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PATIENT PROFILE & PATIENT COUNSELING
C. DRUG PROFILE OF ATLEAST 25
IMPORTANT MEDICATIONS
DIGOXINE
CLINICAL PHARMACY
BY
Zul Kamal
DEPARTMENT OF PHARMACY
SHAHEED BENAZIR BHUTTO UNIVERSITY, SHERINGAL
DIGOXIN
+Ionotropic (Inc. Force of Contractility).
-Chronotropic effects (Dec. HR) Vegal stimulation.
Cardiac Glycosides (Digitalis, Fox Glove).
Cardiac glycosides influence the sodium and calcium ion flows
in the cardiac muscle
PHARMACOKINETICS
 ADMINISTERATION
• Orally,
• Parentrally via IV Injection
• METABOLISM
Only 16% is metabolized Liver
 EXCRETION
Most of Digoxine is excreted unchanged in Urine
PHARMACODYNAMIC
MECHANISM OF ACTION
 Digoxin inhibit an Enzyme Na/K ATPase. This Enzyme
carries Na to the exterior of the cell and K to the
anterior of the cell.
 There is another system called Ca/Na Exchanger
system. When Na/K ATPase is blocked by digoxin
then there will be excess of Na inside the cell and
increases level of Na is trigger for Ca Influx.
 Thus Ca increases the contractility of heart and thus
pump blood to all parts of the body.
INDICATIONS
It is used as
 CHF or CCF
 Atrial Flutter (A condition in which heart rate incraeses
from 240-400 beats i,.e irregular heart beat).
 Atrial Fibrillation (Both are cardiac arrhythmias and can
be diagnosed by the absence of p-waves in ECG).
 Paraoxysmal supraventricular tacchycardias
(Paraoxymal mean that it can occur at regular interval of
time; supraventricular mean that the problem is above
the ventrical i.e SA node)
CONTRAINDICATIONS
 Ventricular Tacchycardia
 Ventricular Subaortic stenosis (narrowing of the artery)
 Ventricular Fibrillation
ADVERSE EFFECTS
 SA and AV Block
 It can also induce ventricular tacchycardia
NOTE: The common cardiac side effect is arrhythmia, characterized
by slowing of atrioventricular conduction associated with atrial
arrhythmias. A decrease in intracellular potassium is the primary
predisposing factor in these effects.
 CNS: Headache, Fatigue, Delirium, Hallucination.
 Endocrine System: Enlargement of Breast in Female and
Gynecomastia in Male.
 GIT: Nausea, Vomiting and Diarrhea.
DRUG INTERACTION
 Diuretics like Thiazide and Loop Diuretics Which
increases the excretion of K and thus incresea the toxicity
of Digoxin; resulting Hypokalemia.
 Calcium Channel Blockers like Verapamil which displaces
Digoxin from its binding site and inc. the level of Digoxin
from 50-75% and thus causing toxicity by ventricular
arrhythmia and heart block.
 Quinidine (Class-I Antiarrhytmic) displace Digoxin from its
binding site which causes Toxicity.
DOSE AND DOSAGE FORM
 DOSES
 250-500 µg/day in Two to Three divided doses.
 0.75-1 mg in the form of infusion in EMERGENCY
SITIUATION
 BRAND NAME:
 Lanoxin (GSK), Tabs and Injection
 Digox (Platinum), 250 µgTabs or 0.25 mg
 Doxin (Xenon Pharma), Syrup of 60mL
Digoxine Dr.Z Pharmacy Practice Lecture

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Digoxine Dr.Z Pharmacy Practice Lecture

  • 1. PATIENT PROFILE & PATIENT COUNSELING C. DRUG PROFILE OF ATLEAST 25 IMPORTANT MEDICATIONS DIGOXINE CLINICAL PHARMACY BY Zul Kamal DEPARTMENT OF PHARMACY SHAHEED BENAZIR BHUTTO UNIVERSITY, SHERINGAL
  • 2. DIGOXIN +Ionotropic (Inc. Force of Contractility). -Chronotropic effects (Dec. HR) Vegal stimulation. Cardiac Glycosides (Digitalis, Fox Glove). Cardiac glycosides influence the sodium and calcium ion flows in the cardiac muscle
  • 3.
  • 4. PHARMACOKINETICS  ADMINISTERATION • Orally, • Parentrally via IV Injection • METABOLISM Only 16% is metabolized Liver  EXCRETION Most of Digoxine is excreted unchanged in Urine
  • 5. PHARMACODYNAMIC MECHANISM OF ACTION  Digoxin inhibit an Enzyme Na/K ATPase. This Enzyme carries Na to the exterior of the cell and K to the anterior of the cell.  There is another system called Ca/Na Exchanger system. When Na/K ATPase is blocked by digoxin then there will be excess of Na inside the cell and increases level of Na is trigger for Ca Influx.  Thus Ca increases the contractility of heart and thus pump blood to all parts of the body.
  • 6.
  • 7. INDICATIONS It is used as  CHF or CCF  Atrial Flutter (A condition in which heart rate incraeses from 240-400 beats i,.e irregular heart beat).  Atrial Fibrillation (Both are cardiac arrhythmias and can be diagnosed by the absence of p-waves in ECG).  Paraoxysmal supraventricular tacchycardias (Paraoxymal mean that it can occur at regular interval of time; supraventricular mean that the problem is above the ventrical i.e SA node)
  • 8. CONTRAINDICATIONS  Ventricular Tacchycardia  Ventricular Subaortic stenosis (narrowing of the artery)  Ventricular Fibrillation
  • 9. ADVERSE EFFECTS  SA and AV Block  It can also induce ventricular tacchycardia NOTE: The common cardiac side effect is arrhythmia, characterized by slowing of atrioventricular conduction associated with atrial arrhythmias. A decrease in intracellular potassium is the primary predisposing factor in these effects.  CNS: Headache, Fatigue, Delirium, Hallucination.  Endocrine System: Enlargement of Breast in Female and Gynecomastia in Male.  GIT: Nausea, Vomiting and Diarrhea.
  • 10. DRUG INTERACTION  Diuretics like Thiazide and Loop Diuretics Which increases the excretion of K and thus incresea the toxicity of Digoxin; resulting Hypokalemia.  Calcium Channel Blockers like Verapamil which displaces Digoxin from its binding site and inc. the level of Digoxin from 50-75% and thus causing toxicity by ventricular arrhythmia and heart block.  Quinidine (Class-I Antiarrhytmic) displace Digoxin from its binding site which causes Toxicity.
  • 11. DOSE AND DOSAGE FORM  DOSES  250-500 µg/day in Two to Three divided doses.  0.75-1 mg in the form of infusion in EMERGENCY SITIUATION  BRAND NAME:  Lanoxin (GSK), Tabs and Injection  Digox (Platinum), 250 µgTabs or 0.25 mg  Doxin (Xenon Pharma), Syrup of 60mL