Примери за използване на Adverse reactions observed на Английски и техните преводи на Български
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Adverse reactions observed from clinical trials.
The most common adverse reactions observed were LARs.
Adverse reactions observed with Timolol monotherapy.
After administration of up to 5 times the recommended dose for 6 months to young adult healthy cats, adverse reactions observed were consistent with those mentioned in section 4.6.
Adverse reactions observed with Bimatoprost monotherapy.
Antidotes After administration of up to 5 times the recommended dose for 6 months to young adult healthy cats, adverse reactions observed were consistent with those mentioned in section“Adverse reactions”.
Adverse reactions observed in the clinical development of Numient.
Table 1 gives the adverse reactions observed from clinical trials.
Adverse reactions observed during clinical studies and post-marketing.
The most frequent adverse reactions observed with Rasitrio are hypotension and dizziness.
Adverse reactions observed in the two studies are listed below.
The clinically relevant adverse reactions observed in the CAPRIE study are discussed below.
Adverse reactions observed were diarrhoea, abdominal pain and vomiting.
The below table gives the adverse reactions observed from placebo-controlled and active-controlled clinical trials.
Adverse reactions observed with darunavir/cobicistat in adult patients.
The most common local and systemic adverse reactions observed in clinical trials were pain at the injection site and headache.
The adverse reactions observed are shown in the table below.
Frequency, type and severity of adverse reactions observed in the paediatric population are similar to those in the adult population.
Adverse reactions observed in clinical trials or post-marketing.
Additional adverse reactions observed in paediatric studies(aged 1to 17 years).
Adverse reactions observed with ivacaftor alone are also provided in Table 4.
Also listed are adverse reactions observed post-marketing in association with stavudine-containing antiretroviral treatment.
Adverse reactions observed during clinical studies to date.
The most common adverse reactions observed include hypersensitivity reactions(including cases of rash, urticaria and angioedema) and headache.
Adverse reactions observed only during post-marketing are marked(*).
The most common adverse reactions observed were weight increase(18%), IRRs(9%), diarrhoea(12%), headache(9%), arthralgia(9%), increased appetite(6%) and pain in extremity(6%).
Adverse reactions observed are listed below, by system organ class and frequency.
Table 6 Adverse reactions observed in paediatric patients with severe osteogenesis imperfecta.
Adverse reactions observed with darunavir/ritonavir in clinical trials and post-marketing.
Adverse reactions observed during clinical studies are listed below by frequency category.