The pills are not FDA approved, with research still in its infancy.
此外由于此类保健品的研究仍处于初始阶段，食品药品管理局也不批准它上市。
FDA approved - The only U. S. Food and Drug Administration approved HIV-1 test system.
FDA批准-唯一的美国食品和药物管理局批准的HIV - 1测试系统。
They are selling fast on the Internet but illegal in the United States and not FDA approved.
在网上，该隐形眼镜销售火爆，但是在美国这是违法的，因为该隐形眼镜没有经过食品及药物管理局（FDA）的批准。
So let's assume that a drug has passed the stringent testing requirements and is now FDA approved.
所以，让我们假设一种药物已通过严格的测试要求，FDA也批准了。
In 2008 the FDA approved its use as a food additive, previously it was sold only as a dietary supplement.
2008年，美国食品药品管理局批准它作为一种食品添加剂，以前它只作为一种食品补充剂出售。
Furthermore, several of these drugs are already FDA approved or currently in clinical trials for other diseases.
此外，其中一些药物已FDA批准或目前在临床试验中的其他疾病。
Avoid Overpriced, Unproven supplements - Most people assume that FDA approved nutritional supplements are proven products.
回避那些定价过高又未经证明的补品——多数人认为食品及药物管理局批准的营养补品就是经过验证的产品。
The FDA approved Nexium on the basis of exploratory research demonstrating the drug's effectiveness and safety for use with children.
FDA在探索性的研究基础上批准了耐信证明了儿童应用这一药物的有效性和安全性。
Ultrasound is a safe, non-invasive, FDA approved diagnostic test that USES sound waves to measure blood-flow velocity in large arteries.
超声波是FDA认可的一种安全的非侵入性诊断实验项目，利用声波来测量大动脉血管中的血液流速。
In 2004, the FDA approved its use as a "bridge" device before a transplant. In all, surgeons have implanted more than 900 man-made hearts.
2004年，FDA允许全人工心脏作为心脏移植前的过渡装置，植入数总计已超过900颗。
Rapamycin, the other big candidate, has one clear advantageover resveratrol: it's already FDA approved as a drug — but as animmunosuppressant.
雷帕霉素，另外一种抗衰老的重要健将，与白藜芦醇相比有一个非常明确的优点：雷帕霉素已经被美国食品药品管理局认可，但是是作为一种免疫抑制剂认可的。
In March 2010, FDA approved a labeling revision for simvastatin based on interim results from an ongoing clinical trial - the Heart Protection Study 2 (HPS2).
2010年3月，FDA基于一项正在进行的临床研究——心脏保护研究2 (HPS2)的中期结果，修改了辛伐他汀产品说明书中的标识。
Although the use of this medicine to manage pain has been common practice for many years, this form and concentration of morphine was not FDA approved until now.
虽然这种药物用于疼痛多年来一直是普遍的做法，但这种剂型和浓度的吗啡直到现在才被美国FDA批准。
Thirty-four of 35 were approved on or before the review time targets agreed to with industry under PDUFA, including three cancer drugs that FDA approved in less than six months.
34/35个药物是与药业工业在PDUFA下同意目标审评时间时或前被批准的，包括3个癌症药物FDA在短于6个月内批准。
The FDA approved Voltaren Gel based on studies that together included more than 900 patients with knee or hand osteoarthritis, according to Novartis, which makes Voltaren Gel.
据扶他林乳胶剂的生产商诺华公司声称，FDA是在其对900多名患者的膝和手关节炎的研究基础之上批准扶他林乳胶剂的。
The FDA approved the PSA test for use in conjunction with a DRE to help detect prostate cancer in men 50 and older, and for monitoring prostate cancer patients after treatment.
FDA同意直肠指(DRE)与PS A测试一起进行，用以帮助检测50岁及以上男性前列腺癌病症，从而在治疗后用以监督前列腺癌患者。
If approved, the FDA said Cymbalta would be the first nontraditional analgesic approved for chronic pain.
FDA称，如果欣百达获得批准，它将是第一个非传统慢性疼痛止痛药。
The FDA has already approved DBS as a treatment for neurologic disorders, including essential tremor, Parkinson's disease, dystonia, and severe obsessive-compulsive disorder.
FDA已经批准DBS用于治疗神经系统疾病，其中包括原发性震颤、帕金森症、肌张力障碍及重度强迫症。
The FDA has approved nine of its drug candidates in 2009 alone.
美国食品药品管理局（FDA）仅在2009年就批准了该公司的9种药物。
The FDA recently approved this drug, which works by reducing activity in cells responsible for bone breakdown.
食品及药物管理局最近证明这种药，可以通过减少细胞在骨头变脆弱的活动来起作用。
Valproate was FDA-approved in 1995 for treatment of mania.
1995年，丙戌酸钠被FDA核准用于治疗躁狂。
Mithoefer considers the findings especially notable given that 20 of the 21 participants had previously failed to obtain relief from FDA-approved treatments.
米索弗认为，鉴于这21名受试者中的20人此前接受FDA批准的治疗方法后均无效果，所以这一研究结果尤其值得重视。
Pfizer released Chantix, a drug the Food and drug Administration (FDA) approved in May of that year to help smokers quit.
辉瑞公司的Chantix研发成功，并在五月通过了美国食品与药物管理局的验证说这种药物能帮助吸烟者禁烟。
The group chose the PLGA polymer and the pHEMA hydrogel because both materials are FDA-approved for use in the eye.
该研究小组采用的PLGA和pHMA是因为这两种都是FDA（美国食品药物管理局）批准用于眼病的材料。
Drugs made by compounders, including those made at human drug compounding outsourcing facilities, are NOT FDA-approved.
由制药公司制作的药物，包括在人用药调制外包场所制作的，都不是FDA批准的。
Drugs made by compounders, including those made at human drug compounding outsourcing facilities, are NOT FDA-approved.
由制药公司制作的药物，包括在人用药调制外包场所制作的，都不是FDA批准的。
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