ACTIVITY 1 Flashcards

1
Q

blockade of neuronal T-type Ca2+ channel

A

valproic acid

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2
Q

GABAA receptor–chloride ion channel macromolecular complex (opening of Cl channel) Increase duration

A

clonazepam and benzodiazepines

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3
Q

GABAA receptor–chloride ion channel macromolecular complex (opening of Cl channel) Increase frequency

A

phenobarbital and barbiturates

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4
Q

(TCA) = inhibits re-uptake of NE and 5-HT

A

Clomipramine

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5
Q

(heterocyclics) = inhibits re-uptake of NE and 5-HT

A

Duloxetine

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6
Q

(heterocyclics) = α2-receptor antagonism

A

Mirtazapine

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7
Q

(SSRI) = inhibits re-uptake of 5-HT

A

Fluoxetine

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8
Q

(TCA) = inhibits re-uptake of NE and 5-HT

A

Trimipramine

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9
Q

inhibit protein synthesis by binding, with high affinity, to the A-site on the 16S ribosomal RNA of the 30S ribosome

A

Aminoglycosides

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10
Q

reversibly inhibit nerve transmission by binding voltage-gated sodium channels (Nav) in the nerve plasma membrane

A

Local anesthetics

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11
Q

inhibit synaptic activity partly through direct activation of μ, δ, and κ receptors that confers antinociceptive mechanisms at the spinal level.

A

Opioid analgesics

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12
Q

a medication is an assessment of the risk of fetal injury due to the pharmaceutical, if it is used as directed by the mother during pregnancy.

A

Pregnancy category

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13
Q

Fetal risks are evident; there are no situations where the risk/benefit justifies use

A

Pregnancy Category X

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14
Q

Insufficient human studies, but animal studies show problems or: No animal studies, and insufficient human studies

A

Pregnancy Category C

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15
Q

Appropriate human studies - no risk

A

Pregnancy Category A

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16
Q

Human studies, with/without animal research show fetal risks, but the drug is important to some women to treat their conditions

A

Pregnancy Category D

17
Q

Insufficient human studies, but animal research suggests safety or: Animal studies show issues but human studies show safety

A

Pregnancy Category B

18
Q

a solid dosage form containing medicinal substance(s) with or without diluents.

A

Tablet

19
Q

a solid dosage form in which the drug is enclosed within a hard or soft soluble container or shell.

A

Capsule

20
Q

drug in the form of a capsule prepared in such a way that, when taken orally, its contents are released slowly

A

Spansules

21
Q

tablet dosage form in the shape of a capsule.

A

Caplet

22
Q

a two-phase system in which one liquid is dispersed throughout another liquid in the form of small droplets.

A

Emulsion

23
Q

a solution containing a high concentration of sucrose or other sugars

A

Syrup

24
Q

a liquid preparation that consists of solid particles dispersed throughout a liquid phase in which the particles are not soluble; it may be oral, topical, otic, or ophthalmic.

A

Suspension