Pharma Flashcards

1
Q

Used to treat RA & bowel diseases such as crohn’s

A

Sulfasalazine

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2
Q

Competitive inhibition of DHFR

A

Methotrexate

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3
Q

Inhibit AICAR transformylase —> inhibit purine synthesis

A

Methotrexate

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4
Q

Metabolized to mercaptopurine —> inhibit DNA
Has drug interaction w allopurinol

A

Azathioprine

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5
Q

Converted to teriflunomide -> inhibit DHOD -> inhibit pyrimidine this inhibiting RNA synthesis

A

Leflunomide

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6
Q

Leflunomide

A

Well absorbed orally
Long half life
Active metabolite goes enterohepatic circulation
Risk of hepatic failure

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7
Q

inhibit IL-2 & not cytotoxic

A

Cyclosporin A

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8
Q

Phosphoramide mustard which Alkylate DNA and inhibit dna , RNA cross linking

A

Cyclophosphamide

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9
Q

Inhibit JAK

A

Tofacitinib

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10
Q

Bind to TNF - a and inhibit it’s effects
Side effects; upper respiratory infection

A

Infliximab

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11
Q

Inhibit IL-1
Metal chelator in wilsons disease

A

D-pinicillamine

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12
Q

Anti-malaria and used in Sjögren’s syndrome

A

Chlorquine

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13
Q

Drugs that causes bone more suppression

A

Methotrexate
Azathioprine
Leflunomide
D-penicillamine

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14
Q

Drug that doesn’t cause Bone marrow suppression

A

Cyclosporin - A

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15
Q

Irreversible non selective cox inhibitor

A

Aspirin

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16
Q

St high doses causes hyperventilation and res alkalosis

A

Aspirin

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17
Q

What drug interact with aspirin to reduce the rate of absorption ?

A

Antacids

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18
Q

What drug interact with aspirin to increase the risk of bleeding

A

Heparin

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19
Q

What drug interact with aspirin to reduce urate excretion!

A

Probencid

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20
Q

What drug interact with aspirin to increase it half life ?

A

Naproxen

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21
Q

Reye disease is a side effect of which drug ?

A

Aspirin

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22
Q

Non competitive non selective reversible COX inhibitor

A

Paracetamol (acetaminophen)

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23
Q

Paracetamol pathway used for children

A

Conjugation with sulfate

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24
Q

Predominat pathway for paracetamol in adults

A

Conjugation with glucuronide

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25
Competitive non selective reversible cox inhibitor Indol derivative
Indomethacin
26
Competitive non selective cox inhibitor Propionic acid
Ibuprofen Naproxen
27
Competitive non selective cox inhibitor Phenylacetic acid derivative
Diclofenac
28
Selective cox 2 inhibitor Dipyridinyl derivative
Etoricoxib
29
Selective cox 2 inhibitor Pyrazole derivative
Celecoxib
30
Oral synthetic prostaglandin Used to treat and prevent peptic ulcers
Misoprotosol
31
Normalize the hypothalamic’thermostat’ altered by pg’s in the brain Reduce fever by inhibiting PG synthesis
Antipyretic action
32
Alleviate pain by removing hyperalgesic effects of PGs
Analgesic action
33
Prevent thrombosis by reducing formation of platelet aggregating theomboxane A2
Aspirin
34
Effect of inhibiting cox 2
Decrease the release of anti-aggregatory prostaglandin I2 But it does not affect Thromboxane bcz it lacks cox2
35
PTH synthetic analog increases osteoblast proliferation, differentiation and activity o for parenteral treatment of osteoporosis
Teriparatide
36
1αHydroxyvitamin D2 , converted in the liver to 1,25dihyroxyvitamin D active form of Vit D that selectively inhibits PTH formation
Doxercalciferol
37
19nor1,25dihydroxyvitamin D2 - An analog of calcitriol active form of Vit D that selectively inhibits PTH formation
Paricalcitol
38
An active form of Vit D that selectively inhibits PTH formation - Uses: o topical treatment of psoriasi
Calcipotriol
39
salmon calcitonin is most often selected for clinical use (not human calcitonin), why?
longer half-life and greater potency
40
Selective estrogen receptor modulator (SERM) - prevent or delay bone loss in postmenopausal women Inhibit PTH - stimulated bone resorption
Raloxifene
41
human monoclonal antibody binds to and prevents the action of RANKL -> inhibits osteoclast formation and activity
Denosumab
42
Calcimimetic lowers PTH by activating the calcium-sensing receptor in the parathyroid gland
Cinacalcet
43
short-chain organic polyphosphate compounds that reduce both the resorption and the formation of bone by an action on the basic hydroxyapatite crystal structure
Bisphosphonates
44
Have direct effects on osteoclasts, including inhibition of farnesyl pyrophosphate
Bisphosphonate
45
Morphine MOA
its mechanism will lead to reduction in transmitter release and pain
46
Codeine vs. morphine
Codeine better absorbed orally Morphine iv or im
47
Codeine is a weak opiod
can be used to supplement NSAIDs in alleviating mild inflammatory pain or arthritis
48
Mode of administration of fentanyl
Sublingual or transdermally bcz its liphophilic
49
partial m receptor agonist - an inhibitor of serotonin- norepinephrine reuptake from the neuronal synaptic cleft
Tramadol
50
Sides effects of opiods
Respiratory depression Constipation Pupillary constriction Histamine release
51
Uricostatic drugs , (xanthine oxidase inhibitor)
Allopurinol Febuxostat
52
lower uric acid levels by inhibiting its synthesis a Uricostatic Drug (xanthine oxidase inhibitor)
Allopurinol
53
a Uricostatic Drug (xanthine oxidase inhibitor) - a non-purine inhibitor of xanthine oxidase
Febuxostat
54
alkaloid extracted from the autumn crocus - used to both prevent and relieve acute attacks
Colchicine
55
Colchicine MOA
binds to tubulin preventing microtubule polymerization, effectively acting as a mitotic poison Preventing microtubule polymerization -> disrupts the mobility of granulocytes and inhibits their migration to the joint
56
Drugs of choice to treat acute attacks of gout Contraindicated in patients with: o peptic ulcer disease
Indomethacin
57
used to treat acute gout in patients that cannot use NSAIDs
Prednisone
58
Uricosuric drug
Probencid Losartan
59
Losartan MOA
Angiotensin II antagonist Inc ph dec risk of stones
60
Uricolytic drug
Rasburicase
61
Converted to allantoin
Rasburicase