Wondering if anyone else is a long term user of imitrex/sumatriptan & have retinal vein occlusion?
Wondering if anyone else is a long term user of imitrex/sumatriptan & have retinal vein occlusion?
I guess most of us have our share of worrying about side effects of the migraine meds we take but some of those side effects are more serious than others. I've kind of come to terms that I'm somewhat spacey, forgetful and "lose" my words for example. It's a trade off for a reduction in pain and frequency of migraines. But earlier this year I was diagnosed with retinal vein occlusion (blood clot in the eye)… read more
Interesting as I am just recovering from an unexplained detached retina and dense vitreous haemorrhage but not sure if related to the Sumatriptan injections I have been using for over 20 years.
Yes, I have seen a eye specialist for a vascular burn out behind my eye. I do not reach for sumatriptan or rizatriptan as a first medication any more. It is my last choice if fiorecet fails. With my nsaid allergy I have few options. Your post resonates with me.
I’ve not heard of this I’m on this drug tablet form, I get the aura in my eyes, I will keep a watch on it now, thanks for the heads up ,
It is a matter of what works the best for each person and with the least side effects. I can share that with the nasal mist, you are not suppose to inhale when you spray. (It does taste awful running down the back of the throat). I often find the migraine will move to the opposite side of my head, after about a hour of relief, especially if I waited too long to use it.
I started with the pills which didn't work well because of nausea, then tried nasal mist which I couldn't stand and also didn't work well, so about 10 years ago I was changed over to injections. Interesting you have scarring in your eye! Wow...I'm sorry:(
