Examples of 'following subcutaneous' in a sentence
Meaning of "following subcutaneous"
following subcutaneous: Pertaining to something that occurs or is located beneath the skin's surface
How to use "following subcutaneous" in a sentence
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following subcutaneous
Residues of nitroxinil in milk following subcutaneous administration to cattle.
Following subcutaneous administration, the terminal half-life is slightly prolonged.
There was no incidence of hypotension following subcutaneous administration of amifostine.
Following subcutaneous administration to patients with type 2 diabetes, exenatide reaches median peak plasma concentrations in 2 h.
The acute toxicity was studied following subcutaneous administration in rats.
Following subcutaneous administration of Hizentra, peak serum levels are achieved after approximately 2 days.
The apparent volume of distribution in patients following subcutaneous administration was.
Local tolerability studies following subcutaneous and intramuscular administration in rabbits gave no remarkable findings.
Etanercept has been reported to be excreted in human milk following subcutaneous administration.
The plasma concentration of PTH following subcutaneous delivery and transdermal delivery is compared in Fig.
The resulting preparations release insulin slowly following subcutaneous injection.
Following subcutaneous administration, the absolute bioavailability is about 70.
The typical activity profile following subcutaneous injection is illustrated below.
Following subcutaneous administration, the absolute bioavailability is approximately 60.
Acute toxicity of insulin human was studied following subcutaneous administration in rats.
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Following subcutaneous administration, the absolute bioavailability of icatibant is 97.
Residues of nitroxinil in milk following subcutaneous administration to sheep and goats.
Following subcutaneous administration the bioavailability of belimumab was approximately 74 %.
Transitory discomfort has been observed in some cattle following subcutaneous administration.
Following subcutaneous administration, terminal elimination half-life is approximately 2 to 5 weeks.
None of the protein was detected in the serum following subcutaneous administration.
Following subcutaneous administration, elimination half-life for inotersen is approximately 1 month.
The novel preparations release insulin slowly following subcutaneous injection.
Following subcutaneous injection, peak plasma concentrations of volanesorsen are typically reached in 2 to 4 hours.
The mean serum interferon concentrations following subcutaneous and intramuscular injections were comparable.
Following subcutaneous administration, peak plasma levels are attained 2 to 6 hours after injection.
The proteins were below the threshold of detection in the serum following subcutaneous administration.
Following subcutaneous injection, plerixafor is absorbed quickly and peak concentrations are reached after 30 to 60 minutes.
Trastuzumab washout period was assessed following subcutaneous administration using the population PK model.
Following subcutaneous administration to patients with type 2 diabetes, dulaglutide reaches peak plasma concentrations in 48 hours.
Absolute bioavailability of liraglutide following subcutaneous administration is approximately 55.
Following subcutaneous administration, the absolute bioavailability is approximately 60 % ; the terminal half-life is slightly prolonged.
Residues of rafoxanide in milk following subcutaneous administration - cattle.
Following subcutaneous dosing in GCA patients, the absorption t ½ was around 4 days.
Residues of clorsulon in milk following subcutaneous administration - cattle.
Following subcutaneous administration of 2.25 µg / kg to adult cancer patients a mean peak ic.
Residues of closantel in milk following subcutaneous administration - cattle.
Following subcutaneous administration, bioavailability was 62 %.
In cattle, doramectin is rapidly absorbed following subcutaneous administration.
The median Tmax following subcutaneous administration was approximately 3 days, with high interindividual variability range 1-14 days.
In addition, serum follistatin levels were increased following subcutaneous injection.
The absorption of liraglutide following subcutaneous administration is slow, reaching maximum concentration 8-12 hours post dosing.
This local reaction resolved within 8 hours following subcutaneous administration.
Insulin PK parameters following subcutaneous administration with or without rHuPH20 Humalog ® insulin lispro.
Figure 10 is a graphical representation of antibody titre in chickens following subcutaneous inoculation with S. typhimurium STM-1.
The half-life following subcutaneous injection in cattle is 2-3 days.
Figure 9 shows the pharmokinetic profile of IFN-B and PEG-IFN in mice following subcutaneous administration.
High bioavailability was observed following subcutaneous administration of Compound 6 relative to IV.
Following subcutaneous administration, the elimination half-life was approximately 15.5 days.
In this case, the withdrawal period following subcutaneous injection applies.
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Examples of using Subcutaneous
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