Seroquel has helped Dad's hallucinations, but he sleeps a lot more. Should we adjust the dosage?

When is the next follow up with the neurologist?

seroquel was like an elephant tranquilizer for mom and did little to tone down her behavior issues so we switched to another antipsychotic which works much better for her and we are in process of tapering the dosage down / she’s 95

seroquel is also used as a sleep
aid and oftentimes is increased as the person becomes adjusted to it

many posters here have had good results with it but it just wasn’t the right one for my mom

How often does he take 50 mg? My mom took Seroquel. She was started on 12.5 mg once a day at 4 pm to help with sundowning. The amount increased very gradually to 75 mg once a day over the course of 3.5 years. Maybe the amount your dad is taking should be decreased. Check with his doctor. Or it very easily could be his heart problem causing him to be very sleepy.

My mom was prescribed Seroquel for her anxiety and sundowning I personally discontinued her taking the medication as it made her too tired she was sleeping all day and was lethargic and the more and more I watched her on this medication it also began to affect her ability to walk. for me I think Seroquel was too strong of a drug . As a reminder older persons metabolism slows and so it takes a lot longer for the medications to be broken down in there system. the effects tend to stay a little longer or seems more profound because of their ability or lack thereof to process the medication at a faster rate. when I stopped the drug her ability to walk returned however she developed what's called ticks otherwise known as tardive dyskinesia so now she has random jerking of her hands and her body but then I decide sometimes the behavior can be attributed to her trying to communicate when she gets anxious or agitated so I don't have her on any medication as she too is entitled to express her emotions and I'm pretty okay with that. I find that playing music of the genre that I remember that she used to like when she was in her right state of mind has totally helped and calms her down during her sundowning.

My dad's dose started as 3 - 12.5mg (1/2 tablet) per day. That seemed to make him 'out of it' during the day so he's been on two 1/2 tablets per day for about 6 months and that seems to be good. One in the morning, one before bed. I think he had 'forgotten' how to sleep and this has helped a lot, although he says he doesn't remember sleeping! It has also calmed down his anxiety, however, I have seen lately he seems to be more a little more anxious than usual and I have discussed this with is doctor. Might be time for a slight increase.

I empathize with your scenario

My mother 89, has vascular dementia which was not into the hardest or advanced phase until she fell and was in an out of hospital - psychosis worsening with behavioral changes in hospital and medications.

Seroquel was added and it seemed to stop most of the screaming etc - hallucinations still present...shes making no sense and its not doing much - she is in a twilight psychosis so I cannot give more feedback as it has been a wk on seroquel.

My heart goes out to you and your family

sometimes I hesitate to add my experience.
but when my mom(dementia) was repeatedly hearing music and TV noise (in evening), when there was NONE. . . the AL said take your mom to see her Dr.

I did  - and you know what Dr did? he cleaned out my moms ears.(yeah there was wax) Then Dr. sent out a authorization for a referral for a hearing test. We went and she did ok I guess. They said she ~could~ choose to get a hearing aid. I choose no hearing aid.

I read online about musical ear syndrome. (because I found it so weird my mom was hearing things)that means you have a hearing loss and then you develop auditory hallucinations. I don't know if its true or not. But my mom eventually stopped complaining about it thank goodness.

im not saying anyone does or doesn't need medication. just how my moms Dr (not a geriatric at that time) handled her issue.

Thanks everyone for the great answers!  I don't think it's affected his ability to walk, but it's hard to judge because his feet were swollen last week; that slowed him down.  Now that the swelling is gone, he's able to walk better (he refuses to use a walker and I've stopped trying to get him to use it).  He takes a single 50mg tablet in the evening.  When he's awake during the day, he doesn't seem drugged like he did on Risperdal (which didn't help at all). I had his hearing tested a few years ago and got him fitted with a hearing aid, but he doesn't wear it. The doctor checked his ears yesterday and they were clear.

He's got a followup scheduled with the neurologist in a few weeks, so I'll see how he does in the mean time. Thanks again!

my mom stayed in bed a lot will cut a lot out ..what i did was google what is good vitamins for a person with dementia vitamin E is a good one ..i suggest you do it & see ..but i also gave her a lot of salt .to she got low on sodium a lot so i gave her the sodium pills i made from getting cinnamon pills that are capsule form took out the cinnamon part & put in table salt ..in a week she got out of bed & did not do that for 3 months @ least but the second round i did try but no effect so much ..but i wonder if salt can be a big help .but then if salt issues need to watch it can cause high blood pressure ..if so need to talk to a doctor on that ..

My MIL is on the Quetiapine version and she was sleeping during the day a lot. I moved it to the evening meds and she is up every day around 9:30 or 10:00 and hits the bed around 8:30. Much better in the last few months since the change.

My mother is 83 and lives with me. I wake her for meds and meals but she won't stay up. We turn our back and she's right back in the bed. If she has an appointment I wake her two hours earlier and she's always trying to get back in bed. She won't watch TV, read or do word searches anymore. She may not be asleep but she's in the bed. Best of Luck!

If he's 91 years old, reasonably happy, active and not hallucinating,........Do you think that he's not active enough? I'm not sure what the goal is. Most people with dementia are supervised and eventually need prompting to get up, go the bathroom, eat meal, etc. I might discuss his daily schedule and health with the AL staff and get their input. I wouldn't base modifying medication that is helping him based on what you might see one day a month during your visit.

My husband is also on Seroquel to help with delusions and hallucinations. He does sleep a lot, but I'm willing to go with that as he was threatening the caregivers and anyone who came into his room, even the Dr when he visited. He is 88 years old, and needs total care. He is able to feed himself so they take him to ding room 3 times a day and to activities in the Commons area that he does enjoy. I'm satisfied, at least I can visit with him and not be accused of all kinds of things that are not true.

Man, I hope when I am 91 my kids leave me the heck alone.

J/K. But not really.

Getting old is exhausting. Not everyone goes 'gently into that good night'...they are tired from simply living. They'e not happy or interested in anything--

My mother's last friend is in Hospice. When this woman dies, my mom will have zero friends. She's outlived everyone she knows. She's basically housebound now herself, and her options for socialization are nil. She doesn't WANT to go anywhere. She is happy with her tvs and her birds and working on puzzles. If she wanted to sleep all day everyday, I'd let her.

EVERYTHING hurts on her now. She's mobile, but barely so...creeping along so slowly....takes all day long to do 3 tiny loads of laundry. Why should we harangue her about getting up and out more? At 88....( and a HARD 88) she just wants to have her stuff around her and be peaceful.

BTW- Seroquel has a very long "after effect" of sleepiness into the next day. But it works very well to calm and to help sleep. a 50 mg dose is pretty small.

I just went through a nightmare of two weeks with 83 year-old husband with frontal temporal lobe/vascular dementia. He was becoming violent both night and day, but mostly at night, resulting in my needing to call 911 on three occasions in two weeks. The hospital would send him home because all of his tests came back normal and vitals were good. The last time I called his PC doc first and he said this time to make it very clear that I would refuse to take him home until he had a full psych eval and meds were checked. He spent five days as an "outpatient under observation" and had the eval as well as swallow therapy and eval and they added depekote to the meds. He was already on seroquel, and they upped that doseage. At home now, he sleeps so much, has so little ability to do the things he was doing before being hospitalized. His care at home is now multiplied to the point where my exhaustion and ability to care for him is much less than before. They suggested placement in a board and care facility, but our finances are in ruin now, and that is just not possible. He needs better care than I can give him and I am feeling completely lost. We do not qualify for any programs. I was advised to declare bankruptcy, which I am going to do, but emotionally I am overwhelmed and feeling paralyzed. It is 9:00 am and he has been sleeping since 11 pm, is still combative just before he falls asleep, is completely unreasonable throughout the long days. But at least he has stayed in bed during the rest of the night. I feel so badly for him and I wish I could do more, be less agitated myself, feel real affection towards him. I hug, I rub his arms and back to try and soothe him, telling him that I love him, though I do not feel it like before, but nothing I do seems to help. I am sad.

Dear Linkabit,

How fortunate you’ve found a treatment for the hallucinations.

Adjusting the dosage is best discussed with the prescribing physician.

I am repeatedly told by physicians and nurses that the rule of thumb with geriatric patients and medication is “dose low and go slow.”

So, whether we have added, increased,or decreased and eliminated a medication for my Mom, it has always been in small increments.

It has worked best for my mom to start below the desired dose, let her adjust to it for days to weeks, then gradually increase in the same way.

Same goes for lowering it or eliminating medications - incremental reductions in dosage over longer periods of time.

The only time we have stopped a medication immediately/entirely is when the side effects have been intolerable or dangerous.

Again, best to iscuss this with your dad’s physician.

All best to you.

My mother uses it ...prescribed by Neurologist for combativeness from Dementia...calms her

Seroquel is a sedative so it's doing what it's designed for. However, since at the very end of your post you mention that he is a heart patient, I would definitely get him to his cardiologist as early as possible to check heart functionality.

Seroquel is an anti-psychotic with sedative effects. It works well for some, like my mom, and not so much for others. It is prescribed to calm agitation and delusions. Sometimes the dosage will cause sleepiness. I would prefer sleepiness to agitation and delusions.

My mom is on 25 mg of Seroquel. I have to crush it and put it in her dinner or she won't take it. She doesn't like taking ANY meds. She gets sound sleep and I get good rest. If she is hyper/ anxious prior to dinner then the 25 mg will not work. Two months ago her neurologist prescribed 50 mg. He said if she has a very bad day with aggressive behavior prior to bedtime, then give her the 50 mg. Because the 25 mg works within 20 min on good days, I am too afraid to give her the 50 mg. I just make sure I give her the other calming drug (lexapro), which we were able to get in liquid form so I put it in her H2o or drizzled over her dinner. This combination seems to calm her and she sleeps good. On really bad days, if she won't eat or drink, I just let her work herself up because she eventually runs out of gas and falls asleep or is more compliant.