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Buprenorphine (with or without naloxone)
Buprenorphine (with or without naloxone)

... or without Naloxone) in the Treatment of Opioid Dependence, provide a framework for the effective, safe and responsive delivery of opioid substitution treatment. They will be appended to Opioid Substitution Treatment: New Zealand Practice Guidelines (Ministry of Health 2008). Similar to the national ...
Specials information pack - Barking and Dagenham Clinical
Specials information pack - Barking and Dagenham Clinical

... safety testing, this risk should not be underestimated. Prescribers must be able to justify and feel competent in using unlicensed medicines. The General Medical Council (http://www.gmc-uk.org/guidance/) have guidance on prescribing unlicensed medicines within good practice in prescribing and managi ...
a contemporary history of ibogaine in the united states and europe
a contemporary history of ibogaine in the united states and europe

... putative efficacy of ibogaine in opioid withdrawal and possibly other drug dependence syndromes. An important question is whether clinical observations regarding opioid withdrawal made in this setting can be methodologically valid. The idea of a lay psychotropic user’s group as a means of drug disco ...
2012 Medical Marijuana for the Treatment of Migraine Headaches:
2012 Medical Marijuana for the Treatment of Migraine Headaches:

... article is summarized in table 1. Articles that were listed in the search but that did not meet the inclusion criteria are listed in table 2. Only one article was submitted by the public and it was in the list uncovered by the search and is indicated by an * in table 1. There were a total of 6 artic ...
EFNS guideline on the drug treatment of migraine
EFNS guideline on the drug treatment of migraine

... or only a little more effective than ASA. In about 60% of nonresponders to NSAID, triptans are effective [46]. Sumatriptan 6 mg subcutaneously is more effective than intravenous ASA 1000 mg s.c. but has more side effects [47]. Triptans can be effective at any time during a migraine attack. However, there ...
TAG Mail 30 November 2007
TAG Mail 30 November 2007

... - Anti-Vascular Endothelial Growth Factor Drugs for the Treatment of Retinal Conditions: A Review of Safety https://www.cadth.ca/anti-vascular-endothelial-growth-factor-drugs-treatment-retinal-conditions-reviewsafety ...
advanced sedation techniques
advanced sedation techniques

... dentistry is fairly poor in its access and availability. S Need for such services is indisputable. S Due to the severe burden on the NHS hospital sector and the high ...
Methadone Assisted Recovery Guidelines for Saskatchewan
Methadone Assisted Recovery Guidelines for Saskatchewan

... reduction strategy to prevent the transmission of HIV and other blood-borne pathogens, while assisting those using opioids to reduce illicit use, needle sharing and criminal activity associated with opioid use. Addiction counsellors can be involved in several key areas of methadone assisted recovery ...
British Association of Dermatologists` guidelines
British Association of Dermatologists` guidelines

... respiratory tract, and skin conditions, such as atopic dermatitis, urticaria and erythema nodosum. Nail changes are an important medical concern for patients and, therefore, nail diseases should raise attention and receive proper care from both physicians and other healthcare providers.22 Approximat ...
Botulinum Toxin Injection for Facial Wrinkles
Botulinum Toxin Injection for Facial Wrinkles

... onabotulinumtoxinA (Botox), abobotulinumtoxinA (Dysport), and incobotulinumtoxinA (Xeomin), which are summarized in Table 2.19,20 All three serotype A products have a 150 kDa core botulinum toxin protein and differ in whether they have complexing proteins surrounding the core neurotoxin. Onabotulinu ...
Guidelines of care for acne vulgaris management
Guidelines of care for acne vulgaris management

... Journal of Family Practice, and BMJ-USA). This strategy was supported by a decision of the Clinical Guidelines Task Force in 2005 with some minor modifications for a consistent approach to rating the strength of the evidence of scientific studies.1 Evidence was graded using a three-point scale based ...
Botulinum Toxins A and B - UnitedHealthcareOnline.com
Botulinum Toxins A and B - UnitedHealthcareOnline.com

... sole discretion, to modify its Policies and Guidelines as necessary. This Drug Policy is provided for informational purposes. It does not constitute medical advice. UnitedHealthcare may also use tools developed by third parties, such as the MCG™ Care Guidelines, to assist us in administering health ...
Prescribing Information
Prescribing Information

... Read the Patient Information that comes with VUSION Ointment before you use it on your child. This leaflet does not take the place of talking to your healthcare provider about your child’s medical condition or treatment. If you have any questions or if you are not sure about any of the information o ...
AusPAR Attachment 2: Extract from the Clinical Evaluation Report
AusPAR Attachment 2: Extract from the Clinical Evaluation Report

... The TGA relies on the public, healthcare professionals and industry to report problems with medicines or medical devices. TGA investigates reports received by it to determine any necessary regulatory action. ...
Guidelines that are no longer current are archived as
Guidelines that are no longer current are archived as

... may, however, benefit from such testing. In prepubertal children, the signs include acne, early-onset body odor, axillary or pubic hair, accelerated growth, advanced bone age, and genital maturation. After puberty, common virilizing signs and symptoms are infrequent menses, hirsutism, male or female ...
QA248_4Pyridostigmine_neostigmine_FINAL
QA248_4Pyridostigmine_neostigmine_FINAL

... given by IM or SC injection every 2-4 hours.(3) Oral neostigmine doses are usually 15 – 30mg at regular intervals throughout the day, with up to 5-20 tablets taken daily.(4) Higher doses may be needed in some patients. (2-4) Patients with myasthenia gravis suffer with weak and easily fatigued muscle ...
Medication Safety, October 2012 (Word 4.23MB)
Medication Safety, October 2012 (Word 4.23MB)

... method for evaluating a process to identify where and how it might fail, and to assess the relative impact of different failures in order to identify the parts of the process that are most in need of change. 6 Governance: The set of relationships and responsibilities established by a health service ...
Polyethylene Glycol 3350 (PEG 3350) Frequently Asked
Polyethylene Glycol 3350 (PEG 3350) Frequently Asked

... No. PEG 3350 is currently approved by the U.S. Food and Drug Administration (FDA) for use in adults, for no longer than seven days, and is not approved for use in children. However, a drug that does not have FDA approval for use in children does not mean that the drug is unsafe. It usually means the ...
Review of the Available Evidence on “Newer”
Review of the Available Evidence on “Newer”

... complementary list). The same drugs, except for magnesium sulfate, are in the WHO EMLc. These drugs are intended to treat generalized and partial epilepsy, mostly as first-line therapies. [1] In 2009, a WHO/EML Expert Committee recommended a review of second-line anticonvulsants for an update of the ...
Guideline for the Quality, Safety, and Efficacy Assurance of Follow
Guideline for the Quality, Safety, and Efficacy Assurance of Follow

... follow-on biologic using the same vector system is thought to be difficult. In particular, the follow-on biologic is likely to be developed using a gene expression construct in which the promoter/enhancer and signal sequence, etc. are different from those of the original biologic. In accordance with ...
S F R SAMHSA
S F R SAMHSA

... • whether such Waivers have significantly increased (relative to the beginning of such period) the availability of maintenance treatment and detoxification treatment; and • whether such Waivers have adverse consequences for the public health (e.g., adverse consequences, diversion for abuse). Based ...
What factors need to be considered when prescribing for lactose
What factors need to be considered when prescribing for lactose

... The lactose content of oral medications is generally small in comparison to the amount of lactose in many dietary substances, particularly dairy products (2). The dose of lactose in most pharmaceuticals is usually less than 2g per day. Therefore, unless an adult has severe lactose intolerance, it is ...
HIGHLIGHTS OF PRESCRIBING INFORMATION
HIGHLIGHTS OF PRESCRIBING INFORMATION

... twice per week induced squamous cell skin tumors in transgenic TgAC mice in a study using 20 weeks of topical treatment. The clinical significance of this is unknown. In a 2-year dermal carcinogenicity study in mice, treatment with DUAC Gel at doses up to 8,000 mg/kg/day (16 times the highest recomm ...
JANUARY 1, 2015 TREATMENT AUTHORIZATION (TAR) CRITERIA
JANUARY 1, 2015 TREATMENT AUTHORIZATION (TAR) CRITERIA

... stimulant abuse/diversion by the patient or a family member residing in the home. Adult use (age 17 and older): (1) Documentation of a history of abuse/diversion by the patient, OR, (2) Adequate trial and unsatisfactory result with formulary methylphenidate, non-formulary ...
Why Do We Use 600 mg of Rifampicin in
Why Do We Use 600 mg of Rifampicin in

... isoniazid-pyrazinamide regimens over equally active isoniazid-rifampicin regimens as rifampicin cost more than £110 for 6 months, which was .4 times the cost of pyrazinamide. The benefit of their study was formulated giving ‘‘good prospects of developing practical short-course regimens which do not ...
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National Institute for Health and Care Excellence

The National Institute for Health and Care Excellence (NICE) is an executive non-departmental public body of the Department of Health in the United Kingdom. It serves both the English NHS and the Welsh NHS. It was set up as the National Institute for Clinical Excellence in 1999, and on 1 April 2005 joined with the Health Development Agency to become the new National Institute for Health and Clinical Excellence (still abbreviated as NICE). Following the Health and Social Care Act 2012, NICE was renamed the National Institute for Health and Care Excellence on 1 April 2013 reflecting its new responsibilities for social care, and changed from a special health authority to an Executive Non-Departmental Public Body (ENDPB).NICE publishes guidelines in four areas: the use of health technologies within the NHS (such as the use of new and existing medicines, treatments and procedures); clinical practice (guidance on the appropriate treatment and care of people with specific diseases and conditions); guidance for public sector workers on health promotion and ill-health avoidance; and guidance for social care services and users. These appraisals are based primarily on evaluations of efficacy and cost–effectiveness in various circumstances.NICE was established in an attempt to defuse the so-called postcode lottery of healthcare in England and Wales, where treatments that were available depended upon the NHS Health Authority area in which the patient happened to live, but it has since acquired a high reputation internationally as a role model for the development of clinical guidelines. One aspect of this is the explicit determination of cost–benefit boundaries for certain technologies that it assesses. NICE also plays an important role in pioneering technology assessment in other healthcare systems through NICE International, established in May 2008 to help cultivate links with foreign governments.
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