Sitagliptin emea

Common Questions and Answers about Sitagliptin emea

januvia

Avatar n tn m asking please if is it possable that if i take the drug sitagliptin it would mean i could reduce the gliclazide and stop the mrtformin my Diabetes is well controlled on the whole but my nurse as requested i increase the glicazide
Avatar m tn Of the total number of subjects [N=3884] in Phase II and III clinical studies of Sitagliptin, 725 patients were 65 years and over, while 61 patients were 75 years and older. No overall differences in safety or effectiveness were observed between subjects 65 years and over and younger subjects. While this and other clinical experience have not identified differences in responses between the elderly and younger patients, greater sensitivity of some older individuals cannot be ruled out.
Avatar f tn Ben Weintraub, director of research, Wolters Kluwer inThought We expect that 2011 will be the year for novel oral anticoagulants, as the FDA gets over its hesitation in approving Xarelto (rivaroxaban) and we begin to get mature data for apixaban, edoxaban, and others. Physicians in Europe and the U.S. will begin to replace heparin with Xarelto and Pradaxa (dabigatran).
488724 tn?1253551235 I take 1000mg of Metformin twice a day, 100mg of Januvia(Sitagliptin) once a day and i take 25mg of Levothyroxin once a day. I also just started 150mg of Ranitidine twice a day for my stomach pain that makes me always feel nauseaous, and 100mg of Loratidine once a day for allergies. and today im starting taking Vitamins that i had stopped for a while.
Avatar f tn I recommend you research for yourself on teh FDA website, the EMEA (european FDA) website as well as runnign a google on it. There are many un-nerving entries on teh internet about this drug. However, it is good to do your own research and then se this information to discuss with your cardiologist or EP. Best wishes.
401554 tn?1270213756 Be very careful about any product intended (or with a label claim) to have a pharmacological effect on the body that is not approved by a regulatory body (e.g. FDA for U.S.A., EMEA for Europrean Union). Wishing you well.
Avatar m tn Alternatively the European Medicines Agency (EMEA) handles licencing for the EU. If a product is licensed by the EMEA then it is valid in all 27 Member states of the EU and will carry the CE mark.
Avatar n tn In Hong Kong, the risk fo your partner being infected with HIV is certainly lower than if she were an IV drug user. How much lower is hard to say. Thus again., your risk of infection is lower, and probably far lower than 1 in a million.
408795 tn?1324935675 But its FDA equivalent, the European Medicines Agency (EMEA), still rejects as many as fifty percent of the drug names it receives. The EMEA’s Name Review Group watches out for name confusion, misleading implicit claims about the drug’s efficacy or purpose, and misinformation about what the drug is made of...." ..."Consonants play a weaker but still influential role. Voiced consonants like “g” and “v” use the vocal cords, while their voiceless equivalents like “k” and “f” don’t.
1972385 tn?1343827076 Aloprim), Zyloprim, Dilantin, Depakote, Levaquin, diclofenac, etravirine, isotretinoin (a.k.a. Accutane), fluconazole,[4] valdecoxib, sitagliptin, oseltamivir, penicillins, barbiturates, sulfonamides, phenytoin, azithromycin, oxcarbazepine, zonisamide, modafinil,[5] lamotrigine, nevirapine, pyrimethamine, ibuprofen,[6] ethosuximide, carbamazepine, nystatin, and gout medications.
1542388 tn?1293851813 He is on Lantus 50 units qd and 1 table of Janumet (which is 50mg Sitagliptin/1000mg Metformin) qd and sometimes BID. Just bought a book by Dr. Neal Barnard hoping to get the DM where it should be. I think the Inf/Reb tx had something to do with the onset of the DM-everything was just too coincidental! I worry too all these DM meds are hard on the liver. His kidneys seem to be OK so far; GFR's are 100 from Oct and 117 from April, but he does have Htn with BP on the 27th 162/87.
Avatar f tn Available therapies have no contraindication in children if otherwise healthy. The US FDA and EMEA have recently approved combined pegylated-IFN-α2b plus ribavirin treatment for children, who should be over 3 years of age in order to avoid severe side effects. Experiences in pilot trials and international studies indicate a response rate of 50% in genotype 1 patients, and more than 90% in genotype 2 or 3 patients, indicating resolution of chronic disease.