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Antidepressant medication table for Adults
Antidepressant medication table for Adults

... Standard Dose (mg/day) ...
DETERMINATION OF LEVOCETIRIZINE CONFIGURATIONAL STABILITY IN TABLETS USING  CHIRAL HPLC METHOD  Research Article 
DETERMINATION OF LEVOCETIRIZINE CONFIGURATIONAL STABILITY IN TABLETS USING  CHIRAL HPLC METHOD  Research Article 

Enteropeptidase: A Gene Associated with a Starvation
Enteropeptidase: A Gene Associated with a Starvation

... considered to be negligible after oral administration. Therefore, the weak off-target activity alluded-to earlier is of little or no concern, and few – if any – side effects are anticipated. The results of our animal studies suggest that partial inhibition of EP through chemotherapeutic intervention ...
Full Prescribing Information
Full Prescribing Information

... of patients in the placebo group. These effects were dose-related and generally appeared within the first 6 weeks of treatment, although new events continued to be observed through more than 37 weeks. FYCOMPA-treated patients experienced more hostility- and aggression-related adverse reactions that ...
Respiratory drugs-nursing
Respiratory drugs-nursing

... • decreases frequency of asthma exacerbation and severity of symptoms The corticosteroids commonly used are hydrocortisone, predinisolone, beclomethasone, triamcinolone and etc. The drugs can be taken by inhalation as aerosol, oral, or an IV administration ...
Goat Parasites: Management and Control
Goat Parasites: Management and Control

... is a more typical time. Clinical signs include increased respiratory rate, difficult breathing and coughing. Ivermectin, levamisole and fenbendazole will kill larval stages and adults. Muellerius and Protostrongylus - have an indirect life cycle with a snail intermediate host. Protostrongylus lives ...
Digoxin
Digoxin

... Description ...
Neonatal Abstinence Syndrome Objectives Objectives, continued
Neonatal Abstinence Syndrome Objectives Objectives, continued

... • Clonidine: added to regimen if phenobarbital and morphine do not control symptoms • Dose: 0.1 mcg/kg q 4-6 hours • Clonidine is well studied and used in adult addicts, and has been shown to be effective in newborns as well ...
Memorin - Beximco Pharmaceuticals Ltd.
Memorin - Beximco Pharmaceuticals Ltd.

... for some patients. Accordingly, whether or not to employ a dose of 10 mg is a matter of prescriber and patient preference. Side Effects The rates of discontinuation from controlled clinical trials of Donepezil hydrochloride due to adverse events for the Donepezil hydrochloride 5 mg/day treatment gro ...
Anithypertensive_drugs_and_its_classifications
Anithypertensive_drugs_and_its_classifications

... (especially sodium) or are not easily absorbed from the nephron themselves (mannitol). Consequently solutes remain within the filtrate and exert an osmotic effect that inhibits the reabsorption of water. ◦ This effect can also be seen if blood plasma levels of glucose become very high (e.g. in hyper ...
Inflammatory Bowel Disease
Inflammatory Bowel Disease

... • Inhibitor of calcineurin, preventing clonal expansion of T-cell subsets • Rapid onset of action • Used in mx severe UC • Can be used as IV salvage therapy in those heading for colectomy • Measurement of blood pressure, full blood count, renal function, and CsA concentration at 0, 1, and 2 weeks, t ...
ASSESSMENT OF DRUG DOSE ADJUSTMENT IN PATIENTS WITH KIDNEY DISEASE:
ASSESSMENT OF DRUG DOSE ADJUSTMENT IN PATIENTS WITH KIDNEY DISEASE:

... One hundred and forty two patients were recruited in the study. Patients’ files were studied on random basis during hospital stay and patients with elevated serum creatinine (above 1.1 mg/dl) were selected for further analysis. The inclusion criteria consisted of 1) age older than 16, 2) GFR less th ...
Drugs That Significantly Increase Blood Glucose
Drugs That Significantly Increase Blood Glucose

... Clinicians may be surprised by the number of drugs that can cause an increase in blood glucose. In certain patient populations, such as those with glucose intolerance, this may be more likely to be of significance. It may also be of more significance for drugs that are used chronically, such as anti ...
Slajd 1
Slajd 1

... Levels of AT II, bradykinin, TNF Assesment at baseline and after 1 year of treatment ...
BSH`s formal response to MHRA - British Society for Heart Failure
BSH`s formal response to MHRA - British Society for Heart Failure

... •Suspected adverse reactions should be reported to us on a Yellow Card ...
Pharmacologic treatment of Parkinson disease:
Pharmacologic treatment of Parkinson disease:

... Examine the effect of diet, and avoid taking levodopa with high protein meals. A sustained-release levodopa formulation may be beneficial, but only in the early stages of wearing "off" in patients with less advanced PD. In patients with more advanced PD, reduce the levodopa dose interval by 30 to 60 ...
ISMP Medication Safety Alert - Institute For Safe Medication Practices
ISMP Medication Safety Alert - Institute For Safe Medication Practices

... emergency department. AJHP. ...
intramuscularly
intramuscularly

...  CNS effects subside, following redistribution to less well-perfused tissues (re-distribution half-life 2.7 min.). ...
Glossary - Remodulin
Glossary - Remodulin

... In patients with mild or moderate hepatic insufficiency, decrease the initial dose of Remodulin to 0.625 ng/kg/min ideal body weight. Remodulin has not been studied in patients with severe hepatic insufficiency [see Warnings and Precautions (5.3), Use In Specific Populations (8.6) and Clinical Pharm ...
Prescribing Information
Prescribing Information

... Drug-induced liver injury, hepatocellular injury, hepatic steatosis, hepatitis cholestatic and hepatotoxicity have each been reported in < 1% of patients treated with NINLARO. Events of liver impairment have been reported (6% in the NINLARO regimen and 5% in the placebo regimen). Monitor hepatic enz ...
Glucocorticoids
Glucocorticoids

... Prednisone is a commonly used glucocorticoid. Prednisone is a pro-drug, therefore it must be metabolized to prednisolone to elicit its pharmacologic effect. Cats are variable metabolizers of prednisone to prednisolone, so the effect will also be variable and less predictable in cats. Prednisolone is ...
rajiv gandhi university of health sciences, karnataka, bangalore
rajiv gandhi university of health sciences, karnataka, bangalore

... effectiveness and side effects of intravenous patient controlled morphine,pethidine and tramadol were compared. All the three drug have equivalent pain scores and side effects but tramadol group required more frequent use of rescue analgesic.5 In another study comparing nalbuphine hydrochloride with ...
Appropriate Use of Ergotamine and Dihydroergotamine
Appropriate Use of Ergotamine and Dihydroergotamine

... studies although there were several class I studies. The incidence of nausea and vomiting is high. Reducing the dosage or adding antinauseants may improve tolerance to the drug. Twenty-one studies concerning DHE efficacy were reviewed; these studies were difficult to interpret because they did not u ...
Female Reproductive Disorders
Female Reproductive Disorders

... • Oligomenorrhea – long interval between menses • Amenorrhea - absence of menses • Menorrhagia – prolonged menstrual bleeding • Metrorrhagia – irregular bleeding – Complication is low hemoglobin ...
January 2017 - WSU College of Pharmacy
January 2017 - WSU College of Pharmacy

... The FDA warned consumers not to purchase or use PNC-27 promoted and sold online as a treatment or cure for cancer. A FDA lab discovered the bacteria Variovorax paradoxus in a sample from the PNC-27 solution. No form of PNC-27 has been evaluated or approved by the FDA. Implantable Infusion Pumps in M ...
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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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