Welcome, Guest. Please login or register.
April 19, 2024, 11:00:08 am

Login with username, password and session length


Members
  • Total Members: 37644
  • Latest: Aman08
Stats
  • Total Posts: 773210
  • Total Topics: 66337
  • Online Today: 581
  • Online Ever: 5484
  • (June 18, 2021, 11:15:29 pm)
Users Online
Users: 3
Guests: 471
Total: 474

Welcome


Welcome to the POZ Community Forums, a round-the-clock discussion area for people with HIV/AIDS, their friends/family/caregivers, and others concerned about HIV/AIDS.  Click on the links below to browse our various forums; scroll down for a glance at the most recent posts; or join in the conversation yourself by registering on the left side of this page.

Privacy Warning:  Please realize that these forums are open to all, and are fully searchable via Google and other search engines. If you are HIV positive and disclose this in our forums, then it is almost the same thing as telling the whole world (or at least the World Wide Web). If this concerns you, then do not use a username or avatar that are self-identifying in any way. We do not allow the deletion of anything you post in these forums, so think before you post.

  • The information shared in these forums, by moderators and members, is designed to complement, not replace, the relationship between an individual and his/her own physician.

  • All members of these forums are, by default, not considered to be licensed medical providers. If otherwise, users must clearly define themselves as such.

  • Forums members must behave at all times with respect and honesty. Posting guidelines, including time-out and banning policies, have been established by the moderators of these forums. Click here for “Do I Have HIV?” posting guidelines. Click here for posting guidelines pertaining to all other POZ community forums.

  • We ask all forums members to provide references for health/medical/scientific information they provide, when it is not a personal experience being discussed. Please provide hyperlinks with full URLs or full citations of published works not available via the Internet. Additionally, all forums members must post information which are true and correct to their knowledge.

  • Product advertisement—including links; banners; editorial content; and clinical trial, study or survey participation—is strictly prohibited by forums members unless permission has been secured from POZ.

To change forums navigation language settings, click here (members only), Register now

Para cambiar sus preferencias de los foros en español, haz clic aquí (sólo miembros), Regístrate ahora

Finished Reading This? You can collapse this or any other box on this page by clicking the symbol in each box.

Author Topic: SUSTIVA vs. VIRAMUNE (AND TRUVADA) ??  (Read 5594 times)

0 Members and 1 Guest are viewing this topic.

Offline mrtallguy

  • Member
  • Posts: 199
SUSTIVA vs. VIRAMUNE (AND TRUVADA) ??
« on: December 28, 2006, 05:50:40 am »
I have been on the Sustiva and Truvada combo for 6 months and my sleep issues are getting progressively worse.  Responses from another posting lead me to believe that the Sustiva is the problem child for me and I am thinking of talking to my doc about switching to Viramune as my NNRTI....any thoughts about side effects...good or bad....on VIRAMUNE??

BE WELL!!

MRTALLGUY
I AM DETERMINED TO SEE THINGS DIFFERENTLY!
--ACIM

Offline penguin

  • Member
  • Posts: 747
  • The Penguin Whisperer
Re: SUSTIVA vs. VIRAMUNE (AND TRUVADA) ??
« Reply #1 on: December 28, 2006, 07:37:19 am »
Hey..

sustiva, just don't agree with some people.

Viramune, a non nuke like sustiva, sans the screwy head effects - can be bit tougher on the liver, & a small chance of causing a serious allergic reaction at the start of treatment. No food restrictions. Dose is 200mg once a day for the first 2 weeks then increased to 400mg/day if all goes well, usually split into 2 doses.
You can read more about it here

Does it have to be viramune though? There are other, PI based choices for a once daily combo..boosted reyataz or lexiva, kaletra..

Re the sleep, or not sleep, from your other post - mirtazapine can be a useful anti depressant, due to its sedative properties. If the primary issue is anxiety, then a low dose of zyprexa or summat similar might be more helpful than the sleeping tabs/tranquillisers you've been downing..just a thought.

kate

Offline J.R.E.

  • Member
  • Posts: 8,207
  • Positive since 1985, joined forums 12/03
Re: SUSTIVA vs. VIRAMUNE (AND TRUVADA) ??
« Reply #2 on: December 28, 2006, 08:01:29 am »
Hello Mrtallguy,

You need to open up with your doctor, and discuss the sleep issues that you are having. I've been on Viramune since October of 03 ( first line of meds ), and had no problem with it. There are other options available to you.

From the drug Section :

"Taking Viramune is a two-step process. For the first two weeks (14 days) of treatment, the dose is one 200mg tablet once a day. Two weeks after starting treatment, the dose of Viramune is increased to one 200mg tablet twice a day. Following this schedule – which you should do under your doctor's guidance – can reduce the chance of developing a rash or other side effects.

"Liver problems have been reported in HIV-positive people treated with Viramune. The greatest risk of liver problems is during the first six weeks of treatment. Liver problems are more likely to occur in women (including pregnant women) with T-cell counts greater than 250 at the time of starting anti-HIV treatment for the first time. As for men, liver problems are more likely to occur if the T-cell count is above 400 at the time of starting anti-HIV treatment for the first time. HIV-positive people should work with their doctors very carefully if they have T-cell counts above these levels and are planning on starting therapy for the first time with a drug regimen that contains Viramune.


For complete info on this drug, click here :

https://www.poz.com/drug/viramune-viramune-xr



I can only share with you my experiences of being on viramune. So far...so good !! I have very little issues with sleeping. Of course I sleep in the day and work at night, but still I have very little issues.

No wild dreams, just the usual stuff. I have had most of my life!  How about reyataz,- norvir and truvada?

I believe that could be a possible combination for you. Talk to your doctor, and see what he may suggest to you. I wouldn't put it off. If you can't handle the Sustiva, check out your options.


Take care/ Let us know what you decide on-----Ray


« Last Edit: May 08, 2019, 11:14:25 am by iana5252 »
Current Meds ; Viramune / Epzicom Eliquis, Diltiazem. Pravastatin 80mg, Ezetimibe. UPDATED 2/18/24
 Tested positive in 1985,.. In October of 2003, My t-cell count was 16, Viral load was over 500,000, Percentage at that time was 5%. I started on  HAART on October 24th, 2003.

 UPDATED: As of April, 2nd 2024,Viral load Undetectable.
CD 4 @593 /  CD4 % @ 18 %

Lymphocytes,total-3305 (within range)

cd4/cd8 ratio -0.31

cd8 %-57

72 YEARS YOUNG

Offline Pippet

  • Member
  • Posts: 135
  • Life is drawing without an eraser.
Re: SUSTIVA vs. VIRAMUNE (AND TRUVADA) ??
« Reply #3 on: December 28, 2006, 10:06:00 am »
  I had a bad reaction to Viramune.  I developed a rash (from face to waist) along with a fever at day 10. It was unbearable by day 12. I will soon be trying Reyataz / Norvir with Truvada.

  I have a friend who swears by Truvada / Viramune combo.  He has had no side effects, to speak of, and his numbers have been great for years.  I was hoping for the same results...

  I am new to this, but one thing I have learned is that the combo that is right for one person may not be what's right for you.  All we can do is give it a shot, and hope for the best.

Be well, Pippet  ;)
Diagnosed Aug. 2006
CD4 246, VL 202,000
Started Truvada/ Viramune 11-23-06
Taken off meds 12-06-06 (Bad Rash)
Started Truvada/ Reyataz, Norvir 1-18-07
Taken off Norvir 3-1-07 (Jaundice)
New doc 3-22-07
CD4 229  VL 1031
My latest cocktail...  Truvada and Kaletra (4-6-07)
CD4 289 VL 350 (5-15-07)
CD4 308 VL 115 (8-06-07)
CD4 349 VL 511 (11-5-07)
CD4 489 VL 383 (2-4-08)
CD4 483 VL <50 (5-6-08) YEAH
CD4 545 VL 108 (9-12-08)
CD4 409 VL <48 (1-27-09) YEAH
CD4 505 VL <48 (5-20-09)
CD4 385 VL <48 (9-15-09)
CD4 609 VL  159 (2-28-10)

Offline mrtallguy

  • Member
  • Posts: 199
Re: SUSTIVA vs. VIRAMUNE (AND TRUVADA) ??
« Reply #4 on: December 28, 2006, 07:29:52 pm »
Hey Kate, Ray, & Pippet....
THANKS for the feedback!  I was thinking about Viramune since it also is an NNRTI but since my CD4 is at 725 I don't think I will risk starting on that one now....it could be saved for a time if and when my CD4 drops to a lower level.  I want to get away from the sleep drugs so I'll be talking to my doc about trying a low dose anti-depressant to see how that goes....the Sustiva has done great things for my CD4 so I don't want to dump it pre-maturely....but if it is not for me then I will dump her and review options.  Pippet...you hit it on the head with your comment about what works for one may be a disaster for another!  Are we having fun yet? :)

Be Well,

Craig
I AM DETERMINED TO SEE THINGS DIFFERENTLY!
--ACIM

Offline JasonintheOC

  • Member
  • Posts: 3
Re: SUSTIVA vs. VIRAMUNE (AND TRUVADA) ??
« Reply #5 on: January 02, 2007, 06:47:05 pm »
I started Atripla last summer as soon as it was available.  It was my first crack at drug treatment and thought it would be really nice to have 1 pill once a day.

I had heard about the wild and vivid dreams that Sustiva tends to cause or the opposite, sleeplessness.

My experience with Sustiva ended with switching my meds to Truvada (2 of the 3 drugs in Atripla) and Viramune.

Sustiva created short episodes of panic, fear, and depression.  With incredible in-tenseness I would all of a sudden feel depression and sometimes feel so hopeless that I had suicidal thoughts.  These episodes lasted 5-10 minutes and happened several times a week.

I stayed with the medication through the 3rd month.  My numbers dramatically improved after month 1.  My viral load went from 100,000 to less than 50 and my CD4 count rose from 350 to 450.  I figured that I would eventually get used to the medication and the mental side effects would subside.  I also really wanted to stick with a one pill once a day regimen.  The episodes didn't let up and I didn't want to put up with them any longer.

I've been using the Truvada and Viramune combo now for a couple months and have no known side effects.  I've gotten over having to take 3 pills (2 Viramune, 1 Truvada) instead of 1.

I'm definitely in the Viramune camp!

Offline mrtallguy

  • Member
  • Posts: 199
Re: SUSTIVA vs. VIRAMUNE (AND TRUVADA) ??
« Reply #6 on: January 02, 2007, 09:35:15 pm »
Hey Jason...
Thanks for the reply! And WELCOME to the AM forum!  It is great that you found this venue to find and share information....I joined a few weeks ago and have found the members here to be quite amazing in their desire to share and help eachother.  Of course, as with any endeavor, what you GET from this group will be in direct preportion to what you GIVE this group.  So stop back and let us know about your progress, trials, and tribulations.  We are all in this together....there is strength in numbers!

I have learned through this site that Sustiva does not have to be taken in the recommended 600mg "insanity" dose....it also is available in 200mg capsules so I will start with those tomorrow.  I will try one in the AM, one an hour after lunch and one at bedtime...hopefully a smaller hit will not affect the sleep.  If this approach does not work it is good to know that the Viramune is a good alternative.

Be Well!

Craig
I AM DETERMINED TO SEE THINGS DIFFERENTLY!
--ACIM

 


Terms of Membership for these forums
 

© 2024 Smart + Strong. All Rights Reserved.   terms of use and your privacy
Smart + Strong® is a registered trademark of CDM Publishing, LLC.