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Blood pressure abnormalities

Tretinoin (Vesanoid] Acute promyelocytic leukemia Cardiac arrhythmias edema blood pressure abnormalities (hypotension, hypertension] phlebitis respiratory tract problems muscle pain paresthesias CNS toxicity (depression, anxiety, confusion] skin rash Gl distress (abdominal distension nausea, vomiting]... [Pg.581]

Emergency treatment depends on the immediate toxic effects of BZP and TFMPP. High blood pressure, abnormal heart rate or rhythm, seizures or convulsions, fever, and abnormal movements all have specific treatments and may require hospitalization for intravenous medications and general supportive care. Coma or decreased level of consciousness, respiratory depression, difficulty breathing, and severe allergic reaction may require treatment in an intensive care unit and assisted respiration. If a user experiences any untoward effects, or if someone inadvertently takes a much larger dose of medicinal piperazines than prescribed, it is prudent to contact a doctor, emergency medical services, or poison control. [Pg.80]

Children who had been exposed to excessive amounts of mercurous chloride tablets for worms or mercurous chloride-containing powders for teething discomfort had increased heart rates and elevated blood pressure. Abnormal heart rhythms were also seen in children who had eaten grains contaminated with very high levels of methylmercury. [Pg.36]

Cardiovascular Effects. No atypical heart sounds or blood pressure abnormalities were observed in 24 employees occupationally exposed to concentrations as high as 130 mg zinc/m of metallic zinc dust, zinc oxide dust, zinc sulfide dust, or lithophone dust (a combination of barium sulphate and -5-30% zinc sulphide) for 2-35.5 years (Batchelor et al. 1926). However, this study is limited because only selected employees were examined, and they were not compared to controls. [Pg.28]

Other symptoms may Include low blood pressure, abnormal breathing, reduced body temperature, reduced body pH, convulsions, collapse and death. [Pg.126]

It is well accepted that hypertension is a multifactorial disease. Only about 10% of the hypertensive patients have secondary hypertension for which causes, ie, partial coarctation of the renal artery, pheochromacytoma, aldosteronism, hormonal imbalances, etc, are known. The hallmark of hypertension is an abnormally elevated total peripheral resistance. In most patients hypertension produces no serious symptoms particularly in the early phase of the disease. This is why hypertension is called a silent killer. However, prolonged suffering of high arterial blood pressure leads to end organ damage, causing stroke, myocardial infarction, and heart failure, etc. Adequate treatment of hypertension has been proven to decrease the incidence of cardiovascular morbidity and mortaUty and therefore prolong life (176—183). [Pg.132]

Hypotension is defined as abnormally low blood pressure. In most cases, hypotension is adequately treated with general measures (e.g. physical exercise), dtug treatment is rarely required. Drugs used for the treatment of hypotension include a-adrenoceptor agonists and compounds which activate both a and (3 adrenoceptors. [Pg.609]

B2 knockout embryos subjected to salt stress in utero show suppressed renin expression and an abnormal kidney phenotype and develop early postnatal hypertension. Consistently, although basal bradykinin formation is defective tissue kallikrein-null mice have normal blood pressure however suffer from cardiovascular abnormalities. However suggesting a function of kinin signaling during development. [Pg.675]

Identify normal and abnormal blood pressure levels for adults. [Pg.393]

Table VI summarizes the material presented in the previous discussion. It correlates the changes in oxygen and carbon dioxide partial pressures, showing the pathological causes for the imbalances. In addition, it contains the various diagnoses of acid-base abnormality (using same numbers as in Figures 1 and 2 and Table I). Considering the format of Table VI as a tic-tac-toe set-up, we can label the nine portions by the letters A-I for identification in Table VII which gives examples of various conditions associated with such blood gas abnormalities (20-30). Table VI summarizes the material presented in the previous discussion. It correlates the changes in oxygen and carbon dioxide partial pressures, showing the pathological causes for the imbalances. In addition, it contains the various diagnoses of acid-base abnormality (using same numbers as in Figures 1 and 2 and Table I). Considering the format of Table VI as a tic-tac-toe set-up, we can label the nine portions by the letters A-I for identification in Table VII which gives examples of various conditions associated with such blood gas abnormalities (20-30).
In addition to excess sodium intake, abnormal renal sodium retention may be the primary event in the development of hypertension, and it includes abnormalities in the pressure-natriuresis mechanism. In hypertensive individuals, this theory proposes a shift in the control mechanism preventing the normalization of blood pressure. The mechanisms behind the resetting of the pressure-natriuresis curve may include afferent arteriolar vasoconstriction, decreased glomerular ultrafiltration, or an increase in tubular sodium reabsorption.4 Other theories supporting abnormal renal sodium retention suggest a congenital reduction in the number of nephrons, enhanced renin secretion from nephrons that are ischemic, or an acquired compensatory mechanism for renal sodium retention.9... [Pg.13]

Monitor electrocardiogram continuously in patients with cardiac abnormalities until serum potassium levels drop below 5 mEq/L (5 mmol/L) or cardiac abnormalities resolve. Evaluate serum potassium and glucose levels within 1 hour in patients who receive insulin and dextrose therapy. Evaluate serum potassium levels within 2 to 4 hours after treatment with SPS or diuretics. Repeat doses of diuretics or SPS if necessary until serum potassium levels fall below 5 mEq/L (5 mmol/L). Monitor blood pressure and serum potassium levels in 1 week in patients who receive fludrocortisone. [Pg.382]

Sepsis The systemic inflammatory response syndrome and documented infection (culture or Gram stain of blood, sputum, urine, or normally sterile body fluid positive for pathogenic microorganisms Severe sepsis Sepsis associated with organ dysfunction, hypoperfusion, or hypotension (systolic blood pressure less than 90 mm Hg). Hypoperfusion and perfusion abnormalities may include, but are not limited to, lactic acidosis, oliguria, or acute alteration in mental status. [Pg.1186]

Another observation during the study was that at the beginning of the program 39 people had high blood pressure and 7 had low blood pressure. Of these 46 people with abnormal blood pressure, 41 had reached normal levels by the end of the week. Those who started with normal readings were still normal at the end of the week. [Pg.43]

Septic shock Sepsis with hypotension (a systolic blood pressure of <90 mm Hg or a reduction of <40 mm Hg from baseline), despite adequate fluid resuscitation, along with the presence of perfusion abnormalities as seen by severe sepsis. Patients who are receiving inotropic or vasopressor agents may not be hypotensive at the time that perfusion abnormalities are measured. [Pg.58]

NOx levels are increased in plasma and urine of septic animals. Many nonse-lective NO synthase inhibitors (e.g., L-NMMA) are used in several models with experimental induced sepsis (S40). In most studies it was shown that the cardiovascular abnormalities associated with sepsis were reversed, increasing blood pressure and systemic vascular resistance (F7, K9, M26, N5), together with a improvement in renal function (B42, H24). Also, selective inhibition of iNOS prolonged survival in septic rats (A7). [Pg.75]

In a particularly dramatic case of placebo-induced side effects, doctors at a hospital in Jackson, Mississippi, treated a young man who came into the emergency room, said to the receptionist, Help me, I took all my pills and then collapsed to the floor, dropping an empty prescription container. His blood pressure was abnormally low, and he was treated with intravenous fluids, which brought it back to within a normal range. The prescription bottle bore a label indicating that the medication was part of a clinical trial of antidepressants. Further investigation revealed that he had... [Pg.127]

This material is hazardous through inhalation, penetration through broken skin, and ingestion. Symptoms include headache, fever and chills, seizures, slow heart rate (bradycardia), abnormal blood pressure, vomiting, and death. [Pg.484]

Cirrhosis results in elevation of portal blood pressure because of fibrotic changes within the hepatic sinusoids, changes in the levels of vasodilatory and vasoconstrictor mediators, and an increase in blood flow to the splanchnic vasculature. The pathophysiologic abnormalities that cause it result in the commonly encountered problems of ascites, portal hypertension and esophageal varices, HE, and coagulation disorders. [Pg.252]

Yellow Rain A lethal yellow substance thought to have been dispersed aerially as a warfare agent in Southeast Asia and Afghanistan the lethal component is though to have been a trichothecene mycotoxin that was reported to produce severe nausea and vomiting, disturbances in the central nervous system. Fever, chills, and abnormally low blood pressure with a case mortality of approximately 50 percent. [Pg.338]


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