Pharmacology Flashcards

1
Q

Schedule I drugs

A

Highly addictive,not accepted in medical use in United States. Examples of drugs heroin peyote LSD

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2
Q

Schedule II drugs

A

High risk for potential abuse.

Morphine, oxycodone, amphetamine, cocaine, methadone

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3
Q

Schedule III drugs

A

Less potential for abuse than schedule two drugs. Examples codeine hydrocodone or anabolic steroids

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4
Q

Schedule IV drugs

A

Low potential abuse relative to schedule three drugs. Darvon,
Benzodiazepines

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5
Q

First pass effect

A

Absorption of drugs in intestinal tract and the drug’s entry into portal circulation. First pass through liver detoxifies substances.

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6
Q

Why do mg of medications sometimes differ when given iv or IM as opposed to PO?

A

Because PO meds go through first pass effect and med gets biotransformed.

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7
Q

Prodrugs

A

Drugs that, upon biotransformation in liver, produce active metabolites.

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8
Q

iatrogenic effect

A

Illness induced by medication given for tx.

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9
Q

Common symptoms of bone marrow suppression:

A
  • anemia characterized by weakness, dyspnea, fatigue, syncope
  • neutropenia (low neutrophils) characterized by fever chills, sore throat, malaise and opportunistic infection
  • thrombocytopenia (low platelets) characterized by eccymosis, petechiae, unusual bleeding
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10
Q

Symptoms of neurotoxic reactions of meds

A

CNS
-confusion, excitation, sedation, delusions, depression
Autonomic Nervous system-
-constipation, diarrhea
Peripheral NS
- paresthesias, peripheral neuritis, cranial nerve deficits( diplopia)

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11
Q

Symptoms of nephrotoxicity

A
Oliguria
Anuria
Edema
Weight gain
Hematuria
Crystakluria
Azotemia (azo=nitrogen, so it means nitrogen blood condition)
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12
Q

Symptoms of hepatotoxicity

A
Anorexia
Malaise, fatigue
Nausea
Fever
Hepatic tenderness
Jaundice
Hepatomegaly
Elevated LFT
Dark urine
Light colored stools
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13
Q

Ototoxicity

A

Tinnitus
Sensitive to noise
Vestibular toxicity- nystagmus,vertigo, n/v

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14
Q

Cardiotoxicity

A
Tachyarrhythmias
Bradyarrhythmias
Cardiomyopathy
Chf
Severe hypo or hypertension
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15
Q

Symptoms of resp depression

A

Decreased resp rate and shallow resps

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16
Q

Stevens-Johnson Syndrome

A

Caused by pcn, sulfa drugs, cotrimoxazole, carbamazepine, hydantoins, allopurinol…
S/sx- erythema multiforme, erosive involvement of mucous membranes of mouth, nose, bronchial tree and genitalia

17
Q

Toxic epidermal necrolysis

A

Caused by pcn, sulfa drugs, cotrimoxazole, carbamazepine, hydantoins, allopurinol…
Initially resembles Stevens -Johnson, but progresses to greater than 30% loss of epidermis due to necrosis.

18
Q

Hypersensitivity syndrome

A

Caused by carbamazepine, phenytoin, phenobarb, sulfa drugs, allopurinol.
S/sx- skin rash and fever
Hepatitis, arthralgia, lymphadenopathy, blood abnormalities

19
Q

Drug induced vasculitis

A

Caused by allopurinol, pcn, sulfa drugs, thiazides, pyrazolones…
-s/sx- Palpable purpuric papular rash usually on lower extremities but can be present in kidneys, gi tract, CNS

20
Q

Anticoagulant induced skin necrosis

A

Caused by warfarin and heparin
S/sx: occlusive thrombi of vessels supplying skin and subcutaneous tissue of areas with large amounts of adipose tissue (breast, butt)

21
Q

Type 1 allergic reaction

A

Result from IgE
Mast cells release large quantities of histamines.
Rapid onset- 30 min.
S-sx difficulty swallowing or breathing as bronchi become edematous.
rhinitis, sneezing
Treatment is epinephrine and resp support

22
Q

Type 2 drug reaction

A

IgG or IgM
-hemolysis (destruction of RBCs)
-Hemolytic reaction to blood transfusion
-immediate reaction is fever
- flank pain, wheezing, n/v, chest pain
Treatment- D/C blood transfusion, maintain BP,
Control bleeding and prevent renal damage, possibly IV diuretics

23
Q

Type 3 drug reaction

A

Caused by formation of immune complexes when antigens interact with antibodies, resulting in Serum sickness
Serum sickness occurs with a few days of injection of a protein.
Usually resolve spontaneously within 7-14 days. Antihistamines may help or if severe can use corticosteroids

24
Q

Type 4 drug reaction

A

Rash secondary to topical agents.
Mediated by T cell.
Treatment is d/c use of product and use calamine for itch

25
Q

Carcinogenic drugs

A

Drug induced changes in DNA from meds such as cyclophosphamide (antineoplastic)
Drug related cancer may not occur until years after administration

26
Q

Teratogenic reactions

A

Drugs affecting fetus

27
Q

List some of the many uses of cholinergic drugs

A

Slowing a fast heart rate,
relieving spasms of respiratory system

relieving nasal discharge, treat nausea and vomiting, motion sickness and dizziness,

decrease a gastric secretions and increase esophageal sphincter muscle tone,
treating eye and urinary tract disorders, neurological disorders

28
Q

Uses of antineoplastic drugs

A

Fight new growth caused by cancer,

used against auto immune diseases such as rheumatoid arthritis

29
Q

Difference between
1-anticoagulants
2-antiplatelet drugs
3.thrombolytics

A

Anticoagulants Prevent blood from clotting, cause a prolonged bleeding time. Heparin and warfarin, apixiban(Eliquis), enoxaparin

Antiplatelet drugs prevent thromboembolic events. (Traveling clots that can cause CVA or MI.) ASA and clopidogrel(plavix)

Thrombolytics Promote lysis of fiber in strands causing dissolution of thrombi. Alteplase, streptokinase

30
Q

Antiretrovirals

A

Manage HIV infections.

Increase the CD4 cell count and decrease the viral load.

31
Q

Uses for Beta blockers

A

BP, chest pain, fast heart rate, vessel narrowing

Migraine, glaucoma, heart failure.

can prevent heart attacks and can manage symptoms of low thyroid function

32
Q

Uses for calcium channel blockera

A

BP, chest pain, coronary artery spasm.

Control the rhythm of the heart and to prevent neurological damage

33
Q

Tall man lettering

A

buPROPion vs busPIRone

Prevents errors with LASA (look alike sound alike)

34
Q

30g = how many ounces?

A

30g =1 oz

35
Q

1g = how many gr? (Grains)

A

1 g equals 15 gr

36
Q

Buccal route for administering meds

A

In the cheek
Absorbed though mucosa
Not swallowed when

37
Q

Parenteral route

A

administration means any non-oral means of administration, but is generally interpreted as relating to injecting directly into the body, bypassing the skin and mucous membranes. The common parenteral routes are intramuscular (IM), subcutaneous (SC) and intravenous (IV).