pegasys pfs

Yes, Pegasys is no more available in market. What is MRP of Exxura 180mcg? Are you getting any offer or discount on this?

Anyone who responds to this, do you think i will need get surgery on the other knee. And last question. Is PFS common in black people and can PFS result in a patella tendon rapture.

18 mos) (significant) hazard ratio 0.71 Concerned over bev affecting CA 125 levels I OS 39 mos II OS 39 mos III OS 39 mos Follow up 17.

X-rays and blood tests will not show any soft tissue problems. I would have ordered a MRI ASAP. This sounds like PFS (patellar-femoral-syndrome) or a problem with your lateral collateral ligament. Get the MRI! Best of luck!

t know what a normal dose is but my dr always gave me the ovidrel 250 mcg pfs (.5 ml) is that lower? I am going to wait to test but was wondering how long that shot was going to be in my system lol.

Hello and Welcome to the MedHelp Orthopedic Community! Well, don't drag me into court over this as I am only trying to give you my personal opinion! You realize you should always consult your physician for a diagnosis/ treatment plan. That being said, Worker's Comp (in this situation) is full of ....! I am doubting the PFPS (Patella-Femoral Pain Syndrome, we - I am a Orthopedic Surgical First Assistant - just call it PFS) was a "genetic defect"!

Well, this is puzzling! The PFS could explain your knee pain, but that would be all. You could have bilateral carpal tunnel syndrome (which could explain the wrists). Sorry, but I would have to see all the x-rays and do an examination to do you justice. I hope you are seeing a Orthopod and having a Radiologist reading these films. I would like to hear the end result when/if you get one. Best wishes, jd1963!

I treat quite a lot of men for post-finasteride syndrome (PFS). It is not possible to answer your question since there are no rules with this horrible condition.

The nurse gave me the Pegasys injection intramuscular in my arm instead of subcutaneous? Will that have any effect on the course of treatment? Does it have the same efficacy?will I still benefit from the injection in the same intended way?

I came from Afghanistan .I want to buy pegasys because it wouldnt found in my country, How can I get pegasys ???

then he recommend Pegasys, injection po siya for 48 weeks, Salamat sa Dios kasi he lead me to my new Dr. I believe that God has a plan for all of us. inform you guys what will happen. after I'm going on my third week now taking this medicine after the fourth week I will have my sgpt test. I will update you guys on the result.

Make sure you emphasize that there are floating particles in the Pegasys. A light yellow color is normal but floating particles are not. Drug company literature states (see page 2) http://www.medhelp.org/posts/show/638650?post_id=post_3464276 1. DO NOT USE Pegasys if it is cloudy, 2. DO NOT USE Pegays if it has particles in it. 3. DO NOT USE Pegasys if it is any color but clear or light yellow.

I start pegasys in July. Are the side effects really bad? I know everyone is different.. Do most people lose some of their hair? I just wanted info from someone that has been on this.

Has anybody out there been treated with COPEGUS and PEGASYS? I saw a gastroentoligist today and he has ordered all sorts of blood work, but says if I start treatment this is what he would give me. I asked about the new VERTEX drug coming out next year and he said it probably wouldent be out that soon.

//www.gene.com/gene/products/information/pegasys/pdf/copegus_pi.pdf These will cover all possible adverse reactions caused by pegasys and copegus. It would be best to discuss this with your doc as he knows your prior medical history.

I tolerated Pegasys much better than Peg Intron.

I was wondering if there have been any studies comparing Pegasys and Pegintron, and if one has better SVR numbers than the other or was more tolerable. I am new here so I hope I am posting this in the correct forum.

24 weeks of total treatment, with RG7128 500 mg BID [twice daily] in combination with Pegasys and ribavirin for 12 weeks, followed by 12 weeks of Pegasys and ribavirin ("12+12") 24 weeks of total treatment, with RG7128 1000 mg BID in combination with Pegasys and ribavirin for 12 weeks, followed by 12 weeks of Pegasys and ribavirin ("12+12") 24 weeks of total treatment, with RG7128 1000 mg BID in combination with Pegasys and ribavirin for 8 weeks, followed by a further 16

The first time (2008) was a trial with Roche 1626 polymerase inhibitor, Pegasys and Ribavarin. I was UND between 7 or 8 weeks, relapsed 6 weeks after being pulled from tx at 43 of 48 weeks as the trial drug was too harsh on my system. Back then they refused to give me rescue drugs so I had no choice. I have diabetes which may have contributed to my relapse, during tx my sugar was so low I stopped checking it, DUH!

Hi All, Well it looks like my docs office wants to treat me with Peg Intron (80 mg) and Ribaviron 1000mg tablets. She said the Peg Intron in her experience causes a more "predictable" decline in red blood cells than pegasys. I am only 110 lbs, so she said because it is weight based too, that is better for me. Any thoughts on Pegasys vs. Peg Intron? My stats again - female, mid 20s, type 3a, VL 950,000. I have been infected since birth (my mom was HCV). Thanks!

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