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H1 antihistamines have been reported to have a beneficial effect in a variety of other disorders, including mastocytosis, local reactions to mosquito bites, polycythemia vera, neurofibromatosis, eosinophilic gastroenteritis, eosinophilic fasciitis, interstitial cystitis, aphthous ulceration, lichen nitidus, rheumatoid arthritis, scleroderma, myotonic congenita, topical analgesia, chronic fatigue syndrome, and even malaria.267-273 In some of these disorders, there is a sound rationale, supported by one or more prospective, randomized, double-blind, placebo-controlled studies, for H1 antihistamine use. For example, in mastocytosis, plasma histamine concentrations are elevated and H1 antihistamines are effective in symptom relief267; cetirizine, ebastine, and, to a lesser extent, loratadine, significantly reduce mosquito biteinduced local reactions268; and hydroxyzine is one of the most effective medications available for control of pruritus in polycythemia vera.269 Interestingly, the mechanism by which an H1 antihistamine such as chlorpheniramine delays development of resistance to chloroquine during malaria treatment in children, as confirmed in randomized, placebo-controlled, double-blind studies, involves a pharmacokinetic interaction between the drugs, leading to decreased chloroquine clearance and increased plasma chloroquine concentrations.273 In most of the other disorders listed, however, claims of H1 antihistamine efficacy are anecdotal and are not supported by randomized, placebo-controlled, double-blind trials: either such trials have not been performed, or they have been performed with negative results.

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EENT Preparations: Antiallergic Agents AHFS Class 520200 ; Manufacturer comments on behalf of these products: Astelin-MedPointe Pharmaceuticals Elestat-Inspire Pharmaceuticals Optivar-MedPointe Pharmaceuticals Patanol-Alcon Laboratories Dr. Ferris explained there are 11 drugs in this class of which 10 drugs are available for ophthalmic administration and 2 products are available for nasal administration. Ophthalmic cromolyn is available generically. Nasal cromolyn is available over-the-counter. The agents included in this review demonstrate antihistaminic, mast-cell stabilizing or combination antihistaminic and mast-cell stabilizing properties. Dr. Ferris noted that agents with antihistaminic properties have a faster onset of action, provide quicker relief and will treat the acute symptoms. Agents with mast-cell stabilizing properties have a slower onset of action and are more effective when used chronically in the prevention of allergic symptoms. Drug interactions are minimal or have not been reported due to low systemic bioavailability of the ophthalmic and nasal preparations. Adverse events are comparable for all of the products with local transient burning and headache most frequently reported. Nasal azelastine was associated with a higher incidence of bitter taste than nasal cromolyn. The dosing schedules for the ophthalmic antiallergic products range from twice daily azelastine, epinastine, ketotifen, nedocromil, olopatadine ; to four times a day cromolyn, emedastine, levocabastine, lodoxamide, pemirolast ; . Nasal azelastine is dosed twice daily while nasal cromolyn is dosed three to four times a day. There is limited data on the effects of dosing frequency on clinical outcomes. There are limited clinical studies comparing brand antiallergic products to each other. Most of the studies used an allergen challenge model and measured relief of acute symptoms. The clinical significance of these studies is difficult to interpret as there are not any clinical studies that have demonstrated differences in clinical outcomes among these products. There are limited clinical studies comparing brand antiallergic products to generic ophthalmic cromolyn. One study reported olopatadine was significantly more effective in reducing itching and redness compared to cromolyn 2%; however, cromolyn is commercially available as a 4% solution and its effects are concentration dependent. A recent study found that OTC pheniramine + naphazoline was more effective than olopatadine for alleviating the acute signs and symptoms associated with ocular allergies in the allergen challenge model. There are no studies comparing nasal azelastine to nasal cromolyn. There are studies comparing nasal azelastine to oral antihistamines and nasal corticosteroids. In conclusion, the OTC antihistamine decongestant combinations used along with generic cromolyn sodium 4% can be considered options to the treatment and prevention of acute and delayed ocular allergy symptoms. This combination is first-line alternative to brand products within this class. As a result of the. Women shall be instructed not to douche or use any vaginal creams for several days prior to having a pap smear. Patients are to be rescheduled if menses occurs. Laboratory requisition forms for pap smears should be filled out completely and include: patient name, EF number, birthdate, age, date of last menses, hormonal supplementation if any, notation of previous abnormal pap smear results or GYN surgery or radiation. All laboratory results are to be dated when received, initialed by a registered nurse or advanced level provider and an entry made into the progress notes. This shall occur regardless of whether the test results are normal or abnormal. Abnormal findings will be documented and referred as indicated. Following annual assessments the inmate will be reprofiled. If no significant changes have occurred, the profile will be updated to reflect the most recent assessment date. There are no data base or flow sheets for the annual health assessment. A thorough progress note should be made and the inmate reprofiled. Patients will be counseled regarding the meaning of their test results and measures they can take for health promotion. Topics might include: Eliminating or reducing risk factors for heart a. disease maintaining normal weight and blood pressure, importance of lowering dietary fat etc. ; . b. Smoking cessation. c. Health benefits of exercise. d. Monthly breast self exam. e. Recognition of symptoms suggestive of reproductive cancers. If patients are approaching their release date, additional topics may include: Reproductive decision making and family planning. a. HIV risk reduction. b. Referral to health agencies, including alcohol and drug c. treatment and counseling agencies, for example, antihistamine. 11.1% Pfizer GlaxoSmKl 5.1% 4.5% Novartis Roche 4.1% 3.9% As traZeneca Aventis 3.9% Johns nJohns n 3.5% Merck 3.4% Bris tolMySq 3.0% Lilly 3.0% 2.7% Wyeth Amgen 2.3% 2.1% S anofi ScheringPlough 1.6% Abbott 1.5% Takeda 1.4% Genentech 1.3% AkzoNobel 1.1% NovoNordis k 1.0% ScheringA G 0.9% Eis ai MerckKGaA 0.9% 0.8% Yamanouchi Bayer 0.8% Fores t 0.8% 0.7% Altana Fujis awa 0.6% Teva 0.6% Sankyo 0.6% Solvay 0.6% Chugai 0.5% Biogen Idec 0.5% Allergan 0.4% S erono Daiichi 0.4% Genzyme Tais ho 0.4% Gilead 0.4% Shire 0.4% Banyu 0.3% Lundbeck 0.3% S hionogi Elan 0.3% Medimmune 0.3% King 0.3% UCB 0.3% Schwarz 0.3% Chiron 0.3% Ranbaxy 0.2% Alcon 0.2% Cephalon Tanabe 0.2% Celltech 0.2% Biovail 0.2% Ono 0.2% Pliva 0.2% Cipla 0.1% Dr. Reddy's Galen 0.1% Recordati 0.1% Kyorin 0.1% Valeant 0.1% Kis s ei 0.1% Actelion 0.1% Sun Pharma 0.1% KV Pharma 0.1% Zydus Cadila 0.1% Nicholas Piramal 0.1% Egis 0.1% Medicis 0.1% W ockhardt 0.1% 0.0% S alix Enzon 0.0% Matrix Labs 0.0% Torrent 0.0% Unichem 0.0% 45.6% 19.9. For basic information on solution preparation and compatibility, see Chemotherapy Chart in Appendix. Injection: 50 mcg mL, 100 mcg mL or 500 mcg mL of SC octreotide ampules; 200 mcg mL 5 mL vial ; of SC octreotide multidose vials; 10 mg, 20 mg or 30 mg of octreotide LAR vials with two vehicle ampules. For prolonged storage, keep under refrigeration. Avoid freezing of SC multidose vials. For day-to-day use, ampules and SC multidose vials may be stored at room temperature for up to 2 weeks. LAR vials can remain at room temperature on the day of injection but the suspension should be prepared immediately before administration. Do not use heat to bring solution rapidly to room temperature, as octreotide may be damaged. Protect from light. Discard unused 4 portion of SC ampules. Reconstitute octreotide LAR powder: Allow octreotide LAR and vehicle vials to warm at room temperature for 3060 minutes.8 Suspend powder with 2 mL of vehicle immediately before injection. Each kit contains a reserve vehicle ampule. Without disturbing the powder, gently inject the vehicle into the vial by running the it down the inside wall of the vial. Withdraw any excess air from the vial. Do not disturb the vial until the vehicle has wetted the powder. Once complete wetting has occurred about 2-5 minutes ; , the vial should be moderately swirled until a uniform suspension is achieved. Do not shake the vial vigorously. Slowly withdraw the entire vial contents into the syringe. 4 Immediately change the needle supplied ; . Gently invert the syringe as needed to maintain a uniform suspension. Reconstituted octreotide LAR suspension for injection: should be injected immediately.4 Diluted solution for infusion: For continuous IV infusion, dilute octreotide SC solution in NS. Stable for 24 hours at room temperature. Discard unused portion. Reconstituted octreotide LAR suspension must never be given IV.4 and progesterone. Cefadroxil Hydrate.10 Cefadroxil.10 Cefdinir.10 Ceftin.10 Cefuroxime Axetil .10 Celexa .28 CellCept.17 Cephalexin Monohydrate .10 Cephulac.52 Cetaphil .42 Chemstrip K.49 Children's Advil.21, 56 Chlor-Trimeton OTC .71 Chloral Hydrate .27 Chlorambucil .16 Chloramphenicol .68 Chlordiazepoxide HCl.30 Chlorhexidine Gluconate .44 Chloroptic S.O.P 68 Chloroquine Phosphate.15 Chlorothiazide .34 Chlorpheniramine.71 Chlorpromazine HCl .29 Chlorpropamide.48 Chlorthalidone.34, 36 Chlorzoxazone.26, 58 Cholestyramine Aspartame.37 Cholestyramine Sucrose .37 Choline Salicylate Magnesium Salicylate.22, 57 Chronulac .90 Ciloxan.68 Cimetidine HCl .50 Cinacalcet.46 Cipro.11 Ciprodex .43 Ciprofloxacin HCl.11, 68 Ciprofloxacin HCl Dexamethasone.43 Citalopram HBr .28 Citric Acid Potassium Citrate .80 Citric Acid Sodium Citrate .80 Clarithromycin.11 Claritin OTC .71 Claritin-D OTC.75 Clemastine Fumarate.71. Chlorhexidine gluconate solution Miscellaneous Products chlor-mal methscopolamine nit tab. sr 12h Cough Cold Preparations chloroquine phosphate tablet Antiinfectives Antifungal Antiviral chlorothiazide tablet Diuretics chloroxylenol p-chlor-m-xylen ; soln Eye, Ear, Nose & Throat Agents chlorpheniramine maleate capsule sa Antihistamines chlorpheniramine maleate syrp Antihistamines chlorpheniramine tannate and p susp Antihistamines chlorpromazine hcl ampul Psychotherapeutic Drugs chlorpromazine hcl tablet Psychotherapeutic Drugs chlorpropamide tablet Hypoglycemics Diuretics chlorthalidone tablet chlorzoxazone tablet Muscle Relaxants Analgesics chol sal magnesium salicylate liquid Pain Management Analgesics chol sal magnesium salicylate tablet Pain Management cholestyramine aspartame packet Cardiovascular cholestyramine aspartame powder Cardiovascular cholestyramine sucrose packet Cardiovascular Cardiovascular cholestyramine sucrose powder ciclopirox olamine cream Skin Preps ciclopirox olamine suspension Skin Preps cilostazol tablet Blood Products Modifiers Thinners cimetidine hcl liquid Gastrointestinal Gastrointestinal cimetidine hcl vial cimetidine tablet Gastrointestinal CIPRO I.V. PIGGYBACK Antiinfectives Antifungal Antiviral CIPRO I.V. VIAL Antiinfectives Antifungal Antiviral CIPRODEX DROPS SUSP Eye, Ear, Nose & Throat Agents ciprofloxacin hcl drops Eye, Ear, Nose & Throat Agents ciprofloxacin hcl tablet Antiinfectives Antifungal Antiviral 43 Effective Date 1 07 and propafenone.

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Chlorpheniramine 1 mg, dextromethorphan 7.5 mg, pseudoephrine 15 mg; 2 -5 yrs: 5 mL PO q6h prn 6-11 yrs: 10 mL PO q6h prn 12 yrs: 20 mL PO q6h prn Tobradex; Corticosteroid, Antibacterial; Ophth susp: dexamethasone 0.1%, tobramycin 0.3% [2.5, 5, 10 mL] Ophth oint: dexamethasone 0.1%, tobramycin 0.3% [3.5 gm]; Ophth susp: Instill 1-2 drops into affected eye s ; q4-6h. Ophth oint: Apply into conjunctival sac of affected eye s ; q6-8h. Trizivir; Nucleoside Analog Reverse Transcriptase Inhibitors; Tab: abacivir 300 mg, lamivudine 150 mg, zidovudine 300 mg; 40 kg: one tablet PO bid Tylenol Children's Cold Plus Cough Suspension; Analgesic, Antihistamine, Antitussive, Decongestant; Liq per 5 mL: Acetaminophen 160 mg, chlorpheniramine 1 mg, dextromethorphan 5 mg, pseudoephedrine 15 mg; 2-5 yrs: 5 mL PO q6h prn 6-11 yrs: 10 mL PO q6h prn 12 yrs: 20 mL PO q6h prn Maximum 4 doses per day Tylenol Children's Flu Suspension; Analgesic, Antihistamine, Antitussive, Decongestant; Susp per 5 mL: Acetaminophen 160 mg, chlorpheniramine 1 mg, dextromethorphan 7.5 mg, pseudoephedrine 15 mg; 2-5 yrs: 5 mL PO q6h prn 6-11 yrs: 10 mL PO q6h prn 12 yrs: 20 mL PO q6h prn Maximum 4 doses per day Tylenol Infant's Cold Concentrated Drops; Analgesic, Decongestant; Drops per 1 mL: Acetaminophen 100 mg, pseudoephedrine 9.375 mg; Dose per pseudoephedrine component: 4 mg kg day PO q6h prn Tylenol Children's Sinus Suspension; Analgesic, Antihistamine, Decongestant; Susp per 5 mL: Acetaminophen 160 mg, pseudoephedrine 15 mg; 2-5 yrs: 5 mL PO q6h prn 6-11 yrs: 10 mL PO q6h prn 12 yrs: 20 mL PO q6h prn Maximum 4 doses per day Tylenol Children's Cold Liquid; Analgesic, Antihistamine, Decongestant; Liq per 5 mL: Acetaminophen 160 mg, chlorpheniramine 1 mg, pseudoephedrine 15 mg; 2-5 yrs: 5 mL PO q6h prn 6-11 yrs: 10 mL PO q6h prn 12 yrs: 20 mL PO q6h prn Maximum 4 doses per day Tylenol Cold Children's Cold Chewable Tablets; Analgesic, Antihistamine, Decongestant; Tab: Acetaminophen 80 mg, chlorpheniramine 0.5 mg, pseudoephedrine 7.5 mg; 2-5 yrs: 2 tablets PO q4h prn 6-11 yrs: 4 tablets PO q6h prn 12 yrs: 8 tablets PO q6h prn Tylenol Infants' Cold Decongestant & Fever Reducer Plus Cough Concentrated Drops; Analgesic, Antitussive Decongestant; Drops per 1 mL: acetaminophen 100 mg, dextromethorphan 3.125 mg, pseudoephedrine 9.375 mg; 2-3 yrs: 1.6 mL PO q4-6h prn max 6.4 mL day ; Tylenol Children's Cold Plus Cough Chewable Tablets; Analgesic, Antihistamine, Antitussive, Decongestant; Tab: Acetaminophen 80 mg, chlorpheniramine 0.5 mg, dextromethorphan 2.5 mg, pseudoephedrine 7.5 mg; 2-5 yrs: 2 tablets PO q6h prn 6-11 yrs: 4 tablets PO q6h prn 12 yrs: 8 tablets PO q6h prn Tylenol w Codeine C-III Analgesic, Opioid Narcotic; Elix per 5 mL: Acetaminophen 120 mg, codeine 12 mg No. 2 Tab: Acetaminophen 300 mg, codeine 15 mg No. 3 Tab: Acetaminophen 300 mg, codeine 30 mg No. 4 Tab: Acetaminophen 300 mg, codeine 60 mg; 0.5-1 mg kg dose of codeine PO q4-6h Maximum 60 mg dose Unasyn; Antibacterial, Penicillin; Inj: Ampicillin 1 gm sulbactam 0.5 gm; ampicillin 2 gm sulbactam 1 gm; 100-200 mg of ampicillin component kg day IM IV q6h; in meningitis, may use 200-400 mg kg day IV q6h max 8 gm ampicillin day ; Vasocon-A; Ophth Decongestant, Antihistamine; Ophth soln: Naphazoline 0.05%, antazoline 0.5% [5, 15 mL]; Instill 1-2 drops in each eye q4-6h prn Do not use for more than 3-4 days. Vicks Pediatric 44M Cough & Cold Relief Liquid; Antihistamine, Antitussive, Decongestant; Liq per 5 mL: chlorpheniramine 0.67 mg, dextromethorphan 5 mg, pseudoephedrine 15 mg; 2-5 yrs: 5 mL PO q6h prn 6-11 yrs: 10 mL PO q6h prn 12 yrs: 20 mL PO q6h prn Vicks 44M Cough, Cold & Flu Relief Liquid; Analgesic, Antihistamine, Antitussive, Decongestant; Liq per 5 mL: Acetaminophen 162.5 mg, chlorpheniramine 1 mg, dextromethorphan 7.5 mg, pseudoephedrine 15 mg; 2-5 yrs: 5 mL PO q6h prn. Was, however, no trend of successive injections suppressing craving F [1, 5] 2.66, P 0.16 ; , nor did the post injection minimum CRAVING change significantly with repeated injections t 1.05 with 60 d.f., P 0.3 ; . Except for injection five, CRAVING ratings tended to peak 1 min prior to each injection and then immediately decreased to nadir in 2 min; they rose again before the subsequent injection. Group behavioral ratings of ANXIOUS and RUSH relative to each injection were quite variable within and between subjects and were not further analyzed. Neural correlates of cocaine's subjective effects Based upon a voxel-wise whole brain correlation analysis of the entire 1 h SA session BOLD time-course data with individual behavioral ratings, a number of brain regions correlated with ratings of HIGH n 19 ; , followed by those of CRAVING n 13 ; , RUSH n 6 ; , and ANXIETY n 3 ; , with the majority of these significant clusters localized to the right hemisphere Table 1 ; . Several clusters significantly correlated with self-reports of both HIGH and CRAVING, and as these constructs tended to be inversely related, an inverse relationship was also seen between the constructs and brain activity. Structures correlating with HIGH Several limbic, paralimbic, and mesocortical clusters correlated significantly with HIGH Table 1, Fig. 5 ; . In general, more inferior limbic and frontal regional activity was negatively related and rythmol.

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Oral decongestants Provide no benefit for sneezing, itching, and rhinorrhea; provide modest benefit in relieving congestion. ; Pseudoephedrine Phenylephrine Intranasal topical decongestants Provide no benefit for sneezing, itching, and rhinorrhea; provide substantial benefit for congestion. ; Oxymetazoline hydrochloride Phenylephedrine Ephedrine Intranasal corticosteroids Provide substantial benefit in relieving sneezing, itching, congestion, and rhinorrhea. ; Beclomethasone Budesonide Flunisolide Fluticasone propionate Momentasone Triamcinolone Intranasal mast cell stabilizers Provide modest benefit in relieving sneezing, itching, congestion, and rhinorrhea. ; Cromolyn sodium Intranasal topical anticholinergics Provide substantial benefit in relieving rhinorrhea; no benefit in relieving sneezing, itching, and congestion. ; Ipratropium bromide Antihistamines Oral formulations provide substantial benefit in relieving sneezing, itching, and rhinorrhea and minimal benefit in relieving congestion. Intranasal formulations provide moderate benefit in relieving sneezing, itching, and rhinorrhea and minimal benefit in relieving congestion. ; First generation Side effects may be prohibitive. ; -- chlorpheniramine -- diphenhydramine -- tripelennamine -- clemastine fumarate Second generation Nonsedating ; -- terfenadine * -- astemizole * -- loratadine -- cetirizine hydrochloride Next generation Nonsedating ; -- fexofenadine hydrochloride -- desloratadine -- tecastemizole investigational ; -- levocetirizine investigational ; Leukotriene modifiers Indicated for the treatment of asthma, these agents are being investigated for efficacy in reducing the symptoms of allergic rhinitis. ; Zileuton Pranlukast available in Japan ; Zafirlukast Montelukast sodium * Not available in United States because of.

Formulary Status Generic Generic Generic Non-Formulary Non-Formulary Non-Formulary Non-Formulary Brand Preferred Brand Preferred Brand Preferred Brand Preferred Non-Formulary Non-Formulary Brand Preferred Brand Preferred Generic Brand Preferred Generic Generic Brand Preferred Brand Preferred Brand Preferred Generic Generic Brand Preferred Generic Generic Generic Generic Brand Preferred Generic Generic Generic Generic Non-Formulary Non-Formulary Non-Formulary Non-Formulary Non-Formulary Brand Preferred Brand Preferred Generic Generic Generic Generic Non-Formulary Generic Generic DESQUAM-X DESQUAM-X 10 DESQUAM-X 5 DESYREL DESYREL DESYREL DESYREL DETROL DETROL DETROL LA DETROL LA DETUSS DEX PC DEXAMETHASONE DEXAMETHASONE DEXAMETHASONE DEXAMETHASONE DEXAMETHASONE DEXAMETHASONE DEXAMETHASONE DEXAMETHASONE DEXAMETHASONE DEXAMETHASONE DEXAMETHASONE DEXAMETHASONE INTENSOL DEXAMETHASONE SODIUM PHOSPHATE DEXAPHEN DEXASOL DEXCHLOR DEXCHLORPHENIRAMINE MALEATE DEXCHLORPHENIRAMINE MALEATE DEXCHLORPHENIRAMINE MALEATE DEXCON-DM DEXCON-PE DEXEDRINE DEXEDRINE DEXEDRINE DEXEDRINE DEXFOL DEXPAK DEXPAK JR. DEXTROAMPHETAMINE SULFATE DEXTROAMPHETAMINE SULFATE DEXTROAMPHETAMINE SULFATE DEXTROAMPHETAMINE SULFATE DEXTROAMPHETAMINE SULFATE DEXTROAMPHETAMINE SULFATE DEXTROMETHORPHAN-CP-PHENYL BRAND NAME GENERIC NAME BENZOYL PEROXIDE BENZOYL PEROXIDE BENZOYL PEROXIDE TRAZODONE HCL TRAZODONE HCL TRAZODONE HCL TRAZODONE HCL TOLTERODINE TARTRATE TOLTERODINE TARTRATE TOLTERODINE TARTRATE TOLTERODINE TARTRATE P-EPHED HCL HYDROCODONE CP D-METHORPHAN HB PE CHLORPHENIR DEXAMETHASONE DEXAMETHASONE DEXAMETHASONE DEXAMETHASONE DEXAMETHASONE DEXAMETHASONE DEXAMETHASONE DEXAMETHASONE DEXAMETHASONE DEXAMETHASONE DEXAMETHASONE DEXAMETHASONE DEXAMETHASONE SOD PHOSPHATE P-EPHED SUL D-BROMP MAL DEXAMETHASONE SOD PHOSPHATE DEXCHLORPHENIRAMINE MALEATE DEXCHLORPHENIRAMINE MALEATE DEXCHLORPHENIRAMINE MALEATE DEXCHLORPHENIRAMINE MALEATE GUAIFEN D-METHORPHAN HB PE GUAIFEN D-METHORPHAN HB PE D-AMPHETAMINE SULFATE D-AMPHETAMINE SULFATE D-AMPHETAMINE SULFATE D-AMPHETAMINE SULFATE FOLIC ACID VITAMIN B COMP W-C DEXAMETHASONE DEXAMETHASONE D-AMPHETAMINE SULFATE D-AMPHETAMINE SULFATE D-AMPHETAMINE SULFATE D-AMPHETAMINE SULFATE D-AMPHETAMINE SULFATE D-AMPHETAMINE SULFATE D-METHORPHAN HB PE CHLORPHENIR GUAIFEN DM HB P-EPHEDRINE and pyrazinamide. Chlorpheniramine and diphenhydramine both category b ; have been considered the antihistamines of choice for oral and parenteral use, respectively, in pregnancy, 20 although one case-control study showed an association between the use of diphenhydramine in the first trimester and cleft palate. This pro establishment status quoist tendency in law is a direct fallout of our colonial days. Take a look at the British influence on the law. There were over 400 British statutes since 1927. Rather than a repeal of these laws, we had Article 372 of the Constitution which continued them. 258 British statutes were repealed by the British Statutes Repeal Act, 1960. But nearly 150 British Statutes continued to be in operation. The 96 report of the Law Commission and quetiapine.

Australia is seen as a highly successful sporting nation but paradoxically it is succumbing to sedentary activities. The incidence of obesity and being overweight is following the same trends as North America and the UK. The Australian Diabetes, Obesity and Lifestyle Study AusDiab ; surveyed lifestyle factors, socio-economic factors, obesity and the incidence of diabetes between 1999 and 2000. It was a cross sectional study of over 20, 000 people from 42 sites throughout Australia, and showed that 67% of males and 52% of females aged 25 and over were overweight, with 191% and 218%, respectively, being considered obese. Perhaps even more worrying were the figures from the Sentinel Site for Obesity Prevention in Victoria which reported last year that 267% of children aged between 7 and 11 are overweight with 79% of this total considered to be obese. This compares badly with the national data from 1985 giving figures of 121% overweight with 17% obese. A recent report from the Organisation for Economic Co-operation and Development ranked Australia fourth in the world for obesity and growing at the fastest rate. As in every other country where obesity is an increasing problem, the healthcare costs for individuals and states mount with the growing levels of associated morbidity. So what has gone wrong in Australia and what is being done about it? The Federal Government has set up a National Obesity Prevention Group and similar initiatives exist at State level. There is no doubt that obesity is much higher on the health agenda now, and increasing amounts of health funds are being directed towards research. This is, as yet, not being translated into significant improvement in the overall figures. The promise of funds by politicians lags behind their delivery, and there is a suspicion that hospital deficits take priority over funding for prevention. There are local centres of excellence that are having some impact. For instance the Sentinel Sites for Obesity Prevention are seeking to produce effective collaboration between health professionals and the community in order to try and prevent obesity in children. Here and in other areas of Victoria an increase in nutritional advice and back up is helping schools to provide guidance on healthy lunches, and educational sessions for parents are hoping to promote healthier eating patterns at home see Table 1 ; . School-based programs that promote healthier lifestyles, with increased activity and healthier food choices have been shown to be effective in a controlled trial. However, changes are only sustainable where the input is multifocused. For instance, individual education is provided for both children and parents, together with population-based education, and popular myths about diet and weight gain are addressed and challenged, because pamabrom. 1. STEINBERG AD, KARLINER JS: The clinical spectrum of heroin pulmonary edema. Arch Intern Med Chicago ; 122: 1968 DUBERSTEIN JL, KAUFMAN DM: A clinical study of an epidemic of heroin intoxication and heroin-induced pulmonary edema. Amer J Med 51: 704, 1971 KATZ S, ABERMAN AM, STEIN IM, FRAND Y, FULOP M: Heroin pulmonary edema: Evidence for increased pulmonary capillary permeability. Amer Rev Resp Dis. In press 4. CLEMMESEN C, LASSEN NA: Treatment of circulatory shock in narcotic poisoning. Danish Med Bull 10: 100, 1963 HULTGREN HN, GROVER RF, HARTLEY LH: Abnormal circulatory responses to high altitude in subjects with a previous history of highaltitude pulmonary edema. Circulation 44: 759, 1971 WIHAYNE TF JR, SEVERINGHAUS JW: Experimental hypoxic pulmonary edema in the rat. J Appl Physiol 25: 729, 1968 PIETRA GG, SZ1ON JP, LEVENTHAL MM, FISHMAN AP: Histamine and interstitial pulmonary edema in the dog. Circ Res 26: 323, 1971 HAUGE A: Role of histamine in hypoxic pulmonary hypertension in the rat: I. Blockade or potentiation of endogenous amines, kinins, and ATP. Circ Res 22: 371, 1968 ILLIFF LD: Extra-alveolar vessels and edema development in excised dog lungs. Circ Res 28: 524, 1971 WOOD JE, Roy SB: The relationship of peripheral venomotor responses to high altitude pulmonary edema in man. Amer J Med Sci 259: 56, 1970 SUSMANO A, CARLETON RA: Prevention of hypoxic pulmonary hypertension by chlorpheniramine. J Appl Physiol 31: 531, 1971 LUISADA AA: Paroxysmal pulmonary edema and the acute cardiac lung. Amer J Cardiol 20: 69, 1967 SIMMONs RL, HEISTERKAMP CA III, COLLINs JA, BREDENBURG CE, MARTIN AM: Acute pulmonary edema in battle casualties. J Trauma 9: 760, 1969 and seroquel.

While most women recognize the importance of healthy eating, some find it particularly challenging to achieve. Many women say they have little time and energy to devote to meal planning and preparation. For some women, healthy food choices are not affordable. Healthy eating messages often conflict, resulting in a lack of clear, reliable and relevant information Health Canada, 2000b ; . In addition, social pressures encourage women to strive for unhealthy weights. Our culture associates beauty with being female from the earliest days of a child's life. Long before puberty, girls learn that beauty is a basic dimension of the female gender role Rice, 1995 ; . Most women are dissatisfied with their body size and shape. Many women eat less in an effort to control their weight, putting them at greater risk of inadequate intake. Women may attempt to alter their size through dieting, self-starvation, self-induced vomiting, laxatives, diuretics or strenuous exercise. Close to 70% of Canadian women are weight preoccupied and almost 40% are continually gaining and losing weight. Most women who practice weight control activities are of childbearing age Rice, 1995 ; . Media images, with their underlying messages about the importance of appearance, are particularly harmful to adolescents and young adult women. A healthy body weight promotes general health, reduces the incidence of disease and is a major positive influence in the management and outcome of pregnancy Cefalo & Moos, 1995 ; . Weight related problems can negatively influence the mother's and unborn baby's health and, if possible, should be addressed through appropriate information and supports prior to pregnancy Health Canada, 2000b ; . Being overweight puts women at risk for poor health and pregnancy outcomes Carmichael et al., 1997 ; . Women who are underweight have an increased risk of infertility and anaemia and are also more likely to have an infant with a low birth weight Rice, 1995 ; . The higher rate of low birth weight in the adolescent population may be partially due to the vulnerability of adolescents to cultural pressures, for instance, polaramine.
Adult male ICR mice weighing 20 to 24 were obtained from Flow Research Animals Inc., Dublin, Va. Adult male BDF, mice weighing 21 to 23 g, male DBA mice weighing 20 to 21 g, and male BALB c mice weighing 17 to 19 were obtained from Simonson Laboratories, Gilroy, Calif. Adult female C3H HeCr mice weighing 20 to 23 were obtained from Charles River Breeding Laboratories, Wilmington, Mass. Adult female CDF, mice weighing 17 to 19 were obtained from Laboratory Supply Co., Inc., Indianapolis, Ind. They were acclimated to their new environment for 1 week before experimentation and were allowed free access to food Purina Lab Chow; Ralston Purina Co., St. Louis, Mo. ; and water. All drug solutions were prepared so that the required quantity was administered as 0.01 ml g of mouse weight. E. coli 026: B6 LPS Boivin preparation [B]; Difco Laboratories, Detroit, Mich. ; was suspended in 0.15 M NaCl. The other LPS preparations were also obtained from Difco. Pseudomonas vaccine lot X41667 ; was generously provided by M. W. Fisher, Parke, Davis & Co., Detroit, Mich. A9THC was obtained from the National Institute of Drug Abuse Rockville, Md. ; and dissolved in Emulphor-ethanol at a stock concentration of 20 mg ml. This stock was diluted in 0.15 M NaCl as appropriate and quinine.

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MIMS Group MIMS Description RESPIRATORY SYSTEM Decongestants RESPIRATORY SYSTEM Decongestants RESPIRATORY SYSTEM Decongestants RESPIRATORY SYSTEM Decongestants RESPIRATORY SYSTEM Decongestants RESPIRATORY SYSTEM Glucocorticoids RESPIRATORY SYSTEM Methylxanthines & Combinations RESPIRATORY SYSTEM Methylxanthines & Combinations RESPIRATORY SYSTEM Mucolytics RESPIRATORY SYSTEM Mucolytics RESPIRATORY SYSTEM Mucolytics RESPIRATORY SYSTEM Mucolytics RESPIRATORY SYSTEM Mucolytics RESPIRATORY SYSTEM Mucolytics RESPIRATORY SYSTEM Mucolytics RESPIRATORY SYSTEM Mucolytics RESPIRATORY SYSTEM Other Anti-asthmatics RESPIRATORY SYSTEM Sympathomimetics RESPIRATORY SYSTEM Sympathomimetics RESPIRATORY SYSTEM Sympathomimetics THERAPEUTIC VITAMINS & OTHER SUPPLEMENTS Electrolytes THERAPEUTIC VITAMINS & OTHER SUPPLEMENTS Electrolytes URINARY TRACT Diuretics URINARY TRACT Diuretics URINARY TRACT Diuretics URINARY TRACT Diuretics URINARY TRACT Others URINARY TRACT Others URINARY TRACT Urinary Alkalinizers URINARY TRACT Urinary Antiseptics URINARY TRACT Urinary Antiseptics URINARY TRACT Urinary Antiseptics URINARY TRACT Urinary Antiseptics URINARY TRACT Urinary Antiseptics URINARY TRACT Urinary Antiseptics URINARY TRACT Urinary Antiseptics Active Ingredient Nappi6 Product Description Chlorpheniramine maleate 4mg; phenylpropanolamine HCI 5mg; phenylephrine HCI 5mg 5ml 760773 RINEX SYR Phenylpropanolamine HCI 2.5mg; Phenylephrine HCI 2.5mg; Chlorpheniramine maleate 2mg 5ml syr 760803 RINEX PAED SYR Pseudoephedrine HCI 30mg; Triprolidine HCI 1.25mg 5ml 794295 ACUGEST SYR Pseudoephedrine HCI 60mg 796972 ADCO-SUFEDRIN 60MG TAB Psuedoephedrine 30mg 5ml 796964 ADCO-SUFEDRIN 30MG 5ML SYR Beclomethasone dipropionate 50mcg Aerosol 819611 BECLATE 50MCG INHALER Theophylline & ethylenediamine 200mg 769320 NORSTAN-TED 200MG TAB Theophylline anhydr.syr 701750 ALCOPHYLLIN 80MG 15ML Carbocisteine 375mg caps 726478 FLEMEX-20 PLUS CAP Carbocisteine 375mg caps 805335 MUCOLESS 375MG CAP Carbocisteine. Adult Syr 787078 MUCOLINCT 250MG 5ML SYR Carbocisteine. Paed Syr 781169 MUCOSPECT PAED SYR N-acetylcysteine 100mg lozenge 809306 SOLMUCOL 100MG LOZ N-acetylcysteine 200mg effervescent tab 824291 ACC 200MG EFF TAB N-acetylcysteine 400mg sachet 809292 SOLMUCOL 400MG SACHET Sorbimacrogol laurate [300] 36.33mg; Ammonium chloride 34mg; alcohol 7.4% v v 10ml EXPIGEN SYR 725323 Ketotifen hydrogen fumarate 1mg 5ml syr 854905 ZETOFEN 1MG 5ML SYR Salbutamol 2mg tab 775398 VENTEZE 2MG TAB Salbutamol sulph.syr 824186 ASTHAVENT 2MG 5ML SYR Salbutamol sulphate 100mcg Inhaler 819603 ASTHAVENT INH 200 DOSE Potassium chloride 335.8mg; Na citrate 469.8mg; Na chloride 473.68mg; dextrose762873 SCRIPTOLYTE SOLUTION monohydrate 3.96g 30ml Rehydration solution 871915 SOROL CITRATE 28G Amiloride HCl 5mg; hydrochlorothiazide 50mg 780618 ADCO-RETIC TAB Furosemide 40mg 731668 SANDOZ FUROSEMIDE 40MG TAB Hydrochlorthiazide 25mg 890470 HEXAZIDE 25MG TAB Hydrochlorthiazide 50mg; KCl 300mg 774057 URIREX-K TAB Flavoxate HCl 200mg 820113 URISPAS 200MG TAB Phenazopyridine HCl 100mg 758647 PYRIDIUM 100MG TAB Sodium citrate 613mg; Citric acid 702mg; Tartaric acid 858mg; Sodium Bicarbonate 2.452g 5g 820059 ADCO-SODASOL GRANULES Nalidixic acid 250mg 5ml 778672 WINLOMYLON SUSP Nalidixic acid 500mg 745685 PUROMYLON 500MG TAB Nitrofurantoin 100mg; macrocrystals 739847 MACRODANTIN 100MG CAP Nitrofurantoin 25mg 5ml 727601 FURANDANTIN 25MG 5ML Nitrofurantoin 50mg; macrocrystals 739839 MACRODANTIN 50MG CAP Nitroxoline 100mg 824453 NICENE N 100MG TAB Pipemidic acid trihydrate 200mg 717770 DEBLASTON 200MG CAP Status.
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Revised Current MRP with MRP with ED and ED and Local Taxes Local Taxes Reduction Therapeutic Rs. ; in % Category Composition Pack Size Rs. ; Ofloxacin 200 + Tinidazole 600 10x10 856.00 Paracetamol IP 500mg 50 x 10 390.55 320.42 Pantoprazole Sodium Sesquihydrate 10 x 10 524.30 406.60 eq. to Pantozole 20mg + Domperidone B.P. 10mg Excipients Q.S. Pantoprazole Sodium Sesquihydrate 10 x 10 1005.80 845.30 eq. to Pantozole 40mg + Domperidone B.P. 10mg Excipients Q.S. Para + PPH + CPM + Magnisium 25 x 2 856.00 802.05 Triclicate Sparfloxacin 200 mg 10x6 749.00 588.50 Paracetamol I.P. 500mg, 25 x 10 481.50 336.93 Dicyclomine Hydrochloride IP 20mg Tadalafil tablets Sildenafil Citrate eq to Slidenafil 100mg Sildenafil Citrate eq to Slidenafil 50mg Paracetamol I.P. 500mg, Ceffeine anhydrous I.P. 25mg, Chlorpheniramine Hydrochloride B.P. 12.5mg, Excipients q.s. Albendazole I.P. 400mg, excipient qs 20 x 24X4 342 Amoxil Dry Susp. 343 Becomed Forte Syrup 344 Boss - Q Syp. 1. Maleate 2. Toluamide 3. Chlorpheniramine 4. Propranolol and ribavirin and pheniramine.

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Check with your doctor as soon as possible if any of the following side effects occur: for both females and males less common acne dark-colored urine increased oiliness of hair or skin muscle cramps or spasms swelling of feet or lower legs unusual tiredness or weakness weight gain rapid ; rare bleeding gums bloating, pain or tenderness of abdomen or stomach blood in urine burning, numbness, pain, or tingling in all fingers except the smallest finger changes in vision chest pain chills complete or partial numbness or weakness on one side of body cough coughing up blood diarrhea difficulty in speaking difficulty in swallowing discharge from nipple eye pain fast heartbeat fever headache hives or other skin rash joint pain light-colored stools loss of appetite continuing ; loss of muscle coordination more frequent nosebleeds muscle aches nausea purple- or red-colored, or other spots on body or inside the mouth or nose restlessness shortness of breath sore throat sweating tingling, numbness, or weakness in legs, which may move upward to arms, trunk, or face unusual bruising or bleeding unusual tiredness, weakness, or general feeling of illness vomiting yellow eyes or skin for females only more common decrease in breast size irregular menstrual periods weight gain rare enlarged clitoris hoarseness or deepening of voice unnatural hair growth for males only rare changes in semen decrease in size of testicles some side effects may occur that usually do not need medical attention.

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Es, social workers, pharmacists, care coordinators, therapists, chaplains and physicians. Antipsychotic drugs "have a `more favorable side effect profile, '" as the expert testimony in Weston established and Dr. Wolfson's testimony in this case reiterates. Weston, 255 F.3d at 877 n.3.10 It is important to avoid generalizations that either oversimplify or get ahead of the research, which is necessarily specific to particular medications. Accordingly, we attach to this brief several documents describing particular drugs and what is known about them, including their own risks of side effects often of a different sort from the older drugs ; : 1 ; excerpts from J. Gorman, The Essential Guide to Psychiatric Drugs 3d ed. 1997 2 ; excerpts from P. Weiden et al., Breakthroughs in Antipsychotic Medications: A Guide for Consumers, Families, and Clinicians 1999 ; , a publication of the National Alliance for the Mentally Ill; 3 ; two summary tables from J. Preston et al., Handbook of Clinical Psychopharmacology for Therapists 2d ed. 2001 4 ; detailed chapters on some of the newer drugs from A. Breier et al., eds., Current Issues in the Psychopharmacology of Schizophrenia 2001 and 5 ; the APA's Practice Guideline for the Treatment of Patients With Schizophrenia, 154 Am. J. Psychiatry No. 4 April 1997 Supp. ; . This and other literature establish the correctness of Dr. Wolfson's testimony.

Discussion Several studies have reported high recurrence rates of H. pylori infection after apparently successful eradication 20 ; . In most of these studies, however, recurrence occurred in the first year after the completion of treatment, suggesting that these recurrences in fact represented resurgence of a suppressed infection rather than a new one 21-24 ; . Therefore, the reliability of the tests used to establish eradication of the infection in these studies is to be questioned. Several studies examined the reliability of a negative test after treatment, but only four of them were published as full paper 2539 ; . In most studies one single test was selected as the gold standard, resulting in an a priori accuracy of that test of 100%. This makes interpretation of these studies difficult. A few studies tried to avoid that bias and classified the H. pylori status of each patient on an individual basis 27, 29, 38 ; . Comparable to three other studies 32, 34, 39 ; , we avoided to select a single test as the gold standard, by stipulating that a positive test should be confirmed by another positive test. A possible drawback of this study is that true eradication of the infection in patients classified as 'H. pylori negative' was not confirmed by long term follow-up. In a similar treatment study performed in our hospital, however, the same endoscopic follow-up protocol was used and all but one of one of ninety successfully treated patients were still H. pylori negative after a median follow-up of 6 years chapter 11 ; . This suggests that.
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After the drug treatments, neutrophils were fixed and stored in 3.2% PFA at 4C overnight for F-actin analysis by fluorescence microscopy and flow cytometry. The changes in neutrophil intracellular F-actin were measured by the method of Wallace et al. 1987 ; . The intracellular F-actin was labeled with the fluorescent probe BODIPY FL-phallacidin Molecular Probes, Eugene, OR ; , which specifically binds to F-actin filaments, but not monomeric G-actin, in a stoichiometric ratio of one phallacidin per actin subunit De La Cruz and Pollard, 1994 ; . Fixed cells were washed twice with PBS-BSA and incubated in PBS containing 165 nM BODIPY FLconjugated phallacidin in the dark for 45 60 min at room temperature. Labeled cells were rinsed with PBS-BSA and suspended at 5 105 cells ml for cytoskeletal analysis. The quantification of neutrophil intracellular F-actin content was carried out on a Coulter Elite ESP flow cytometer Coulter Electronics, Miami, FL ; . The fluorophore BODIPY FL was excited at a wavelength of 488 nm with a 25-mW argon laser and the emitted fluorescence by BODIPY FL was collected at a wavelength of 520 530 nm. A small population of red, for instance, pheniraamine maleate tablets.
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ALLEGRA-D ASTELIN ATARAX 100 mg brompheniramine pseudoephedrine 4 mg 45 mg per 5 mL brompheniramine pseudoephedrine ext-rel 12 mg 120 mg brompheniramine pseudoephedrine ext-rel 6 mg 60 mg carbinoxamine pseudoephedrine 1 mg 15 mg per mL chlorpheniramine pseudoephedrine ext-rel 8 mg 120 mg CLARINEX clemastine 2.68 mg cyproheptadine CYPROHEPTADINE syrup diphenhydramine diphenhydramine inj fexofenadine hydroxyzine HCl 10 mg, 25 mg NonPreferred Preferred Preferred Generic Generic Generic Generic Generic Preferred Generic Generic Preferred Generic Generic Generic Generic 39 and progesterone.
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Global Initiative for Asthma, " Global strategy for asthma management and prevention NHLBI WHO workshop report , 1995: No. 95-3659 ; . National Institutes of Health. This review was supported by the Saving Newborn Lives Initiative of Save the Children USA through a grant from the Bill & Melinda Gates Foundation and the Department of Child and Adolescent Health and Development, World Health Organization. We thank Dr Jose Martines of the World Health Organization and Anne Tinker of Save the Children USA for technical input and encouragement during the review process; Chitra Krishnan for assistance in locating relevant articles for review; Fauzia Aman Malik for technical and editorial assistance; and Sarah Holland and Charlotte Storti for editorial expertise. We also thank the following individuals who reviewed the manuscript and provided technical and editorial review on behalf of the World Health Organization: Dr Martin Weber, Dr Jelka Zupan, and Dr Bernadette Daelmans World Health Organization, Geneva, Switzerland Professor Robert Black Department of International Health, Johns Hopkins University Bloomberg School of Public Health, Baltimore, MD Dr Douglas McMillan University of Calgary Calgary Health Region, Calgary, Alberta, Canada and Dr Steven Wall and Dr Vinod Paul Save the Children USA, Washington, DC. 4 tablets daily ; . After 2 weeks, fever, painful oedema and erythema of the face, bilateral conjunctivitis, lip erosions ensued followed by generalised erythema, multiple, flaccid bullae. Rupture of the bullae was followed by sloughing of large sheets of skin exposing an intensely erythematous, moist, exuding base, characteristic of TEN. Nikolsky's sign was produced with only slight pressure. Laboratory Investigations: Routine tests were normal. Urine culture, blood urea, serum proteins total and differential ; were also normal. X-ray chest favoured lesions of pulmonary tuberculosis bilateral infiltrations ; . Sputum for acid fast-bacilli was positive. However, skin biopsy could not be performed. Patient was immediately started on oral Prednisolone 30 mg daily, antihistaminics Pheniram8ne maleate, orally 25 mg four times daily ; and soframycine eye drops for conjuctivitis. After 7-10 days, her general condition bettered and discharge from the eyes ceased. Cutaneous blisters also resolved. The prednisolone was diminished gradually as the condition improved. After 2 weeks, strepto.
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Drug Name ALTACE 2.5MG CAPSULE ALTACE 5MG CAPSULE ALTACE 10MG CAPSULE SILVADENE 1% CREAM SILVADENE 1% CREAM SILVADENE 1% CREAM LORABID 200MG PULVULE CORZIDE 80 5 TABLET DELESTROGEN 20MG ML VIAL DELESTROGEN 40MG ML VIAL FLORINEF ACETATE 0.1MG TAB CORGARD 40MG TABLET CORGARD 160MG TABLET ANUSOL-HC 2.5% CREAM GUAIFENESIN TABLET SA GUAIFENESIN TABLET SA CHLORPHENIRAMINE 12MG CP SA METHOTREXATE 25MG ML VIAL AMINOCAPROIC ACID 500MG TAB DIABETIC TUSSIN DM LIQUID DIABETIC TUSSIN EX LIQUID DIABETIC TUSSIN MAX-STR LIQ DIABETIC TUSSIN C LIQUID ABELCET 5MG ML VIAL P F DOXYCYCLINE 100MG CAPSULE HYDROCODONE APAP 5 500 TAB DOXYCYCLINE 100MG TABLET DOXYCYCLINE 100MG TABLET VIREAD 300MG TABLET HEPSERA 10MG TABLET EMTRIVA 200MG CAPSULE EMBREX 600 COMBO PACK ENTEX PSE 600 120 TABLET SA ENTEX PSE 400-120 CAPSULE HISTEX PD 4MG 5ML LIQUID ENTEX LA TABLET SA. Concepts: diagnosis, localization and management. N Engl J Med 1984; 311: 1298-1303. Loh KC, Shlossberg AH, Abbott EC et al. Pheochromocytoma: a ten-year survey. QJM 1997; 90: 51-60. Cullen ML, Staren ED, Straus AK et al. Pheochromocytoma: Operative strategy. Surgery 1985; 98: 927-930. Gifford RW Jr, Kvale WF, Maher FT et al. Clinical features, diagnosis and treatment of phaeochromocytoma: A review of 76 cases. Mayo Clinic Proceedings 1964; 4: 281-302. Modlin IM, Farndon JR, Shepherd A et al. Pheochromocytoma in 72 patients. Clinical and diagnostic features, treatment and long term results. Br J Surg 1979; 66: 456-465. Remine WH, Chong GC, Van Heerden JA et al. Current Management of Phaeochromocytoma. Ann Surg 1974; 179: 740-748. Ross NS, Aron DC. Hormonal Evaluation of the patient with an incidentally discovered adrenal mass. N Engl J Med 1989; 323: 1401-1405. Stein PP, Black HR. A simplified diagnostic approach to pheochromocytoma: A review of the literature and one institution's experience. Medicine Baltimore ; 1991; 70: 46-66. Dunnick NR, Schaner EG, Doppman JL et al. Computed tomography in adrenal tumors. AJR J Roentgenol 1979; 132: 43-46. Epstein AJ, Patel SK, Petasnick JP. Computed tomography of the adrenal gland. JAMA 1979; 242: 2791-2794. Dunnik NR, Korobkin M, Francis I. Adrenal Radiology: distinguishing benign from malignant adrenal masses. AJR 1996; 167: 861-867. Fink IJ, Reinig JW, Dwyer AJ et al. MR Imaging of pheochromocytoma. J Comput Assist Tomogr 1985; 9: 454458. Sjoeddsma A, Engelman K, Waldmann TA. Phaeochromocytoma: Current Concepts of Diagnosis & Treatment. Ann Intern Med 1996; 6: 1302-1326. Scott HW, Dean RH, Oates JAet al. Surgical management of pheochromocytoma. Surg 1981; 47: 8-13. Daly PA, Landsberg L. Phaeochromocytoma: diagnosis and management. Baillieres Clin Endocrinol Metabolism 1992; 6: 143-166. Orchard T, Grant CS, van Heerden JA, Weaver A. Pheochromocytoma-continuing evolution of surgical therapy. Surgery 1993; 114: 1158-1159. Pezzulich RA, Mannix H Jr. Immediate complication of adrenal surgery. Ann Surg 1970; 172: 125-130. Witkiewicz W, Kosinski M, Paprocka M et al. Surgical results in adrenal tumours. Pol Przeg Chir 1994; 66: 10121015. Brzezinski T, Szostek M. The lateral extraperitoneal access in surgery of the adrenal glands. Pol Merkuriusz Lek 2000; 8: 124-126. Foo M, Burton BJ, Ahmed R. Phaeochromocytoma. Br J Hosp Med 1995; 54: 318-321. Chodakowska J, Jakubowskia W, Januszewicz A et al. Diagnosis and treatment of phaeochromocytoma. Med. Prak 1998; 5: 19-25.
All 24 children 14 boys, 10 girls ; enrolled completed the study. The mean age was 9.87 standard deviation 1.85 years, and age range was 7 to 14 years. The mean weight was 38.12 standard deviation 11.44 kg with a range of 20 to kg. There were 19 Chinese, 4 Malays, and 1 Indian. The hours of sleep the night before each study day and baseline rhinitis scores did not differ significantly among the 3 groups Table 1 ; . Baseline P300 latencies in the 3 electrodes also did not differ significantly from each other. Using Pearson correlation, we found no significant correlation between body weight and percentage change in P300 latency in all 3 electrodes for both cetirizine and chlorpheniramine P .05 ; . Compared with baseline, we observed an increase in P300 latency for chlorpheniramine Fz: P .01; Cz: P .01; Pz: P .04 ; and cetirizine Fz: P .02; Cz: P .03 ; but not for placebo Fig 1 AC ; . However, the mean percentage change in P300 latency for cetirizine and chlorpheniramine did not differ significantly from placebo. On the basis of previous studies, an increase in the P300 latency of 5% after H1-receptor antagonist administration is clinically relevant.20, 24 At the Fz electrode, cetirizine and chlorpheniramine increased P300 latency by at least 5% in 8 33% ; and 11 46% ; patients, respectively, whereas for placebo, the increase in P300 latency was at least 5% in only 1 4. EPITOL. See CARBAMAZEPINE. EQUAGESIC. See MEPROBAMATE. EQUANIL. See MEPROBAMATE. ERGOMAR See ERGOTAMINE TARTRATE. ERGOTAMINE TARTRAm. Description and cases, p. 306. ERYTHROMYCIN ESTOLAlX. Description and cases, p. 310. ERYTHROMYCIN Topical Solution ; . Description and cases, p. 309. ESKALITH. See LITHIUM CARBONATE. ESTOMUL. See MAGNESIUM CARBONATE WITH ALUMINUM HYDROXIDE. ESTROGENS CONJUGATED ; . Description and cases, p. 311. ETHAMRUTOL HYDROCHLORIDE. Description and cases, p. 313. ETHCHLORVYNOL. Description and cases, p. 316. ETHINYL ESTRADIOL WITH DIMETHISTERONE. Description and cases, p. 318. ETHINYL ESTRADIOL WITH NORETHINDRONE ACETATE. See NORETHINDRONE ACETATE WITH ETHINYL ESTRADIOL. ETHOSUXIMIDE. Description and cases, p. 321. ETHYNODIOL DIACETAflE WITH ETHINYL ESTRADIOL. Description and cases, p. 322. ETHYNODIOL DIACETATF, WITH MESTRANOL. Description and cases, p. 323. ETRAFON. See AMITRIPTYLINE; PERPHENAZINE. EUCALYPTUS OIL AND MEW.l'HOL. Description and cases, p. 329. EUTRON. See METHYCLOTHIKZIDE. EXCEDRIN. See ASPIRIN. EXTENDRYL. See CHLORPHENIRAMINE MALEATE. 1021. From page 1 Divergent rates of success for stone removal may be related to the fact that there are two underlying explanations for pain associated with chronic calcific pancreatitis. In pancreatic duct obstruction, pain results from parenchymal hypertension. This scenario responds well to ductal decompression. Pain associated with pancreatic and peripancreatic neural inflammation, most often associated with long-standing chronic disease, does not. Careful imaging can point to whether endoscopic treatment should be undertaken and in some cases, bring to light massive stones and strictures that could be managed only by lithotripsy or surgical Whipple resection. "I would strongly recommend if you see patients with chronic pancreatitis, that you switch your gears from a reflex of just getting a CT scan to talking to your radiologist and getting geared up for high-quality MRI scanning . with secretin stimulation, " he said. No other modality gives such clear or important information in treatment planning for patients with chronic pancreatitis, Dr. Hawes said. He disclosed that he has received grants from Olympus America Inc. and research support from Wilson-Cook Medical Inc. and Boston Scientific Corp., and he is a consultant for InScope. s. Answer: christie, it is not always possible or healthier for the baby to have a med-free 9 months. Sub-Chapter: ANTIHISTAMINES $ $ $$$ $ $ $ $ $$ $$$$ $$$ $$$ cyproheptadine promethazine supp, syrup, tabs fexofenadine Sub-Chapter: COUGH COLD ALLERGY chlorpheniramine pseudoephedrine codeine soln, 2-30-10 5mL codeine guaifenesin soln, syrup, 10-100 5mL; tabs, 10 300 hydrocodone guaifenesin syrup, 2.5-200 5mL, 5-100 pseudoephedrine guaifenesin ER caps 60 300; ER tabs 45 600, 60 brompheniramine pseudoephedrine ER caps, 6 60, 12 acetylcysteine Sub-Chapter: NASAL AGENTS - SYSTEMIC AND TOPICAL flunisolide 25 mcg spray fluticasone 50 mcg spray $$$ $$$ $$$$ ASTELIN BACTROBAN nasal NASONEX.

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