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The 443 prescriptions listed 136 different drugs; 118 prescriptions were "as required" 26.6% ; . The most common drugs were: paracetamol 74 ; , gluco-saline 29 ; , co-amoxiclav 29 ; , morphine 26 ; , ondansetron 26 ; , mefenamic acid 26 ; , ibuprofen 22 ; , and salbutamol 21 ; . 33.4% of drugs were given intravenously, 27.1% orally, 18.5% rectally, 7.2% via an aerosol, and 13.8% by another route of administration. Of the prescriptions, for mandatory criteria, 12.6% were safe Fig. 1 ; and 77.0% were unambiguous Table 2. The drug list is a guide within select therapeutic categories for plan participants. Generics should be considered the first line of prescribing. If there is no generic available, there may be more than one brand name medicine to treat a condition. These preferred brand name medicines are listed to help identify products that are clinically appropriate and cost-effective. Generics listed in therapeutic categories are for representational purposes only and not meant to be all-inclusive. This list represents brand products in CAPS and generic products in lower case italics, because pulvinal salbutamol.Subjects Sixteen clinically stable patients with COPD forced expiratory volume in 1 second FEV1 ; 60% predicted, FEV1 forced vital capacity FVC ; , 70% ; who were not hypoxic resting arterial oxygen tension PaO2 ; .65 mm Hg 8.7 kPa ; , exercise oxygen saturation SaO2 ; 88% ; and had significant activity related breathlessness modified Baseline Dyspnoea Index score 6 ; 14 were studied. Patients with significant cardiovascular disease, other pulmonary disease, or other disorders that could contribute to dyspnoea or exercise limitation were excluded. Study design This randomised, double blind, placebo controlled, crossover study was approved by the local university hospital research ethics committee. Subjects were recruited from a list of patients who had participated in previous exercise studies. After giving informed consent and screening of medical history, patients were familiarised with all procedures and completed pulmonary function tests and a symptom limited incremental cycle exercise test. During four subsequent visits conducted 27 days apart, subjects received one of four treatment combinations in random order: bronchodilator BD ; + room air RA ; , placebo PL ; + RA, BD + O2, or PL + O2. At these visits subjects were given either PL or BD, they waited 105 15 ; minutes before performing pulmonary function tests, then completed a constant load cycle endurance test at 75% of their maximal incremental work rate while breathing either RA or 50% O2. Subjects adhered to the standard withdrawal of bronchodilators before testing: short acting b2 agonists 4 hours ; , short acting anticholinergics 6 hours ; , long acting b2 agonists 12 hours ; , long acting anticholinergics 48 hours ; , theophyllines 48 hours ; , and antileukotrienes 48 hours ; . Subjects avoided caffeine, alcohol, and heavy meals for 4 hours before testing and avoided major physical exertion entirely on visit days. Interventions PL and BD were administered by nebuliser Parimaster compressor with Pari LC Jet + nebuliser; PARI Respiratory Equipment Inc, Richmond, VA, USA ; in a double blind fashion. The BD used was Combivent 0.5 mg ipratropium bromide + 2.5 mg salbutamol ; and PL was sterile 0.9% saline solution. Subjects breathed either RA 21% O2 ; or 50% O2 on demand from a 200 l Douglas bag reservoir for at least 10 minutes at rest before starting exercise and throughout exercise; they were blinded to the gas mixture being breathed at each test. Procedures Pulmonary function measurements were collected using automated equipment Vmax229d with Autobox 6200 DL; SensorMedics, Yorba Linda, CA, USA ; and expressed as percentages of predicted normal values; 1520 predicted IC was calculated as predicted total lung capacity TLC ; minus predicted functional residual capacity FRC ; . Symptom limited exercise tests were conducted on an electrically braked cycle ergometer Ergometrics 800S; SensorMedics ; using a cardiopulmonary exercise testing system Vmax229d; SensorMedics ; . Incremental testing was performed at the first visit. Subsequent constant load tests were conducted at 75% of the maximal incremental work rate. Exercise test measurements included intensity of dyspnoea breathing discomfort ; and leg discomfort using the 10-point modified Borg scale; 21 operating lung volumes derived from IC manoeuvres; 22 23 arterialised capillary blood samples taken from. TABLE 4. Tocolytic magnesium sulfate exposure among children with cerebral palsy and control children, by birth weight, Atlanta, Georgia, 19911992, for instance, salbutamol side effect. 1. What led you to write this book? 2. How is DRUGS FOR LESS different from other books out there? 3. Why don't people hear about the alternatives to brand-name drugs? 4. Why do people pay so much for their drugs? 5. Do people with prescription drug coverage have to worry about the cost of prescription drugs? 6. Briefly, what are the Seven Strategies for obtaining cheaper medication? 7. A lot of people are turning to online pharmacies to get their medicine. Is this really safe?. When apples or potatoes are peeled and sliced for eating or cooking, a relatively rapid change depending on the time of year ; takes place, and the tissues brown. The purpose of the series of experiments associated with this section is to determine the conditions which affect the rate of this reaction and to determine whether it is microbial or biochemical. Then you can try to devise methods of avoiding or controlling the spoilage without harming the texture and flavour of the food and introducing toxic additives. Fruit-browning reactions are studied because they are relatively simple and safe ; when compared with more complicated types of food spoilage, such as fat oxidation, maturation of meat, and pectin changes in vegetables. But the same principles apply in all these cases and alfacalcidol.
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Bronchoalveolar lavage BAL ; fluid from patients treated with placebo or salbutamol on wound closure was determined. Cell proliferation in response to control media or 10-6 M salbutamol was measured using the MTT assay. Results: Salgutamol increased wound repair salbutamol 75 4.1 ; % vs control 44.7 7.1 ; %, P 0.001 ; . This effect was blocked 10-5 M propranolol 55.5 4.6 ; %, P 0.008 ; . Salbtamol had no effect on A549 cell proliferation 1.30 0.3 ; OD vs 1.33 0.3 ; OD, P 0.8 ; . Compared to saline control, BAL fluid from patients at the onset of ARDS significantly increased wound repair BAL fluid 40.1 4 ; % vs saline 20.2 3 ; %, P 0.001 ; . Wound closure following incubation of BAL fluid from patients after 4 days treatment with IV salbutamol was significantly greater than for placebo treated patients salbutamol 52.7 4.4 ; % vs placebo 46.2 4.3 ; % respectively, P 0.008 ; . Conclusion: Physiological concentrations of salbutamol significantly increased wound repair. BAL fluid from patients treated in a randomized controlled trial with IV salbutamol stimulated significantly greater wound repair than BAL fluid from patients in the placebo arm suggesting salbutamol may have an effect on repair of the alveolar capillary barrier and calciferol.
Oxygen Give oxygen to all children with asthma who are cyanosed or whose difficulty in breathing interferes with talking, eating or breastfeeding. See page 86. Rapid-acting bronchodilators Give the child one of the three rapid-acting bronchodilators--nebulized salbutamol, salbutamol by metered-dose inhaler with a spacer device, or subcutaneous epinephrine adrenaline ; , as described below. 1 ; Nebulized salbutamol The driving source for the nebulizer must deliver at least 69 litres minute. Recommended methods are an air compressor or oxygen cylinder. If neither is available, use a durable and easy-to-operate foot-pump, although this is less effective.
In prison it is not uncommon for a woman to discover she is pregnant at the same time she discovers she has HIV infection. The psychological burden of being in prison, leaving behind her family, a new pregnancy and discovering her HIV status can be devastating for women who are often fragile and vulnerable. They may also have apprehensions about their pregnancy, about infecting their baby, and about losing custody of the newborn. Ethical dilemmas can arise if the woman refuses to disclose her diagnosis of HIV to the baby's father. In all cases, much empathy and patient counselling are paramount to ensure the best conditions possible for mother and baby in what is always a complicated situation. The patient's confidentiality should not be waived under the pretext that she is a prisoner, but some informed disclosure may be necessary to those who need to know, so as to obtain the best possible medical care for example, in planning a caesarean section ; . Immune function is suppressed as a normal effect of pregnancy in both HIV-positive and -negative women. In early pregnancy, levels of both immunoglobulin and complement are reduced, and there is a significant decrease in cell-mediated immunity during pregnancy. Research has shown, however, that these normal changes do not and alpha-lipoic.
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While drug therapy is effective in relieving the biological component of depression, it is recommended that a combination of drug and psychological therapy be used and amantadine.
Received October 23, 2003; de novo received March 22, 2004; revision received June 1, 2004; accepted June 23, 2004. From the Departments of Biochemistry and Molecular Biology T.M.T., S.G.S., B.M.S., Y.X., R.E.K. ; and Obstetrics, Gynecology, and Reproductive Sciences M.-C.D., L.C.G. ; , The University of Texas Health Science Center at Houston. Guest Editor for this article was Joseph Loscalzo, MD, PhD. Correspondence to Dr Rodney E. Kellems, Department of Biochemistry and Molecular Biology, University of Texas Health Science Center at Houston, 6431 Fannin St, Houston, TX 77030. E-mail rodney.e.kellems uth.tmc 2004 American Heart Association, Inc. Circulation is available at : circulationaha DOI: 10.1161 01.CIR.0000142855.68398.3A.
Salactol 13.7 salbutamol 3.1.1.1 salcatonin 6.6.1 salmeterol 3.1.1.1 sandocal 9.5.1.1 saquinavir 5.3.1 Scheriproct 1.7.2 Sebco 13.9 selegiline 4.9.1 selenium sulphide 13.9 semisodium valproate 4.2.3 senna 1.6.2 Seretide 3.2 sermorelin 6.5.1 sertraline 4.3.3 sevoflurane 15.1.2 sildenafil 7.4.5 silver sulfadiazine 13.10.1.1 simple linctus 3.9.2 simvastatin 2.12 Sinemet 4.9.1 sodium aurothiomalate 10.1.3 sodium bicarbonate 9.2.1.2 9.2.1.3 12.1.3 sodium chloride 9.2.1.2 12.3.4 13.11.1 sodium clodronate 6.6.2 sodium cromoglicate 3.3.1 11.4.2 12.2.1 sodium feredetate 9.1.1.1 sodium fluoride 9.5.3 sodium nitroprusside 2.5.1 sodium picosulfate 1.6.2 1.6.5 sodium polystyrene sulphonate 9.2.1.1 sodium tetradecyl sulphate 2.13 sodium valproate 4.8.1 somatropin 6.5.1 sotalol 2.3.2 2.4 spironolactone 2.2.3 stavudine 5.3.1 streptokinase 2.10.2 streptomycin 5.1.9 sucralfate 1.3.3 Sudocrem 13.2.2 sulfasalazine 1.5 10.1.3 sulpiride 4.2.1 4.9.3 Sultrin 7.2.2 sumatriptan 4.7.4.1 Sunsense Ultra 13.8.1 surgical spirit 13.11.1 suxamethonium 15.1.5 Symbicort 3.2 Synalar C 13.4 Synalar 13.4 syntometrine 7.1.1 Sytron 9.1.1.1 and amiloride.
Pleural empyema in a 14-year-old adolescent with cystic fibrosis Griffiths AL, Massie J. J Paediatr Child Health 42: 396397, 2006, for example, salbutamol abuse.
Abstract The purpose of this study was to measure serum magnesium Mg ; levels in order to determine the effect of salbutamol on them and correlate the Mg levels to the reduction of clinical severity scores in acute severe asthma. Thirty three patients met the inclusion criteria. The mean serum Mg levels were significantly lower than the normal population [1.45 SD 0.22 ; VS 1.64 SD 0.04 ; mEq L, p 0.001]. In the MgSO4 treated group, the mean percentage reduction in severity score correlated negatively to the percentage change of Mg levels from the baseline correlation coefficient -0.38, p 0.549 ; . In the control group, the cumulative doses of salbutamol correlated weakly and negatively to the change in serum Mg levels after 240 min correlation coefficient - 0.005, p 0.431 ; . This study concluded that Serum Mg levels in severe asthmatic patients were significantly lower than those in the normal population. The improvement of clinical severity score did not significantly correlate to the increment of serum Mg levels. The administration of nebulized salbutamol in acute severe asthma did not significantly affect serum Mg levels. Chiang Mai Med Bull 2001; 40 1 ; : 1-5 and amiodarone.
In this paper, affordability is calculated in terms of the number of days the lowest paid unskilled government worker would have to work to pay for one treatment course for an acute condition or one month's treatment for a chronic condition. At the time of the survey, 4 the lowest paid unskilled government worker earned ETB 6.7 US$ 0.80 ; per day. According to a Ministry of Finance and Economic Development report, 44.2% of Ethiopians earn less than 5 US$1 per day . Overall, purchasing treatments for chronic conditions was found to require many more days' work than purchasing treatments for acute conditions. The burden is especially great for a family needing treatment for several conditions at the same time, e.g. using the lowest priced generic medicines, it would take just under 5 days' wages for the lowest paid unskilled government worker to purchase in the private sector a salbutamol inhaler for a child with asthma, a course of cotrimoxazole suspension for a child with a respiratory tract infection, glibenclamide tablets for an adult with diabetes and hydrochlorothiazide tablets for an adult with hypertension. If the innovator brands are bought, the month's salary would not be sufficient as 32.5 days wages would be needed.
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Place ; in boxes as appropriate and fill in blanks. Place patient in resuscitation area immediately. Notify physician and RT. Oxygen to maintain SpO2 Adult 92% Peds 95% Adult Continuous 5.0 mg Salgutamol by neb until improvement and 0.5mg Ipratropium Bromide with the first 2 neb treatments Peds 5.0 mg Salbutamol, then continuous 2.5 mg Albutamol 0.25 mg Ipratropium Bromide Q 30 min.
Drug Administration. The drugs used were salbutampl a 2-AR partial agonist ; , alprenolol a 1 2 antagonist with partial 2 agonist activity; refs. 1921 ; , nadolol and carvedilol both 1 2 antagonist with inverse agonist activity at the 2-AR' refs. 22 and 23 ; . To examine the effects of duration of -AR ligand therapy on the phenotype of the murine model of asthma, the experimental drugs were administered either acutely or chronically to different groups of asthmatic mice. Asthmatic mice on acute therapy were given a single i.v. bolus infusion of either -AR ligand or normal saline on protocol day 28, 15 min before airway responsiveness to methacholine was determined. The doses of carvedilol, nadolol, alprenolol, and salbutamol administered to the mice were 24 mg kg 1, 72 mg kg 1, 72 mg kg 1, and 1.2 mg kg 1, respectively. Asthmatic mice on chronic therapy were treated with -AR ligand from protocol days 1 to 28. Those on -blocker therapy had free access to chow treated with carvedilol, nadolol, or alprenolol at concentrations of 2, 400 ppm, 250 ppm, or 7, 200 ppm, respectively. These concentrations were chosen because they had previously been shown to produce effects in mice 24, 25 ; . The i.v. bolus doses were calculated to approximate the loading dose required to achieve similar blood levels to those obtained at steady-state with chronic treatment. The nontreated asthmatic mice were fed normal chow. Salbutajol was delivered for 28 days at a dose of 0.5 mg kg 1 day 1 by using an osmotic minipump Alzet no. 2004, Durect, Cupertino, CA ; . Animal Preparation, Lung Physiology, and Bronchoalveolar Lavage and elavil.
Summary: in contrast to asthma, inhaled corticosteroids should not be used as a first-line medication in patients with copd.
University of Colorado School of Pharmacy and at kaiser Permanente, both in Denver. AliSon E. DoBBiE, M.D., is the vice chair of and a professor in the Department of Family and Community Medicine at the University of Texas Southwestern Medical School at Dallas. She received her medical degree from the University of Glasgow in Scotland and completed her family medicine residency in Edinburgh, Scotland. Dr. Dobbie also completed a fellowship in academic medicine at the Faculty Development Center in Waco, Tex. Address correspondence to Madelyn Pollock, M.D., University of Kansas Medical Center, Dept. of Family Medicine, 3901 Rainbow Blvd., MS# 4010, Kansas City, KS 66160 e-mail: madelyn.pollock gmail ; . Reprints are not available from the authors. Author disclosure: nothing to disclose. REFERENCES and endep and salbutamol, for example, buy salbutamol inhaler.
Prescribing notes for topical psoriasis preparations 1 Vitamin D analogues do not smell or stain clothing. The use of emollients before treatments should be encouraged to ensure that the cream or ointment reaches the affected area. 2 Notes on the use of Dithrocream: Dithrocream needs to be applied carefully to lesions. Hands should be washed carefully after use. When using a higher concentration of Dithrocream it is advisable to use a wooden spatula or disposable gloves; Dithrocream will burn any surrounding non-psoriatic skin. Applying Vaseline as a barrier will help prevent this; Dithrocream should only be applied to psoriatic plaques, avoiding flexural areas. Application in the flexures causes smudging onto clear skin, which results in burning and soreness; Dithrocream can be left on psoriatic plaques for 30 minutes or longer but preferably not overnight to avoid the risk of it spreading onto healthy skin; If required for the face it should be applied with caution. On the scalp it may stain fair or grey hair pink which is permanent until the hair grows out. The brown staining of Dithranol on the skin is temporary and will usually disappear approximately 14 days after treatment. It will, however, stain clothing, furniture and bedding permanently. The bath and shower should be cleaned immediately after use to help prevent staining; Where scalp application is required it should be combed against the direction of growth to help lift the scale. For overnight use, bed clothing should be protected. A tar-based shampoo should be used in the morning to remove the treatment; Dithrocream is a long-term treatment for psoriasis. It is important to continue with daily applications for several weeks, increasing the strength as necessary.
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This association of salbutamol and beclomethasone is specially provided for those patients who require regular doses of both drugs for treatment of their obstructive airways disease.
SYNAPTOGENESIS IN MATURE BRAIN ing 8 hours in vitro when synaptic transmission was blocked. These findings suggest that blocking synaptic transmission prolonged the process of synaptogenesis on mature hippocampal dendrites, preventing them from progressing to their more mature forms. An open question is how long can the immature forms remain synaptogenic before they are lost in the absence of synaptic activity? The observation that multiple synapses continue to form in the dentate gyrus of adult rats during several months after destruction of the entorhinal cortex Steward and Vinsant, 1983 ; implies that under these conditions of reduced overall synaptic activity immature forms continue to appear for an extended period of time. Live-imaging with multiphoton microscopy shows that mature hippocampal dendrites also produce more elongated filopodia after exposure to cold for only 20 13 minutes Kirov et al., 2004a ; . Additional experiments are required to determine the exact dynamics and turnover rate of filopodia on mature hippocampal neurons and whether reinstatement of synaptic activity will induce spine maturation and or competitive elimination of the immature forms. Mature neurons of mentally retarded adults exhibit numerous dendritic filopodia Fiala et al., 2002b ; , suggesting that the failure of filopodia to mature leads to aberrant synaptic networks. Further understanding of the exact mechanisms by which dendritic spines are induced and how they establish appropriate synaptic connections in the mature brain are crucial to the development of appropriate treatments. If, indeed, reduced synaptic activity is required in the intact mature brain, then knowing when to tap into this responsive synaptogenesis, for example, after a stroke, could also mean the difference between loss and recovery of function. Variation in brain activity during the sleepwake cycle may also provide a mechanism for the induction and preservation of spine synapses or the elimination of unconsolidated synapses in the mature brain.
ABSTRACT Albumin microspheres AMS ; have found many applications in the diagnosis and treatment in recent years and more than 100 diagnostic agents and drugs have been incorporated into AMS. In the present study Bovine Serum Albumin BSA ; based microspheres bearing propranolol hydrochloride were prepared by an emulsion-internal phase stabilization technique. The prepared microspheres were studied for particle size distribution, drug loading, release characteristics, bioadhesion and in-vitro controlled diffusion across the rat intestine. The microspheres had mean diameters between 1-25 m of which more than 50 percent were below 5 m. The encapsulated drug was found to be about 9% w w of that initially added to microspheres and the superficial drug was 25% of the total amount of the encapsulated drug. Also AMS were noted to possess good bioadhesion in such a way that about 70% of microspheres remained adherent on the surface mucosa of rat jejunum.The drug release from albumin microspheres was mainly controlled by diffusion and showed a biphasic pattern with a high initial release burst effect ; , followed by a more gradual terminal release. The total amount of drug released from microspheres after 12h was 70%. In vitro experiments on the rat intestinal segments revealed that the microspheres could effectively pass their content through intestinal membrane. Key words: Albumin microspheres, Propranolol, Bioadhesion, Release, Size distribution INTRODUCTION Microspheres can be defined as solid, approximately spherical particles ranging in size from 1 to 1000 m 1 ; . They are made from polymeric, waxy, or other protective materials such as starches, gums, proteins, fats and waxes and used as drug carrier matrices for drug delivery. Albumin and gelatin are among the natural polymers which are used in preparation of microspheres. Preparation of uniformly sized AMS was first reported in the late 60's and early 70's 2, 3, ; . AMS have received wide attention during the recent decades due to their specificity 5 ; , biodegradability 6 ; and other desirable characteristics such as non-toxicity and biocompatibility 7 ; as an ideal drug carrier. More than 100 therapeutic and diagnostic agents have been incorporated into albumin microspheres and drugs of various therapeutic categories such as nifedipine 8, 9 ; , mitoxantrone 10 ; , dexamethasone 11 ; , salbutamol sulfate 12 ; have been prepared and characterized as AMS delivery systems. Two methods have been developed for the preparation of albumin microspheres which include heat stabilization and chemical cross-linking by using glutaraldehyde 13 ; . Propranolol is a beta adrenergic blocking agent which is widely used in the treatment of angina pectoris, high blood pressure and migraine prophylaxis. The need for controlled systemic delivery of propranolol by some convenient delivery system is well established and a microsphere prepared from Human Serum Albumin HSA ; was one of those systems which were studied for its nasal delivery 14 ; . Due to variable absorption rates and high first pass metabolism of the oral route, several other researchers have also attempted to deliver propranolol via nasal route 15, 16 ; . The aim of the present study was to prepare and characterize Bovine Serum Albumin BSA ; microspheres loaded with propranolol HCl. BSA microspheres were prepared by an emulsification technique and stabilized by heat denaturation. The prepared microspheres were then studied for their particle size, size distribution, release characteristics, bioadhesion and drug diffusion profile across the rat intestine. MATERIALS AND METHODS Chemicals Bovine Serum Albumin and sorbitan mono.
In Vitro Aerosol Deposition Profiles The in vitro ACI deposition of salbutamol and BDP determined from 10 actuations of the Ventide inhaler are summarized in Table 1. Figure 1 shows the relative deposition masses for salbutamol and BDP on the ACI stages. A mean shot weight of 83.2 1.6 mg was recorded for the 30 actuations. Scanning Electron Microscopy A representative electron photomicrograph from Plate 3 is reproduced in Figure 2. The image shown is the same deposit and the area is of a similar size to that analyzed by Raman mapping, but with a different orientation. In general, irregu.
Antithrombotic flufosal 42 ; various: antituberc. fenamisal 15 ; , thiomersal 1 ; disinfect. ; , triflusal 37 ; antithrombotic ; -salanalgesic anti-inflammatory A.4.2.0 acetaminosalol 1 ; , acetylsalicylic acid IP ; , carbasalate calcium 27 ; , carsalam 13 ; , etersalate 50 ; , etosalamide 14 ; , parsalmide 32 ; , talosalate 43 ; various amotosalen 85 ; , calcium benzamidosalicylate 10 ; , homosalate 28 ; sunscreen agent ; , lasalocid 30 ; antibiotic. vet. ; , mersalyl 4 ; mercurial diuretic ; , octisalate 83 ; sunscreen ; , osalmid 15 ; choleretic ; , xenysalate 12 ; antiseborrheic ; salazophenylazosalicylic acid derivatives antibact. S.5.l.0 salazodine 22 ; , salazosulfadimidine 11 ; , salazosulfamide 1 ; , salazosulfathiazole 1 ; -salazine -salazide dersalazine 86 ; , mesalazine 52 ; , olsalazine 52 ; , sulfasalazine 55 ; , balsalazide 48 ; , ipsalazide 48 ; -salan brominated salicylamide derivatives disinfect. S.2.l.0 bensalan 18 ; , dibromsalan 14 ; , flusalan 16 ; , fursalan 18 ; , metabromsalan 16 ; , tiosalan 18 ; , tribromsalan 14 ; b ; non-salicylic acid derivatives macrosalb 99mTc ; 33 ; , trioxysalen l6 ; pigmenting agent ; bronchodil. levosalbutamol 78 ; , salbutamol 20 ; , salmefamol 23 ; c ; analgesic, anti-inflammatory A.4.2.0 aloxiprin 13 ; , anilamate 13 ; , benorilate 21 ; , brosotamide 29 ; , cresotamide 28 ; , dibusadol 24 ; , dipyrocetyl 6 ; , ethenzamide 10 ; , fenamifuril 16 ; , hydroxytoluic acid 17 ; , sodium gentisate 1 ; , sodium glucaspaldrate 17 ; various 4-aminosalicylates of the -caine series D.1.0.0: ambucaine 6 ; , hydroxyprocaine 1 ; , hydroxytetracaine 1 ; , propoxycaine 4 ; antihypertensives H.3.0.0 labetalol 35 ; antitussives K.1.0.0 alloclamide l6 ; , flualamide 20 ; saluretics N.l.2.0 xipamide 22 ; sulfamoyl deriv and alfacalcidol.
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