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Pharmacologie générale PHAR-G2000 > Partie 1 > Flashcards

Partie 1 Flashcards

1
Q

Pharmacologie def

A

4

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2
Q

Médicament def

A

4

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3
Q

Pharmacologie > grec

A

5

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4
Q

Médicament

A

6

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5
Q

Excipients

A

7

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6
Q

Formes galéniques

A

8

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7
Q

Origines des médicaments

A

9; 10

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8
Q

L’homéopathie

A

11

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9
Q

Statut des produits homéopathiques

A

12

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10
Q

2 procédures d’enregistrement

A

13

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11
Q

Phytothérapie

A

14

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12
Q

Phytothérapie non conventionnelle

A

15

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13
Q

Plantes médicinales

A

16

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14
Q

Un extrait végétal

A

17

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15
Q

Aristolochiae Fangch

A

18 -> 35

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16
Q

Produit

naturel

A

36

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17
Q

Intoxication

A

37

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18
Q

huiles essentielles

A

38, 39

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19
Q

Levure de riz rouge

A

40

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20
Q

Effets indésirables

A

41

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21
Q

Médecine traditionnelle vs Médecine conventionnelle

A

42

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22
Q

Médicaments de synthèse

A

43

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23
Q

Médecine traditionnelle vs Médicament de synthèse

A

44

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24
Q

Développement d ’un médicament

A

45, 46

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25
Q

Dossier analytique

A

47

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26
Q

Dossier toxicologique

A

48

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27
Q

Etude de toxicité aiguë

A

49

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28
Q

courbe dose /réponse

A

50

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29
Q

Dose létale 50

A

51

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30
Q

Classes de toxicité : Échelle de Hodge et Sterner

A

52

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31
Q

Facteurs modulant la DL50

A

53

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32
Q

Etude de toxicité subaiguë

A

54, 55

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33
Q

Etude de toxicité chronique

A

56

34
Q

Etudes de mutagénèse

A

57

35
Q

Recherche de mutation de gènes

A

58

36
Q

Corrélation mutagénèse/cancérogénèse

A

59

37
Q

Etudes de cancérogénèse

A

60; 61; 62

38
Q

Evaluation des tumeurs

A

63

39
Q

Classification de l’Union européenne cancérigènes

A

64

40
Q

Etudes de la fonction reproductrice; Etude de fertilité

A

65

41
Q

Etude de tératogénicité

A

66

42
Q

Pour l’alcool

A

67

43
Q

Mode d’action des agents tératogènes :

A

68

44
Q

Etude de tératogénicité; Observations

A

69

45
Q

Extrapolation à l ’homme:

A

70

46
Q

Etude de péri et post-natalité

A

71

47
Q

Dossier clinique

A

72

48
Q

Etude de phase IV

A

73; 74

49
Q

Expiration du brevet

A

75

50
Q

Les génériques

A

76

51
Q

Etude clinique de bioéquivalence

A

77

52
Q

Principe de bioéquivalence

A

78, 79

53
Q

Génériques -> prescription

A

80

54
Q

Les biomédicaments

A

81; 82

55
Q

Médicaments issus de la biotechnologie

A

83 -> 85

56
Q

L’érythropoïèse

A

86, 87

57
Q

Classification de la maladie rénale chronique

A

88, 89, 90

58
Q

Médicaments composés de protéines fabriquées à l’aide du génie génétique

A

91

59
Q

Lors de l’expiration du brevet (biomédicament)

A

92

60
Q

Médicament biosimilaire

A

93

61
Q

Conditions nécessaires à l’obtention d’une autorisation de mise sur le marché (AMM) pour un médicament biosimilaire.

A

94

62
Q

« Timing » de fabrication d’un médicament biosimilaire:

A

95, 96

63
Q

Indications biosimilaire

A

97

64
Q

Pharmacovigilance médicament biologique

A

98

65
Q

Coûts

A

99

66
Q

Proportion des biosimilaires mis sur le marché

A

100

67
Q

Domaines de la pharmacologie

A

103

68
Q

Pharmacologie clinique

A

104

69
Q

La prescription médicale

A

105

70
Q

Qu’entend-on par « médicament »

A

106

71
Q

Original ou générique

A

107

72
Q

Le remboursement de référence

A

108

73
Q

Quels sont les critères légaux qu’une prescription doit remplir?

A

109

74
Q

Originale / générique / en DCI ou magistrale

A

110

75
Q

La prescription au nom de la molécule (DCI)

A

111

76
Q

Qu’est-ce qu’une préparation magistrale ?

A

112

77
Q

Sous quels conditions l’assurance soins de santé rembourse-t-elle un médicament ?

A

113

78
Q

Qui paie quoi ?

A

114

79
Q

L’assurance soins de santé rembourse partiellement ou totalement certains médicaments :

A

115

80
Q

Les plans gouvernementaux : E-Health, DPI, SNOMED CT et Recip-e

A

116 -> 122

Pharmacologie générale PHAR-G2000 (10 decks)

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