that does
not respond to paracetamol. Short unpleasant periods of crushing sensation
on chest and not being able to breath. AND my neck, shoulders and elbows
feel like there is sand inside the joints - I can almost hear the grating
sound as I move!.
DAY SEVEN - stopped Montelukast and all symptoms go within 36 hours.
However, I have a pain in my left elbow that startde on day 5 and has not
gone. Two months later the pain is still there and my GP says I have tennis
elbow. Now its almost 8 months later and the elbow still hurts.
Sorry its such a long posting. But its a serious matter as I have damage to
my elbo which I think is linked to this medication. Secondly, many of these
side effects are not officially acknowledged which seems very bad indeed.
Thirdly, 5mg Montelukast is regularly given to kids where all the side
effcts that I describe can be put down to growing pains.
I would like that anyone who has shared this experience come out and put it
in writting for other people to see it, it may be that its an issue that is
yet to be fully appreciated. Finally, can anyone suggest what I can do to
fix my elbow?! I am going aboraod in a cuople of days so won't be able
to respond to any replies until the end of the month.
Cheers
Michael k
Dragonfly - 04 Nov 2007 03:29 GMT
> Sorry its such a long posting. But its a serious matter as I have damage to
> my elbo which I think is linked to this medication. Secondly, many of these
> side effects are not officially acknowledged which seems very bad indeed.
> Thirdly, 5mg Montelukast is regularly given to kids where all the side
> effcts that I describe can be put down to growing pains.
Tennis Elbow, correctly diagnosed that is, is a repetitive strain
injury. It cannot be caused by medication, though I believe that
genetics, past history, and certain medications can pre-dispose one to
certain injuries. Pain in one's elbow, that is not a repetitive
strain injury, could be caused by medication. There is a HUGE
difference between the two. Knowing which it is will probably be
difficult, but its crucial that you and your doctor figure it out.
Tenis Elbow is a severe injury that absolutely must be treated as an
injury, and not just silenced with pain medication. A lot of people
"treat" or self-diagnose and self-"treat" repetitive strain injuries
with painkillers, both OTC and prescription, and this only leads to
even worse and ocasionally evn permanent damage.
Important to know why the pain is there, before you can start fixing
it. Look up tennis elbow on a reputable medical site online and check
out specifically how one gets tennis elbow (not just from tennis,
that's just the first place it cropped up enough times to be given the
name, if I remember correctly), and the specific symptoms of that
injury to see if you match the actual diagnosis. If you feel its been
wrongly diagnosed, then seek a second opinion or go back and talk to
your doctor about it if you feel he or she is open to hearing your
opinion about it. A lot of doctors aren't. If you feel like the
diagnosis does fit, I believe the general means to healing tennis
elbow is easily found online. And of course, talk to your doctor
about it! The one who diagnosed you with tennis elbow should be
setting up a healing strategy including scans of various sorts to get
an idea on how extensive the damage is (MRI, X-rays, that kind of
thing), daily exercises, probably heat and/or ice pack routines, and
what movements to avoid. Also, a referral to a specialist would be a
good idea.
If your doctor isn't doing such things, ask why. If he or she doesn't
give a satisfactory answer, find a new doctor and ask the new doctor
to start new with the elbow pain, explaining that you did not have
confidence in the diagnosis from your previous doctor.
There isn't much one single patient can do about drugs being badly
prescribed, though I think personally the most effective is to get it
heard. Send letters to the local medical oversight people, your
representatives in the government, the media, anyone who you think
might listen and would be in a position to get something done about
it. Sending letters of complaint to the licensing board for medical
doctors might be worthwhile also, though I doubt the drug company
would even read such a letter.
Good luck.
Dragonfly
TRN - 05 Nov 2007 20:07 GMT
I've been around awhile and I can tell you some of the common reasons people
have reported going off the med include very odd dreams, high blood pressure
and heartburn. Never heard of anyone having the reactions you report. But
you know that we are all different in our response to medications. Sounds
like you should leave that one alone.
> I would like to know if anyone has had any of the following problems
> relating to Montelukast medication. I was prescribed 5mg daily by my GP,
[quoted text clipped - 65 lines]
>
> Michael k