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[BizJournal]
See Also: Protalix Asked to Widen Gaucher-Drug Supply
[Wall Street Journal; $$$]
See Also: Protalix's New Carrot Derived Drug Likely to Win FDA Approval
[CNBC]
7/7 Generic Maker Caraco Lays Off 1/2 Workforce; Quality Control Lapse
Caraco Pharmaceuticals lays off 350
jobs indefinitely after federal authorities shut down distribution at all the company's Michigan plants last month citing faulty manufacturing practices
[Detroit News]
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That research, from the University of Maryland School of Pharmacy and funded by Novartis Pharmaceuticals, found "small but statistically significant" improvements in health status, based on daily activity levels, of those enrollees who previously had no prescription drug coverage. |
Customs. |
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Customs official, DEA official, or FDA official. |
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7/7 Lilly Gets Nod For Expanded Use Of Alimta
Lilly Receives Fourth FDA Approval for ALIMTA(R) (pemetrexed for injection)
maintenance therapy for locally advanced or metastatic non-small cell lung cancer (NSCLC) . |
"We can make it better and get more savings and, of course, keep people's health better maintained. They were randomly assigned to receive losartan (Cozaar), enalapril (Vasotec), or placebo for five years
[ MedpageToday]
Renal and Retinal Effects of Enalapril and Losartan in Type 1 Diabetes
5-year cumulative incidence of microalbuminuria was 6% in the placebo group; the incidence was higher with losartan (17%, P=0. |
| 96 by the log-rank test)
[NEJM]
7/6 Sepracor: 2 Lunesta For Kids Experiments Put On Hold
Sepracor Provides Update on Clinical Trials for SEP-225289 and LUNESTA(R) Pediatrics
FDA has notified us that these two studies have been put on clinical hold due to its concerns regarding non-clinical data that could be relevant to the administration of eszopiclone in children
[Sepracor Press Release]
See Also: Safety & Efficacy Study in Children and Adolescents With Attention-Deficit/Hyperactivity Disorder - Associated Insomnia
[ClinicalTrials. |
* In many cases, you do not know where the drugs were made or how they were handled.gov]
7/6 Zevalin: Complete Response Letter
Spectrum Pharmaceuticals Receives Complete Response Letter from FDA for Zevalin
Does Not Involve New Clinical Studies or New Data Analyses
FDA requested the Company to submit data files from the FIT study to support and verify a subset of the data that are currently under review
[Spectrum Pharmaceuticals Press Release]
7/6 Provenge Approval Possible Mid-1010 Launch;
Efficacy = Extra 4 Months Vs. |
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* You have no recourse if the drugs you purchase are worthless or do you harm. |
Food and Drug Administration
U. |
At the same time, each of the groups also decreased the amount spent on other medical care by $33, $46 and $30, respectively.
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WEDNESDAY, July 1 (HealthDay News) -- Older people who signed up for Medicare's prescription drug coverage, called Part D, spent more on drugs after enrolling than they had before but less on other types of medical care, researchers have found.
At the same time, each of the groups also decreased the amount spent on other medical care by $33, $46 and $30, respectively. |
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Likely FDA Approval Gives Dendreon A Lift
extended survival by a median 4.
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7/7 Genzyme's Pain Is Upstart Israeli's Gain
FDA considers new Gaucher drug to offset Genzyme's plant shutdown
not yet been approved for use in the U.S. |
| Customs permits people to bring back reasonable amounts of medications for personal use, but does not allow stockpiling or purchasing large amounts of drugs for what will be assumed is a commercial or resale purpose. I am not a doctor, nor am I a U. |
"We can make it better and get more savings and, of course, keep people's health better maintained. |
| laws regarding importation of foreign drugs may lead to your arrest in the U. |
gov]
See Also: Long Term Safety Study in Children and Adolescents With Attention Deficit Hyperactivity Disorder -Associated Insomnia
[ClinicalTrials. |
| S. Food and Drug Administration last month seized more than 30 of its generic drugs for QC violations such as oversized pills. |
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