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Adverse Drug
Effect
By
Arijit Chakraborty
M-Pharm (Pharmacology)
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Definition: Adverse effect is ‘any undesirable or
unintended consequence of drug administration. It
is a broad t...
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DRUG ADVERSE EFFECT
Diethyl carbamazepine Mazzoti reaction
Mebendazole Abdominal pain, diarrhea
Chloroquinine Ga...
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Types of adverse drug effect
All drugs can produce harmful as
well as beneficial effects. These are either
relat...
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Adverse effect related to the main
pharmacological action of the drug:
Many adverse effects related to the main
...
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Such effects are sometimes serious
(e.g. intracerebral bleeding caused by
anticoagulants, hypoglycemic coma from...
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Adverse effects unrelated to the main
pharmacological action of the drug:
Adverse effects unrelated to the main
...
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Drug Toxicity
Toxicity testing: Toxicity testing in animals is
carried out on new drugs to identify potential
ha...
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Types of drug toxicity
Toxic effects of drugs can be:
 Related to the principal pharmacological action, e.g.
bl...
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GENERAL MECHANISMS OF TOXIN-
INDUCED CELL DAMAGE AND CELL
DEATH:Toxic concentrations of drugs or drug
metabolite...
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The liver is of great importance in drug
metabolism and hepatocytes are exposed to
high concentrations of nascen...
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NON-COVALENT INTERACTIONS: Reactive
metabolites of drugs can be involved in several
related, potentially cytotox...
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Covalent reaction: Some of effects produced by
covalent reaction,
 Lipid per-oxidation.
 Reactive oxygen speci...
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HEPATOTOXICITY
Many therapeutic drugs cause liver
damage, manifested clinically as hepatitis or
only as laborato...
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General mechanisms of cell damage and
cell death:
 Drug-induced cell damage or death is usually caused by
react...
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Modification of sulfhydryl groups on key
enzymes, e.g. Ca2+-ATPase and structural
proteins.
 Covalent interact...
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Adverse effects of non-steroidal anti-
inflammatory drugs on the kidney:
Cause Adverse effects
Principal pharmac...
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MUTAGENESIS AND CARCINOGENICITY
Mutation changes the genotype of a
cell, and the change is passed on when the ce...
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BIOCHEMICAL MECHANISMS OF
MUTAGENESIS
 Most chemical carcinogens act by
modifying bases in DNA, particularly gu...
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 The importance of drugs, in comparison with
other chemicals such as pollutants and food
additives, as a causat...
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CARCINOGENESIS
Alteration of DNA is the first step in the
complex, multistage process of carcinogenesis.
Carcino...
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TERATOGENESIS AND DRUG-INDUCED FETAL
DAMAGE
Teratogenesis signifies the production
of gross structural malformat...
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MECHANISM OF TERATOGENESIS
The timing of the teratogenic insult in
relation to fetal development is critical in
...
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SOME DEFINITE AND PROBABLE HUMAN
TERATOGENS
Although many drugs have been found
to be teratogenic in varying deg...
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 Warfarin: Administration of warfarin in the first
trimester is associated with nasal hypoplasia
and various ce...
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ALLERGIC REACTIONS TO DRUGS
Allergic reactions of various kinds are a
common form of adverse response to drugs.
...
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 The reaction conforms to one of the clinical
syndromes associated with allergy-types I, II, III
and IV of the ...
Your Logo
Hypersensitivity reactions – originally
divided into 4 types.
 Type I: classical immediate hypersensitivity
 T...
Your Logo
Hypersensitivity reaction depends on:
1) chemical nature of allergen
2) route involved in sensitization i.e. inh...
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Allergic reactions to drugs
 Drugs or their reactive metabolites can bind
covalently to proteins to form immuno...
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Anaphylactic shock (type I): Many drugs
can cause this, and most deaths are caused by
penicillin
Hematological...
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Rashes (type I, IV): It is usually mild but can
be life-threatening (e.g. Stevens-Johnson
syndrome).
Drug-indu...
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 Rang, Dale’s, Pharmacology, Elsevier, 6th
edition, 2008 ( 751-764).
 K. D. Tripathi, Essentials of Medical
Ph...
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Transcript of "Adverse drug effect"

  1. 1. Ihr Logo Adverse Drug Effect By Arijit Chakraborty M-Pharm (Pharmacology)
  2. 2. Your Logo Definition: Adverse effect is ‘any undesirable or unintended consequence of drug administration. It is a broad term, includes all kinds of noxious effect – trivial, serious or even fatal. Another term ‘adverse drug effect’ has been use to mean ‘ any untoward medical occurrence that many present during treatment with a medicine, but which does not necessary have a casual relationship with the treatment’.
  3. 3. Your Logo DRUG ADVERSE EFFECT Diethyl carbamazepine Mazzoti reaction Mebendazole Abdominal pain, diarrhea Chloroquinine Gastrointestinal upset, purities Mefloquine Abdominal pain, epigastric distress Quinine Tinitus, headache Metronidazole Headache, dry mouth Ciprofloxacin Abdominal discomfort, dizziness, headache Ampicillin Maculoccular rash, anaphylaxis, loose motion Chloramphenicol Gray baby syndrome, Bone marrow depression, pancytopenia
  4. 4. Your Logo Types of adverse drug effect All drugs can produce harmful as well as beneficial effects. These are either related or unrelated to the principal pharmacological action of the drug. Adverse effects are of great concern to drug regulatory authorities, which are charged with establishing the safety as well as the efficacy of drugs before these are licensed for marketing.
  5. 5. Your Logo Adverse effect related to the main pharmacological action of the drug: Many adverse effects related to the main pharmacological action of the drug are predictable. They are sometimes referred to as type A ('augmented') adverse reactions. For example, postural hypotension occurs with α1- adrenoceptor antagonists, bleeding with anticoagulants, sedation with anxiolytics.
  6. 6. Your Logo Such effects are sometimes serious (e.g. intracerebral bleeding caused by anticoagulants, hypoglycemic coma from insulin), and occasionally they are not easily reversible, for example drug dependence produced by opiate analgesics. Drugs that block cyclo-oxygenase-2 ('coxibs', for example rofecoxib, celecoxib, valdecoxib) predictably increase the risk of thrombotic events such as myocardial infarction.
  7. 7. Your Logo Adverse effects unrelated to the main pharmacological action of the drug: Adverse effects unrelated to the main pharmacological effect may be predictable when a drug is taken in excessive dose. e.g. paracetamol hepatotoxicity, aspirin- induced tinnitus.
  8. 8. Your Logo Drug Toxicity Toxicity testing: Toxicity testing in animals is carried out on new drugs to identify potential hazards before administering them to humans. It involves the use of a wide range of tests in different species, with long-term administration of the drug, regular monitoring for physiological or biochemical abnormalities, and a detailed postmortem examination at the end of the trial to detect any gross or histological abnormalities.
  9. 9. Your Logo Types of drug toxicity Toxic effects of drugs can be:  Related to the principal pharmacological action, e.g. bleeding with anticoagulants.  Unrelated to the principal pharmacological action, e.g. liver damage with paracetamol.  Some adverse reactions that occur with ordinary therapeutic dosage are unpredictable and serious, e.g. agranulocytosis with carbimazole.
  10. 10. Your Logo GENERAL MECHANISMS OF TOXIN- INDUCED CELL DAMAGE AND CELL DEATH:Toxic concentrations of drugs or drug metabolites can cause necrosis; however, programmed cell death is increasingly recognized to be of paramount importance, especially in chronic toxicity. Chemically reactive drug metabolites can form covalent bonds with target molecules or alter the target molecule by non-covalent interactions.
  11. 11. Your Logo The liver is of great importance in drug metabolism and hepatocytes are exposed to high concentrations of nascent metabolites as these are formed by cytochrome P450- dependent drug oxidation. Drugs and their polar metabolites are concentrated in renal tubular fluid as water is reabsorbed, so renal tubules are exposed to higher concentrations than are other tissues.
  12. 12. Your Logo NON-COVALENT INTERACTIONS: Reactive metabolites of drugs can be involved in several related, potentially cytotoxic, non-covalent interactions, including:  Lipid per-oxidation.  Generation of toxic reactive oxygen species.  Reactions causing depletion of glutathione (GSH).  Modification of sulfhydryl groups.
  13. 13. Your Logo Covalent reaction: Some of effects produced by covalent reaction,  Lipid per-oxidation.  Reactive oxygen species.  Depletion of glutathione.  Modification of sulfhydryl groups.
  14. 14. Your Logo HEPATOTOXICITY Many therapeutic drugs cause liver damage, manifested clinically as hepatitis or only as laboratory abnormalities. Paracetamaol, Isoniazid cause hepatoxicity by the mechanisms of cell damage. Genetic deficiency in drug metabolism have been implicated in some instances, e.g. phenytoin.
  15. 15. Your Logo General mechanisms of cell damage and cell death:  Drug-induced cell damage or death is usually caused by reactive metabolites of the drug, involving non-covalent and covalent interactions with target molecules.  Non-covalent interactions include:  Lipid per-oxidation via a chain reaction.  Generation of cytotoxic reactive oxygen species.  Depletion of reduced glutathione.
  16. 16. Your Logo Modification of sulfhydryl groups on key enzymes, e.g. Ca2+-ATPase and structural proteins.  Covalent interactions, for example adduct formation between a metabolite of paracetamol (NAPBQI:N-acetyl-p-benzoquinone imine) and cellular macromolecules. Covalent binding to protein can produce an immunogen ; binding to DNA can cause carcinogenesis and teratogenesis.
  17. 17. Your Logo Adverse effects of non-steroidal anti- inflammatory drugs on the kidney: Cause Adverse effects Principal pharmacological action (i.e. inhibition of prostaglandin biosynthesis) Acute ischaemic renal failure. Sodium retention (leading to or exacerbating hypertension and/or heart failure) Water retention Hyporeninaemic hypoaldosteronism (leading to hyperkalaemia) Unrelated to principal pharmacological action Renal failure (allergic-type interstitial nephritis) Proteinuria Unknown whether or not related to principal Papillary necrosis pharmacological action (analgesic nephropathy) Chronic renal failure
  18. 18. Your Logo MUTAGENESIS AND CARCINOGENICITY Mutation changes the genotype of a cell, and the change is passed on when the cell divides. Chemical agents cause mutation by covalent modification of DNA. Growth factors are polypeptide mediators that stimulate cell division; examples are epidermal growth factor and platelet-derived growth factor. The receptors for these growth factors regulate a number of cellular processes through tyrosine phosphorylation.
  19. 19. Your Logo BIOCHEMICAL MECHANISMS OF MUTAGENESIS  Most chemical carcinogens act by modifying bases in DNA, particularly guanine, the O6 and N7 positions of which readily combine covalently with reactive metabolites of chemical carcinogens.  The accessibility of bases in DNA to chemical attack is greatest when DNA is in the process of replication (i.e. during cell division). The likelihood of genetic damage by many mutagens is therefore related to the frequency of cell division.
  20. 20. Your Logo  The importance of drugs, in comparison with other chemicals such as pollutants and food additives, as a causative factor in mutagenesis has not been established, and such epidemiological evidence as exists suggests that they are uncommon (but not unimportant) causes of fetal malformations and cancers.
  21. 21. Your Logo CARCINOGENESIS Alteration of DNA is the first step in the complex, multistage process of carcinogenesis. Carcinogens are chemical substances that cause cancer, and can interact directly with DNA or act at a later stage to increase the likelihood that mutation will result in a tumor.
  22. 22. Your Logo TERATOGENESIS AND DRUG-INDUCED FETAL DAMAGE Teratogenesis signifies the production of gross structural malformations during fetal development, in distinction from other kinds of drug-induced fetal damage such as growth retardation, dysplasia (e.g. iodide-associated goiter), or the asymmetrical limb reduction resulting from vasoconstriction caused by cocaine in an otherwise normally developing limb.
  23. 23. Your Logo MECHANISM OF TERATOGENESIS The timing of the teratogenic insult in relation to fetal development is critical in determining the type and extent of damage. Mammalian fetal development passes through three phases –  Blastocyst formation.  Organogenesis .  Histogenesis and maturation of function.
  24. 24. Your Logo SOME DEFINITE AND PROBABLE HUMAN TERATOGENS Although many drugs have been found to be teratogenic in varying degrees in experimental animals, relatively few are known to be teratogenic in humans. Some of the more important are discussed below.  Cytotoxic drugs: Many alkylating agents (e.g. chlorambucil and cyclophosphamide) and ant-imetabolites (e.g. azathioprine and mercaptopurine) cause malformations when used in early pregnancy but more often lead to abortion.
  25. 25. Your Logo  Warfarin: Administration of warfarin in the first trimester is associated with nasal hypoplasia and various central nervous system abnormalities, affecting roughly 25% of exposed babies.  Anti-emetics: Anti-emetics have been widely used to treat morning sickness in early pregnancy, and some are teratogenic in animals. Results of surveys in humans are inconclusive, providing no clear evidence of teratogenicity. Nevertheless, it is prudent to avoid the use of these drugs in pregnant
  26. 26. Your Logo ALLERGIC REACTIONS TO DRUGS Allergic reactions of various kinds are a common form of adverse response to drugs. Most drugs, being low-molecular-weight substances, are not immunogenic in themselves.  The time course differs from the main action of the drug; it is either delayed in onset or occurs only with repeated exposure to the drug  Allergy may result from doses that are too small to elicit pharmacodynamic effect.
  27. 27. Your Logo  The reaction conforms to one of the clinical syndromes associated with allergy-types I, II, III and IV of the Gell and Coombs classification and is unrelated to the pharmacodynamic effect of the drug. Penicillin's, which are the commonest cause of drug-induced anaphylaxis, produce this response in an estimated 1 in 50000 patients exposed.
  28. 28. Your Logo Hypersensitivity reactions – originally divided into 4 types.  Type I: classical immediate hypersensitivity  Type II: cytotoxic hypersensitivity  Type III: immune-complex mediated hypersensitivity  Type IV: cell mediated or delayed hypersensitivity
  29. 29. Your Logo Hypersensitivity reaction depends on: 1) chemical nature of allergen 2) route involved in sensitization i.e. inhalation, ingestion, injection… 3) physiological state of individual / genetic potential
  30. 30. Your Logo Allergic reactions to drugs  Drugs or their reactive metabolites can bind covalently to proteins to form immunogens. Penicillin (which can also form immunogenic polymers) is an important example.  Drug-induced allergic (hypersensitivity) reactions may be antibody-mediated (types I, II, III) or cell-mediated (type IV). Important clinical manifestations.
  31. 31. Your Logo Anaphylactic shock (type I): Many drugs can cause this, and most deaths are caused by penicillin Hematological reactions (type II, III or IV): Including hemolytic anemia (e.g. methyldopa), agranulocytosis (e.g. carbimazole), thrombocytopenia (e.g. quinine) and aplastic anemia (e.g. chloramphenicol) Hepatitis (types II, III): For example halothane, phenytoin.
  32. 32. Your Logo Rashes (type I, IV): It is usually mild but can be life-threatening (e.g. Stevens-Johnson syndrome). Drug-induced systemic lupus erythematosus (mainly type II): Antibodies to nuclear material are formed (e.g. hydralazine).
  33. 33. Your Logo  Rang, Dale’s, Pharmacology, Elsevier, 6th edition, 2008 ( 751-764).  K. D. Tripathi, Essentials of Medical Pharmacology, Jaypee, 6th edition, 2010 (78- 86).
  34. 34. Ihr Logo
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