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Vet Info 1 Noromectin PLUS
Vet Info 1 Noromectin PLUS

... or by improper disposal of drug containers. Dispose of containers in an approved landfill or by incineration. As with other avermectins, ivermectin is excreted in the dung of treated animals and can inhibit the reproduction and growth of pest and beneficial insects that use dung as a source of food ...
NIMODIPINE USE IN M.E. / CFS Page 1 N I M O D I P I N E use in
NIMODIPINE USE IN M.E. / CFS Page 1 N I M O D I P I N E use in

... of arteries at the base of the skull was successfully treated with nimodipine, measured by transcranial Doppler ultrasonography. (Ref. 17.) From the information that I presently have, the longest nimodipine human trial was for a length of seven years, although this was not continuous usage. That tri ...
Lovastatin and beyond
Lovastatin and beyond

... at its maximal recommended dose of 80 mg daily produced a mean reduction in LDL cholesterol of 40%23–26, a far greater reduction than could be obtained with any of the treatments available at the time. Equally important, the drug produced very few adverse effects, and with once- or twice-daily dosin ...
Pharmacodynamic Profile of Enadoline, A Selective Kappa (k
Pharmacodynamic Profile of Enadoline, A Selective Kappa (k

... maintenance buprenorphine dose (a theoretical option, but no studies to date on this and may find ceiling effect limits amount of analgesia ...
Windtree Therapeutics (WINT)
Windtree Therapeutics (WINT)

... exhalation, do not begin to form in the lungs until very late in the gestation period. RDS was a leading cause of death among premature infants before the introduction of surfactants via endotracheal intubation in the late 1980s. This has already led to a significant decrease in RDS-related mortalit ...
Amvasc 2.5 mg Capsule REGIONAL ADMINISTRATIVE INFORMATI
Amvasc 2.5 mg Capsule REGIONAL ADMINISTRATIVE INFORMATI

... For both hypertension and angina the usual initial dose is 5 mg Amlodipine once daily which may be increased to a maximum dose of 10 mg depending on the individual patient's response. Paediatric The recommended antihypertensive oral dose in paediatric patients ages 6-17 years is 2.5 mg once daily as ...
alkylating agent
alkylating agent

... * procarbazine metabolized in liver and possibly in tumor cells to yield a variety of free radical and alkylating species; - beside myelosuppression, it causes hypnotic and other CNS effects, including vivid nightmares; - can cause disulfiram - like syndrome on ingestion of ethanol (disulfiram = dru ...


... via the right jugular vein 30 min prior to antigen challenge. The preparation was also administered using an infusion pump, at a continuous dose of 0.5mg·kg-1·h-1, throughout the experiment. On the controlled occasion, the sheep were given phosphate-buffered saline (PBS) by inhalation instead of A. ...
product monograph - Eli Lilly Canada
product monograph - Eli Lilly Canada

... previously undiagnosed/mildly symptomatic) respiratory infections (see CONTRAINDICATIONS and WARNINGS AND PRECAUTIONS, Congenital Disorders). ...
Lecture 4: Hepatic Variability
Lecture 4: Hepatic Variability

... cancer, is excreted primarily through metabolism (95%). In patients in normal hepatic function, the average total body clearance is 62 L/hr, the t½ is 5.5 hours and the normal daily dose is 250 mg every 8 hours. ...
Age
Age

... Concurrent Medications (cytochrome P450 isoenzymes mutation) ...
Performance enhancement at the cost of potential brain plasticity
Performance enhancement at the cost of potential brain plasticity

... educated approximation. It is also possible that, although many studies found no overt cognitive differences between the effects of low-dose MPH on normal individuals and ADHD patients, molecular or cellular differences may exist that await detection by the development of more advanced technology. T ...
Macrolid es, Ketolid es, a nd Glyc ylc yclines : Azithromyc in,
Macrolid es, Ketolid es, a nd Glyc ylc yclines : Azithromyc in,

... fluids and tissues. Mean tissue concentrations are 2- to 20-fold greater than serum concentrations for clarithromycin and are 10- to 100-fold greater than serum concentrations for azithromycin.31,32 Tissue concentrations do not peak until 48 hours after administration of azithromycin and persist for ...
Adult Diabetes
Adult Diabetes

... Annually if diabetic retinopathy is present, if planning pregnancy or are pregnant. If no evidence of retinopathy for one or more exams, then every 2 years may be considered. Initiate dilated and comprehensive eye examination at diagnosis of type 2 and within 5 years after diagnosis for type 1. Annu ...
Mykofenolatmofetil Actavis capsule, hard ENG SmPC
Mykofenolatmofetil Actavis capsule, hard ENG SmPC

... recommended dose in renal transplant patients is 1 g administered twice daily (2 g daily dose). Paediatric population aged 2 to 18 years The recommended dose of mycophenolate mofetil is 600 mg/m2 administered orally twice daily (up to a maximum of 2 g daily). Mykofenolatmofetil Actavis capsules shou ...
Dialectical behavior therapy versus comprehensive validation
Dialectical behavior therapy versus comprehensive validation

... subjects. Further, those assigned to DBT had significantly better treatment retention (64% retention in DBT; 27% retention in TAU). In social and global adjustment, there were no significant between-group differences during treatment or at 12-month follow-up, but DBT subjects did show significantly ...
Reinforcing Effects of Benzodiazepines
Reinforcing Effects of Benzodiazepines

... patients with panic disorder in Harvard/Brown Anxiety Research Project followed prospective over 10 years to examine their use of psychotropic ‹ Only a modest increase in use of SSRIs over 10 years was found ‹ Benzodiazepines were the most commonly used medication for panic disorder and SSRI use has ...
Chemical Peels
Chemical Peels

... primary outcome was clinical response according to a blinded evaluator, categorized as good (>50% improvement), fair (21%-50% improvement), poor (10%-20% improvement), no change, or worse. A total of 17 of the 20 patients were included in the analysis; 1 patient dropped out and 2 were lost to follow ...
ARF in Sepsis
ARF in Sepsis

...  No improvement of survival. Clinical studies with selective thromboxane or leukotriene inhibitors have not been performed. ...
soung_htn
soung_htn

... patients >80yo included in previous HTN trials  JNC 7 recommends same management for elderly (but w/ lower initial drug doses)  Previous meta-analysis of HTN treatment in pts >80yo suggested reduced CVA risk but trend towards increase mortality JAMA 2003;289:2560-2572 NEJM 2008;358:1887-98 ...
product monograph
product monograph

Update on Alcohol, Other Drugs, and Health
Update on Alcohol, Other Drugs, and Health

Cannabis
Cannabis

... • Effects can generally be felt within 15 minutes and peak effects occur within 30 to 60 minutes post-smoking and last 2-4 hours • Spectrum of effects precludes classification as a stimulant, sedative or hallucinogen. ...
Selective serotonin reuptake inhibitor discontinuation syndrome: A
Selective serotonin reuptake inhibitor discontinuation syndrome: A

... marked autoinhibition properties, however, the long half-life and active metabolite of fluoxetine prevent significant occurrence of SSRI discontinuation syndrome.1 Another serotonergic hypothesis suggested that the reuptake blockade of serotonin will result over time in the down-regulation (desensit ...
Pain Management
Pain Management

... Warn the patient it may take some time to determine if the drug will be effective. Upward titration of the dose should stop when either pain is relieved or side effects become intolerable. Optimal dose is when patient experiences analgesic efficacy (10-30% pain reduction), minimal benefit from fur ...
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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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