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Feline Dermatitis.do..
Feline Dermatitis.do..

... should be used for a 10-week trial. This is often the quickest way to collect the most information regarding a dermatosis. Even if not diagnostic, enough information can be gathered to guide additional diagnostic tests or therapeutic trials Allergy testing for in vitro blood assays can provide usefu ...
Breakthrough Pain
Breakthrough Pain

...  More patients reported ≥30% reduction in pain intensity with Abstral than with placebo (p<0.0001) ...
Opioid Prescribing: Many Questions and Few Answers
Opioid Prescribing: Many Questions and Few Answers

...  Mono-therapy rarely effective  More data shows improvement with decreased doses  Controversy persists among groups ...
somatropin (recombinant) (soe-ma-troe-pin)
somatropin (recombinant) (soe-ma-troe-pin)

... growth hormone deficiency. Replacement of somatropin in deficient adults. In- Turner syndrome— 0.33 mg/kg/wk divided into 6– 7 daily doses. Idiopathic short creased bone density in adult growth hormone– deficient patients. stature— 0.47 mg/kg/wk divided into 6– 7 daily doses. Subcut (Adults): 0.04mg ...
HIGHLIGHTS OF PRESCRIBING INFORMATION •
HIGHLIGHTS OF PRESCRIBING INFORMATION •

... antibacterial agents alters the normal flora of the colon leading to overgrowth of C. difficile. 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 these infections can be refracto ...
Click here - Journal of Clinical and Diagnostic Research
Click here - Journal of Clinical and Diagnostic Research

... traditional NSAIDs and opioids and shows a prolonged action with lesser adverse effects like gastric irritation [9]. [10]. Reviews of published studies have noted that at least 50% pain relief was reported by 64% users of etoricoxib 120 mg. Also, significantly fewer participants opted for rescue med ...
Epinephrine Administration by the EMT
Epinephrine Administration by the EMT

Octaplas For	Coagulation	Disorders NEW	DRUGS
Octaplas For Coagulation Disorders NEW DRUGS

... has been approved to treat overactive bladder in adults who cannot use or do not adequately respond to anticholinergic agents. Botox is also used to treat facial wrinkles, cervical dystonia, hyperhidrosis, blepharism, spasticity, strabismus, and chronic migraine. When injected into the bladder, Boto ...
Assessing the clinical value of fast onset and sustained duration of
Assessing the clinical value of fast onset and sustained duration of

... sometimes twice-daily [46]. Duration of effect can be dosedependent [47]. Aclidinium was originally investigated as a oncedaily drug given at doses of 200 or 400 mg but was found to be suboptimal in terms of effect size and duration; 400 mg twice daily showed greater efficacy than the 200 mg dose and ...
EFFECT OF SEPTILIN - A HERBAL PREPARATION ON
EFFECT OF SEPTILIN - A HERBAL PREPARATION ON

... and tonic-clonic seizures (4). It is absorbed slowly after oral administration, with peak concentration around 4 hours after oral dose. Mean systemic availability is approximately 90% (5). CBZ is metabolized primarily in the liver by cytochrome p450 (CYP450) isozyme 3A4 to carbamazepine-lO, ll-epoxi ...
Psychopharmacology of Mood Disorders
Psychopharmacology of Mood Disorders

... headache, insomnia, sexual dysfunction) ...
Clinical Pharmacology
Clinical Pharmacology

... Safe, effective pharmacotherapy is one of the greatest challenges in clinical geriatrics. Special considerations are necessary when prescribing drugs (see Table 6-1). The elderly have many chronic disorders and consequently use more drugs than any other age group. Their diminished physiologic reserv ...


... it should be noted that HALDOL may be capable of potentiatingONSdepressants such as anesthetics opiates, and alcohoL CarcinogenesI Mutagenesis andlmpairment olFertility: No mutagenic potential of haloperidol decanoatewasfound in theAmes Salmonella microsomal activation assay. Carcmnogenicity studies ...
Bitter Leaf
Bitter Leaf

Pharmacogenetics of response to antiresorptive therapy
Pharmacogenetics of response to antiresorptive therapy

... Genetic markers could allow identification of those more or less likely to – fracture – respond to a specific treatment – suffer side effects from a specific treatment ...
Pdf version
Pdf version

... prevent the occurrence of stent thrombosis in patients undergoing stenting [2]. Since then the clinical efficacy of clopidogrel treatment has been demonstrated in various settings of cardiovascular diseases either as an alternative or complimentary to aspirin. Based on the marginal superiority over ...
Enrocare 10% Injection
Enrocare 10% Injection

... The pharmacokinetics of enrofloxacin in dogs and cats are such that oral and parenteral administration leads to similar serum levels. Enrofloxacin possesses a high distribution volume. Tissue levels 2-3 times higher than that found in the serum have been demonstrated in laboratory animals and target ...
AusPAR: Pitavastatin - Therapeutic Goods Administration
AusPAR: Pitavastatin - Therapeutic Goods Administration

... cells is close to the respective clinical dose ratios of 2 mg/5 mg/10 mg. In guinea pig livers, the 50% effective doses (ED50s) for inhibition of sterol synthesis were 0.33 mg/kg for pitavastatin and 5.1 mg/kg for simvastatin. Pitavastatin showed a more sustained effect than simvastatin and pravasta ...
product monograph
product monograph

... In patients receiving higher therapeutic dalteparin doses (such as 100IU/kg -120 IU/kg every 12 hours or 200 IU/kg once daily), the interval for the insertion or removal of the epidural or spinal catheter should be a minimum of 24 hours. Extreme vigilance and frequent monitoring must be exercised t ...
What public health benefits could be secured by using universal
What public health benefits could be secured by using universal

... recommended to reduce the timelines and increase the supply chain flexibility in and outside Europe: ƒ “Specific QRD template for pandemic vaccines” with a simplified labelling content for outer packaging, labels and the package leaflet (shortened package leaflet) ƒ Early approval with only the esse ...
DUEXIS® (ibuprofen 800mg/famotidine 26.6mg) oral tablet
DUEXIS® (ibuprofen 800mg/famotidine 26.6mg) oral tablet

... Safety and effectiveness in pediatric patients have not been established. ...
Serotonin Syndrome - Clinician`s Brief
Serotonin Syndrome - Clinician`s Brief

... mg/kg SC q24h) should be administered after emesis or gastric lavage and before activated charcoal. ■ Activated charcoal with sorbitol should be administered. ❏ Benefits of charcoal administration over aspiration risk should be considered in symptomatic patients. ❏ Repeat doses without sorbitol can ...
Cordarone® Intravenous - Amiodarone-IV
Cordarone® Intravenous - Amiodarone-IV

... in vitro studies, the protein binding of amiodarone is >96%. In clinical studies of 2 to 7 days, clearance of amiodarone after intravenous administration in patients with VT and VF ranged between 220 and 440 mL/h/kg. Age, sex, renal disease, and hepatic disease (cirrhosis) do not have marked effects ...
SERC PM
SERC PM

... dihydrochloride was also found to have a dose dependent inhibiting effect on spike generation of neurons in lateral and medial vestibular nuclei. Pharmacodynamics In ten healthy male volunteers, single oral doses of 8, 16, and 32 mg of betahistine dihydrochloride given in a placebo-controlled, doubl ...
Indocin - Iroko Pharmaceuticals
Indocin - Iroko Pharmaceuticals

... at any time, with or without warning symptoms, in patients treated with NSAIDs. Only one in five patients who develop a serious upper GI adverse event on NSAID therapy is symptomatic. Upper GI ulcers, gross bleeding, or perforation caused by NSAIDs occurred in approximately 1% of patients treated fo ...
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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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