Restasis adverse effects
Common Questions and Answers about Restasis adverse effects
restasis
About 2 months ago I was prescribed Restasis Eye drops and after being on the dug for about 2-3 weeks I noticed that my mouth got extremely dry. So I looked up all the side effects and none included dry mouth. so I called the Dr. that prescribed it to me and I was told that 1% of patients get this dry mouth and I was told to discontinue use of the drug and come see the Dr in 1 month. It's been a month and I went to the Dr but the symptoms has gotten worse instead of better.
m wondering about the side effects of Restasis as I have to use it for 6 months. I know it is an immunosuppressive drug and I really don't know what that means? Does that leave my body open for other diseases because it suppresses my system so the eyes can make the tear film that was partially lost when the nerves were cut during the cataract operations? I don't want to be dependent on drugs for the rest of my life.
My eye doctor just Rx'd Lotemax (4 weeks) & Restasis (for life) for my extremely dry eyes. They feel like sand is in them. I am concerned because from what I can understand Restasis works through the auto immune system. I am in week 38 of standard treatment and since week 16 of treatment have had a hypothyroid. Any advice? I also was told this morning to increase Procrit from 20,000 to 40,000 a week because Hgb was only 8.5 on this weeks lab.
I have been prescribed teva-cyclosporine 0.05%, I was wondering if it is okay to put the eye drops in my eye, and then after like 10 minutes or more use a warm eye compress, I am very stressed due to my bloodshot eyes from dry eye, and I find that the warm compress helps me to fall asleep but do not want to "wash" away or eliminate the effects of the eye drops with the moisture from the warm compress. any thoughts will be appreciated !
Is this the best solution? Could you please explain the pros and cons of this recommendation? Are there any side-effects or potential adverse consequences? Are the installation or removal procedures,or the plugs themselves, painful? Are there any other safe and effective alternatives? Thanks in advance for any advice or insight you can offer.
I just got back from my optomologist & he prescribed for me Restasis. He mentioned that once you're on Restasis, it's an on going thing it's not really temporary. Is that the case, do I have to stay on it. I was hoping that once my eye is feeling better, I could just use artificial tears to keep my eyes from drying so badly. He also changed my contact lenses to Acuvue Oasys. Any advice or info would be great.............................
My ophthalmologist recently prescribed restasis for dry eyes. I read that cyclosporin can causes cancer. Is this true? Are these drops safe?
I'm on restasis, my wife is on restasis, I use restasis in my practice. the medicine does not cause floaters. Floaters can occur at any time. If they start and you are doing something else like mowing the yard, reading a book or starting restasis the relationship is COINCIDENTAL. On the other hand if you are hit in the eye with a fist and note floaters the relationship is CAUSATIVE.
dry eyes, dry mouth, throat feels swollen, constantly chapped lips. In fact, I never thought anything of my constant need to reapply chapstick every few hours for months until now! I've also had some acid reflux that comes and goes over the last few months. I discovered in the summer that I have an unusually low IGA, meaning my salivary gland production is very low. Could a low IGA cause Sjogren's Syndrome? Am I just being paranoid or does this seem likely?
Rare anyone to be too sensitive to restasis. My wife and I have been on restasis for many years with fabulous results. restasis works with both forms of dry eyes. Many people have stinging with restasis for several weeks which can be helped by using steroid drops for a couple of weeks. there is a new medication that works like restasis called Xidra it is supposed to kick in faster (3-4 months) than restasis (4-6 months) but has not been shown to be better than restasis and is more costly.
I firmly believe that my psychiatrist should have warned me about the side effects of this med or any meds he prescribes. By God, they are sure to warn against effects of Viagra and other drugs on TV!!!!!! I would have never thought of telling him about mouth sores and a sore throat. I made no connection at all. I don't know how long it's going to take to get out of my system, but we stopped it on Friday and I hope I don't have any untoward effects from that.
Hotflashes (of on) since 08
Off / on mild moderate joint pain and stiffness in 38 of 40 joints with idiopathic pheriperal neuropathy UE LE 05 present with 2 point differential
I have found no articles mentioning differentating side effects radiation therapy with Sjogrens and fibromyalgia Recent increase fatigue (radiation tx?) with increase sporadic low back siatic pain, muscle pain and joint stiffness UE LE (flare of Sjogrens and Fibromyalgia?
After extensive testing (hormonal and auto-immune) came back normal, my doctors can not figure out how a 20 year old can have such sudden severe dry eye. I am on restasis, have punctal plugs, tried steroid drops, warm compresses, lid massages, and I have not gotten relief. They said my tear break up time is low, but I don't have much meibomitis, my schmimer fluctuates every time (from 4 to 20) so the doctors say is not a really reliable measure.
I have a moderate to serious dry eye. I am going to start my Restasis today and I know that I will not see the result till 2 months or more from now. I am also planning for a cataract surgery in 1 to 2 months. I also foresee that I will use some steroid or antibotics for a few weeks after the surgery. Do I need to stop Restasis once I start the steroid ?
Recommended
