A 3:1 mixture of alfaxalone with alfadolone acetate that previously had been used as a general anesthetic. It is no longer actively marketed. (From Martindale, The Extra Pharmacopoeia, 30th ed, p1445)
Pregnane derivatives in which two side-chain methyl groups or two methylene groups in the ring skeleton (or a combination thereof) have been oxidized to keto groups.
A species of sheep, Ovis aries, descended from Near Eastern wild forms, especially mouflon.

Anaesthesia for injection of bleeding oesophageal varices. (1/19)

Patients with haemorrhage from oesophageal varices associated with portal hypertension are poor risks for anaesthesia and surgery. One method of controlling such haemorrhage is injection of the oesophageal varices (sclero-therapy) via an oesophagoscope. Careful preoperative preparation and use of the Sengstaken-Blakemore tube in combination with the anaesthetic technique of intermittent Althesin and suxamethonium with artificial ventilation with nitrous oxide and oxygen enables sclerotherapy to be carried out successfully.  (+info)

Recovery and simulated driving after intravenous anesthesia with thiopental, methohexital, propanidid, or alphadione. (2/19)

Recovery from anesthesia was assessed in a double-bind manner in 40 healthy volunteer students after intravenous anesthesia with thiopental (6.0 mg/kg), methohexital (2.0 mg/kg), propanidid (6.6 mg/kg), or alphadione (Althesin), 85 mul/kg using a driving simulator 2,4, 6, and 8 hours after injection of the drugs. Clinical recovery was faster after propanidid and methohexital than after thiopental or alphadione. Driving performances remained significantly (P less than 0.05) worse than in a control group for 6 hours after thiopental and for 8 hours after methohexital, and reaction times 8 hours after thiopental remained worse than in the control subjects. After alphadione driving skills were impaired at 6 hours only. Propanidid produced no impairment in driving skills at any time during the experiment. It is concluded that after the doses used in this study patients should not drive or operate machinery for at least 2 hours after propanidid and for at least 8 hours after alphadione. After methohexital and thiopental patients should probably not drive for 24 hours because of the severity of the disturbances at 8 hours.  (+info)

Evidence that central 5-HT2A and 5-HT2B/C receptors regulate 5-HT cell firing in the dorsal raphe nucleus of the anaesthetised rat. (3/19)

1. Systemic administration of phenethylamine-derived, 5-hydroxytryptamine(2) (5-HT(2)) receptor agonists inhibits the firing of midbrain 5-HT neurones, but the 5-HT receptors involved are poorly defined, and the contribution of peripheral mechanisms is uncertain. This study addresses these issues using extracellular recordings of 5-HT neurones in the dorsal raphe nucleus of anaesthetised rats. 2. The 5-HT(2) receptor agonists DOI ((+/-)-2,5-dimethoxy-4-iodoamphetamine hydrochloride) and DOB ((+/-)-2,5-dimethoxy-4-bromoamphetamine hydrobromide), caused a dose-related (10-100 micro g kg(-1) i.v.) inhibition of 5-HT neuronal activity, with the highest dose reducing firing rates by >80%. 3. Pretreatment with the 5-HT(2) receptor antagonist ritanserin (1 mg kg(-1) i.v.) completely blocked the action of DOI. The 5-HT(2A) receptor antagonist MDL 100,907 (0.2 mg kg(-1) i.v.) blocked the action of both DOI and DOB. In comparison, the 5-HT(2B/C) receptor antagonist SB 206553 (0.5 mg kg(-1) i.v.) caused a small, but statistically significant, shift to the right in the dose response to DOI and DOB. 4. Pretreatment with the peripherally acting 5-HT(2) receptor antagonist BW 501C67 (0.1 mg kg(-1) i.v.) had no effect on the DOI-induced inhibition of 5-HT cell firing, but completely blocked the DOI-induced rise in mean arterial blood pressure. 5. These data indicate that the inhibition of 5-HT cell firing induced by systemic administration of DOI and DOB is mediated predominantly by the 5-HT(2A) receptor-subtype, but that 5-HT(2B/C) receptors also play a minor role. Moreover, central and not peripheral mechanisms are involved. Given evidence that 5-HT(2) receptors are not located on 5-HT neurones, postsynaptic 5-HT feedback mechanisms are implicated.  (+info)

The effect of ketamine and saffan on the beta-endorphin and ACTH response to hemorrhage in the minipig. (4/19)

The endocrine response is an important component of the physiological response to blood loss. There is some variability in reported levels of certain hormones during hemorrhage such as the stress hormone adrenocorticotrophic hormone (ACTH). Therefore, the effect of two anesthetic agents, ketamine and saffan, on ACTH and beta-endorphin levels during hemorrhage was assessed in 12 minipigs. The animals were divided into two groups, group I saffan and group II ketamine (n=6). Pigs were subjected to a continuous fixed volume hemorrhage under one of the above anesthetics while spontaneously breathing. Blood pressure and heart rate responses were recorded together with beta-endorphin and ACTH levels both before and at 10, 20, 30, 40 min after the onset of bleeding. ACTH levels were higher in the ketamine-anesthetized pigs and rose significantly faster with falling blood pressure than ACTH measured in pigs under saffan anesthesia. In contrast, the hemorrhage induced beta-endorphin increase was not significantly different between the two anesthetic groups. These results indicate that choice of anesthetic agent is important when investigating the hormone response to hemorrhage and may account for the variable hormone levels in the published literature to date.  (+info)

Absence of coronary artery calcification and all-cause mortality. (5/19)

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Anaesthetic suppression of transmitter actions in neocortex. (6/19)

1. The effects of general anaesthetics were investigated on neuronal sensitivities to transmitter substances, which were determined by iontophoretic applications of acetylcholine, glutamate, N-methyl-D-aspartate (NMDA) and gamma-aminobutyrate (GABA) during intracellular recording in in vitro slice preparations of neocortex (guinea-pig). 2. In most of the 65 neurones studied, perfusion of isoflurane (0.5-2.5 minimum alveolar concentration (MAC)) or Althesin (25-200 microM) and, in some cases, halothane (0.5-2 MAC), markedly reduced the depolarizing responses and associated membrane conductance changes evoked by dendritic applications of acetylcholine, glutamate, NMDA and GABA. 3. The order of depression was acetylcholine greater than glutamate or NMDA much greater than GABA. This selectivity could also be assessed from the EC50 for the isoflurane-induced depression of the just-maximal responses to acetylcholine, which was 0.9 MAC compared with an EC50 = 1.9 MAC for the suppression of glutamate responses. The selectivity was less pronounced in the case of the actions of Althesin, where the EC50s were 75 microM for the depression of acetylcholine responses and 90 microM for the depression of glutamate responses. 4. The hyperpolarizing responses observed when GABA was applied near the perikaryon in 7 neurones, were slightly reduced (approximately 15%) in 4, and unchanged in 3 neurones during anaesthetic application. 5. The pronounced depression of the responsiveness to the putative arousal transmitters and an observed blockade of acetylcholine-induced potentiation of glutamate actions suggest that anaesthetics produce unconsciousness, at least in part, by interfering with subsynaptic mechanisms of neocortical activation.  (+info)

Facilitation of synaptic transmission by general anaesthetics. (7/19)

1. The actions of five structurally different intravenous and inhalation anaesthetics (alphaxalone/alphadolone, halothane, ketamine, methohexitone, and pentobarbitone) have been studied on synaptic transmission through the cuneate nucleus of the dorsal column-lemniscal afferent pathway in the decerebrate cat. 2. Synaptic input and output were estimated from antidromic and orthodromic potentials, which were evoked by either afferent volleys from the periphery or micro-electrode excitation of the presynaptic fibre terminals in the cuneate and recorded at forelimb nerves and the medial lemniscus. 3. Each of the anaesthetic agents potentiated the efficiency of synaptic transmission, as shown by the elevation of input-output curves constructed from the integrals of the potentials evoked by varying intensities of either peripheral or cuneate stimulation. 4. The excitability of the afferent terminals, as measured at the peripheral nerves by the antidromic responses to micro-electrode stimulation, was depressed by the anaesthetics. Post-synaptic excitability, which was assessed from the direct lemniscal response to intra-nuclear stimulation, did not appear to change. 5. Hypotensive states (mean arterial levels less than 60 torr) produced depolarization of presynaptic terminals and depression of synaptic efficiency and transmission; these changes opposed the primary effects of the general anaesthetics. 6. It is concluded that anaesthetics do not depress activity at all synapses of the central nervous system. Their facilitatory action on cuneate transmission is attributed to an enhanced release of excitatory transmitter; the underlying mechanism may be hyperpolarization of the primary afferent terminals, secondary to an increase in K+ conductance.  (+info)

Effects of saffan on cardiopulmonary function in healthy cats. (8/19)

The effects of saffan on cardiopulmonary function were evaluated in eight healthy adult cats. Measured values were cardiac output by thermodilution, heart rate by electrocardiogram, arterial blood gases, respiratory rate and systolic, diastolic and mean arterial blood pressures by arterial catheterization. Calculated values included cardiac index, stroke volume and systemic vascular resistance. Statistical analysis employed paired t-tests comparing pre saffan anesthetic induction and post saffan anesthetic parameters over a 120 minute time sequence. Thirty min after saffan induction, significant depression in cardiac output was evident while stroke volume was significantly depressed at 45 and 60 min, systolic blood pressure at 15 min and respiratory rate at 5, 10 and 15 min. No significant changes occurred in cardiac index, heart rate, arterial blood gases, diastolic and mean arterial blood pressure or systemic vascular resistance. It was concluded that saffan causes significant depression of cardiopulmonary function in normal adult cats.  (+info)

Althesin information about active ingredients, pharmaceutical forms and doses by GlaxoSmithKline, Althesin indications, usages and related health products lists
Boeryd, B; Lundin, P; and Norrby, K, Tumour growth after intravenous, intraperitoneal and subcutaneous injection of syngeneic monodispersed tumour-cell suspension. (1971). Subject Strain Bibliography 1971. 1706 ...
Looking for online definition of althesin in the Medical Dictionary? althesin explanation free. What is althesin? Meaning of althesin medical term. What does althesin mean?
TY - JOUR. T1 - Effect of body posture on cardiopulmonary function in horses during five hours of constant-dose halothane anesthesia. AU - Steffey, Eugene. AU - Kelly, A. B.. AU - Hodgson, D. S.. AU - Grandy, J. L.. AU - Woliner, M. J.. AU - Willits, N.. PY - 1990/3/23. Y1 - 1990/3/23. UR - http://www.scopus.com/inward/record.url?scp=0025266649&partnerID=8YFLogxK. UR - http://www.scopus.com/inward/citedby.url?scp=0025266649&partnerID=8YFLogxK. M3 - Article. C2 - 2301808. AN - SCOPUS:0025266649. VL - 51. SP - 11. EP - 16. JO - American Journal of Veterinary Research. JF - American Journal of Veterinary Research. SN - 0002-9645. IS - 1. ER - ...
Intravenous anaesthetics 1.Thiopentone- agent of choice for neurosurgery - c/i in hypovolemia & shock - truth serum 2-Propofol- preferred agent for day care surgery - intravenous anaesthetic agent of choice in malignant hyperthermia - iv anaesthetic of choice for intubation 3-Etomidate- agent of choice for cardiovascular surgeries 4-Ketamine- dissociative anaesthesia -c/i in head injury , space occupying lesions - c/i hypertensive and ischaemic heart diseases - iv anaesthetic of choice in pt with shock and hypovolemia - iv anaesthetic of choice in asthmatic ...
The main goal of the pectus multicenter outcomes study is to document the utility of PEx repair in improving health and quality of life and to test the prevailing belief that the two predominant surgical procedures currently in use for PEx repair are essentially equivalent in terms of long-term outcomes.. We believe the uncertainty about the impact of PEx on cardiopulmonary function is due to part to the fact that the previous studies have not measured the physiological parameters mostly likely affected by the defect. A protocol to test this was developed. Thus, we propose to use these measures as well as conventional output of progressive exercise test to examine cardiopulmonary function before and after surgical repair of PEx within the context of the original study. ...
Cancer cells possess a broad spectrum of migration and invasion mechanisms. These include both individual and collective cell-migration strategies. Cancer therapeutics that are designed to target adhesion receptors or proteases have not proven to be effective in slowing tumour progression in clinica …
In order to provide the best care possible, C-O2 partners with the C-era and C-endo clinics to offer complete and comprehensive care.. ...
OBJECTIVE To determine the pharmacokinetics and pharmacodynamics of the neurosteroid anaesthetic, alfaxalone, in neonatal foals after a single intravenous (IV) injection of alfaxalone following premedication with butorphanol tartrate. STUDY DESIGN Prospective experimental study. ANIMALS Five clinically healthy Australian Stock Horse foals of mean ± SD age of 12 ± 3 days and weighing 67.3 ± 12.4 kg. METHODS Foals were premedicated with butorphanol (0.05 mg kg(-1) IV) and anaesthesia was induced 10 minutes later by IV injection with alfaxalone 3 mg kg(-1) . Cardiorespiratory variables (pulse rate, respiratory rate, direct arterial blood pressure, arterial blood gases) and clinical signs of anaesthetic depth were evaluated throughout anaesthesia. Venous blood samples were collected at strategic time points and alfaxalone plasma concentrations were assayed using liquid chromatography-mass spectrometry (LC/MS) and analysed by noncompartmental pharmacokinetic analysis. RESULTS The harmonic, mean ±
The binding affinities of two steroid anaesthetics, alphaxalone (Alfx) and alphadolone acetate (Alfd), for testosterone-oestradiol-binding globulin (TeBG) and corticosteroid-binding globulin (CBG)...
The hemodynamic effects of alfaxalone and propofol on the cardiovascular system during anesthetic maintenance in experimental medicine were investigated in pigs.
The major finding of the present study is that the inhibition of spontaneous firing of 5-HT cells in the rat DRN induced by systemic administration of risperidone is associated with, and probably caused by, increased 5-HT output within the DRN.. Based on the high affinity of risperidone for 5-HT2A receptors and less, but still relatively high, affinity for D2 receptors as shown with both ex vivo (Leysen et al., 1992; Schotte et al., 1996) and in vivo (Matsubara et al., 1993; Sumiyoshi et al., 1994) methods, the doses of risperidone used in the present study were selected to yield a high 5-HT2A receptor occupancy throughout the major part of the dose spectrum and a gradually increasing D2 receptor occupancy. Consequently, both antagonism of 5-HT2A and D2 receptors by risperidone could, theoretically, underlie the observed inhibition of 5-HT cell firing in the DRN. However, this explanation seems less likely since both the highly selective 5-HT2A receptor antagonist MDL 100,907 (Palfreyman et al., ...
General anaesthesia in pigs maintained with intravenous drugs such as propofol may cause respiratory depression. Alfaxalone gives less respiratory depression than propofol in some species. The aim of the investigation was to compare respiratory effects of propofol-ketamine-dexmedetomidine and alfaxalone-ketamine-dexmedetomidine in pigs. Sixteen pigs premedicated with ketamine 15 mg/kg and midazolam 1 mg/kg intramuscularly were anaesthetised with propofol or alfaxalone to allow endotracheal intubation, followed by propofol 8 mg/kg/h or alfaxalone 5 mg/kg/h in combination with ketamine 5 mg/kg/h and dexmedetomidine 4 µg/kg/h given as a continuous infusion for 60 min. The pigs breathed spontaneously with an FIO2 of 0.21. Oxygen saturation (SpO2), end-tidal CO2 concentration (PE′CO2), respiratory rate (fR) and inspired tidal volume (VT) were measured, and statistically compared between treatments. If the SpO2 dropped below 80% or if PE′CO2 increased above 10.0 kPa, the pigs were recorded as failing to
1. Systemic administration of phenethylamine-derived, 5-hydroxytryptamine(2) (5-HT(2)) receptor agonists inhibits the firing of midbrain 5-HT neurones, but the 5-HT receptors involved are poorly defined, and the contribution of peripheral mechanisms is uncertain. This study addresses these issues using extracellular recordings of 5-HT neurones in the dorsal raphe nucleus of anaesthetised rats. 2. The 5-HT(2) receptor agonists DOI ((+/-)-2,5-dimethoxy-4-iodoamphetamine hydrochloride) and DOB ((+/-)-2,5-dimethoxy-4-bromoamphetamine hydrobromide), caused a dose-related (10-100 micro g kg(-1) i.v.) inhibition of 5-HT neuronal activity, with the highest dose reducing firing rates by |80%. 3. Pretreatment with the 5-HT(2) receptor antagonist ritanserin (1 mg kg(-1) i.v.) completely blocked the action of DOI. The 5-HT(2A) receptor antagonist MDL 100,907 (0.2 mg kg(-1) i.v.) blocked the action of both DOI and DOB. In comparison, the 5-HT(2B/C) receptor antagonist SB 206553 (0.5 mg kg(-1) i.v.) caused a small,
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Practical imaging constraints restrict the number of wavelengths that can be measured in a single Biolumines- cence Tomography imaging session, but it is unclear which set of measurement wavelengths is optimal, in the sense of providing the most information about the bioluminescent source. Mutual Information was used to integrate knowledge of the type of bioluminescent source likely to be present, the optical properties of tissue and physics of light propagation, and the noise characteristics of the imaging system, in order to quantify the information contained in measurements at different sets of wavelengths. The approach was applied to a two-dimensional sim- ulation of Bioluminescence Tomography imaging of a mouse, and the results indicate that different wavelengths and sets of wavelengths contain different amounts of information. When imaging at a single wavelength, 580nm was found to be optimal, and when imaging at two wavelengths, 570nm and 580nm were found to be optimal. Examination of the ...
Patients with myasthenia gravis (MG) initially have their condition diagnosed and medically stabilized by a neurologist, who then refers the patient to our surgeons. The surgeon first arranges for the patient to have a computed tomography (CT) scan to look for a potential thymoma as MG has about a 25 percent chance of being associated with a thymoma. Based on the findings of this test and other factors, we work with the patient to determine the most appropriate surgical course of treatment.. Our divisions physicians are highly skilled in performing transcervical thymectomy and video-assisted thoracoscopy (VATS), two minimally invasive procedures for thymus removal. We also perform standard open (i.e. transsternal) procedures. Recently, robotic-assisted minimally invasive thymectomy has been introduced as an additional option for selected patients. We have an excellent track record with all techniques in terms of patient outcomes.. Following surgery, the patients neurologist will provide ...
Assessment of anaesthetic depth is vital for safe anaesthesia, and has traditionally been based on clinical signs including eye position, ocular and palpebral reflexes, changes in heart and respiratory rate, muscle tone and response to noxious stimuli (Guedel 1927, Gillespie 1943, Hall and others 2001). During inhalant anaesthesia, the eye is ventromedially rotated during light or moderate planes of anaesthesia, and is central during inadequate or excessively deep planes of anaesthesia (Guedel 1927, Hall and others 2001). The aim of this study was to determine the eye position of cats anaesthetised with alfaxalone (AFX) or propofol (PRO) to a sufficient depth to perform orotracheal intubation.. The study was approved by the University of Bristol Ethics Committee, and informed, written, owner consent was obtained. Healthy cats (American Society of Anesthesiologists physical status 1) presented for routine neutering were enrolled in the study. Cats were randomly allocated to receive either AFX or ...
Dogs are often placed under general anesthesia for diagnostic and surgical procedures. Aside from the well-known risks of anesthesia, such as heart or lung depression, anesthetic agents can also suppress immune function. This poorly understood phenomenon is especially important in dogs that may already suffer from immune compromise, such as those with critical illness or cancer. The role of commonly used anesthetic agents, such as ketamine and propofol, on immune function in patients with cancer is being investigated in laboratory animals and humans, with ketamine increasing the spread of cancer to the lungs in rats compared to propofol. Unfortunately, there is no current research in dogs comparing these two anesthetic agents. Additionally, a newer anesthetic agent, alfaxalone, is gaining popularity for use in both healthy and critically ill dogs, but there is no research available on the effects of alfaxalone on immune function in dogs. Given the lack of information of the immune effects of these three
Global General Anaesthetics Key Trends and Opportunities to 2026. General Anesthesia Drugs, also known as general anaesthetics, is a kind of drug that can inhibit the central nervous system function, make the consciousness, feeling and reflection temporarily disappeared, skeletal muscle relaxation, mainly used for anesthesia before surgery.. COVID-19 outbreak will affect upstream, midstream, downstream of General Anesthesia Drugs in many ways. The promotion effect of short-term occupant economy factors in General Anesthesia Drugs market is obvious.. The major General Anaesthetic player in the market. Astrazeneca. Fresenius-Kabi. Abbott. Bayer. AbbVie. Baxter Healthcare. B.Braun. Maruishi. Piramal. Hikma Pharmaceuticals. Mylan. Lunan. Humanwell Healthcare. Nhwa Pharmaceutical. Guangdong Jiabo Pharmaceutical. Sichuan Guorui Pharmaceutical. Xian Libang Pharmaceutical. Sichuan Kelun Pharmaceutical. Hengrui Pharmaceutical. Shanghai United Imaging Healthcare. Wandong Medical Technology. The major ...
Döbeli, Alexandra. Apgar score of dog puppies deliverd by cesarean section using alfaxalone or propofol for anesthesia induction. 2013, University of Zurich, Vetsuisse Faculty. ...
The Drug Enforcement Administration (DEA) proposes the placement of 5[alpha]-pregnan-3[alpha]-ol-11,20-dione (alfaxalone) including its salts, isomers, and salts of isomers whenever the existence of such salts, isomers, and salts of isomers is possible, into Schedule IV of the Controlled...
Phaxan™ is an intravenous general anaesthetic and sedative containing alphaxalone as the active pharmaceutical ingredient. Alphaxalone is a neuroactive steroid anaesthetic. It is a pregnanedione with no endocrine hormonal activity. This water-insoluble drug was initially formulated using CremophorEL and marketed as Althesin® from 1972 to 1984. It was found to be a safe and versatile intravenous anaesthetic used in clinical practice in anaesthesia and intensive care in many countries until it was withdrawn from clinical practice because of hypersensitivity to the CremophorEL.. Many subsequent attempts to make an aqueous formulations of neuroactive steroids suitable for human use have failed. Drawbridge Pharmaceuticals proprietary and patented formulation, Phaxan™, is a solution of alphaxalone 10mg/ml dissolved in 13% SBECD (7- sulfobutylether β-cyclodextrin); a molecule with a lipophilic cavity that enables drug dispersal in water for human use. The use of SBECD as the excipient preserves ...
Source: Pharmarket sales statistics 1-12/2019. Orion is a significant player also in the Scandinavian generics market.. According to IQVIA pharmaceutical sales statistics, in Europe total sales of the most common intravenous anaesthetics and intensive care sedatives (propofol, midazolam, remifentanil and dexmedetomidine) in the 12-month period ending in September 2019 were up by 4% at EUR 595 (570) million. The active ingredient in Orions Dexdor® intensive care sedative is dexmedetomidine. The total sales of dexmedetomidine wasEUR 72 (69) million in Europe, according to IQVIA pharmaceutical sales statistics... Published on 23 October 2019. Finland is the most important individual market for Orion, generating about one-third of the Groups net sales. According to Pharmarket statistics (1-9/2019), the total sales of Orions human pharmaceuticals, including both medicinal and non-medicinal products, was behind market trend. The growth in the Finnish pharmaceuticals market has mostly been ...
General anaesthetic can make the pain of operations worse for patients recovering after surgery by activating the bodys mustard receptors, researchers have found. Many of the drugs that send surgical patients to sleep are known to make them more sensitive to pain when they wake up. Scientists now believe they have discovered the reason for the side effect. The findings may help researchers develop new anaesthetics that are kinder to recovering patients. General anaesthetics all suppress the central nervous system to cause unconsciousness and paralysis. But they can also activate pain-sensing cells in the peripheral nervous system, leading to post-operative discomfort. The new research focused on two of these pain receptors, TRPV1 and TRPA1, which often appear together and also react to irritants such as the chilli chemical capsaicin and mustard. Study leader Dr Gerard Ahern, from Georgetown University Medical Centre in Washington DC, said: Plants produce chemicals such as capsaicin, ...
How is Diazepam and Methohexital (drug combination) abbreviated? D-M stands for Diazepam and Methohexital (drug combination). D-M is defined as Diazepam and Methohexital (drug combination) very rarely.
Looking for online definition of methohexital in the Medical Dictionary? methohexital explanation free. What is methohexital? Meaning of methohexital medical term. What does methohexital mean?
Methohexital - Get up-to-date information on Methohexital side effects, uses, dosage, overdose, pregnancy, alcohol and more. Learn more about Methohexital
A Hysterectomy is a surgical procedure to remove the uterus from women. It is a major surgery that requires general anaesthetics, multiple days in hospital and weeks of rest and recovery.
Alfadolone was not included in the mixture, as its hypnotic effects were quite weak. An aqueous form of Alfaxan was released in ... Most of these efforts were aimed at making alfaxalone more water-soluble. In 1971, a combination of alfaxalone and alfadolone ... Alfaxalone was marketed in 1971 in combination with alfadolone acetate under the brand name Althesin for human use and Saffan ... Alfaxalone is mostly excreted in the urine, though some is excreted in the bile as well. Alfaxalone, also known as 11-oxo-3α,5α ...
... alfaxalone alfadolone mixture MeSH D04.808.745.558.783 - tetrahydrocortisone MeSH D04.808.745.620 - pregnanetriol MeSH D04.808. ...
... alfadolone (INN) alfaprostol (INN) alfaxalone (INN) Alfenta (Taylor) redirects to alfentanil alfentanil (INN) alferminogene ... mixture of fexofenadine and pseudoephedrine Allegra (Sanofi-Aventis), also known as fexofenadine Aller-Chlor Allercon Tablet ...
Alfaxalone Alfadolone Mixture D4.808.745.558.50 D4.210.500.745.558.50 Algestone D4.808.745.745.654.829.25 D4.210.500.745. ...
ALFAXALONE ALFADOLONE MIXTURE. APROCARB. PROPOXUR. CHOLERA VACCINE. CHOLERA VACCINES. CREATINE KINASE ISOENZYMES. CREATINE ...
ALFAXALONE ALFADOLONE MIXTURE. APROCARB. PROPOXUR. CHOLERA VACCINE. CHOLERA VACCINES. CREATINE KINASE ISOENZYMES. CREATINE ...
ALFAXALONE ALFADOLONE MIXTURE. APROCARB. PROPOXUR. CHOLERA VACCINE. CHOLERA VACCINES. CREATINE KINASE ISOENZYMES. CREATINE ...
ALFAXALONE ALFADOLONE MIXTURE. APROCARB. PROPOXUR. CHOLERA VACCINE. CHOLERA VACCINES. CREATINE KINASE ISOENZYMES. CREATINE ...
Alfaxalone Alfadolone Mixture - Preferred Concept UI. M0362311. Scope note. A 3:1 mixture of alfaxalone with alfadolone acetate ... Mélange alfaxalone alfadolone Entry term(s):. Alfadolone Mixture, Alfaxalone. Alfatesine. Alfathesin. Alphadione. Alphathesin. ... A 3:1 mixture of alfaxalone with alfadolone acetate that previously had been used as a general anesthetic. It is no longer ... Alfaxalone Alfadolone Mixture Entry term(s). Alfadolone Mixture, Alfaxalone Alfathesin - Narrower Concept UI. M0351497. ...
ALFAXALONE ALFADOLONE MIXTURE. APROCARB. PROPOXUR. CHOLERA VACCINE. CHOLERA VACCINES. CREATINE KINASE ISOENZYMES. CREATINE ...
ALFAXALONE ALFADOLONE MIXTURE. APROCARB. PROPOXUR. CHOLERA VACCINE. CHOLERA VACCINES. CREATINE KINASE ISOENZYMES. CREATINE ...
ALFAXALONE ALFADOLONE MIXTURE. APROCARB. PROPOXUR. CHOLERA VACCINE. CHOLERA VACCINES. CREATINE KINASE ISOENZYMES. CREATINE ...
ALFAXALONE ALFADOLONE MIXTURE. APROCARB. PROPOXUR. CHOLERA VACCINE. CHOLERA VACCINES. CREATINE KINASE ISOENZYMES. CREATINE ...
ALFAXALONE ALFADOLONE MIXTURE. APROCARB. PROPOXUR. CHOLERA VACCINE. CHOLERA VACCINES. CREATINE KINASE ISOENZYMES. CREATINE ...
ALFAXALONE ALFADOLONE MIXTURE. APROCARB. PROPOXUR. CHOLERA VACCINE. CHOLERA VACCINES. CREATINE KINASE ISOENZYMES. CREATINE ...
ALFAXALONE ALFADOLONE MIXTURE. APROCARB. PROPOXUR. CHOLERA VACCINE. CHOLERA VACCINES. CREATINE KINASE ISOENZYMES. CREATINE ...
ALFAXALONE ALFADOLONE MIXTURE. APROCARB. PROPOXUR. CHOLERA VACCINE. CHOLERA VACCINES. CREATINE KINASE ISOENZYMES. CREATINE ...
ALFAXALONE ALFADOLONE MIXTURE. APROCARB. PROPOXUR. CHOLERA VACCINE. CHOLERA VACCINES. CREATINE KINASE ISOENZYMES. CREATINE ...
ALFAXALONE ALFADOLONE MIXTURE. APROCARB. PROPOXUR. CHOLERA VACCINE. CHOLERA VACCINES. CREATINE KINASE ISOENZYMES. CREATINE ...
... alphadolone and alphaxalone (also known as alfaxalone). Last idea seems odd to us in that extent their labia had injection ... especially teens irreversible stretch marks a heightened tendency for hair it is composed of a mixture of two neurosteroids, ...
Alfaxalone Alfadolone Mixture Preferred Concept UI. M0362311. Registry Number. 8067-82-1. Scope Note. A 3:1 mixture of ... Alfaxalone Alfadolone Mixture Preferred Term Term UI T414229. Date05/15/2000. LexicalTag NON. ThesaurusID NLM (2001). ... A 3:1 mixture of alfaxalone with alfadolone acetate that previously had been used as a general anesthetic. It is no longer ... Alfaxalone Alfadolone Mixture. Tree Number(s). D04.210.500.745.558.050. Unique ID. D000530. RDF Unique Identifier. http://id. ...
ALFAXALONE ALFADOLONE MIXTURE. APROCARB. PROPOXUR. CHOLERA VACCINE. CHOLERA VACCINES. CREATINE KINASE ISOENZYMES. CREATINE ...
Alfaxalone Alfadolone Mixture Preferred Concept UI. M0362311. Registry Number. 8067-82-1. Scope Note. A 3:1 mixture of ... Alfaxalone Alfadolone Mixture Preferred Term Term UI T414229. Date05/15/2000. LexicalTag NON. ThesaurusID NLM (2001). ... A 3:1 mixture of alfaxalone with alfadolone acetate that previously had been used as a general anesthetic. It is no longer ... Alfaxalone Alfadolone Mixture. Tree Number(s). D04.210.500.745.558.050. Unique ID. D000530. RDF Unique Identifier. http://id. ...
Aldrin N0000010038 alefacept N0000010039 alemtuzumab N0000006657 Alendronate N0000167424 Alfaxalone Alfadolone Mixture ... Complex N0000169269 Complement System Proteins N0000169351 Complementarity Determining Regions N0000011165 Complex Mixtures ...
Alfaxalone Alfadolone Mixture D4.808.745.558.50 D4.210.500.745.558.50 Algestone D4.808.745.745.654.829.25 D4.210.500.745. ...
Alfaxalone Alfadolone Mixture D4.808.745.558.50 D4.210.500.745.558.50 Algestone D4.808.745.745.654.829.25 D4.210.500.745. ...
Alfaxalone Alfadolone Mixture D4.808.745.558.50 D4.210.500.745.558.50 Algestone D4.808.745.745.654.829.25 D4.210.500.745. ...
Alfaxalone Alfadolone Mixture D4.808.745.558.50 D4.210.500.745.558.50 Algestone D4.808.745.745.654.829.25 D4.210.500.745. ...
Alfaxalone Alfadolone Mixture D4.808.745.558.50 D4.210.500.745.558.50 Algestone D4.808.745.745.654.829.25 D4.210.500.745. ...
Saffan use Alfaxalone Alfadolone Mixture Safflower use Carthamus tinctorius Safflower Oil Safflower Oils use Safflower Oil ...
Alfaxalone Alfadolone Mixture Alfentanil Algal Proteins Algeria Algestone Algestone Acetophenide Alginates Algorithms TERM ... Complex Mixtures Complex Regional Pain Syndromes Compliance Complicity Compomers Composite Lymphoma Composite Resins Composite ... Ampholyte Mixtures Amphotericin B Ampicillin Ampicillin Resistance Amplified Fragment Length Polymorphism Analysis Amplifiers, ...
... orbignyi borborygmi borborygmus Bordeaux bordeaux mixture Bordeaux mixture border border cell border cells border disease ... alexithymic alexithymics alexomycin Aleyrodidae AlF ALF alfa alfa-2b AlFABdCTP alfacalcidol alfacon-1 alfacron alfadolone ... alfalfa weevil alfalfa weevils alfamovirus Alfamovirus alfamoviruses alfaprostol alfare alfas alfatesine alfathesin alfaxalone ... acid analyzer aminoacid analyzer amino acid analyzers aminoacid analyzers aminoacidemia amino acid mixture amino acid mixtures ...
... orbignyi borborygmi borborygmus Bordeaux bordeaux mixture Bordeaux mixture border border cell border cells border disease ... alexithymic alexithymics alexomycin Aleyrodidae AlF ALF alfa alfa-2b AlFABdCTP alfacalcidol alfacon-1 alfacron alfadolone ... alfalfa weevil alfalfa weevils alfamovirus Alfamovirus alfamoviruses alfaprostol alfare alfas alfatesine alfathesin alfaxalone ... acid analyzer aminoacid analyzer amino acid analyzers aminoacid analyzers aminoacidemia amino acid mixture amino acid mixtures ...
The most commonly used catalyst is a mixture of potassium chloride and aluminum chloride. However, various forms of porous ... Alfadolone. * Alfaxalone. * Anabolic steroids. * 3α-Androstanediol. * Androstenol. * Androsterone. * Cholesterol. * DHDOC. * 3α ...

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