What is the translation of " JEDNOKRATNE DOZE " in English?

• single dose
• the single-dose
• single doses
• single-dose
• the single dose

Examples of using Jednokratne doze in Croatian and their translations into English

Antihipertenzivni učinak jednokratne doze kombinacije održao se 24 sata.
The antihypertensive effect of a single dose of the combination persisted for 24 hours.

Farmakokinetika lijeka IDELVION ocjenjivala se nakon intravenske injekcije jednokratne doze od 25, 50 i 75 IU/kg.
The pharmacokinetics(PK) of IDELVION were evaluated following an intravenous injection of a single dose of 25, 50 and 75 IU/kg.

Volumen distribucije jednokratne doze od 500 mikrograma roflumilasta je oko 2, 9 l/kg.
Volume of distribution for single dose of 500 micrograms roflumilast is about 2.9 l/kg.

Nije primijećen učinak na krvni tlak kad se nitroglicerin uzeo 24 sata nakon primjene jednokratne doze vardenafil 20 mg filmom obložene tablete.
No effect on blood pressure was observed when nitroglycerin was taken 24 hours after administration of a single dose of vardenafil 20 mg film-coated tablet.

Manje od 1% jednokratne doze nintedaniba se izlučuje putem bubrega vidjeti dio 5.2.
Less than 1% of a single dose of nintedanib is excreted via the kidney see section 5.2.

Zdravi ispitanici koji su primali do 20 mg/dan do 14 dana i jednokratne doze do 40 mg nisu imali neočekivane nuspojave.
Healthy subjects who received up to 20 mg/day for up to 14 days, and single doses up to 40 mg had no unexpected adverse reactions.

Ispitivanje jednokratne doze u ispitanika s različitim stupnjevima ciroze jetre Child-Pugh stadij A, B.
A single-dose study in subjects with varying degrees of liver cirrhosis Child-Pugh Classes A, B, and.

U kliničkim ispitivanjima bolesnici su primili jednokratne doze abakavira do 1200 mg te dnevne doze do 1800 mg.
Single doses up to 1,200 mg and daily doses up to 1,800 mg of abacavir have been administered to patients in clinical studies.

Nakon jednokratne doze rufinamida hrana povećava njegovu bioraspoloživost(AUC) za približno 34%, a njegovu vršnu koncentraciju u plazmi za 56.
After single doses food increases the bioavailability(AUC) of rufinamide by approximately 34% and the peak plasma concentration by 56.

Bioraspoloživost fenofibrične kiseline je niža nakon primjene jednokratne doze kombinacije fenofibrat-pravastatin 160/40 mg natašte.
The bioavailability of fenofibric acid is lower in fasting conditions after a single dose administration of the Fenofibrate-Pravastatin 160/40 mg combination.

Štakori su podnosili jednokratne doze od 1500 mg/kg(9000 mg/m2), a psi od 720 mg/kg(14 400 mg/m2) bez značajne toksičnosti.
Single doses of 1500 mg/kg(9000 mg/m2) and 720 mg/kg(14,400 mg/m2) were tolerated without significant toxicity in rats and dogs.

Ne postoji farmakokinetička interakcija između zaleplona i difenhidramina nakon primjene jednokratne doze(10 mg odnosno 50 mg) svakoga lijeka.
There is no pharmacokinetic interaction between zaleplon and diphenhydramine following the administration of a single dose(10 mg and 50 mg, respectively) of each drug.

Antihipertenzivni učinak jednokratne doze kombinacije održan je tijekom 24 sata.
The antihypertensive effect of a single dose of the combination persisted for 24 hours.

Jednokratne doze od 80 mg/kg deferasiroksa u formulaciji tablete za oralnu suspenziju u bolesnika s talasemijom i preopterećenjem željezom uzrokovale su blagu mučninu i proljev.
Single doses of 80 mg/kg of the deferasirox dispersible tablet formulation in iron-overloaded thalassaemic patients caused mild nausea and diarrhoea.

Postoje malobrojni klinički podaci o sigurnosti primjene jednokratne doze lijeka CIALIS u bolesnika s insuficijencijom jetre Child-Pugh stadij C.
There is limited clinical data on the safety of single-dose administration of CIALIS in patients with severe hepatic insufficiency Child-Pugh Class C.

Toksičnost jednokratne doze glikopironija ispitana je u raznim ispitivanjima, iako su dostupni samo ograničeni eksperimentalni podaci.
The single dose toxicity of glycopyrronium has been tested in a range of investigations, although only limited experimental details are available.

Istodobna primjena s vorapaksarom nije izmijenila farmakokinetiku jednokratne doze roziglitazona(8 mg), supstrata za CYP2C8 koji se ne nalazi na tržištu u EU.
Co-administration with vorapaxar did not alter the single-dose pharmacokinetics of rosiglitazone(8 mg), a CYP2C8 substrate not marketed in the EU.

Nakon jednokratne doze KE/bazedoksifena ukupan estron po početnoj vrijednosti(predstavlja KE) eliminira se s poluživotom od otprilike 17 sati.
After a single dose of CE/bazedoxifene, baseline-adjusted total estrone(representing CE) is eliminated with a half-life of approximately 17 hours.

Ispitivanja ponovljenih doza u štakora, koja su uključila i procjenu toksičnosti jednokratne doze i lokalnu podnošljivost, nisu ukazala na poseban rizik za ljude.
A repeat dose toxicity study in rats, which included an evaluation of single-dose toxicity and local tolerance, revealed no special hazards to humans.

U ispitivanju jednokratne doze na dobrovoljcima s blagim oštećenjem jetre(Child-Pugh zbroj bodova 5 do 6) nisu uočene klinički značajne promjene AUC-a retigabina.
In a single-dose study, there were no clinically significant effects on retigabine AUC in volunteers with mild hepatic impairment Child-Pugh score 5 to 6.

Nije primijećen značajan utjecaj fluoksetina(inhibitora CYP2D6), jednokratne doze antacida(aluminij, magnezij) ili cimetidina na farmakokinetiku olanzapina.
Fluoxetine(a CYP2D6 inhibitor), single doses of antacid(aluminium, magnesium) or cimetidine have not been found to significantly affect the pharmacokinetics of olanzapine.

Nakon primjene jednokratne doze Odomza(100 mg do 3000 mg) bez hrane u bolesnika s rakom, medijan vremena do vršne koncentracije(Tmax) bio je 2 do 4 sata.
Following the administration of a single dose of Odomzo(100 mg to 3000 mg) without food in patients with cancer, the median time-to-peak concentration(Tmax) was 2 to 4 hours.

U zdravih je ispitanika sistemska izloženost takrolimusu(AUC) za Modigraf iznosila približno 18% više nego za Prograf kapsule kad su se primijenjeni kao jednokratne doze.
In healthy subjects the systemic exposure to tacrolimus(AUC) for Modigraf was approximately 18% higher than that for Prograf capsules when administered as single doses.

Kohorta 0 dizajnirana je kako bi se ocijenila podnošljivost jednokratne doze posakonazol koncentrata za otopinu za infuziju primijenjene kroz centralnu liniju.
Cohort 0 was designed to evaluate the tolerability of a single dose of posaconazole concentrate for solution for infusion when administered via a central line.

Nakon jednokratne doze(25-150 mg) primijenjene intramuskularno injekcijom u deltoidni mišić, zabilježena je prosječno 28% viša Cmax u usporedbi s injekcijom u glutealni mišić.
Following intramuscular injection of single doses(25-150 mg) in the deltoid muscle, on average, a 28% higher Cmax was observed compared with injection in the gluteal muscle.

Istodobna primjena karbamazepina 600 mg dvaput na dan u stanju dinamičke ravnoteže i jednokratne doze fingolimoda 2 mg smanjila je AUC fingolimoda i njegovog metabolita za otprilike 40.
Co-administration of carbamazepine 600 mg twice daily at steady-state and a single dose of fingolimod 2 mg reduced the AUC of fingolimod and its metabolite by approximately 40.

Pri slučajnom gutanju jednokratne doze od 200 mg imikvimoda, što je otprilike sadržaj 16 vrećica, mogu se pojaviti slabost, glavobolja, mijalgija i vrućica.
Following accidental ingestion, nausea, emesis, headache, myalgia and fever could occur after a single dose of 200 mg imiquimod which corresponds to the content of approximately 16 sachets.

Imunogenost sadašnje formulacije koja je postojana na hladnom pokazala se sličnom imunogenosti ranije formulacije cjepiva ProQuad šest tjedana nakon jednokratne doze cjepiva.
The immunogenicity of the current refrigerator-stable formulation was shown to be similar to the immunogenicity of the earlier formulation of ProQuad six weeks after a single dose of the vaccine.

Kada su se jednokratne doze 0, 625 mg KE/20 mg bazedoksifena davale uz obrok koji je sadržavao visok postotak masnoća, Cmax bazedoksifena se nije mijenjao, ali se AUC povećao za otprilike 25.
When single doses of CE 0.625 mg/bazedoxifene 20 mg were administered with a high-fat meal, bazedoxifene Cmax was unaffected, but AUC increased by approximately 25.

U zdravih ispitanika doziranje ketokonazola(400 mg na dan) ili cimetidina(1200 mg na dan) u stanju dinamičke ravnoteže nije imalo klinički relevantne učinke na farmakokinetiku jednokratne doze zonisamida.
Steady-state dosing of either ketoconazole(400 mg/day) or cimetidine(1200 mg/day) had no clinically relevant effects on the single-dose pharmacokinetics of zonisamide given to healthy subjects.