Paliperidone fda

Common Questions and Answers about Paliperidone fda

invega

Avatar n tn Finally, since about year he began giving him INVEGA (paliperidone) injection 50 mg which he is fine with it. The problem is that he has become sperm non-existent as he told me. Will it disappear in case he stop taking the injection after a long period of use???? I am very confused, particularly as he wants to get married and be a father.
Avatar n tn For the past couple years I have been on paliperidone which is generic for invega which I know can cause extreme weight gain. Couple that with my increasingly poor eating habits, I definitely ballooned in weight. For about the past two months I have gone on a heavy calorie restriction that I know is deemed to be unsafe and unhealthy. I want to say now that with respect, I would prefer you focus on my question at hand and not about telling me to eat more food than I currently do. Thanks.
Avatar m tn Well will wonders never cease? Are we surprised about the information? I guess they had to spend money on something after they couldn't buy donuts for doctors offices anymore.
Avatar f tn 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.
438514 tn?1305734140 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.
29837 tn?1414534648 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.
Avatar m tn 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.
356929 tn?1246389756 I don't know if I can forward this link but evidently there is a fda warning re: possible salmonella in raw tomatoes. I'll try to copy and paste link, but if it doesn't work, go to the FDA website. I know that some of my friends having chemo had to be very careful when eating raw fruits or vegetables. Just thought I'd pass it along. I heard this on CNN as well. It's not a hoax...http://www.fda.gov/bbs/topics/NEWS/2008/NEW01848.
4705307 tn?1447970322 GILD), with a proposed indication for the treatment of chronic hepatitis C infection, in combination with other agents in adult patients with genotypes 1 to 6 and/or adult patients awaiting liver transplantation. FDA intends to make background material available to the public no later than 2 business days before the meeting.
757137 tn?1347196453 The FDA has issued a stern warning concerning the use of Advair. Not only can it worsen asthma, but the side effects can be fatal. Other forms of treatment should be sought and, if the product is used at all, it should be for short periods of time. Advair affected my adrenals, harmed my eyes, and worsened my asthma. It caused such serious choking that I feared it would kill me. I stopped taking it last August and am doing fine on natural anti-inflammatories.
Avatar m tn For people with 1b Sovaldi and Riba seems to be the ticket. Later this year the FDA should approve the companion drug for Sovaldi and do away with the Riba. Do you know what your IL28B Polymorphism is? You could wait until later this year and do the 2 drug combo or do Sovaldi and riba now.
Avatar n tn ALL ELISA tests are FDA approved. All tests marketed in the US are FDA approved. All tests are 3 month tests to obtain a conclusive negative test result. Now move on.
572651 tn?1530999357 At the close of the inspection, the FDA investigator presented an inspectional observations Form FDA 483 for your review and discussed the observations listed on the form with you. The deviation noted on the Form FDA 483, your written response to the noted violation dated November 7, 2011,and our subsequent review of the inspection report is discussed below. This letter also requests prompt corrective action to address the violation cited.
393685 tn?1425812522 Here is the information I received today from both RLC labs ( the makers of Naturethroid) and the FDA. YES!!! - I really talked to a live person with both of them:) Now remember - this is ONLY the most up to date information I have. It sounded a bit hairy on the phone with the FDA - but I'll explain below. First - both organizations were the best people I have spoken to in a long time. 1. RLC labs....... "There is NO ceasing of desiccated thyroid medication.
110225 tn?1272727888 The FDA is accepting comments regarding expanded access to the Direct acting anti-virals for Hep C at http://www.regulations.gov/search/Regs/home.html#submitComment?R=0900006480ab98ce. Will those of us who cannot or will not take interferon post comments demanding greatly expanded trials with combinations of the best STAT-C drugs, in the public health interest?
Avatar m tn IDX719 Receives Fast Track Designation From the FDA for the Treatment of Chronic Hepatitis C Infection CAMBRIDGE, Mass., July 25, 2012 (GLOBE NEWSWIRE) -- Idenix Pharmaceuticals, Inc. (Nasdaq:IDIX), a biopharmaceutical company engaged in the discovery and development of drugs for the treatment of human viral diseases, today announced the U.S. Food and Drug Administration (FDA) has granted Fast Track designation for IDX719 for the treatment of chronic hepatitis C infection (HCV).
789572 tn?1334424879 Vertex asked for fast track status several years ago. The FDA made them add another trial. The point I was trying to make along with the article is that the FDA approval process STINKS and cost many people their lives! If a drug is proven safe and tested then there is no reason you should have to wait 8-10 years to be approved. All this does is make the drugs cost more money.
Avatar n tn No the military would not use a test that is not FDA approved. For further discussions on this I suggest you talk with your medic.