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Biological Therapies
Biological Therapies

An Overview of the Pharmaceutical Development Process
An Overview of the Pharmaceutical Development Process

... Leak Rate ...
ANAFRANIL® 25 mg Coated tablets, 75 mg Sustained
ANAFRANIL® 25 mg Coated tablets, 75 mg Sustained

... Antidepressants increased the risk of suicidal thinking and behaviour (suicidality) in shortterm studies in children, adolescents and young adults less than 25 years old with depressive disorders and other psychiatric disorders. Short-term studies did not show an increase in the risk of suicidality ...
File
File

... When constant dose of a drug is repeated before 5 t1/2. it would achieve higher peak concentration, because some remnant of the previous dose will be present in the body  This continues with every dose until progressively increasing rate of elimination balances the amount administered over the do ...
Enough of Clinical…Let’s talk Pre-Clinical!
Enough of Clinical…Let’s talk Pre-Clinical!

... (c) At the initiation of a nonclinical laboratory study, animals shall be free of any disease or condition that might interfere with the purpose or conduct of the study. If, during the course of the study, the animals contract such a disease or condition, the diseased animals shall be isolated, if n ...
cyanocobalamin - DavisPlus
cyanocobalamin - DavisPlus

... IM, Subcut (Adults): 100 mcg/day for 6– 7 days; if improvement, give same dose every other day for 7 doses, then every 3– 4 days for 2– 3 wk; once hematologic values return to normal (remission), can give maintenance dose of 100 mcg/month (doses up to 1000 mcg have been used for maintenance) (could ...
Product Information: Lurasidone hydrochloride
Product Information: Lurasidone hydrochloride

... and race did not reveal any clear evidence of differential responsiveness. An analysis of patients with a ≥30% reduction from baseline PANSS score (clinical response analysis) was performed in three of these studies. The placebo response rate was around 35% across the studies and the response rates ...
opioid conversions - Palliativedrugs.com
opioid conversions - Palliativedrugs.com

... It is standard practice at The Rowans Hospice to use a 30ml syringe in drivers, giving a drug volume capacity of up to 22mls, although is possible to use a 50ml syringe (32ml capacity for drugs), or to use two syringe drivers. Volume is likely to be an issue for morphine doses approaching 600mg (30m ...
Clofibric acid
Clofibric acid

... Carcinogenesis (http://www.rxlist.com/cgi/generic2/clofibrate.htm) Administration of clofibrate to mice and rats in long-term studies at 1 to 2 times the maximum recommended human dose (based on surface area, mg/m2 ), resulted in a higher incidence of benign and malignant liver tumors than in contro ...
36pt Trebuchet MS Bold
36pt Trebuchet MS Bold

... also envisaged ...
Telenzepine is at least 25 times more potent than pirenzepine
Telenzepine is at least 25 times more potent than pirenzepine

... peptone stimulated gastric acid secretion (xZ±SEM) of 10 male healthy subjects (58±6 mmol H+/3 h for placebo) was significantly and dose dependently inhibited by oral telenzepine (2 mg: 31+5, 3 mg: 23±5, 5 mg: 21±4 mmol H+/3 h). Telenzepine 3 and 5 mg were significantly stronger than pirenzepine 50 ...
Remeron (mirtazapine)
Remeron (mirtazapine)

... significant benefits from their antidepressants until after 3–4 weeks, and it can sometimes take as long as 8 weeks for the medication to produce its full effects. Thus it is critical that patients continue to take their antidepressant long enough for the medication to be beneficial and that patient ...
Full Prescribing Information
Full Prescribing Information

... neurologic changes and gastrointestinal symptoms if concomitant treatment is clinically warranted (5.5, 7.3) Medication overuse headache: Detoxification may be necessary (5.6) Increase in blood pressure, very rarely associated with significant clinical events (4.4, 5.7) Use with caution in patients ...
Rebamipide - PIO Nas - Badan Pengawas Obat dan Makanan
Rebamipide - PIO Nas - Badan Pengawas Obat dan Makanan

... plasma was about 1.5 hours. Repeated-administration studies have shown that the drug does not accumulate in humans. The absorption of rebamipide tended to be slow when the drug was administered orally at a dose of 150 mg to 6 healthy subjects after a meal. However, food did not affect bioavailabilit ...
Allergic Rhinitis Marshall Plaut, M.D., and Martin D. Valentine, M.D.
Allergic Rhinitis Marshall Plaut, M.D., and Martin D. Valentine, M.D.

12 Why are the elderly often overdosed?
12 Why are the elderly often overdosed?

... almost 94 percent of those ages 75 to 84 received a prescription medication in ...
Diphenhydramine Hydrochloride Injection, USP
Diphenhydramine Hydrochloride Injection, USP

... MAO inhibitors prolong and intensify the anticholinergic (drying) effects of antihistamines. Carcinogenesis, Mutagenesis, Impairment of Fertility: Long-term studies in animals to determine mutagenic and carcinogenic potential have not been performed. Pregnancy: Pregnancy Category B: Reproduction stu ...
2nd T. 5th L. Updated
2nd T. 5th L. Updated

... salicylic acid. It is weakly COX-1-selective It is almost completely absorbed after oral administration, and peak plasma concentrations occur within 2 to 3 hrs It is extensively bound to plasma albumin (99%). At the usual analgesic dose, the plasma t1/2 averages between 8 and 12 hours (cf. salicyl ...
XDR-TB
XDR-TB

... deteriorates and during end-of-life care. Nausea and vomiting or any other conditions that interfere with nutritional support should be treated. ...
The SmartPak™ Pharmacy Equine Product Information Sheet
The SmartPak™ Pharmacy Equine Product Information Sheet

... the tip of the syringe, and insert the syringe into the horse’s mouth at the interdental space. Depress the plunger until stopped by the knurled ring. The dose should be deposited on the back of the tongue or deep into the cheek pouch. Care should be taken to ensure that the horse consumes the compl ...
Area - Wyre Forest CCG
Area - Wyre Forest CCG

... (WAHT Consultant request to consider) both GP and patient consultation time. Vesomni® (solifenacin The APC supported the niche use of Vesomni® only in men who are 6mg/tamsulosin; Astellas Pharma) stabilised on both solifenacin and tamsulosin. In these cases there would be a small cost saving by pres ...
The Treatment of Hyperkalemia - Georgia Society of Health
The Treatment of Hyperkalemia - Georgia Society of Health

... SPS superior to placebo in reduction of mean serum K+ between groups; 1.07 mEq/L (95% CI -1.37 to -0.71) Trend toward more hypomagnesemia, hypocalcemia, and constipation vs placebo Lepage, CJASN 2015 ...
Disclosures Objectives: Pharmacists Objectives: Pharmacy
Disclosures Objectives: Pharmacists Objectives: Pharmacy

... o Higher dose of 10 mg appears more effective with higher rates of side effects o Two studies with no difference in primary outcome for active control (duloxetine) ...
Deficiency of IL-1 Receptor Antagonist (DIRA)
Deficiency of IL-1 Receptor Antagonist (DIRA)

... protein that DIRA patients lack. Daily injection with anakinra is the only therapy that has been effective in the treatment of DIRA. In this way, the shortage of natural IL-1RA is corrected and the disease can be brought under control. Disease recurrence can be prevented. With this therapy, after th ...
Randomized, Double-blind, Placebo
Randomized, Double-blind, Placebo

... to receive CoQ10 and 67 to receive placebo. The strata consist of 21 subjects without levodopa treatment in both groups and 43 and 46 subjects receiving levodopa in the CoQ10 and placebo groups, respectively. Baseline demographic and background characteristics are summarized in the Table; there were ...
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Bilastine



Bilastine (trade name Bilaxten) is a second generation antihistamine drug for the treatment of allergic rhinoconjunctivitis and urticaria (hives).It exerts its effect as a selective histamine H1 receptor antagonist, and has a effectiveness similar to cetirizine, fexofenadine and desloratadine. It was developed in Spain by FAES Farma.Bilastine is approved in the European Union for the symptomatic treatment of allergic rhinoconjunctivitis and urticaria, but it is not approved by the U.S. Food and Drug Administration for any use in the United States. Bilastine meets the current European Academy of Allergy and Clinical Immunology (EAACI) and Allergic Rhinitis and its Impact of Asthma (ARIA) criteria for medication used in the treatment of allergic rhinitis.Bilastine has been effective in the treatment of ocular symptoms and diseases of allergies, including rhinoconjuctivitis. Additionally, bilastine has been shown to improve quality of life, and all nasal and ocular symptoms related to allergic rhinitis.
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