Traducción de «Medicamento » (Español → Inglés) :

over-the-counter drug [ non-prescription drug | non-prescription medicinal product | OTC drug | OTC medicine | over-the-counter medicine ]

medicinal product not subject to medical prescription | non-prescription drug | non-prescription medicinal product | OTC drug | OTC medicine | over-the-counter drug | over-the-counter medicine

medicament [ medication ]

Do not take indigestion remedies or medicines containing iron or zinc at the same time of day as this medicine

manage a person's medication | manage a person's medicines | administer prescribed drugs | administer prescribed medication

analyze a medication's impact on the brain | analyze medication's impact on brain | analyse a medication's impact on the brain | analyse medication's impact on brain

drug surveillance [ pharmaceutical surveillance | supervision of medicinal products | supervision of pharmaceutical drugs ]

medical sales market | medical sales markets | medical sales industries | medical sales industry

Food and Drug Administration | United States Food and Drug Administration | US Food and Drug Administration | FDA [Abbr.] | US FDA [Abbr.]

In view of the risks of carcinogens, mutagens and substances toxic to reproduction, the Commission will request the Committee for Medicinal Products for Human Use of the European Medicines Agency to draw up an opinion on the use of these categories of substances as excipients of medicinal products for human use, on the basis of Articles 5(3) and 57(1)(p) of Regulation (EC) No 726/2004 of 31 March 2004 laying down Community procedures for the authorisation and supervision of medicinal products for human and veterinary use and establishing a European Medicines Agency.

The report promotes the following: a global fund financed by G8, the EU, oil-rich nations and others to finance access to and supply of medication and treatment; a global strategy to implement a programme of action to treat and prevent communicable diseases; tiered pricing of medicines from the pharmaceutical industry to ensure wide access to treatment; support for health infrastructure to scan, diagnose, treat and monitor patients, as supply of medicines in itself is inadequate; use of incentives – both financial and legislative – to enhance research and development to produce new medicines and vaccines by both industry and the publ ...[+++]ic sector; the European Commission to work closely with the governments of developing countries, UN agencies, NGOs and civil society to implement the programme.

– Mr President, on a point of order, when the Commissioner quotes the WHO Essential Medicines' List he knows that includes not just essential medicines, but the affordability of those medicines.

(1) Council Directive 81/851/EEC of 28 September 1981 on the approximation of the laws of the Member States relating to veterinary medicinal products(3), Council Directive 81/852/EEC of 28 September 1981 on the approximation of the laws of the Member States relating to analytical, pharmaco-toxicological and clinical standards and protocols in respect of the testing of veterinary medicinal products(4), Council Directive 90/677/EEC of 13 December 1990 extending the scope of Directive 81/851/EEC on the approximation of the laws of the Member States relating to veterinary medicinal products and laying down additional provisions for immunolog ...[+++]ical veterinary medicinal products(5), and Council Directive 92/74/EEC of 22 September 1992 widening the scope of Directive 81/851/EEC on the approximation of provisions laid down by law, regulation or administrative action relating to veterinary medicinal products and laying down additional provisions on homeopathic veterinary medicinal products(6) have been frequently and substantially amended; in the interests of clarity and rationality, the said Directives should therefore be codified by assembling them in a single text.