Name: Md. Zahirul Islam
Department of pharmacy
World University of Bangladesh
Presentation of
Drug interaction
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To
Our Presentation
DEFINITION
Drug interaction is defined as the
pharmacological activity of one drug is altered by
the concominant use of another drug or by the
presence of some other substance.
โ€ขThe Drug whose Activity is effected by such an
Interaction is called as a โ€œObject drug.โ€
โ€ข The agent which precipitates such an interaction
is refered to as the โ€œPrecipitantโ€.
Types of drug Interactions
1.Drug-drug interactions.
2.Drug-food interactions.
3.Chemical-drug interactions.
4.Drug-laboratory test interactions.
5.Drug-disease interactions.
The Net effect of a Drug Interaction is
โ€ขGenerally quantitative i.e.increased or decreased effect.
โ€ขSeldom qualitative i.e.rapid or slower effect.
โ€ขPrecipitation of newer or increased adverse effect.
Factors contributing to drug interactions:
1.Multiple drug therapy.
2.Multiple prescribers.
3.Multiple pharmacological effects of drug.
4.Multiple diseases/predisposing illness.
5.Poor patient compliance.
6.Advancing age of patient.
7.Drug-related factors.
Mechanisms of drug interactions:
The three mechanisms by which an interaction
can develop are-
1.Pharmaceutical interactions.
2.pharmacokinetic interactions.
3.Pharmacodynamic interactions.
Pharmaceutical interactions:
Also called as incompatibility.it is a physicochemical
interaction that occous when drugs are mixed in i.v .
Infusions causing precipitation or inactivation of active
principles .
Example:-
Ampicillin ,chlorpromazine &barbituates interact with
dextran in solutions and are broken down.
Pharmacokinetic Interactions:
โ€œThese interactions are those in which adme properties
of the object drug is altered by the precipitant and hence
such interactions are also called as ADME interactionsโ€.
โ€ขThese are classified as:
1.Absorption interactions
2.Distribution interactions
3.Metabolism interactions
4.Excretion interactions.
Absorption interactions
.
Are those where the absorption of the object
drug is altered. The net effect of such an interaction is:
โ€ข Faster or slower drug absorption.
โ€ข More, or, less complete drug absorption.
Major mechanisms of absorption interactions are:
1.Complexation and adsorption.
2.Alteration in GI pH.
3.Alteration in gut motility.
4.Inhibition of GI enzymes.
5.Alteration of GI micro flora.
6.Malabsorption syndrome.
Distribution interactions
Are those where the distribution pattern of the
object drug is altered :
โ€ขThe major mechanism for distribution interaction is
alteration in protein-drug binding.
METABOLISM INTERACTIONS:
Are those where the metabolism of the object drug
is altered.
Mechanisms of metabolism interactions include:
1.Enzyme induction:
Increased rate of metabolism.
2.Enzyme inhibition:
Decreased rate of metabolism. It is the most
significant interaction in comparison to other
interactions and can be fatal.
EXCRETION INTERACTIONS
Are these where the excretion pattern of the
object drug is altered. Major mechanisms of excretion
interactions are-
๏ƒ˜Alteration in renal blood flow
๏ƒ˜Alteration of urine PH
๏ƒ˜Competition for active secretions
๏ƒ˜Forced diuresis
Pharmacodynamic interactions:
Are those in which the activity of the object
drug at its site of action is altered by the precipitant.
Such interactions may be direct or indirect.
1.These are of two types1.direct pharmacodynamic
interactions.
2.Indirect pharmacodynamic interactions.
DIRECT PHARMACODYNAMIC
INTERACTIONS:
In which drugs having similar or opposing
pharmacological effects are used concurrently.
The three consequences of direct interactions are
1.Antagonism.
2.Addition or summation.
3.Synergism or potentiation.
Indirect pharmacodynamic interaction:
In which both the object and the precipitant drugs
have unrelated effects.but the latter in Some way
alerts the effects but latter in some way alerts the
Effects of the former.
Example: salicylatesdecrease the ability of the
platelets to aggregate thus impairing the Homeostasis
if warfarin indused bleeding occurs.
REDUSING THE RISK OF DRUG
INTERACTIONS:
1.Identify the patients risk factors.
2.Take through drug history.
3.Be knowledge about the actions of the drugs being
used.
4.Consider therapeutic alternatives.
5Avoid complex therapeutic regiments when possible.
INFLUENCE OF SMOKING ON DRUG
INTERACTIONS:
Smoking increases the activity of drug metabolizing
enzymes in the liver, With the result that certain
therapeutic agents.
Example: Diazepam, propoxyphene, theophylline,
olanzapine.Are metabolized more rapidly,and their
effect is decreased.
INFLUENCE OF ALCOHOL ON DRUG
INTERACTION:
Chronic use of alcohol beverages may increases the rate of
metabolism of drugs such as warfarin and phenytoin, probably
by increasing the activity of hepatic enzymes.
โ€ขAcute use of alcohol by non alcoholic individuals may
โ€ข cause an inhibition of hepatic enzymes.
โ€ขUse of alcoholic beverages with sedatives and other
โ€ขdepressants drugs could result in an excessive
โ€ข depressant response.
INFLUENCE OF FOOD ON DRUG
INTERACTION:
Food effects the rate and extent of absorption of drugs
from the GI tract.
Example: Many anti biotics should be given atleast 1hr
before or 2hr after meals to achieve Optimal absorption.
โ€ขThe type of food may be important with regard to the
โ€ขabsorption of concurrently administered Drugs.
Example: Dietary items such as milk and other dairy products
that contain calcium may decrease .
Thanks
To
All

Drug interaction

  • 1.
    Name: Md. ZahirulIslam Department of pharmacy World University of Bangladesh Presentation of Drug interaction
  • 2.
  • 3.
    DEFINITION Drug interaction isdefined as the pharmacological activity of one drug is altered by the concominant use of another drug or by the presence of some other substance.
  • 4.
    โ€ขThe Drug whoseActivity is effected by such an Interaction is called as a โ€œObject drug.โ€ โ€ข The agent which precipitates such an interaction is refered to as the โ€œPrecipitantโ€.
  • 5.
    Types of drugInteractions 1.Drug-drug interactions. 2.Drug-food interactions. 3.Chemical-drug interactions. 4.Drug-laboratory test interactions. 5.Drug-disease interactions.
  • 6.
    The Net effectof a Drug Interaction is โ€ขGenerally quantitative i.e.increased or decreased effect. โ€ขSeldom qualitative i.e.rapid or slower effect. โ€ขPrecipitation of newer or increased adverse effect.
  • 7.
    Factors contributing todrug interactions: 1.Multiple drug therapy. 2.Multiple prescribers. 3.Multiple pharmacological effects of drug. 4.Multiple diseases/predisposing illness. 5.Poor patient compliance. 6.Advancing age of patient. 7.Drug-related factors.
  • 8.
    Mechanisms of druginteractions: The three mechanisms by which an interaction can develop are- 1.Pharmaceutical interactions. 2.pharmacokinetic interactions. 3.Pharmacodynamic interactions.
  • 9.
    Pharmaceutical interactions: Also calledas incompatibility.it is a physicochemical interaction that occous when drugs are mixed in i.v . Infusions causing precipitation or inactivation of active principles . Example:- Ampicillin ,chlorpromazine &barbituates interact with dextran in solutions and are broken down.
  • 10.
    Pharmacokinetic Interactions: โ€œThese interactionsare those in which adme properties of the object drug is altered by the precipitant and hence such interactions are also called as ADME interactionsโ€. โ€ขThese are classified as: 1.Absorption interactions 2.Distribution interactions 3.Metabolism interactions 4.Excretion interactions.
  • 11.
    Absorption interactions . Are thosewhere the absorption of the object drug is altered. The net effect of such an interaction is: โ€ข Faster or slower drug absorption. โ€ข More, or, less complete drug absorption.
  • 12.
    Major mechanisms ofabsorption interactions are: 1.Complexation and adsorption. 2.Alteration in GI pH. 3.Alteration in gut motility. 4.Inhibition of GI enzymes. 5.Alteration of GI micro flora. 6.Malabsorption syndrome.
  • 13.
    Distribution interactions Are thosewhere the distribution pattern of the object drug is altered : โ€ขThe major mechanism for distribution interaction is alteration in protein-drug binding.
  • 14.
    METABOLISM INTERACTIONS: Are thosewhere the metabolism of the object drug is altered. Mechanisms of metabolism interactions include: 1.Enzyme induction: Increased rate of metabolism. 2.Enzyme inhibition: Decreased rate of metabolism. It is the most significant interaction in comparison to other interactions and can be fatal.
  • 15.
    EXCRETION INTERACTIONS Are thesewhere the excretion pattern of the object drug is altered. Major mechanisms of excretion interactions are- ๏ƒ˜Alteration in renal blood flow ๏ƒ˜Alteration of urine PH ๏ƒ˜Competition for active secretions ๏ƒ˜Forced diuresis
  • 16.
    Pharmacodynamic interactions: Are thosein which the activity of the object drug at its site of action is altered by the precipitant. Such interactions may be direct or indirect. 1.These are of two types1.direct pharmacodynamic interactions. 2.Indirect pharmacodynamic interactions.
  • 17.
    DIRECT PHARMACODYNAMIC INTERACTIONS: In whichdrugs having similar or opposing pharmacological effects are used concurrently. The three consequences of direct interactions are 1.Antagonism. 2.Addition or summation. 3.Synergism or potentiation.
  • 18.
    Indirect pharmacodynamic interaction: Inwhich both the object and the precipitant drugs have unrelated effects.but the latter in Some way alerts the effects but latter in some way alerts the Effects of the former. Example: salicylatesdecrease the ability of the platelets to aggregate thus impairing the Homeostasis if warfarin indused bleeding occurs.
  • 19.
    REDUSING THE RISKOF DRUG INTERACTIONS: 1.Identify the patients risk factors. 2.Take through drug history. 3.Be knowledge about the actions of the drugs being used. 4.Consider therapeutic alternatives. 5Avoid complex therapeutic regiments when possible.
  • 20.
    INFLUENCE OF SMOKINGON DRUG INTERACTIONS: Smoking increases the activity of drug metabolizing enzymes in the liver, With the result that certain therapeutic agents. Example: Diazepam, propoxyphene, theophylline, olanzapine.Are metabolized more rapidly,and their effect is decreased.
  • 21.
    INFLUENCE OF ALCOHOLON DRUG INTERACTION: Chronic use of alcohol beverages may increases the rate of metabolism of drugs such as warfarin and phenytoin, probably by increasing the activity of hepatic enzymes. โ€ขAcute use of alcohol by non alcoholic individuals may โ€ข cause an inhibition of hepatic enzymes. โ€ขUse of alcoholic beverages with sedatives and other โ€ขdepressants drugs could result in an excessive โ€ข depressant response.
  • 22.
    INFLUENCE OF FOODON DRUG INTERACTION: Food effects the rate and extent of absorption of drugs from the GI tract. Example: Many anti biotics should be given atleast 1hr before or 2hr after meals to achieve Optimal absorption. โ€ขThe type of food may be important with regard to the โ€ขabsorption of concurrently administered Drugs. Example: Dietary items such as milk and other dairy products that contain calcium may decrease .
  • 23.