The document discusses various drugs used for anticoagulation and antiplatelet therapy. It provides details on unfractionated heparin (UFH) including its indications, pharmacokinetics, dosing and monitoring. It also discusses aspirin and clopidogrel, describing their combined mechanisms of action and differences versus each other. The document then presents several case studies describing patients' conditions, lab results, treatments including various anticoagulant and antiplatelet drugs administered, and outcomes.
A talk covering epidemiology, diagnosis and management of primary headache disorders, common cases of secondary headache disorders and when to order brain imaging, lumbar puncture in headaches.
A talk covering epidemiology, diagnosis and management of primary headache disorders, common cases of secondary headache disorders and when to order brain imaging, lumbar puncture in headaches.
This PPT focuses on the diagnosis and treatment of the primary headache disorders, with special emphasis on migraine, the headache most likely to bring patients to physicians and pharmacists. warning signs of the ominous headache, which, although rare, can herald a life-threatening condition. Clinical characteristics of the primary headache types, migraine, tension-type headache, and cluster headache, are described
Please find the power point on Tension Type Headache (TTH). I tried to present it on understandable way and all the contents are reviewed by experts and from very reliable references. Thank you
This PPT focuses on the diagnosis and treatment of the primary headache disorders, with special emphasis on migraine, the headache most likely to bring patients to physicians and pharmacists. warning signs of the ominous headache, which, although rare, can herald a life-threatening condition. Clinical characteristics of the primary headache types, migraine, tension-type headache, and cluster headache, are described
Please find the power point on Tension Type Headache (TTH). I tried to present it on understandable way and all the contents are reviewed by experts and from very reliable references. Thank you
Seizures which affect initially only one hemisphere of the brain. Symptoms include:
Contractions on just one side of the body
unusual head or eye movements
Numbness, tingling, or a feeling that something is crawling on the skin
Abdominal pain
Rapid heart rate or pulse
Sweating
Nausea
Explore natural remedies for syphilis treatment in Singapore. Discover alternative therapies, herbal remedies, and lifestyle changes that may complement conventional treatments. Learn about holistic approaches to managing syphilis symptoms and supporting overall health.
Ozempic: Preoperative Management of Patients on GLP-1 Receptor Agonists Saeid Safari
Preoperative Management of Patients on GLP-1 Receptor Agonists like Ozempic and Semiglutide
ASA GUIDELINE
NYSORA Guideline
2 Case Reports of Gastric Ultrasound
TEST BANK for Operations Management, 14th Edition by William J. Stevenson, Ve...kevinkariuki227
TEST BANK for Operations Management, 14th Edition by William J. Stevenson, Verified Chapters 1 - 19, Complete Newest Version.pdf
TEST BANK for Operations Management, 14th Edition by William J. Stevenson, Verified Chapters 1 - 19, Complete Newest Version.pdf
- Video recording of this lecture in English language: https://youtu.be/lK81BzxMqdo
- Video recording of this lecture in Arabic language: https://youtu.be/Ve4P0COk9OI
- Link to download the book free: https://nephrotube.blogspot.com/p/nephrotube-nephrology-books.html
- Link to NephroTube website: www.NephroTube.com
- Link to NephroTube social media accounts: https://nephrotube.blogspot.com/p/join-nephrotube-on-social-media.html
MANAGEMENT OF ATRIOVENTRICULAR CONDUCTION BLOCK.pdfJim Jacob Roy
Cardiac conduction defects can occur due to various causes.
Atrioventricular conduction blocks ( AV blocks ) are classified into 3 types.
This document describes the acute management of AV block.
Factory Supply Best Quality Pmk Oil CAS 28578–16–7 PMK Powder in Stockrebeccabio
Factory Supply Best Quality Pmk Oil CAS 28578–16–7 PMK Powder in Stock
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Ethanol (CH3CH2OH), or beverage alcohol, is a two-carbon alcohol
that is rapidly distributed in the body and brain. Ethanol alters many
neurochemical systems and has rewarding and addictive properties. It
is the oldest recreational drug and likely contributes to more morbidity,
mortality, and public health costs than all illicit drugs combined. The
5th edition of the Diagnostic and Statistical Manual of Mental Disorders
(DSM-5) integrates alcohol abuse and alcohol dependence into a single
disorder called alcohol use disorder (AUD), with mild, moderate,
and severe subclassifications (American Psychiatric Association, 2013).
In the DSM-5, all types of substance abuse and dependence have been
combined into a single substance use disorder (SUD) on a continuum
from mild to severe. A diagnosis of AUD requires that at least two of
the 11 DSM-5 behaviors be present within a 12-month period (mild
AUD: 2–3 criteria; moderate AUD: 4–5 criteria; severe AUD: 6–11 criteria).
The four main behavioral effects of AUD are impaired control over
drinking, negative social consequences, risky use, and altered physiological
effects (tolerance, withdrawal). This chapter presents an overview
of the prevalence and harmful consequences of AUD in the U.S.,
the systemic nature of the disease, neurocircuitry and stages of AUD,
comorbidities, fetal alcohol spectrum disorders, genetic risk factors, and
pharmacotherapies for AUD.
ARTIFICIAL INTELLIGENCE IN HEALTHCARE.pdfAnujkumaranit
Artificial intelligence (AI) refers to the simulation of human intelligence processes by machines, especially computer systems. It encompasses tasks such as learning, reasoning, problem-solving, perception, and language understanding. AI technologies are revolutionizing various fields, from healthcare to finance, by enabling machines to perform tasks that typically require human intelligence.
Couples presenting to the infertility clinic- Do they really have infertility...Sujoy Dasgupta
Dr Sujoy Dasgupta presented the study on "Couples presenting to the infertility clinic- Do they really have infertility? – The unexplored stories of non-consummation" in the 13th Congress of the Asia Pacific Initiative on Reproduction (ASPIRE 2024) at Manila on 24 May, 2024.
Title: Sense of Taste
Presenter: Dr. Faiza, Assistant Professor of Physiology
Qualifications:
MBBS (Best Graduate, AIMC Lahore)
FCPS Physiology
ICMT, CHPE, DHPE (STMU)
MPH (GC University, Faisalabad)
MBA (Virtual University of Pakistan)
Learning Objectives:
Describe the structure and function of taste buds.
Describe the relationship between the taste threshold and taste index of common substances.
Explain the chemical basis and signal transduction of taste perception for each type of primary taste sensation.
Recognize different abnormalities of taste perception and their causes.
Key Topics:
Significance of Taste Sensation:
Differentiation between pleasant and harmful food
Influence on behavior
Selection of food based on metabolic needs
Receptors of Taste:
Taste buds on the tongue
Influence of sense of smell, texture of food, and pain stimulation (e.g., by pepper)
Primary and Secondary Taste Sensations:
Primary taste sensations: Sweet, Sour, Salty, Bitter, Umami
Chemical basis and signal transduction mechanisms for each taste
Taste Threshold and Index:
Taste threshold values for Sweet (sucrose), Salty (NaCl), Sour (HCl), and Bitter (Quinine)
Taste index relationship: Inversely proportional to taste threshold
Taste Blindness:
Inability to taste certain substances, particularly thiourea compounds
Example: Phenylthiocarbamide
Structure and Function of Taste Buds:
Composition: Epithelial cells, Sustentacular/Supporting cells, Taste cells, Basal cells
Features: Taste pores, Taste hairs/microvilli, and Taste nerve fibers
Location of Taste Buds:
Found in papillae of the tongue (Fungiform, Circumvallate, Foliate)
Also present on the palate, tonsillar pillars, epiglottis, and proximal esophagus
Mechanism of Taste Stimulation:
Interaction of taste substances with receptors on microvilli
Signal transduction pathways for Umami, Sweet, Bitter, Sour, and Salty tastes
Taste Sensitivity and Adaptation:
Decrease in sensitivity with age
Rapid adaptation of taste sensation
Role of Saliva in Taste:
Dissolution of tastants to reach receptors
Washing away the stimulus
Taste Preferences and Aversions:
Mechanisms behind taste preference and aversion
Influence of receptors and neural pathways
Impact of Sensory Nerve Damage:
Degeneration of taste buds if the sensory nerve fiber is cut
Abnormalities of Taste Detection:
Conditions: Ageusia, Hypogeusia, Dysgeusia (parageusia)
Causes: Nerve damage, neurological disorders, infections, poor oral hygiene, adverse drug effects, deficiencies, aging, tobacco use, altered neurotransmitter levels
Neurotransmitters and Taste Threshold:
Effects of serotonin (5-HT) and norepinephrine (NE) on taste sensitivity
Supertasters:
25% of the population with heightened sensitivity to taste, especially bitterness
Increased number of fungiform papillae
Pulmonary Thromboembolism - etilogy, types, medical- Surgical and nursing man...VarunMahajani
Disruption of blood supply to lung alveoli due to blockage of one or more pulmonary blood vessels is called as Pulmonary thromboembolism. In this presentation we will discuss its causes, types and its management in depth.
Tom Selleck Health: A Comprehensive Look at the Iconic Actor’s Wellness Journeygreendigital
Tom Selleck, an enduring figure in Hollywood. has captivated audiences for decades with his rugged charm, iconic moustache. and memorable roles in television and film. From his breakout role as Thomas Magnum in Magnum P.I. to his current portrayal of Frank Reagan in Blue Bloods. Selleck's career has spanned over 50 years. But beyond his professional achievements. fans have often been curious about Tom Selleck Health. especially as he has aged in the public eye.
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Introduction
Many have been interested in Tom Selleck health. not only because of his enduring presence on screen but also because of the challenges. and lifestyle choices he has faced and made over the years. This article delves into the various aspects of Tom Selleck health. exploring his fitness regimen, diet, mental health. and the challenges he has encountered as he ages. We'll look at how he maintains his well-being. the health issues he has faced, and his approach to ageing .
Early Life and Career
Childhood and Athletic Beginnings
Tom Selleck was born on January 29, 1945, in Detroit, Michigan, and grew up in Sherman Oaks, California. From an early age, he was involved in sports, particularly basketball. which played a significant role in his physical development. His athletic pursuits continued into college. where he attended the University of Southern California (USC) on a basketball scholarship. This early involvement in sports laid a strong foundation for his physical health and disciplined lifestyle.
Transition to Acting
Selleck's transition from an athlete to an actor came with its physical demands. His first significant role in "Magnum P.I." required him to perform various stunts and maintain a fit appearance. This role, which he played from 1980 to 1988. necessitated a rigorous fitness routine to meet the show's demands. setting the stage for his long-term commitment to health and wellness.
Fitness Regimen
Workout Routine
Tom Selleck health and fitness regimen has evolved. adapting to his changing roles and age. During his "Magnum, P.I." days. Selleck's workouts were intense and focused on building and maintaining muscle mass. His routine included weightlifting, cardiovascular exercises. and specific training for the stunts he performed on the show.
Selleck adjusted his fitness routine as he aged to suit his body's needs. Today, his workouts focus on maintaining flexibility, strength, and cardiovascular health. He incorporates low-impact exercises such as swimming, walking, and light weightlifting. This balanced approach helps him stay fit without putting undue strain on his joints and muscles.
Importance of Flexibility and Mobility
In recent years, Selleck has emphasized the importance of flexibility and mobility in his fitness regimen. Understanding the natural decline in muscle mass and joint flexibility with age. he includes stretching and yoga in his routine. These practices help prevent injuries, improve posture, and maintain mobilit
6. INTRO:
Clinically obtained from 1937, when sufficient degree of purification was
achieved
It contains a polymer of two sulphated disaccharide unit
D-glycosylmine-L-iduronic acid
D-glycosylamine-D-glucorinic acid
It present in all tissue containing mast cells
Rich in lung, liver and intestinal mucosa
Commersionally produced from Ox lung and pig intestinal mucosa
7. MECH OF ACTION:
It bind and activate antithrombin factor.
That prevent the conversion of prothrombin to thrombin.
But not having direct effect on coagulation and its gone to inactivate
factors II,IX,X,XI.
PHARMACOKINETIC:
Available in injection form.
Normally administered in s/c or IV not in intramuscular route.
Metabolised in liver .
Onset of action- After 60min.
Half life – 1-4hrs .
THERAPEUTIC USES :
Anticoagulation effect.
Antiplatelet effect.
Reduced triglyceride and LDL level.
8. MONITORING PARAMETER:
Closure monitoring of a PTT level .
TOXICITY:
Bleeding.
Heparin causing thrombocytopenia.
CONTRA INDICATION:
Purpura.
Hypertension.
Intracranial haemorrhage.
Active TB.
Renal disease.
9. CASE – 2
FOOT ULCER
DOA : 23/10/18
ADE : 59 yrs
SEX : male
PAST HISTORY : Coronary artery disease
DM past 10 yrs
10. DRUGS
DRUG DOSE FREQUE
NCY
ROUTE START
DATE
END
DATE
INDICATION
INJ.HEPARIN
(Unfractionated
heparin)
25000
IU
BD IV 24/10 26/10 ANTICOAGULANT
T.ECOSPIRIN
(Aspirin)
75mg OD oral 23/10 26/10 ANTIPLATELET
11.
12. Discharge Medication :
Tab. Clopilet A – 75mg – Morning – After food - 14 days
Tab. Stiloz - 50mg – Morning – After food – 14 days
( cilostazol) &Night
Platelet count : 295000 on 23/10/18
Drug interaction chart :
Tab. Stiloz interact moderately with aspirin and severe
incase of anticogulant drugs
13.
14. CASE-3
CELLUITIS TOE GANGRENE
AGE : 62 yrs
SEX : Male
DOA : 12/11/18
PAST DIAGNOSIS : Stroke ( cerebrovascular
disease )
DM for 8 yrs on treatment
CASE TYPE : Cellulitis toe gangrene (
amputation ) done on 15/11/18
15. DRUG
DRUG DOSE FREQU
ENCY
ROUTE START
DATE
END DATE INDICATION
INJ.HEPARIN
(Unfractionated
heparin)
5000IU BD IV 13/11 15/11
Stopped on
2nd dose on
15/11
ANTICOAGU
LANT
T.Deplatt A
(clopidogrel)
75mg OD oral 13/11 16/11 ANTIPLATEL
ET
16.
17. AGE : 44 yrs.
SEX : Female.
DOA : 10/11/18.
BLOOD GROUP : A positive.
CASE TYPE : Respiratory disease (tracheostomy ).
CASE 4
RESPIRATORY DISORDER
18. Progress Notes :
12/11/18 DONE A PTT – 35 seconds
INR – 1.16
Drug : Inj . Heparin – 5000IU ( S/C ) – BD
12/11, bed ridden DVT prophylaxis TED stocking
Therapy provided :
Heparin .
TED stocking .
Clinical condition :
INR – 1.16.
PTT – 35 seconds.
bed ridden DVT prophylaxis.
19. Clinical indication Vs Drug preferred :
a) Prophylaxis of DVT and PE in high risk , bed – ridden medical
/ surgical patients
b) Treatment of DVT and/or PE
c) Primary PCI in patients of STEMI or in high risk cases of
NSTEMI/UA
d) Along with aspirin +_ clopidogrel to prevent reocclusion
following fibrinolytic of STEMI/ high risk NSTEMI
Drugs Preferred:
a) Fonda./LMW heparin/ rivaroxaban/UFH followed by
warfarin/TED stockings.
20.
21.
22.
23. CASE – 5
ACUTE ISCHEMIC STROKE
AGE : 72 yrs.
SEX : Male.
DOA : 25/1/19.
CASE TYPE : Acute ischemic stroke.
SOCIAL HABITS:smoker and alcoholic.
24.
25. Lab Test :
TEST 25/1 26/1 NORMAL RANGE
Total count 22200 19600 (4000-11300)cells/cubicmm.
Polymorph 88 % 85 % 45-75%
Lymphocytes 10% 12% 20-40%
Eosinophil 00% 01% 02-06%
26.
27. DRUG
DRUG DOSE FREQ
UENC
Y
ROUT
E
START
DATE
END DATE INDICATION
T.Clopilet
(clopidogrel)
( 9 am )
75mg OD oral 25/1 30/1 ANTIPLATELET
Discharge Medication :
Tab. Ecospirin – 75mg – Morning – After food- 20 days
28.
29.
30.
31. HEPARIN
INDICATION :
Treatment and prophylaxis of deep vein thrombosis and pulmonary
embolism ;atrial fibrillation with embolism ; treatment and
prophylaxis of peripheral aterial embolism ; prophylaxisof deep vein
thrombosis in major surgery ; lipemia clearing
AVAILABILITY :
INJECTIONS vials 1000, 5000 and 25,000 IU/ml
DOSE :
ADULT – Treatment of deep vein thrombosis and pulmonary
embolism ; loading dose of 5000 units (10.000 units in severe
pulmonary emboloism ) followed by continuous intravenous
infusion of 15 to 25 units/kg/h. CHILD – 50 to 100U/kg every 4 to
6 h
32. SUBCUTANEOUS INJECTION :
15,000 units every 12 h ; laboratory monitoring is
essential , preferably on a daily basis and dose adjusted
accordingly.
prophylaxis in general surgery ; 5000 units 2 h before
surgery , then every 8 to 12 h for 7 days or until patient
is ambulant ( monitoring not needed ) during pregnancy
( with monitoring ) 5000 to 10000 units every 12 h
CHILD – 250 units/kg every 12 h
Intravenously injection and continuous intravenous
infusion
CHILD – By IV injection ; lower loading dose , then by
continuous intravenous infusion ;15 to 25 units/kg/h
33. INDICATION :
Prophylaxis in thromboembolic disorder including myocardial
infraction, peripheral aterial disease and stroke . Acute
coronary syndrome
AVAILABILITY :
Tablets 75 and 150mg
DOSE :
ADULTS – 75mg once daily
Non-ST segment elevation myocardial infraction ; loading
dose 300 mg followed by 75 mg once daily
34. PRECAUTIONS :
Patient with increased risk of bleeding from trauma , surgery
or other pathological conditions , ulcers, renal impairments ,
hepatic impairment , history of bleeding hemostatic disorder ,
pregnancy ( Appendix 7c ) ; interactions ( Appendix 6c )
ADR :
Bleeding, neutropenia, thrombocytopenia ,
other bone marrow toxicity , diarrhoea
epigastric pain , rashes, paraesthesia , vertigo
35. CONTRAINDICATION :
Bleeding disorders, history of HIT
Severe hypertension ( risk of cerebral haemorrhage ),
threatened abortion , piles, g.i. ulcers ( risk of aggravated
bleeding )
Subcute bacterial endocarditis ( risk of embolism ), large
malignancies ( risk of bleeding in the central necrosed are of
the tumour ), tuberculosis ( risk of haemoptysis )
Ocular and neurosurgery , lumbar puncture.
Chronic alcoholics , cirrhosis , renal failure .
aspirin and other antiplatelet drugs should be used very
cautiously during heparin therapy
36. INDICATION :
Management of mild to moderate pain such as
headache , acute migraine attacks , transient
musculoskeletal pain , dysmenorrhoeal pain
and for reducing fever
Pain and inflammation of rheumatoid arthritis ,
anti platelet agent for prophylaxis of MI ,
stroke , angina pectoris , stroke prophylaxis
AVAILABILITY :
Tablets : 50, 60, 75, 80, 150, 300, and 325 mg
37. DOSE :
Oral
Adult - Analgesic and antipyretic including migraine attacks
:0.3 to 0.9 g , 3 to 4 times a day ( max. 4g daily ).
Anti platelet : 75 to 325 mg/day
rheumatic fever : 4 to 6 g or 75 to 100 mg/kg daily in
divided dises
Child – under 16 yrs : not recommended ( cause reye’s
syndrome )
CONTRAINDICATION :
Hypersensitivity
gastrointestinal ulceration
haemophilia
38. PRECAUTION :
Asthma ,
allergic disease ,
impaired renal or hepatic function
ADR :
Gastrointestinal discomfort or nausea
hearing disturbances such as tinnitus , confusion
hypersensitivity reactions
myocarditis , Reye’s syndrome
STORAGE :
Store in protected from moisture at a temperature not
exceeding 30 degree Celsius
39.
40. AGE : 47 yrs
SEX : Male
DOA : 29/3/19
CASE TYPE : AWMI ( thrombolysed )
ECHO IMPRESSION:
Moderate LVdysfunction EF( 35-40%),Mild,distal
anterior wall and apex are akinetic moderate size pericardial
effusion seen (7am) ,no evidence of tamponade,mild mitral
regurgitation.
CORONARY ANGIOGRAM:
Thrombolysed anterior wall myocardial infarction.
41. DRUG
DRUG
DOSE FREQUE
NCY
ROUTE START
DATE
END DATE
ANTIPLATELET (THROMBOXINE A2 INHIBITOR )
T.Ecospirin
(Aspirin)
75mg BD Oral 29/3 2/4
ANTICOAGULANT INDIRECTLY ACTING THROMBIN
Inj.Clexane
(enoxaparin)
60mg BD
OD
S/C
S/C
29/3 TO
30/3
31/3 TO
2/4
2/4
(FREQ CHANGED
ON 31/3)
42.
43. Low molecular weight heparin (LMWH) licensed in UK :
o enoxaparin (standard prophylactic dose 40mg daily ; minimum 20mg daily to
maximum 60mg twice daily )
o dalteparin (standard prophylactic dose 5000 units ; minimum 1250 units once
daily to maximum 5000 units twice daily ; obese patients – maximum 7500 twice
units daily)
o tinzaparin (standard prophylactic dose 3500 units once daily ; minimum 2500
units once daily to max. 4500 units twice daily ; obese patients – max. 6750
twice daily )
LMWH , licensed in countries other than UK :
o Bemiparin ( standard 2500 units daily ; mini. 2500 units daily to max. 3500
units daily )
o Certoparin ( 3000 units daily ) & Reviparin (mini. 1750 units once daily to max.
4200 units once daily )
o Nadroparin ( standard 2850 units once daily ; mini. 2850 once daily to max.up to
57 units/kg once daily )
o Parnaparin ( standard 3200 units once daily ; mini. 3200 units daily to max. 4250
units once daily )
51. Drug chart:
DRUG DOSE FREQUE
NCY
ROUT
E
START
DATE
END
DATE
INDICATION
Tab. Ecospirin
(Aspirin)
75mg OD oral 11/2 13/2 ANTIPLATELET
Tab. Aspisol
(aspirin+Glycin)
75mg OD oral 11/2 13/2 ANTIPLATELET
Inj.UFH 5000IU TID I.V 11/2 13/2 ANTICOAGULANT
52. CASE CONDITIONS FOR PREFERRING UFH:
Adults and young people ( 16years and older ) who are acutely ill
patients admitted to hospital
MECHANICAL:
Anti – embolism stockings (AES) ( above or below knee)
Intermittent pneumatic compression (IPCD) devices ( full leg or
below knee
Foot pumps or foot impulse devices( FID)
Electrical stimulation ( including Geko devices )
Continuous passive motion
PHARMACOLOGICAL :
Unfractionated heparin (UFH) ( low dose , administrated
subcutaneously)
53.
54. CASE TYPE : Coronary artery disease
Age. : 50yrs
Sex : Male
DOA. : 13.11.2018
PAST HISTORY :DM for 4 yrs
ECG IMPRESSION :
ST segment elevation in the inferior leads .
PRESENT SURGICAL PROCODURE :
CAG done on (14/11/18).
CASE 8 (CAD)
55. Lab Investigations:
TEST OBSERVED VALUE NORMAL VALUE
Total WBC count 17700
(cells/cumm)
4000-
11300(cells/cumm)
Basophils 00% 0-1%
Eosinophils 00% 2-6%
Lymphocytes 11% 20-40%
Monocytes 02% 2-10%
Polymorphs 87% 45-75%
56.
57. ABOUT THE DISEASE :
Definition:
Occurs when anterior myocardial tissue usually supplied
by the left anterior descending coronary artery suffers
injury due to lack of blood supply.
It's also known as anterior ST elevated myocardial
infarction (STEMI)
58. SYMPTOMS:
Pressure or tightness in the
chest
Sweating
Vomitting
Chest pain
Shortness of breath
Nausea
59. Heparin or LMWH
With PCI.
With Lytics ( if getting asa and alteplase ).
Without reperfusion.
24-48 hrs.
Evidence for use one to three months post – MI
in patients at high risk for embolization ,
especially those with an anterior wall MI.
62. TICAGRELOR :
Ticagrelor is a faster
more potent
more consistent acting P2Y12 inhibitor
anti platelet drug
DOSE : For ACS requiring urgent PCI 180mg loading dose
followed by 90 mg BD ; may be continued for upto 12 months
MOA :
It is the P2Y12 receptor inhibitor which acts directly without
needing metabolic activation
Ticagrelor is not a thienopyridine but blocks platelet aggregation
by inhibiting binding of ADP to the P2Y12 receptor
Unlike clopidogrel and prasugrel the action of ticagrelor is
reversible
63.
64. PHARMACOKINETICS :
It is a faster onset
quicker offset of action
biological half life is 12 hrs
it needs twice daily administration
ADVERSE EFFECT :
The risk of intracranial bleeding was faster with ticagrelor ,
but that of all major bleeds was similar