Each pharmaceutical company to carry out the responsibilities and commitment towards the products j

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In the winter of 1961, the world experienced the thalidomide disaster. The drug thalidomide as a sedative (sleep aid) was used. About 4 years after the release of the drug in many countries consumed a sharp increase in the prevalence of congenital birth defects were observed.
In the winter of 1961, the world experienced the thalidomide disaster. The drug thalidomide as a sedative (sleep aid) was used. About 4 years after the release of the drug in many countries consumed a sharp increase in the prevalence of congenital birth defects were observed. Epidemiological studies have revealed that the cause of this increase has been the drug thalidomide during pregnancy. The disaster trigger the formation of national centers to record and evaluate the effects of drugs in different countries of the world. The main purpose of rapid identification centers and supernatural complications are necessary precautions regarding their occurrence.
In today's world where millions of people every day are taking various medications and their side effects are very difficult to collect information about, how can the use of products medication complications related j mendel to the probable destructive traced?
The key to solving j mendel this problem, careful and ongoing monitoring of drug consumption by medical personnel, and so the people j mendel involved in the letter in any part of the world unwanted effects deleteriotis need to be aware of the drug any complications j mendel Drug suspect to a single center in their country report. In order to evaluate the side effects of medications center and subordinate units of the Office of Research and Development Food and Drug Department of the Ministry of Health as the national center for the collection and registration of drug side effects by the community of the center since will 1377 as a full member of the World Health Organization () WHO Programme for International Drug Monitoring products have been accepted and since then the organization and other Member States to exchange information on drug side effects and pays according to international standards International, yellow forms provided by the center, which is in contact with the center, the number of necessary medical and applicants will be considered and then fill out the forms to the address of the center of medicine unintentional side-effects review Unit,'s subsidiary Office of Research and Development Department of the Food and Drug Administration sent the postage is already paid. What should j mendel be reported?
All adverse events suspected to taking any health products, including drugs (both prescription and self-medication or under treatment), j mendel blood products, vaccines, contrast agents, substances j mendel used in dentistry or surgery, herbal products, contact lens solutions and reporting to the center, and the important thing is that even when reporting a problem except where the manufacturer's name and number search batches, and the report.
Identification, assessment, reporting and prevention of adverse drug effects in humans, called the main objectives Farmakvvyzhyla Farmakvvyzhyla te te, quick and timely detection of adverse effects and drug Tdakhla unknown Adverse j mendel drug preventing, identifying risk factors involved in the occurrence of adverse effects of drugs and pharmaceutical products is reasonable and safe. The duties and responsibilities of pharmaceutical companies
Each pharmaceutical company to carry out the responsibilities and commitment towards the products j mendel are required to record the appropriate systems in Farmakvvyzhyla Ness (Drug Watch) should be necessary than using appropriate measures to deal with the problems Pharma is committed. The goal is to be able to assess side effects, drug safety regulations and assess the benefits and harms of specific pharmaceutical products and the accuracy j mendel of the respective company and have enclosed necessary and, more importantly, pharmaceutical companies before making any drug product, especially Drugs under license from other states to peer review and scrutiny of adverse effects j mendel associated with those drugs act. Hope that it Farmakvvyzhyla part of te (watch drug) Pharmaceutical companies increasingly j mendel more bold and more intricate work.
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