Invegavictim
Greenlighter
- Joined
- Apr 1, 2017
- Messages
- 44
How long untill sexual dysfunction stops? I think my balls shrinked and all i can ejaculate is smelly water. Anyone else in this?
Because I have never seen such a one-sided thread as this one thread on bluelight. Demonizing one/two substances or even a whole class is plain ridiculous. I have been on many neuroleptics, have more than one friend who has been on risperidon, have seen plenty of patients on maintenance and have not seen a single one who showed the symptoms you are describing. I am convinced most (!) of the negative experiences are due toI highly doubt that your friend on Risperdal Consta is "in a romantic relationship", " agile", or "emotional"
Risperdal consta makes you a fat, emotionless zombie. The opposite of agile and emotional. It eventually after long term use gives almost all men man tits and sever impotence. This is a fact.
They give that shit to severly "manic" patients and also people who experience vivid hallucinations. Giving Risperdal Consta to any human for any indication is in my opinion cruel and barbaric.
Also you have made it very clear that you are not recovering from invega, neuroleptics or any psychiatric drugs so why do you feel the need to continue posting here? This is not the right thread for you to express your views. You are only upsetting people who are severly suffering and have lost their lives to psychiatry, many of who are on the verge of suicide because of forced drugging
with the poisons you endorse.
Please post somewhere else.
Has anyone developed racing thoughts from this drug?
I keep failing at breathing meditation where you focus on your breathing to clear thoughts. I always get a random thought popped in my head or am conversing with myself even when I don't want to. Pretty sure I wasn't like this before the drug. It gets ten times worse whe I tried to stop taking the drug. Endless racing thoughts.
Anyone know what I can do?
Willl this go away if I get off the drug for a few months?
Yes. This is by far the most distressing effect I experience - even worse than testicle shrinkage. Because it makes it near-impossible to live my usual life... How can I have a meaningful conversation with someone, for example, when I'm always preoccupied thinking of pointless shit?
Try auditory or guided meditations. YouTube has plenty. It's difficult to meditate in general on drugs designed to induce non-meditative states; but, at least for me, focusing on listening to something is far easier than focusing on shutting my mind up. I also experience the conversations... relentlessly, day in, day out... I can confirm, we weren't like this before the drug. It got worse when I came off the neuroleptics the first time, but after 8 or so months, I did experience happiness and was overall more chill. The racing thoughts/mind chatter subsides.
Yeah, it goes away but for me got worse before it got better.
- ZM
@Crook;
There is no reason to stir the hornets nest. This thread is for people who have had extreme adverse reactions to Invega. There is no reason to point out that not all people have the same reaction.
You have not been affected by this medication, and merely knowing of someone who has taken it is not grounds to speak in this thread. No offense but you are completely ignorant to what we are going through.
I haven't posted in a few days. I am doing well. I am still dealing with anhedonia, poor complexion and constant sweating. However it has been 8 and 1/2 months and I am slowly coming around.
Today also marks the 3rd week I have excersized daily. I am not seeing too much improvement from this but I will press on. I noticed all the early recovery stories share excersize as part of the recovery.
I hope you all are doing well, and I am glad we have this place to share our stories. I hope everyone recovers quickly. Try doing what I do and fill your days with work or school so that you are making progress in your life.
I recently graduated CDL school and I now have my Class A CDL. Monday I am starting a job driving a water truck in the oil fields. This has been the hardest tims of my life but I am accomplishing things and I will feel great when I finally come around.
Thanks again,
-Benjamin
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4977821/ said:Tolerability and Safety of Paliperidone Palmitate for Schizoaffective Disorder
Interpreting differences in tolerability outcomes versus placebo in the randomized phase is complicated because subjects with tolerability problems may have dropped out during the prior open-label treatment phase. In the paliperidone palmitate relapse prevention study, 28.2% of the placebo group discontinued treatment during the double-blind phase, compared with 23.8% of those in the paliperidone group. Higher rates of subjects discontinued because of withdrawal of consent and being lost to follow-up in the control groups, but 5.5% of subjects in the paliperidone group discontinued due to an adverse event, as opposed to 1.8% on placebo (NNH 27). There were 2 deaths in the paliperidone group during the double-blind phase, as well, one by overdose of sleeping medication and one due to coronary artery disease, neither judged by the investigator as caused by the investigational product.
The common (≥5%) treatment-emergent adverse events (TEAEs) reported more frequently in the paliperidone group than in the placebo group were: weight increased (8.5% paliperidone, 4.7% placebo, NNH 27), nasopharyngitis (5.5% paliperidone, 3.5% placebo, NNH 50), and headache (5.5% paliperidone, 3.5% placebo, NNH 50). Extrapyramidal symptom-related TEAEs were reported in 8.5% of the paliperidone group, compared with 7.1% of the placebo group (NNH 72). Prolactin-related TEAEs occurred in 13.9% of women in the paliperidone group, compared with 5.8% of women in the placebo group (NNH 13). Thirteen percent of paliperidone-treated compared with only 6% of placebo-treated subjects gained ≥7% of their weight during the study (NNH 15), although there was only minimal mean weight change reported for both groups.
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3383636/ said:Treatment of schizophrenia in patients with comorbid substance use (alcohol/illicit drug use, abuse or dependence) presents challenges for public health systems. Substance use in people with schizophrenia is up to four times greater than the general population and is associated with medication nonadherence and poor outcomes. Therefore, continuous antipsychotic treatment in this population may pose more of a challenge than for those with schizophrenia alone. Many clinical trials and treatment recommendations in schizophrenia do not take into consideration substance use as people with comorbid substance use have typically been excluded from most antipsychotic trials. Nonetheless, antipsychotic treatment appears to be as efficacious in this population, although treatment discontinuation remains high. The objective of this review was to highlight the importance and utility of considering long-acting injectable antipsychotics for patients with schizophrenia and comorbid substance use.
No, not at the time. I've been on numerous other neuroleptic drugs though and take olanzapine as needed. Most of the people I know are struggling with mental illness and some have seen the worst side psychiatric treatment.@cr00k: are you currently taking or recovering from invega, invega sustenna, paliperidone, invega trinza, xeplion or trevicta?