Experiences with

Scopolamine

I now have in my possession oral scopolamine (works faster than the patches). I searched the archives and could find no mention of this drug. Does anyone know if this drug will affect my RLS and if so will it make it better or worse? Thank you.

just need to get it out! We have reached end of life. Emergency meds are being used and Jon now has pneumonia. Day 3 of meds, day 2 of pneumonia and date 2 of hyoscine via a drip from the awful box! Last night was relatively easy from the 3 previous nights. I’m not sure what’s hardest, will today

Hi - with a heavy heart tell you that TC died on Sunday 3rd March. We managed to keep him at home, as he wanted, and it was peaceful at the end. I know that it's difficult to know when the end will come so I will document how it was for us.TC deteriorated quite dramatically after Christmas. His stomach

The effect of combined oral treatment, for 28 successive days, on cognitive function and other AD-like alterations was studied in scopolamine-heavy metal mixtures (SCO + HMM) AD model in rats. The combination reversed at least, partially on the learning and memory impairment induced by SCO + HMM.

Her GP saw her and assessed that her chest was clear but gave her a new medication to try that might help with fluid in her throat - Scopolamine in a patch. She became even more unwell, very confused and weak and ultimately became very distressed and appeared to be hallucinating.

Sorry for the english, this is my second language I have this kind of soft stool for about 1 month and I have this kind of stomach pain, for 1 week, started July 26. A stomach spams that usually goes away, but I didn't care of it and i feel it everyday, but last Wednesday, i feel sudden stomach cramps

I am sorry for the graphic. I just want to know because it legit scares me so much. Hi, I am 22 years old female resided in Philippines. Sorry for my bad english. I have recently been in the doctor last friday and I have this specific abdominal pain that is hard to press and kinda painful too. I dont

Does anyone happen to know why those with thyroid problems or heart conditions and those over 60, (I have all three) should speak to their doctor before taking these for motion sickness. A pharmacist who was aware of my medical conditions suggested Kwells for me. Only just read the pil in full. I haven

I'm stage 4 terminal without possibility of a Tx, have a TIPSS, and have an active DNACPR. I was referred to St Marys who said it was an inappropriate referral, and I'm supposed to have a fitted syringe driver with morphine, midazolam, levomepromazine, and hyoscine (busco). For some reason the meds are

- https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6804255/ Sulforaphane-Enriched Broccoli Sprouts Pretreated by Pulsed Electric Fields Reduces Neuroinflammation and Ameliorates Scopolamine-Induced Amnesia in Mouse Brain through Its Antioxidant Ability via Nrf2-HO-1 Activation - https://www.ncbi.nlm.nih.gov

Put the patch on Tuesday and Thursday 4:00 am it started.this is the guy who has not been able to get himself out of bed for well over a year,he got himself out of bed 4 times moving things, trying to do things such as get a towel for our Granddaughter who is 29 and dose not live with us ,trying to

Has anyone ever had the hyoscine patch to dry up mucus if so can you tell me your experience please, they are planning to try it on my because nothing else is helping this copious mucus issues. Thanks.

Hello all and Thankyou for all the wonderful posts full of advice for caring with adults with psp. I would like your ideas on how to help my father in law who was diagnosed with psp about 3 years ago & is now struggling with excessive saliva & problems swallowing especially liquids. He had been on hyoscine

I get Botox shots every 12 weeks in my salivary glands and wear a scopolamine patch that gets changed every 72 hours! My neurologist suggested that I go to an ENT doctor to discuss having my salivary gland removed! Has anyone had this done?

I’m waiting to get scopolamine patches to help but hoping someone has found a solution and can advise us. Thank you!

Morning everyone I hope that everyone here on this Group are in best of health, and enjoying the sun quick question to anyone who may be aware of injection and what are they used for they are called CYCLIZINE, HYOSCINE, MIDAZOLAM Thank you in advance

Scopolamine patches are highly effective but they require a prescription. If you have experienced dizziness, tinnitus or hearing loss in connection with PD this is a good place to tell your story.

Mum is deteriorating fast. She is end stage with a peg, sleeping 24hrs. We're having serious problems with secretions, saliva and moaning. Suction is taking place multiple times during the day, the night is always worse with us having to use suction on and off over a period of 2hrs. It builds up so

my problems started after chemo cycle 18, I had what I thought was just the flu but now the nausea will not go away even after recovering from some flu/cold thing I had, I just cant get over the nausea , I am currently taking Zofran and I am also using a patch behind my ear called Scopolamine, these

Syringedriver been in place a couple of weeks. Hyoscine to help dry up secretions created by the terrible coughing and morphine for the pain caused by the coughing. Extra stat doses are also being given by needle as only so much hyoscine can be given in the driver. This must be painful as hubby has