Примери за използване на Additional adverse на Английски и техните преводи на Български
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Additional adverse reactions4.
In clinical studies for other indications, the following additional adverse reactions were commonly dic.
No additional adverse reactions were identified.
In clinical studies for other indications,the following additional adverse reactions were commonly reported.
An additional adverse reaction was tremor(common).
Хората също превеждат
NNT: Number of patients who need to be treated to prevent one additional adverse outcome.
The following additional adverse reactions were seen.
The number needed to treat(NNT)is the average number of patients who need to be treated to prevent one additional adverse outcome.
No additional adverse reactions were identified with Glyxambi.
As NB is a fixed combination of two active ingredients,in addition to the terms listed in Table 1, additional adverse reactions seen with one of the active substances may potentially occur.
Additional adverse reactions from Trial 6 are included in Table 4.
Peripheral oedema adverse reaction observed with SIMBRINZA 2 additional adverse reaction observed with brinzolamide monotherapy additional adverse reaction observed with brimonidine monotherapy.
Additional adverse reactions from postmarketing spontaneous reporting.
Table 3 Frequency of additional adverse reactions by system organ class.
No additional adverse reactions have been identified for ADROVANCE.
The following additional adverse reactions were reported from post-marketing surveillance with.
An additional adverse reaction reported in children was psychomotor hyperactivity.
The following additional adverse reactions have been identified during post-approval use of HUMULIN N.
Additional adverse reactions observed in paediatric studies(aged 1to 17 years).
Table 3 shows additional adverse reactions which have been spontaneously reported post-marketing.
The additional adverse reactions in Table 2 have been reported from postmarketing surveillance or no.
Table 1 also includes additional adverse events which have been spontaneously reported during the post-marketing use of Gardasil worldwide.
Additional adverse reactions reported during post-marketing surveillance are listed below.
The following additional adverse reactions have been observed with Prometax transdermal patches: anxiety, delirium, pyrexia(common).
Additional adverse events that have been seen with one of the components and may potentially occur with DuoTrav.
No additional adverse reactions have been identified for the combination of alendronate and colecalciferol.
Additional adverse reactions have been evaluated in a clinical study including 16 UCD patients less than 2 months of age.
Additional adverse reactions that have been seen with one of the active substances and may potentially occur with DuoTrav.
The additional adverse reactions in Table 2 have been reported from postmarketing surveillance or Phase IV clinical trials.
No additional adverse reactions were identified for the dapagliflozin plus metformin group compared with those reported for the individual components.