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adverse drug reactions
nervous system disorders
Laatste Update: 2008-03-04
Gebruiksfrequentie: 1
Kwaliteit:
Gelieve het te verwijderen indien je dit meent.
management of adverse event reports vich:
management of adverse event reports vich:
Laatste Update: 2011-10-23
Gebruiksfrequentie: 1
Kwaliteit:
Gelieve het te verwijderen indien je dit meent.
elintarvikkeiden aiheuttamat yliherkkyysreaktiot (adverse reactions to foods)
adverse reactions to foods
Laatste Update: 2014-02-06
Gebruiksfrequentie: 1
Kwaliteit:
toksisuuden vaikeusasteluokitus: nci common terminology criteria for adverse events
nci common terminology criteria for adverse events
Laatste Update: 2017-04-26
Gebruiksfrequentie: 1
Kwaliteit:
toksisuuden vaikeusasteluokitus: national cancer institute common terminology criteria for adverse events.
toxicity grades are in accordance with national cancer institute common terminology criteria for adverse events.
Laatste Update: 2017-04-26
Gebruiksfrequentie: 1
Kwaliteit:
rotilla ei todettu noael-arvoa (no observed adverse effect level).
in rats, a no observed adverse effect level (noael) was not observed.
Laatste Update: 2017-04-26
Gebruiksfrequentie: 1
Kwaliteit:
toksisuuden vaikeusasteluokitus: national cancer institute (nci) common terminology criteria for adverse events.
national cancer institute (nci) common terminology criteria for adverse events
Laatste Update: 2017-04-26
Gebruiksfrequentie: 1
Kwaliteit:
ctcae-luokitus (worst national cancer institute common terminology criteria for adverse events grade)
worst national cancer institute common terminology criteria for adverse events grade.
Laatste Update: 2017-04-26
Gebruiksfrequentie: 1
Kwaliteit:
the c o u n of justice is adverse , the agreement may enter into force only in accordance with article n of the treary o n european union .
the c o u n of justice is adverse , the agreement may enter into force only in accordance with article n of the treary o n european union .
Laatste Update: 2011-10-23
Gebruiksfrequentie: 1
Kwaliteit:
noael (no observed adverse effect level) – testatun aineen taso tai pitoisuus, joka ei aiheuta havaittavaa haittavaikutusta.
noael (no observed adverse effect level) — dose or concentration of a substance tested at which no adverse effect is found.
Laatste Update: 2014-11-21
Gebruiksfrequentie: 1
Kwaliteit:
lyhennys määritelmälle "no observed adverse effect level" eli korkein annostaso, jolla ei havaita mitään haitallisia käsittelyyn liittyviä vaikutuksia.
is the abbreviation for no observed adverse effect level and is the highest dose level where no adverse treatment-related findings are observed.
Laatste Update: 2014-11-21
Gebruiksfrequentie: 1
Kwaliteit:
Waarschuwing: Bevat onzichtbare HTML-opmaak
sitten valitaan asteittain alenevat annostasot annostukseen liittyvän vasteen ja noael-arvon (no observed adverse effect) osoittamiseksi alhaisimmalla annostasolla.
thereafter, a descending sequence of dose levels should be selected with a view to demonstrating any dosage related response and no-observed-adverse effects at the lowest dose level (noael).
fda käytti päätelmiä tehdessään joukkoa tieteellisiä tietoja efedriinin vaikutuksista sekä ei-toivottuja vaikutuksia koskevia ilmoituksia( adverse event reports, aer).
to reach its conclusions the fda used a combination of scientific evidence on the effects of ephedrine and a set of adverse event reports( aers).
lausuntoa varten toimitetut ohjeet management of adverse event reports (cvmp/ vich/ 547/ 00) efficacy of anthelmintics:
the survey showed that there is a high level of satisfaction with the operation and results of the centralised procedure from all sides.
näiden haitattomien annosten (no observed adverse effect level, noael) aikaansaama systeeminen altistus oli enintään 2,5-kertainen odotettuun kliiniseen altistukseen verrattuna.
these no observed adverse effect level (noael) doses were associated with systemic exposures up to 2.5 times greater than anticipated clinical exposure.
suurimman haitattoman annoksen (no observed adverse effect level, noael) katsottiin olevan alle 75 mg/kg/vrk, mikä on noin 25 kertaa suurempi kuin auc-altistukseen perustuva ihmisen vuorokausialtistus.
the no observed adverse effect level (noael) was considered to be less than 75 mg/kg/day, and is approximately 25-fold greater than the human daily exposure based on auc exposure.