filgrastim fda

Filgrastim is also prescribed as pegfilgrastim (called Neulasta). My doctor used the 500 neutrophill count as a cut-off, so every time I got down around 500 I used Neulasta. The interferon drops neutrophils and platelets. Some people can do okay with low neutrophils but just as many end up with kidney and sinus infections, etc., that make you even more miserable.

my stats seem to go up and down so I only have to take it now every 2 wks. It is unknown whether filgrastim (Neupogen) increases or decreasses an individual's risk of developing cancer. Based on limited long-term data from healthy people ( if a person is healthy why would they need neupogen in the first place ) who have received filgrastim, no long-term risks have been found so far. good luck to you....hope this helped!

, the primary ‘rescue’ meds are (generic) epoetin alpha (brand names Epogen, Procrit, Aransp), and filgrastim (generic) (brand name Neupogen). We do have a platelet booster here that has been approved for cancer treatment; it is generically known as oprelvekin (brand name Neumega), but its use has not been FDA approved for HCV treatment to my knowledge; it tends to worsen hemolytic anemia, although we have had a few patients in forum that have tried it.

Do you mean filgrastim? And are you saying Dengue fever? It would be a surprising though perhaps not impossible use of filgrastim. Dengue is usually treated by pain managers and sometimes hospitalization and a blood transfusion. Anyway, if you have a legitimate prescription from a doctor, you should be able to fill it in the United States.

For this reason, patients are prescribed antibiotics and even receive injections to increase white blood counts (such as filgrastim or lenograstim). If this 0.4 value really pertains to your white counts, then I believe this is really low and what you are experiencing is a condition called 'febrile neutropenia'. I would suggest you ask your doctor about filgrastim or lenograstim injections aside from the Levaquin. Regards.

Doctors unable to give any explanation for such wide variations on a dose to dose basis. Till date, I have also taken 5 doses of Filgrastim - the WBC Stimulator. Can you pleae advice possible reasons for such wide fluctuations.

Neulasta® (pegfilgrastim) or NEUPOGEN® (Filgrastim) may reduce your chance of getting an infection, but it does not prevent all infections. An infection can happen anytime your neutrophil counts are low. Look for signs of infection, such as fever, chills, rash, sore throat, diarrhea, or redness, swelling, or pain around a cut or sore. If you have any of these signs, contact your health care professional immediately. http://www.neulasta.com/starting-chemo-with-neulasta/about-neulasta-neupogen.

Fda, getting movin! I have already written to my senators congressional rep , people will decompensate and probably die while we are waiting for sofo/ledip/sime.

Musculoskeletal symptoms have been the most frequently reported adverse effects of filgrastim therapy. Bone pain has been reported in approximately 22% of patients. Reactivation of pseudogout occurred in a patient receiving chemotherapy. Postmarketing reports have included decreased bone density and osteoporosis in pediatric severe chronic neutropenia (SCN) patients receiving chronic treatment with filgrastim.

Hi, With modern medical advances, especially effective anti-emetics, and growth factors (filgrastim), chemotherapy has become safer and more tolerable over the last decade or so. Hair loss will be your major side effect, and some intermittent illnesses may also be expected during the course of chemotherapy. But your overall long-term benefit will be much more than these temporary effects. All the Best!

You can discuss ‘Neupogen (filgrastim) with the doc; this is a GCSF drug that stimulates bone marrow production of white cells. It is generally initiated when absolute neutrofils reach .500 or that vicinity; some docs allow closer to .350, depending on occupation and other matters.

Listen, I am NOT trying to scare anyone half to death. I am sharing information that was sent to me by the FDA. If you don't want to read the latest up-to-date info, don't read it. But plenty of people like to be in the loop. If you want to stick your head in the sand, go right ahead. The censoring on this site by some of you is appaling to me. I think this will be the last time I will share anything I receive. For Willy. There is no link but here is the entire email I received.

Hello, this is my first time on this forum. I just wanted to see if anyone is having or has had some of the same problems. Five weeks ago I started a 48 week treatment for hep b with 180 mg Pegasys. The nurse gave me my first injection in my arm which hurt for two weeks. Since then, I've alternated the injection sites. Twice in my thighs and twice in my belly. I have these big, round, red rashes with bruises in the middle. They just seem to be getting worse.

That's pretty standard of the FDA, they do this all the time (in other words, it's not earth shattering). Law requires any claims at cures (or more precisely 'treatment') be backed up by clinical trials, FDA clinical trials to be precise. That is why nobody can say any drug, supplement, etc, is a treatment or cure without first completing a multi-million dollar FDA clinical trial that will last for 10 to 20 years.

Today I got not one but two calls from the FDA, so apparently my persistence is paying off. They are going to do whatever the pharmaceutical companies suggest, especially since there are no other alternative drugs except Interferon and Ribavirin. My contact at Vertex, who I just spoke to, is going to look once more into the IND application (Compassionate Use), and see if there's been any changes in their (Vertex) policy for allowing it.

Daily visits to selected websites, subscriptions to selected scientific and medical podcast as well as my monthly magazines such as Nature, Scientific American, Physics Today, Science Magazine and Science Readers. respirate just convinced me to add the FDA website into my dailies. What is good with technology these days is that you can be very selective regarding the kind of information you want to get and newspapers make me angry for some reasons that are totally personal.

NEUPOGEN® ( Filgrastim ) Program is designed to assist those patients who are medically indigent (patients may be uninsured or underinsured). Eligibility is based on patient's insurance status and income level.

I used Neulasta, the pegylated form of filgrastim. More expensive but supposed to hold your neuts up longer when they are getting stomped by the IFN (I have good insurance). No side effect problems with it at all and it took my neut level from .640 to 12 overnight and kept me out of danger level for about 6 weeks. Better than an interferon reduction if patient is responsive to it.

Neulasta is a peglated version of Neupogen which is also know as filgrastim. It's used to stimulate production of neutrophils, a component of whilte blood cells. It can be taken less often than regular 'ol Neupogen. I found it rougher than Neupgen in that it had some side effects, mainly bone pain. I found Neupogen to be side-less. Aranesp is Darbepoetin Alfa which is like Procrit (epo). It is also taken less often than Procrit.

Neulasta is the expensive pegylated counterpart of neupogen. Same drug (filgrastim). Otherwise all you can do is reduce the interferon and it's generally considered better not to do that before you've cleared the virus. I don't know of any ways to reduce your risk of infection. What are you thinking of when you say that, please?

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