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An ABC of Drug-Related Problems RHB Meyboom, M Lindquist, ACG Egberts Drug Safety 2000;22:415-23
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Introduction The percentage of hospital admissions due to adverse drug reactions in some countries is about or more than 10% Br J Clin Pharmacol 1998, 45(3), 301- 308. Thèrapie, 1999, 54(1) 21-27. Ad Drug React Toxico Rev., 1998, 17(1), 19-50. Norway11.5%, France13%, UK 16%
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6.7% of hospital patients have serious adverse drug reactions (medication error excluded) Lazarou J. Pomeranz BH, Corey PN. JAMA 1998;279:1200-5 16.2% of hospital admissions are drug-related Therapeutic failure 54.8% Adverse reactions32.9% Overdose12.3% Avoidable49.3% Nelson KM, Talbert RL. Pharmacotherapy 1996;16:701-7
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Some countries spend up to 15-20% of their hospital budget dealing with drug complications. – White T et al. Counting the cost of drug-related adverse events. Pharmacoeconomics, 1999, 15(5). 445- 458.
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Type A adverse effects Drug actions Interactions Type B adverse effects Patient reactions Type C adverse effects Statistical effects Ineffectiveness Poisoning Noncompliance Medication error Dependence Late effects Carcinogenesis Organ selective injury Risk situations The Zodiac of Drug-Related Problems
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Type A adverse effects - Drug actions Pharmacological side effects Common (> 1 %) Dose relationship Suggestive time relationship (kinetics) Reproducible Drug actions Type A adverse effects Interactions Patient reactions Type B adverse effects Statistical effects Type C adverse effects Non-compliance Overdose Therapeutic failure Dependence Organ selective toxicity Delayed effects Special situations
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Type A adverse effects - Drug actions Examples: Sedation Constipation Diarrhoea Urinary retention Impotence Hypoglycaemia (antidiabetics) Hypokalaemia (diuretics) Baldness (oncolytics) Drug actions Type A adverse effects Interactions Patient reactions Type B adverse effects Statistical effects Type C adverse effects Non-compliance Overdose Therapeutic failure Dependence Organ selective toxicity Delayed effects Special situations
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Drug actions Type A adverse effects Interactions Patient reactions Type B adverse effects Statistical effects Type C adverse effects Non-compliance Overdose Therapeutic failure Dependence Organ selective toxicity Delayed effects Special situations Type A adverse effects - Drug actions Organ selective injury Long-term use effects Carcinogenesis Risk situations, e.g. - childhood - elderly - pregnancy - lactation - renal failure - haemodialysis Interactions
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Type A adverse effects - Drug actions Methods of study: Clinical trial / follow-up study Spontaneous reporting Prescription event monitoring Hospital studies Experiments Drug actions Type A adverse effects Interactions Patient reactions Type B adverse effects Statistical effects Type C adverse effects Non-compliance Overdose Therapeutic failure Dependence Organ selective toxicity Delayed effects Special situations
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Drug actions Type A adverse effects Interactions Patient reactions Type B adverse effects Statistical effects Type C adverse effects Non-compliance Overdose Therapeutic failure Dependence Organ selective toxicity Delayed effects Special situations Type B adverse effects - Patient reactions Rare (< 1 %) No dose relationship Unexpected Mechanism uncertain Causality uncertain Not reproducible Characteristic, serious Suggestive time relationship Low background frequency
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Type B adverse effects - Patient reactions Immunoallergic reactions Pseudoallergy Metabolic intolerance Idiosyncrasy Examples: Anaphylaxis Stevens-Johnson syndrome Blood dyscrasias Hepatitis Drug actions Type A adverse effects Interactions Patient reactions Type B adverse effects Statistical effects Type C adverse effects Non-compliance Overdose Therapeutic failure Dependence Organ selective toxicity Delayed effects Special situations
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Drug actions Type A adverse effects Interactions Patient reactions Type B adverse effects Statistical effects Type C adverse effects Non-compliance Overdose Therapeutic failure Dependence Organ selective toxicity Delayed effects Special situations Type B adverse effects - Patient reactions Methods of study: Spontaneous reporting Prescription event monitoring Case control surveillance Large databases / record linkage
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Type C adverse effects - 'statistical effects' Increased frequency of 'spontaneous' disease High background frequency Less typical for a drug reaction No suggestive time relationship Often long latency Mechanism unknown Not reproducible Drug actions Type A adverse effects Interactions Patient reactions Type B adverse effects Statistical effects Type C adverse effects Non-compliance Overdose Therapeutic failure Dependence Organ selective toxicity Delayed effects Special situations
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Type C adverse effects - 'statistical effects' Examples: Thromboembolic events GI haemorrhage Pancreatitis Drug actions Type A adverse effects Interactions Patient reactions Type B adverse effects Statistical effects Type C adverse effects Non-compliance Overdose Therapeutic failure Dependence Organ selective toxicity Delayed effects Special situations
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Drug actions Type A adverse effects Interactions Patient reactions Type B adverse effects Statistical effects Type C adverse effects Non-compliance Overdose Therapeutic failure Dependence Organ selective toxicity Delayed effects Special situations Type C adverse effects - 'statistical effects' Methods of study: Follow up studies (large scale, long-term) Case control studies Large databases / record linkage Spontaneous Reporting of limited use
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Ineffectiveness 55% of drug related problems Limited efficacy Noncompliance Pharmaceutical defect (counterfeit; generic) Interaction Resistance Tolerance Drug actions Type A adverse effects Interactions Patient reactions Type B adverse effects Statistical effects Type C adverse effects Non-compliance Overdose Therapeutic failure Dependence Organ selective toxicity Delayed effects Special situations
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Drug actions Type A adverse effects Interactions Patient reactions Type B adverse effects Statistical effects Type C adverse effects Non-compliance Overdose Therapeutic failure Dependence Organ selective toxicity Delayed effects Special situations Inappropriate use Wrong dose Wrong duration Wrong indication Wrong administration Wrong patient Wrong attitude or expectations - Noncompliance - Medication error - Negligence (contraindication) - Failure of information, counseling or monitoring
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Medication Error > 7000 deaths per year from medication error in the USA To Err is Human: Building a Safer Health System. National Academy Press, 1999
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Inappropriate use Methods of study: Spontaneous reporting Questionnaire Hospital studies Follow-up studies Drug actions Type A adverse effects Interactions Patient reactions Type B adverse effects Statistical effects Type C adverse effects Non-compliance Overdose Therapeutic failure Dependence Organ selective toxicity Delayed effects Special situations
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Dependence hidden not only narcotics Drug actions Type A adverse effects Interactions Patient reactions Type B adverse effects Statistical effects Type C adverse effects Non-compliance Overdose Therapeutic failure Dependence Organ selective toxicity Delayed effects Special situations
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Poisoning (overdose) iatrogenic accidental intentional Drug actions Type A adverse effects Interactions Patient reactions Type B adverse effects Statistical effects Type C adverse effects Non-compliance Overdose Therapeutic failure Dependence Organ selective toxicity Delayed effects Special situations
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Type A adverse effects Drug actions Interactions Type B adverse effects Patient reactions Type C adverse effects Statistical effects Ineffectiveness Poisoning Noncompliance Medication error Dependence Late effects Carcinogenesis Organ selective injury Risk situations The Zodiac of Drug-Related Problems
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Definitions (WHO) Side Effect: any unintended effect of a drug occurring at normal doses, which is related to the pharmacological properties of the drug Adverse Event: any untoward medical occurrence that may present during treatment with a drug but does not necessarily have a causal relationship Adverse Reaction: any response to a drug which is noxious and unintended and occurs at normal doses Often only suspicions! Edwards IR, Biriell C. Drug Safety 1994;10:93-102
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