Литература для музыкальных школ. ББК 83.0я73 Рубрики: Теория литературы--Учебники для вузов Кл.слова (ненормированные): Литературная иерархия -- Теория литературы -- Литература -- Учебники для вузов -- Литературоведение -- Искусство -- Литературное произведение -- Жанры. В последние годы издательством «Музыка — осуществлено несколько проектов, связанных с выпуском учебников по музыкальной литературе для разных ступеней и уровней Полезными окажутся эти страницы и для студентов некоторых специальностей вузов.
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Drug Safety and Availability; Drug Recalls; Drug Recalls. Share; Tweet; Linkedin; Pin it. FDA began a pilot program to notify people of drug recalls before they are classified. Superpotent and subpotent test results. PharmaTech is voluntarily. Safety pharmacology services by WuXi AppTec help deliver high-quality drug candidates faster and at a lower cost. Services include electrophysiology and in vitro pharmacology. Drug Formulation, Solubility & Bioavailability 2016. Lophius Biosciences Performs Successful Clinical Validation for T-Track. Nanion Starts Shipping the SyncroPatch 384 Patch Engine. Shop for At Home Drug Test For Multi Drug Test, By Phamatech - 1 Test, Earn reward points on your purchase. The half life of any drug, medication or substance is the period of time necessary for 1/2 the drug to be eliminated or disintegrated by natural processes in the body. The half life of Valium is particularly long, 2. However, Valium’s typical half life in a young, healthy person is about 2. This is due to the nature of the medication. Valium (diazepam) is a long acting benzodiazepine that starts inactive and becomes active as the normal metabolic process of the body occur and introduce the drug throughout the body (including the liver and the blood brain barrier). Should I mix Valium with other drugs? No. Valium SHOULD NOT be taken with other medications, drugs or alcohol. This is because Valium can interact with other substances to extend and increase the effects of Valium, causing it to stay in the bloodstream for even longer amounts of time. Likewise, the effects of Valium are decreased with the use of caffeine or cigarettes. Drug Testing for Valium. If you are avoiding a drug test and think that you may have a problem with Valium. Waiting for 5 days is a total precaution to make sure that the drug is totally out of your system. But as a Class IV drug, there is a relatively low risk for addiction when compared to other drugs (like Vicodin, Codeine or Oxycodone). But if you take a larger dose of Valium than prescribed or more often that prescribed, you may develop tolerance to the drug. Long- term or excessive use can also result in withdrawal (a sign of physical dependence) when you stop taking the drug. But does this mean that you are addicted? Click here to take a self- survey and see if you are addicted to Valium, or not. Consumers with questions regarding this recall can contact 8. Monday through Friday, 9 AM to 6 PM EST or email WPNQuality@wellsrx. A complete list of recalled products can be found at http: //www. Safety/Recalls/ucm. Invokamet XR labeling includes a Boxed Warning regarding the risk of lactic acidosis. View page. Lomaira Approved for Weight Reduction. The FDA has approved KVK Tech’s Lomaira (phentermine hydrochloride) 8 mg (Schedule IV) to be used for a short period of time (a few weeks) for weight reduction in adults with an initial body mass index of 3. Lomaira should be used together with regular exercise and a reduced- calorie diet. View page. Kyleena Approved for Prevention of Pregnancy. The FDA has approved Bayer’s Kyleena (levonorgestrel- releasing intrauterine system) 1. Kyleena will be available by prescription only in October 2. View page. Exondys 5. Approved for Duchenne Muscular Dystrophy. The FDA has approved Sarepta Therapeutics’ Exondys 5. Exondys 5. 1 is the first drug approved to treat patients with Duchenne muscular dystrophy and was approved under the FDA’s accelerated approval program. View page. Hyoscyamine Sulfate Recall. Virtus Pharmaceuticals Opco II is voluntarily recalling 7 batches (http: //www. Safety/Recalls/ucm. The affected lots were distributed throughout the US and Puerto Rico starting March 1. Virtus is notifying distributors and retailers by letter and email and arranging for the product return. Customers with affected lots should discontinue use and distribution and return the product to place of purchase. Consumers with questions regarding this recall can contact Virtus at 1- 8. Monday through Friday, 8 AM to 5 PM EST or email rxrecalls@inmar. View page. Influenza A (H5. N1) Vaccine Expanded Indication. The FDA has approved an expanded indication for Glaxo. Smith. Kline’s Influenza A (H5. N1) virus monovalent vaccine, adjuvanted emulsion for intramuscular injection to include patients 6 months and older for the prevention of disease caused by the influenza A virus H5. N1 subtype contained in the vaccine. The vaccine was previously indicated in patients 1. View page. Cuvitru Approved for Primary Immunodeficiency. The FDA has approved Shire’s Cuvitru (immune globulin subcutaneous . Cuvitru labeling includes a Boxed Warning regarding the risk of thrombosis. View page. Krystexxa Expanded Boxed Warning. The FDA has expanded the Boxed Warning for Crealta Pharmaceuticals' Krystexxa (pegloticase) injection to include information regarding reports of hemolysis and methemoglobinemia in patients with G6. PD deficiency in addition to statements regarding the risk of anaphylaxis and infusion reactions. View page. Eye Wash/Eye Irrigating Solutions Recall. United Exchange Corporation, in cooperation with the FDA, is voluntarily recalling specific lots (http: //www. Safety/Recalls/ucm. Safety/Recalls/ucm. Rugby Eye Irrigating Solution (NDC 0. Major Eye Wash (NDC 0. Family Care Eye Wash due to microbial contamination. United Exchange is notifying its distributors and customers by recall letter and is arranging for return of all recalled products. Consumers with questions regarding these should contact Rugby's Customer Support Department at 1- 8. Monday through Friday, 8 AM to 8 PM EST. Consumers with questions regarding the Family Care recall should contact the United Exchange Customer Service Department at 8. Monday through Friday, 8: 3. AM to 5: 3. 0 PM PST. Arzerra is also indicated in combination with chlorambucil for previously untreated patients with CLL for whom fludarabine- based therapy is considered inappropriate; for extended treatment of patients who are in complete or partial response after at least 2 lines of therapy for recurrent or progressive CLL; and for the treatment of patients with CLL refractory to fludarabine and alemtuzumab. Arzerra labeling contains a Boxed Warning regarding the risk of hepatitis B virus reactivation and progressive multifocal leukoencephalopathy. Blincyto is dispensed with a patient Medication Guide. View page. Benzodiazepines and Opioid Medicines Safety Alert. An FDA review has found that the combined use of opioid medicines with benzodiazepines or other drugs that depress the CNS resulted in serious adverse reactions, including slowed or difficult breathing and deaths. Based on these findings, the FDA is requiring that new Boxed Warnings be added to the labeling of prescription opioid pain and prescription opioid cough medicines, and benzodiazepines, as well as new or revised patient Medication Guides. The FDA will also continue to evaluate the evidence regarding combined use of benzodiazepines or other CNS depressants with medication- assisted therapy drugs used to treat opioid addiction and dependence, and whether labeling changes will be needed for other CNS depressants. Health care providers should limit prescribing opioid pain medicines with benzodiazepines or other CNS depressants only to patients for whom alternative treatment options are inadequate. If these medicines are prescribed together, the dosages and duration of each drug should be limited to the minimum needed to achieve the desired clinical effect. Patients and caregivers should be warned about the risks of slowed or difficult breathing and/or sedation, and the associated signs and symptoms. The prescribing of opioid cough medicines for patients taking benzodiazepines or other CNS depressants, including alcohol, should also be avoided. Patients taking opioids with benzodiazepines, other CNS depressant medicines, or alcohol, and caregivers of these patients, should seek medical attention immediately if symptoms of unusual dizziness or lightheadedness, extreme sleepiness, slowed or difficult breathing, or unresponsiveness occur. This action is part of the FDA’s Opioids Action Plan, which focuses on policies aimed at reversing the prescription opioid abuse epidemic while still providing patients in pain access to effective and appropriate pain management. Safety/Med. Watch/Safety. Information/Safety. Alertsfor. Human. Medical. Products/ucm. Unit- of- use blister packs may contain 1. The blister card within the blister pack is properly labeled as 1. ODT, however, the plastic shell pack containing the 1. ODT. The affected lot was distributed to wholesale distributors and retail pharmacies nationwide from June 1. August 1. 0, 2. 01. Pharmacists and wholesalers should check their inventories for the affected lot, segregate any material from the lot, and contact Stericycle at 1- 8. Monday through Friday, 8 AM to 5 PM EST) for instructions on product return. View page. Afluria Quadrivalent. The FDA has approved Seqirus’ Afluria Quadrivalent (influenza vaccine, inactivated) suspension for intramuscular injection for use in patients 1. A subtype viruses and type B viruses contained in the vaccine. View page. Trokendi XR Expanded Indication. The FDA has approved an expanded indication for Supernus Pharmaceuticals’ Trokendi XR (topiramate) extended- release oral capsules as an initial monotherapy treatment in patients 6 years and older with partial onset or primary generalized tonic- clonic seizures. Trokendi XR was previously approved for monotherapy treatment in patients 1. Trokendi XR is also approved as adjunctive therapy in patients 6 years and older with partial onset, primary generalized tonic- clonic seizures, or seizures associated with Lennox- Gastaut syndrome. It is dispensed with a patient Medication Guide. View page. Troxyca ER Approved for Pain Management. The FDA has approved Pfizer’s Troxyca ER (oxycodone hydrochloride and naltrexone hydrochloride) extended- release oral capsules for the management of pain severe enough to require daily, around- the- clock, long- term opioid treatment and for which alternative treatment options are inadequate. Troxyca ER contains a Boxed Warning regarding the risk for addiction, abuse, and misuse; life- threatening respiratory depression; accidental ingestion; neonatal opioid withdrawal syndrome; and cytochrome P4. A4 interaction. Troxyca ER is dispensed with a patient Medication Guide. Troxyca ER capsules are designed to be abuse- deterrent, as the sequestered naltrexone is released only upon crushing or chewing the capsules. The excipient talc may also cause significant issues if injected parenterally. View page. Eyesaline Eyewash Recall. Honeywell, in cooperation with the FDA, is voluntarily recalling 1 lot (F1. Eyesaline Eyewash solution due to a risk of product contamination with Klebsiella pneumoniae. No injuries have been reported, and no contamination was found in batch testing. Distributors must stop distribution of the affected product and return it to Honeywell for credit or replacement. Customers with questions regarding this recall should contact their distributor or Honeywell Customer Care at 1- 8. Monday through Friday, 8 AM to 6: 3. PM EST. View page. Oxacillin Recall. Sagent Pharmaceuticals has voluntary recalled 1 lot of oxacillin 1. OXT5. 12, expiration date March 2. NDC 2. 50. 21- 1. The particulate matter was identified as iron oxide, which may result in local swelling, irritation of blood vessels or tissue, or blockage of blood vessels if administered. The affected lot was distributed to hospitals, wholesalers, and distributors nationwide from June through July 2. Those with the affected lot should discontinue use and distribution and quarantine the product immediately. For additional assistance, customers can call 1- 8. Monday through Friday, 8 AM to 7 PM CST. View page. Cetylev Recall. Arbor Pharmaceuticals has voluntarily recalled three lots of Cetylev (acetylcysteine) 5. C1. 6, 0. 06. C1. C1. 6; expiration date February 2. NDC 2. 43. 38- 7. 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