mtm detailed Flashcards

1
Q

Pharmaceutical equivalent (3)

A

contain the same active ingredient(s)

have the same dosage form and route of administration

are identical in strength or concentration.

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2
Q

pharmaceutical alternatives (3)

A

are different salts, esters, or complexes (e.g. tetracycline hydrochloride and tetracycline phosphate complex)

have different dosage forms (e.g. capsules vs. tablets) or strengths

data are generally not available for FDA to make the determination of tablet to capsule

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3
Q

bioavailability

A

refers to the rate and extent to which an active ingredient is absorbed after administration and becomes available at the drug’s site of action

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4
Q

bioequivalence

A

the rate of absorption may differ, but this is intentional, is reflected in the product labeling, is not essential to the attainment of effective body

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5
Q

biosimilars

A

have been shown to have no clinically meaningful differences in safety, purity, and potency from the reference product

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6
Q

The Orange Book

A

The FDA’s list of therapeutic drug equivalence-drugs containing the same active ingredients

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7
Q

Therapeutic equivalence (5)

A

The FDA criteria require that they:

(1) are approved drugs shown to be safe and effective; expected to have the same clinical effect and safety profile when administered to patients under the conditions specified in the labeling

(2) are pharmaceutical equivalents which (a) contain identical amounts of the same active ingredient in the same dosage form and route of administration, and (b) meet required standards of strength, quality, purity, and identity

(3) are bioequivalent - either the drugs do not present a known or potential bioequivalence problem and meet an acceptable in vitro standard, or may present a known or potential bioequivalencce problem but it is within acceptable bioequivalence standards

(4) have adequate labeling

(5) are manufactured in compliance with current Good Manufacturing Practice regulations

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8
Q

“A” rating

A

drugs that are therapeutically equivalent to the reference drug, with no known bioequivalence problems

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9
Q

AA

A

conventional dosage forms

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10
Q

AN

A

solutions and powders for aerosolization

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11
Q

AO

A

Injectable oil solutions

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12
Q

AP

A

injectable aqueous / IV solutions

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13
Q

AT

A

topical products

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14
Q

AB

A

therapeutically equivalent to each other; known or potential bioequivalence problems may exist but have been found to meet standards for bioequivalence

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15
Q

B

A

not therapeutically equivalent to other pharmaceutical products; actual or potential bioequivalence problems have not been resolved

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16
Q

B*

A

requires FDA investigation to review equivalence

17
Q

BC

A

Extended-release dosage forms (capsules, injectables and tablets)

18
Q

BD

A

active ingredient and dosage forms with DOCUMENTED bioequivalence problems

19
Q

BE

A

delayed-release oral dosage forms

20
Q

BN

A

aerosol nebulizer delivery systems

21
Q

BP

A

potential bioequivalence problems

22
Q

BS

A

products shown by the FDA to have deficient standards

23
Q

BT

A

topical products that are not bioequivalent

24
Q

BX

A

products for which the data are insufficient to determine therapeutic equivalence

25
Q

INR

A

international normalized ratio

<1.1 is normal for healthy people
2.0-3.0 is effective therapeutic range for warfarin; may need to be higher for L-VAT patients

26
Q

A1C

A

glycosylated hemoglobin

normal <5.7%
prediabetes = 5.7% - 6.4%
diabetes >6.5%

A1C = BG
7=152
8-183
9=212
10=240

27
Q

sodium levels

A

133-145

28
Q

potassium levels

A

3.6-5.2

29
Q

Chloride levels

A

96-106

30
Q

magnesium levels

A

1.7-2.2

31
Q

serum levels

A

8.6-10.3

32
Q

TSH (thyroid stimulating hormone)

A

0.4-4.0, with 4.0-5.0 being high, and higher than 5.0 likely representing hypothyroidism

33
Q

BUN (blood urea nitrogen) levels

A

7-20 mg/dL (2.5-7.1 mmol/L)

34
Q

creatinine levels

A

women: 0.74-1.35mg/dL
men: 0.59-1.04mg/dL

35
Q

glucose

A

80-130

36
Q

CO2 levels

A

23-29