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Dr. Kiran G. Piparva,
Assistant professor, Pharmacology,
All India Institute of Medical Science (AIIMS), Rajkot.
Date: 12/02/21
Learning objectives….
• Classification of anticholinergic drugs
• Pharmacological actions
• Pharmacokinetics
• Side effects of Atropine
• Drug drug interaction
• Atropine substitutes
Cholinergic Receptors blockers
Muscarinic receptors (Nm) Nicotinic receptors
(Nn) (Nm)
Anticholinergic drugs: Drugs are which blocks the actions of Ach action of on
autonomic effectors and in the CNS exerted through muscarinic receptors.
Though nicotinic antagonists also block certain actions of ACh, they are generally
referred to as ‘ganglion blockers’ and ‘neuromuscular blockers’
ANTICHOLINERGIC DRUGS
Antimuscarinic agents (Nm) Antinicotinic agents (Nn)
Ganglionic blockers Neuromuscular blockers
(NN blockers) (NM blockers) Skeletal muscle relaxants
 Anticholinergic drugs- Antimuscarinic drugs
 Neuromuscular blockers- Skeletal muscle relaxants
Ganglionic blockers- NOT USED
Hyoscine niger
• Cimetropium
bromide
• Isopropamide
• Atropine- Racemic mixture
• Atropine- Competitive antagonist of Ach
• Atropine - Don’t differentiate between
M1, M2, M3, M4 subtypes
• Wide spread actions on multiple system
Atropine – Mechanism of Action
Atropine – Pharmacological action
CNS (M1): Atropine- less entry → stimulation of CNS -medullary centers
- High dose- excitation, disorientation, hallucination
Hyoscine - freely enters → depression of CNS
↓ of vestibular excitation- emesis –Antimotion sickness
CVS (M2): Tachycardia due to ↓ vagal tone
- Facilitation of AV conduction
- Blood Pressure – minor change
SMOOTH MUSCLES (M3 block)
GIT
 Relaxation- relieve
spasm
No effect on peristalsis-
Impact on local mediators
(5-HT, Enkephalin)
Constipation (S/E)
Biliary tract
Weak relaxation
Urinary
↓ tone of ureter
↓tone of fundus→
↓contraction (prostate)
Urinary retention (S/E)
 Bronchi
 Relaxation
Bronchodilation
 Drying of secretion
 Mucus plug
EYE
Eye
Active mydriasis:
• Contraction of dilator pupillae
(Radial muscle)
• Don’t affect accommodation
• Light reflex present
• ɑ1 adrenergic drugs
Passive mydriasis:
• Relaxation of Sphinctor pupillae
• Don’t affect accommodation
• Light reflex absent
• Antimuscarinic drugs
Exocrine glands: ↓ secretions
↓ Salivary ≥ Sweat ≥ Bronchial ˃˃ Lacrimal ≥ Gastric
• Dry skin/ eye- difficulty in talking and swallowing √
• Gastric secretion– only volume decreases- mild action & at higher dose
Body temperature: ↑ at higher dose : ↑ Thermostat + ↓ Sweating
Local anaesthetic action: Mild anesthetic action on cornea only
Sensitivity of different organ and tissues to atropine-
Saliva, Sweat, Bronchial secretion > Eye > Bronchial muscle, Heart>
Smooth muscle of intestine, bladder> gastric glands
Pharmacokinetics of Atropine
• Atropine- poor blood brain barrier
• Hyoscine- better blood brain barrier penetration
• Dose of Atropine available: 0.6-2mg I.M., I.V.
1-2 % topically eye drop
• Combination of atropine and analgesic and antipyretics are banned
in India .
Atropine side effects
Part 2: Atropine substitutes
Atropine substitutes……
• Why there is need of atropine substitute ?
- Nonspecific action
- Ocular side effects- mydriasis, Cycloplegia
- Difficulty in micturition: urinary retention
- Drying of skin & difficulty in swallowing
- Constipation
Quaternary ammonium atropine substitute
• Poor absorption from G.I. track
• Poor penetration into cornea
• Poor penetration into brain
• Slower elimination –longer acting
• Higher nicotinic blocking property
• At high dose- Nm blockage occurs
Part 2 Atropine substitutes….
Atropine substitutes:
1. Antispasmodic antisecretory
2. Respiratory
3. Vesicoselective
4. Ophthalmic
5. Antiparkinsonian
Atropine substitutes:
1. Antispasmodic antisecretory antimuscarinic:
2. Respiratory antimuscarinic: Ipratropium bromide, Tiotropium bromide
Tertiary Amine:
Dicyclomine,
Valethamate,
Pirenzepine
Quaternary compound (GOCCIP):
Glycopyrrolate, Oxyphenonium, Clinidium,
Cimetropium bromide, Isopropamide,
Propanthaline (GOCCIP)
3. Vesicoselective antimuscarinic:
Oxybutynin, Flavoxate, Tolterodine, Deriphenacin, Solifenacin
4. Ophthalmic antimuscarinic:
Homatropine, Tropicamide, Cyclopentolate
5. Antiparkinsonian antimuscarinic:
Trihexyphenidyl, Benztropine, Benzhexol.
• Hyoscine butylbromide: Esophageal and gastrointestinal spastic conditions:
PREP: 10 mg tab, 20 mg/ml inj.
• Atropine methonitrate: Abdominal colic and hyperacidity
• Propantheline: peptic ulcer and gastritis
• Use has declined due to availability of H2 blockers which are more efficacious.
• Oxyphenonium: Similar to propantheline, recommended in peptic ulcer and gastric
hypermotility
1. Antispasmodic Antisecretory (Quaternary amine)drugs
Gastric spastic
condition
Hyperacidity
• Clinidium/ Isopropamide: Hyperacidity, Nervous dyspepsia, irritable
bowel syndrome (IBS) and other G.I. disturbances especially associated
with mental and emotional disorder.
• Cimetropium bromide: especially for IBS –dryness of mouth is
commonest side effect
• Glycopyrrolate: Exclusively used for preanaesthetic medication
during anesthesia
1. Antispasmodic (Tertiary amine)drugs
• Dicyclomine: Anticholinergic, antispasmodic, antiemetic with few atropinic side
effects. Used in Abdominal colic, dysmenorrhea and irritable bowel, morning
sickness and motion sickness.
 Not recommended below 6 months of age.
• Valethamate: visceral anti-spasmodic: (urinary, biliary and intestinal colic)+
Hasten dilatation of cervix when the same is delayed during labor.
• Pirenzepine: peptic ulcer: use is declined due to availability of H2 blocker
2. Respiratory antimuscarinic drugs……..
1. Ipratropium bromide
2. Tiotropium bromide
Ipratropium bromide
• Advantages of ipratropium bromide over atropine
- It has selective action on bronchial smooth muscle >secretion
- Don’t depress mucociliary clearance
• Advantages over sympathomimetic (bronchodilator)
- Gradual onset and late peak-good for regular prophylactic use
- Acts on receptors on larger bronchioles.
• COPD: higher parasympathetic tone so ipratropium bromide is more
effective in COPD than in bronchial asthma.
• ADR: less- dryness of mouth, scratching sensation in trachea, bad taste
and nervousness
• 250ug/ml, 2 puffs , 3-4 times daily.
Tiotropium bromide
• Tightly binding to
M1/M3- Longer acting
• High bronchial selectivity
• Less ADR- Not absorbed
from respiratory and G.I.
mucosa
3. Vesicoselective anticholinergic(M3/ M1 selective)
• Oxybutynin
• Tolterodine
• Flavoxate
• Darifenacin
• Solifenacin
Therapeutic use
• Detrusor instability- urinary frequency and
urge incontinence
• Post prostatectomy vasical spasm
• Neurogenic bladder
• Nocturnal enuresis
• Spina bifida
• Oxybutynin/ Flavoxate:
• M3/M1 selectivity
• Oral: anticholinergic side effect
Intravesical instillation: few side effect
• Tolterodine
• Selective M3 - less ADR (M1 –dryness of
mouth - other anticholinergic action)
Metabolized by CYP3A4
Dose reduction with CYP34 inhibitors
CYP3A4 inhibitors:
Clarithromycin, erythromycin,
diltiazem, itraconazole,
ketoconazole, ritonavir, grapefruit
• Derifenacin/ Solifenacin: M3 selective, long t1/2 - 24hrs by SR preparation
Drotaverine:
• Non anticholinergic antispasmodic
• M/A:
PDE-4 (phosphodiesterase-4 inhibitors) inhibitors- increases cAMP/cGMP
• Use:
Intestinal/biliary and renal colic, IBS
• ADR:
- No anticholinergic side effect
- Headache, dizziness, constipation, flushing
- fall in BP (I.V.)
4. Mydriatics
• Limitation of Atropine :
Potent and long lasting mydriatic and cycloplegic – subject is visually
handicap.
• Short acting agents:
Homatropine
Cyclopentolate
Tropicamides
Mydriasis Cycloplegia Remarks/ADR
Atropine
30-40 minutes 1 week
Visually handicap for 1 week
Undesirable for refraction
testing
Homatropine (10times
less potent)
45- 60 minutes 1-3days Accommodation recovers in
2 days
Cyclopentolate 30-60 minutes 1 day
Potent and rapidly acting
Transient behavioural
abnormalities in children
Tropicamide
20-40minutes
3-6hrs,
unreliable
cycloplegia
Best for refraction error
testing and short acting
mydriatic for fundoscopy
Therapeutic uses of Atropine/ atropine substitute
• Antisecretory
• Antispasmodic
• Bronchial asthma
• Mydriatic and cycloplegic
• Cardiac vagolytic
• Central action
• To antagonize muscarinic effects if drugs and poisons
1. Antisecretory
1. Preanesthetic medication:
- Irritant GA - check increased salivary and tracheobronchial
secretion
- Along with halothane –vagal slowing- NA mediated ventricular
arrhythmias
- prevent reflex laryngospasm
- Prevent vasovagal attack
2. Pulmonary embolism
- reduces pulmonary secretions
3. Antiparkinson: to check excessive sweating or salivation
4. Peptic ulcer: NOT USED
2. antispasmodic
Intestinal colic –abdominal cramps
Spastic constipation, IBS, Pyolorspasm, Nervous dyspepsia
Renal colic – Opioid/NSAID better
To relieve urinary urgency/frequency – increases bladder capacity
Dysmenorrhoea – Not effective
3. Bronchial asthma, COPD
• COPD: reflex vagal activity Bronchoconstriction Bronchodilation Anticholinergic
increased secretion
• Oral route: ADR- drying up of secretion, mucus plug- alveolar collapse
• Inhalation route: NO ADR
• Slow onset- long duration- suitable for regular prophylactic use
• Acute exacerbation of asthma/COPD: in combination with sympathomimetic through
nebulizer
• Ipratropium bromide - OD
• Regular intake reduces episodes of COPD exacerbation
4. Ophthalmic use: Mydriatic & Cycloplegic
4. Ophthalmic use: Mydriatic & Cycloplegic
• Diagnostic:
• Refraction error testing: both
mydriasis & cycloplegia both required
• Best- tropicamide –faster and stronger
action
• For children- atropine/cyclopentolate
• For fundoscopy: only mydriasis is
required
• sympathomimetic preferred
• Therapeutic:
• Irits/ iridocyclitis/ chorioiditis/
keratitis / corneal ulcer
• Atropine
• Long lasting mydriatic-cycloplegic
• Local anodyne action on cornea
• Rest to intraocular muscles- cut down
painful spasm
• Along with miotics- break adhesion
between iris and lens
5. Cardiac vagolytic
• Increased vagal tone (myocardial infraction / digitalis toxicity) - sinus
bradycardia, partial heart block
• Only in selected cases.
6. Central action
• Parkinsonism:
• Central anticholinergic used in “ Drug induced
parkinsonism”
• Motion sickness:
• Most effective – hyoscine, Dicyclomine(2nd option)
• Start before journey
• Prophylactic use: 0.2mg oral –action last 4-6hrs
• TDS: applied behind pina 4hrs before journey-
protect 3 days
7. To antagonize muscarinic effects of drugs and poisons…
• In mashroom poisoning
• To reverse muscarinic action neostigmine for mysethenia gravis,
decurarization, cobra envenomation.
Belladonna poisoning
• Overdose /overconsumption of seeds / barriers of belladonna/
dhatura plant
• Children
• Symptoms: exaggerated pharmacological
action of atropine- 7Ds
• Diagnosis: Methacholine/neostigmine-
fail to produce muscarinic action
• Rx: Symptomatic Mx only
• Gastric lavage
• Patient should be kept in dark quite room
• Cold sponging
• ABC management – no ChE effective- more ADR
•Rapid fire….
• Atropine produces active mydriasis or passive mydriasis?
• Atropine induced cycloplegia last for????
• Best substitute for Irritable bowel syndrome???
• Best substitute for preanesthetic medication??
• Best short acting mydriatic?
• Mydriatic of choice in pediatric?
• Non anticholinergic smooth musce relaxant?
• Y anticholinergic is better for COPD than BA?
• Drug of choice for motion sickness?
Anticholinergic part 1, Dr. Kiran Piparva, AIIMS,Rajkot

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Anticholinergic part 1, Dr. Kiran Piparva, AIIMS,Rajkot

  • 1. Dr. Kiran G. Piparva, Assistant professor, Pharmacology, All India Institute of Medical Science (AIIMS), Rajkot. Date: 12/02/21
  • 2. Learning objectives…. • Classification of anticholinergic drugs • Pharmacological actions • Pharmacokinetics • Side effects of Atropine • Drug drug interaction • Atropine substitutes
  • 3. Cholinergic Receptors blockers Muscarinic receptors (Nm) Nicotinic receptors (Nn) (Nm) Anticholinergic drugs: Drugs are which blocks the actions of Ach action of on autonomic effectors and in the CNS exerted through muscarinic receptors. Though nicotinic antagonists also block certain actions of ACh, they are generally referred to as ‘ganglion blockers’ and ‘neuromuscular blockers’
  • 4. ANTICHOLINERGIC DRUGS Antimuscarinic agents (Nm) Antinicotinic agents (Nn) Ganglionic blockers Neuromuscular blockers (NN blockers) (NM blockers) Skeletal muscle relaxants  Anticholinergic drugs- Antimuscarinic drugs  Neuromuscular blockers- Skeletal muscle relaxants Ganglionic blockers- NOT USED
  • 6.
  • 8. • Atropine- Racemic mixture • Atropine- Competitive antagonist of Ach • Atropine - Don’t differentiate between M1, M2, M3, M4 subtypes • Wide spread actions on multiple system Atropine – Mechanism of Action
  • 9.
  • 10. Atropine – Pharmacological action CNS (M1): Atropine- less entry → stimulation of CNS -medullary centers - High dose- excitation, disorientation, hallucination Hyoscine - freely enters → depression of CNS ↓ of vestibular excitation- emesis –Antimotion sickness CVS (M2): Tachycardia due to ↓ vagal tone - Facilitation of AV conduction - Blood Pressure – minor change
  • 11. SMOOTH MUSCLES (M3 block) GIT  Relaxation- relieve spasm No effect on peristalsis- Impact on local mediators (5-HT, Enkephalin) Constipation (S/E) Biliary tract Weak relaxation Urinary ↓ tone of ureter ↓tone of fundus→ ↓contraction (prostate) Urinary retention (S/E)  Bronchi  Relaxation Bronchodilation  Drying of secretion  Mucus plug
  • 12. EYE
  • 13.
  • 14. Eye
  • 15. Active mydriasis: • Contraction of dilator pupillae (Radial muscle) • Don’t affect accommodation • Light reflex present • ɑ1 adrenergic drugs Passive mydriasis: • Relaxation of Sphinctor pupillae • Don’t affect accommodation • Light reflex absent • Antimuscarinic drugs
  • 16.
  • 17. Exocrine glands: ↓ secretions ↓ Salivary ≥ Sweat ≥ Bronchial ˃˃ Lacrimal ≥ Gastric • Dry skin/ eye- difficulty in talking and swallowing √ • Gastric secretion– only volume decreases- mild action & at higher dose
  • 18. Body temperature: ↑ at higher dose : ↑ Thermostat + ↓ Sweating Local anaesthetic action: Mild anesthetic action on cornea only Sensitivity of different organ and tissues to atropine- Saliva, Sweat, Bronchial secretion > Eye > Bronchial muscle, Heart> Smooth muscle of intestine, bladder> gastric glands
  • 19. Pharmacokinetics of Atropine • Atropine- poor blood brain barrier • Hyoscine- better blood brain barrier penetration • Dose of Atropine available: 0.6-2mg I.M., I.V. 1-2 % topically eye drop • Combination of atropine and analgesic and antipyretics are banned in India .
  • 20.
  • 22.
  • 23.
  • 24. Part 2: Atropine substitutes
  • 25. Atropine substitutes…… • Why there is need of atropine substitute ? - Nonspecific action - Ocular side effects- mydriasis, Cycloplegia - Difficulty in micturition: urinary retention - Drying of skin & difficulty in swallowing - Constipation
  • 26. Quaternary ammonium atropine substitute • Poor absorption from G.I. track • Poor penetration into cornea • Poor penetration into brain • Slower elimination –longer acting • Higher nicotinic blocking property • At high dose- Nm blockage occurs
  • 27. Part 2 Atropine substitutes….
  • 28. Atropine substitutes: 1. Antispasmodic antisecretory 2. Respiratory 3. Vesicoselective 4. Ophthalmic 5. Antiparkinsonian
  • 29. Atropine substitutes: 1. Antispasmodic antisecretory antimuscarinic: 2. Respiratory antimuscarinic: Ipratropium bromide, Tiotropium bromide Tertiary Amine: Dicyclomine, Valethamate, Pirenzepine Quaternary compound (GOCCIP): Glycopyrrolate, Oxyphenonium, Clinidium, Cimetropium bromide, Isopropamide, Propanthaline (GOCCIP)
  • 30. 3. Vesicoselective antimuscarinic: Oxybutynin, Flavoxate, Tolterodine, Deriphenacin, Solifenacin 4. Ophthalmic antimuscarinic: Homatropine, Tropicamide, Cyclopentolate 5. Antiparkinsonian antimuscarinic: Trihexyphenidyl, Benztropine, Benzhexol.
  • 31. • Hyoscine butylbromide: Esophageal and gastrointestinal spastic conditions: PREP: 10 mg tab, 20 mg/ml inj. • Atropine methonitrate: Abdominal colic and hyperacidity • Propantheline: peptic ulcer and gastritis • Use has declined due to availability of H2 blockers which are more efficacious. • Oxyphenonium: Similar to propantheline, recommended in peptic ulcer and gastric hypermotility 1. Antispasmodic Antisecretory (Quaternary amine)drugs Gastric spastic condition Hyperacidity
  • 32. • Clinidium/ Isopropamide: Hyperacidity, Nervous dyspepsia, irritable bowel syndrome (IBS) and other G.I. disturbances especially associated with mental and emotional disorder. • Cimetropium bromide: especially for IBS –dryness of mouth is commonest side effect • Glycopyrrolate: Exclusively used for preanaesthetic medication during anesthesia
  • 33. 1. Antispasmodic (Tertiary amine)drugs • Dicyclomine: Anticholinergic, antispasmodic, antiemetic with few atropinic side effects. Used in Abdominal colic, dysmenorrhea and irritable bowel, morning sickness and motion sickness.  Not recommended below 6 months of age. • Valethamate: visceral anti-spasmodic: (urinary, biliary and intestinal colic)+ Hasten dilatation of cervix when the same is delayed during labor. • Pirenzepine: peptic ulcer: use is declined due to availability of H2 blocker
  • 34. 2. Respiratory antimuscarinic drugs…….. 1. Ipratropium bromide 2. Tiotropium bromide
  • 35. Ipratropium bromide • Advantages of ipratropium bromide over atropine - It has selective action on bronchial smooth muscle >secretion - Don’t depress mucociliary clearance • Advantages over sympathomimetic (bronchodilator) - Gradual onset and late peak-good for regular prophylactic use - Acts on receptors on larger bronchioles. • COPD: higher parasympathetic tone so ipratropium bromide is more effective in COPD than in bronchial asthma. • ADR: less- dryness of mouth, scratching sensation in trachea, bad taste and nervousness • 250ug/ml, 2 puffs , 3-4 times daily.
  • 36. Tiotropium bromide • Tightly binding to M1/M3- Longer acting • High bronchial selectivity • Less ADR- Not absorbed from respiratory and G.I. mucosa
  • 37. 3. Vesicoselective anticholinergic(M3/ M1 selective) • Oxybutynin • Tolterodine • Flavoxate • Darifenacin • Solifenacin Therapeutic use • Detrusor instability- urinary frequency and urge incontinence • Post prostatectomy vasical spasm • Neurogenic bladder • Nocturnal enuresis • Spina bifida
  • 38. • Oxybutynin/ Flavoxate: • M3/M1 selectivity • Oral: anticholinergic side effect Intravesical instillation: few side effect • Tolterodine • Selective M3 - less ADR (M1 –dryness of mouth - other anticholinergic action) Metabolized by CYP3A4 Dose reduction with CYP34 inhibitors CYP3A4 inhibitors: Clarithromycin, erythromycin, diltiazem, itraconazole, ketoconazole, ritonavir, grapefruit • Derifenacin/ Solifenacin: M3 selective, long t1/2 - 24hrs by SR preparation
  • 39. Drotaverine: • Non anticholinergic antispasmodic • M/A: PDE-4 (phosphodiesterase-4 inhibitors) inhibitors- increases cAMP/cGMP • Use: Intestinal/biliary and renal colic, IBS • ADR: - No anticholinergic side effect - Headache, dizziness, constipation, flushing - fall in BP (I.V.)
  • 40. 4. Mydriatics • Limitation of Atropine : Potent and long lasting mydriatic and cycloplegic – subject is visually handicap. • Short acting agents: Homatropine Cyclopentolate Tropicamides
  • 41. Mydriasis Cycloplegia Remarks/ADR Atropine 30-40 minutes 1 week Visually handicap for 1 week Undesirable for refraction testing Homatropine (10times less potent) 45- 60 minutes 1-3days Accommodation recovers in 2 days Cyclopentolate 30-60 minutes 1 day Potent and rapidly acting Transient behavioural abnormalities in children Tropicamide 20-40minutes 3-6hrs, unreliable cycloplegia Best for refraction error testing and short acting mydriatic for fundoscopy
  • 42. Therapeutic uses of Atropine/ atropine substitute • Antisecretory • Antispasmodic • Bronchial asthma • Mydriatic and cycloplegic • Cardiac vagolytic • Central action • To antagonize muscarinic effects if drugs and poisons
  • 43. 1. Antisecretory 1. Preanesthetic medication: - Irritant GA - check increased salivary and tracheobronchial secretion - Along with halothane –vagal slowing- NA mediated ventricular arrhythmias - prevent reflex laryngospasm - Prevent vasovagal attack 2. Pulmonary embolism - reduces pulmonary secretions 3. Antiparkinson: to check excessive sweating or salivation 4. Peptic ulcer: NOT USED
  • 44. 2. antispasmodic Intestinal colic –abdominal cramps Spastic constipation, IBS, Pyolorspasm, Nervous dyspepsia Renal colic – Opioid/NSAID better To relieve urinary urgency/frequency – increases bladder capacity Dysmenorrhoea – Not effective
  • 45. 3. Bronchial asthma, COPD • COPD: reflex vagal activity Bronchoconstriction Bronchodilation Anticholinergic increased secretion • Oral route: ADR- drying up of secretion, mucus plug- alveolar collapse • Inhalation route: NO ADR • Slow onset- long duration- suitable for regular prophylactic use • Acute exacerbation of asthma/COPD: in combination with sympathomimetic through nebulizer • Ipratropium bromide - OD • Regular intake reduces episodes of COPD exacerbation
  • 46. 4. Ophthalmic use: Mydriatic & Cycloplegic
  • 47. 4. Ophthalmic use: Mydriatic & Cycloplegic • Diagnostic: • Refraction error testing: both mydriasis & cycloplegia both required • Best- tropicamide –faster and stronger action • For children- atropine/cyclopentolate • For fundoscopy: only mydriasis is required • sympathomimetic preferred • Therapeutic: • Irits/ iridocyclitis/ chorioiditis/ keratitis / corneal ulcer • Atropine • Long lasting mydriatic-cycloplegic • Local anodyne action on cornea • Rest to intraocular muscles- cut down painful spasm • Along with miotics- break adhesion between iris and lens
  • 48. 5. Cardiac vagolytic • Increased vagal tone (myocardial infraction / digitalis toxicity) - sinus bradycardia, partial heart block • Only in selected cases.
  • 49. 6. Central action • Parkinsonism: • Central anticholinergic used in “ Drug induced parkinsonism” • Motion sickness: • Most effective – hyoscine, Dicyclomine(2nd option) • Start before journey • Prophylactic use: 0.2mg oral –action last 4-6hrs • TDS: applied behind pina 4hrs before journey- protect 3 days
  • 50. 7. To antagonize muscarinic effects of drugs and poisons… • In mashroom poisoning • To reverse muscarinic action neostigmine for mysethenia gravis, decurarization, cobra envenomation.
  • 51. Belladonna poisoning • Overdose /overconsumption of seeds / barriers of belladonna/ dhatura plant • Children • Symptoms: exaggerated pharmacological action of atropine- 7Ds • Diagnosis: Methacholine/neostigmine- fail to produce muscarinic action • Rx: Symptomatic Mx only • Gastric lavage • Patient should be kept in dark quite room • Cold sponging • ABC management – no ChE effective- more ADR
  • 52. •Rapid fire…. • Atropine produces active mydriasis or passive mydriasis? • Atropine induced cycloplegia last for???? • Best substitute for Irritable bowel syndrome??? • Best substitute for preanesthetic medication?? • Best short acting mydriatic? • Mydriatic of choice in pediatric? • Non anticholinergic smooth musce relaxant? • Y anticholinergic is better for COPD than BA? • Drug of choice for motion sickness?