Results 261 to 270 of about 4,880,179 (312)
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Drug safety, drug quality, drug analysis

Journal of Pharmaceutical and Biomedical Analysis, 2008
Controlling and minimizing the side effects of drugs are the key issues in assuring the safety of drug therapy. Since side effects are inherent properties of the drug material, these cannot be influenced by drug analysts. At the same time drug analysts play a predominant role in assuring the quality of bulk drug materials and drug formulations and this
Sándor Görög
exaly   +3 more sources

Safety of obesity drugs

Expert Opinion on Drug Safety, 2005
The safety of obesity drugs has historically been poor. This and the stigmatisation of obesity in society ensured that a higher standard of safety for obesity drugs must be met. The authors review the safety disasters of obesity drugs that were withdrawn.
Frank L, Greenway, Mary K, Caruso
openaire   +2 more sources

Advances in Drug Safety

Current Pharmaceutical Design, 2012
The operating room offers a unique setting where anesthetics, preoperative medications, patient comorbidities, and surgery all merge. Anesthesiologists are responsible for combining these concerns into a dependable and safe approach. From formulation to administration, enhancements in nearly every aspect of a given drug have improved the ability of ...
J Adam, Cartwright   +5 more
openaire   +2 more sources

Drug safety in claudication

Nursing Standard, 1991
Atenolol or nifedipine can probably be used safely in patients with claudication and coexisting hypertension and angina.
openaire   +2 more sources

Safety in New Drugs

JAMA, 1964
NOW, BY LAW, new drugs must be both effective and relatively safe. But I think a new drug must be more than a tolerable cipher in an already overcrowded list. The hope of significant new knowledge which may lead to therapeutic progress is, in my view, the only defense for studying the effects of as yet poorly understood new drugs in human subjects. How
openaire   +2 more sources

The Future of Drug Safety

Clinical Pharmacology & Therapeutics, 2007
To provide a European perspective, I was invited to sit on the Institute of Medicine (IOM) committee that was charged with assessing the current system for evaluating and ensuring postmarketing drug safety in the United States. My colleagues on the committee came from a variety of professional backgrounds (health care, epidemiology, law, and economics),
openaire   +2 more sources

The safety of antiretroviral drugs

Expert Opinion on Drug Safety, 2008
Antiretroviral (ARV) medications have been in clinical use for 20 years in the treatment of HIV and our knowledge about the safety of these medicines continues to grow. The potential side effects of ARVs can be either short term, such as hypersensitivity reactions, drug-induced hepatitis, anemia and lactic acidosis, or long term, including dyslipidemia,
Christopher N, Tymchuk   +1 more
openaire   +2 more sources

Drugs and the Public Safety

Annals of Internal Medicine, 1966
The basic Food Drug and Cosmetic Act of 1938 together with its accompanying amendments through 1965 now gives the Food and Drug Administration (FDA) sweeping authority to monitor and control the development production and use of drugs. The law provides the U.S.
openaire   +2 more sources

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