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Seizure threshold psychotropics (powerpoint file)
Seizure threshold psychotropics (powerpoint file)

... • Generalised tonic-clonic (3-20% have some focality), no aura. • 40% single seizure, 90% have < 5 in 6 hr period • Only 3% develop status epilepticus (should prompt search for other causes) (Shockley, 2007). ...
Significance of syncope in patients with Alzheimer`s disease treated
Significance of syncope in patients with Alzheimer`s disease treated

... syncope in 2 patients and dizziness (and eventual syncope) in another because the symptoms occurred soon after the initiation of therapy. Atropine (1 mg) was administered to patient 1 during electrophysiological study without any significant change in measured data. But at baseline these data were sl ...
11SUN Handouts.indd - The Collaborative Education Institute
11SUN Handouts.indd - The Collaborative Education Institute

... antidepressants or serum concentrations higher than 150 nanograms/milliliter may increase the risk of asymptomatic electrocardiographic changes in children and adolescents. As little as 15mg/kg may be fatal in a child. ...
October 2012 - Kaiser Permanente
October 2012 - Kaiser Permanente

...  Pantoprazole 20mg and 40mg delayed-release tablets will be added to Commercial formulary, effective November 6, 2012  Studies have shown that pantoprazole 40mg is equally effective as omeprazole 20mg for various indications  Pantoprazole inhibits CYP2C19 the least of all the Proton Pump Inhibito ...
OLMESARTAN MEDOXOMIL/HYDROCHLOROTHIAZIDE 20/12
OLMESARTAN MEDOXOMIL/HYDROCHLOROTHIAZIDE 20/12

... had no clinically-relevant effects on the pharmacokinetics of either component in healthy subjects. Absorption and Distribution Olmesartan medoxomil: Following oral administration, olmesartan medoxomil is rapidly converted to its pharmacologically active metabolite, olmesartan. The mean absolute bio ...
Guideline on Fixed Combinations - EMA
Guideline on Fixed Combinations - EMA

... The indications claimed for a fixed-combination medicinal product should be such that the presence of each active substance makes a contribution to the claimed effect. The product should be formulated so that the dose and proportion of each substance present is appropriate for the intended use. An i ...
skeletal muscle relaxants
skeletal muscle relaxants

... treating acute neck pain compared to placebo. Although fair quality evidence demonstrates improved global functioning and sleep in fibromyalgia patients, no improvement in fatigue or tender points has been observed. Furthermore, these studies are limited by their high drop-out rates and short durati ...
Small Animal Veterinary Medicine – Treatment Of Dogs And
Small Animal Veterinary Medicine – Treatment Of Dogs And

... Treatment of Dogs and Cats with Human Pharmaceutical Products Speaker: Peter A. Kreckel R.Ph. is a graduate of the University of Pittsburgh, Bachelor of Science in Pharmacy, Magna Cum Laude, Class of 1981. He served as the President of the Pharmacy School Class of 1981 for 3 years, and President of ...
Epilepsy - Touch Neurology
Epilepsy - Touch Neurology

... (DR) AEDs that are dosed as twice daily or more frequently to extendedrelease (ER) preparations that are dosed as once daily.13,26 ER formulations (also denoted as XR) have the advantages of minimizing peak to trough variations seen with IR formulations, thereby reducing AEs associated with peak con ...
PREDICTION OF RENAL IMPAIRMENT INDUCED BY STATIN THERAPY IN CARDIAC OUTPATIENTS
PREDICTION OF RENAL IMPAIRMENT INDUCED BY STATIN THERAPY IN CARDIAC OUTPATIENTS

IOSR Journal of Agriculture and Veterinary Science (IOSR-JAVS)
IOSR Journal of Agriculture and Veterinary Science (IOSR-JAVS)

MorphoSys Company Presentation JPM 150114
MorphoSys Company Presentation JPM 150114

... Global Assessment (PGA) score of cleared or minimal disease at week 16 (primary endpoint)  Significantly higher efficacy than comparator Humira NEXT ...
Macugen, INN-pegaptanib sodium
Macugen, INN-pegaptanib sodium

... Pegaptanib sodium has not been adequately studied in patients with creatinine clearance below 20 ml/min. A decrease in creatinine clearance down to 20 ml/min may be associated with up to a 2.3-fold increase in pegaptanib AUC. No special considerations are needed in patients with creatinine clearance ...
Free PDF
Free PDF

... cytochrome P (CYP) 450 substrates, inducers or inhibitors, co-administration with other metabolized drugs could result in drug accumulation and possible toxicity or decreased efficacy of one or both treatments. Cancer patients receive a large number of drugs during their treatment including those fo ...
darbepoetin - Cancer Care Ontario
darbepoetin - Cancer Care Ontario

... Darbepoetin alfa is contraindicated for prophylactic use in surgical patients, in patients who  developed pure red cell aplasia (PRCA) following treatment with any erythropoiesis regulating  hormone, with uncontrolled hypertension, and with known hypersensitivity to mammalian cell­ derived products  ...
Prevex® B - GlaxoSmithKline
Prevex® B - GlaxoSmithKline

... patients. Some published studies of 0.1% betamethasone valerate creams have reported that clinical outcomes in pediatric patients more than 1 year and less than 18 years of age were consistent with those of the general adult population.1, 2, 3, 4, 5 Administration of topical corticosteroids to child ...
Nilotinib in Imatinib-Resistant CML and Philadelphia Chromosome
Nilotinib in Imatinib-Resistant CML and Philadelphia Chromosome

Clinical Pharmacology of Drugs Acting on the Respiratory Organs
Clinical Pharmacology of Drugs Acting on the Respiratory Organs

... When mast cells become activated, they release a host of preformed chemical mediators which initiate an asthma attack consisting of increasing cough, wheeze, and difficulty breathing. The job of the mast cells is not complete with this act. Mast cells begin to produce a different mixture of chemical ...
Stimulant fact sheet
Stimulant fact sheet

... medication is taken as prescribed, but represents a significant risk if the medication is abused, i.e. taken at high doses to produce a “high”. At high doses, usually far beyond medical limits, most stimulants can induce euphoria, personality changes, chronic sleep deprivation, paranoia, and even ps ...
BIOCOMPATIBLE SILVER NANOPARTICLES SYNTHESIZED
BIOCOMPATIBLE SILVER NANOPARTICLES SYNTHESIZED

... production. In our study the diabetic rats that were treated with GSNPs attenuate the increasing in the blood glucose level in the glucose tolerance test, suggesting that the GSNPs exert a protective effect. Previous work studied the therapeutic effect of ZnO and SNPs on STZ-induced diabetic rats [2 ...
Bupropion/naltrexone fixed-dose combination for
Bupropion/naltrexone fixed-dose combination for

... with a maximal weight loss achieved between weeks 28 and 36. Improvements from baseline in waist circumference, insulin resistance, HDL-cholesterol, triglycerides and high-sensitivity C-reactive protein were also seen in the treatment groups. NB32 was also associated with an improvement in fasting g ...
Other Major Side Effects to Immunomodulators and/or Biologics in
Other Major Side Effects to Immunomodulators and/or Biologics in

... • Much less common but much more serious: • Nodular regenerative hyperplasia: 1.2% at 10 years of AZA (but there may be a baseline of NRH in thiopurine-naïve IBD • Veno-occlusive disease of liver ...
Challenges in Lipid Management.
Challenges in Lipid Management.

... C) Maintain current drug regimen without changes D) Change fenofibrate to gemfibrozil 600 mg twice daily E) Add cholestyramine resin 8 g twice daily A) Doubling simva dose only yields an additional 6% LDL reduction, when goals is additional ~20%, and 80 mg dose is assoc. with increased risk of muscl ...
NUROFEN PLUS
NUROFEN PLUS

... In cross-study comparisons with doses ranging from 1200-3200 mg daily for several weeks, a slight dose-response decrease in hemoglobin/hematocrit was noted. Aseptic meningitis with fever and coma has been observed on rare occasions in patients on ibuprofen therapy. Although it is probably more likel ...
Investigational New Drug (IND) Submission checklist
Investigational New Drug (IND) Submission checklist

... 18. Toxicology: Integrated Summary An Integrated Summary is only used for drugs and well-characterized, therapeutic biotechnologyderived products. For novel biotechnology-derived products, the review division should be consulted first. Need for studies depend on the nature of the drug and the phase ...
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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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