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On the Discovery and Development of Pimavanserin
On the Discovery and Development of Pimavanserin

... symptoms are equally disturbing to the patient [2]. The most common non-motor symptoms include depression, sleep problems, psychosis and dementia. Parkinson’s disease psychosis (PDP) [3, 4], which is characterized by hallucinations and/or delusions, may develop in up to 60 % of PD patients [5], is p ...
BuSpar (buspirone)
BuSpar (buspirone)

... General Information BuSpar (buspirone) is an antianxiety medication indicated for management of selected anxiety disorders or for short-term relief of anxiety symptoms. It is not chemically related to the benzodiazepines (e.g., Valium) or barbiturates. In addition, unlike those medications, BuSpar n ...
racial-diff-pharm-treatments
racial-diff-pharm-treatments

... – Also important in determining proper doses for nicotine patches. ...
Shared Care Protocol for the use of Dexamfetamine
Shared Care Protocol for the use of Dexamfetamine

... remedial behavioural methods alone have failed. Various trials show that the most effective treatments are those combining treatments with medication, but the resource implications of this means that many children would receive no care and medication alone does show significant gains1. Dexamfetamine ...
Document
Document

... controlled release capsules. Adults with OCD are often started at a dose of 50 mg administered at bedtime. The dose may be increased by 50 mg every 4 to 7 days. The effective dosing range in premarketing trials with OCD was 100 to 300 mg per day, although, clearly, some patients do respond to higher ...
Attachment: Product Information: Linagliptin
Attachment: Product Information: Linagliptin

... (AUC) of linagliptin increased approximately 33% following 5 mg doses at steady-state compared to the first dose. The intra-subject and inter-subject coefficients of variation for linagliptin AUC were small (12.6% and 28.5%, respectively). Plasma AUC of linagliptin increased in a less than dosepropo ...
Clinical experiences with cannabinoids in spasticity management in
Clinical experiences with cannabinoids in spasticity management in

... This study was designed to evaluate THC/CBD effectiveness and safety in clinical practice as a symptomatic treatment for refractory spasticity in patients diagnosed with MS. Regarding our first objective, we can state that THC/CBD was highly effective (80%) in our series of 50 cases. This finding is s ...
PDF
PDF

... immunoglobulin M syndrome 5 years ago with complaints of recurrent fever until 6 month-year-old. He was treated with IVIG every 3-4 weeks according to his Ig levels and clinical evaluations. He weighs at 19.5 kilograms and was taking 10g IVIG every 2-3 weeks. For 2 months he has been treated with 5g ...
Clinical Challenges when using Pharmacolgo
Clinical Challenges when using Pharmacolgo

... Thirty day duration of action ...
Switching opioids using equivalence tables
Switching opioids using equivalence tables

... Calculate dose needed for PRN immediate release rescue opioid o If patient is started on Hydromorph Contin 9 mg BID, rescue dose is 10 to 15 % x 18 mg = 0.1 to 0.15 x 18mg hydromorphone = 1.8 to 2.7 mg hydromorphone. The patient can be provided with hydromorphone immediate release 2 mg with instruct ...
Help to inform an important clinical trial for patients with follicular
Help to inform an important clinical trial for patients with follicular

... patients consists of stopping the disease from growing back during the two years of drug treatment. Ideally, R maintenance would be given only to the 1 in 5 patients who are likely to benefit from it, sparing the rest from unnecessary side effects. However, until now we have not had a test that can ...
Volume 6 Number 18 (Issue 195) Tuesday, Jul yy 22,, 2008 NEW
Volume 6 Number 18 (Issue 195) Tuesday, Jul yy 22,, 2008 NEW

... http://www.pharmacistactivist.com/2008/may_2008.shtml [Free subscription also available here] Guidelines – Screening for Type 2 Diabetes … The U.S. Preventive Services Task Force has issued a recommendation that those patients whose blood pressure exceeds 135/80 mmHg (treated or untreated) should be ...
Vm - Veterinary Medicines Directorate
Vm - Veterinary Medicines Directorate

... Do not administer to pregnant mares. Do not use in animals showing hypersensitivity to flunixin meglumine. Do not use in animals suffering from cardiac, hepatic or renal disease, where there is a possibility of gastro-intestinal ulceration or bleeding. 4.4. Special warnings for each target species N ...
Vol. 22, No. 1 Infertility Therapy
Vol. 22, No. 1 Infertility Therapy

... production.11 It is taken daily starting on day 2 of the menstrual cycle continuing until ovulation. Methylprednisolone may also be used for anti-inflammatory treatment after IVF oocyte retrieval. It is usually taken daily beginning on the day of retrieval and ending on day or embryo transfer.12 5. ...
Respiratory Drug Agents
Respiratory Drug Agents

... Work by inhibiting the action of histamine through out the body. Prevent stimulation of chemo trigger receptor zone (CTZ). ...
Dose translation from animal to human studies revisited
Dose translation from animal to human studies revisited

... Shannon Reagan-Shaw,* Minakshi Nihal,*,† and Nihal Ahmad*,†,‡,1 *Department of Dermatology, †Paul P. Carbone Comprehensive Cancer Center; ‡Molecular and Environmental Toxicology Center, University of Wisconsin, Madison, Wisconsin, USA As new drugs are developed, it is essential to appropriately tran ...
Attachment: Product Information: Avanafil
Attachment: Product Information: Avanafil

... changes from baseline in systolic/diastolic blood pressure of -5.3/-3.7 mmHg at 1 hour after dosing, compared to mean changes from baseline in the placebo group of 2.7/-0.4 mmHg. Effects on Cardiac Electrophysiology The effect of single 100 or 800 mg doses of avanafil on the QT interval were evaluat ...
Mechanism of Action
Mechanism of Action

... vinorelbine if the patient experiences pain on administration. • Acute dyspnea and severe bronchospasm – occur infrequently and respond to bronchodilators. – Risk factor : concurrent use of mitomycin, Subacute pulmonary reactions occur within one hour after drug administration and may be characteriz ...
47 CONSUMER INFORMATION DIFLUCAN
47 CONSUMER INFORMATION DIFLUCAN

... to treat infections caused by fungi including yeasts and may also be used to stop you from getting a fungal infection. The most common cause of fungal infection is a yeast called Candida. What it does: DIFLUCAN selectively interferes with the normal sterol production in fungi and helps to stop funga ...
Management of Geriatric Psychiatric Disorders
Management of Geriatric Psychiatric Disorders

... subsequent response after 6-8 weeks • No Response or Partial Response after 2- 4 weeks ...
CanFite BioPharma Completes $12 Million Financing
CanFite BioPharma Completes $12 Million Financing

... Continued Dr. Frank Rauscher, Professor and Deputy Director of the Wistar Institute Cancer Center at Penn State University and Editor-in-Chief of Cancer Research, the flagship journal of the American Association of Cancer Research: “This, coupled with the drug's oral bioavailability, its efficacy i ...
Impaired Renal Function Clinical Trial
Impaired Renal Function Clinical Trial

... • the target patient populations ...
T Thalidomide
T Thalidomide

... Oral bioavailability of thalidomide is not known due to poor aqueous solubility. Slowly absorbed from the GI tract with peak plasma levels reached 3–6 hours after oral administration. ...
Restoril (temazepam)
Restoril (temazepam)

... General Information Restoril (temazepam) is a benzodiazepine sedative-hypnotic medication approved for short-term treatment of insomnia. Similar to other benzodiazepines, Restoril has anxiolytic effects (i.e., relieves anxiety), but it is seldom prescribed for this use. It has an intermediate durati ...
American Academy of Ophthalmology 2015 Annual Meeting
American Academy of Ophthalmology 2015 Annual Meeting

... In a new study presented at the AAO meeting, five years of treatment with low-dose 0.01% atropine eye drops slowed the progression of nearsightedness in children and caused fewer adverse effects compared with higher doses. The research was led by Donald T. Tan, MD, of the Singapore Eye Research Inst ...
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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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