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71 Cards in this Set

  • Front
  • Back
GENERIC NAME

diazepam
diazepam
BRAND NAME

diazepam
Valium
CLASS

diazepam
benzodiazepine
INDICATIONS AND FIELD USE

diazepam
Grand mal seizures, especially status epilepticus

Transient analgesia/amnesia for medical procedures (e.g., fracture reduction, cardioversion, pacing)

Delirium tremens

Treat the cause first
ADULT DOSAGE

diazepam
2 mg increments slow IV/IO push. Administer no faster than 2 mg/minute
BONUS

diazepam
Incompatibilities/drug interactions:
Do not mix or dilute diazepam with other solutions or drugs in syringe, tubing or IV container

Special notes:
Valium must be injected slowly and small veins such as those on the dorsum of the hand or wrist should be avoided

Risk of venous thrombosis, phlebitis, local irritation, swelling and vascular spasm is increased

Extreme care must be taken to avoid intra-arterial injection or extravasation

Diazepam may cause prolonged CNS depression in the neonate (30 days of age or less)
GENERIC NAME

etomidate
etomidate
BRAND NAME

etomidate
Etomidate
CLASS

etomidate
sedative/hypnotic agent
INDICATIONS AND FIELD USE

etomidate
Induction of anesthesia for rapid sequence intubation (RSI)
ADULT DOSAGE

etomidate
0.3 mg/kg IV/IO over 30-60 seconds
BONUS

etomidate
Onset of action:
1 minute

Duration of action:
3-5 minutes
GENERIC NAME

lorazepam
lorazepam
BRAND NAME

lorazepam
Ativan
CLASS

lorazepam
antianxiety; benzodiazepine, short or intermediate acting
INDICATIONS AND FIELD USE

lorazepam
Status epilepticus

Seizure

Agitation
ADMINISTRATION

lorazepam
IM: Should be administered deep into the muscle mass

IV/IO: Do not exceed 2 mg/minute or 0.05 mg/kg over 2-5 minutes

**Inadvertent intra-arterial injections may produce arteriospasm resulting in necrosis and potential amputation
ADULT DOSAGE

lorazepam
Status epilepticus: 2 mg to 4 mg IV/IO given slowly (over 2-5 minutes. May repeat dose in 10-15 minutes if needed (maximum 8 mg). May give IM if no IV access
BONUS

lorazepam
Incompatibilities/drug interactions:
Concomitant use of CNS sedatives such as phenothiazines, narcotic analgesics, barbiturates, antidepressants, and alcohol should be assessed prior to administration of IV lorazepam

Special notes:
Care must be used when administering lorazepam IV to elderly patients, seriously ill patients, and those with limited pulmonary reserve as apnea and/or cardiac arrest may occur

Patients over the age of 50 years may have a more profound and prolonged sedation with IV lorazepam

All patients should be monitored for respiratory depression and hypotensive effects

Stability above room temperature has not been established
GENERIC NAME

midazolam hydrochloride
midazolam hydrochloride
BRAND NAME

midazolam hydrochloride
Versed
CLASS

midazolam hydrochloride
central nervous system depressant, benzodiazapine
INDICATIONS AND FIELD USE

midazolam hydrochloride
Anti-convulsant

Sedation

Management of acute agitation/treat cause first

Induction for intubation
ADULT DOSAGE

midazolam hydrochloride
Patients 14 to 60 years of age: 1 to 5 mg IV (2 to 5 mg IM), titrate to effect, administer slowly in small increments of no more than 2.5 mg over at least 2 minutes

Patients over 60 years of age: 1 to 3.5 mg IV (1 to 3 mg IM), titrate to effect, administer slowly in small increments of no more than 1.5 mg over at least 2 minutes

Total dose: Should not exceed 20 mg

For emergency intubation: 0.1 mg/kg up to 0.3 mg/kg with dosage limit of 20 mg

Seizures: 0.2 mg/kg IM for status seizures if no IV access
BONUS

midazolam hydrochloride
Incompatibilities/drug interactions:
Midazolam may potentiate other CNS depressants, including opiate agonists or other analgesics, barbiturates or other sedatives, anesthetics, or alcohol

Erythromycin may double the half-life of midazolam

Special Notes:
Flumazenil is the accepted antagonist for midazolam
GENERIC NAME

morphine sulfate
morphine sulfate
BRAND NAME

morphine sulfate
Morphine Sulfate
CLASS

morphine sulfate
narcotic agonist
INDICATIONS AND FIELD USE

morphine sulfate
Analgesia, especially in patients with burns, myocardial infarction, or renal colic

Pulmonary edema (cardiogenic)
ADULT DOSAGE

morphine sulfate
Administer 2-4 mg increments slow IV/IO PUSH until pain is relieved up to 20 mg, if systolic is > 90

IM: 5-10 mg if no IV access if systolic > 90
BONUS

morphine sulfate
Incompatibilities/drug interactions: CNS side effects (including respiratory depression) can be reversed by naloxone

Special notes:
Schedule II narcotic

Watch for histamine effects (wheals, urticaria) proximal to IV site; contact medical control

Correct hypotension before administration

Maximum respiratory depression 7-10 minutes after administration; can be reversed with naloxone; caution in patients with emphysema

IV infusions of morphine sulfate may be transported, however an infusion pump is required
GENERIC NAME

nitrous oxide 50%
nitrous oxide 50%
BRAND NAME

nitrous oxide 50%
Nitronox
CLASS

nitrous oxide 50%
analgesic, inhalation
INDICATIONS AND FIELD USE

nitrous oxide 50%
Moderate to severe pain from musculoskeletal trauma, burns, AMI
ADULT DOSAGE

nitrous oxide 50%
Self-administer and self-regulated by the patient, who must hold the mask to face to create an airtight seal until the pain is significantly relieved or the patient drops the mask
BONUS

nitrous oxide 50%
Dosage forms/packaging: Nitrous oxide machine that delivers a fixed ratio of nitrous oxide and oxygen (50:50) utilizing a mixing valve with separate tanks of N2O and O2 with a fail safe device (O2 tank empty, no nitrous flows) and a self-administation mask
GENERIC NAME

succinylcholine
succinylcholine
BRAND NAME

succinylcholine
Succinylcholine
CLASS

succinylcholine
ultra-short acting depolarizing-type skeletal muscle relaxant
INDICATIONS AND FIELD USE

succinylcholine
Endotracheal intubation requiring paralysis (RSI) by a qualified EMT-P
ADULT DOSAGE

succinylcholine
1.5 mg/kg IV push, may repeat in 2-3 minutes to achieve paralysis
BONUS

succinylcholine
Incompatibilities/drug interactions: Beta-blockers, procainamide, lithium, and quinidine prolong the effects

Duration of action: Muscle paralysis lasting 4-6 minutes

Special Notes: *Succinylcholine should not be given to patients for the period from 24 hours to 21 days after significant burns or crush injury due to elevated potassium levels and potential for cardiac dysrhythmias
MECHANISM OF ACTION

Diazepam
Acts on parts of the limbic system, the thalamus, and hypothalamus producing calming effects; decreases seizures by increading the seizure threshold; transient analgesia; amnesic; sedative
CONTRAINDICATIONS

Diazepam
Hypersensitivity (allergy)

Glaucoma, acute narrow angle (relative)
ADVERSE REACTIONS

Diazepam
CV: Bradycardia, hypotension, cardiovascular collapse; venous thrombosis; phlebitis; vascular spasm

Resp: Respiratory arrest; may be prolonged in neonates

CNS: Somnolence, confusion, coma, diminished reflexes

Other: Burning proximal to IV injection site; local irritation; swelling; extravasation will cause tissue necrosis
PEDIATRIC DOSAGE

Diazepam
IV/IO Dose: 0.1 - 0.2 mg/kg (max of 2.0 mg/dose); may repeat x 3 every 5 minutes

Rectal dose (< or = 6 years): 0.5 mg/kg rectally via ANGIOCATH (max of 10 mg)
MECHANSIM OF ACTION

Lorazepam
Agent bings highly to the gamma-amino butyric acid (GABA) benzodiazepine receptor complex without displacing GABA, (GABA is the major inhibitory neurotransmitter in the brain). It exerts tranquilizing action on the central nervous system.
CONTRAINDICATIONS

Lorazepam
Known sensitivity to the benzodiazepines

Acute narrow angle glaucoma or myasthenia gravis

Known hypersensitivity to polyethylene glycol, propylene glycol, or benzyl alcohol

Pregnancy
ADVERSE REACTIONS

Lorazepam
Most frequent adverse reaction is sedation

Transient amnesia or memory impairment

Confusion

Hypotension

Respiratory depression

Dizziness

Headache
PEDIATRIC DOSAGE

Lorazepam
Status epilecticus: 0.05 - 0.1 mg/kg IV/IO over 2-5 minutes (maximum 4 mg). May repeat in 10-15 minutes
MECHANISM OF ACTION

midazolam hydrochloride
CNS effects are mediated through the inhibitory neurotransmitter gamma-aminobutyric acid (GABA).

Acts at the limbic, thalamic, and hypothalamic levels of the CNS, producing anxiolytic, sedative, hypnotic, and anticonvulsant effects.

Capable of producing all levels of CNS depression, from mild sedation to coma
CONTRAINDICATIONS

midazolam hydrochloride
Hypersensitivity to midazolam

Relative contraindication in: myasthenia gravis or other neuromuscular disorders; acute alcohol intoxication; sever COPD; and acute pulmonary insufficiency
ADVERSE REACTIONS

midazolam hydrochloride
CV: hypotension (especially in patients premedicated with narcotic); cardiac arrest; irregular or fast heartbeat

Resp: Apnea; respiratory depression, respiratory arrest; hyperventilation; wheezing or difficulty in breathing; hiccups; coughing

CNS: emergence delirium; muscle tremor; uncontrolled or jerky movements of body; unusual excitement, irritability, or restlessness; dizziness, light-headedness, or feeling faint; prolonged drowsiness; headache

GI: nausea and/or vomiting
PEDIATRIC DOSAGE

midazolam hydrochloride
Pediatric patients: 0.05 to 0.1 mg/kg slow IV push

0.2 mg/kg IM for status seizures if no IV access
MECHANISM OF ACTION

morphine sulfate
Alleviates pain by acting on the pain receptors in the brain; elevates pain threshold

Depresses central nervous system; depresses brainstem respiratory centers; decreases responsiveness to changes in PaCO2

Increases venous capacitance (venous pooling), vasodilates arterioles, reducing preload and afterload

Histamine release
CONTRAINDICATIONS

morphine sulfate
Respiratory depression

Head injuries

Elevated intra cranial pressure

Asthma, relative

Abdominal pain, relative
ADVERSE REACTIONS

morphine sulfate
CV: brady or tachydysrhythmias, orthostatic hypotension

Resp: Respiratory depression or arrest

CNS: Excess sedation, seizures to coma and arrest, pupillary constriction

GI: nausea and vomiting, GI spasm

Derm: Histamine release may cause local urticaria
PEDIATRIC DOSAGE

morphine sulfate
Age < 14 years: IV/IO 0.1 mg/kg. May repeat to a max total dose or 0.2 mg/kg. Max total dose of 10 mg.
MECHANISM OF ACTION

etomidate
Produces hypnosis rapidly causing CNS depression and anesthesia

No analgesic effect
CONTRAINDICATIONS

etomidate
Hypersensitivity
ADVERSE REACTIONS

etomidate
Transient muscle movements

Apnea

Causes minimal but not clinically significant suppression of cortisol levels

May cause myoclonus and tremors that can resemble seizure activity
PEDIATRIC DOSAGE

etomidate
None
MECHANISM OF ACTION

nitrous oxide 50%
Centrally acting agent that produces CNS depression and elevation of the pain threshold
CONTRAINDICATIONS

nitrous oxide 50%
Unconscious patient

Poor respiratory drive, compromise of respiratory status (i.e. pneumothorax)

Abdominal pain unless intestinal obstruction has been completely ruled out

Severe head injury
ADVERSE REACTIONS

nitrous oxide 50%
Resp: worsening or pre-existing pneumothorax; may cause hypercarbia in oxygen sensitive patients (CO2 retainers)

GI: nausea and vomiting, may lead to rupture of intestine if administered to patient with intestinal obstruction
PEDIATRIC DOSAGE

nitrous oxide 50%
Must be old enough to follow the instructions for use and large enough that the mask creates an airtight seal
MECHANISM OF ACTION

succinylcholine
Combines with cholinergic receptors of the motor end plate to produce depolarization

Hydrolyzed by acetylcholinersterase
CONTRAINDICATIONS

succinylcholine
Muscle disorders

Personal or family history of malignant hyperthermia

History of hyperkalemia

Burn injured patients

Ocular injuries

Patients in whom successful endotracheal intubation is doubtful
PEDIATRIC DOSAGE

succinylcholine
None
ADVERSE REACTIONS

succinylcholine
vagal stimulation leading to bradycardia or systole

hyperkalemia

rhabdomyolysis

hypersalivation

elevated intraocular pressure

release of histamine