-
Ondansetron Classification
Antiemetic
-
Ondansetron Indications
N/V with chemotherapy, gastroenteritis, head injury or refractory to other Tx.
-
Ondansetron Mechanisms of Action
Blocks serotonin (5-HT3) receptors in CTZ, GI tract and VC (vomiting centre = medulla)
-
Ondansetron Adverse Effects
QT prolongation
-
Ondansetron Contraindications
Hypersensitivity
-
Ondansetron Dosage
Adult:
Peds:
8mg IM or in 50ml over 15min
- Peds: <4y/o 2mg PO
- >y/o 4mg PO
or 0.1mg/kg IV max 4mg in 50ml over 15min
-
Ondansetron Onset/Peak/Duration
- Onset: 15-30min
- Peak: 1-1.5hr
- Duration: 6-12hrs
-
Oxytocin Classification
Hormone
-
Oxytocin Indications
- 1. Delivery
- 2. Post partum hemorrhage
-
Oxytocin Mechanisms of Action
- 1. Stimulates contraction of uterine smooth muscle.
- 2. Has vasopressor/antiduiretic effects
-
Oxytocin Side Effects
- 1. Fluid retension ↠ hyponatremia and hypochloremia
- 2. Hypotension
- 3. Uterine rupture
-
Oxytocin Contraindications
- 1. Hypersensitivity
- 2. Uterine inversion
- 3. Placenta previa
- 4. Placenta abruptio
- 5. If subsequent fetus not yet delivered
-
Oxytocin Dosing
- Delivery: 10u IM
- Hemorrhage: 6u/hr = 40u in 1000ml = 150ml/hr
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Pancuronium (Pavulon) Classification
Long acting nondeplolarizing neuromuscular blocking agent.
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Pancuronium (Pavulon) Indications
-
Pancuronium (Pavulon) Mechanisms of Action
- 1. Blocks ACh from binding to postsynaptic receptors by competitively binding to without stimulating depolarization.
- 2. Selectively blocks Vagus nerve resulting in tachycardia, arrhythmias and HTN
-
Pancuronium (Pavulon) Side Effects
- 1. Bronchospasm
- 2. Tachycardia
- 3. HTN
- (4. ↑ ICP - preferable to use vecuronium in theres pts.)
-
Pancuronium (Pavulon) Contraindications
Hypersensitivity to bomides
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Pancuronium (Pavulon) Onset/Peak/Duration
- Onset: 30-45sec
- Peak: 3-5min
- Duration: 30-60min
-
Pancuronium (Pavulon) Dosing
- 0.04-0.1mg/kg
- infusion of 0.1mg/kg/hr
Peds is the same
-
Pentastarch (Pentaspan) Classification
Plasma Volume Expander
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Pentastarch (Pentaspan) Indication
Shock, volume depletion. Situations where volume expansion is needed.
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Pentastarch (Pentaspan) Mechanisms of Action
Hypertonic solution that increases osmotic force and pulls fluid into vascular space from interstital space for 18-24hrs.
-
Pentastarch (Pentaspan) Side Effects
- 1. Coagulation disorders
- 2. H/A
- 3. Edema
- 4. CP
- 5. Fever
-
Pentastarch (Pentaspan) Contraindications
- 1. Hypersensitivity to hydroxyethyl
- 2. Bleeding disorders
- 3. CHF
- 4. Renal failure with anuria/oliguria
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Pentastarch (Pentaspan) Dosage
500-2000ml bolus
No ped dose
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Phenobarbital (Luminal) Classification
- Long acting Barbiturate
- Anticonvulsant
- Hypnotic
- Sedative
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Phenobarbital (Luminal) Indications
- 1. Tx of status epilepticus refractory to standard Tx - 2nd line agent.
- 2. Febrile seizure
-
Phenobarbital (Luminal) Mechanisms of Action
- 1. Prosuces all levels of CNS depression - sensory cortex, motor activity and alters cerebellar function.
- 2. Increases seizure threshold by mimicking GABA effects.
- 3. Speeds up liver enzymes that metabolize drugs and bilirubin.
-
Phenobarbital (Luminal) Side Effects
- 1. Sedation
- 2. Resp Depression
- 3. Hypotension
- 4. Bronchospasm
- 5. N/V
- (6. Neuralgia, myalgia)
-
Phenobarbital (Luminal) Contraindications
- 1. Hypersensitivity
- 2. COPD/Asthma/resp difficulties
- 3. Uncontrolled severe pain
- 4. Severe liver disease
-
Phenobarbital (Luminal) Dosage
- Adult: 20mg/kg SIVP
- Maintenance 1-3mg/kg/day
- Peds: 20mg/kg SIVP
- Maintenance of 6mg/kg/day
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Phentolamine (Rogitine) Classification
Alpha adrenergic blocker
-
Phentolamine (Rogitine) Indications
- 1. HTN Crisis due to primarily pheochromocytoma
- 2. Prevention of dermal necrosis/sloughing following extravasation of catecholamine administration (epi/norepi/dope/dobut)
-
Phentolamine (Rogitine) Side Effects
- 1. Cerebrovascular spasm
- 2. Hypotension
- 3. Tachycardia
- 4. Angina/MI
- 5. Arrhythmias
- 6. N/V/D
- 7. Abd pain
-
Phentolamine (Rogitine) Contraindications
- 1. Hypersensitivity
- 2. PVD
- 3. CAD
- 4. cerebral atherosclerosis
-
Phentolamine (Rogitine) dosing
5-10mg IV
-
Phentolamine (Rogitine) Onset/Peak/Duration
- Onset: immediate
- Peak: 2min
- Duration: 15-30min
-
Phenylephrine (Neo-Synephrine) Classification
Sympathetic agonist
-
Phenylephrine (Neo-Synephrine) Indications
BP <70mmHg due to decreased peripheral vascular resistance (distributive shock), not a first line agent
-
Phenylephrine (Neo-Synephrine) Mechanisms of action
Acts almost exclusively of alpha receptors increasing vascular resistance and BP
-
Phenylephrine (Neo-Synephrine) Onset/Peak/Duration
- Onset: immediate
- Peak: <1min
- Duartion: 15-20min
-
Phenylephrine (Neo-Synephrine) Contraindications
1. Cardiogenic shock
-
Phenylephrine (Neo-Synephrine) Side Effects
- 1. Angina
- 2. HTN
- 3. Nervousness/H/A
- 4. blurred vision
- 5. lacrimation
- 6. urinary retention
- 7. arrhythmias
- 8. N/V
-
Phenylephrine (Neo-Synephrine) Dosage
- 100-180mcg/min
- Maintenance of 46-60mcg/min
-
Phenytoin Classifications
- 1. Anticonvulsant
- 2. Class 1B Antiarrythmic
-
Phenytoin Indications
- 1. Status epilepticus refractory of other Tx (benzos etc)
- 2. Neuropathic pain
- 3. Ventricular arrhythmias due to digitalis toxicity
-
Phenytoin Mechanisms of Action
- 1. Blocks Na and Ca channels in neurons, stabilizing cell membranes. This increases threshold activity in brain, prevents spread of seizure activity and decreases speed of conduction through a neuron.
- 2. Highly bound to plasma protein so a low serum concentration of albumin (malnourishment or chronic renal failure) there is an increased in free, unbound active phenytoin in blood.
- 3. Antiarrhythmic: normalizes Na and Ca influx in Purkinje fibers and accelerates repolarization period.
-
Phenytoin Side Effects
- 1. Hypotension
- 2. Arrhythmias
- 3. Ataxia
- 4. Nystagmus
- 5. Slurred speech
- 6. Encephalophathy
Green = OD (narrow therapeutic index)
-
Phenytoin Contraindication
- 1. Hypersensitivity to hydrantoins, propylene glycol, and ethanol
- 2. Bradycardia/Severe Heart blocks
- 3. TCA ingestion - promotes further seizures.
- 4. Chronic admin
-
Phenytoin Dosing
Adult:
Peds
Adult: 15-20mg/kg IV no faster than 50mg/min
Peds: 15-20mg/kg no faster than 1mg/kg/min or 50mg/min.
-
Phenytoin Onset/Duration/ Half Life
- Onset 5-30min
- Duration: 12-24hrs
- Half Life: 10-60hrs
-
Potassium Chloride (Slow-K, K-Dur) Classification
Electroly
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Potassium Chloride Indication
Hypokalemia
-
Potassium Chloride Mechanisms of Action
- Potassium is needed for:
- - Metabolic enzymatic reactions
- - conduction of nerve impulses
- - renal function
- - acid-base balance
- - tissue synthesis
- - carbohydrate metabolism
-
Potassium Chloride Side Effects
- 1. Arrhythmias/cardiac arrest
- 2. Confusion
- 3. Restlessness
- 4. N/V/D
- 5. Abd pain
-
Potassium Chloride Contraindications
- 1. Severe renal impairment
- 2. Hyperkalemia
-
Potassium Chloride Dosage
Adult:
Peds:
Adult: 20-40mEq/day depending on severity, not to exceed 10-20mEq/hr.
Peds: 0.5-1mEq/kg, max 30mEq
-
Prednisone Classification
corticosteriod
-
Prednisone Indications
- 1. Bronchospasm
- 2. Immunosuppressant purposes
-
Prednisone Mechanisms of action
- 1. Prevents accumulation of inflammatory cells, including macrophages and leukocytes.
- 2. Inhibits lysosomal enzyme release and synthesis of chemical mediators of inflammation.
-
Prednisone Side Effects
- 1. Increased intraocular pressure
- 2. HF, cardiac edema
- 3. HF
- 4. HTN
- 5. tooo many to list
-
Prednisone Contraindications
- 1. Pts already taking prednisone
- 2. Hypersensitivity
- 3. Systemic infections
-
Prednisone Dosage
50mg PO
-
Procainamide (Procan) Classification
Class 1A antiarrhythmic
-
Procainamide (Procan) Indications
- 1. VT
- 2. WPW
- 3. SVTs/A-fib
- 4. Suppression of PVCs
-
Procainamide (Procan) Mechanisms of Action
- 1. Stabilizes cell membranes by blocking Na channels depressing myocardial excitability
- 2. Increases action potential duration
- 3. Prolongs effective refractory period time by decreasing repolarization
- 4. Decreases or eliminates ectopic foci stimulation
- 5. Anticholinergic activity
- 6. Negative inotropic effect
-
Procainamide (Procan) Side effects
- 1. ++ CNS effects including seizures, confusion
- 2. ++ Arrhythmias - ventricular, QT prolongation
- 3. Blood disorders
- 4. N/V/D
- 5. Fever
- 6.... Lots more
-
Procainamide (Procan) Contraindications
- 1. Hypersensitivity
- 2. 2nd and 3rd degree blocks
- 3. Torsades
-
Procainamide (Procan) Dosing
- 20-50mg/min until :
- 1. Arrhythmia suppressed
- 2. Hypotension
- 3. QRS widens by 50%
- 4. Max of 17mg/kg
Maintenance of 1-4mg/min
-
Prochlorperazine (Stemetil) Classifications
- 1. Antiemetic
- 2. Antipsychotic
-
Prochlorperazine (Stemetil) Indications
-
Prochlorperazine (Stemetil) Mechanisms of Action
- 1. Blocks Dopamine D2 receptors in CTZ.
- 2. Blocks Vagus nerve in GI tract
- 3. Alpha blocking activity
-
Prochlorperazine (Stemetil) Side Effects
- 1. EPS
- 2. Anticholinergic effects
- 3. Neuroleptic malignant syndrome
- 4. Hypotension
-
Prochlorperazine (Stemetil) Contraindications
- 1. Hypersensitivity to or to bisulfites or benzyl alcohol
- 2. Seizures
- 3. Encephalopathy
- 4. Parkinson's
-
Prochlorperazine (Stemetil) Dosing
- 2.5-10mg IV tid-qid
- 5-10mg IM tid-qid
-
Propranolol (Inderal) Classification
Non-selective β blocker
-
Propranolol (Inderal) Indications
- 1. HTN
- 2. MI/Angina
- 3. Rate control with SVTs/Afib
- 4. Tachyarrhythmias with cardiac glycoside ingestion, thyrotoxicosis (excessive thyroid hormones)
- 5. Migraines
-
Propranolol (Inderal) Side Effects
- 1. Bronchospasm
- 2. Hypotension
- 3. Bradycardia/Heart Blocks
- 4. CHF/pul edema
- 5. Arrhythmias
- 6. Fatigue/dizziness/weakness
-
Propranolol (Inderal) Contraindications
- 1. Hypersensitivity
- 2. Bradycardia/Heart blocks
- 3. Asthma/COPD
- 4. CHF/Cardiogenic shock
-
Propranolol (Inderal) Dosing
Adult:
Ped:
Adult: 1-3mg in D5W (10-30ml) over 2min. May repeat x1 in 2min.
Ped: 10-100mcg/kg, max 1mg over 2min q6-8hrs prn
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Propofol (Diprivan) Classification
- General Anesthetic
- Ultra short acting hypnotic
-
Propofol (Diprivan) Indications
- Anesthesia
- Sedation/maintenance of
-
Propofol (Diprivan) Mechanisms of Action
- 1. Specific mechs are ukn, ultra short acting sedative
- 2. Potent resp and cardiovascular depressant
- 3. No analgesic properties
- 4. Vasodilation
-
Propofol (Diprivan) Side Effects
- 1. Severe resp depression/apnea
- 2. Bradycardia
- 3. Hypotension
- 4. Pain/stinging at injection site
- 5. Twithcing extremities
-
Propofol (Diprivan) Contraindications
- 1. Hypersensitivity to or to soybean oil, egg lecithin, or glycerol
- 2. Peds <3y/o
-
Propofol (Diprivan) Dosage
- Induction: 1-3mg/kg in D5W only
- or 40mg prn until sedation
- Maintenance: 100-200mcg/kg/min for first 30min, then reduce dose by 30-50%.
- or: 25-50mg prn
Degrades plastic
Vents: 5-50mcg/kg/min
Peds = same as adult
-
Propofol (Diprivan) Onset/Duration
- Onset: immediate
- Duration: 3-5min
-
Racemic Epinephrine (Vaponefrin) Indications
1. Laryngo/bronchospasm - croup mainly, asthma, bronchitis, bronchiolitis
-
Racemic Epinephrine (Vaponefrin) Dosing
0.25-5ml 2.25% solution (mixed with 3ml NS if necessary) neb q 5min prn.
-
Ranitidine (Zantac) Classification
Histamine H2 receptor antagonist
-
Ranitidine (Zantac) Indications
- 1. GERD
- 2. Peptic ulcers
- 3. Indigestion
- 4. Zollinger-Ellison Syndrome (excessive HCl secreting)
-
Ranitidine (Zantac) Side Effects
-
Ranitidine (Zantac) Mechanisms of Action
- 1. Copetitively blocks H2 receptors of parietal cells, decreasing responsiveness to histamine, ACh and gastrin. This reduced acid secretion by up to 90%.
- 2. Stomach pH increases
- 3. Increases prolactin secretion from anterior pituitary
-
Ranitidine (Zantac) Contraindications
Hypersensitivity
-
Ranitidine (Zantac) Dosing
Adult:
Ped:
Adult: 50mg IV/IM q4-6hrs, max 400mg/day
Peds: 2-4mg/kg/day divided into 3-4 doses/day
-
Reteplase (Retavase) Classification
Fibrinolytic
-
Reteplase (Retavase) Indication
AMI
-
Reteplase (Retavase) Mechanisms of action
1. Catalyzes conversion of plasminogen into plasmin. Plasmin degrades the fibrin matrix of clots.
-
Reteplase (Retavase) Side Effects
- 1. Bleeding
- 2. Reperfusion arrhythmias
- 3. N/V
- 4. Fever
- 5. Anaphylaxis
-
Reteplase (Retavase) Contraindications
- 1. Prior intracranial hemorrhage
- 2. CVA lesion
- 3. Malignant intracranial neoplasm
- 4. Ischemic stroke within 3 months except acute within 3 hrs
- 5. Aortic dissection
- 6. Active bleeding
- 7. Significant closed head trauma of facial trauma within 3 months
- Relative:
- 1. Poorly/uncontrolled HTN
- 2. Uncontrolled HTN sys >180 or DBP >110
- 3. Ischemis stroke >3 months
- 4. Traumatic or prolonged CPR or major bleed within 3 weeks
- 5. Recent intracranial bleed (2-4wks)
- 6. Noncompressible vascular punctures
- 7. Strptokinase/anitrplase greater than 5 days
- 8. Pregnancy
-
Reteplase (Retavase) Dosing
10u IV over 2min q30min max 20u.
-
Rocuronium (Zemuron) Classification
Intermediate acting Nondepolarizing neuromuscular blocking agent
-
Rocuronium (Zemuron) Indications
- RSI
- Surgery
- Maintenance of paralysis
-
Rocuronium (Zemuron) Mechanisms of Action
1. Blocks ACh from binding to postsynaptic receptors by competitively binding to without stimulating depolarization.
-
Rocuronium (Zemuron) Side Effects
1. Bronchospasm
-
Rocuronium (Zemuron) Contraindications
Hypersensitivity to or to bromide
-
Rocuronium (Zemuron) Dosing
1mg/kg repeat 0.5mg/kg q10min prn
Peds = same
-
Rocuronium (Zemuron) Onset/Peak/Duration
- Onset: 1-3min
- Duration 30-60min
-
Ritodrine (Yutopar) Info
Discontinued tocolytic
β2 agonist that relaxes uterine smooth muscle and supression of preterm labour.
50-350mcg/min IV
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