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What does C2 stand for?

C2 stands for 2 hours postdose

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In controlled clinical trials, first-degree AV block after the first dose occurred in 4. 7% of patients receiving GILENYA and 1. 6% of patients on placebo. In a study of 697 patients with available 24-hour Holter monitoring data after their first dose (N=351 receiving GILENYA and N=346 on placebo), second-degree AV blocks (Mobitz Types I [Wenckebach] or 2:1 AV blocks) occurred in 4% (N=14) of patients receiving GILENYA and 2% (N=7) of patients on placebo. Of the 14 patients receiving GILENYA, 7 patients had 2:1 AV block (5 patients within the first 6 hours postdose.
In controlled clinical trials, first-degree AV block after the first dose occurred in 4. 7% of patients receiving Gilenya and 1. 6% of patients on placebo. In a study of 697 patients with available 24-hour Holter monitoring data after their first dose (N=351 receiving Gilenya and N=346 on placebo), second-degree AV blocks (Mobitz Types I [Wenckebach] or 2:1 AV blocks) occurred in 4% (N=14) of patients receiving Gilenya and 2% (N=7) of patients on placebo. Of the 14 patients receiving Gilenya, 7 patients had 2:1 AV block (5 patients within the first 6 hours postdose.
c. every 12 hours but ranges from 15 000 to 20 000 units s. c. every 12 hours. The APTT should be taken at 6 hours postdose (midpoint of dosing interval) and dosage adjusted to maintain APTT between 1. 5 and 2 times control. Prevention of Venous Thromboembolism (Fixed-Dose Therapy) (see Table II): The usual prophylactic dose for general surgical and medical patients at risk for thromboembolism is 5 000 units s.
It was routine in the 1980s to obtain serum levels of several of our limited armamentarium of psychotropic medications. The standard was either a 12- or 24-hour postdose level, or in some cases, a trough level before the morning dose. Therapeutic ranges were established for lithium, many of the TCAs, valproic acid, and carbamazepine. After FDA approval of clozapine in 1989, its therapeutic serum range was established.
Vildagliptin orally dosed with 10 µmol/kg both significantly decreases glucose excursions and stimulates insulin secretion in Obese male Zucker rats. Maximum inhibition of plasma DPP-IV activity (95%) is observed approximately 2 hours postdose.
14 L/kg/hr and 0. 83±0. 13hr, respectively post IV administration. After IV administration of a 0. 2 mg radiolabeld glycopyrrolate, 85% of dose recovered was recovered in urine 48 hours postdose and some of the radioactivity was also recovered in bile. After IM administration of glycopyrrolate to adults, the mean T1/2 vaule is reported to be between 0. 55 to 1. 25 hours. Over 80% of IM dose administered was recovered in urine and the bile as unchanged drug and half the IM dose is excreted within 3 hrs.
It was developed for the treatment of osteoarthritis, rheumatoid arthritis and acute pain. The acidic nature of lumiracoxib allows it to penetrate well into areas of inflammation. It has shown to be rapidly and well absorbed, with peak plasma concentration occurring in about 1–3 hours. [15] A study showed that when a subject was given 400 mg dose, the amount of unchanged drug in the plasma 2. 5 hours postdose.