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Directly Observed Therapy (DOT) for the Treatment of Tuberculosis
Directly Observed Therapy (DOT) for the Treatment of Tuberculosis

... ○ notifying the physician if the patient has side effects, clinical problems or misses DOT visits. • DOT should be initiated when TB treatment starts. Do not allow the patient to try selfadministering medications and missing doses before providing DOT. If the patient views DOT as a punitive measure, ...
Document
Document

... anti-arrhythmic agent. It has been used in humans to treat atrial fibrillation (AF), atrial flutter, and ventricular tachyarrhythmias. In horses, amiodarone has been successfully used to treat chronic atrial fibrillation and refractoryventriculartachycardia.8,9 Amiodarone blocks sodium and calcium c ...
Memorandum
Memorandum

... Thus, we concludethat the evidenceof safety from the article was minimal or lacking and no conclusionsof safety can be drawn from the report. We also cannot draw any safety conclusionsfrom the other publishedreport on the hyperglycemic activity of polypeptidesof a plant source (fruit, seeds,and tiss ...
III. Pipeline
III. Pipeline

... TAK-438 is a potassium-competitive acid blocker (P-CAB) that suppresses gastric acid secretion by inhibiting the proton pump, the final step of acid secretion from gastric parietal cells. PPIs are activated in an acid environment and bind irreversibly to the proton pump whereas TAK-438 suppresses ac ...
March 2016
March 2016

... The PBAC noted the submission’s claim of superior efficacy and noninferior safety was based on an indirect comparison between a single-arm denosumab observational study and a pooled subgroup analysis of zoledronic acid 8 mg retreatment from two randomised controlled trials. The PBAC considered that ...
5-HT1A Receptor Null Mutant Mice Responding Under a Differential
5-HT1A Receptor Null Mutant Mice Responding Under a Differential

... freezer until day of administration. The vehicle for all the drugs was distilled water and all injections were administered intraperitoneally (i.p.). Doses were expressed as the salt or in mg/kg and injections of drug or vehicle administered at a volume of 6.25 ml/kg. All injections of drugs were ad ...
Chloramphenicol 0.5% Eye Drops
Chloramphenicol 0.5% Eye Drops

... Date Approved: Review Date: ...
Managing Pharmaceuticals to Reduce Medication Errors
Managing Pharmaceuticals to Reduce Medication Errors

... A covering physician admitted a patient with Hodgkin’s lymphoma to a medical unit. At home, the patient had been taking hydromorphone (DILAUDID) 2 to 4 mg orally for pain. The covering physician prescribed the same medication, but also wrote an order for hydromorphone 2 to 4 mg IV every 3 hours for ...
click here to the doc
click here to the doc

... acebutolol, have less effect on the beta2 (bronchial) receptors and are, therefore, relatively cardioselective, but they are not cardiospecific. They have a lesser effect on airways resistance but are not free of this side effect. ...
Hypnotics in clinical practice - South West Yorkshire Partnership
Hypnotics in clinical practice - South West Yorkshire Partnership

... GABA site making it easier for GABA to open the chloride channel. As a result the channel opens more quickly. The benzodiazepines contain a benzene ring linked to a seven-member diazepine ring. They are rapidly absorbed from the gastro-intestinal tract, although this absorption is slowed by food and ...
Ceftin (cefuroxime axetil) tablets USP - GlaxoSmithKline
Ceftin (cefuroxime axetil) tablets USP - GlaxoSmithKline

... toxicity in the rabbit. Reproduction studies that have been performed in mice and rats at oral doses of up to 50 to 160 times the human dose have revealed no evidence of impaired fertility or harm to the fetus due to cefuroxime axetil. There are, however, no adequate and well-controlled studies in p ...
IOSR Journal of Pharmacy and Biological Sciences (IOSR-JPBS) ISSN: 2278-3008.
IOSR Journal of Pharmacy and Biological Sciences (IOSR-JPBS) ISSN: 2278-3008.

Analgesics Pharm I - Colorado Mesa University
Analgesics Pharm I - Colorado Mesa University

... ◦ Least effective opioid out there ◦ No more effective than APAP, but causes sedation and resp depression like other opiates ◦ Toxic metabolite (norpropoxyphene) can accumulate and cause arrhythmias, pulmonary edema, apnea, and CV events. ◦ Often used in suicides ◦ Should be avoided in kids, older a ...
hepatoprotective activity of root bark of azima tetracantha lam
hepatoprotective activity of root bark of azima tetracantha lam

... p.o and the standard drug Liv.52 (40mg/kg,p.o) were administered orally for 7 days in CCl4 intoxicated rats. The hepatoprotective activity was assessed by using various biochemical parameters like SGOT, SGPT, alkaline phosphatase (ALP) and acid phosphatase (ACP), also total bilirubin along with hist ...
02D Reading Medication Labels WS
02D Reading Medication Labels WS

... 8. How much vaccine should I administer to him and where? How often should I revaccinate? 1 ml dose, under the skin (SubQ) or in the muscle (IM). Vaccinate 3 times over 3 week intervals, then once a year. 9. What other diseases does this vaccine prevent? adenovirus type 2 (and hepatitis), parainflue ...
details - Global Pharmaceuticals Pakistan
details - Global Pharmaceuticals Pakistan

... Sodium Bicarbonate is contraindicated in patients with metabolic alkalosis and hypocalcemia. Sodium bicarbonate should be used with caution in patients with Bartter's syndrome, hypokalemia , respiratory alkalosis and problems with acid-base balance. Pregnancy: There are no adequate and well-controll ...
Cleocin Pediatric
Cleocin Pediatric

... USAGE section. It should not be used in patients with nonbacterial infections such as most upper respiratory tract infections. C.difficile produces toxins A and B which contribute to the development of CDAD. Hypertoxin producing strains of C.difficile cause increased morbidity and mortality, as thes ...
new oral anticoagulant drugs (noac) and their
new oral anticoagulant drugs (noac) and their

... hepatic impairment. It is not recommended in patients with a creatinine clearance of less than 15 mL/min. Limited clinical  data for patients with severe renal impairment (creatinine clearance 15 ‐ 29 ml/min) indicate that rivaroxaban plasma  concentrations are significantly increased therefore, riv ...


... Perhaps the first issue that the general practitioner will have to address is how to inculcate in the patient an appropriate expectation of withdrawal. Should a full account of all the symptoms that could be encountered be given, thereby incurring the risk of overinterpretation of symptoms and antic ...
Conclusion - Computing Services
Conclusion - Computing Services

... Background: DNCB is a potent skin sensitiser in humans. The structural analogue DNTB has been implicated as a specific skin toleriser in animals, but its activity in humans is unknown Aim: To: 1) define the sensitising potency of DNTB in humans and 2) examine mechanisms that impact on this. Methods: ...
SAFE n Smart* Use of Sulfonylureas
SAFE n Smart* Use of Sulfonylureas

... C. SUs In Co-morbid Conditions C1. Shorter acting drugs, especially those metabolized in the liver (glipizide), should be the preferred SU in patients with moderate/severe renal impairment. In mild/ moderate renal impairment, gliclazide and glimepiride may also be used, preferably at lower doses. C ...
Spectinomycin - American Academy of Veterinary Pharmacology
Spectinomycin - American Academy of Veterinary Pharmacology

... and systemic infections caused by organisms sensitive to spectinomycin.{R-5} Extra-label withdrawal recommendation: U.S. and Canada— Pigs: Because injectable spectinomycin is not labeled for use in pigs, there are no established withdrawal times in the U.S. or Canada. If spectinomycin is administere ...
cataflam - Novartis
cataflam - Novartis

... Mechanism of Action Diclofenac has analgesic, anti-inflammatory, and antipyretic properties. The mechanism of action of CATAFLAM, like that of other NSAIDs, is not completely understood but involves inhibition of cyclooxygenase (COX-1 and COX-2). Diclofenac is a potent inhibitor of prostaglandin syn ...
Analogues
Analogues

... other functional groups - only suitable for simple esters. Hydrolysis leads to a dramatic increase in polarity which may influence ability of analogue to reach target if in vivo tests are used Reduction to alcohol removes carbonyl group and can establish importance of the carbonyl oxygen, but reacti ...
patrick_ch10_p1
patrick_ch10_p1

... other functional groups - only suitable for simple esters. Hydrolysis leads to a dramatic increase in polarity which may influence ability of analogue to reach target if in vivo tests are used Reduction to alcohol removes carbonyl group and can establish importance of the carbonyl oxygen, but reacti ...
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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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