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The surveys indicate that a high percentage recall seeing risk information as part of the ad. In the FDA survey 40 per cent said they read half or more of the risk information in print ads and 85 per cent said they would read all or almost all of the information if they were especially interested in the drug.
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ABSTRACT To test the hypothesis that the long-term antihypertensive action of furosemide is mediated by a renomedullary vasodepressor substance, we measured mean arterial pressure MAP ; by radiotelemetry in Dahl-S rats with either intact or bromoethylamine-induced BEA, 100 mg kg i.p. ; lesion of the renal papilla and medulla. Seven days of recovery after BEA administration, the rats diet was changed from 1 to 4% NaCl, and during days 8 to 31, rats were randomized to daily treatment with placebo or furosemide 50 mg kg p.o. ; . Then furosemide treatment was stopped and the rat food was changed to 1% NaCl diet. After a 10-day wash-out period, renal function was measured. BEA produced a rapid within min ; and sustained increase in MAP which was accelerated during 4% NaCl diet. Furosemde prevented 4% NaCl-induced hypertension in both rats with intact.
National Pharmaceutical Council United Healthcare of Florida, Inc. 13621 N.W. 12th Street Sunrise, FL 33323 800 910-3224 Vista South Florida FKA Foundation Health Plan ; 300 South Park Road Hollywood, FL 33021 800 441-5501 DUR Contact.
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Drug Req. Drug Name Tier Limits DIOVAN 2 QL DIOVAN HCT 2 QL HYZAAR 2 QL MICARDIS 2 QL MICARDIS HCT 2 QL BETA BLOCKERS Generics metoprolol tartrate 1 Brands COREG 2 INNOPRAN XL 2 TOPROL XL 2 CALCIUM CHANNEL BLOCKERS Generics diltiazem HCl 1 felodipine ER 1 nifedipine ER 1 verapamil HCl 1 Brands DYNACIRC CR 2 NORVASC 2 SULAR 2 OTHER ANTIHYPERTENSIVE COMBINATIONS Generics lisinopril hydrochlorothiazide 1 QL Brands LOTREL 2 QL TARKA 2 QL UNIRETIC 2 QL THIAZIDE & RELATED DIURETICS Generics furosemide 1 hydrochlorothiazide 1 metolazone 1 VASODILATORS Generics hydralazine HCl 1 minoxidil 1 and glucophage.
ABSTRACT Clonidine was nonhypotensive in conscious unrestrained rats maintained on a normal sodium intake. In contradistinction, clonidine caused a dose-related hypotension in conscious unrestrained rats subjected to sodium depletion via furosemide. The plasma renin activity of normal and sodium-depleted rats was reduced after the administration of clonidine 100 Mg kg, iv ; by 22.8% and 34.4%, respectively. Intravenous infusion of an angiotensin II antagonist, l-Sar-8-Ala-angiotensin II, caused a significant reduction of arterial blood pressure in sodium-depleted rats but not in normal rats. Similarly, bilateral nephrectomy reduced arterial blood pressure and completely abolished the hypotensive effect of clonidine in sodium-depleted rats. Subcutaneous administration of chlorisondamine caused a significantly greater reduction of arterial blood pressure in sodiumdepleted rats than it did in normal rats. Treatment of normal and sodium-depleted rats with 6-hydroxydopamine reduced the arterial blood pressure of both groups to approximately 85 mm Hg and completely abolished the hypotensive effect of clonidine in the sodium-depleted rats. The data presented in this paper are consistent with the conclusion that clonidine acts at some site in the sympathetic nervous system of sodium-depleted rats to inhibit renal nerve activity with a resultant suppression of renin secretion and a reduction of the angiotensin II-maintained arterial blood pressure. A similar sequence of events occurring in normal rats would not result in hypotension because their arterial blood pressure is not maintained by angiotensin II.
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Table 1. Macroscopic Assessment of Animals Control Clinical signs % of mice ; Wet peri-anal area fluid-filled lumen Semi-solid fecal pellet Hyperemic colon occult blood bloody diarrhea Colon length mm ; Change in body weight g 5 days and glyburide.
Baseline anthropometric, clinical, and functional results are shown in Table 1. Seventeen of 24 subjects 71 percent ; were atopic at least one immediate skin reaction to 15 common inhalants with skin prick testing ; and 19 79 percent ; were taking inhaled steroid preparations. Baseline FEV, was less than 80 percent predicted and the ratio of FEV, to forced vital capacity was less than 85 percent predicted" in 11 of subjects 46 percent ; . The PC20 for histamine and methacholine as assessed on the third day of the baseline period was reproducible within a 3.2-fold difference in 22 of subjects 92 percent ; , the exceptions being subjects 13 and 15. Baseline FEV, remained constant throughout the study period p 0.05 ; , with only five subjects showing changes between 10 and 20 percent comparing the lowest with the highest FEV, value before the histamine test on any of the study days. The PC20 methacholine results also remained unchanged throughout the study period p 0.05 ; , with only two.
15. MacLennan AH, Taylor AW, Wilson DH, Wilson D. The prevalence of pelvic floor disorders and their relationship to gender, age, parity and mode of delivery. BJOG, 107: 1460-1470, 2000 Nelson RL, Norton N, Cautley E and Furner S. Community based prevalence of anal incontinence. JAMA, 274: 559-562, 1995. Enck P, Bielefeld K, Rathmann W, PurrmannJ, Tschope D, Erkenbrecht JF. Epidemiology of faecal incontinence in selected patient groups. Int J Colorectal Dis., 6: 143-146, 1991 Wisconsin Family Health Survey, Center for Health Statis-tics, Division of Health, Department of Health and Social Serv-ices, P.O. Box 309, Room 172, Madison Wisconsin 53701-0309, 1994. 19. Nelson RL, Furner S, Jesudason V. Fecal incontinence in Wisconsin nursing homes. Dis Colon & Rectum, 41: 1226-1229, 1998 Borrie MJ, Davidson HA. Incontinence in institutions: costs and contributing factors. CMAJ, 147: 322-328, 1992. Hojberg KE, Salvig JD, Winslow NA, Bek KM, Laurberg S, Secher NJ. Flatus and faecal incontinence: prevelence and risk factors at 16 weeks of gestation. BJOG, 107: 1097-1103, 2000. Donnelly V, Fynes M, Campbell D, Johnson H, OConnel PR, OHerlihy C. Obstetric events leading to anal sphincter damage. Obstet Gynecol., 92: 955-961, 1998. Donnely VS, OHerlihy C, Campbell DM, OConnel PR. Postpartum fecal incontinence is more common in women with irritable bowel syndrome. Dis. Colon & Rectum, 41: 586-589, 1998. Nygaard IE, Rao SSC, Dawson JD. Anal incontinence after anal sphincter disruption: a 30 year perspective. Obstet. Gynec., 89: 896-901, 1997. Wald A. Systemic diseases causing disorders of defecation and continence. Sem Gastroint Dis., 6: 194-202, 1995. MacKenzie WR, Hoxie NJ, Proctor ME, Gradus MS, Blair KA, Petersen DE, Kazmierczak JJ, Addiss DG, Fox KR, Rose JB and Davis JP. A massive outbreak in Milwaukee of cryptosporidium infection transmitted through the public water supply. NEJM, 331: 161-7, 1994. Sullivan SN, Wong C. Runners diarrhea. Different patterns and associated factors. J. Clin Gastroent., 14: 101-104, 1992 and hydrochlorothiazide.
Ness et al. 13 ; published a reanalysis of pooled data from seven case-control studies with 4, 644 cases diagnosed from 1989 to 1999 and 7, 182 population controls. Among nulligravid women with infertility for more than 5 years compared with those treated for less than 1 year, the risk of ovarian cancer was increased 2.67-fold 95% CI 1.913.74 ; . However, no association between fertility drug use and the overall risk of invasive ovarian cancer was found odds ratio [OR] 0.97; 95% CI 0.76 1.25 ; . In addition, increasing duration of fertility drug use CC and hMG ; was not associated with increased risk. Separate analyses of cancer in nulligravid and gravid women showed a nonsignificant increase in the OR for nulligravid women exposed to fertility drugs OR 1.60; 95% CI 0.90 2.87 ; . However, Ness et al. found that fertility drug use was associated with a significantly increased risk of borderline serous ovarian tumors when analysis by histologic subtypes of cancer was performed OR 2.43; 95% CI 1.015.88 ; . An elevated risk was not noted with any other borderline or invasive subtypes. In the case-control study by Franceschi et al. 14 ; , a medical diagnosis of infertility was not associated with an increased risk of ovarian cancer. The RR of ovarian cancer in the exposed infertile population compared with the unexposed population was 1.3 with 95% CI 0.72.4. However, this study was limited by lack of information on cause of infertility and type of fertility treatment. Shushan et al. 15 ; conducted a case-control study on a combined case group of invasive and borderline epithelial ovarian tumors and a case group including only women with borderline tumors. Compared with women without a history of infertility, infertile women who had never used fertility drugs had a crude RR of 1.3 95% CI 0.6 2.7 ; of an ovarian tumor, whereas the RR for infertile women who had ever used fertility drugs was 1.8 95% CI 1.0 3.3 ; . When adjustment was made for confounding factors, the risk associated with fertility drugs became nonsignificant. When the analysis was restricted to borderline tumors, the RR was 3.5 95% CI 1.210.1 ; . The adjusted RR with CC use was 0.9 P NS ; for epithelial ovarian cancers and 1.3 P NS ; for borderline tumors. However, the RR with hMG use was 3.2 95% CI 0.9 11.8 ; for the combined case group and 9.4 95% CI 1.752.1 ; for the borderline tumors. As mentioned earlier, this is contrary to the findings of Rossing et al. 3 ; . The investigators provided no information on types of infertility. Although this study had the strength of including cases through Israel Cancer Registry with histologic verification in all cases, it was limited by lack of information on specific causes of infertility and the fact that 36% of cases had died before contact was established, which could have caused selection bias. Mosgaard et al. 16 ; conducted the largest case-control study with 684 cases of epithelial and non-epithelial ovarian cancer and 1, 721 controls. The risk of ovarian cancer was not increased among treated infertile women compared with, for example, furosemide brand name.
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Drug costs rising faster in Canada than rest of World IMS HEALTH data for the 12 months ending September 2002 shows that Canada's drug costs are increasing faster than any country in the world. Canada's expenditures were up 16%, while costs were up 13% in the U.S., 12% in the U.K., 10% in Spain, 9% in Germany, 5% in Italy and 3% in France. The price of pharmaceuticals: Brand vs. Generic A price comparison based on data from IMS HEALTH comparing brand name and generic prices of virtually every multi-source product on the Canadian market shows that the average price differential between generic and brand products is 45%. According to data from IMS HEALTH, the average cost of a brand-name prescription has increased by 76% from $31.52 in 1992 to $55.56 in 2002. During the same period of time, the average cost of a generic prescription increased from $16.35 to $21.57, or 32%. Price per prescription 1992 2002 % Increase Brand $31.52 $55.56 76% Generic $16.35 $21.57 32, because furosemide mg.
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42. FLOMAX 0.4MG CAPSULE 43. FLOVENT 11OMCG INHALER 44. FLUOXETINE 20MG CAPSULE 45. FOSAMAX 10MG TABLET 46. FOSAMAX 70MG TABLET 47. FUROSEMIDE 40MG TABLET 48. GEMFIBROZIL 600MG TABLET 49. GLUCOPHAGE 1000MG TABLET 50. GLUCOPHAGE 500MG TABLET 51. GLUCOPHAGE 850MG TABLET 52. GLUCOPHAGE XR 500MG 53. GLUCOTROL XL 10MG TABLET 54. GLUCOVANCE 5 500MG TABLET 55. GLYBURIDE 5MG TABLET 56. HUMULIN 70 30 VIAL 57. HUMULIN N 100U ML VIAL 58. HYDROCODONE APAP 5 59. HYZAAR 100-25 TABLET 60. HYZAAR 5O-12.5 TABLE 61. ISOSORBIDE MN 30MG TABLET 62. ISOSORBIDE MN 60MG TABLET 63. K-DUR 2OMEQ TABLET SR 64. KLOR-CON M20 TABLET 65. LESCOL 40MG CAPSULE 66. LEVAQUIN 500MG TABLE 67. LIPITOR 10MG TABLET 68. LIPITOR 20MG TABLET 69. LIPITOR 40MG TABLET 70. LORAZEPAM 0.5MG TABLET 71. LORAZEPAM 1MG TABLET 72. LOTREL 5 10MG CAPSULE 73. LOTREL 5 20MG CAPSULE 74. METOPROLOL 50MG TABLET 75. MIACALCIN 200U NASAL 76. NEURONTIN 300MG CAPSULE 77. NEXIUM 40MG CAPSULE 78. NIFEDIPINE ER 30MG TABLET 79. NORVASC 10MG TABLET 80. NORVASC 5MG TABLET 81. OXYCONTIN 20MG TABLET 82. OXYCONTIN 40MG TABLET.
NAME OF DRUG CALCIMAR SOLUTION Calcitonin-Salmon ; THERAPEUTIC OR PHARMACOLOGICAL CLASSIFICATION Synthetic Salmon Calcitonin ACTION Calcimar participates in the regulation of the homeostasis of calcium by acting primarily on the bone; in Paget's disease presumably by an initial blocking effect on accelerated bone resorption. The rate of bone turnover appears to be decreased. Calcimar participates in the regulation of urinary excretion of phosphate and calcium. Administration of Calcimar decreases the volume and acidity of the gastric juice and decreases the volume as well as trypsin and amylase content of the pancreatic juice. For further details see Clinical Pharmacology section ; . INDICATIONS 1. Paget's Disease Treatment of symptomatic Paget's disease of the bone. 2. Hypercalcemia: Calcitonin is indicated for early treatment of hypercalcemic emergencies, along with other appropriate agents, when a rapid decrease in serum calcium is required, until more specific treatment of the underlying disease can be accomplished. It may also be added to existing therapeutic regimens for hypercalcemia such as intravenous fluids and furosemide, oral phosphate or corticosteroids, or other agents. Calcitonin may be used in patients with azotemia and those with limited cardiac reserve in whom intravenous fluids may be contraindicated. CONTRAINDICATIONS Known hypersensitivity to salmon calcitonin and ibuprofen.
13, 2002 depomed, inc amex: dmi ; today announced the results of a phase i human trial comparing its internally developed, extended release dosage form, furosemode gr tm ; , with the currently marketed immediate release furosemude formulation.
MANAGEMENT OF CHRONIC OBSTRUCTIVE PULMONARY DISEASE COPD ; Pathophysiology Most of the increased resistance to airflow is due to irreversible pulmonary damage and is unresponsive to medication. A degree of reversible airway resistance is superimposed onto this and therapy is aimed at reducing this to a minimum and hence proving maximum pulmonary function. Acute deteriorations in function are common and often associated with viral and bacterial infection. Principles of drug therapy and imitrex and furosemide, for example, furosrmide picture.
Patents Office Journal precious metal or coated therewith combs and sponges; brushes except paint brushes brush-making materials; articles for cleaning purposes; unworked or semi-worked glass except glass used in building glassware, porcelain and earthenware included in this class ; . Textiles and textile goods included in this class bed and table covers; curtains of textile or plastic.
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That the Planning and Budget Committee Recommend to the Academic Board: 1. THAT the Project Planning Report for the Multi-faith Centre for Study and Spiritual Practice be approved in principle to be located on the second and third floors of the Koffler Institute for Pharmacy Management Building at 569 Spadina Avenue including the renovation of approximately 615 net assignable square metres; 2. THAT the space program to accommodate expanded training facilities in support of the Administrative Management Systems AMS ; and Human Resources HR ; activities that is to be relocated to the ground floor at 256 McCaul and isosorbide.
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Operation of Conventional Coating Pan 48 inches pan ; Start the compressor and open the compressed air inlet valve Put on the main switch. Put on the control panel switches TC and TI Open the steam inlet valve. Start the air inlet blower. Set inlet air opening diaphragm in the 3rd hole from closed end. Open the steam by-pass valve and then close it. Start the exhaust blower and set outlet air diaphragm in the 3rd hole from closed end. Put ON the pan light. Dry the coating pan. Rotate the pan for 5 minutes Draw out the retractable arm assembly using the Pneumatic System Put on inlet air, outlet air and coating pan. Set atomisation air pressure on '0'. Start peristaltic pump. Set air pressure on the pump to 1.0 kg cm2 and check the spray rate of.
He risks to patients from government-regulated products really depend on the balance of power between the government, industry, and patients. This risk relationship is often naively portrayed as an equilateral triangle, but it really is not. Sometimes the government is much closer, appropriately so, to the corner of the patients. More often, unfortunately, it is closer to the corner of industry. In these circumstances we have tried, with some success over the years, to get drugs or other products that are too dangerous off the market, or to warn people about hazards of various products, mostly FDA-regulated, despite resistance from the FDAindustry alliance not to do so. The regulation of blood is an example of a situation in which we believe the government has, more recently, properly aligned itself with patients and has taken on the industry. In this case, it is the industry of blood and blood products and blood collection. These were the findings from an FDA inspection of the American Red Cross ARC ; Headquarters completed almost four years ago [in 2000]: deficient quarantine system to prevent release of unsuitable products; improper release of CMV- cytomegalovirus.
Semide kinetics and dynamics in patients with cirrhosis. Clin Pharmacol Ther 40: 14 20, Verbeeck RK, Patwardhan RV, Villeneuve JP, Wilkinson GR, Branch RA: Fueosemide disposition in cirrhosis. Clin Pharmacol Ther 31: 719 725, Mees EJD: Does it make sense to administer albumin to the patient with nephrotic oedema? Nephrol Dial Transplant 11: 1224 1226, Akcicek F, Yalniz T, Basci A, Ok E, Mees EJD: Diuretic effect of furosemide in patients with nephrotic syndrome: Is it potentiated by intravenous albumin? Br Med J 310: 162163, 1995 Fliser D, Zurbruggen, Mutschuler E, Bischoff I, Nussberger J, Franek E, Ritz E: Coadministration of albumin and furosemide in patients with the nephrotic syndrome. Kidney Int 55: 629 634, Kirchner KA, Voelker JR, Brater DC: Tubular resistance to furosemide contributes to the attenuated diuretic response in nephrotic rats. J Soc Nephrol 2: 12011207, 1992 Keller E, Hoppe-Seyler G, Schollmeyer P: Disposition and diuretic effect of furosemide in the nephrotic syndrome. Clin Pharmacol Ther 32: 442 449, Prandota J: Urinary elimination kinetics and diuretic effect of intravenous furosemide in nephrotic children. Dev Pharmacol Ther 5: 98 108, Smith DE, Hyneck ML, Berardi RR, Port FK: Urinary protein binding, kinetics, and dynamics of furosemide in nephrotic patients. J Pharm Sci 74: 603 607, Sjostrom PA, Odlind BG, Beermann BA, Karlberg BE: Pharma cokinetics and effects of furosemide in patients with the nephrotic syndrome. Eur J Clin Pharmacol 37: 173180, 1989.
Consistent with the findings from short-term diuretic studies, there was no increase in uv when anuric furosemide-treated patients were challenged with an additional diuretic.
Figure 2. Real and projected global sales of antipsychotics, 1990-2009. Source: IMS Health Inc reproduced with permission and gemfibrozil.
Erythromycin Ethylsuccinate Escitalopram Escitalopram Escitalopram Estradiol patch Estradiol patch Estrogen Conj. Estrogen Conj. Estrogen Conj. Estrogen Conj. Estrogen Conj. medroxyprogesterone Estrogen Conj. medroxyprogesterone Estrogen Ester. methyltestosterone Estrogen vaginal Etidronate Famotidine Famotidine Fentanyl Fentanyl Fentanyl Fentanyl Ferrous Gluconate Ferrous Sulfate Ferrous Sulfate Finasteride Fluconazole Fluconazole Fludrocortisone Fluocinonide 30 gm Fluocinonide 60 gm Fluocinonide 60 gm Fluocinonide emulsified 60 gm Fluoride sodium 5000 Flurometholone Fluticasone Fluticasone Fluticasone Fluticasone nasal Fluticasone salmeterol Fluticasone salmeterol Folic acid Furosemiide Furosemide.
4th european conf. Health Economics - July 02 SL-2417 02.
They may become infected. Only 10 percent of persons infected will develop active or contagious TB. A TB infection can become active in a short period of time, or it may take years to become active depending on an individual's health status. The following factors increase one's risk for both TB exposure and infection: being in close contact with someone who is infectious, being an immigrant from areas where TB is common e.g., Asia, Africa or Latin America ; , being poor, homeless, and or medically underserved, being a racial ethnic minority, living in congregate settings like correctional facilities or residential AOD programs, being a person who is alcoholic or injects drugs, having HIV AIDS, and being exposed on the job.
Date: 06 05ISR Number: 4686969-9Report Type: Expedited 15-DaCompany Report #2005079018 Age: 74 YR Gender: Female I FU: I Outcome Dose Duration Hospitalization 750 MG 250 Initial or Prolonged MG, 3 IN 1 D ; Blood Creatine Increased Creatinine Renal Clearance Increased Drug Interaction 6.25 MG Glasgow Coma Scale Abnormal 30 MG Neurological Symptom Therapeutic Agent 0.5 MG 0.25 Toxicity MG, 2 IN 1 D ; Escitalopram Escitalopram ; 10 MG Irbesartan Irbesartan ; 300 MG Lormetazepam Lormetazepam ; Metformin Metformin ; Furosemid4 C C SS Risperidone Risperidone ; SS Lisinopril Lisinopril ; SS Report Source Foreign Literature Health Professional Levomepromazine Levomeromazine ; Product Lithium Lithium ; Role PS Manufacturer Route.
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It belongs to the families of drugs called antidepressant agents and selective serotonin reuptake inhibitors ssris, for example, furosemide interactions.
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Statistical Analysis Results are presented as mean SD, unless otherwise stated. Survival status of all subjects after 5 years was assessed. The duration from entry to the last attendance or death was recorded. The survival time was calculated using the life table method. Univariate and multivariate Cox proportional hazards analyses were performed to investigate the relationship between the clinical indices and mortality. Postbronchodilator FEV1 was used as an index of airflow limitation, because it is regarded as a better predictor of mortality than prebronchodilator FEV1 2 ; . Clinical variables were used as continuous variables, except that the categorical variables of smoking status and the use of inhaled.
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Table 4. Reclassification of Flavobacterium spp.
This medication should not be used if you have certain medical conditions. Before using this medicine, consult your doctor or pharmacist if you have: high potassium blood levels, severe kidney disease e.g., chronic kidney failure, inability to make urine ; , untreated underactive adrenal gland, sudden loss of body fluids acute dehydration ; , severe conditions of tissue breakdown e.g., severe burns, traumatic injury ; . Before using this medication, tell your doctor or pharmacist your medical history, especially of: kidney problems, certain types of heart disease e.g., atrioventricular block ; , esophagus stomach intestinal problems e.g., stomach ulcers, slowed movement, blockage ; . Kidney function declines as you grow older. This medication is removed by the kidneys. Therefore, elderly people may be more sensitive to the effects of this drug. This medication should be used only when clearly needed during pregnancy. Discuss the risks and benefits with your doctor. It is not known whether this drug passes into breast milk. Consult your doctor before breast-feeding. DRUG INTERACTIONS: Your healthcare professionals e.g., doctor or pharmacist ; may already be aware of any possible drug interactions and may be monitoring you for it. Do not start, stop or change the dosage of any medicine before checking with them first. Before taking potassium supplements, check with your doctor if you are taking other medications products that may also increase the potassium level in your blood. A potassium level in the blood that is too high may cause serious side effects. Follow your doctor's instructions carefully and continue medications for your condition as directed. Keep all medical laboratory appointments so your doctor can monitor your potassium levels. Consult with your doctor if you are taking any of the following: ACE inhibitors e.g., captopril, lisinopril ; , angiotensin receptor blockers ARBs such as candesartan, losartan ; , eplerenone, potassium-sparing "water pills" diuretics such as amiloride, spironolactone, triamterene ; , salt substitutes containing potassium. Before using this medication, tell your doctor or pharmacist of all prescription and nonprescription herbal products you may use, especially of: digoxin, drospirenone, "water pills" diuretics such as furosemide, hydrochlorothiazide ; . Also tell your doctor or pharmacist if you take medications that may slow down the movement of potassium capsules tablets in your digestive system, possibly increasing the risk of side effects. These drugs include: anticholinergic drugs e.g., atropine, scopolamine ; , certain antihistamines e.g., diphenhydramine ; , antispasmodic drugs e.g., dicyclomine, hyoscyamine ; , certain anti-Parkinson's drugs e.g., benztropine, trihexyphenidyl ; , belladonna alkaloids, bladder control drugs e.g., oxybutynin, tolterodine ; . NOTES: Do not share this medication with others. Laboratory and or medical tests e.g., potassium blood level, kidney function tests ; should be performed periodically to monitor your progress or check for side effects. Consult your doctor for more details. Eat a well-balanced diet. Foods high in potassium include: bananas, oranges, watermelon, cantaloupe, raisins, dates, prunes, avocados, apricots, beans, broccoli, leafy green vegetables, spinach, potatoes, lentils, fish, chicken, turkey, ham, beef, and milk. Consult your doctor or pharmacist regarding your specific dietary plan. OVERDOSE: If overdose is suspected, contact your local poison control center or emergency room immediately. US residents can call the US national poison hotline at 1-800-222-1222. Canadian residents should call their local poison control center directly. Symptoms of overdose may include irregular heartbeat, muscle weakness, confusion, numbness tingling of the hands feet, chest pain.
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