My mom is a PSP patient for 6-7 years. Recently, we have needed to use Clonazepam for her agitation etc. Regret, we do not have certain indormation about the max recommended dose of it. Do you have any idea about the Clonazepam dosage? Do you have any suggestion/ experience about it?
Many thanks
Esra
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Esra
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Have you Googled it to find out ? It's a strong drug and should only be used as prescribed. I suggest you contact her doctor to find the exact dose he/she recommends.
Ask a pharmacist not a doctor concerning the drug, (any drug really) they are the specialists Doctors do not know full effects side effects and contra indications, maximum dose etc. The doctor should accept pharmacist queries/suggestions.
Also there should be a drug description script in all boxes of medicine, that should tell you the chemical breakdown of the drug, what it is used for any side effects etc usually very wordy.
My wife still on Lorazapam: a related drug but shorter acting only in system for about 4 hrs, compared to 8+ for your drug.
My husband uses it as needed for anxiety. Like everyone said, I would check with you GP. Our GP said if the dosage is too high, all my husband will do is sleep. (sometimes that wouldn't be a bad idea!!)
My wife is given 1 tablet (0.5mg), but I only give it to her when I suspect a restless night might ensue. When she takes it, it seems to carryover into the daytime, which I don't want to occur. I started her out on a half of tablet, but have gone up to 2 when she was at her worst at night. I had discussed this prior with her neurologist. But as she has progressed with PSP, she is a lot weaker and sleeps most of the time (day and night). So now I'm giving her Ritlin to keep her more alert during the day.
Hi Esra, I'm so sorry for the late reply. I haven't checked my emails the last week, just haven't had the time. My mum was prescribed Clonazepam by the consultant last year to try to help with her agitation/anxiety at bedtime. I can't remember the dosage but I do know that unfortunately it didn't help her. I know everyone responds totally different to medication, as yet we are still to find something that relaxes her enough to get her to sleep. I find the sleepless nights the worse thing about psp, it's not just her not sleeping but she doesn't let me or my dad sleep either. I can't imagine what's going on in her mind. Good luck love xxx
As yoı know, this is an awful disease for patients and also their families. I am feeling sometimes very bad and sad beacuse of her situation... I am praying for all PSP patients and their families in all over the world
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