Pharmacology High Yield
Pharmacology High Yield
Pharmacology High Yield
High-yield
Index
Sl.No. Chapter Pg.No.
1. Autonomic Nervous System 09
2. General Pharmacology 28
3. Neuropharmacology 43
4. CVS Pharmacology 70
5. Nephrology 83
6. Haematology 93
7. Anti Cancer Drugs 100
8. Hormonal Therapies, DMARDS & Biologicals 107
9. Antibiotics 117
10. Endocrinology 145
Autonomic Nervous System
Basic Idea
Sympathetic Parasympathetic
Parasympathetic system
MCQ Bulletins Synthesis
1) Source of Choline Choline Choline MCQ Bulletins
is Serine. +
Na+ Acetyl
•
Rate Limiting Step
2) Defect in this channel CoA
causes
Ach
LAMBERT EATON SYNDROME Ca 2+
Rx : 3,4 - diaminopyridine
by increasing Ach release. Vesicle
MOA
i) Ca2+ channel activation. -
Channel
M1, M3, M5 - Gq Nm, Nn
(Blocker) -
Puffer fish M2, M4 - Gi
- Ligand Gated
Toxin Skeletal
Receptor
Muscle “G” Protein Coupled
Paralysis Receptor
Previous Year Questions AIIMS 2018
M1 M2
a
Location - Stomach Location - In Myocardium, maximally located at AV Node
v.
a
Releases HCL Action - Decreases Myocardial contractility
v.
a
Selective M1 Agonist
- Oxetremorine Bradycardia
a
C/I - Gastritis v.
:
Tripitramine
- Pirenzepine
- Telenzepine
:
B) Ejaculation
C) Bronchodilation
D) Increased myocardial contractility
M3 Receptors location
Smooth Muscle
Visceral Muscle
: Eye
M3
Location - a) Smooth Muscle
b) Visceral Muscle
c) Eye
Visceral Muscle
- Intestine and Bladder
M3 agonists on eye
Pilocarpine
: Ecothiophate
Sphincter
M3
Pupillae
Muscle In Organophosphate poisoning
Constriction
They are irreversible
Miosis cholineseterase inhibitors
Increase in Ach
Miosis
:
ii) Increases uveosclreal outflow
Prostaglandin Analogues
(Pilocarpine)
Sympathomimetics Conjunctival hyperemia
Sympathomimetics Alpha 2 agonists CNS depression in infants
:
iii) Increases Trabecular Outflow
Miotics
(Brimonidine, Apraclonidine)
Beta Blockers Corneal hypoesthesia
a
Rhokinase inhibitors (Netarsudil) (Timolol) Systemic S/E
Carbonic anhydrase Systemic S/E
Inhibitors Corneal Oedema
Prostaglandin Eyelash Hypertrichosis
Analogues Macular Oedema
(Latanoprost) Iris pigmentation
Periorbital fat
Previous Year Questions AIIMS 2018
:
Previous Year Questions AIIMS 2019
Anticholinergic.
Used in the treatment for motion sickness
: Scopolamine patch is the preferred mode of administration and is most effective.
Patch should be applied the night before the journey.
: Not given to children less than 10 years of age.
Place patch behind the ears at least 4 hours before travel and lasts for 3 days.
: S/E : Dry mouth, Sedation.
Other anticholinergic used in motion sickness - Dicyclomine.
: Other drugs used in Motion Sickness -
: Promethazine
Cinnarizine
Diphenhydramine
:
Cyclizine
Meclizine
: Dimenhydrinate
You and your friend plan for a mountain trip for the day after. What medication
would you advise him to help with his motion sickness?
A) Ranitidine tablet before start of trip
B) Dimenhydrinate before start of trip
C) Scopolamine patch the night before trip
✓
D) Omeprazole the night before and before start of trip
C) Misolastin
D) Loratidine
Nicotine receptors
ACh SCh
Na+ Succinylcholine
Structure mimics Ach structure
Nm Nn
Membrane depolarised
Skeletal
Muscle
Persistent
Anticholineesterases
Reversible
1) Physostigmine (Natural Origin)
Highly lipid soluble. So can cross Blood Brain Barrier.
DOC - Atropine (Belladona) Poisoning
2) Pyridostigmine
Orally given drug, longer acting in myasthenic patients.
3) Neostigmine
Has direct action on Nm, for myasthenic patients in injection form.
4) Edrophonium
Water soluble. So can’t cross Blood Brain Barrier.
Edrophonium Challenge Test - Short Acting, If after injecting, symptoms improve, then
it’s positive test.
Other drugs are : Rivastigmine Used in Alzheimer’s disease
Donepezil Pathology - Deficiency of ACh
Galantamine
Previous Year Questions AIIMS & INICET 2020
:
B) 2 and 3
C) 1 and 3
D) 1 only
Irreversible
Mnemonics
Organophosphorous Compounds (OPCs) Drugs that can’t cross BBB
1) Dyflos Goa on SuNDay
2) Parathion
3) Malathion G - Glycopyrrolate
4) Diazinon S - Streptomycin
OPCs inhibit cholinesterase enzyme by binding N - Neostigmine
with esteric site of cholineseterase enzyme. D - Dopamine
ACh accumulation
•
Carbamate
1) Carbaryl
2) Propoxur
Drugs used in Organophosphorous poisoning
i) Atropine
First line drug of choice.
Max dose 200 mg.
Signs and symptoms of Atropinisation
- Until the HR > 100/min
- Pupil size : dilated
- Pulmonary secretions and other secretions decreases
ii) Oximes
Bind to anionic site - reactivation of cholineseterase enzyme.
Eg : Pralidoxime
Obdoxime
Diacetyl monooxime (more potent)
Tyrosine Tyr
Tyrosine Hydroxylase
Dopa
DOPA Decarboxylase
Dopamine
Dop
NE
The 2 enzymes that cause metabolism
:
of NE : i) MonoAmine Oxidase (MAO)
ii) Catechol - O - Methyl transferase
NE
(COMT)
Alpha Beta
Alpha 1 - Gq Beta 1
Gs
Alpha 2 - Gi Beta 2
Beta 3
Alpha 2
NE Inhibits release of NE
Alpha 2
Controls release
A patient was treated for septicemia with norepinephrine infusion. Which of the following
best explains the benefit of this drug?
A) Bradycardia
B) Tachycardia
C) Increases urine output
D) Increases mean arterial blood pressure
Examples of Alpha 2 Agonists and Uses
1) Clonidine
Uses of Clonidine
- As autoreceptor : inhibited release of NE
i) Hypertension
- As heteroreceptor : inhibits release of ACh
ii) Opiod Withdrawal symptoms
S/E : a) Mental depression
iii) Useful in controlling smoking habits
b) Sedation
iv) Analgesic action
c) Impotence
v) Prophylaxis of chronic migraine
d) Dry mouth, nose, eye.
ACh vi) For controlling loose motion d/t Diabetes.
e) Constipation
Sudden Withdrawal : Rebound Hypertension
2) Moxonidine
Used as anti HTNs but has much lesser incidence for rebound HTN.
3) Rilmonidine
4) Apraclonidine Aqueous humor Uveoscleral Treatment of
5) Brimonidine formation Outflow Glaucoma
in
6) Tizanidine - Centrally acting SMR
7) Dexmedetomidine - Sedation in ICU patients.
Creative BP
Mood So used in
Sexual hypertension
Stimulation
Alpha 1 - Sites and Action
1) Vascular Smooth muscle - Vasoconstriction
:
D) Flutamide
A patient with diabetes and COPD developed post-operative urinary retention. Which of
the following drugs can be used for short-term treatment of the condition?
A) Tamsulosin
B) Bethanechol
C) Terazosin
D) Methacoline
Non - Selective Alpha Blocker
Irreversible Reversible
Beta 1
β1 Heart Increase HR
Increased force of contraction.
Increased Cardiac Output.
Synthetic Catecholamines
Isoprenaline - β1, β2, β3
: Dopexamine - D1, β2
Dobutamine - β1 : Stress Echo & ECG
: Fenoldopam - D1 : Given as IV infusion in HT emergency with renal impairment.
Beta 2
Beta 2 Vascular - Vasodilatation
Visceral Uterus
(Relaxation)
Tocolytic Agents
Bronchus Ritodrine
: Isoxsurpine
n
Bronchodilatation
The following table gives BP values before and after administration of drug 'X'.
What would be the probable mechanism of action of drug 'X'?
A) a1 agonist and ß1 agonist Drug X
B) M2 agonist and M3 agonist SBP 120 150
C) a1 antagonist and ß2 agonist DBP 80 68
D) B1 agonist and ß2 agonist
:
HR 72 86
:
C) 1:1000 1.M. - 1 ml
D) 1:1000 I.V. - 0.5 ml
Reflux Tachycardia
DBP increases
5) Adrenaline (Alpha 1, Alpha 2, Beta 1, Beta 2)
In very high concentration, Adrenaline acts on Alpha 1.
: In very low concentration, Adrenaline acts on Beta 2.
Beta Blockers
a) Non selective Beta blockers - First generation
b) Cardioselective Beta blockers - Second generation
(Predominantly blocks Beta 1)
c) Beta blockers with additional properties - Third Generation (Blocks Beta + Alpha)
Cardioselective Beta blockers
i) Nebivolol - Most cardioselective Releases NO
Causes Vasodilatation
:
B) Torsades de pointes
C) Tachycardia
D) Ventricular fibrillation
A drug was given IV at a rate of 1.6mg/min. The clearance of the drug is 640ml/min. The half
life of the drug is 1.8 hour. Calculate the plasma concentration of the drug.
A) 2.88mg/ml
B) 0.004mg/ml
C) 3.55mg/ml
D) 0.002mg/ml
✓
I -
Basic Idea of Drug Absorption
Drug absorption is favourable when there is lipid solubility & non ionisation
So, if any drug toxicity occurs, we need to think about the pH of the drug
We need to inject acidic agent (Eg : NH4Cl or We need to inject basic agent (Eg : NaHCO3) to
Ascorbic Acid) to make the drug ionised, hence make the drug ionised, hence decreasing
decreasing absorption. absorption.
“P” Glycoprotein
Reduces the bioavailability of digoxin
Mnemonics
Mnemonics
“P” Glycoprotein Inhibitors “P” Glycoprotein Inducers
Eat - Erythromycin St. John’s - St. John’s wart
All - Amiodarone Baby - Barbiturate
V - Verapamil needs
I - Itraconazole C - Carbamazepine
Q - Quinidine P - Phenytoin
R - Rifampicin
:
Previous Year Questions NEET PG 2021
:
B) Efficacy
C) Potency
D) Toxicity
:
D) 8
:
D) Both A and B
The graph below shows the relationship between the log (dose) and the response
of three drugs, A, B, and C. Which of these drugs has the highest potency?
A) A
B) B
C) Both A and B
D) C
Cmax
Area under the curve - Bioavailability
Concentration
Tmax
Time
Drug Distribution
If any drug gets distributed only in plasma - Low volume of distribution.
Lipid insoluble
Ionised
In this kind of drug poisoning,
Highly protein bound
Large Size
We need hemodialysis
Lipid Soluble
Non ionised Large volume of distribution Mnemonics
Free form AVOID
So it gets distributed in A - Amphetamine
cellular component also. V - Verapamil
O - Opioids
There is no role of dialysis I - Imipramine
in such poisoning D - Digoxin
:
C) Intravenous
D) Transdermal
Biotransformation
Previous Year Questions AIIMS 2018 Previous Year Questions AIIMS 2019
Drugs following
Zero Order Kinetics Microsomal Enzyme Inducers
Zero G - Griseofulvin
W - Warfarin P - Phenytoin
A - Alcohol R - Rifampicin
A - Aspirin S - Smoking
T - Tolbutamide Cell - Carbamazepine
T - Theophylline Phone - Phenytoin
Power - Phenytoin Chronic Alcoholism
:
C) Isoniazid
D) Amiodarone
A female patient on oral contraceptive pills (OCP) was diagnosed to have tuberculosis
and started on antitubercular therapy (ATT). She was advised to use an additional barrier
method of contraception. What is the reason for this advice?
A) Teratogenic
B) Failure of ATT
C) Rifampicin decreases OP metabolism
D) Rifampicin induces CP metabolism and cause failure
11
100
Constant 75
amount T1/2 - 2 hours
is eliminated. 50
No fixed T1/2 T1/2 - 1 hour
25
0
First Order Kinetics
100
1st T1/2 50% drug eliminated
Constant 50 +
fraction 2nd T1/2 25% drug eliminated
is eliminated 25 = 75% drug eliminated
with constant 3rd T 1/2 12.5 %
interval. 12.5
So fixed T1/2. 4th T1/2
6.25%
6.25
A patient requires Ceftriaxone 180 mg. You have a 2 ml syringe with 10 divisions per ml. The
vial contains 500 mg/5ml of ceftriaxone. How many divisions in the 2 ml syringe will you fill
to give 180 mg ceftriaxone?
A) 18
✓
B) 1.8
C) 20
D) 2
Previous Year Questions AIIMS 2017
For which of the following drugs, is absorption increased after a fatty meal?
A) Griseofulvin
÷
B) Amphotericin B
C) Ampicillin
D) Aspirin
The package description of a drug states that 500mg of paracetamol is present in each unit of
the tablet formulation, but in reality, each unit contains only 200mg. What is the terminology
used to refer to these kinds of drugs?
A) Counterfeit drug
B) Adulterated drugs
C) Spurious drugs
D) Mislabelled drugs
A drug solution containing 500 mg/5 ml of the drug is given to you. You are provided with a
2 ml syringe (having 10 divisions for each mi). How many divisions of the 2 ml syringe need
to be administered to deliver 180 mg of the drug to a patient?
A) 1.8
B) 10
C) 14
D) 18
Previous Year Questions AIIMS 2018
;
Previous Year Questions AIIMS & INICET 2020
:
C) Phase 3
D) Phase 4
αβ αγ
BZD
Causing
Hyperpolerisation
GABA facilitatory action
Causing hyperpolarisation
Benzodiazepines Actions
Barbiturates GABA A
Cl- Receptor
αβ αγ
MCQ Boost
Three important Benzodiazepenes that can be used in Hepatic failure also :
i) Temazepam
ii) Oxazepam
i
iii) Lorazepam
Barbiturates
•
General properties
•
They itself causes pain. So general anaesthesia using these cause pain.
• Narrow therapeutic index.
• Used only for two purposes - Epilepsy, Anaesthesia.
Examples of Barbiturates
Ultrashort acting Barbiturates Short Acting Barbiturates
i) Thiopentone Sodium i) Secobarbitone
t1/2 is slow because of redistribution. ii) Pentobarbitone
Highly lipid soluble, so can cause BBB.
Uses : a) i.v induction for GA.
b) Narcoanalysis
c) Status Epilepticus
ii) Methohexitone
Causes : Convulsion
Use : Electroconvulsive therapy
Long Acting
i) Phenobarbitone
ii) Primidone (Active Metabolite)
Use : Anticonvulsive agent in pregnancy and paediatric use.
Adv effects : Hyperkinesia in children.
Clinical symptoms of barbiturate poisoning MCQ BOOSTEr
1) Flabiness of muscle. It is a Microsomal Enzyme Inducer,
2) Comatose, shallow and falling respiration. so it reduces the level other drugs
3) Bullous eruption - Hallmark skin lesion for poisoning. given along with it.
Barbiturate poisoning has no specific antidote. So if given with OCP, contraceptive
failure can occur.
GABA analogues
Valproate
Glutamate
Glutamate +
Decarboxylase Induces
GABA
Inhibits
Tigabine Reuptake
- GABA
Inhibits
Valproate
Digestion by
GABA transaminase
Vigabatrin Used in
Inhibits Infantile spasm
In Tuberous Sclerosis
Gabapentin Treatment of i) DM neuropathies
Pregabalin MCQ BOOSTER
ii) Post Hepatic neuralgia ACTH is the DOC
for Simple Infantile
Spasm.
Promotes synthesis and release of GABA
GABA B receptor
•
G protein coupled receptor.
•
Agonist : Baclofen
•
Uses : i) Centrally Acting SMR
ii) Rx of hiccup
iii) Central craving of alcohol
•
Antagonist : Saclofen
Glutamate
Has action on CNS Excitatory Neurotransmitter
:
S/E - Acute toxicity
High i.v dose - Cardiac arrest
Chronic Adverse Effects
Fetal Hydantoin Syndrome Hyperplasia of gums
Hirsuitism
Hypotension and
H
Hypersensitivity Reaction -
on iv cause arrhythmias Rashes, Lymphadenopathy
Hyperglycaemia, Hypocalcemia
Cerebella Ataxia and
vestibular nystagmus Hallucination, Behavioural
Abnormality
Hepatotoxicity
Non epileptic use
i) Trigeminal Neuralgia
ii) Digoxin induced VT.
Carbamazepine
¥
,
÷
B) Agranulocytosis
C) Rash
D) Steven Johnson Syndrome
A patient who was diagnosed with epilepsy was put on retigabine TDS. Now phenytoin is
being added. Which of the following changes should be made to retigabine?
A) Increase the dose
B) Decrease the dose
C) Stop the drug
D) Stop retigabine and start on carbamazepine
MCQ Boost
Absence seizure
Pathology - Abnormal T Type Calcium Channels
T/t of absence seizures - i) Ethosuccimide
ii) Sodium Valproate
iii) Trimethadione
Antiepileptics having Carbonic Anhydrase activity
i) Topiramate
ii) Zonisamide
First line goals in different types of seizures
l
Types of Seizures First Line Drugs
Generalised Onset Tonic Clonic Lamotrigene
Valproate
Focal Lamotrigene
Oxcarbazepine
Carbamazepine
Phenytoin
Levetiracetam
Typical Absence Valproic Acid
Ethosuccimide
Lamotrigene
Atypical, Absence, Valproic Acid
Myoclonic, Atonic, Lamotrigene
Topiramate
Dopamine
Acts on
- Nigrostriatal Pathway : Initiation of movement
- Mesolimbic fibre : Controls behaviour
- Tuberoinfundibular fibre : Inhibits pituitary for prolactin secretion
Previous Year Questions AIIMS 2017
A known epileptic patient on levetiracetam has been seizure-free for 2 years. But he develops
agitation and anger issues
interfering with his day-to-day activities as a result of the drug intake. Which of the following
measures is to be taken next?
A) Slowly taper the drug over next 6 months
✓
B) Continue levetriacetam since a 5 year seizure free interval is needed
C) Stop levetiracetam and start on a different anti-epileptic
D) Discontinue the drug as he is seizure free
Antipsychotics
Antipsychotics
•
Extrapyramidal signs more prominent
Extra Edge
Extra Pyramidal Side effects - Common side
Effect of Typical Antipsychotics
Types Treatment
i) Drug induced Parkinsonism Promethazine
ii) Acute Muscular dystopia Benzhexol
Benztropin
iii) Tardive dyskinesia Valbenazine
Deuterabenazine
iv) Akathesia (Restless urge Propranolol
to move)
(Most Common EPS)
v) Neuroleptic Malignant Dantrolene Sodium
Syndrome
Previous Year Questions AIIMS 2018
A patient presented to the casualty with signs of dehydration due to severe vomiting. The intern
gave the patient a parenteral medication, following which the patient developed grimacing and
abnormal posturing. What could have been the inciting drug for this reaction?
A) Atropine
B) Ranitidine
C) Metoclopramide
:
D) Domperidone
Levodopa
In peripheral circulation,
Dopa
Levodopa Dopamine
Decarboxylase
Alpha 1 - Vasoconstriction
Beta 1 - HR increases, Increase in Cardiac contraction
CTZ - Nausea and Vomitting, Altered taste sensorium
Amantadine
It’s an antiviral drug used for influenza A.
: Mechanism of Action : i) Anticholinergic
ii) Dopaminergic Agonist
iii) NMDA Antagonism
Adverse Reactions : i) Ankle Edema
:
ii) Levido Reticularis (Net like skin rashes on extremities)
(Imp NEET MCQ visual)
Ergot D2 Agonist
They all have vasoconstrictor property.
So Side effects of erythromyalgia and increased anginal pain.
: Eg : i) Bromocriptine
ii) Pergolide
iii) Cabergoline
Serotonin
Source - Tryptophan MCQ Booster
Tryptophan Carcinoid Tumour
Increased Serotonin/ 5 HT production
5 - hydroxy Tryptophan
Urinary Estimation of
5 - hydroxy Tryptamine 5 - hydroxy Indole Acetic Acid
(Serotonin)
Action of serotonin
G Protein Ligand
Coupled Gated
Receptors Receptors
5HT, 5HT2, 5HT4 5HT3
5HT1 -
5 HT3
- Nausea, Vomitting.
So 5 HT3 blocker has use as antiemetic.
Eg : Ondansetron, Granisetron
Migraine
An elderly woman on treatment for migraine presents with chest pain. She has a
previous history of angina/MI. Which of the following mechanism of the prescribed
drug for migraine might have caused this presentation?
A) 5-HT antagonist
B) 5-HT agonist
:
C) Calcium Channel Blocker action
D) Nitric oxide mediated vasodilation
:
- Olcegepant (i.v)
- Telcegepant (oral)
Monoclonal Antibodies
- Erenumab
- Fremanezumab
Anxiety Disorder
- Overaction of Serotonin
- Poor action of GABA
- Performance Anxiety
DOC - Propranolol
- Anxiety with Panic Attack
SSRI + Benzodiazepine
- 5 HT1A Agonist - causes auto regulation
i) Buspirone
ii) Ipsapirone
iii) Gepirone
Advantage
- Non sedative
- Non habit forming
Disadvantage
- Delay in onset of action.
Antidepressants
SSRI
Main treatment of depression.
i
i) Fluoxetine
(Longest acting SSRI, Least chances of having “discontinuation”)
ii) Fluoxamine
iii) Paroxetine
- Causing weight gain
- Teratogenicity
- T/t of Premenstrual tension
iv) Citalopram - QT Prolongation
v) Escitalopram - Highly Selective SSRI
vi) Sertraline - Safe in cardiac patients
- Less drug interaction
Uses of SSRI
1) Depression - Juvenile Depression
2) OCD
3) PTSD
4) Bullimia
5) Premature Ejaculation
6) Premenstrual Tension
S/E Drug Interactions
:
5 HT2 - i) Insomnia Combination of SSRI with MAO Inhibitor
ii) Anxiety
iii) Delayed Ejaculation
5 HT3 - Nausea, Vomitting Serotonin Level increases
T/t - Cyproheptadine
TCA
Blocks - Histaminic, Muscarinic and Alpha 1 receptors
: Examples :
- Clomipramine - Used for OCD
- Doxepine - Strongest Antihistamine
- Imipramine - Strong anticholinergic
- Amitryptiline - Antidepressant, Prophylaxis of Migraine, DM Neuropathy
- Maprotiline
- Amoxapine - Additional D2 blockage + Antipsychotic
- Nortriptylline - S/E : EPS, Galactorrhea.
Antihistamine Side Effects
:
- Sedation
- Increase in appetite
- Weight Gain
Anti Muscarinic side effects
- Dryness of mouth
- Constipation
- Tachycardia
- Retention of urine.
:
Vasodilatation
Postural Hypotension
TCA Poisoning
i) Cardiac Arrhythmia
ii) Convulsion
iii) Coma
iv) Metabolic Acidosis
A patient was treated with TCA for a major depressive episode in the hospital for 4
weeks. What is the main concern while considering his discharge from the hospital?
A) Need for drug monitoring
B) ECG monitoring for arrhythmias
C) Suicidal risk
✓
D) Sedation being the side effect
Previous Year Questions AIIMS & INICET 2020
Snri
i) Venlafexine - Can cause HTN in severe form due to increased NE.
ii) Duloxetine - T/t of i) Neuropathic Pain
ii) Fibromyalgia
iii) Stress Incontinence
iii) Milnacipran
iv) Vilazodone
v) Vortioxetine
NDRI
Bupropion
T/t of i) ADHD
ii) Obesity
iii) Smoking Control
S/E : More Anxiogenic
Seizure
Bipolar Disorder
Mania
+
Depression
BPD Type 1 BPD Type 2
T/t of acute mania T/t of depressive phase - Lamotrigene
- Valproate
- Lithium
- Carbamazepine
- Olanzapine
- Risperidone
- Aripiprazole
- Diazepam
Lithium
Narrow Therapeutic Index - Unsafe
: T 1/2 - 24 hours
Hyponatremia, Diuretics, NSAIDs - Aggravates Lithium Toxicity (NEET 2020)
: Lithium Plasma Concentration
- Maintenance margin safety for BPD : 0.5 - 0.8 meq/L
- Maintenance margin safety For Acute Mania : 0.8 - 1.2 meq/L
- Toxic symptoms arise : > 1.5 meq/L
- Hemodialysis needed : 4 meq/L
Drug Interactions with Lithium :
:
Aggregation of Action of Succinylcholine : SCh Apnoea
Aggregation of Action of Pancuronium : Tachycardia
Adverse Reaction
Li - Leukocytes increase in number.
T - Tremor (Most Common of 8 - 10 Hz)
H - Hypothyroidism - Inhibit release of T3/T4 from follicle.
IU - Increased Urination - T/t : Amiloride
M - Pregnant Mother - Ebstein’s Anomaly : Box Shaped Heart
Previous Year Questions AIIMS 2017
÷
D) Valproate
A patient is started on lithium therapy. Which of the following side effects should the
patient be asked to watch out for to monitor for toxicity?
A) Malaise and sore throat
B) Vertigo and Diarrhoea
C) Fever
D) Breathlessness
A psychiatric patient was started on lithium for the management of bipolar disorder. To
monitor the blood lithium levels, at what time interval should the blood sample be collected
after the administration of lithium tablets?
A) After 24 hours
B) After 12 hours
C) After 6 hours
D) Immediately after taking tablets
Previous Year Questions NEET PG 2020
:
D) Thiazides cause water loss therby increase lithium levels
A female patient was on lithium therapy for bipolar disorder for 6 months. She
kept a fast for few days due to religious reasons and presented with seizures,
coarse tremors, confusion and weakness of limbs. Which of the following
investigations should be done to help diagnose her condition?
A) Serum electrolytes
B) Serum lithium level
C) ECG
D) MRI
Opiod Receptors
-
Prolactin release
M - Miosis
:M - Miosis
A - Analgesia
-
C - Constipation -
R - Resp. Depression
Convulsion -
D - Diuresis
-
A - Analgesia -
S - Sedation
-
R - Resp. Depression
-
E - Euphoria
-
S - Sedation
MCQ Booster
All the actions of Morphine will produce tolerance on chronic therapy except
3 Cs
i) Constipation
ii) Convulsion
iii) Miosis
Pure Agonist
•
Natural Opiod
- Morphine : Controls pain
- CodEine : Antitussive
•
Semisynthetic
- Diacetylmorphine (Heroin)
- Pholcodine
•
Synthetic
- Pethidine (Meperdine)
- Analgesic : Used in post op pain
- Antimuscarinic : C/I in MI pain
- Metabolite is Norpethidine - Causes seizures
- Methadone
- Longer acting Opiod
- MOA : NMDA blocking action, Inhibits Reuptake of NE, Serotonin.
- Use : Neuropathic pain and Cancer pain
- DOC in Opiod deaddiction.
Pure Antagonist
Nalmefene
: Naloxone (i.v) - Specific antidote of Opiod poisoning
Naltrexone - Oral, long acting
: Peripheral Opiod Antagonist - Useful for treating Opiod induced constipation.
Eg : Methyl Naltrexone, Alvimopan, Naloxegol
A patient presented with biliary colic. The intern has administered an analgesic, following
which the pain got aggravated. Which of the following could be responsible for the
aggravation of the patient's symptoms?
A) Morphine
✓
B) Diclofenac
C) Nefopam
D) Etoricoxib
Classification of few opioids on their action on Opiod
Receptors (INICET 2020)
Receptors : µ δ K
Drugs
Buprenorphine +/- - -
Butorphanol +/- +++
Nalbuphine - ++
Pentazocine +/- +
+++ : Strong Agonist
+/- : Partial/ Weak agonist
- : Antagonist
Which of the following opioids is a partial agonist at mu and a full agonist at kappa receptors?
A) Pentazocine
✓
B) Buprenorphine
C) Tramadol
D) Fentanyl
:
Crosses BBB
Risk of addiction
So cautiously used
Severe Asthma.
Previous Year Questions AIIMS & INICET 2020
:
D) Can be used to treat cough effectively
A patient presented with pelvic fracture and head trauma after a road traffic accident. He
was given IV morphine for pain relief following which he developed respiratory difficulty.
What could be the most likely cause?
A) Pelvic Fracture
B) CO2 retention due to opioid use
C) Cerebral Edema
D) Pulmonary embolism
Nitrates
:
Glyceryl Trinitrate
NO Amyl Nitrate
:
Accumulation Isosorbide Mononitrate (6 - 10 hours)
Receptor Downregulation
Tolerance
Nitrate Action
It is a Smooth Muscle Relaxant.
Nitrates are useful in cyanide poisoning as they can form Methaemoglobin.
Action on
Vascular Smooth muscle
Decrease in Preload
So by reducing Oxygen
demand,
Angina is relieved.
:
Headache
Aphthous Ulcer
Role of Betablockers
•
in Angina
Inhibits Beta 1 receptor
•
in Acute MI
- To control fear by reducing Catecholamines.
- Reducing the size of infarct by controlling HR.
- Additional Antiarrythmic Property (Class V)
Reduces Mortality
Sodium Nitroprusside
Only iv infusion
: Short Acting ( <10 min)
•
Treatment of i) Hypertensive Emergency
ii) Dissection of Aorta
It is a cyanide containing drug, so contraindicated in pregnancy.
: Thiocyanate - Inhibits uptake of Iodine by thyroid gland causing hypothyroidism.
Previous Year Questions AIIMS 2018
:
Types of Calcium Channels
L Type - All cardiac CCBs
N Type
: T Type - Ethosuximide
- Treatment of Absence Seizures
Calcium Channel Blockers
Type of Calcium channels :
- L Type - All cardiac CCBs
- N Type
- T Type - Ethosuximide - Treatment of Absence Seizures
•
These CCBs maximally dilate Artery •
Verapamil
- Controls HR.
Peripheral Vasodilatation - Acts predominantly on AV Node.
- Additional antiarrythmic property.
Reduction in BP - Used mainly in i) SVT
ii) AT
Useful in the treatment of : - SE
:
i) HTN i) Bradycardia
ii) Peripheral vascular disease ii) AV block
Approved for Hypertensive emergency. iii) Ankle Edema
i.v use : Clevidipine iv) Constipation
Nicardipine - Contraindicated in the
Adverse Reactions : i) Hypotension treatment of Arrythmia due to
ii) Reflex tachycardia Wolf Parkinson White Syndrome
iii) Ankle Edema (Aberrant Conducting fibre).
•
Diltiazem
MCQ Booster
- Acts on both SA and AV Node and
First line drugs for Angina
peripheral blood vessel.
- Beta blockers
- Treatment of angina
- CCB (Diltiazem)
by reducing Oxygen demand
- Nitrates
and increased Oxygen supply due to
Second line drugs for Angina vasodilatation.
•
pFOX inhibitors - Trimetazidine •
Ivabradine
- Ramolazine
Causes bradycardia.
•
If Na + channel blocker
- “I funny current” (Na+ channel
- Ivabradine
blocker) in SA Node.
- Uses - Angina, Heart failure.
- Adverse Reaction - Bradycardia.
Antiarrythmic Drugs
Rapid closure
ST Segment
of Na channels
Phase I
Ca2+ influx
Phase II
T wave
APD
If K + blocker is
R (Duration of Action Potential) added
T
P Increase in
Action Potential
duration
QT prolongation
Q
S
Classification of Antiarrythmic drugs
•
Class I - Na+ channel blockers + K+ channel blocker (Class IA)
OR
K+ channel opener (Class IB)
Class II - Beta Blockers
: Class III - K Channel Blocker
Class IV - Ca channel blocker - (Verapamil, Diltiazem)
: Miscellaneous and unclassified agents - Adenosine, Atropine, Digoxin, MgSO4, KCl
:
i) Quinidine
ii) Procainamide - Acetylation : S/E - SLE, Rheumatic Arthritis
iii) Disopyramide - Has highest anticholinergic activity.
Dryness of mouth
Constipation
Retention of urine (Not suitable for elderly patients with BPH).
Class I B
Na channel blockers & K channel openers.
QT interval reduces & Action Potential duration decreases.
: Acts upon Purkinje fibres at ventricles.
Used for Ventricular Tachycardia.
: Examples for Class Ib Antiarrythmics
Lignocaine Phenytoin
For treatment of digoxin induced VT (first line drug). Only in digoxin induced VT .
Mexilitine Tocainide
Derivative of lignocaine. This drug causes agranulocytosis.
Can be given orally. Not in use
Useful for i) Ventricular Arrythmia
ii) Diabetic Neuropathy
iii) Phantom Limb
Side Effects i) Bradycardia
ii) Tremor
iii) Nausea
Class Ic
0
Na+ blocking with negligible effect on K+ channel.
No change in ECG.
: Maximum proarrythmic property.
Examples :
:
i) Flecainide
ii) Encainide Useful for controlling arrhythmia due to
iii) Propafenone aberrant pathway in
iv) Moricizine Wolf Parkinson White syndrome
Class II
Beta Blocker.
a
Useful for Atrial and Ventricular Arrythmia.
Adverse Reaction : Bradycardia
-
Heart block
Hypotension
Class III
K+ channel blocker.
QT Prolongation
Examples of Class III
Antiarrythmic drugs
i) Amiodarone Previous Year Questions AIIMS 2017
ii) Dronederone
Dofetilide belongs to which
iii) Bretylium
class of anti-arrhythmic drugs?
iv) Sotalol
A) Class I
v) Ibutilide
B) Class II
vi) Vernakalant
C) Class Ill
= vii) Dofetilide
D) Class IV
Examples of Class III Antiarrythmic drugs
Amiodarone
:
- Broad Spectrum antiarrythmic.
- It has multiple mechanisms of action :
Na+ blocking
Beta blocker
Calcium channel blocker
K+ blocking
- Long T1/2 - 53 days
- Iodine containing drugs
- S/E
PLZ - Photosensitivity - Pigment of skin
Check - Whorl like pattern in Cornea : Cornea Verticillata
Pft - Pulmonary fibrosis, Peripheral Neuropathy
Lft - Liver damage : Hepatitis
TFT - Thyroid : Hypothyroidism (Inhibits peripheral conversion of T4 - T3)
: Hyperthyroidism (As, it is an Iodine containing drug)
Dronederone - No Iodine
Bretylium - Chemical defibrillator.
: Sotalol - Beta blocking property & K+ channel blocker.
Normal
Ibutilide Converts
: Vernakalant AF
Sinus
Rhythm
Class IV
CCB having Antiarrhythmic activity.
Verapamil
: Diltiazem
Miscellaneous Antiarrythmics
Atropine
•
Anticholinergic agent
•
Useful for treatment of : Symptomatic bradycardia
1° Heart block
Digoxin induced AV block
Adenosine
•
DOC for supraventricular tachycardia.
•
IV (Rapid i.v bolus) - 12 mg
•
Shortest Acting - < 10 seconds
•
Actions
a) Adenosine in brain - Antiepileptic Action
b) Adenosine in bronchus - Bronchoconstrictor
c) Adenosine in kidney - Na+ absorption from PCT.
•
Adenosine Antagonist
- Theophylline S/E - Seizures
- Aminophylline - Diuresis
- Bronchodilator
•
Adenosine Agonist - Dipyridamol
:
C) Spironolactone
D) Triamterene
Ionotropic effect
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•µpkeg_Bs•µ.q¥•••ÉB! BB.mbgmo.ae iBook
HCO3-
qzE'Y amazon.eaah-z-g.bg
•••Ñ
DCT
(Na+_Cl- Symporter)
!kB•m!Ba•
PCT
Collecting
a.q.ae#ttNhnoamaRBgBaoa.z
Loop part of DCT
Of Henle
(Na+_K+_Cl- Symporter) qamar
.
Metabolic Acidosis
ii) Inhibit secretion/retention of H+ in collecting duct.
Convulsions
iii) Hypokalemia
Eg : i) Acetazolamide
:
ii) Dorzolamide
iii) Brinzolamide
Adverse Reaction
Sulpha derivative - Hypersensitivity, Bone marrow suppression
Contraindicated in Liver Disease, Severe COPD, Metabolic acidosis
: Other Uses : i) Treatment of Glaucome
ii) Mountain Sickness
iii) Catamenial Seizure
iv) Periodic Paralysis
Previous Year Questions AIIMS 2018
:
Loop Diuretics
H
Inhibits Na+ - K+ - Cl- Symporter
Furosemide
Uses
1) Renal failure
2) Left ventricle failure ( To promote urination with oligura/Anuria)
Additional vasodilatory property
Increased Renal
Helps in shifting pulmonary fluid to systemic circulation
Blood Supply
Bumetamide
Torsemide - Longest t1/2
O Ethacrynic acid - S/E : Ototoxicity
S/E of loop diuretics
Water Loss - Reduction in ECF Volume
i. Electrolyte Abnormality .
Metabolism
- Hyponatremia - Hypouricemia
- Hypokalemia - Hyperglycemia
- Hypocalcemia - Hyperlipidemia
- Increased H+ : Metabolic Acidosis
Thiazide Diuretics
Inhibits Na - Cl symporter @ DCT
: Loss of Na+, K+, H+, Cl-
Calcium reabsorption, so safe in renal failure patients.
: Preferred drug of HTN in post menopausal women.
Examples of Thiazide Diuretics
: - Indapamide
- Chorthalidone
Uses : Mild edema
HTN
Antidiuretic property - Use in nephrogenic diabetes insipidus
: S/E of Thiazide Diuretics :
Water loss
Electrolyte Abnormalities
- Hyponatremia
- Hypokalemia
- Hypochlorinemia
- Decreased H+
- Hypercalcemia
A patient with gout develops hypertension. The uric acid level was found to be
elevated. Which of the following is not administered?
A) Hydrochlorothiazide
✓
B) Atenolol
C) Enalapril
D) Prazosin
A 34-year-old hypertensive man is diagnosed with stage 4 CKD, with eGFR<30. His doctor
wants to prescribe a thiazide diuretic. Which of the following can be given?
A) Chlorothiazide
B) Chlorthalidone
C) Metolazone
D) Hydrochlorothiazide
✓
Previous Year Questions NEET PG 2021
A patient with renal insufficiency presented with very low urine output, pedal
edema, headache and BP 160/90. Which anti-hypertensive can be administered?
A) Aliskiren
B) Chlorthalidone
:
C) Amlodipine
D) Prazosin
Gynaecomastia
(Eplerenon doesn’t cause)
They are the only group of diuretics that work from the interstitium.
3 Na+ ENAC
Na+
Antidiuretic
Mannitol
a
Site of action
- Loop of Henle Previous Year Questions NEET PG 2019
- PCT
Intravenous mannitol is used in
a
Used in the treatment of
A) Pulmonary edema
- Glaucoma
B) Congestive cardiac failure
- Cerebral Edema
C) Acute kidney injury with anuria
- Cisplatin toxicity
a
C/I D) Glaucoma
✓
- Pulmonary Oedema
- Cerebral Haemorrhage
Vasopressin Receptors
V1 V2
V2
:
2) Vascular Endothelium
SIADH
co
Increase in ADH. Previous Year Questions NEET PG 2019
Increase in water retention.
: Treatment by V2 Antagonist The best approach in the treatment of chronic SIADH is
- Lixivaptan A) Tolvaptan
✓
- Mozavaptan B) Reducing fluid intake to <500 ml per day
- Tolvaptan C) Demeclocycline
- Satavaptan D) Fludrocortisone
V1
Sites And Action :
:
Vascular Smooth Muscle Platelet Hepatocytes Myometrium
:
- Relcovaptan
- Nelivaptan
- Conivaptan
ACE
Direct -
Renin Inhibitor ACEI (Angiotensin
- Converting Enzyme)
- By acting on
ARB Angiotensin
Receptor
Direct Renin Inhibitor
MCQ Bulletins
Aliskiren
Enalkiren Any drug blocking RAAS Vasoconstriction
: Remikiren pathway will cause hyperkalemia.
A patient who was diagnosed with ADPKD was prescribed tolvaptan. After a few weeks, he
presented with dry mouth. and increased thirst. What is the likely cause?
A) Increased free water clearance
✓
B) V2 receptor agonism
C) Increased renal cAMP levels
D) Increase in urine osmolality
ACE Inhibitor
e
Captopril
e
Lisinopril
e
Ramipril
e
Fosinopril
e
Trandolapril
e
Enalapril
e
All ACEIs are prodrugs except Captopril and Lisinopril.
e
Use in e
S/E & C/I
i) HTN C - Cough and Angioedema
ii) CCF A - Anaemia
iii) MI P - Potassium (Hyperkalemia)
iv) DM T - Taste Change
v) Proteinuria O - Orthostatic Hypotension
vi) Scleroderma P - Pregnancy (C/I)
Enalapril - Best drug for HTN, DM R - Renal Artery Stenosis (C/I)
I - Increased Creatinine
L - LAAL (Red) Skin Rashes
A 35-year-old chronic hypertensive woman visits the outpatient department for pre-
conceptional counseling. Which of the following anti-hypertensives should she discontinue?
A) Labetalol
B) Calcium channel blockers
C) Angiotensin-converting enzyme inhibitors
✓
D) Alpha methyldopa
: - TXA2 Antagonism
T/t in HTN and gout
Vasopeptide
Example ANP BNP Urodilatin
Natriuresis Natriuresis
Function
Diuresis Diuresis
Vasodilatation Vasodilatation
Nesiritide
Can’t be taken orally.
: Only as iv infusion.
T/t of CHF.
: Metabolised by Vasopeptidase/ Neprilysin ( Neutral Endopeptidase).
Selective Neprilysin Inhibitors - Ecadotril, Sacubitril
: Neprilysin Inhibitors with additional ACE Inhibition - Omapatrilat, Sampatrilat
Previous Year Questions NEET PG 2018
:
D) 5
: Plasminogen
Examples :
Plasmin Breaks Cut
1) Streptokinase
2) Urokinase
3) Alteplase
4) Reteplase
5) Tenecteplase
Indication :
: - Acute MI
- Pulmonary Embolism
S/E :
- Bleeding (Most Common)
- Severe Intracerebral Haemorrhage (Rare)
Antithrombolytic Therapy
Increases clotting action
i) Epsilon Aminocaproic Acid
ii) Tranexamic Acid
iii) Aprotinin
Anticoagulant Drugs
:
- Fondaparinux
- Idraparinux
- Idrabiotaparinux
Rivaroxaban
: Edoxaban
Betrixaban
Oxidised Reduced
Vit K Vit K
Gamma carboxylation
Precursor Functioning
Clotting Clotting Factors
Factors II, VII, IX, X
Protein C, Protein S
Due to deactivation
Hypercoagulation
S/E of Warfarin Therapy
Purple Toe Syndrome
: Dermal Necrosis
Narrow Therapeutic Index
: Warfarin safety assessed by INR
Antiplatelet drugs
Cyclogenase 1 Inhibitor
:
Low dose aspirin.
Inhibition of TXA2 production.
Thromboxane synthase enzyme inhibitor - DAZOXIBEN
Thromboxane Receptor blockers : LOSARTAN
DALTROBAN
IFETROBAN
SULTROBAN
Irreversible P2Y12 inhibitors : TICLODIPINE
CLOPIDOGREL
ADP Receptor PRASUGREL
ADP mediated
action of GPIIb/IIIa
Reversible P2Y12 Inhibitors : TICAGRELOR
: CANGRELOR
GP IIb/IIIa Inhibitors : ABCIXIMAB
EBTIFIBATIDE
TIROFIBAN
Thrombin (PAR - 1) Receptor Antagonist : VORAPAXAR
: ATOPAXAR
:
D) Omeprazole interferes in its activation to an active metabolite
A patient on aspirin presented with occult blood in the stool. This is due to
inhibition of __________ by aspirin.
A) Phospholipase A2
B) Thromboxane
C) Phospholipase C
D) Phospholipase D
Anticancer Drugs
Cell cycle specific Anticancer Agents
G2
Cell G1
Cycle
Drugs Acting on G2
• Acts on Topoisomerase I
Bleomycin - Only anticancer antibiotic which is cell cycle specific.
: Campothecins : Irinotecan
Topotecan
S/E : Diarrhoea
M Phase
Vinka Alkaloids (Polymerisation Inhibitors)
: Vinblastin - Maximum myelosuppression
Vincristin - Maximum neurotoxicity
: Taxames
- Stabilise microtubules.
- Paclitaxel
- Docitaxel
- Cobazitaxel
- Can be used as stent eluting.
Previous Year Questions
AIIMS & INICET 2020
A boy presents with pallor and lymphadenopathy, the X-ray of his skull is given below. Which
of the following drug is not used for the management of the suspected diagnosis?
A) Cyclosporine
B) Methotrexate
C) Vinblastine
D) Vincristine
✓
G1 Phase
L - Asparagine
:
Use - ALL
S/E - Hypercoagulation, Haemorrhagic Pancreatitis
Palbociclib
CDK 4 - 6 Inhibitor
Amebaciclib
Used in the treatment of Breast CA
:
Ribociclib
Steroids : Apoptosis of t and B Cell.
Used in Lymphoma.
S Phase
Topoisomerase II Inhibitors
- Etoposide
- Tenoposide
Pyramidine Antimetabolite
Cytarabine
: 5 - Fluorouracil : Given along with Levamisole in the treatment of Colorectal Ca.
Floxuridine
: Gemcitabine - T/t for pancreatic cancer.
Capecitabine - T/t of AML and Paediatric ALL.
: Adverse Reaction - Hand Foot Syndrome
Purine Antimetabolite
6 - Thioguanine
: 6 - Mercaptopurine
6 - Mercaptopurine 6 Mercaptothiouric Acid (Inactive)
:
Xanthine
Oxidase
IMP AMP
Fludarabine
: Cladribin Hairy Cell Leukaemia
Pentostatin
:
Fludarabine and Pentostatin also used in CLL.
Levatinib - Thyroid Ca
~
Dasatinib
:
EGFR Blockers VGFR Blockers PDGFR Blockers
Vandetanib Axitinib
T/t of T/t
Medullary Ca Thyroid Renal Cell Carcinoma
Multitarget TKIs
Alkylating Agents
General properties Nitrosureas
N7 guanine residue as target. Temozolomide
Cell cycle non - specific. : Cyclophosphamide
Can be used for T/t of Ca. Ifosfamide - T/t of Beast Ca, Lymphoma
o
Adverse effects of Alkylating Agents : : Procarbazine
L - Leukaemia (Secondary) Dacarbazine
-
G - GI Toxicity
S - Sterility
T - Teratogenic
A - Alopecia
M - Myelosuppression
P - Pulmonary Toxicity
Anticancer Antibiotics
Actinomycin D (Dactinomycin)
: Daurorubicin
Doxorubicin
: Mitoxantrone
S/E of Doxorubicin : Cardiomyopathy Heart Failure
:
Doxorubicin in the presence of Iron forms free radicals.
NitrosOureas Temozolomide
a
Lomustine Highly lipid soluble
a
a
Semustine Crosses BBB
a
Cyclophosphamide Aldophosphamide
Phosphoramide Acrolein
Haemorrhagic Cystitis
:
Drugs for Multiple Myeloma
Melphalan
Drugs for Malignant Melanoma
Vemurafenib
i
•
BRAF -
•
Thalidomide &
Dabrafenib
&
Lenolidomide Trametinib
&
&
Bortezomib (DOC) Cobimetinib
&
SERM
Antagonistic Action on some oestrogen receptors.
: Agonistic action on some other oestrogen receptors.
Tamoxifen
:
- Has only antagonistic action on Estrogen Receptor of breast.
- So used in the treatment of Breast Ca.
- Agonistic action on Estrogen receptors :
- Vasodilatory action on blood vessels - Hot Flush
- Endometrial Proliferation - Ca Uterus
- Hypercoagulation (Increased clotting factor syntheis) - DVT
Toremifene
Doloxifen Breast Ca
: Raloxifen
Ospemifene - Dyspareunia
: Clomiphene - Ovulation Induction
Ormeloxifene - Contraception, Dysfunctional Uterine Bleeding.
:
(Centchroman)
SPRM
Ulipristal (Emergency Contraceptive) : Can be taken 5 days after unsafe coitus.
Asoprisnil
: Telapristone Use in Uterine Fibroid/Endometriosis
Aromatase Inhibitors
Peripheral Androgen Oestrogen Post Menopausal Bleed
Aromatase
Enzyme
Exemestane
:
Irreversible Aromatase Inhibitor
Formestane
Vorozole
:
Fadrozole To reduce Androgen induced Prostate Ca
Letrozole
Anastrozole
:
Drugs for Inhibiting Testosterone
GnRH Analogues
: No Histamine release
S/E of GnRH analogues - Hot flush
Loss of libido
Impotence
Sarcopenia (Decreased muscle mass)
Osteoporosis
Previous Year Questions AIIMS 2019
i
B) Endometriosis
C) Precocious puberty
D) Prostate cancer
Thalidomide
MOA : Anti Ca + Immune Modulation
In Multiple Myeloma
R Isomer - Therapeutic use and teratogenicity.
S Isomer - Sedation.
Previously used as antiemetic sedative.
Most common S/E :
i) Constipation
ii) Aphthous Ulcer
iii) Peripheral sensory neuropathy
iv) Never use in pregnancy (Phocomelia - Baby with no limbs)
Highly teratogenic - Category X Drug
MCQ Boosters
Anticancer drugs Antidote
Methotrexate Foilinic acid, Glucarpidase
Doxorubicin Dexrazoxane (Iron Chelator)
Cyclophosphamide Mensa in Haemorrhagic cystitis
Cisplatin Amifostine
Given in ITP
Eltrombopag - Oral
: Caplacizumab - Anti VWF, used in Acquired Thrombotic Thrombocytopenic Purpura.
Drugs for Anemia
Epoietin
:)
Darbopoietin
Recombinant Erythropoietin
:
Drugs for Anti Ca/ Radiation induced Vomitting
5 HT3 Antagonists
Ondansetron
: Granisetron
Tropisetron
: Palonosetron - Most selective 5HT3 blocker; Also used in late phase Vomitting.
Dolasetron - S/E : QT Prolongation and
:Supportive Antiemetics for Emesis Management due to Ca Chemotherapy
D2 blocker
: Benzodiazepine
Steroids - Dexamethasone, Methyl prednisolone
:Drugs for late phase Vomiting (Vomiting after 48 hours following chemotherapy)
Aprepitant - Oral Neurokinin 1 Antagonist
:
Fosaprepitant - i.v
Cancer Cachexia
IL - 1 Antagonist : Anakinra
IL - 6 blocker : Tocilizumab, Sarilumab
Fusion Protein (Target - CD 80/86) : Abatacept, Belatacept
Adverse Reaction
Secondary Infections.
: All TNF α blocker may cause liver damage - C/I in Hep B patients.
All TNF α blocker cause cardiotoxicity - C/I in Heart failure patients.
:
Rarely cause 2° cancer.
MCQ Booster
Uses of Rituximab - Target : CD - 20
C - CLL
A - Autoimmune Haemolytic Anemia
N - NHL
T - TTP
M - Marginal Zone Lymphoma, Mantle Cell Lymphoma
I - ITP
Ss - SLE
RITU - Rheumatic Arthritis
: Commonly used NSAIDs for acute gout are Naproxen, Indomethacin, Sulindac.
Aspirin shouldn’t be used due to its Uric Acid retention property.
Colchicine
MOA : Disruption of microtubule of Neutrophil.
A
Steroids
C) Psoriatric arthritis
D) Paralytic ileus
Previous Year Questions NEET PG 2020
Immunosuppressants
e
Calcineurin Inhibitors
Inhibits synthesis of IL - 2
: Examples : Cyclosporine, Tacrolimus Unique S/E of Cyclosporine
Indication : Autoimmune patients, Organ transplant patients. n
Hypertrophy of gums
: S/E : Dose limiting S/E - Nephrotoxicity Hirsutism
Neurotoxicity
Diabetes/Diarrhoea
: Hypertension
Hyperkalemia
Alopecia
Hepatotoxicity
IL - 2 receptor inhibitors
:
Sirolimus
Everolimus
Monoclonal Antibodies
Name Analysis
U - Full Human
ZU - Humanised (90% Human, 10% Animal) MAB
Xi - Chimerical (50% Human, 50% Animal)
Receptor Blockade Target Example
IL - 2 Li - Lowering Immunity BasiLiximab
GP IIB - IIIA Ci - Circulation AbCiximab
Respiratory Syncitial Virus Vi - Virus PaliVizumab
RANK - L Ligand OS - Osleo DenOsumab
PCSK - 9 OC - Over Cholesterol AlirOcumab, EvolOcumab
What is basiliximab?
A) IL-1 receptor antagonist
B) Anti-CD3 antibody
C) IL-2 receptor antagonist
:
D) TNF inhibitor
Other MABs
Ramucizumab - Target : VGFR
Uses : Gastric Ca
Omalizumab - Target : IgE ; Uses - Bronchial Asthma
: Reslizumab
Target : IL - 5
Mepolizumab Uses : Bronchial Asthma, Churg Strauss Syndrome
: Duplilumab -Target : IL - 4; Uses - Moderate and severe atopic dermatitis.
Ibalizumab - Entry Inhibitor; Used in HIV patients
: Cetuximab - Target : EGFR; Used in Menetrier’s disease.
Panitumumab - Target : EGFR; Used in Colorectal Ca.
: Eculizumab - Target : Complement component C5;
Used in Paroxysmal Nocturnal Haemoglobinuria
Antibiotics
Inhibition of cell wall synthesis Mnemonics
Drug Mechanism of Action
Cycloserine Inhibition of Alanine Ligase/Racemase BBCVan
S/E - Psychosis
Fosfomycin Inhibition of Enol Pyruvate/Transferase B - Beta Lactam
S/E - Diarrhoea B - Bacitracin
Bacitracin Inhibition of dephosphorylation of Bactoprenol C - Cycloserine
Vancomycin Inhibition of Transglycolase
Van - Vancomycin
Beta Lactam Transpeptidase
Penicillin
Penicillin G
Oldest One
: Limitations : i) Not effective orally (As it is acid sensitive, destroyed by HCl).
ii) Narrow spectrum only - UNSAFE.
iii) Resistance develops easily.
Newer Penicillins
Acid Resistant Penicillins/Orally Used
:
V - Penicillin V
O - Oxacillin
D - Dicloxacillin
C - Cloxacillin
A - Ampi/ Amoxycillin
Extra Edge
Probenecid added with Penicillin - Prolongs duration of action.
Most of the penicillins are excreted by renal route.
: Ampicillin and Nafcillin are excreted by bile.
Duration of Action of Procaine Penicillin : 12 - 24 hours.
: Duration of Action of Benzathine Penicillin : 4 weeks.
Previous Year Questions AIIMS 2017
Penicillin Resistance
Mechanism 1 - Enzymatic degradation by Penicillinase or β - Lactamase.
: Mechanism 2 - Alteration of Penicillin Binding Protein (Seen in MRSA, VRSA)
Aminopenicillins
Ampicillin
: Amoxycillin (Prodrug - Becampicillin)
C/I : Infectious Mononucleosis (Causes Skin Rash)
Thioacetazone : C/I for treating TB in HIV patients due to risk of Steven Johnson’s Syndrome.
:
Previous Year Questions AIIMS & INICET 2020
A known asthmatic patient with fever and sore throat was prescribed an antibiotic. Two
days later he presents with a maculopapular rash. Which of the following drugs might
have caused this?
A) Prednisolone
B) Salbutamol
C) Fexofenadine
D) Amoxicillin
✓
Carboxypenicillins Ureidopenicillins
e
Carbenicillin Azlocillin
e
e
Ticarcillin Piperacillin
e
e
Effective against Pseudomonas. Mezlocillin
e
i
Previous Year Questions NEET PG 2018
Carbopenems Monobactam
Carbopenems
Imipenem
÷
Meropenem
Broad spectrum of antibiotics are short acting, as they are rapidly degraded by
Dehydropeptidase I.
So it is administered along with Cisplatin to get longer duration of action.
Monobactam
Aztreonam
:Doesn’t show cross reaction with other β - Lactam drugs.
Use : Aerobic gram negative.
Previous Year Questions NEET PG 2019
Cephalosporins
How to memorise the names.
1st Generation : Cefazolin, Cefalexin, Cefaloridine
: (If ‘a’ is present after ‘Cef’ - Exception is Cefaclor which is 2nd generation.
3rd Generation
Contains ‘me’ - Ceftizoxime, Ceftazidime ( Exception : Cefuroxime - 2nd Gen)
Contains ‘one’ - Cefoperazone, Ceftriaxone
Contains ‘ten’ - Ceftibuten
4th Generation - Name contains ‘pi’ : Cefepime, Cefpirone
: 5th Generation - Name contains ‘rol’ in it : Ceftobiprole, Ceftaroline.
All the other Cephalosporins are 2nd Generation.
Glycopeptide Antibiotics
Vancomycin
Uses - Taken orally in Pseudomembranous colitis caused by Clostridium.
: Taken i.v - DOC for MRSA
S/E - Red Man Syndrome due to histamine release.
- Neurotoxicity
- Ototoxicity
Other Gylcopeptide Antibiotics
Teicoplanin - Least chances of histamine release.
Oritavancin - No need of modifying dose in CRF.
Telavancin
Dalbavancin - Longest Acting (6 - 10 days)
Linezolid
-
NE Increases
Cheese Reaction
Streptogranin
9
Quinupristin + Daltopristin
9
Given as i.v.
9
Daptomycin Tigecycline
T
Lipopeptide Antibody n
i.v Tetracycline
T
Acting on cell membrane. n
Excretion by bile - Safe in renal failure.
n
Resistance to efflux, pump.
MCQ Booster
Pseudomonas Colitis
Most commonly caused by 3rd Gen Cephalosporins, Clindamycin.
e
Match the following bacteria with the drug of choice used for each.
A. Bacteroides
B. MRSA
C. Hemophilus
D. Klebsiella
1. Vancomycin
2. Metronidazole
3. Meropenem
4. Penicillin
A) A-1, B-3, C-4, D-2
B) A-2, B-1, C-4, D-3
✓
C) A-3, B-4, C-1, D-2
D) A-4, B-1, C-2, D-3
Sulfonamides
Mechanism of action - Inhibits Fatty acid synthesis.
: Sulfazaline : 5 - Aminosalicylic acid + Sulfapyridine
Used in the treatment of bowel pathology of ulcerative colitis.
S/E - Oligospermia and infertility.
Topical Sulfonamides : Sulfactamide - Eyedrop
An infant had a serum bilirubin level of 33 mg/dL. The mother might have taken which of the
following drugs during the third trimester for this to occur?
A) Ampicillin
B) Co-trimoxazole
:
C) Azithromycin
D) Chloramphenicol
•
Tetracyclines are first drug of choice for : Rickettsial Infection
Lymphogranuloma Venereum
Chlamydial Infection
•
Treatment Used as prophylaxis in : Cholera
Brucellosis
Plague (T/t - Streptomycin)
•
Tetracyclines are C/I in pregnancy
.
In Mother - Hepatic Failure
•
In Baby - Bone and Teeth problem.
MCQ Booster
Gonorrhoea/Syphilis/Chancroid Eravacycline is used in the t/t
: Chlamydia
of Severe Combined
Legionella Intraabdominal Infection.
: Campylobacter jejuni
Spiramycin : Toxoplasma in pregnancy
:
S/E : GI Toxicity
Hearing Problem
Hepatitis
Cholestatic Jaundice
Erythromycin is most potent Microsomal
enzyme inhibitor.
:
- Kanamycin
- Capreomycin Second Line
- Amikacin
In Pseudomonas Infection
T - Tobramycin
A - Amikacin
G - Gentamicin
Other uses of Streptomycin
ATT - Category 1
÷
Prophylaxis of Plague.
÷
T/t of Tularemia.
÷
Other Aminoglycosides
Paromomycin
:
Oral - In Amoebiasis
IV - In Kala Azar ( For Indian Population - DOC is Liposomal Amphotericin B)
Neomycin
Oral - Gut sterilisation (In Hepatic Encephalopathy)
S/E of Aminoglycosides
Ototoxicity : First affects base of hair cells.
:
First high frequency are affected followed by low frequency.
K - Kanamycin
A - Amikacin
N - Neomycin
Vestibular Toxicity : Streptomycin, Gentamicin, Tobramycin
Nephrotoxicity
: Neuromuscular block
Previous Year Questions AIIMS & INICET 2020
MCQ Bullets
Aminoglycoside follows “concentration dependent killing pattern.”
: So, don’t split the dose.
G Also have post antibiotic effect, whereas β - Lactam shows time dependent killing pattern.
Quinolones
Mechanism of Action - Inhibits DNA Gyrase in Gram negative Bacteria.
Inhibits Topoisomerase in Gram positive Bacteria.
Excretion - Through Renal Route.
Pefloxacin, Moxifloxacin, Trovafloxacin excreted through bile.
Ciprofloxacin : First line drug for Typhoid fever.
S/E : Chance for Tendinitis, Tendon rupture.
Microsomal Enzyme Inhibitor - Increases drug level of concurrently
administered drug.
Previous Year Questions NEET PG 2020
Uses of Quinolones
Treatment of MDR - TB : Levofloxacin, Moxifloxacin.
: Treatment of Leprosy Infection : Ofloxacin, Ciprofloxacin.
C) Magnesium sulfate
D) All of the above
÷ Rifampicin
Pyrazinamide
Ethambutol
:
CNS side effects
Rifampicin
MOA : Inhibition of DNA dependent RNA polymerase.
Action : Bactericidal (Intracellular + Extracellular Action)
: Excretion through liver.
Mechanism of Resistance : Mutation of HPO B gene - β subunit of RNA polymerase.
: Unique side effects :Microsomal Enzyme Inducer - Other drug failure
Orange yellow urine.
Flu like symptoms with intermittent dosing.
:
C) Nitrofurantoin
D) Novobiocin
Pyrazinamide
MOA : Inhibition of Fatty Acid Synthase I - Inhibition of Cell membrane synthesis.
Action : Bactericidal (Intracellular)
: Excretion through liver.
Mechanism of Resistance : Mutation of Pn Ca gene.
: Unique side effects : Hepatotoxicity (Max)
Hyperuricemia
Ethambutol
MOA : Inhibition of Arabians transferase - Inhibition of cell wall synthesis.
: Action : Bactericidal (Extracellular)
Excretion through kidney.
: Mechanism of Resistance : Mutation of emb B gene.
~
Unique side effects : Optic neuritis, Hyperuricemia.
Second Line Anti TB Drugs
Thiacetazone - C/I in HIV : Can cause Steven Johnson’s Syndrome.
Paramino salicylic acid - Bacteriostatic
Ethionamide : S/E - Hepatitis, Hypothyroidism, Cross resistance to INH.
Cycloserine - Neuropsychosis
Aminoglycoside - Used in MDR cases. (Kanamycin, Amikacin, Capreomycin)
Fluoroquinolone - Ciprofloxacin, Moxifloxacin, Levofloxacin, Ofloxacin.
:
C) Acyclovir
D) Vancomycin
:
Psychosis - INH, Cycloserine
Uveitis - Rifabutin
Clofazamine
Bacteriostatic drug of Leprosy.
Anti Inflammatory action - So used for Lepra reaction also.
: Adverse Reaction : Dermatological - Reddish black discolouration.
Dapsone
Sulphonamide drug (S containing)
:S/E : Can cause allergy.
Also used as DOC for Dermatitis Herpetiformis.
New Form : Injection Acadapsone (IM) - 3 months dosage.
:
Previous Year Questions AIIMS 2018
Lepra Reaction
Type II Reaction
Type I Reaction (Erythema Nodosum Leprosum)
±
Mainly seen in Borderline spectrum. ±
Mainly seen in LL (50%) > BL.
(BT,BB,BL)
*
Type 4 Hypersensitivity - Inflammation *
Type 3 Hypersensitivity - New erythematous
of existing skin lesion. and tender lesions.
±
T/t : *
T/t :
Supportive therapy for Mild Reaction. Oral corticosteroid (1st line drug).
Severe Reaction - Oral Corticosteroids. Clofazimine (Steroid dependent ENL).
Thalidomide (Most effective but not used first).
Antifungal Drugs
Mechanism of Action
Fungal Cell
Griseofulvin
DNA & RNA
- synthesis
-
Microtubule
Flucytosine
Assembly
Squalene
Squalene
Cell Membrane Cell Wall
Epoxidase
-
Squalene Epoxide Terbinafine
Squalene
Amphotericin B
Epoxidase Nystatin
Lanosterol Ergosterol
- 14 α Demthylase
Azoles
Cyt P450 1,3, β-D - Glucan
Synthase
-
Echinocandin
Identify the wrongly matched pair of antifungals with its mechanism of action:
A) Ketoconazole : Lanosterol-14-demethylase inhibition
B) Flucytosine : Inhibits microtubule synthesis and thus hinders mitosis
✓
C) Terbinafine : Squalene epoxidase inhibition
D) Amphotericin B : Sequesters ergosterol
Previous Year Questions NEET PG 2018
Polyene Antibiotic
Eg : Amphotericin B
: MOA - Binds with Ergosterol to form multiple pores in fungal cell membrane.
Not absorbed through GIT - So given as IV infusion (Chance of Infusion reaction).
Poor distribution into CNS.
: Adverse Reaction
- Dose limited toxicity - Nephrotoxicity : Manifests as
hypokalemia, hypomagnesemia.
- Anaemia (Rare)
- CNS Toxicity (Rare) - Seizure, Neurological Change.
To reduce Nephrotoxicity
Maintain hydration.
÷ Targeted drug delivery
- Colloid Dispersion (Remember as ‘ABCD’)
- Lipid Complex (Remember as ‘ABLC’)
Azoles
e)
Ketoconazole
Acid medium required for absorption.
: Can also be used for Cushing’s syndrome.
Microsomal Enzyme Inhibitor - Increases effect of other concurrent drugs.
:
S/E - Hepatotoxic, Gynaecomastia, Adrenal Insufficiency.
Fluconazole : Treatment of Candidiasis, Cryptococcal Meningitis.
: Voriconazole : S/E - Hepatotoxic, Visual Problems, QT Prolongation.
Posaconazole : Alternate drug in the treatment of Mucormycosis in renal failure patients.
: Terbinafine : Squalene epoxidase inhibitor.
Use - Superficial + Systemic Fungal Infection.
Griseofulvin: Inhibit microtubule assembly of fungus.
:
Use - Only for superficial fungal infection.
Given orally.
Microsomal Enzyme Inducer - Reduces effect of concurrently administered drug.
Shows Disulfiram Reaction.
Echinocandins
Acts on cell wall by inhibiting 1,3 - β - D Glucan Synthase.
-
-
Used in Systemic Candidiasis + Aspergillosis.
-
Nikkomycin
-
Acts on cell wall by inhibiting Chitin synthesis.
-
÷
G/I Side effects Vision Loss
Eye - Bull’s Eye Maculopathy
Not used nowadays due to its S/E profiles.
CVS - Bradycardia, Hypotension
Liver damage
Safest antimalarial drug in pregnancy.
:
Halofantrine
Uses : To treat Falciparum Malaria in a combination with Artemisinin.
Lumefantrine : Absorption increases with food.
Halofantrine is the more cardiotoxic.
Primaquine
Vivax curative drug.
Kills dormant Hypnozoite phase also to prevent recurrence.
: C/I in pregnancy and G - 6 - PD deficiency (Haemolytic Anaemia).
: Cerebral/Falciparum Malaria
Not used in chemoprophylaxis.
Adverse Reaction : GI - Nausea, Vomitting, Diarrhoea
CVS - QT Prolongation, 1st degree heart block
Haematology - Reversible Leucopenia
Artemisinin, Artemether, Arteether - All are fast acting drugs.
: Artemisinin Combination Therapies
Artemether + Lumefantrine
: Artesunate + Amodiaquine
Artesunate + Sulphadoxine - Pyrimethamine
: Artesunate + Medloquine
Before Entry
①
Target
HIV CD 4 Cells
CCR -5
GP -120
: Eg : Enfuvirtide (S/C)
Adverse effects : Infection Site Reaction, Pneumonia (Rare)
GP - 120 Blocking Receptor : Fostemsavir
CCR - 5 Inhibitor : Maraviroc
: Aplaviroc
Vicriviroc
Entry Blocking MAB - Ibalizumab
After Entry Reverse Transcriptase Inhibitors
-
Reverse Transcriptase Inhibitor Nucleoside Reverse Transcriptase Inhibitors
-
✗
Integrase Inhibitor Non - Nucleoside Reverese Transcriptase Inhibitors
✗
Protease Inhibitor
: Maturation Inhibitor
Reverse Tanscriptase Inhibitors
Zidovudine - S/E : Myelosuppression - Macrocytic Anaemia
: Lipoatrophy
Nail Hyperpigmentation
Didanosine - S/E : Pancreatitis, Severe Diarrhea
Stavudine - S/E : Severe Neuropathy
Abacavir - S/E : Can cause Steven Johnson Syndrome in patients with HLA B 5701
allele.
Genetic screening test should be done before administering.
Severe hyper cholesterolemia : Can cause MI
Lamivudine : Best tolerated drug.
:
Do not cause any severe adverse reaction.
Can be used in HIV as well as HBV.
Prophylactic use in pre exposure prophylaxis.
Emtricitabine : Can be used in HIV as well as HBV.
Prophylactic use in pre exposure prophylaxis.
Tenofovir : Can be used in HIV as well as HBV.
:
Prophylactic use in pre exposure prophylaxis.
First line drug for HBV.
S/E - GI Toxicity, Fanconi Syndrome
Integrase Inhibitor
Raltegravir
: Elvitegravir
n
Dolutegravir
Protease Inhibitor ±
.
Saquinavir - Best tolerated Protease Inhibitor
Indinavir - S/E : Nephrolithiasis (Radioluscent Stones)
: Nelfinavir
Ritonavir - Most powerful Microsomal enzyme Inhibitor
: Amprenavir
Acts as a booster for other drugs
S/E : Circumoral Parasthesia
Fosamprenavir
: Atazanavir - Least chance of Lipodystrophy.
Lopinavir
: Common S/E of Protease Inhibitor : Hyperglycemia
Fat redistribution - T/t : Tesamorelin
(Synthetic form of GHRF)
Lipid abnormality
A patient with AIDS was treated with zidovudine, lamivudine, indinavir, ketoconazole and
cotrimoxazole. He developed nephrolithiasis, central obesity, hyperlipidemia and insulin
resistance. Which of the drugs could have been the cause?
A) Ketoconazole
B) Indinavir
:
C) Lamivudine
D) Zidovudine
Hypothalamus
Anterior Pituitary
Growth Hormone
Liver
Somatomedin
(Insulin Like Growth Factor)
Tissue
Octreotide
Forty times more potent than Somatostatin.
÷
It is longer acting - 12 hours.
Given as S/C or IV (in emergencies).
Not used orally.
Uses
Acromegaly
Carcinoid Diarrhoea
i. AIDS
Variceal Bleeding
S/E
Vit B12 deficiency
: Gallstone
Diabetes Mellitus
Treatment of Acromegaly
- Increase in GH
r
Drugs inhibiting release of Growth Hormone
(Somatostatin Analogue)
r
Octreotide
r
Lanreotide
S/C
r
Vapreotide
r
Seglitide
r
Ergot D2 analogues
r
Bromocriptine
Orally
Cabergoline
r
r
Growth Hormone Receptor Blocker
r
Pegvisomant - S/C
27-year-old female came for treatment of infertility to OPD. Bromocriptine was prescribed.
What could be the possible reason?
A) Hyperprolactinemia
v
B) PCOD
C) Hypogonadotrophic hypogonadism
D) PID
GH analogues
Somatrem
: Somatropin
Uses - Dwarfism
Less teratogenicity
Lugol’s Iodine
Inhinits release of T3, T4 from follicle.
: Fastest symptom relieving drug.
Use : For pre operative preparation before Thyroid surgery
:
Reduces vascularity
:
5’ Deiodinase Enzyme Inhibitors
Beta blockers
Amiodarone
: Propylthiouracil (Also Inhibits peripheral conversion of T4 to T3 - Dual MOA)
Dexamethasone
: Ipodate
Radioiodine Therapy
I 131
: T1/2 - 8 days
Emits 2 Rays - β Ray for Therapeutic Index.
: γ Ray for diagnostic purpose.
Damage the gland from inside to outside.
Total destruction - Permanent hyperthyroidism
:
(Not useful for Medullary Ca as it doesn’t accumulate in parafollicular cells)
Lenvatinib
Inhibits VGFR
A Tyrosine Kinase Inhibitor useful for well differentiated Thyroid Ca.
:
Vandetanib
Inhibits EGFR, VGFR
Useful for Medullary Ca thyroid.
Previous Year Questions AIIMS 2018
=
C) Ion channel receptor
D) G protein coupled receptor
Insulin Preparations
Glargine (pH - 4)
I
Detemir
Short Acting
All are neutral insulins except Glargine.
Onset : 30 mins
5
I
So can’t be mixed with any other insulin.
5
Duration 5 - 8 hours
I
Regular Insulin
Previous Year Questions AIIMS 2017
Longest Acting - Degludec
Composition of Lente insulin is:
A) 70% amorphous 30% crystalline
B) 70% crystalline 30% amorphous
✓
C) Only 70% amorphous
D) Other name of NPH insulin
New update in Insulin preparation (AIIMS Update)
Inhalational Insulin
: Exubera
Afrezza - Ultrarapid acting : Action within 15 minutes.
: S/E : Hypoglycemia, Weight Gain
Newer Antidiabetics
GLP - 1 Analogue
-
Promotes insulin release.
Glucagon like peptide.
: Exenatide - Origin : Salivary gland of Gil’s monster in sea.
-
÷ Albiglutide
Dulaglutide
Adverse Reaction : GIT - Nausea, Vomitting, Diarrhoea
- Necrotising Pancreatitis
DPP - 4 Inhibitors
Metabolism of GLP - 1 is by DPP - 4.
: Accumulation of GLP - 1 therefore increases.
Oral drug.
: Sitagliptine
Saxagliptin
Linagliptin
Vidagliptin
: Alogliptin
Excretion is by renal route.
Linagliptin is excreted through bile, so it is safe in renal failure.
: Adverse Reactions - Nasopharyngitis (URTI), Liver Damage, Pancreatitis.
Previous Year Questions AIIMS 2017
In a middle-aged diabetic patient with chronic kidney disease stage 5, which of the following
drugs can be given safely without altering the dose?
A) Vildagliptin
B) Linagliptin
✓
C) Saxagliptin
D) Sitagliptin
In a middle-aged diabetic patient with chronic kidney disease stage 5, which of the following
drugs can be given safely without altering the dose?
A) Vildagliptin
B) Linagliptin
✓
C) Saxagliptin
D) Sitagliptin
SGLT - 2 Blockers
Inhibition of Sodium Glucose Cotransporter at PCT of neuron (Responsible for 90% of
: Glucose Absorption).
Can cause Glycosuria (So caution in patients with Renal Failure).
: Canagliflozin
Sergliflozin
: Dapagliflozin
Empagliflozin
: Adverse Reaction - Urinary Tract Infection
- Risk of Bladder Ca and Breast Ca
Previous Year Questions NEET PG 2019
Meglitinide Analogues
'
MOA : Acts on pancreas to increase Insulin release.
To control post prandial glucose
: Eg : Repaglinide, Nateglinide
Biguanides
Mechanism of Action - AMP activated protein kinase activation : Insulin sensitisation.
: Drug is not acting on Pancreas, so no increase in Insulin release and no chances of hypoglycemia.
Reduces both micro and macro vascular complications.
: Eg : Metformin
Excretion through renal route.
: So C/I in renal failure patients.
Adverse Reaction
: GI Toxicity - Diarrhoea, Indigestion.
Inhibits Intestinal Absorption of Glucose, Hexose, Vit B12
: Deficiency of Vitamin B12 - Megaloblastic Anaemia
Increases chances of Lactic Acidosis.
:
Alpha Glucosidase Inhibitors
Inhibits polysaccharide to monosaccharide conversion by inhibiting Alpha Glucosidase enzyme.
Helps to reduce post prandial glucose.
: S/E
Flatulence, Abdominal distension, Diarrhoea,
: Unsafe in renal failure due to excretion by renal route.
Examples
: Acarbose
Voglibose
:
Miglitol
:
- Weight Gain
- Macular Oedema
- Osteoporosis
- Bladder Ca
PCSK 9 Inhibitors
MOA : Increase in LDL Receptors.
: Eg : Alirocumab, Evolocumab.
Nicotinic Acid (Vitamin B3)
MOA - Decrease in LDL and Increase in Lipoprotein and HDL.
: S/E
Cutaneous Flushing (Most Common) - Due to increase in Prostaglandins.
: Hyperuricemia
Diabetes due to Insulin resistance.
: Hepatotoxicity.
Ezetimibe
Inhibit cholesterol absorption from Intestine.
Bile Acid Sequestrants Mipomersen
I
Cholestyramine z
Given S/C.
s
Colestipol 2
Given Once in a week.
•
Colesevelam ,
MOA : Inhibits VLDL secretion from liver.
Newer Drugs
Cholesterol Ester Transport Protein Inhibitor (“cetrapib in suffix”)
÷
Dalcetrapib
Evacetrapib
Anacetrapib
Microsomal Triglyceride Transport Protein Inhibitor
Eg : Lomitapide
Avasimibe
Inhibits conversion of Cholesterol to Cholesterol Ester by
blocking LCAT - 1 (Lecithin Cholesterol Acyl Transferase)
Drugs in Orthopaedics
Bisphosphonates
DOC for osteoporosis
: - In post menopausal women, Hypercalcemia, Paget’s disease.
Zolindronate
IV infusion once in a year.
S/E : Infusion reaction, Nephrotoxicity, Osteonecrosis of Jaw (Rare)
Ibandronate
: Given once in a month.
Risedronate
Given once in a week.
Previous Year Questions NEET PG 2020
Bronchodilators
t
β2 Agonist
M3 Blocker
: Methyl Xanthines
Theophylline Non selective - Increases Cyclic AMP
Aminophylline PDE Inhibitors
Other actions of Methyl Xanthines
Increase strength of contraction of diaphragm.
: CNS Stimulation (Insomnia, Seizure)
Cardiac stimulation
: Diuresis
S/E
Nausea, Vomitting
: Headache, Gastritis PDE4 Blocking
Diuresis - A1 Receptor Antagonism
: Epileptic Seizures
PDE3 Inhibition/A1 Receptor Antagonism
Cardiac Arrythmias
:
Mast Cell Stabilisers
Sodium Chromoglycate
Ketotifen
: Nedocromil
Previous Year Questions NEET PG 2021
Leuokotriene Antagonists
Leukotriene Receptor Blockers
Arachidonic Acid
- Monteleukast
Zileuton 5 - lipoxygenase
Zafirleukast
LTA4 Used for prophylaxis.
BLT Receptor
LTD4
LTE4
÷Mepolizumab : IL - 5
Reslizumab
Dupilumab : IL - 4 (Also used in Atopic Dermatitis)
Inhalational Steroids
Beclomethasone
: Budesonide Antiinflammatory by inhibiting Phospholipase A2
i
Fluticasone Increase the responsiveness of β receptors.
Mometasone
: S/E
i
Hoarseness
Dysphonia
: Oral Thrush
i
For severe asthma DOC : Inhalational steroids + Long Acting Beta Agonist (LABA)
Previous Year Questions AIIMS & INICET 2020
Oseltamivir
^
Neuraminidase inhibitor.
^
Given for the treatment of Influenza A and B.
^
Competitively and reversibly interact with the enzyme sites to inhibit the activity of viral
neuraminidase.
^
This interferes with the release of the progeny from infected host cells, stopping the spread
of infection.
^
Therefore, early administration is needed.
^
Can be given for treatment and prophylaxis.
^
Other neuraminidase inhibitor - Zanamivir
Previous Year Questions AIIMS 2017
:
Drugs reducing acid formation and ulcer formation
H2 Antihistaminics
Cimetidine : Antiandrogenic action (So can cause Gynaecomastia)
Microsomal Enzyme Inhibitor
Famotidine - Most potent H2 blocker.
: Ranitidine
Roxatidine
: Nizatidine
Loratadine
: All given at bedtime to reduce nocturnal acid output and basal acid output.
Excretion through renal route, so contraindicated in renal failure patients.
: Lafutidine : Reduces acid secretion and promotes ulcer healing by NO release and
mucous production. (Ulcer healing property)
M1 blockers
MCQ BOOSTER
Pirenzepine
Sodium Bicarbonate/Calcium Bicarbonate + Milk : Telenzepine
Carbenoloxone
^
Drugs in IBS
Pain Relief Medications For Diarroea dominant cases
TCAs d
Opiods
: Imipramine Loperamide, Diphenoxylate
Desmipramine d
Kappa Agonists
: Nortriptylline Fedotozine
Citalopram
C d
µ Agonist and δ Antagonist
c
Anticholinergics Eluxadoline
Dicyclomine d
Reserpine Analogue
: Hyoscine
Mebeverine
d
5HT3 Antagonists
Alosetron
For Constipation Dominant Cases
Previous Year Questions AIIMS 2019
~
5 HT4 Agonists
Tegaserod
: Prucalopride Prucalopride is a
CCK 1 Antagonist A) 5HT2a agonist
: Loxiglumide
Chloride Channel Stimulant
B) 5HT2b agonist
C) 5HT4 antagonist
Lubiprostone D) 5HT4 agonist
✓
Guanylyl Cyclase Agonist
: Linaclotide
SSRI
Paroxetine
Miscellaneous Drugs
PDE inhibitors
PDE inhibitors Drugs Clinical Application
-
A - Aceclofenac
M - Meloxicam R - Retardation of Growth
: E - Etodolac
-
D - Diclofenac ÷ T - Thin Skin and easy bruisability
I - Infection and Immunosuppression
C - Cataract
Drugs Precipiating gout O - Oedema
7
C - Cyclosporine/Anti Ca Drugs
A - Aspirin
: S - Suppression of HPA Axis
T - Thinning and ulceration of Gastric Mucosa
: N - Niacin -
E - Emotional Disturbance
7
T - Thiazide R - Rise in BP
.
L - Lasix (Frusemide)
: O - Other fatal Abnormality like Hypokalemia
I - Increase in Hair Growth
7
E - Ethambutol -
D - Diabetes Mellitus precipitation
7
A - Alcohol -
S - Striae
7
P - Pyrizinamide
Drugs Precipitating Porphyria
B - Barbiturate
Drugs Causing Pulmonary Fibrosis : O - OCPs
n
A - Amiodarone n
O - Orphenadrine
n
A - Azathioprine n
S - Sulphonamide
n
B - Bleomycin ^
T - Tetracycline
n
B - Busulfan
C - Carmustine C - Chloramphenicol, Carbamazepine
÷
C - Chloramphenicol H - Haloperidol, Hydralazine
C - Cyclophosphamide A - Alcohol
D - Doxorubicin P - Phenytoin
M - Methysergide
: M - Methotrexate Drugs which need
Therapeutic Drug Monitoring
D - Digoxin
Previous Year Questions NEET PG 2018
: A - Antiarrhythmic
A - Antiepileptic
Which of the following inhibits the
T - Theophylline
synthesis of glucocorticoid?
A) Mifepristone : A - Aminoglycoside
L - Lithium
B) Flutamide
C) Finasteride
T - TCAs
D) Metyrapone
✓
: M - Methotrexate
C - Calcineurin Inhibitors
Teratogenic Drugs and Birth Defects
Drugs Adverse Effects
Pencillamine Cutis Laxa Syndrome
:
C) PGH2
D) PGI2
:
D) Methylcellulose