Si può desiderare di provare un trattamento naturale disfunzione erettile come un diverso per i problemi di costruzione. Al giorno d oggi ci sono diverse terapie sul mercato, ma un trattamento naturale disfunzione erettile è stato confermato qualche ora e ora di nuovo per dare risultati efficienti e permanenti. Cos è la disfunzione sessuale? L incapacità di sviluppare o sostenere una costruzione abbastanza lungo per fare l amore è chiamato disfunzione erettile, ED https://farmacia-senzaricetta.it/ o (maschio) problemi di erezione. Tutti gli uomini possono avere problemi di costruzione di volta in volta e gli scienziati considerano ED essere presenti se si verificano problemi di costruzione almeno il 25% del tempo. Alcuni fatti duri: ED Può essere dovuto a problemi emotivi. Stress, pressione, giltiness, depressione, bassa autostima e ansia prestazioni può essere la causa dei vostri problemi di costruzione. La ricerca ha confermato che il 90 per cento della disfunzione erettile è fisica in origine, non emotiva. L impotenza colpisce la maggior parte degli uomini durante la loro vita e può essere dovuto a troppo colesterolo, problemi cardiaci, diabete, ipertensione, fumo o alcol. Alcuni rimedi possono essere la ragione. Le questioni legate al movimento sono collegate. Se ti occupi dei tuoi problemi di movimento, hai piu possibilita di risolvere questo problema. Qui ci sono 5 consigli facili su come aumentare la circolazione: 1. Mangia i pasti giusti. Questo ti rendera il flusso sanguigno ovvio. Una grande parte di rimanere sani e anche mantenere il flusso sanguigno ovvio è legato al vostro piano di alimentazione quotidiana e quello che si mangia. Una buona cura per la disfunzione erettile è mangiare un piano a basso contenuto di grassi e grande alimentazione di fibre. Mangiare fibre tutti i giorni e questo viene scoperto in prodotti cerealicoli cereali integrali, frutta e verdura. Evitare il più possibile pasti pronti o pasti non sani. 2. Wonder herbal rimedi. Molti rimedi vegetali per ED eseguire bene come possono migliorare il movimento. Hanno molto meno reazioni avverse rispetto ai farmaci convenzionali e si svolgono in modo efficiente per migliorare hardons e la forza, troppo. Erbe naturali come Ginkgo Biloba sono utilizzati come una strategia per ED. Gli specialisti di erboristeria credono anche che le spezie o le erbe come noce moscata, portano al movimento intorno al corpo, tra cui il pene. 3. Vitamine naturali vitali. Gli scienziati sanitari hanno scoperto che una mancanza di supplemento è tipico tra gli uomini con ED in particolare vitamina A. Se si ha una mancanza del nutriente ossido di zinco, Questo è stato confermato per portare alla disfunzione erettile. Queste inadeguatezze derivano dal fatto che molti valori nutrizionali in quello che mangiamo piano non sono sufficienti. Aggiungere al vostro fabbisogno di nutrienti aumenterà la circolazione del sistema e migliorare questa condizione. Gli integratori alimentari sono completamente naturali, quindi non dovrete preoccuparvi dei rischi di reazioni avverse. Inoltre, queste vitamine naturali sono utili per il vostro benessere over-all. Oltre a questi vantaggi benessere, disfunzione erettile vitamine naturali e integratori costano molto meno di farmaci rimedi. 4. Esercitare. Fai una mossa e non un tablet vibrante. Camminare farà di più per migliorare e sostenere hardons di qualsiasi altra compressa chimica nel lungo periodo. Il fitness fisico manterrà bassi livelli di pressione e mantenere grandi stadi di movimento. Andando per un 20-30 minuti di movimento rapido ogni giorno, può affrontare questo problema e può sostenere la vostra libido senza l uso di qualsiasi farmaco. 5. Sottolineare. Questo è il peggior attaccante per problemi di erezione. Scopri diversi metodi per riposare. Alcuni metodi tipici per riposare includono la lettura di un libro, la meditazione, un bagno rilassante o allenamenti di respirazione. Sto solo imparando alcuni semplici allenamenti di respirazione che possono migliorare significativamente il movimento nel reparto pantaloni. Una naturale disfunzione erettile soluzioni di trattamento stanno diventando sempre più popolare con gli uomini. Questi rimedi a base di erbe sono preferiti perché non hanno reazioni avverse e sono confermati essere efficiente come il farmaco. La maggior parte degli uomini combattere parlano dei loro problemi, in particolare la disfunzione erettile come c è poca discussione sui problemi di erezione. La verita e che ED ha un impatto su piu di dieci milioni di uomini solo negli Stati Uniti. Non siete soli e l aiuto è disponibile.

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Adverse drug reactions from psychotropic medicines in the paediatric
population: analysis of reports to the Danish Medicines Agency over a decade
BMC Research Notes 2010, 3:176
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Adverse drug reactions from psychotropic medicines in the paediatric population: analysis of reports
to the Danish Medicines Agency over a decade
1Department of Pharmacology and Pharmacotherapy, Section for Social Pharmacy, Faculty of Pharmaceutical Sciences, University of Copenhagen and FKL Research Centre for Quality in Medicine Use, Universitetsparken 2, DK- 2100 Copenhagen, Denmark Abstract
Background
The prescribing of psychotropic medicines for the paediatric population is rapidly increasing. In attempts to curb the use of psychotropic medicine in the paediatric population, regulatory authorities have issued various warnings about risks associated with use of these products in childhood. Little evidence has been reported about the adverse drug reactions (ADRs) of these medicines in practice. As spontaneous reports are the main source for information about previously unknown ADRs, we analysed data submitted to a national ADR database. The objective was to characterise ADRs reported for psychotropic medicines in the Danish Findings
All spontaneous ADR reports from 1998 to 2007 for children from birth to 17 years of age were included. The unit of analysis was one ADR. We analysed the distribution of ADRs per year, seriousness, age and gender of the child, suspected medicine and type of reported ADR. A total of 429 ADRs were reported for psychotropic medicines and 56 % of these were classified as serious. Almost 20 % of psychotropic ADRs were reported for children from birth up to 2 years of age and one half of ADRs were reported in adolescents, especially for antidepressants and psychostimulants. Approximately 60 % of ADRs were reported for boys. Forty percent of all ADRs were from the category ‘nervous and psychiatric disorders’. All but one ADR reported for children below two years were serious and two of these were fatal. A number of serious ADRs reported in children from birth up to 2 years of age were presumably caused by mothers’ use of psychotropic medicines during pregnancy. Conclusion
The high number of serious ADRs reported for psychotropic medicines in the paediatric population should be a concern for health care professionals and physicians. Considering the higher number of birth defects being reported greater care has to be given while prescribing these drugs for pregnant women. Findings
Background
The prescribing of psychotropic medicines for the paediatric population is rapidly increasing in many countries including Denmark. In attempts to curb the use of psychotropic medicine in the paediatric population, regulatory authorities have issued various warnings about risks associated with use of these products in childhood [1-4]. A systematic review detected seventeen studies since 2000 that reported information about the occurrence of ADRs in paediatric populations [5]. Nearly one third of all ADRs reported in children were due to psychotropic medicines, especially CNS stimulants and antidepressants. However, more detailed information about the characteristics of ADRs from psychotropic medicines in the general paediatric population is lacking and little evidence has been reported about safety and long-term effects of these medicines in practice [6-8]. Lack of knowledge of adverse drug reactions (ADRs) at the point of licensing of new medicines renders spontaneous ADR reporting an important contributor to knowledge about safety of medicines [9]. As spontaneous reports are the main source for information about new and previous unknown ADRs we conducted an analysis of all spontaneous ADR reports for psychotropic We used data from the national Danish ADR database, which contains information about all spontaneous reports submitted to the Danish Medicines Agency (DKMA) [10]. ADRs reported for children from 0 to 17 years of age were included. We analysed the distribution of ADRs per year, seriousness, age and gender of the child, suspected medicine and type of reported ADR (system organ class [SOC]). ADRs were classified as serious on the following criteria: death, life-threatening, requiring hospitalisation or prolongation of existing hospitalisation, resulting in persistent or significant disability/incapacity, a congenital anomaly/birth defect and other medically important conditions. From 1998 to 2007 a total of 2437 individual ADR reports containing information about 4500 ADRs were reported for children. Of these, 210 reports corresponding to 429 ADRs were submitted for psychotropic medicines. Figure 1 shows the annual distribution of the reported ADRs. There were wide fluctuations in the number of ADRs reported annually, with an increase in number from 2003 to 2005 followed by a decrease in Table 1 shows the distribution of reported ADRs by therapeutic group and medicine, age of patient and seriousness. Almost one fifth of ADRs were reported for children below 2 years and one half of all ADRs were reported for adolescents (from 11 to 17 years of age), and 45% of these were serious. Totally, 59% of all ADRs were reported for boys. More than one half of all ADRs were classified as ‘serious’. Table 2 displays characteristics of ADRs reported for children below two years. Two deaths were reported for citalopram and fluoxetin due to chorioamnionitis and persistent foetal circulation, respectively. ADRs among children up to 2 years of age encompassed a wide range of reactions, e.g. convulsion, feeding disorder, neonatal priapism, apnoea and ventricular septal defects. Seven ADRs: drug exposure during pregnancy, neonatal respiratory depression, apnoea and pallor were reported as “maternal drugs affecting foetus”. However, the remaining ADRs were probably also caused by mothers’ use of psychotropic medicines during pregnancy, as the indications for use were reported as depression, anxiety, panic disorder and schizophrenia. The share of serious psychotropic ADRs was higher than the share of serious ADRs in Danish children in general (40%) [11]. In the general Danish paediatric population, half of all ADRs were reported in children from birth up to 2 years of age, but for psychotropic medicines more than half of all ADRs were reported for adolescents which reflect a more extensive use of psychotropic medicine in 11 to 17- year-olds [9]. The majority of serious ADRs were reported in infants in contrast to reports submitted to Health Canada where 60% of all ADRs for psychotropic medicines were reported in 13 to 19-year-olds, and only 12% in infants [12]. A number of ADRs were reported for Danish children below 2 years, probably due to the mother’s intake of psychotropic medicine, primarily antidepressants and antipsychotics, during pregnancy. Serious ADRs such as ‘neonatal withdrawal syndrome’, ‘ventricular septal defects’ and ‘premature labour’ were reported. The risks of malformations as well as preterm delivery of babies due to use of antidepressants during pregnancy have been reported previously in the literature and is supported by our results [13-16]. The largest share of ADRs (42%) was reported for psychostimulants (ATC group N06B), followed by 31% for antidepressants (ATC group N06A) and 24% for antipsychotics (ATC group N05A). More than one half of the ADRs reported for antipsychotics were caused by the drugs ziprasidone, olanzapine and risperidone. Although only 2.5% of ADRs were reported for anxiolytics and sedatives (ATC group N05B and N05C), predominantly in infants, all these ADRs were serious. Two-thirds of the ADRs reported for antidepressants (ATC group N06A) were reported for infants and adolescents and exclusively for the medicines sertraline, citalopram and fluoxetine and seventy-five percent of these were serious. For psychostimulants (ATC group N06B) 50% of ADRs were serious and reported for children from six to nine years of age, and 40% of the reports were associated with methylphenidate and atomoxetine. With one exception, all 70 ADRs reported for children less than one year of age were serious. Table 3 shows the distribution of reported ADRs by system organ class (SOC). The largest shares of ADRs were reported for the SOCs ‘psychiatric disorders’ (20% of total), ‘nervous system disorders’ (20% of total) and ‘general disorders and administration site conditions’ (12% of total). Less than 1% of the total number of reports concerned the following SOCs: ‘ear and labyrinth disorders’, ‘endocrine disorders’, ‘hepatobiliary disorders’, ‘immune system disorders’, ‘pregnancy, puerperium and perinatal conditions’ and ‘surgical and medical procedures’. The largest shares of serious ADRs, about 25% of all were reported for the SOCs: ‘psychiatric disorders’ and ‘nervous system disorders’. The distribution between serious and non-serious ADRs within SOCs varied. More than seventy-five percent of ADRs reported from the SOCs: ‘nervous system disorders’, ‘musculoskeletal and connective tissue disorders’ and ‘congenital, familial and genetic There are huge gaps in the evidence on the safety of medicines in children as only few medicines prescribed for children are tested in clinical trials and licensed for use in this population. In addition, information about serious and long-term ADRs is sparse due to the limitations embedded in the design of randomised, controlled clinical trials which are used primarily to test hypotheses about efficacy rather than safety and children are usually excluded from clinical trials of medicines for ethical reasons [17]. Therefore, it is very important to systematically analyse and evaluate data reported to the spontaneous reporting programmes as these reports are the major source for new information about possibly serious and previously unknown ADRs [18]. Several of the reported ADRs were birth defects, an area where we have very limited knowledge. Conclusions
The high number of serious ADRs reported for psychotropic medicines in the paediatric population should be a concern for health care professionals and physicians. Considering the higher number of birth defects being reported greater care has to be given while prescribing these drugs for pregnant women. Competing interests
The authors declare that they have no competing interests. Authors' contributions
LA and EHH designed the study, analysed data and wrote the first version of the manuscript. LA did the sampling. Both authors read and approved the final version of the manuscript. Acknowledgements
We would like to thank the Danish Medicines Agency for placing data at our disposal. References
1. European Medicines Agency/CHMP/128918/2005. Press Release: European Medicines Agency finalises review of antidepressants in children and adolescents. Available at: http://www.ema.europa.eu/pdfs/human/press/pr/12891805en.pdf [Accessed 18 February 2010]. 2. Meeting highlights from the Committee for Medicinal Products for Human Use (EMEA/431407/2007). Available at: www.emea.europa.eu/pdfs/human/press/pr/43140707en.pdf. [Accessed 18 February 2010]. 3. European Medicines Agency makes recommendations for safer use of Ritalin and other methylphenidate-containing medicines in the EU (EMEA/22315/2009). Available at: www.ema.europa.eu/pdfs/human/referral/methylphenidate/2231509en.pdf. [Accessed 18 February 2010] 4. Cheung A, Sacks D, Dewa CS, Pong J, Levitt A: Paediatric prescribing practices and the FDA Black-box
warning on antidepressants. J Dev Behav Pediatr.2008;29:213-15.
5. Aagaard L, Christensen AC, Hansen EH: Information about adverse drug reactions reported in children: a
qualitative review of empirical studies. Br J Clin Pharmacol 2010: In press.
6. Garland EJ: Facing the evidence: antidepressant treatment in children and adolescents. CMAJ 2004;170:489-91.
7. Riddle MA, Labellarte MJ, Walkup JT: Paediatric psychopharmacology: problems and prospects. J Child
Adolesc Psychopharmacol 1998;8:87-97.
8. Neubert A, Dormann H, Weiss J, Egger T, Criegee-Rieck M, Rascher W, Brune K, Hinz B: The impact of
unlicensed and off-label drug use on adverse drug reactions in paediatric patients. Drug Saf 2004;27:1059-67.
9. Aagaard L, Thirstrup S, Hansen EH: Opening the white boxes: The licensing documentation of efficacy and
safety of psychotropic medicines for children. Pharmacoepidemiol Drug Saf 2009;18:401-11.
10. Aagaard L, Stenver DI, Hansen EH: Structures and processes in spontaneous reporting systems: a comparative
study of Australia and Denmark. Pharm World Sci 2008;30:563-70.
11. Aagaard L, Weber CB, Hansen EH: Adverse drug reactions in the paediatric population in Denmark: a
retrospective analysis of reports made to the Danish Medicines Agency from 1998 to 2007. Drug Saf 2010:33:327-
12. Carleton BC, Smith MA, Gelin MN, Heathcote SC: Paediatric adverse drug reaction reporting: understanding
and future directions. Can J Clin Pharmacol 2007;14:e45-e57.
13. Dobson R: SSRI use during pregnancy is associated with fetal abnormalities. BMJ 2006;333;824.
14. Wogelius P, Nørgaard M, Gislum M, Pedersen L, Munk E, Mortensen PB, Lipworth L, Sørensen HT: Maternal Use of Selective Serotonin Reuptake Inhibitors and Risk of Congenital Malformations. Epidemiology.
2006;17:701-4.
15. Cuevas DC, Sanz EJ: Safety of selective serotonin reuptake inhibitors in pregnancy. Curr Drug Saf 2006;1:17-
16. Lund N, Pedersen LH, Henriksen TB: Selective serotonin reuptake inhibitor exposure in utero and pregnancy
outcomes. Arch Pediatr Adolesc Med 2009;163:949-54.
17. Hansen EH: Technology assessment in a user perspective- experiences with drug technology. Int J Techn Assess
Health Care 1992; 8:150-65.
18. Aagaard L, Hansen EH: Information about adverse drug reactions explored by pharmacovigilance
approaches: a qualitative review of studies on antibiotics, SSRIs and NSAIDs. BMC Pharmacology 2009;9:4.
Figure 1: Annual number of adverse drug reactions (ADRs) for psychotropic medicines reported in the Danish
paediatric population
Table 1: Number of adverse drug reactions reported for psychotropic medication in the paediatric population by age
and seriousness (in italic) (1998 to 2007)
Age groups (years)
11<17
Antipsychotics (N05A)
Hypnotics and sedatives (N05B/N05C)
Antidepressants (N06A)
Psychostimulants (N06B)
Total N05 and N06
Table 2: Serious ADRs from psychotropic medicines reported for children below two years of age (1998 to 2007)
ATC Medicines
Adverse drug reaction
Indication of use
Age of child
Zuclopemthixol Supraventricular tachycardia *Indication for use not listed, but recorded as “Maternal drugs affecting foetus”; NA: not available
Table 3: Adverse drug reactions from psychotropic medicines by system organ class (descending order)
System Organ Class (SOC)
All ADRs (%) Serious as % of all
Serious as % of
General disorders and administration site conditions Respiratory, thoracic and mediastinal breast disorders Metabolism and nutrition disorders Musculoskeletal and connective tissue disorders Congenital, familial and genetic disorders Reproductive system and breast disorders

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