Meds Flashcards

1
Q

Induction Dose of Versed

A

1-4 mg

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2
Q

Induction Dose of Fentanyl:

A

1-3 mcg/kg

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3
Q

Induction dose for Propofol

A

2 mg/kg

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4
Q

Induction dose for Lidocaine

A

1-1.5 mg/kg

Max of 100 mg

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5
Q

Induction dose for Roc:

A

0.6 mg/kg

1.2 mg/kg for RSI

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6
Q

Induction dose for Sucs:

A

1 mg/kg

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7
Q

Induction dose for Ketamine:

A

0.5 - 1.5 mg/kg

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8
Q

Induction dose for Etomidate

A

0.3 mg/kg

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9
Q

Dose for Neo:

A

100 mcg IVP
or
gtt of 40-80 mcg/min

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10
Q

Dose for Ephedrine:

A

5-10 mg IVP

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11
Q

IVP dose for Vaso:

A

1-2 units

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12
Q

Dose for Precedex:

A

1 mcg/kg over 10 min followed by gtt @ 0.2-0.7 mcg/kg/hr

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13
Q

MOA for Versed:

A

Binds to the alpha/gamma subunits on GABA receptor

Enhances receptor’s affinity for GABA

Enhanced opening of Cl- channels

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14
Q

MOA for Fentanyl:

A

Mu Opioid Agonist

Increases K+ conductance, decreases Ca conductance (↓ cAMP)

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15
Q

MOA for Lidocaine:

A

Blocks VG Na+ channels and prevents AP conduction

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16
Q

MOA for Propofol

A

Modulates GABA through through GABA-A receptors

↑ Cl- conductance = hyperpolarization of postsynaptic membrane & neuron = sedative & hypnotic effects

17
Q

MOA for Roc:

A

Blocks Ach release from pre-junctional sites

Competes for alpha subunits on post-junctional nAch R’s

prevents conformational change - inhibition of Na+ conduction - no impulses

18
Q

MOA for Sucs:

A

Attaches to 1 or both alpha subunits on nACh Rs

Mimics Ach @ NMJ - causes depolarization of the post-junctional membrane

Post-junctional membrane cannot respond to subsequent release of Ach

19
Q

MOA for Ketamine:

A
  • NMDA antagonist: blocks Ca influx - ↓ release of glutamate
  • Opioid receptor antagonist
20
Q

MOA for Etomidate

A

Binds to GABA-A receptor & increases receptor’s affinity for GABA

21
Q

MOA for Neo:

A

Alpha 1 Agonist
(mimics the alpha effects of Norepi but not as potent)

22
Q

MOA for Ephedrine:

A

Non-catecholamine Sympathomimetic

Direct acting: alpha & beta agonist (non-selective)
Indirect: NE & endogenous catechol. release

23
Q

MOA for Precedex

A

Stimulates a2 receptors & causes presynaptic inhibition (turns down SNS)

a2A: sedation, hypnosis, sympatholysis

a2B: Vasoconstriction, anti-shivering, analgesia, Ca-linked

a2C: learning, startle response

24
Q

Onset, DOA of Versed:

A

Onset: <1 min
DOA: 2-6 hrs

25
Q

Onset, DOA of Fent (induction)

A

Onset: 30-60 secs
DOA: 10-20 min

26
Q

Onset, DOA of Lidocaine (Induction)

A

Onset: 1 min
DOA: 10-20 min

27
Q

Onset, DOA of Propofol (induction)

A

Onset: 30-60 sec
DOA: 1-8 min

28
Q

Onset, DOA for ROC

A

Onset- 2-3 mins
DOA: 30-40 min

29
Q

Onset, DOA for Sucs

A

Onset: 30-60 secs
DOA: 3-5 mins (5-10 mins)

30
Q

Onset, DOA for Ketamine:

A

Onset: 1 min
DOA: 10-20 min

31
Q

Onset, DOA for Etomidate

A

Onset: 1 min
DOA: 3-10 min

32
Q

Onset, DOA for Neo:

A

Onset: 10-15 min
DOA: 15 min

33
Q

Onset for Vaso:

A

10-15 mins

34
Q

Doses: Anti-Emetics

Zofran
Phenergan
Dexamethasone
Inapsine
Reglan
Pepcid

A

Zofran: 4-8mg
Phenergan: 6.25-25 mg
Dexamethasone: 4 mg
Inapsine: 0.625 mg
Reglan: 10-20 mg
Pepcid: 20 mg

35
Q

Dose for Sugammadex:

A

2 mg/kg for moderate block (2/4 TOF twitches)

4 mg/kg for deep block (no TOF, 1-3 PTF)

8-16 mg/kg for Extreme block (no TOF or PTF)