Literature DB >> 2878346

Adverse reactions and interactions with beta-adrenoceptor blocking drugs.

R V Lewis, D G McDevitt.   

Abstract

beta-Blocking drugs are widely used throughout the world and serious adverse reactions are relatively uncommon. Most of those which do occur are pharmacologically predictable and may be avoided by ensuring that patients who are to be given beta-blockers do not have a predisposition to the development of bronchospasm, cardiac failure or peripheral ischaemia. In some situations, the use of a beta 1-selective blocking drug may reduce the risk of a severe adverse reaction, but there is little evidence that other ancillary properties such as partial agonist activity are of relevance in this context. Long term experience with many of the beta-blockers in current use suggests that unpredictable major adverse reactions such as the practolol oculomucocutaneous syndrome are unlikely to be repeated, although some of these drugs may be associated with immunological disturbances and some have been implicated in the development of retroperitoneal fibrosis. beta-Blocking drugs appear to be associated with a number of subjective side effects including muscle fatigue, peripheral coldness and some neurological symptoms. These side effects are highly subjective and are therefore difficult to quantify and it is not known whether they are of major importance in terms of their effect upon patients' overall well-being. It cannot be assumed that simply because such side effects can be elicited that they do, in fact, matter. However, because beta-blockers are often prescribed for patients who have no symptoms and for whom the benefits of therapy are generally small, such side effects would be of considerable importance if they had an overall effect upon quality of life. There are theoretical reasons to suppose that the incidence and severity of such side effects may be related to the ancillary properties of the individual drugs, but there is little evidence that parameters such as beta 1-selectivity, or partial agonist activity are clinically important determinants of the severity of these side effects. Lipophilicity, however, may be associated with an increased incidence of neurological symptoms. beta-Blocking drugs may cause a variety of metabolic disturbances including an increase in serum VLDL-cholesterol concentrations. However, long term studies have not shown that such disturbances are associated with an increased risk of cardiovascular disease, indicating that such metabolic changes may not be of major importance in practice. beta-Blocking drugs may be involved in a number of interactions with other drugs, but few of these have been shown to be of clinical significance.(ABSTRACT TRUNCATED AT 400 WORDS)

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Year:  1986        PMID: 2878346     DOI: 10.1007/bf03259848

Source DB:  PubMed          Journal:  Med Toxicol        ISSN: 0112-5966


  134 in total

1.  Plasma binding and the affinity of propranolol for a beta receptor in man.

Authors:  D G McDevitt; M Frisk-Holmberg; J W Hollifield; D G Shand
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2.  Increased antidepressant use in patients prescribed beta-blockers.

Authors:  J Avorn; D E Everitt; S Weiss
Journal:  JAMA       Date:  1986-01-17       Impact factor: 56.272

3.  The effects of acute or chronic ingestion of propranolol or metoprolol on the physiological responses to prolonged, submaximal exercise in hypertensive men.

Authors:  R G Wilcox; T Bennett; I A Macdonald; M Herbert; A M Skene
Journal:  Br J Clin Pharmacol       Date:  1984-03       Impact factor: 4.335

Review 4.  Serum lipoproteins and ischemic vascular disease: on the interpretation of serum lipid versus serum lipoprotein concentrations.

Authors:  S Rössner
Journal:  J Cardiovasc Pharmacol       Date:  1982       Impact factor: 3.105

5.  Satalol-induced torsade de pointes.

Authors:  A Kontopoulos; A Filindris; F Manoudis; P Metaxas
Journal:  Postgrad Med J       Date:  1981-05       Impact factor: 2.401

6.  Attenuation of hypotensive effect of propranolol and thiazide diuretics by indomethacin.

Authors:  J Watkins; E C Abbott; C N Hensby; J Webster; C T Dollery
Journal:  Br Med J       Date:  1980-09-13

7.  Propranolol interactions with diazepam, lorazepam, and alprazolam.

Authors:  H R Ochs; D J Greenblatt; B Verburg-Ochs
Journal:  Clin Pharmacol Ther       Date:  1984-10       Impact factor: 6.875

8.  Immediate cardiovascular responses to oral prazosin--effects of concurrent beta-blockers.

Authors:  H L Elliott; K McLean; D J Sumner; P A Meredith; J L Reid
Journal:  Clin Pharmacol Ther       Date:  1981-03       Impact factor: 6.875

9.  A randomized trial of propranolol in patients with acute myocardial infarction. I. Mortality results.

Authors: 
Journal:  JAMA       Date:  1982-03-26       Impact factor: 56.272

10.  Impairment of antipyrine clearance in humans by propranolol.

Authors:  D J Greenblatt; K Franke; D H Huffman
Journal:  Circulation       Date:  1978-06       Impact factor: 29.690

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Review 5.  Clinical pharmacokinetics of pravastatin: mechanisms of pharmacokinetic events.

Authors:  T Hatanaka
Journal:  Clin Pharmacokinet       Date:  2000-12       Impact factor: 6.447

6.  Natriuretic peptide-induced catecholamine release from cardiac sympathetic neurons: inhibition by histamine H3 and H4 receptor activation.

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Review 7.  The pharmacokinetics of lignocaine and beta-adrenoceptor antagonists in patients with acute myocardial infarction.

Authors:  S Nattel; G Gagne; M Pineau
Journal:  Clin Pharmacokinet       Date:  1987-11       Impact factor: 6.447

Review 8.  Guidelines for treating hypertension in the elderly.

Authors:  J P Emeriau
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Review 9.  Adverse reactions with beta-adrenoceptor blocking drugs. An update.

Authors:  R V Lewis; C Lofthouse
Journal:  Drug Saf       Date:  1993-10       Impact factor: 5.606

10.  Clinical pharmacology of chronic atrial fibrillation.

Authors:  R Lewis; J McClay
Journal:  J R Coll Physicians Lond       Date:  1988-10
  10 in total

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